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A HapMap harvest of insights into the genetics of common disease

Teri A. Manolio, … , Lisa D. Brooks, Francis S. Collins

Teri A. Manolio, … , Lisa D. Brooks, Francis S. Collins

Published May 1, 2008
Citation Information: J Clin Invest. 2008;118(5):1590-1605. https://doi.org/10.1172/JCI34772.

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A Genome-wide Pleiotropy Scan for Prostate Cancer Risk OA Panagiotou, RC Travis, D Campa, SI Berndt, S Lindstrom, P Kraft, FR Schumacher, A Siddiq, SI Papatheodorou, JL Stanford, D Albanes, J Virtamo, SJ Weinstein, WR Diver, SM Gapstur, VL Stevens, H Boeing, HB Bueno-de-Mesquita, AB Gurrea, R Kaaks, KT Khaw, V Krogh, K Overvad, E Riboli, D Trichopoulos, E Giovannucci, M Stampfer, C Haiman, B Henderson, LL Marchand, JM Gaziano, DJ Hunter, S Koutros, M Yeager, RN Hoover, SJ Chanock, S Wacholder, TJ Key, KK Tsilidis	European Urology	2015
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How do SNP ascertainment schemes and population demographics affect inferences about population history? EJ McTavish, DM Hillis	BMC Genomics	2015
Genome-wide Association Study on Platinum-induced Hepatotoxicity in Non-Small Cell Lung Cancer Patients S Cao, C Wang, H Ma, R Yin, M Zhu, W Shen, J Dai, Y Shu, L Xu, Z Hu, H Shen	Scientific Reports	2015
Genome-wide association study reveals a locus for nasal carriage of Staphylococcus aureus in Danish crossbred pigs P Skallerup, C Espinosa-Gongora, CB Jørgensen, L Guardabassi, M Fredholm	BMC veterinary research	2015
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes A Teumer, A Tin, R Sorice, M Gorski, NC Yeo, AY Chu, M Li, Y Li, V Mijatovic, YA Ko, D Taliun, A Luciani, MH Chen, Q Yang, MC Foster, M Olden, LT Hiraki, BO Tayo, C Fuchsberger, AK Dieffenbach, AR Shuldiner, AV Smith, AM Zappa, A Lupo, B Kollerits, B Ponte, B Stengel, BK Krämer, B Paulweber, BD Mitchell, C Hayward, C Helmer, C Meisinger, C Gieger, CM Shaffer, C Müller, C Langenberg, D Ackermann, D Siscovick, E Boerwinkle, F Kronenberg, GB Ehret, G Homuth, G Waeber, G Navis, G Gambaro, G Malerba, G Eiriksdottir, G Li, HE Wichmann, H Grallert, H Wallaschofski, H Völzke, H Brenner, H Kramer, IM Leach, I Rudan, HL Hillege, JS Beckmann, JC Lambert, J Luan, JH Zhao, J Chalmers, J Coresh, JC Denny, K Butterbach, LJ Launer, L Ferrucci, L Kedenko, M Haun, M Metzger, M Woodward, MJ Hoffman, M Nauck, M Waldenberger, M Pruijm, M Bochud, M Rheinberger, N Verweij, NJ Wareham, N Endlich, N Soranzo, O Polasek, P der Harst, PP Pramstaller, P Vollenweider, PS Wild, RT Gansevoort, R Rettig, R Biffar, RJ Carroll, R Katz, RJ Loos, SJ Hwang, S Coassin, S Bergmann, SE Rosas, S Stracke, TB Harris, T Corre, T Zeller, T Illig, T Aspelund, T Tanaka, U Lendeckel, U Völker, V Gudnason, V Chouraki, W Koenig, Z Kutalik, JR O'Connell, A Parsa, IM Heid, AD Paterson, IH de Boer, O Devuyst, J Lazar, K Endlich, K Susztak, J Tremblay, P Hamet, HJ Jacob, CA Böger, CS Fox, C Pattaro, A Köttgen	Diabetes	2015
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Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples Q Yan, DE Weeks, HK Tiwari, N Yi, K Zhang, G Gao, WY Lin, XY Lou, W Chen, N Liu	Human Heredity	2015
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Associating Multivariate Quantitative Phenotypes with Genetic Variants in Family Samples with a Novel Kernel Machine Regression Method Q Yan, DE Weeks, JC Celedon, HK Tiwari, B Li, X Wang, WY Lin, XY Lou, G Gao, W Chen, N Liu	Genetics	2015
A Sequence Kernel Association Test for Dichotomous Traits in Family Samples under a Generalized Linear Mixed Model Q Yan, HK Tiwari, N Yi, G Gao, K Zhang, WY Lin, XY Lou, X Cui, N Liu	Human Heredity	2015
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Genome-wide association study of myelosuppression in non-small-cell lung cancer patients with platinum-based chemotherapy. Cao S, Wang S, Ma H, Tang S, Sun C, Dai J, Wang C, Shu Y, Xu L, Yin R, Song X, Chen H, Han B, Li Q, Wu J, Bai C, Chen J, Jin G, Hu Z, Lu D, Shen H	The Pharmacogenomics Journal	2015
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Genetic factors regulating lung vasculature and immune cell functions associate with resistance to pneumococcal infection MS Jonczyk, M Simon, S Kumar, VE Fernandes, N Sylvius, AM Mallon, P Denny, PW Andrew	PloS one	2014
Common and Rare Genetic Risk Factors for Glaucoma R Wang, JL Wiggs	Cold Spring Harbor Perspectives in Medicine	2014
Kernel-Machine Testing Coupled with a Rank-Truncation Method for Genetic Pathway Analysis Q Yan, HK Tiwari, N Yi, WY Lin, G Gao, XY Lou, X Cui, N Liu	Genetic Epidemiology	2014
Testing Gene-Gene Interactions in Genome Wide Association Studies JK Hu, X Wang, P Wang	Genetic Epidemiology	2014
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Association between vascular endothelial growth factor gene polymorphisms and bladder cancer risk Y Yang, X Zhang, D Song, J Wei	Molecular and Clinical Oncology	2014
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Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia D Juraeva, B Haenisch, M Zapatka, J Frank, , , SH Witt, TW Mühleisen, J Treutlein, J Strohmaier, S Meier, F Degenhardt, I Giegling, S Ripke, M Leber, C Lange, TG Schulze, R Mössner, I Nenadic, H Sauer, D Rujescu, W Maier, A Børglum, R Ophoff, S Cichon, MM Nöthen, M Rietschel, M Mattheisen, B Brors	PLoS genetics	2014
Association between FOXO3A gene polymorphisms and human longevity: a meta-analysis JM Bao, XL Song, YQ Hong, HL Zhu, C Li, T Zhang, W Chen, SC Zhao, Q Chen	Asian Journal of Andrology	2014
Exquisite Sequence Selectivity with Small Conditional RNAs JB Sternberg, NA Pierce	Nano letters	2014
Hypothesis-independent pathway analysis implicates GABA and Acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma JN Bailey, BL Yaspan, LR Pasquale, MA Hauser, JH Kang, SJ Loomis, M Brilliant, DL Budenz, WG Christen, J Fingert, D Gaasterland, T Gaasterland, P Kraft, RK Lee, PR Lichter, Y Liu, CA McCarty, SE Moroi, JE Richards, T Realini, JS Schuman, WK Scott, K Singh, AJ Sit, D Vollrath, G Wollstein, DJ Zack, K Zhang, MA Pericak-Vance, RR Allingham, RN Weinreb, JL Haines, JL Wiggs	Human Genetics	2014
A Custom Correlation Coefficient (CCC) Approach for Fast Identification of Multi-SNP Association Patterns in Genome-Wide SNPs Data: Fast Identification of Multi-SNP Patterns in GWAS S Climer, W Yang, L las Fuentes, VG Dávila-Román, CC Gu	Genetic Epidemiology	2014
A statistical framework to guide sequencing choices in pedigrees CY Cheung, EM Blue, EM Wijsman	The American Journal of Human Genetics	2014
LincRNA-uc002yug.2 involves in alternative splicing of RUNX1 and serves as a predictor for esophageal cancer and prognosis H Wu, J Zheng, J Deng, L Zhang, N Li, W Li, F Li, J Lu, Y Zhou	Oncogene	2014
The road from next-generation sequencing to personalized medicine ML Gonzalez-Garay	Personalized Medicine	2014
A Novel Method for Detecting Association Between DNA Methylation and Diseases Using Spatial Information WK Yip, H Fier, DL DeMeo, M Aryee, N Laird, C Lange	Genetic Epidemiology	2014
Identifying genetic relatives without compromising privacy D He, NA Furlotte, F Hormozdiari, JW Joo, A Wadia, R Ostrovsky, A Sahai, E Eskin	Genome research	2014
Identifying Causal Variants at Loci with Multiple Signals of Association F Hormozdiari, E Kostem, EY Kang, B Pasaniuc, E Eskin	Genetics	2014
Variants in Complement Factor H and Complement Factor H-Related Protein Genes, CFHR3 and CFHR1, Affect Complement Activation in IgA Nephropathy L Zhu, YL Zhai, FM Wang, P Hou, JC Lv, DM Xu, SF Shi, LJ Liu, F Yu, MH Zhao, J Novak, AG Gharavi, H Zhang	Journal of the American Society of Nephrology : JASN	2014
TGF Receptor 1: An Immune Susceptibility Gene in HPV-Associated Cancer C Levovitz, D Chen, E Ivansson, U Gyllensten, JP Finnigan, S Alshawish, W Zhang, EE Schadt, MR Posner, EM Genden, P Boffetta, AG Sikora	Cancer research	2014
Guidelines for the tetra-primer ARMS-PCR technique development. Medrano RF, de Oliveira CA	Molecular Biotechnology	2014
Review article: genetic factors that modify the outcome of viral hepatitis. Stättermayer AF, Scherzer T, Beinhardt S, Rutter K, Hofer H, Ferenci P	Alimentary Pharmacology & Therapeutics	2014
InterPregGen: genetic studies of pre-eclampsia in three continents Morgan L, McGinnis R, Steinthorsdottir V, Svyatova G, Zakhidova N, Lee WK, Iversen AC, Magnus P, Walker J, Casas JP, Sultanov S, Laivuori H	Norsk epidemiologi = Norwegian journal of epidemiology	2014
Association of μ-opioid receptor gene (OPRM1) haplotypes with postoperative nausea and vomiting. Sugino S, Hayase T, Higuchi M, Saito K, Moriya H, Kumeta Y, Kurosawa N, Namiki A, Janicki PK	Experimental Brain Research	2014
Cell therapies and regenerative medicine. Blum HE	Hepatology International	2014
Meta-analysis of the association between polymorphisms of estrogen receptor α genes rs9340799 and rs2234693 and Alzheimer's disease: evidence from 23 articles. Pan Y, Li Y, Shen H	American journal of Alzheimer's disease and other dementias	2014
Guilt by rewiring: gene prioritization through network rewiring in Genome Wide Association Studies L Hou, M Chen, CK Zhang, J Cho, H Zhao	Human Molecular Genetics	2013
Genetic Interactions among Idd3 , Idd5.1 , Idd5.2 , and Idd5.3 Protective Loci in the Nonobese Diabetic Mouse Model of Type 1 Diabetes X Lin, EE Hamilton-Williams, DB Rainbow, KM Hunter, YD Dai, J Cheung, LB Peterson, LS Wicker, LA Sherman	Journal of immunology (Baltimore, Md. : 1950)	2013
The genetics of NAFLD QM Anstee, CP Day	Nature Reviews Gastroenterology & Hepatology	2013
Genetic Epidemiology of Type 2 Diabetes and Cardiovascular Diseases in Africa F Tekola-Ayele, AA Adeyemo, CN Rotimi	Progress in Cardiovascular Diseases	2013
GStream: improving SNP and CNV coverage on genome-wide association studies A Alonso, S Marsal, R Tortosa, O Canela-Xandri, A Julià	PloS one	2013
Implementing genomic medicine in the clinic: the future is here TA Manolio, RL Chisholm, B Ozenberger, DM Roden, MS Williams, R Wilson, D Bick, EP Bottinger, MH Brilliant, C Eng, KA Frazer, B Korf, DH Ledbetter, JR Lupski, C Marsh, D Mrazek, MF Murray, PH O’Donnell, DJ Rader, MV Relling, AR Shuldiner, D Valle, R Weinshilboum, ED Green, GS Ginsburg	Genetics in Medicine	2013
Evaluating Rare Variants in Complex Disorders Using Next-Generation Sequencing M Ezewudo, ME Zwick	Current Psychiatry Reports	2013
Anticipating the arrival of low-penetrance genetic testing to primary care medicine BA Tarini, N Exe, BJ Zikmund-Fisher	Journal of Community Genetics	2013
A new way to protect privacy in large-scale genome-wide association studies L Kamm, D Bogdanov, S Laur, J Vilo	Bioinformatics	2013
DNA replication timing and higher-order nuclear organization determine single-nucleotide substitution patterns in cancer genomes L Liu, S De, F Michor	Nature Communications	2013
Genome-wide association studies of maximum number of drinks Y Pan, X Luo, X Liu, LY Wu, Q Zhang, L Wang, W Wang, L Zuo, KS Wang	Journal of Psychiatric Research	2013
GIGI: An Approach to Effective Imputation of Dense Genotypes on Large Pedigrees CY Cheung, EA Thompson, EM Wijsman	The American Journal of Human Genetics	2013
On the simultaneous association analysis of large genomic regions: a massive multi-locus association test D Qiao, MH Cho, H Fier, PS Bakke, A Gulsvik, EK Silverman, C Lange	Bioinformatics	2013
eALPS: Estimating Abundance Levels in Pooled Sequencing Using Available Genotyping Data I Eskin, F Hormozdiari, L Conde, J Riby, CF Skibola, E Eskin, E Halperin	Journal of Computational Biology	2013
Human genome-guided identification of memory-modulating drugs A Papassotiropoulos, C Gerhards, A Heck, S Ackermann, A Aerni, N Schicktanz, B Auschra, P Demougin, E Mumme, T Elbert, V Ertl, L Gschwind, E Hanser, KD Huynh, F Jessen, IT Kolassa, A Milnik, P Paganetti, K Spalek, C Vogler, A Muhs, A Pfeifer, DJ de Quervain	Proceedings of the National Academy of Sciences	2013
Genome wide association studies in presence of misclassified binary responses S Smith, EH Hay, N Farhat, R Rekaya	BMC genetics	2013
Fast association tests for genes with FAST P Chanda, H Huang, DE Arking, JS Bader	PloS one	2013
The geometric increase in meta-analyses from China in the genomic era JP Ioannidis, CQ Chang, TK Lam, SD Schully, MJ Khoury	PloS one	2013
Common dysfunctional variants in ABCG2 are a major cause of early-onset gout H Matsuo, K Ichida, T Takada, A Nakayama, H Nakashima, T Nakamura, Y Kawamura, Y Takada, K Yamamoto, H Inoue, Y Oikawa, M Naito, A Hishida, K Wakai, C Okada, S Shimizu, M Sakiyama, T Chiba, H Ogata, K Niwa, M Hosoyamada, A Mori, N Hamajima, H Suzuki, Y Kanai, Y Sakurai, T Hosoya, T Shimizu, N Shinomiya	Scientific Reports	2013
The power of meta-analysis in genome-wide association studies OA Panagiotou, CJ Willer, JN Hirschhorn, JP Ioannidis	Annual Review of Genomics and Human Genetics	2013
Identification of antithrombin-modulating genes. Role of LARGE, a gene encoding a bifunctional glycosyltransferase, in the secretion of proteins? ME de la Morena-Barrio, A Buil, AI Antón, I Martínez-Martínez, A Miñano, R Gutiérrez-Gallego, J Navarro-Fernández, S Aguila, JC Souto, V Vicente, JM Soria, J Corral	PloS one	2013
Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians H Shen, J Li, J Zhang, C Xu, Y Jiang, Z Wu, F Zhao, L Liao, J Chen, Y Lin, Q Tian, CJ Papasian, HW Deng	PloS one	2013
Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis M Wang, X Jiang, W Wu, D Zhang	PloS one	2013
SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays H Weissensteiner, M Haun, S Schönherr, M Neuner, L Forer, G Specht, A Kloss-Brandstätter, F Kronenberg, S Coassin	PloS one	2013
[Important genodermatoses for the practitioner]. Itin P, Salgado DA		2013
Inflammatory priming predisposes to age−related retinal degeneration in mice Debarshi Mustafi, Tadao Maeda, Hideo Kohno, Joseph Nadeau, Krzysztof Palczewski	Journal of Clinical Investigation	2012
Complement factor H genotypes impact risk of age-related macular degeneration by interaction with oxidized phospholipids PX Shaw, L Zhang, M Zhang, H Du, L Zhao, C Lee, S Grob, SL Lim, G Hughes, J Lee, M Bedell, MH Nelson, F Lu, M Krupa, J Luo, H Ouyang, Z Tu, Z Su, J Zhu, X Wei, Z Feng, Y Duan, Z Yang, H Ferreyra, DU Bartsch, I Kozak, L Zhang, F Lin, H Sun, H Feng, K Zhang	Proceedings of the National Academy of Sciences	2012
A two-SNP IL-6 promoter haplotype is associated with increased lung cancer risk J Chen, RY Liu, L Yang, J Zhao, X Zhao, D Lu, N Yi, B Han, XF Chen, K Zhang, J He, Z Lei, Y Zhou, B Pasche, X Li, HT Zhang	Journal of Cancer Research and Clinical Oncology	2012
Fixing the broken system of genetic locus symbols: Parkinson disease and dystonia as examples C Marras, K Lohmann, A Lang, C Klein	Neurology	2012
Rare and common variants: twenty arguments G Gibson	Nature Reviews Genetics	2012
Inter-chromosomal level of genome organization and longevity-related phenotypes in humans AM Kulminski, I Culminskaya, AI Yashin	AGE	2012
New Genetic Insights from Autoimmune Thyroid Disease TF Davies, R Latif, X Yin	Journal of Thyroid Research	2012
Utility-preserving transaction data anonymization with low information loss G Loukides, A Gkoulalas-Divanis	Expert Systems with Applications	2012
Insights into the Genetic Architecture of Diabetic Nephropathy ND Palmer, BI Freedman	Current Diabetes Reports	2012
Early Determinants of Obesity: Genetic, Epigenetic, and In Utero Influences KE Rhee, S Phelan, J McCaffery	International journal of pediatrics	2012
Technical Reproducibility of Genotyping SNP Arrays Used in Genome-Wide Association Studies H Hong, L Xu, J Liu, WD Jones, Z Su, B Ning, R Perkins, W Ge, K Miclaus, L Zhang, K Park, B Green, T Han, H Fang, CG Lambert, SC Vega, SM Lin, N Jafari, W Czika, RD Wolfinger, F Goodsaid, W Tong, L Shi	PloS one	2012
A Central Role for Long Non-Coding RNA in Cancer SA Mitra, AP Mitra, TJ Triche	Frontiers in Genetics	2012
The mystery of missing heritability: Genetic interactions create phantom heritability O Zuk, E Hechter, SR Sunyaev, ES Lander	Proceedings of the National Academy of Sciences	2012
Data sharing in neuroimaging research JB Poline, JL Breeze, S Ghosh, K Gorgolewski, YO Halchenko, M Hanke, C Haselgrove, KG Helmer, DB Keator, DS Marcus, RA Poldrack, Y Schwartz, J Ashburner, DN Kennedy	Frontiers in Neuroinformatics	2012
The molecular basis of chemoradiosensitivity in rectal cancer:implications for personalized therapies M Grade, HA Wolff, J Gaedcke, BM Ghadimi	Langenbeck's Archives of Surgery	2012
Age of onset and effect size in genome-wide association studies AJ Agopian, LM Eastcott, LE Mitchell	Birth Defects Research Part A: Clinical and Molecular Teratology	2012
The role of large pedigrees in an era of high-throughput sequencing EM Wijsman	Human Genetics	2012
Epistasis and immunity: the role of genetic interactions in autoimmune diseases AM Rose, LC Bell	Immunology	2012
Rare genetic variants and treatment response: sample size and analysis issues JS Witte	Statistics in Medicine	2012
Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder EH Rueckert, D Barker, D Ruderfer, SE Bergen, C O'Dushlaine, CJ Luce, SD Sheridan, KM Theriault, K Chambert, J Moran, SM Purcell, JM Madison, SJ Haggarty, P Sklar	Molecular Psychiatry	2012
CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics D Malhotra, J Sebat	Cell	2012
Meta-analysis of genetic association studies under heterogeneity B Neupane, M Loeb, SS Anand, J Beyene	European Journal of Human Genetics	2012
Genotype imputation in a coalescent model with infinitely-many-sites mutation L Huang, EO Buzbas, NA Rosenberg	Theoretical Population Biology	2012
Genome-wide association studies in mice J Flint, E Eskin	Nature Reviews Genetics	2012
An Exponential Combination Procedure for Set-Based Association Tests in Sequencing Studies LS Chen, L Hsu, ER Gamazon, NJ Cox, DL Nicolae	The American Journal of Human Genetics	2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes A Albrechtsen, N Grarup, Y Li, T Sparsø, G Tian, H Cao, T Jiang, SY Kim, T Korneliussen, Q Li, C Nie, R Wu, L Skotte, AP Morris, C Ladenvall, S Cauchi, A Stančáková, G Andersen, A Astrup, K Banasik, AJ Bennett, L Bolund, G Charpentier, Y Chen, JM Dekker, AS Doney, M Dorkhan, T Forsen, TM Frayling, CJ Groves, Y Gui, G Hallmans, AT Hattersley, K He, GA Hitman, J Holmkvist, S Huang, H Jiang, X Jin, JM Justesen, K Kristiansen, J Kuusisto, M Lajer, O Lantieri, W Li, H Liang, Q Liao, X Liu, T Ma, X Ma, MP Manijak, M Marre, J Mokrosiński, AD Morris, B Mu, AA Nielsen, G Nijpels, P Nilsson, CN Palmer, NW Rayner, F Renström, R Ribel-Madsen, N Robertson, O Rolandsson, P Rossing, TW Schwartz, PE Slagboom, M Sterner, M Tang, L Tarnow, T Tuomi, E Riet, N Leeuwen, TV Varga, MA Vestmar, M Walker, B Wang, Y Wang, H Wu, F Xi, L Yengo, C Yu, X Zhang, J Zhang, Q Zhang, W Zhang, H Zheng, Y Zhou, D Altshuler, LM Hart, PW Franks, B Balkau, P Froguel, MI McCarthy, M Laakso, L Groop, C Christensen, I Brandslund, T Lauritzen, DR Witte, A Linneberg, T Jørgensen, T Hansen, J Wang, R Nielsen, O Pedersen	Diabetologia	2012
'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate H Fier, S Won, D Prokopenko, T AlChawa, KU Ludwig, R Fimmers, EK Silverman, M Pagano, E Mangold, C Lange	Bioinformatics	2012
iLOCi: a SNP interaction prioritization technique for detecting epistasis in genome-wide association studies J Piriyapongsa, C Ngamphiw, A Intarapanich, S Kulawonganunchai, A Assawamakin, C Bootchai, PJ Shaw, S Tongsima	BMC Genomics	2012
Sample size and statistical power calculation in genetic association studies EP Hong, JW Park	Genomics & Informatics	2012
Personalized medicine in cardiovascular diseases MS Lee, AJ Flammer, LO Lerman, A Lerman	Korean Circulation Journal	2012
Cyclin D3 coordinates the cell cycle during differentiation to regulate erythrocyte size and number VG Sankaran, LS Ludwig, E Sicinska, J Xu, DE Bauer, JC Eng, HC Patterson, RA Metcalf, Y Natkunam, SH Orkin, P Sicinski, ES Lander, HF Lodish	Genes & development	2012
Finding a place for genomics in health disparities research SM Fullerton, S Knerr, W Burke	Public health genomics	2012
Human longevity and common variations in the LMNA gene: a meta-analysis KN Conneely, BC Capell, MR Erdos, P Sebastiani, N Solovieff, AJ Swift, CT Baldwin, T Budagov, N Barzilai, G Atzmon, AA Puca, TT Perls, BJ Geesaman, M Boehnke, FS Collins	Aging Cell	2012
Community Engagement about Genetic Variation Research SF Terry, KD Christensen, S Metosky, G Rudofsky, KP Deignan, H Martinez, P Johnson-Moore, T Citrin	Population Health Management	2012
Human Genome-Wide Association and Mouse Knockout Approaches Identify Platelet Supervillin as an Inhibitor of Thrombus Formation Under Shear Stress LC Edelstein, EJ Luna, IB Gibson, M Bray, Y Jin, A Kondkar, S Nagalla, N Hadjout-Rabi, TC Smith, D Covarrubias, SN Jones, F Ahmad, M Stolla, X Kong, Z Fang, W Bergmeier, C Shaw, SM Leal, PF Bray	Circulation	2012
Hepatocellular carcinoma: Towards personalized medicine D Miki, H Ochi, CN Hayes, H Aikata, K Chayama	Cancer Science	2012
Assessment of systematic effects of methodological characteristics on candidate genetic associations. Aljasir B, Ioannidis JP, Yurkiewich A, Moher D, Higgins JP, Arora P, Little J	Human Genetics	2012
Systems genetics in "-omics" era: current and future development. Li H		2012
New routes for transgenesis of the mouse. Belizário JE, Akamini P, Wolf P, Strauss B, Xavier-Neto J	Journal of Applied Genetics	2012
World Congress on Insulin Resistance, Diabetes, and Cardiovascular Disease: Part 3 ZT Bloomgarden	Diabetes care	2011
The Genomic Architecture of Sporadic Heart Failure GW Dorn, AJ Marian, H Watkins, C Seidman	Circulation research	2011
The genetics of asthma and allergic disease: a 21st century perspective C Ober, TC Yao	Immunological Reviews	2011
Quantitative Models for Causal Analysis in the Era of Genome Wide Association Studies SS Coughlin	The open health services and policy journal	2011
Contributions of dopamine-related genes and environmental factors to highly sensitive personality: a multi-step neuronal system-level approach C Chen, C Chen, R Moyzis, H Stern, Q He, H Li, J Li, B Zhu, Q Dong	PloS one	2011
The PhenX Toolkit: Get the Most From Your Measures CM Hamilton, LC Strader, JG Pratt, D Maiese, T Hendershot, RK Kwok, JA Hammond, W Huggins, D Jackman, H Pan, DS Nettles, TH Beaty, LA Farrer, P Kraft, ML Marazita, JM Ordovas, CN Pato, MR Spitz, D Wagener, M Williams, HA Junkins, WR Harlan, EM Ramos, J Haines	American Journal of Epidemiology	2011
Incorporating genetics into your studies: a guide for social scientists DM Dick, SJ Latendresse, B Riley	Frontiers in psychiatry / Frontiers Research Foundation	2011
Quantifying the underestimation of relative risks from genome-wide association studies C Spencer, E Hechter, D Vukcevic, P Donnelly	PLoS genetics	2011
A powerful hybrid approach to select top single-nucleotide polymorphisms for genome-wide association study J Wang, S Shete	BMC genetics	2011
Impact of Phenotype Definition on Genome-Wide Association Signals: Empirical Evaluation in Human Immunodeficiency Virus Type 1 Infection E Evangelou, J Fellay, S Colombo, J Martinez-Picado, N Obel, DB Goldstein, A Telenti, JP Ioannidis	American Journal of Epidemiology	2011
Annotating individual human genomes A Torkamani, AA Zeeland, EJ Topol, NJ Schork	Genomics	2011
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma MA Ferreira, MC Matheson, DL Duffy, GB Marks, J Hui, PL Souëf, P Danoy, S Baltic, DR Nyholt, M Jenkins, C Hayden, G Willemsen, W Ang, M Kuokkanen, J Beilby, F Cheah, EJ de Geus, A Ramasamy, S Vedantam, V Salomaa, PA Madden, AC Heath, JL Hopper, PM Visscher, B Musk, SR Leeder, MR Jarvelin, C Pennell, DI Boomsma, JN Hirschhorn, H Walters, NG Martin, A James, G Jones, MJ Abramson, CF Robertson, SC Dharmage, MA Brown, GW Montgomery, PJ Thompson	The Lancet	2011
Realizing the promise of population biobanks: a new model for translation MJ Murtagh, I Demir, JR Harris, PR Burton	Human Genetics	2011
Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe E Génin, M Schumacher, JC Roujeau, L Naldi, Y Liss, R Kazma, P Sekula, A Hovnanian, M Mockenhaupt	Orphanet Journal of Rare Diseases	2011
Enriching targeted sequencing experiments for rare disease alleles TL Edwards, Z Song, C Li	Bioinformatics	2011
Variable set enrichment analysis in genome-wide association studies W Yang, L las Fuentes, VG Dávila-Román, CC Gu	European Journal of Human Genetics	2011
Direct-to-consumer personalized genomic testing CS Bloss, BF Darst, EJ Topol, NJ Schork	Human Molecular Genetics	2011
Overview of the Development of Personalized Genomic Medicine and Surgery FC Brunicardi, RA Gibbs, DA Wheeler, J Nemunaitis, W Fisher, J Goss, C Chen	World Journal of Surgery	2011
Understanding the contribution of synonymous mutations to human disease ZE Sauna, C Kimchi-Sarfaty	Nature Reviews Genetics	2011
Vaccinomics: Current Findings, Challenges and Novel Approaches for Vaccine Development IG Ovsyannikova, GA Poland	The AAPS Journal	2011
Contemporary human genetic strategies in aging research CS Bloss, L Pawlikowska, NJ Schork	Ageing Research Reviews	2011
Personalized medicine in rheumatoid arthritis: Miles to go before we sleep RM Plenge, SL Bridges	Arthritis & Rheumatism	2011
Genetic analysis of biological pathway data through genomic randomization BL Yaspan, WS Bush, ES Torstenson, D Ma, MA Pericak-Vance, MD Ritchie, JS Sutcliffe, JL Haines	Human Genetics	2011
An efficient hierarchical generalized linear mixed model for pathway analysis of genome-wide association studies L Wang, P Jia, RD Wolfinger, X Chen, BL Grayson, TM Aune, Z Zhao	Bioinformatics	2011
Commentary: Children and Predictive Genomic Testing: Disease Prevention, Research Protection, and Our Future BA Tarini, KP Tercyak, BS Wilfond	Journal of pediatric psychology	2011
The emerging role for rat models in gene discovery MR Dwinell, J Lazar, AM Geurts	Mammalian Genome	2011
Gene- or region-based association study via kernel principal component analysis Q Gao, Y He, Z Yuan, J Zhao, B Zhang, F Xue	BMC genetics	2011
Thrombotic gene polymorphisms and postoperative outcome after coronary artery bypass graft surgery O Emiroglu, S Durdu, Y Egin, AR Akar, YD Alakoc, C Zaim, U Ozyurda, N Akar	Journal of Cardiothoracic Surgery	2011
Pharmacogenomic characterization of US FDA-approved cytotoxic drugs EJ Peters, A Motsinger-Reif, TM Havener, L Everitt, NE Hardison, VG Watson, M Wagner, KL Richards, MA Province, HL McLeod	Pharmacogenomics	2011
Next-generation DNA sequencing-based assay for measuring allelic expression imbalance (AEI) of candidate neuropsychiatric disorder genes in human brain X Xu, H Wang, M Zhu, Y Sun, Y Tao, Q He, J Wang, L Chen, D Saffen	BMC Genomics	2011
Genomics of human health and aging AM Kulminski, I Culminskaya	AGE	2011
Pharmacogenomics: The genetics of variable drug responses DM Roden, RA Wilke, HK Kroemer, CM Stein	Circulation	2011
A Systems Genetics Approach Provides a Bridge from Discovered Genetic Variants to Biological Pathways in Rheumatoid Arthritis H Nakaoka, T Cui, A Tajima, A Oka, S Mitsunaga, K Kashiwase, Y Homma, S Sato, Y Suzuki, H Inoko, I Inoue	PloS one	2011
A Comparison of Association Methods for Cytotoxicity Mapping in Pharmacogenomics C Brown, TM Havener, L Everitt, H McLeod, AA Motsinger-Reif	Frontiers in Genetics	2011
Statistical Optimization of Pharmacogenomics Association Studies: Key Considerations from Study Design to Analysis BJ Grady, MD Ritchie	Current pharmacogenomics and personalized medicine	2011
Next generation genome-wide association tool: Design and coverage of a high-throughput European-optimized SNP array TJ Hoffmann, MN Kvale, SE Hesselson, Y Zhan, C Aquino, Y Cao, S Cawley, E Chung, S Connell, J Eshragh, M Ewing, J Gollub, M Henderson, E Hubbell, C Iribarren, J Kaufman, RZ Lao, Y Lu, D Ludwig, GK Mathauda, W McGuire, G Mei, S Miles, MM Purdy, C Quesenberry, D Ranatunga, S Rowell, M Sadler, MH Shapero, L Shen, TR Shenoy, D Smethurst, SK van Eeden, L Walter, E Wan, R Wearley, T Webster, CC Wen, L Weng, RA Whitmer, A Williams, SC Wong, C Zau, A Finn, C Schaefer, PY Kwok, N Risch	Genomics	2011
An examination of SNP selection prioritisation strategies for tests of gene-gene interaction V Moskvina, N Craddock, B Müller-Myhsok, T Kam-Thong, E Green, P Holmans, MJ Owen, MC O'Donovan	Biological Psychiatry	2011
GATES: A Rapid and Powerful Gene-Based Association Test Using Extended Simes Procedure MX Li, HS Gui, JS Kwan, PC Sham	The American Journal of Human Genetics	2011
Risk Prediction of Complex Diseases from Family History and Known Susceptibility Loci, with Applications for Cancer Screening HC So, JS Kwan, SS Cherny, PC Sham	The American Journal of Human Genetics	2011
Inference of Relationships in Population Data Using Identity-by-Descent and Identity-by-State EL Stevens, G Heckenberg, ED Roberson, JD Baugher, TJ Downey, J Pevsner	PLoS genetics	2011
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE Consortium M Fornage, S Debette, JC Bis, H Schmidt, MA Ikram, C Dufouil, S Sigurdsson, T Lumley, AL DeStefano, F Fazekas, HA Vrooman, DK Shibata, P Maillard, A Zijdenbos, AV Smith, H Gudnason, R Boer, M Cushman, B Mazoyer, G Heiss, MW Vernooij, C Enzinger, NL Glazer, A Beiser, DS Knopman, M Cavalieri, WJ Niessen, TB Harris, K Petrovic, OL Lopez, R Au, JC Lambert, A Hofman, RF Gottesman, M Garcia, SR Heckbert, LD Atwood, DJ Catellier, AG Uitterlinden, Q Yang, NL Smith, T Aspelund, JR Romero, K Rice, KD Taylor, MA Nalls, JI Rotter, R Sharrett, CM van Duijn, P Amouyel, PA Wolf, V Gudnason, A der Lugt, E Boerwinkle, BM Psaty, S Seshadri, C Tzourio, MM Breteler, TH Mosley, R Schmidt, WT Longstreth, C DeCarli, LJ Launer	Annals of Neurology	2011
Personalised medicine in Canada: a survey of adoption and practice in oncology, cardiology and family medicine K Bonter, C Desjardins, N Currier, J Pun, FD Ashbury	BMJ Open	2011
What did we learn from the genome-wide association study for tuberculosis susceptibility? HQ Qu, Q Li, JB McCormick, SP Fisher-Hoch	Journal of medical genetics	2011
Replication and cumulative effects of GWAS-identified genetic variations for prostate cancer in Asians: a case–control study in the ChinaPCa consortium M Wang, F Liu, AW Hsing, X Wang, Q Shao, J Qi, Y Ye, Z Wang, H Chen, X Gao, G Wang, LW Chu, Q Ding, J OuYang, X Gao, Y Huang, Y Chen, YT Gao, ZF Zhang, J Rao, R Shi, Q Wu, Y Zhang, H Jiang, J Zheng, Y Hu, L Guo, X Lin, S Tao, G Jin, J Sun, D Lu, SL Zheng, Y Sun, Z Mo, C Yin, Z Zhang, J Xu	Carcinogenesis	2011
Gene-environment interaction in psychological traits and disorders DM Dick	Annual Review of Clinical Psychology	2011
Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways J Deelen, HW Uh, R Monajemi, D Heemst, PE Thijssen, S Böhringer, EB van Akker, AJ de Craen, F Rivadeneira, AG Uitterlinden, RG Westendorp, JJ Goeman, PE Slagboom, JJ Houwing-Duistermaat, M Beekman	AGE	2011
Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm TJ Hoffmann, Y Zhan, MN Kvale, SE Hesselson, J Gollub, C Iribarren, Y Lu, G Mei, MM Purdy, C Quesenberry, S Rowell, MH Shapero, D Smethurst, CP Somkin, SK van Eeden, L Walter, T Webster, RA Whitmer, A Finn, C Schaefer, PY Kwok, N Risch	Genomics	2011
The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies CA McCarty, RL Chisholm, CG Chute, IJ Kullo, GP Jarvik, EB Larson, R Li, DR Masys, MD Ritchie, DM Roden, JP Struewing, WA Wolf	BMC Medical Genomics	2011
Behavioral Neurogenetics JF Cryan, A Reif	Behavioral Neurogenetics	2011
Recent Advances in Understanding the Role of Nutrition in Human Genome Evolution K Ye, Z Gu	Advances in nutrition (Bethesda, Md.)	2011
Siblings With Ischemic Stroke Study: Results of a Genome-Wide Scan for Stroke Loci JF Meschia, M Nalls, M Matarin, TG Brott, RD Brown, J Hardy, B Kissela, SS Rich, A Singleton, D Hernandez, L Ferrucci, K Pearce, M Keller, BB Worrall	Stroke; a journal of cerebral circulation	2011
Post-Genomic Update on a Classical Candidate Gene for Coronary Artery Disease: ESR1 G Lucas, C Lluís-Ganella, I Subirana, M Sentí, C Willenborg, MD Musameh, SM Schwartz, CJ O'Donnell, O Melander, V Salomaa, R Elosua	Circulation. Cardiovascular genetics	2011
Identification of Cd101 as a Susceptibility Gene for Novosphingobium aromaticivorans -Induced Liver Autoimmunity JP Mohammed, ME Fusakio, DB Rainbow, C Moule, HI Fraser, J Clark, JA Todd, LB Peterson, PB Savage, M Wills-Karp, WM Ridgway, LS Wicker, J Mattner	Journal of immunology (Baltimore, Md. : 1950)	2011
Long Intergenic Noncoding RNAs: New Links in Cancer Progression: Figure 1 MC Tsai, RC Spitale, HY Chang	Cancer research	2011
Giving and withholding of information following genomic screening: challenges identified in a study of primary care physicians in Estonia. Leitsalu L, Hercher L, Metspalu A	Journal of Genetic Counseling	2011
Construction of Japanese BAC library Yamato-2 (JY2): a set of 330K clone resources of damage-minimized DNA taken from a genetically established Japanese individual. Terabayashi Y, Morita K, Park JY, Saito S, Shiina T, Inoko H, Ishiwata I, Fujimori KE, Hirano T	Human Cell	2011
An application and empirical comparison of statistical analysis methods for associating rare variants to a complex phenotype. Bansal V, Libiger O, Torkamani A, Schork NJ	Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing	2011
An Interdisciplinary Approach to Studying Gene–Environment Interactions: From Twin Studies to Gene Identification and Back Dick DM	Research in Human Development	2011
Genome-wide association studies and genetic risk assessment of liver diseases M Krawczyk, R Müllenbach, SN Weber, V Zimmer, F Lammert	Nature Reviews Gastroenterology & Hepatology	2010
Molecular diagnostics in transplantation M Naesens, MM Sarwal	Nature Reviews Nephrology	2010
Quantitative analyses link modulation of sonic hedgehog signaling to continuous variation in facial growth and shape NM Young, HJ Chong, D Hu, B Hallgrímsson, RS Marcucio	Development (Cambridge, England)	2010
Investigation of Variants Identified in Caucasian Genome-Wide Association Studies for Plasma High-Density Lipoprotein Cholesterol and Triglycerides Levels in Mexican Dyslipidemic Study Samples D Weissglas-Volkov, CA Aguilar-Salinas, JS Sinsheimer, L Riba, A Huertas-Vazquez, ML Ordoñez-Sánchez, R Rodriguez-Guillen, R M., T Tusie-Luna, P Pajukanta	Circulation. Cardiovascular genetics	2010
The molecular pathology of cancer TJ Harris, F McCormick	Nature Reviews Clinical Oncology	2010
Human genetics of diabetic retinopathy: current perspectives DP Ng	Journal of Ophthalmology	2010
A knowledge-based weighting framework to boost the power of genome-wide association studies MX Li, PC Sham, SS Cherny, YQ Song	PloS one	2010
Estimating the total number of susceptibility variants underlying complex diseases from genome-wide association studies HC So, BH Yip, PC Sham	PloS one	2010
Breast cancer in the personal genomics era RE Ellsworth, DJ Decewicz, CD Shriver, DL Ellsworth	Current genomics	2010
Being more realistic about the public health impact of genomic medicine WD Hall, R Mathews, KI Morley	PLoS Medicine	2010
Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13q MH Fenstad, MP Johnson, LT Roten, PA Aas, S Forsmo, K Klepper, CE East, LJ Abraham, J Blangero, SP Brennecke, R Austgulen, EK Moses	PloS one	2010
Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies I Fortier, PR Burton, PJ Robson, V Ferretti, J Little, F L'Heureux, M Deschênes, BM Knoppers, D Doiron, JC Keers, P Linksted, JR Harris, G Lachance, C Boileau, NL Pedersen, CM Hamilton, K Hveem, MJ Borugian, RP Gallagher, J McLaughlin, L Parker, JD Potter, J Gallacher, R Kaaks, B Liu, T Sprosen, A Vilain, SA Atkinson, A Rengifo, R Morton, A Metspalu, HE Wichmann, M Tremblay, RL Chisholm, A Garcia-Montero, H Hillege, JE Litton, LJ Palmer, M Perola, BH Wolffenbuttel, L Peltonen, TJ Hudson	International Journal of Epidemiology	2010
Do alterations in mitochondrial DNA play a role in breast carcinogenesis? TE Rohan, LJ Wong, T Wang, J Haines, GC Kabat	Journal of Oncology	2010
Analyze multivariate phenotypes in genetic association studies by combining univariate association tests Q Yang, H Wu, CY Guo, CS Fox	Genetic Epidemiology	2010
Insights into colon cancer etiology via a regularized approach to gene set analysis of GWAS data LS Chen, CM Hutter, JD Potter, Y Liu, RL Prentice, U Peters, L Hsu	The American Journal of Human Genetics	2010
An Environment-Wide Association Study (EWAS) on type 2 diabetes mellitus CJ Patel, J Bhattacharya, AJ Butte	PloS one	2010
Evaluating the transferability of Hapmap SNPs to a Singapore Chinese population AK Andiappan, R Anantharaman, PP Nilkanth, DY Wang, FT Chew	BMC genetics	2010
Interpretation of association signals and identification of causal variants from genome-wide association studies K Wang, SP Dickson, CA Stolle, ID Krantz, DB Goldstein, H Hakonarson	The American Journal of Human Genetics	2010
Curve-based multivariate distance matrix regression analysis: application to genetic association analyses involving repeated measures RM Salem, DT O'Connor, NJ Schork	Physiological genomics	2010
FAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals T Cattaert, V Urrea, AC Naj, LD Lobel, VD Wit, M Fu, JM John, H Shen, ML Calle, MD Ritchie, TL Edwards, KV Steen	PloS one	2010
Genome-wide association studies in diverse populations NA Rosenberg, L Huang, EM Jewett, ZA Szpiech, I Jankovic, M Boehnke	Nature reviews. Genetics	2010
Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression MS Cunnington, MS Koref, BM Mayosi, J Burn, B Keavney	PLoS genetics	2010
Anonymization of electronic medical records for validating genome-wide association studies G Loukides, A Gkoulalas-Divanis, B Malin	Proceedings of the National Academy of Sciences	2010
Polymorphisms in genes of interleukin 12 and its receptors and their association with protection against severe malarial anaemia in children in western Kenya L Zhang, D Prather, JV Eng, S Crawford, S Kariuki, F Kuile, D Terlouw, B Nahlen, AA Lal, L Slutsker, V Udhayakumar, YP Shi	Malaria Journal	2010
Genetics of focal segmental glomerulosclerosis and human immunodeficiency virus-associated collapsing glomerulopathy: the role of MYH9 genetic variation CA Winkler, G Nelson, TK Oleksyk, MB Nava, JB Kopp	Seminars in Nephrology	2010
Genotype-based risk and pharmacogenetic sampling in clinical trials NJ Schork, EJ Topol	Journal of Biopharmaceutical Statistics	2010
Performance of common genetic variants in breast-cancer risk models S Wacholder, P Hartge, R Prentice, M Garcia-Closas, HS Feigelson, WR Diver, MJ Thun, DG Cox, SE Hankinson, P Kraft, B Rosner, CD Berg, LA Brinton, J Lissowska, ME Sherman, R Chlebowski, C Kooperberg, RD Jackson, DW Buckman, P Hui, R Pfeiffer, KB Jacobs, GD Thomas, RN Hoover, MH Gail, SJ Chanock, DJ Hunter	The New England journal of medicine	2010
Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies KC Siontis, NA Patsopoulos, JP Ioannidis	European journal of human genetics : EJHG	2010
Family-based genetic risk prediction of multifactorial disease DM Ruderfer, J Korn, SM Purcell	Genome Medicine	2010
What role for genetics in the prediction of multiple sclerosis? S Sawcer, M Ban, J Wason, F Dudbridge	Annals of Neurology	2010
Genetics of psychiatric disorders methods: molecular approaches D Avramopoulos	The Psychiatric clinics of North America	2010
Genetic and functional dissection of HTRA1 and LOC387715 in age-related macular degeneration Z Yang, Z Tong, Y Chen, J Zeng, F Lu, X Sun, C Zhao, K Wang, L Davey, H Chen, N London, D Muramatsu, F Salasar, R Carmona, D Kasuga, X Wang, M Bedell, M Dixie, P Zhao, R Yang, D Gibbs, X Liu, Y Li, C Li, Y Li, B Campochiaro, R Constantine, DJ Zack, P Campochiaro, Y Fu, DY Li, N Katsanis, K Zhang	PLoS genetics	2010
Efficient evaluation of ranking procedures when the number of units is large, with application to SNP identification TA Louis, I Ruczinski	Biometrical journal. Biometrische Zeitschrift	2010
Bioinformatics challenges for genome-wide association studies JH Moore, FW Asselbergs, SM Williams	Bioinformatics (Oxford, England)	2010
The genetics of ischaemic stroke M Matarin, A Singleton, J Hardy, J Meschia	Journal of Internal Medicine	2010
Methodological challenges of genome-wide association analysis in Africa YY Teo, KS Small, DP Kwiatkowski	Nature Reviews Genetics	2010
Obstructive Sleep Apnoea: From pathogenesis to treatment: Current controversies and future directions PR EASTWOOD, A MALHOTRA, LJ PALMER, EJ KEZIRIAN, RL HORNER, MS IP, R THURNHEER, NA ANTIC, DR HILLMAN	Respirology	2010
Genome-wide association study of recurrent early-onset major depressive disorder J Shi, JB Potash, JA Knowles, MM Weissman, W Coryell, WA Scheftner, WB Lawson, JR DePaulo, PV Gejman, AR Sanders, JK Johnson, P Adams, S Chaudhury, D Jancic, O Evgrafov, A Zvinyatskovskiy, N Ertman, M Gladis, K Neimanas, M Goodell, N Hale, N Ney, R Verma, D Mirel, P Holmans, DF Levinson	Molecular Psychiatry	2010
MicroRNAs: Potential biomarkers in cancer GP George, RD Mittal	Indian Journal of Clinical Biochemistry	2010
Analyzing complex traits with congenic strains H Shao, DS Sinasac, LC Burrage, CA Hodges, PJ Supelak, MR Palmert, C Moreno, AW Cowley, HJ Jacob, JH Nadeau	Mammalian Genome	2010
Conference Scene: The great debate: genome-wide association studies in pharmacogenetics research, good or bad? KR Bailey, C Cheng	Pharmacogenomics	2010
Statistical analysis strategies for association studies involving rare variants V Bansal, O Libiger, A Torkamani, NJ Schork	Nature Reviews Genetics	2010
Pioneering First Steps and Cautious Conclusions FJ McMahon	Biological Psychiatry	2010
Exploring genetic susceptibility to cancer in diverse populations CA Haiman, DO Stram	Current Opinion in Genetics & Development	2010
Individualized medicine 2010 HE Blum	Journal of Cellular and Molecular Medicine	2010
Knowledge gaining by human genetic studies on tuberculosis susceptibility HQ Qu, SP Fisher-Hoch, JB McCormick	Journal of Human Genetics	2010
Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies A Crossett, BP Kent, L Klei, S Ringquist, M Trucco, K Roeder, B Devlin	Statistics in Medicine	2010
Future Health Applications of Genomics CM McBride, D Bowen, LC Brody, CM Condit, RT Croyle, M Gwinn, MJ Khoury, LM Koehly, BR Korf, TM Marteau, K McLeroy, K Patrick, TW Valente	American Journal of Preventive Medicine	2010
Common Variants Near Melanocortin 4 Receptor Are Associated with General and Visceral Adiposity in European- and African-American Youth G Liu, H Zhu, V Lagou, B Gutin, P Barbeau, FA Treiber, Y Dong, H Snieder	The Journal of Pediatrics	2010
Advances in the genetics of endometriosis EC Dun, RN Taylor, F Wieser	Genome Medicine	2010
Human Behavioral Informatics in Genetic Studies of Neuropsychiatric Disease: Multivariate Profile-Based Analysis CS Bloss, KM Schiabor, NJ Schork	Brain Research Bulletin	2010
DataSHIELD: resolving a conflict in contemporary bioscience—performing a pooled analysis of individual-level data without sharing the data M Wolfson, SE Wallace, N Masca, G Rowe, NA Sheehan, V Ferretti, P LaFlamme, MD Tobin, J Macleod, J Little, I Fortier, BM Knoppers, PR Burton	International Journal of Epidemiology	2010
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort L Athanasiu, M Mattingsdal, AK Kähler, A Brown, O Gustafsson, I Agartz, I Giegling, P Muglia, S Cichon, M Rietschel, OP Pietiläinen, L Peltonen, E Bramon, D Collier, DS Clair, E Sigurdsson, H Petursson, D Rujescu, I Melle, VM Steen, S Djurovic, OA Andreassen	Journal of Psychiatric Research	2010
From GWAS to the clinic: risk factors for intracranial aneurysms YM Ruigrok, GJ Rinkel	Genome Medicine	2010
Leveraging informatics for genetic studies: use of the electronic medical record to enable a genome-wide association study of peripheral arterial disease IJ Kullo, J Fan, J Pathak, GK Savova, Z Ali, CG Chute	Journal of the American Medical Informatics Association : JAMIA	2010
Genomics for Disease Treatment and Prevention CS Bloss, DV Jeste, NJ Schork	The Psychiatric clinics of North America	2010
A detailed view on Model-Based Multifactor Dimensionality Reduction for detecting gene-gene interactions in case-control data in the absence and presence of noise T Cattaert, ML Calle, SM Dudek, JM John, FV Lishout, V Urrea, MD Ritchie, KV Steen	Annals of Human Genetics	2010
Direct-to-Consumer Genetic and Genomic Testing: Preparing Nurse Practitioners for Genomic Healthcare JT Loud	The journal for nurse practitioners : JNP	2010
SNPTransformer: A Lightweight Toolkit for Genome-Wide Association Studies C Dong	Genomics Proteomics & Bioinformatics	2010
Power analysis for case-control association studies of samples with known family histories B Peng, B Li, Y Han, CI Amos	Humangenetik	2010
Two-stage case-control designs for rare genetic variants DJ Schaid, JP Sinnwell	Humangenetik	2010
Asthma-susceptibility variants identified using probands in case-control and family-based analyses BE Himes, J Lasky-Su, AC Wu, JB Wilk, GM Hunninghake, B Klanderman, AJ Murphy, R Lazarus, ME Soto-Quiros, L Avila, JC Celedón, C Lange, GT O'Connor, BA Raby, EK Silverman, ST Weiss	BMC Medical Genetics	2010
Laboratory Mouse Models for the Human Genome-Wide Associations GD Kitsios, N Tangri, PJ Castaldi, JP Ioannidis, AE Toland	PloS one	2010
Genetic Variation of DKK3 May Modify Renal Disease Severity in ADPKD M Liu, S Shi, S Senthilnathan, J Yu, E Wu, C Bergmann, K Zerres, N Bogdanova, E Coto, C Deltas, A Pierides, K Demetriou, O Devuyst, B Gitomer, M Laakso, A Lumiaho, K Lamnissou, R Magistroni, P Parfrey, M Breuning, DJ Peters, R Torra, CG Winearls, VE Torres, PC Harris, AD Paterson, Y Pei	Journal of the American Society of Nephrology : JASN	2010
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. McMahon FJ, Akula N, Schulze TG, Muglia P, Tozzi F, Detera-Wadleigh SD, Steele CJ, Breuer R, Strohmaier J, Wendland JR, Mattheisen M, Mühleisen TW, Maier W, Nöthen MM, Cichon S, Farmer A, Vincent JB, Holsboer F, Preisig M, Rietschel M	Nature Genetics	2010
Explaining inter-individual variability in phenotype: is epigenetics up to the challenge? Turan N, Katari S, Coutifaris C, Sapienza C	Epigenetics : official journal of the DNA Methylation Society	2010
Child and adolescent psychiatric genetics. Hebebrand J, Scherag A, Schimmelmann BG, Hinney A	European Child & Adolescent Psychiatry	2010
A genome-wide association study of amygdala activation in youths with and without bipolar disorder. Liu X, Akula N, Skup M, Brotman MA, Leibenluft E, McMahon FJ	Journal of the American Academy of Child and Adolescent Psychiatry	2010
Uncovering the roles of rare variants in common disease through whole-genome sequencing. Cirulli ET, Goldstein DB	Nature reviews. Genetics	2010
Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies. Elliott KS, Zeggini E, McCarthy MI, Gudmundsson J, Sulem P, Stacey SN, Thorlacius S, Amundadottir L, Grönberg H, Xu J, Gaborieau V, Eeles RA, Neal DE, Donovan JL, Hamdy FC, Muir K, Hwang SJ, Spitz MR, Zanke B, Carvajal-Carmona L, Brown KM, Hayward NK, Macgregor S, Tomlinson IP, Lemire M, Amos CI, Murabito JM, Isaacs WB, Easton DF, Brennan P, Barkardottir RB, Gudbjartsson DF, Rafnar T, Hunter DJ, Chanock SJ, Stefansson K, Ioannidis JP	PloS one	2010
CLIA-tested Genetic Variants on Commercial SNP Arrays: Potential for Incidental Findings in Genome-Wide Association Studies Johnson AD, Bhimavarapu A, Benjamin EJ, Fox C, Levy D, Jarvik GP, O\u2019Donnell CJ	Genetics in Medicine	2010
Quality control and quality assurance in genotypic data for genome-wide association studies Laurie CC, Doheny KF, Mirel DB, Pugh EW, Bierut LJ, Bhangale T, Boehm F, Caporaso NE, Cornelis MC, Edenberg HJ, Gabriel SB, Harris EL, Hu FB, Jacobs K, Kraft P, Landi MT, Lumley T, Manolio TA, McHugh C, Painter I, Paschall J, Rice JP, Rice KM, Zheng X, Weir BS	Genetic Epidemiology	2010
Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies. Yoo YJ, Bull SB, Paterson AD, Waggott D, Sun L	Genetic Epidemiology	2010
Statistical significance in genetic association studies. Qu HQ, Tien M, Polychronakos C	Clinical and Investigative Medicine. Medecine Clinique et Experimentale	2010
Analysing biological pathways in genome-wide association studies. Wang K, Li M, Hakonarson H	Nature reviews. Genetics	2010
Can Lessons Learned from Genome-Wide Research be Applied to Nutrition-Wide and Exposure-Wide Evidence? Ioannidis JP	Critical Reviews in Food Science and Nutrition	2010
Pulmonary surfactant: an immunological perspective ZC Chroneos, Z Sever-Chroneos, VL Shepherd	Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology	2009
Cis-regulatory mutations in human disease DJ Epstein	Briefings in functional genomics & proteomics	2009
Modeling molecular and cellular aspects of human disease using the nematode Caenorhabditis elegans GA Silverman, CJ Luke, SR Bhatia, OS Long, AC Vetica, DH Perlmutter, SC Pak	Pediatric Research	2009
Genome-wide association studies--a summary for the clinical gastroenterologist E Melum, A Franke, TH Karlsen	World journal of gastroenterology : WJG	2009
Common genetic variants in sudden cardiac death AL George	Heart rhythm : the official journal of the Heart Rhythm Society	2009
Pathway analysis of GWAS provides new insights into genetic susceptibility to 3 inflammatory diseases H Eleftherohorinou, V Wright, C Hoggart, AL Hartikainen, MR Jarvelin, D Balding, L Coin, M Levin	PloS one	2009
Influence of microbial environment on autoimmunity AV Chervonsky	Nature Immunology	2009
Genetics and the general physician: insights, applications and future challenges JC Knight	QJM : monthly journal of the Association of Physicians	2009
MicroRNA polymorphisms: the future of pharmacogenomics, molecular epidemiology and individualized medicine PJ Mishra, JR Bertino	Pharmacogenomics	2009
MicroRNA polymorphisms: a giant leap towards personalized medicine PJ Mishra	Personalized Medicine	2009
Replication in genome-wide association studies P Kraft, E Zeggini, JP Ioannidis	Statistical science : a review journal of the Institute of Mathematical Statistics	2009
Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies SI Shyn, J Shi, JB Kraft, JB Potash, JA Knowles, MM Weissman, HA Garriock, JS Yokoyama, PJ McGrath, EJ Peters, WA Scheftner, W Coryell, WB Lawson, D Jancic, PV Gejman, AR Sanders, P Holmans, SL Slager, DF Levinson, SP Hamilton	Molecular Psychiatry	2009
Ethical data release in genome-wide association studies in developing countries M Parker, SJ Bull, J Vries, T Agbenyega, OK Doumbo, DP Kwiatkowski	PLoS Medicine	2009
The genetics of Tourette syndrome: a review JA O'Rourke, JM Scharf, D Yu, DL Pauls	Journal of Psychosomatic Research	2009
Genome-wide association studies in cancer--current and future directions CC Chung, WC Magalhaes, J Gonzalez-Bosquet, SJ Chanock	Carcinogenesis	2009
Repertoires of the nucleosome-positioning dinucleotides T Bettecken, EN Trifonov	PloS one	2009
Genome-scale approaches to the epigenetics of common human disease AP Feinberg	Virchows Archiv : an international journal of pathology	2009
Beyond proof of principle: new genes for Alzheimer's disease through collaboration MA Pericak-Vance, JL Haines	Lancet neurology	2009
Information management to enable personalized medicine: stakeholder roles in building clinical decision support GJ Downing, SN Boyle, KM Brinner, JA Osheroff	BMC medical informatics and decision making	2009
Control of fetal hemoglobin: new insights emerging from genomics and clinical implications SL Thein, S Menzel, M Lathrop, C Garner	Human Molecular Genetics	2009
Transgenerational genetic effects on phenotypic variation and disease risk JH Nadeau	Human Molecular Genetics	2009
A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies KB Jacobs, M Yeager, S Wacholder, D Craig, P Kraft, DJ Hunter, J Paschal, TA Manolio, M Tucker, RN Hoover, GD Thomas, SJ Chanock, N Chatterjee	Nature Genetics	2009
Genome-wide association studies: hypothesis-"free" or "engaged"? GD Kitsios, E Zintzaras	Translational research : the journal of laboratory and clinical medicine	2009
Hypothesis-driven candidate gene association studies: practical design and analytical considerations TJ Jorgensen, I Ruczinski, B Kessing, MW Smith, YY Shugart, AJ Alberg	American Journal of Epidemiology	2009
Predicting response to short-acting bronchodilator medication using Bayesian networks BE Himes, AC Wu, QL Duan, B Klanderman, AA Litonjua, K Tantisira, MF Ramoni, ST Weiss	Pharmacogenomics	2009
Genome-wide association studies for atherosclerotic vascular disease and its risk factors K Ding, IJ Kullo	Circulation. Cardiovascular genetics	2009
Genetic scoring analysis: a way forward in genome wide association studies? N Amin, CM van Duijn, AC Janssens	European Journal of Epidemiology	2009
Visualization of shared genomic regions and meiotic recombination in high-density SNP data ED Roberson, J Pevsner	PloS one	2009
Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae EE Kenny, A Gusev, K Riegel, D Lütjohann, JK Lowe, J Salit, JB Maller, M Stoffel, MJ Daly, DM Altshuler, JM Friedman, JL Breslow, I Pe'er, E Sehayek	Proceedings of the National Academy of Sciences	2009
Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer M Yeager, Z Deng, J Boland, C Matthews, J Bacior, V Lonsberry, A Hutchinson, LA Burdett, L Qi, KB Jacobs, J Gonzalez-Bosquet, SI Berndt, RB Hayes, RN Hoover, G Thomas, DJ Hunter, M Dean, SJ Chanock	Human Genetics	2009
The HapMap and genome-wide association studies in diagnosis and therapy TA Manolio, FS Collins	Annual Review of Medicine	2009
Underlying genetic models of inheritance in established type 2 diabetes associations G Salanti, L Southam, D Altshuler, K Ardlie, I Barroso, M Boehnke, MC Cornelis, TM Frayling, H Grallert, N Grarup, L Groop, T Hansen, AT Hattersley, FB Hu, K Hveem, T Illig, J Kuusisto, M Laakso, C Langenberg, V Lyssenko, MI McCarthy, A Morris, AD Morris, CN Palmer, F Payne, CG Platou, LJ Scott, BF Voight, NJ Wareham, E Zeggini, JP Ioannidis	American Journal of Epidemiology	2009
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data RS Vasan, NL Glazer, JF Felix, W Lieb, PS Wild, SB Felix, N Watzinger, MG Larson, NL Smith, A Dehghan, A Grosshennig, A Schillert, A Teumer, R Schmidt, S Kathiresan, T Lumley, YS Aulchenko, IR König, T Zeller, G Homuth, M Struchalin, J Aragam, JC Bis, F Rivadeneira, J Erdmann, RB Schnabel, M Dörr, R Zweiker, L Lind, RJ Rodeheffer, KH Greiser, D Levy, T Haritunians, JW Deckers, J Stritzke, KJ Lackner, U Völker, E Ingelsson, I Kullo, J Haerting, CJ O'Donnell, SR Heckbert, BH Stricker, A Ziegler, T Reffelmann, MM Redfield, K Werdan, GF Mitchell, K Rice, DK Arnett, A Hofman, JS Gottdiener, AG Uitterlinden, T Meitinger, M Blettner, N Friedrich, TJ Wang, BM Psaty, CM van Duijn, HE Wichmann, TF Munzel, HK Kroemer, EJ Benjamin, JI Rotter, JC Witteman, H Schunkert, H Schmidt, H Völzke, S Blankenberg	JAMA : the journal of the American Medical Association	2009
Common variants on chromosome 6p22.1 are associated with schizophrenia J Shi, DF Levinson, J Duan, AR Sanders, Y Zheng, I Pe'er, F Dudbridge, PA Holmans, AS Whittemore, BJ Mowry, A Olincy, F Amin, CR Cloninger, JM Silverman, NG Buccola, WF Byerley, DW Black, RR Crowe, JR Oksenberg, DB Mirel, KS Kendler, R Freedman, PV Gejman	Nature	2009
Complex diseases, complex genes: keeping pathways on the right track P Kraft, S Raychaudhuri	Epidemiology (Cambridge, Mass.)	2009
Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases MJ Khoury, L Bertram, P Boffetta, AS Butterworth, SJ Chanock, SM Dolan, I Fortier, M Garcia-Closas, M Gwinn, JP Higgins, AC Janssens, J Ostell, RP Owen, RA Pagon, TR Rebbeck, N Rothman, JL Bernstein, PR Burton, H Campbell, A Chockalingam, H Furberg, J Little, TR O'Brien, D Seminara, P Vineis, DM Winn, W Yu, JP Ioannidis	American Journal of Epidemiology	2009
Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip CC Spencer, Z Su, P Donnelly, J Marchini	PLoS genetics	2009
Genome-wide association study of bipolar disorder in European American and African American individuals EN Smith, CS Bloss, JA Badner, T Barrett, PL Belmonte, W Berrettini, W Byerley, W Coryell, D Craig, HJ Edenberg, E Eskin, T Foroud, E Gershon, TA Greenwood, M Hipolito, DL Koller, WB Lawson, C Liu, F Lohoff, MG McInnis, FJ McMahon, DB Mirel, SS Murray, C Nievergelt, J Nurnberger, EA Nwulia, J Paschall, JB Potash, J Rice, TG Schulze, W Scheftner, C Panganiban, N Zaitlen, PP Zandi, S Zöllner, NJ Schork, JR Kelsoe	Molecular Psychiatry	2009
Role of GABRA2 in trajectories of externalizing behavior across development and evidence of moderation by parental monitoring DM Dick, SJ Latendresse, JE Lansford, JP Budde, A Goate, KA Dodge, GS Pettit, JE Bates	Archives of general psychiatry	2009
Common vs. rare allele hypotheses for complex diseases NJ Schork, SS Murray, KA Frazer, EJ Topol	Current Opinion in Genetics & Development	2009
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits LA Hindorff, P Sethupathy, HA Junkins, EM Ramos, JP Mehta, FS Collins, TA Manolio	Proceedings of the National Academy of Sciences	2009
The A's, G's, C's, and T's of health disparities E Ramos, C Rotimi	BMC Medical Genomics	2009
Discovery of rare variants via sequencing: implications for the design of complex trait association studies B Li, SM Leal	PLoS genetics	2009
Genome-wide association study of blood pressure and hypertension D Levy, GB Ehret, K Rice, GC Verwoert, LJ Launer, A Dehghan, NL Glazer, AC Morrison, AD Johnson, T Aspelund, Y Aulchenko, T Lumley, A Köttgen, RS Vasan, F Rivadeneira, G Eiriksdottir, X Guo, DE Arking, GF Mitchell, FU Mattace-Raso, AV Smith, K Taylor, RB Scharpf, SJ Hwang, EJ Sijbrands, J Bis, TB Harris, SK Ganesh, CJ O'Donnell, A Hofman, JI Rotter, J Coresh, EJ Benjamin, AG Uitterlinden, G Heiss, CS Fox, JC Witteman, E Boerwinkle, TJ Wang, V Gudnason, MG Larson, A Chakravarti, BM Psaty, CM van Duijn	Nature Genetics	2009
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene BE Himes, GM Hunninghake, JW Baurley, NM Rafaels, P Sleiman, DP Strachan, JB Wilk, SA Willis-Owen, B Klanderman, J Lasky-Su, R Lazarus, AJ Murphy, ME Soto-Quiros, L Avila, T Beaty, RA Mathias, I Ruczinski, KC Barnes, JC Celedón, WO Cookson, WJ Gauderman, FD Gilliland, H Hakonarson, C Lange, MF Moffatt, GT O'Connor, BA Raby, EK Silverman, ST Weiss	The American Journal of Human Genetics	2009
Personalized medicine: a transformative approach is needed TJ Hudson	CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne	2009
The genetic signatures of noncoding RNAs JS Mattick	PLoS genetics	2009
Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility H Lou, M Yeager, H Li, JG Bosquet, RB Hayes, N Orr, K Yu, A Hutchinson, KB Jacobs, P Kraft, S Wacholder, N Chatterjee, HS Feigelson, MJ Thun, WR Diver, D Albanes, J Virtamo, S Weinstein, J Ma, JM Gaziano, M Stampfer, FR Schumacher, E Giovannucci, G Cancel-Tassin, O Cussenot, A Valeri, GL Andriole, ED Crawford, SK Anderson, M Tucker, RN Hoover, JF Fraumeni, G Thomas, DJ Hunter, M Dean, SJ Chanock	Proceedings of the National Academy of Sciences	2009
Imaging phenotypes of major depressive disorder: genetic correlates JB Savitz, WC Drevets	Neuroscience	2009
Systems pharmacology and genome medicine: a future perspective AD Wist, SI Berger, R Iyengar	Genome Medicine	2009
Genome-based prediction of common diseases: methodological considerations for future research AC Janssens, CM van Duijn	Genome Medicine	2009
Psychosis genetics: modeling the relationship between schizophrenia, bipolar disorder, and mixed (or "schizoaffective") psychoses N Craddock, MC O'Donovan, MJ Owen	Schizophrenia Bulletin	2009
Common variants at ten loci modulate the QT interval duration in the QTSCD Study A Pfeufer, S Sanna, DE Arking, M Müller, V Gateva, C Fuchsberger, GB Ehret, M Orrú, C Pattaro, A Köttgen, S Perz, G Usala, M Barbalic, M Li, B Pütz, A Scuteri, RJ Prineas, MF Sinner, C Gieger, SS Najjar, WH Kao, TW Mühleisen, M Dei, C Happle, S Möhlenkamp, L Crisponi, R Erbel, KH Jöckel, S Naitza, G Steinbeck, F Marroni, AA Hicks, E Lakatta, B Müller-Myhsok, PP Pramstaller, HE Wichmann, D Schlessinger, E Boerwinkle, T Meitinger, M Uda, J Coresh, S Kääb, GR Abecasis, A Chakravarti	Nature Genetics	2009
Discovering novel risk factors for venous thrombosis: a candidate-gene approach NL Smith, KM Rice, T Lumley, SR Heckbert, BM Psaty	Thrombosis Research	2009
Genome-wide association study of smoking initiation and current smoking JM Vink, AB Smit, EJ de Geus, P Sullivan, G Willemsen, JJ Hottenga, JH Smit, WJ Hoogendijk, FG Zitman, L Peltonen, J Kaprio, NL Pedersen, PK Magnusson, TD Spector, KO Kyvik, KI Morley, AC Heath, NG Martin, RG Westendorp, PE Slagboom, H Tiemeier, A Hofman, AG Uitterlinden, YS Aulchenko, N Amin, C Duijn, BW Penninx, DI Boomsma	The American Journal of Human Genetics	2009
Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms PA Holmans, B Riley, AE Pulver, MJ Owen, DB Wildenauer, PV Gejman, BJ Mowry, C Laurent, KS Kendler, G Nestadt, NM Williams, SG Schwab, AR Sanders, D Nertney, J Mallet, B Wormley, VK Lasseter, MC O'Donovan, J Duan, M Albus, M Alexander, S Godard, R Ribble, KY Liang, N Norton, W Maier, G Papadimitriou, D Walsh, M Jay, A O'Neill, FB Lerer, D Dikeos, RR Crowe, JM Silverman, DF Levinson	Molecular Psychiatry	2009
Recent advances in genetic predisposition to clinical acute lung injury L Gao, KC Barnes	American journal of physiology. Lung cellular and molecular physiology	2009
Collaborative genome-wide association studies of diverse diseases: programs of the NHGRI's office of population genomics TA Manolio	Pharmacogenomics	2009
Meta-analysis in genome-wide association studies E Zeggini, JP Ioannidis	Pharmacogenomics	2009
An open access database of genome-wide association results AD Johnson, CJ O'Donnell	BMC Medical Genetics	2009
Genetic background comparison using distance-based regression, with applications in population stratification evaluation and adjustment Q Li, S Wacholder, DJ Hunter, RN Hoover, S Chanock, G Thomas, K Yu	Genetic Epidemiology	2009
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels L Xiong, H Catoire, P Dion, C Gaspar, RG Lafrenière, SL Girard, A Levchenko, JB Rivière, L Fiori, J St-Onge, I Bachand, P Thibodeau, R Allen, C Earley, G Turecki, J Montplaisir, GA Rouleau	Human Molecular Genetics	2009
Detecting shared pathogenesis from the shared genetics of immune-related diseases A Zhernakova, CC van Diemen, C Wijmenga	Nature Reviews Genetics	2009
Dissecting the phenotype in genome-wide association studies of psychiatric illness N Craddock, K Kendler, M Neale, J Nurnberger, S Purcell, M Rietschel, R Perlis, SL Santangelo, T Schulze, JW Smoller, A Thapar	The British Journal of Psychiatry	2009
Genome-wide association studies in ADHD B Franke, BM Neale, SV Faraone	Human Genetics	2009
Large-scale analysis of association betweenGDF5andFRZBvariants and osteoarthritis of the hip, knee, and hand E Evangelou, K Chapman, I Meulenbelt, FB Karassa, J Loughlin, A Carr, M Doherty, S Doherty, JJ Gómez-Reino, A Gonzalez, BV Halldorsson, VB Hauksson, A Hofman, DJ Hart, S Ikegawa, T Ingvarsson, Q Jiang, I Jonsdottir, H Jonsson, HJ Kerkhof, M Kloppenburg, NE Lane, J Li, RJ Lories, JB van Meurs, A Näkki, MC Nevitt, J Rodriguez-Lopez, D Shi, PE Slagboom, K Stefansson, A Tsezou, GA Wallis, CM Watson, TD Spector, AG Uitterlinden, AM Valdes, JP Ioannidis	Arthritis & Rheumatism	2009
High marks for GWAS S Chanock	Nature Genetics	2009
Genetics and Genomics of Chronic Obstructive Pulmonary Disease EK Silverman, A Spira, PD Paré	Proceedings of the American Thoracic Society	2009
Genomewide Association Studies and Human Disease J Hardy, A Singleton	The New England journal of medicine	2009
Genomewide association studies: history, rationale, and prospects for psychiatric disorders , S Cichon, N Craddock, M Daly, SV Faraone, PV Gejman, J Kelsoe, T Lehner, DF Levinson, A Moran, P Sklar, PF Sullivan	The American journal of psychiatry	2009
Genetic susceptibility in Parkinson's disease JM Bras, A Singleton	Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease	2009
Emerging Paradigms in Cancer Genetics: Some Important Findings from High-Density Single Nucleotide Polymorphism Array Studies MD Bacolod, GS Schemmann, SF Giardina, P Paty, DA Notterman, F Barany	Cancer research	2009
LD-Spline: Mapping SNPs on genotyping platforms to genomic regions using patterns of linkage disequilibrium WS Bush, G Chen, ES Torstenson, MD Ritchie	BioData mining	2009
The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects AM Molloy, LC Brody, JL Mills, JM Scott, PN Kirke	Birth defects research. Part A, Clinical and molecular teratology	2009
Control Selection Options for Genome-Wide Association Studies in Cohorts: Figure 1 S Wacholder, M Rotunno	Cancer epidemiology, biomarkers & prevention	2009
Systems-based candidate genes for human response to influenza infection L Zhang, JM Katz, M Gwinn, NF Dowling, MJ Khoury	Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases	2009
The Scientific Foundation for Personal Genomics: Recommendations from a National Institutes of Health–Centers for Disease Control and Prevention Multidisciplinary Workshop Khoury MJ, McBride CM, Schully SD, Ioannidis JP, Feero WG, Janssens AC, Gwinn M, Simons-Morton DG, Bernhardt JM, Cargill M, Chanock SJ, Church GM, Coates RJ, Collins FS, Croyle RT, Davis BR, Downing GJ, DuRoss A, Friedman S, Gail MH, Ginsburg GS, Green RC, Greene MH, Greenland P, Gulcher JR, Hsu A, Hudson KL, Kardia SL, Kimmel PL, Lauer MS, Miller AM, Offit K, Ransohoff DF, Roberts JS, Rasooly RS, Stefansson K, Terry SF, Teutsch SM, Trepanier A, Wanke KL, Witte JS, Xu J	Genetics in Medicine	2009
Validating, augmenting and refining genome-wide association signals Ioannidis JP, Thomas G, Daly MJ	Nature reviews. Genetics	2009
The genomic applications in practice and prevention network. Khoury MJ, Feero WG, Reyes M, Citrin T, Freedman A, Leonard D, Burke W, Coates R, Croyle RT, Edwards K, Kardia S, McBride C, Manolio T, Randhawa G, Rasooly R, St Pierre J, Terry S	Genetics in Medicine	2009
Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. Holmans P, Green EK, Pahwa JS, Ferreira MA, Purcell SM, Sklar P, Owen MJ, O'Donovan MC, Craddock N	The American Journal of Human Genetics	2009
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P	Nature	2009
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine. Biesecker LG, Mullikin JC, Facio FM, Turner C, Cherukuri PF, Blakesley RW, Bouffard GG, Chines PS, Cruz P, Hansen NF, Teer JK, Maskeri B, Young AC, Manolio TA, Wilson AF, Finkel T, Hwang P, Arai A, Remaley AT, Sachdev V, Shamburek R, Cannon RO, Green ED	Genome research	2009
A Genome Wide Survey of SNP Variation Reveals the Genetic Structure of Sheep Breeds Kijas JW, Townley D, Dalrymple BP, Heaton MP, Maddox JF, McGrath A, Wilson P, Ingersoll RG, McCulloch R, McWilliam S, Tang D, McEwan J, Cockett N, Oddy VH, Nicholas FW, Raadsma H	PloS one	2009
Biomarker Validation for Aging: Lessons from mtDNA Heteroplasmy Analyses in Early Cancer Detection Barker PE, Murthy M	Biomarker insights	2009
Policy perspectives on the emerging pathways of personalized medicine Downing GJ	Dialogues in clinical neuroscience	2009
Cohort studies and the genetics of complex disease. Manolio TA	Nature Genetics	2009
Beyond odds ratios--communicating disease risk based on genetic profiles. Kraft P, Wacholder S, Cornelis MC, Hu FB, Hayes RB, Thomas G, Hoover R, Hunter DJ, Chanock S	Nature reviews. Genetics	2009
Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how? Wright CF, Kroese M	Human Genetics	2009
Advanced gastric cancer: is laparoscopic gastrectomy safe? Liakakos T, Misiakos EP, Macheras A	Surgical Endoscopy	2009
The genetics of reading disability. Petryshen TL, Pauls DL	Current Psychiatry Reports	2009
Update in endocrine autoimmunity MS Anderson	The Journal of clinical endocrinology and metabolism	2008
Common variants at 30 loci contribute to polygenic dyslipidemia S Kathiresan, CJ Willer, GM Peloso, S Demissie, K Musunuru, EE Schadt, L Kaplan, D Bennett, Y Li, T Tanaka, BF Voight, LL Bonnycastle, AU Jackson, G Crawford, A Surti, C Guiducci, NP Burtt, S Parish, R Clarke, D Zelenika, KA Kubalanza, MA Morken, LJ Scott, HM Stringham, P Galan, AJ Swift, J Kuusisto, RN Bergman, J Sundvall, M Laakso, L Ferrucci, P Scheet, S Sanna, M Uda, Q Yang, KL Lunetta, J Dupuis, PI de Bakker, CJ O'Donnell, JC Chambers, JS Kooner, S Hercberg, P Meneton, EG Lakatta, A Scuteri, D Schlessinger, J Tuomilehto, FS Collins, L Groop, D Altshuler, R Collins, GM Lathrop, O Melander, V Salomaa, L Peltonen, M Orho-Melander, JM Ordovas, M Boehnke, GR Abecasis, KL Mohlke, LA Cupples	Nature Genetics	2008
Cardiovascular genomics, personalized medicine, and the National Heart, Lung, and Blood Institute: part I: the beginning of an era CJ O'Donnell, EG Nabel	Circulation. Cardiovascular genetics	2008
Genetic architecture of complex traits: large phenotypic effects and pervasive epistasis H Shao, LC Burrage, DS Sinasac, AE Hill, SR Ernest, W O'Brien, HW Courtland, KJ Jepsen, A Kirby, EJ Kulbokas, MJ Daly, KW Broman, ES Lander, JH Nadeau	Proceedings of the National Academy of Sciences	2008
Obesity genes: so close and yet so far D Pomp, KL Mohlke	Journal of biology	2008
Invited commentary: from genome-wide association studies to gene-environment-wide interaction studies--challenges and opportunities MJ Khoury, S Wacholder	American Journal of Epidemiology	2008
Intermediacy and gene-environment interaction: the example of CHRNA5-A3 region, smoking, nicotine dependence, and lung cancer S Wacholder, N Chatterjee, N Caporaso	Journal of the National Cancer Institute	2008
Tilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causation KM Weiss	Genetics	2008
Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers M Yeager, N Xiao, RB Hayes, P Bouffard, B Desany, L Burdett, N Orr, C Matthews, L Qi, A Crenshaw, Z Markovic, KM Fredrikson, KB Jacobs, L Amundadottir, TP Jarvie, DJ Hunter, R Hoover, G Thomas, TT Harkins, SJ Chanock	Human Genetics	2008
Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk V Moskvina, N Craddock, P Holmans, I Nikolov, JS Pahwa, E Green, MJ Owen, MC O'Donovan	Molecular Psychiatry	2008
Statistical issues in the analysis of DNA Copy Number Variations NE Wineinger, RE Kennedy, SW Erickson, MK Wojczynski, CE Bruder, HK Tiwari	International Journal of Computational Biology and Drug Design	2008
Public Health Genomics Approach to Type 2 Diabetes MJ Khoury, R Valdez, A Albright	Diabetes	2008
Role of MicroRNA in Pancreatic -Cells: Where More Is Less MD Walker	Diabetes	2008
Promoting Regulatory Gene Variation in Sodium Reabsorption PA Doris	Hypertension	2008
Gene Prospector: An evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases W Yu, A Wulf, T Liu, MJ Khoury, M Gwinn	BMC bioinformatics	2008
Management of High-Throughput DNA Sequencing Projects: Alpheus. Miller NA, Kingsmore SF, Farmer A, Langley RJ, Mudge J, Crow JA, Gonzalez AJ, Schilkey FD, Kim RJ, van Velkinburgh J, May GD, Black CF, Myers MK, Utsey JP, Frost NS, Sugarbaker DJ, Bueno R, Gullans SR, Baxter SM, Day SW, Retzel EF	Journal of computer science and systems biology	2008
Is the time right for translation research in genomics? Janssens AC	European Journal of Epidemiology	2008
Meta-analysis of 32 genome-wide linkage studies of schizophrenia Ng M, Levinson D, Faraone S, Suarez B, DeLisi L, Arinami T, Riley B, Paunio T, Pulver A, Irmansyah, Holmans P, Escamilla M, Wildenauer D, Williams N, Laurent C, Mowry B, Brzustowicz L, Maziade M, Sklar P, Garver D, Abecasis G, Lerer B, Fallin M, Gurling H, Gejman P, Lindholm E, Moises H, Byerley W, Wijsman E, Forabosco P, Tsuang M, Hwu HG, Okazaki Y, Kendler K, Wormley B, Fanous A, Walsh D, O\u2019Neill F, Peltonen L, Nestadt G, Lasseter V, Liang K, Papadimitriou G, Dikeos D, Schwab S, Owen M, O\u2019Donovan M, Norton N, Hare E, Raventos H, Nicolini H, Albus M, Maier W, Nimgaonkar V, Terenius L, Mallet J, Jay M, Godard S, Nertney D, Alexander M, Crowe R, Silverman J, Bassett A, Roy MA, Mérette C, Pato C, Pato M, Roos JL, Kohn Y, Amann-Zalcenstein D, Kalsi G, McQuillin A, Curtis D, Brynjolfson J, Sigmundsson T, Petursson H, Sanders A, Duan J, Jazin E, Myles-Worsley M, Karayiorgou M, Lewis C	Molecular Psychiatry	2008
Current Protocols in Neuroscience CR Gerfen, A Holmes, D Sibley, P Skolnick, S Wray	Current Protocols in Neuroscience	2001

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