The recent identification of multiple dominant mutations in the gene encoding β-catenin in both humans and mice has enabled exploration of the molecular and cellular basis of β-catenin function in cognitive impairment. In humans, β-catenin mutations that cause a spectrum of neurodevelopmental disorders have been identified. We identified de novo β-catenin mutations in patients with intellectual disability, carefully characterized their phenotypes, and were able to define a recognizable intellectual disability syndrome. In parallel, characterization of a chemically mutagenized mouse line that displays features similar to those of human patients with β-catenin mutations enabled us to investigate the consequences of β-catenin dysfunction through development and into adulthood. The mouse mutant, designated batface (
Valter Tucci, Tjitske Kleefstra, Andrea Hardy, Ines Heise, Silvia Maggi, Marjolein H. Willemsen, Helen Hilton, Chris Esapa, Michelle Simon, Maria-Teresa Buenavista, Liam J. McGuffin, Lucie Vizor, Luca Dodero, Sotirios Tsaftaris, Rosario Romero, Willy N. Nillesen, Lisenka E.L.M. Vissers, Marlies J. Kempers, Anneke T. Vulto-van Silfhout, Zafar Iqbal, Marta Orlando, Alessandro Maccione, Glenda Lassi, Pasqualina Farisello, Andrea Contestabile, Federico Tinarelli, Thierry Nieus, Andrea Raimondi, Barbara Greco, Daniela Cantatore, Laura Gasparini, Luca Berdondini, Angelo Bifone, Alessandro Gozzi, Sara Wells, Patrick M. Nolan
Title and authors | Publication | Year |
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Paving the way toward treatment solutions for CTNNB1 syndrome: a patient organization perspective
Miroševič Š, Khandelwal S, Amerson E, Parks E, Parks M, Cochran L, González Hernández A, Ferraro M, Lisowski L, Perez-Iturralde A, Chung W, Jacob MH, Žakelj N, Lainšček D, Forstnerič V, Sušjan P, Maruna M, Jerala R, Osredkar D |
Therapeutic Advances in Rare Disease | 2025 |
Inhibition of GSK3α/β rescues cognitive phenotypes in a preclinical mouse model of CTNNB1 syndrome
Jonathan Alexander, Leeanne Vazquez-Ramirez, Pantelis Antonoudiou, Jamie Maguire, Florence Wagner, Michele H. Jacob |
EMBO Molecular Medicine | 2024 |
A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder
Nagy N, Pál M, Nagy D, Bokor BA, Zimmermann A, Gellén B, Salamon A, Sztriha L, Klivényi P, Széll M |
BMC Pediatrics | 2024 |
CTNNB1 in neurodevelopmental disorders
Zhuang W, Ye T, Wang W, Song W, Tan T |
Frontiers in Psychiatry | 2023 |
Identification of Five Novel Variants in the TSPAN12 Gene in Chinese Families With Familial Exudative Vitreoretinopathy.
Wang Y, Wang Q, Li S, Ding X |
Translational Vision Science & Technology | 2023 |
CTNNB1-related neurodevelopmental disorder mimics cerebral palsy: case report
Lee J, Yoo J, Lee S, Jang DH |
Frontiers in Pediatrics | 2023 |
Tissue tension permits β-catenin phosphorylation to drive mesoderm specification in human embryonic stem cells
Ayad NM, Lakins JN, Ghagre A, Ehrlicher AJ, Weaver VM |
2023 | |
Whole Exome Sequencing Identified two Novel Truncation Mutations in the CTNNB1 Gene Associated with Neurodevelopmental Disorder, Language Dysfunction, and Microcephaly in Chinese Children
Ji Y, Xia Q, Zhang H, Huo H, Cao X, Wang W, Gu Q |
Child Neurology Open | 2023 |
From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome
Onesimo R, Sforza E, Trevisan V, Leoni C, Giorgio V, Rigante D, Kuczynska EM, Proli F, Agazzi C, Limongelli D, Digilio MC, Dentici ML, Macchiaiolo M, Novelli A, Bartuli A, Sinibaldi L, Tartaglia M, Zampino G |
Genes & development | 2023 |
Altered motor learning and coordination in mouse models of autism spectrum disorder
Cording KR, Bateup HS |
Frontiers in cellular neuroscience | 2023 |
Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability
S Dashti, S Salehpour, M Ghasemi, H Sadeghi, M Rostami, F Hashemi-Gorji, R Mirfakhraie, V Yassaee, M Miryounesi |
Neurological Sciences | 2022 |
To Stick or Not to Stick: Adhesions in Orofacial Clefts
A Antiguas, B Paul, M Dunnwald |
Biology : open access journal | 2022 |
Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia
R Taylor, C Soriano, S Williams, D Dzulova, J Ashworth, G Hall, T Gale, I Lloyd, C Inglehearn, C Toomes, S Douzgou, G Black |
Orphanet Journal of Rare Diseases | 2022 |
The Emerging Roles of Long Non-Coding RNAs in Intellectual Disability and Related Neurodevelopmental Disorders
Liaci C, Prandi L, Pavinato L, Brusco A, Maldotti M, Molineris I, Oliviero S, Merlo GR |
International journal of molecular sciences | 2022 |
A novel frameshift variant in the TSPAN12 gene causes autosomal dominant FEVR
Peng L, Dai E, Xiao H, Zhao R, He Y, Li S, Yang M, Yang Z, Zhao P |
Molecular Genetics & Genomic Medicine | 2022 |
The extended clinical and genetic spectrum of CTNNB1-related neurodevelopmental disorder
Lee S, Jang SS, Park S, Yoon JG, Kim SY, Lim BC, Chae JH |
Frontiers in Pediatrics | 2022 |
Tyrosine phosphatase activity is restricted by basic charge substituting mutation of substrates.
Huang CF, Gottardi CJ, Mrksich M |
Scientific Reports | 2022 |
Correlation between Phenotype and Genotype in CTNNB1 Syndrome: A Systematic Review of the Literature.
Miroševič Š, Khandelwal S, Sušjan P, Žakelj N, Gosar D, Forstnerič V, Lainšček D, Jerala R, Osredkar D |
International journal of molecular sciences | 2022 |
Genetic and clinical characteristics of 24 mainland Chinese patients with CTNNB1 loss‐of‐function variants
Yan D, Sun Y, Xu N, Yu Y, Zhan Y |
Molecular Genetics & Genomic Medicine | 2022 |
Startle Disease: An Overlooked Symptom of CTNNB1-Related Neurodevelopmental Disorder With Spastic Diplegia and Visual Defects
Bulot V, Ramond F, Mauguière F, Mazzola L |
2022 | |
Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants
Kayumi S, Pérez-Jurado LA, Palomares M, Rangu S, Sheppard SE, Chung WK, Kruer MC, Kharbanda M, Amor DJ, McGillivray G, Cohen JS, García-Miñaúr S, van Eyk CL, Harper K, Jolly LA, Webber DL, Barnett CP, Santos-Simarro F, Pacio-Míguez M, del Pozo A, Bakhtiari S, Deardorff M, Dubbs HA, Izumi K, Grand K, Gray C, Mark PR, Bhoj EJ, Li D, Ortiz-Gonzalez XR, Keena B, Zackai EH, Goldberg EM, de Nanclares GP, Pereda A, Llano-Rivas I, Arroyo I, Fernández-Cuesta MÁ, Thauvin-Robinet C, Faivre L, Garde A, Mazel B, Bruel AL, Tress ML, Brilstra E, Fine AS, Crompton KE, Stegmann AP, Sinnema M, Stevens SC, Nicolai J, Lesca G, Lion-François L, Haye D, Chatron N, Piton A, Nizon M, Cogne B, Srivastava S, Bassetti J, Muss C, Gripp KW, Procopio RA, Millan F, Morrow MM, Assaf M, Moreno-De-Luca A, Joss S, Hamilton MJ, Bertoli M, Foulds N, McKee S, MacLennan AH, Gecz J, Corbett MA |
Genetics in Medicine | 2022 |
Not All Mice Are Created Equal: Interval Timing Accuracy and Scalar Timing in 129, Swiss-Webster, and C57Bl/6 Mice
Buhusi CV, Meyer AE, Oprisan SA, Buhusi M |
2022 | |
Catenin alpha 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/beta-catenin signaling
Xianjun Zhu, Mu Yang, Peiquan Zhao, Shujin Li, Lin Zhang, Lulin Huang, Yi Huang, Ping Fei, Yeming Yang, Shanshan Zhang, Huijuan Xu, Ye Yuan, Xiang Zhang, Xiong Zhu, Shi Ma, Fang Hao, Periasamy Sundaresan, Weiquan Zhu, Zhenglin Yang |
Journal of Clinical Investigation | 2021 |
Dissecting Molecular Genetic Mechanisms of 1q21.1 CNV in Neuropsychiatric Disorders
J Yoon, Y Mao |
International journal of molecular sciences | 2021 |
Cell–cell coupling and DNA methylation abnormal phenotypes in the after-hours mice
F Tinarelli, E Ivanova, I Colombi, E Barini, E Balzani, CG Garcia, L Gasparini, M Chiappalone, G Kelsey, V Tucci |
Epigenetics & chromatin | 2021 |
Non-Syndromic Intellectual Disability and Its Pathways: A Long Noncoding RNA Perspective
II Barros, V Leão, JO Santis, RC Rosa, DB Brotto, CB Storti, ÁD Siena, GA Molfetta, WA Silva |
Non-Coding RNA | 2021 |
Timing behavior in genetic murine models of neurological and psychiatric diseases
A Karson, F Balcı |
Experimental Brain Research | 2021 |
Exome sequencing in paediatric patients with movement disorders
AK Kwong, MH Tsang, JL Fung, CC Mak, KL Chan, RJ Rodenburg, M Lek, S Huang, S Pajusalu, MM Yau, C Tsoi, S Fung, KT Liu, CK Ma, S Wong, EK Yau, SM Tai, EL Fung, NS Wu, LY Tsung, J Smeitink, BH Chung, CW Fung |
Orphanet Journal of Rare Diseases | 2021 |
Neuronal Cytoskeleton in Intellectual Disability: From Systems Biology and Modeling to Therapeutic Opportunities
C Liaci, M Camera, G Caslini, S Rando, S Contino, V Romano, GR Merlo |
International journal of molecular sciences | 2021 |
Missense variants in CTNNB1 can be associated with vitreoretinopathy—Seven new cases of CTNNB1 ‐associated neurodevelopmental disorder including a previously unreported retinal phenotype
LZ Rossetti, MR Bekheirnia, AM Lewis, HC Mefford, K GoldenGrant, K TarczyHornoch, LC Briere, DA Sweetser, MA Walker, E Kravets, DA Stevenson, G Bruenner, J Sebastian, J Knapo, JA Rosenfeld, PC Marcogliese, MF Wangler |
Molecular Genetics & Genomic Medicine | 2020 |
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
SC Jin, SA Lewis, S Bakhtiari, X Zeng, MC Sierant, S Shetty, SM Nordlie, A Elie, MA Corbett, BY Norton, CL van Eyk, S Haider, BS Guida, H Magee, J Liu, S Pastore, JB Vincent, J Brunstrom-Hernandez, A Papavasileiou, MC Fahey, JG Berry, K Harper, C Zhou, J Zhang, B Li, H Zhao, J Heim, DL Webber, MS Frank, L Xia, Y Xu, D Zhu, B Zhang, AH Sheth, JR Knight, C Castaldi, IR Tikhonova, F López-Giráldez, B Keren, S Whalen, J Buratti, D Doummar, M Cho, K Retterer, F Millan, Y Wang, JL Waugh, L Rodan, JS Cohen, A Fatemi, AE Lin, JP Phillips, T Feyma, SC MacLennan, S Vaughan, KE Crompton, SM Reid, DS Reddihough, Q Shang, C Gao, I Novak, N Badawi, YA Wilson, SJ McIntyre, SM Mane, X Wang, DJ Amor, DC Zarnescu, Q Lu, Q Xing, C Zhu, K Bilguvar, S Padilla-Lopez, RP Lifton, J Gecz, AH MacLennan, MC Kruer |
Nature Genetics | 2020 |
A de novo CTNNB1 Novel Splice Variant in an Adult Female with Severe Intellectual Disability WM Verhoeven, JI Egger, RE Jongbloed, MM van Putten, M de Bruijn-van Zandwijk, AS Zwemer, R Pfundt, MH Willemsen |
International Medical Case Reports Journal | 2020 |
Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits
GT Banks, MC Guillaumin, I Heise, P Lau, M Yin, N Bourbia, C Aguilar, MR Bowl, C Esapa, LA Brown, S Hasan, E Tagliatti, E Nicholson, RS Bains, S Wells, VV Vyazovskiy, K Volynski, SN Peirson, PM Nolan |
Science Advances | 2020 |
Current challenges and possible future developments in personalized psychiatry with an emphasis on psychotic disorders
A Levchenko, T Nurgaliev, A Kanapin, A Samsonova, RR Gainetdinov |
Heliyon | 2020 |
Excessive β-Catenin in Excitatory Neurons Results in Reduced Social and Increased Repetitive Behaviors and Altered Expression of Multiple Genes Linked to Human Autism
JM Alexander, A Pirone, MH Jacob |
Frontiers in synaptic neuroscience | 2020 |
A mouse model for kinesin family member 11 (Kif11)-associated familial exudative vitreoretinopathy
Y Wang, PM Smallwood, J Williams, J Nathans |
Human Molecular Genetics | 2020 |
The Promise of Automated Home-Cage Monitoring in Improving Translational Utility of Psychiatric Research in Rodents
A Mingrone, A Kaffman, A Kaffman |
Frontiers in neuroscience | 2020 |
The RNA helicase DDX3 induces neural crest by promoting AKT activity
M Perfetto, X Xu, C Lu, Y Shi, N Yousaf, J Li, YY Yien, S Wei |
Development (Cambridge, England) | 2020 |
Case Report: A de novo CTNNB1 Nonsense Mutation Associated With Neurodevelopmental Disorder, Retinal Detachment, Polydactyly
Z KE, Y CHEN |
Frontiers in Pediatrics | 2020 |
Wnt signaling in orofacial clefts: crosstalk, pathogenesis and models
K Reynolds, P Kumari, LS Rincon, R Gu, Y Ji, S Kumar, CJ Zhou |
Disease models & mechanisms | 2019 |
Dystonin/BPAG1 modulates diabetes and Alzheimer’s disease cross-talk: a meta-analysis
J Cheng, HP Liu, SL Hwang, LF Hsu, WY Lin, FJ Tsai |
Neurological Sciences | 2019 |
Identification of a novel splice mutation in CTNNB1 gene in a Chinese family with both severe intellectual disability and serious visual defects
H Wang, Y Zhao, L Yang, S Han, M Qi |
Neurological Sciences | 2019 |
PPM 1G forms a PPP ‐type phosphatase holoenzyme with B56δ that maintains adherens junction integrity
P Kumar, P Tathe, N Chaudhary, S Maddika |
EMBO reports | 2019 |
Heterozygous CTNNB1 and TBX4 variants in a patient with abnormal lung growth, pulmonary hypertension, microcephaly, and spasticity
JA Karolak, P Szafranski, D Kilner, C Patel, B Scurry, E Kinning, K Chandler, SN Jhangiani, ZH Akdemir, JR Lupski, E Popek, P Stankiewicz |
Clinical Genetics | 2019 |
Learning impairments and molecular changes in the brain caused by β-catenin loss
RJ Wickham, JM Alexander, LW Eden, M Valencia-Yang, J Llamas, JR Aubrey, MH Jacob |
Human Molecular Genetics | 2019 |
Brain Morphometry and Longitudinal Relaxation Time of Spontaneously Hypertensive Rats (SHRs) in Early and Intermediate Stages of Hypertension Investigated by 3D VFA-SPGR MRI
S Koundal, X Liu, S Sanggaard, K Mortensen, J Wardlaw, M Nedergaard, H Benveniste, H Lee |
Neuroscience | 2019 |
When Rett syndrome is due to genes other than MECP2
AK Percy, J Lane, F Annese, H Warren, SA Skinner, JL Neul |
Translational Science of Rare Diseases | 2018 |
An approach to monitoring home-cage behavior in mice that facilitates data sharing
E Balzani, M Falappa, F Balci, V Tucci |
Nature Protocols | 2018 |
The functional variant rs334558 of GSK3B is associated with remission in patients with depressive disorders
A Levchenko, IS Losenkov, NM Vyalova, GG Simutkin, NA Bokhan, B Wilffert, AJ Loonen, SA Ivanova |
Pharmacogenomics and Personalized Medicine | 2018 |
Spatial Impairment and Memory in Genetic Disorders: Insights from Mouse Models
S Lee, V Tucci, G Vallortigara |
Brain Sciences | 2017 |
Primary Cilia as a Possible Link between Left-Right Asymmetry and Neurodevelopmental Diseases
A Trulioff, A Ermakov, Y Malashichev |
Genes & development | 2017 |
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
HA Stessman, B Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, M Kvarnung, J Gerdts, S Trinh, N Cosemans, L Vives, J Lin, TN Turner, G Santen, C Ruivenkamp, M Kriek, A Haeringen, E Aten, K Friend, J Liebelt, C Barnett, E Haan, M Shaw, J Gecz, BM Anderlid, A Nordgren, A Lindstrand, C Schwartz, RF Kooy, G Vandeweyer, C Helsmoortel, C Romano, A Alberti, M Vinci, E Avola, S Giusto, E Courchesne, T Pramparo, K Pierce, S Nalabolu, DG Amaral, IE Scheffer, MB Delatycki, PJ Lockhart, F Hormozdiari, B Harich, A Castells-Nobau, K Xia, H Peeters, M Nordenskjöld, A Schenck, RA Bernier, EE Eichler |
Nature Genetics | 2017 |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals
M Kharbanda, DT Pilz, S Tomkins, K Chandler, A Saggar, A Fryer, V McKay, P Louro, JC Smith, J Burn, U Kini, AD Burca, DR FitzPatrick, E Kinning |
European Journal of Medical Genetics | 2017 |
A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies
G Banks, G Lassi, A Hoerder-Suabedissen, F Tinarelli, MM Simon, A Wilcox, P Lau, TN Lawson, S Johnson, A Rutman, M Sweeting, JE Chesham, AR Barnard, N Horner, H Westerberg, LB Smith, Z Molnár, MH Hastings, RA Hirst, V Tucci, PM Nolan |
Molecular Psychiatry | 2017 |
Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay: Case report and literature review
N Li, Y Xu, G Li, T Yu, R Yao, X Wang, J Wang |
Medicine | 2017 |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR
ES Panagiotou, CS Soriano, JA Poulter, EC Lord, D Dzulova, H Kondo, A Hiyoshi, BH Chung, YW Chu, CH Lai, ME Tafoya, D Karjosukarso, RW Collin, J Topping, LM Downey, M Ali, CF Inglehearn, C Toomes |
The American Journal of Human Genetics | 2017 |
Synaptic Interactome Mining Reveals p140Cap as a New Hub for PSD Proteins Involved in Psychiatric and Neurological Disorders
A Alfieri, O Sorokina, A Adrait, C Angelini, I Russo, A Morellato, M Matteoli, E Menna, EB Erba, C McLean, JD Armstrong, U Ala, JD Buxbaum, A Brusco, Y Couté, SD Rubeis, E Turco, P Defilippi |
Frontiers in molecular neuroscience | 2017 |
The autism-linked UBE3A T485A mutant E3 ubiquitin ligase activates the Wnt/β-catenin pathway by inhibiting the proteasome
JJ Yi, SR Paranjape, MP Walker, R Choudhury, JM Wolter, G Fragola, MJ Emanuele, MB Major, MJ Zylka |
The Journal of biological chemistry | 2017 |
WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene TCF4
KM Hennig, DM Fass, WN Zhao, SD Sheridan, T Fu, S Erdin, A Stortchevoi, D Lucente, JD Cody, D Sweetser, JF Gusella, ME Talkowski, SJ Haggarty |
Molecular Neuropsychiatry | 2017 |
Early postnatal vocalizations predict sociability and spatial memory in C57BL/6J mice: Individual differences in behavioral traits emerge early in development
K Yoshizaki, K Koike, R Kimura, N Osumi, K Ikeda |
PloS one | 2017 |
Human Accelerated Regions and Other Human-Specific Sequence Variations in the Context of Evolution and Their Relevance for Brain Development
A Levchenko, A Kanapin, A Samsonova, RR Gainetdinov |
Genome Biology and Evolution | 2017 |
PKD1 promotes functional synapse formation coordinated with N-cadherin in hippocampus
C Cen, LD Luo, WQ Li, G Li, NX Tian, G Zheng, DM Yin, Y Zou, Y Wang |
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2017 |
Paternal Aging Affects Behavior in Pax6 Mutant Mice: A Gene/Environment Interaction in Understanding Neurodevelopmental Disorders
K Yoshizaki, T Furuse, R Kimura, V Tucci, H Kaneda, S Wakana, N Osumi, K Ikeda |
PloS one | 2016 |
The old and new face of craniofacial research: How animal models inform human craniofacial genetic and clinical data
EV Otterloo, T Williams, KB Artinger |
Developmental Biology | 2016 |
Deletion of CTNNB1 in inhibitory circuitry contributes to autism-associated behavioral defects
F Dong, J Jiang, C McSweeney, D Zou, L Liu, Y Mao |
Human Molecular Genetics | 2016 |
A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report
A Winczewska-Wiktor, M Badura-Stronka, A Monies-Nowicka, MM Nowicki, B Steinborn, A Latos-Bieleńska, D Monies |
BMC neurology | 2016 |
Deep Genetic Connection Between Cancer and Developmental Disorders: HUMAN MUTATION
H Qi, C Dong, WK Chung, K Wang, Y Shen |
Human Mutation | 2016 |
Molecular subtyping and improved treatment of neurodevelopmental disease
HA Stessman, TN Turner, EE Eichler |
Genome Medicine | 2016 |
Wnt signaling networks in autism spectrum disorder and intellectual disability
V Kwan, BK Unda, KK Singh |
Journal of Neurodevelopmental Disorders | 2016 |
Working-for-Food Behaviors: A Preclinical Study in Prader-Willi Mutant Mice
G Lassi, S Maggi, E Balzani, I Cosentini, C Garcia-Garcia, V Tucci |
Genetics | 2016 |
Automated multi-subject fiber clustering of mouse brain using dominant sets
L Dodero, S Vascon, V Murino, A Bifone, A Gozzi, D Sona |
Frontiers in Neuroinformatics | 2015 |
Identification of Genes That Promote or Inhibit Olfactory Memory Formation in Drosophila
E Walkinshaw, Y Gai, C Farkas, D Richter, E Nicholas, K Keleman, RL Davis |
Genetics | 2015 |
N-cadherin-based adherens junction regulates the maintenance, proliferation, and differentiation of neural progenitor cells during development
Y Miyamoto, F Sakane, K Hashimoto |
Cell adhesion & migration | 2015 |
Cadherins and catenins in dendrite and synapse morphogenesis
E Seong, L Yuan, J Arikkath |
Cell adhesion & migration | 2015 |
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
L Snijders Blok, E Madsen, J Juusola, C Gilissen, D Baralle, MR Reijnders, H Venselaar, C Helsmoortel, MT Cho, A Hoischen, LE Vissers, TS Koemans, W Wissink-Lindhout, EE Eichler, C Romano, H Van Esch, C Stumpel, M Vreeburg, E Smeets, K Oberndorff, BW van Bon, M Shaw, J Gecz, E Haan, M Bienek, C Jensen, BL Loeys, A Van Dijck, AM Innes, H Racher, S Vermeer, N Di Donato, A Rump, K Tatton-Brown, MJ Parker, A Henderson, SA Lynch, A Fryer, A Ross, P Vasudevan, U Kini, R Newbury-Ecob, K Chandler, A Male, S Dijkstra, J Schieving, J Giltay, KL van Gassen, J Schuurs-Hoeijmakers, PL Tan, I Pediaditakis, SA Haas, K Retterer, P Reed, KG Monaghan, E Haverfield, M Natowicz, A Myers, MC Kruer, Q Stein, KA Strauss, KW Brigatti, K Keating, BK Burton, KH Kim, J Charrow, J Norman, A Foster-Barber, AD Kline, A Kimball, E Zackai, M Harr, J Fox, J McLaughlin, K Lindstrom, KM Haude, K van Roozendaal, H Brunner, WK Chung, RF Kooy, R Pfundt, V Kalscheuer, SG Mehta, N Katsanis, T Kleefstra |
The American Journal of Human Genetics | 2015 |
Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing
MM Simon, EM Moresco, KR Bull, S Kumar, AM Mallon, B Beutler, PK Potter |
Mammalian Genome | 2015 |
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement
MK Prasad, V Geoffroy, S Vicaire, B Jost, M Dumas, SL Gras, M Switala, B Gasse, V Laugel-Haushalter, M Paschaki, B Leheup, D Droz, A Dalstein, A Loing, B Grollemund, M Muller-Bolla, S Lopez-Cazaux, M Minoux, S Jung, F Obry, V Vogt, JL Davideau, T Davit-Beal, AS Kaiser, U Moog, B Richard, JJ Morrier, JP Duprez, S Odent, I Bailleul-Forestier, MM Rousset, L Merametdijan, A Toutain, C Joseph, F Giuliano, JC Dahlet, A Courval, ME Alloussi, S Laouina, S Soskin, N Guffon, A Dieux, B Doray, S Feierabend, E Ginglinger, B Fournier, MD la Molla, Y Alembik, C Tardieu, F Clauss, A Berdal, C Stoetzel, MC Manière, H Dollfus, A Bloch-Zupan |
Journal of medical genetics | 2015 |
Actin Out: Regulation of the Synaptic Cytoskeleton
EF Spence, SH Soderling |
The Journal of biological chemistry | 2015 |
DWI and complex brain network analysis predicts vascular cognitive impairment in spontaneous hypertensive rats undergoing executive function tests
X López-Gil, I Amat-Roldan, R Tudela, A Castañé, A Prats-Galino, AM Planas, TD Farr, G Soria |
Frontiers in aging neuroscience | 2014 |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum
A Kuechler, MH Willemsen, B Albrecht, CA Bacino, DW Bartholomew, H Bokhoven, MJ van Boogaard, N Bramswig, C Büttner, K Cremer, JC Czeschik, H Engels, K Gassen, E Graf, M Haelst, W He, JS Hogue, M Kempers, D Koolen, G Monroe, S Munnik, M Pastore, A Reis, MS Reuter, DH Tegay, J Veltman, G Visser, P Hasselt, EE Smeets, L Vissers, T Wieland, W Wissink, H Yntema, AM Zink, TM Strom, HJ Lüdecke, T Kleefstra, D Wieczorek |
Human Genetics | 2014 |
Olanzapine-induced methylation alters cadherin gene families and associated pathways implicated in psychosis
MG Melka, CA Castellani, N Rajakumar, R O’Reilly, SM Singh |
BMC neuroscience | 2014 |