Brett Abrahams, PhD
Advances in autism genetics: on the threshold of a new neurobiology
BS Abrahams, DH Geschwind
Nature reviews genetics 9 (5), 341-355, 2008
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
Common genetic variants on 5p14.1 associate with autism spectrum disorders
K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ...
Nature 459 (7246), 528-533, 2009
Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits
O Peñagarikano, BS Abrahams, EI Herman, KD Winden, A Gdalyahu, ...
Cell 147 (1), 235-246, 2011
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
M Alarcón, BS Abrahams, JL Stone, JA Duvall, JV Perederiy, JM Bomar, ...
The American Journal of Human Genetics 82 (1), 150-159, 2008
A functional genetic link between distinct developmental language disorders
SC Vernes, DF Newbury, BS Abrahams, L Winchester, J Nicod, M Groszer, ...
New England Journal of Medicine 359 (22), 2337-2345, 2008
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
BS Abrahams, DE Arking, DB Campbell, HC Mefford, EM Morrow, ...
Molecular autism 4, 1-3, 2013
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders
B Bakkaloglu, BJ O'Roak, A Louvi, AR Gupta, JF Abelson, TM Morgan, ...
The American Journal of Human Genetics 82 (1), 165-173, 2008
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
C Francks, S Maegawa, J Laurén, BS Abrahams, A Velayos-Baeza, ...
Molecular psychiatry 12 (12), 1129-1139, 2007
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
M Bucan, BS Abrahams, K Wang, JT Glessner, EI Herman, LI Sonnenblick, ...
PLoS genetics 5 (6), e1000536, 2009
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2
AA Scott-Van Zeeland, BS Abrahams, AI Alvarez-Retuerto, LI Sonnenblick, ...
Science translational medicine 2 (56), 56ra80-56ra80, 2010
Connecting genes to brain in the autism spectrum disorders
BS Abrahams, DH Geschwind
Archives of neurology 67 (4), 395-399, 2010
Genome-wide analyses of human perisylvian cerebral cortical patterning
BS Abrahams, D Tentler, JV Perederiy, MC Oldham, G Coppola, ...
Proceedings of the National Academy of Sciences 104 (45), 17849-17854, 2007
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ...
Human genetics 131, 565-579, 2012
Neuronal density in the human retinal ganglion cell layer from 16–77 years
A Harman, B Abrahams, S Moore, R Hoskins
The Anatomical Record: An Official Publication of the American Association …, 2000
Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder
ER Berko, M Suzuki, F Beren, C Lemetre, CM Alaimo, RB Calder, ...
PLoS genetics 10 (5), e1004402, 2014
Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR
A Oguro-Ando, C Rosensweig, E Herman, Y Nishimura, D Werling, ...
Molecular psychiatry 20 (9), 1069-1078, 2015
The disruption of Celf6, a gene identified by translational profiling of serotonergic neurons, results in autism-related behaviors
JD Dougherty, SE Maloney, DF Wozniak, MA Rieger, L Sonnenblick, ...
Journal of Neuroscience 33 (7), 2732-2753, 2013
Aralar sequesters GABA into hyperactive mitochondria, causing social behavior deficits
AK Kanellopoulos, V Mariano, M Spinazzi, YJ Woo, C McLean, U Pech, ...
Cell 180 (6), 1178-1197. e20, 2020
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