Robert D. Nicholls
Title and authors | Publication | Year |
---|---|---|
Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2
Kobayashi H, Igaki T, Kumamoto S, Tanaka K, Takashima T, Nagaoka SI, Suzuki S, Hayashi M, Renfree MB, Kawahara M, Saito S, Kobayashi T, Nagashima H, Matsunari H, Nakano K, Uchikura A, Kiyonari H, Kaneko M, Imai H, Nakabayashi K, Lorincz M, Kurimoto K |
eLife | 2025 |
Transgenerational epigenetic self-memory of Dio3 dosage is associated with Meg3 methylation and altered growth trajectories and neonatal hormones
Martinez ME, Karaczyn A, Wu Z, Bennett CA, Matoin KL, Daigle HM, Hernandez A |
Epigenetics : official journal of the DNA Methylation Society | 2024 |
Inference of putative cell-type-specific imprinted regulatory elements and genes during human neuronal differentiation.
Liang D, Aygün N, Matoba N, Ideraabdullah FY, Love MI, Stein JL |
Human Molecular Genetics | 2023 |
Novel epigenetic molecular therapies for imprinting disorders.
Wang SE, Jiang YH |
Molecular Psychiatry | 2023 |
STAT1 epigenetically regulates LCP2 and TNFAIP2 by recruiting EP300 to contribute to the pathogenesis of inflammatory bowel disease
YL Yu, M Chen, H Zhu, MX Zhuo, P Chen, YJ Mao, LY Li, Q Zhao, M Wu, M Ye |
Clinical Epigenetics | 2021 |
DNA methylome signatures of prenatal exposure to synthetic glucocorticoids in hippocampus and peripheral whole blood of female guinea pigs in early life
A Sasaki, ME Eng, AH Lee, A Kostaki, SG Matthews |
Translational Psychiatry | 2021 |
The sociability spectrum: evidence from reciprocal genetic copy number variations
A López-Tobón, S Trattaro, G Testa |
Molecular autism | 2020 |
Neuroprotective Effect of L-carnitine. Focus on Changing Mitochondrial Function
AV Voronkov, DI Pozdnyakov |
2020 | |
Assessment of maternal and parent of origin effects in genetic variation of economic traits in Iranian native fowl
K Karami, S Zerehdaran, A Javadmanesh, MM Shariati |
British Poultry Science | 2019 |
Insights into in vitro spermatogenesis in mammals: Past, present, future: In vitro spermatogenesis
A Fattahi, Z Latifi, T Ghasemnejad, HR Nejabati, M Nouri |
Molecular Reproduction and Development | 2017 |
Prader-Willi Syndrome: Clinical and Genetic Findings
Merlin G. Butler, Travis Thompson |
The Endocrinologist | 2016 |
Imprinting Disorders: Non-Mendelian Mechanisms Affecting Growth
Merlin G. Butler |
Journal of pediatric endocrinology & metabolism : JPEM | 2016 |
Advanced Concepts in Lumbar Degenerative Disk Disease
JL Pinheiro-Franco, AR Vaccaro, EC Benzel, HM Mayer |
2016 | |
Nanoparticles in food. Epigenetic changes induced by nanomaterials and possible impact on health
B Smolkova, NE Yamani, AR Collins, AC Gutleb, M Dusinska |
Food and Chemical Toxicology | 2015 |
Epigenetic Analysis of Neurocognitive Development at 1 year of Age in a Community-Based Pregnancy Cohort
J Krushkal, LE Murphy, FB Palmer, JC Graff, TR Sutter, K Mozhui, CA Hovinga, F Thomas, V Park, FA Tylavsky, RM Adkins |
Behavior Genetics | 2014 |
Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic Epidemiology
A Li, D Meyre |
Current Psychiatry Reviews | 2014 |
Development and imprinted gene expression in uniparental preimplantation mouse embryos in vitro
M Hu, LC TuanMu, H Wei, F Gao, L Li, S Zhang |
Molecular Biology Reports | 2014 |
Analysis of imprinted gene expression and implantation in haploid androgenetic mouse embryos
M Hu, Z Zhao, LC TuanMu, H Wei, F Gao, L Li, J Ying, S Zhang |
Andrologia | 2014 |
Epigenetics in Psychiatry
AL Gropman |
Epigenetics in Psychiatry | 2014 |
Reference Module in Biomedical Sciences
DL Sackett, RB Haynes |
2014 | |
Epigenetic Factors and Autism Spectrum Disorders
BM Flashner, ME Russo, JE Boileau, DW Leong, GI Gallicano |
NeuroMolecular Medicine | 2013 |
Epigenetic Regulation in the Nervous System
WT Powell, JM LaSalle |
Epigenetic Regulation in the Nervous System | 2013 |
DNA Methylation Patterns in Cord Blood DNA and Body Size in Childhood
CL Relton, A Groom, BS Pourcain, AE Sayers, DC Swan, ND Embleton, MS Pearce, SM Ring, K Northstone, JH Tobias, J Trakalo, AR Ness, SO Shaheen, GD Smith |
PloS one | 2012 |
Characterization, Tissue Expression, and Imprinting Analysis of the Porcine CDKN1C and NAP1L4 Genes
S Li, J Li, J Tian, R Dong, J Wei, X Qiu, C Jiang |
Journal of Biomedicine and Biotechnology | 2012 |
Toxicology and Epigenetics: Sahu/Toxicology and Epigenetics
CA Cooney, KM Gilbert |
Toxicology and Epigenetics: Sahu/Toxicology and Epigenetics | 2012 |
Specific changes in the expression of imprinted genes in prostate cancer--implications for cancer progression and epigenetic regulation
T Ribarska, KM Bastian, A Koch, WA Schulz |
Asian Journal of Andrology | 2012 |
DNA Methylation Patterns in Cord Blood DNA and Body Size in Childhood
CL Relton, A Groom, BS Pourcain, AE Sayers, DC Swan, ND Embleton, MS Pearce, SM Ring, K Northstone, JH Tobias, J Trakalo, AR Ness, SO Shaheen, GD Smith, M Uddin |
PloS one | 2012 |
The Principles of Clinical Cytogenetics
SL Gersen, MB Keagle |
2012 | |
Interindividual differences in placental expression of the SLC22A2 (OCT2) gene: Relationship to epigenetic variations in the 5′-upstream regulatory region
J Saito, T Hirota, N Kikunaga, K Otsubo, I Ieiri |
Journal of Pharmaceutical Sciences | 2011 |
Epigenetic epidemiology of common complex disease: prospects for prediction, prevention, and treatment
CL Relton, GD Smith |
PLoS Medicine | 2010 |
Epigenetics, Copy Number Variation, and Other Molecular Mechanisms Underlying Neurodevelopmental Disabilities: New Insights and Diagnostic Approaches
AL Gropman, ML Batshaw |
Journal of Developmental & Behavioral Pediatrics | 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 |
Sex dependent imprinting effects on complex traits in mice
R Hager, JM Cheverud, LJ Leamy, JB Wolf |
BMC Evolutionary Biology | 2008 |
Genome-wide analysis reveals a complex pattern of genomic imprinting in mice
JB Wolf, JM Cheverud, C Roseman, R Hager |
PLoS genetics | 2008 |
Genomic imprinting in the development and evolution of psychotic spectrum conditions
B Crespi |
Biological Reviews | 2008 |
A search for quantitative trait loci exhibiting imprinting effects on mouse mandible size and shape
LJ Leamy, CP Klingenberg, E Sherratt, JB Wolf, JM Cheverud |
Heredity | 2008 |
Genome-Wide Analysis Reveals a Complex Pattern of Genomic Imprinting in Mice
JB Wolf, JM Cheverud, C Roseman, R Hager, AC Ferguson-Smith |
PLoS genetics | 2008 |
Maternal Effects as the Cause of Parent-of-Origin Effects That Mimic Genomic Imprinting
R Hager, JM Cheverud, JB Wolf |
Genetics | 2008 |
Turner syndrome
SR Kesler |
Child and Adolescent Psychiatric Clinics of North America | 2007 |
Epigenetics in Reproductive Medicine
A Paoloni-Giacobino |
Pediatric Research | 2007 |
Severe presentation of Beckwith–Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15
AC Smith, C Shuman, D Chitayat, L Steele, PN Ray, J Bourgeois, R Weksberg |
American Journal of Medical Genetics Part A | 2007 |
When Puberty is Precocious
OH Pescovitz, EC Walvoord |
2007 | |
RNA Towards Medicine
V Erdmann, J Barciszewski, J Brosius |
2006 | |
RNA Towards Medicine
V Erdmann, J Barciszewski, J Brosius |
2006 | |
RNA Towards Medicine
V Erdmann, J Barciszewski, J Brosius |
2006 | |
Imbalanced genomic imprinting in brain development: an evolutionary basis for the aetiology of autism
C Badcock, B Crespi |
Journal of Evolutionary Biology | 2006 |
Genetics and pathophysiology of mental retardation
J Chelly, M Khelfaoui, F Francis, B Chérif, T Bienvenu |
European Journal of Human Genetics | 2006 |
PERSPECTIVE: MATERNAL KIN GROUPS AND THE ORIGINS OF ASYMMETRIC GENETIC SYSTEMS—GENOMIC IMPRINTING, HAPLODIPLOIDY, AND PARTHENOGENESIS
BB Normark |
Evolution | 2006 |
PERSPECTIVE: MATERNAL KIN GROUPS AND THE ORIGINS OF ASYMMETRIC GENETIC SYSTEMS?GENOMIC IMPRINTING, HAPLODIPLOIDY, AND PARTHENOGENESIS
BB Normark |
Evolution | 2006 |
DNA Methylation: Development, Genetic Disease and Cancer
W Doerfler, P Böhm |
2006 | |
Beckwith-Wiedemann syndrome
R Weksberg, C Shuman, AC Smith |
American Journal of Medical Genetics Part C: Seminars in Medical Genetics | 2005 |
Possible genomic imprinting of three human obesity-related genetic loci
C Dong, WD Li, F Geller, L Lei, D Li, OY Gorlova, J Hebebrand, CI Amos, RD Nicholls, RA Price |
The American Journal of Human Genetics | 2005 |
A new frontier for molecular medicine: Noncoding RNAs
M Szymanski, MZ Barciszewska, VA Erdmann, J Barciszewski |
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer | 2005 |
Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data
DZ Loesch, QM Bui, W Kelso, RM Huggins, H Slater, G Warne, P Bergman, C Rodda, RJ Mitchell, M Prior |
Brain and Development | 2005 |
Genomic imprinting and assisted reproduction
A Paoloni-Giacobino, JR Chaillet |
Reproductive health | 2004 |
Amygdala and hippocampal volumes in Turner syndrome: a high-resolution MRI study of X-monosomy
SR Kesler, A Garrett, B Bender, J Yankowitz, SM Zeng, AL Reiss |
Neuropsychologia | 2004 |
DNA Methylation: Approaches, Methods, and Applications
J Hasskarl, R Claus, M Lubbert |
DNA Methylation: Approaches, Methods, and Applications | 2004 |
Biallelic expression of HRAS and MUCDHL in human and mouse
M Goldberg, M Wei, L Yuan, VV Murty, B Tycko |
Human Genetics | 2003 |
Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome
SR Kesler, CM Blasey, WE Brown, J Yankowitz, SM Zeng, BG Bender, AL Reiss |
Biological Psychiatry | 2003 |
Imprinting evolution and the price of silence
SK Murphy, RL Jirtle |
BioEssays | 2003 |
Imprinting and disease
J Walter, M Paulsen |
Seminars in Cell & Developmental Biology | 2003 |
Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5
M Du, LG Beatty, W Zhou, J Lew, C Schoenherr, R Weksberg, PD Sadowski |
Human Molecular Genetics | 2003 |
Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice
Jun Ren, Syann Lee, Silvia Pagliardini, Matthieu Gérard, Colin L Stewart, John J Greer, Rachel Wevrick |
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2003 |
Absence of Ndn, Encoding the Prader-Willi Syndrome-Deleted Gene necdin, Results in Congenital Deficiency of Central Respiratory Drive in Neonatal Mice
Ren J, Lee S, Pagliardini S, Gérard M, Stewart CL, Greer JJ, Wevrick R |
Journal of Neuroscience | 2003 |
Brain development in Turner syndrome: a magnetic resonance imaging study
WE Brown, SR Kesler, S Eliez, IS Warsofsky, M Haberecht, A Patwardhan, JL Ross, EK Neely, SM Zeng, J Yankowitz, AL Reiss |
Psychiatry Research | 2002 |
Immaculate misconception: Genetics
MA Surani |
Nature | 2002 |
Major Psychosis and Chromosome 22: Genetics Meets Epigenetics
A Petronis, V Popendikyte, P Kan, T Sasaki |
CNS Spectrums | 2002 |
A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues
TK Chibuk, JM Bischof, R Wevrick |
BMC genetics | 2001 |
Fertility preservation for children treated for cancer (1): scientific advances and research dilemmas
R Grundy, RG Gosden, M Hewitt, V Larcher, A Leiper, HA Spoudeas, D Walker, WH Wallace |
Archives of disease in childhood | 2001 |
Paternal uniparental isodisomy of chromosome 20q--and the resulting changes in GNAS1 methylation--as a plausible cause of pseudohypoparathyroidism
M Bastepe, AH Lane, H Jüppner |
The American Journal of Human Genetics | 2001 |
The role of tissue-specific imprinting as a source of phenotypic heterogeneity in human disease
LS Weinstein |
Biological Psychiatry | 2001 |
Future Directions for Neurobehavioral Studies of Environmental Neurotoxicants
DC Bellinger |
NeuroToxicology | 2001 |
New Thoughts on Female Precocious Puberty
SR Ojeda, S Heger |
Journal of Pediatric Endocrinology and Metabolism | 2001 |
Genomic Imprinting, Maternal Care, and Brain Evolution
EB Keverne |
Hormones and Behavior | 2001 |
Imprinting of PEG3, the Human Homologue of a Mouse Gene Involved in Nurturing Behavior
SK Murphy, AA Wylie, RL Jirtle |
Genomics | 2001 |
Ubiquitination, proteasomes and GABAA receptors
B Lüscher, CA Keller |
Nature Cell Biology | 2001 |
Establishment and Maintenance of DNA Methylation Patterns in Mouse Ndn : Implications for Maintenance of Imprinting in Target Genes of the Imprinting Center
ML Hanel, R Wevrick |
Molecular and cellular biology | 2001 |
A GNAS1 imprinting defect in pseudohypoparathyroidism type IB
Jie Liu, Deborah Litman, Marjorie J. Rosenberg, Shuhua Yu, Leslie G. Biesecker, Lee S. Weinstein |
Journal of Clinical Investigation | 2000 |
Imprinted expression of small nucleolar RNAs in brain: time for RNomics
W Filipowicz |
Proceedings of the National Academy of Sciences | 2000 |
Mechanisms of genomic imprinting
K Pfeifer |
The American Journal of Human Genetics | 2000 |
Imprinted expression of small nucleolar RNAs in brain: Time for RNomics
W Filipowicz |
Proceedings of the National Academy of Sciences | 2000 |
Maintaining imprinting
MR Mann, MS Bartolomei |
Nature Genetics | 2000 |
Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder
K Kosaki, T Suzuki, R Kosaki, H Yoshihashi, M Itoh, Y Goto, N Matsuo |
Molecular Psychiatry | 2000 |
Prader-Willi Syndrome: Clinical and Genetic Findings.
Butler MG, Thompson T |
The Endocrinologist | 2000 |
International Review of Cytology
RA Miller |
International Review of Cytology | 1991 |