Brett S. Abrahams - Concepedia

Author

Brett S. Abrahams

Also Known As

Abrahams, Brett S., B S Abrahams, B. Abrahams, B. S. Abrahams, B.S Abrahams, B.S. Abrahams, Brett Abrahams, Brett S Abrahams, Brett S. Abrahams, Brett S. Abrahams

Publications

12.2K

Citations

H-Index

Concepts

All Affiliations

University of California, Los Angeles Albert Einstein College of Medicine Center for Autism and Related Disorders Icahn School of Medicine at Mount Sinai University of British Columbia

About

Brett S. Abrahams is an author at University of California, Los Angeles specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	20	2.9K
2	Social Sciences	11	11	1.5K
3	Natural Sciences	4	4	957
4	Health Sciences	1	1	200
5	Behavioral Sciences	1	1	110

Brett S. Abrahams

Publications

10.1K

Citations

H-Index

Page 1

	Year	Citations
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Absence of CNTNAP2 Leads to Epilepsy, Neuronal Migration Abnormalities, and Core Autism-Related Deficits Olga Peñagarikano, Brett S. Abrahams, Edward I. Herman, Cell Neurodevelopmental DisordersDevelopmental BiologyMolecular NeuroscienceSyndromic AutismNeuroanatomy	2011	1.1K
Common genetic variants on 5p14.1 associate with autism spectrum disorders Kai Wang, Haitao Zhang, Deqiong Ma, Nature Neurodevelopmental DisordersSyndromic AutismGenetic DisorderGeneticsPsychiatric Genetics	2009	968
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs) Brett S. Abrahams, Dan E. Arking, Heather C. Mefford, Molecular Autism	2013	895
Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene Maricela Alarcón, Brett S. Abrahams, Jennifer Stone, The American Journal of Human Genetics Autism-susceptibility GeneSyndromic AutismNatural SciencesGeneticsPsychiatric Genetics	2008	819
A Functional Genetic Link between Distinct Developmental Language Disorders Sonja C. Vernes, Dianne F. Newbury, Brett S. Abrahams, New England Journal of Medicine	2008	684
A genome-wide scan for common alleles affecting risk for autism Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2010	585
Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders Betul Bakkaloglu, Brian J. O’Roak, Angeliki Louvi, The American Journal of Human Genetics Autism Spectrum DisordersSyndromic AutismGeneticsGenetic DisorderMolecular Biology	2008	537
Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes Maja Bućan, Brett S. Abrahams, Kai Wang, PLoS Genetics	2009	432
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia Clyde Francks, Shinji Maegawa, Juha Laurén, Molecular Psychiatry ChromatinPsychiatryGenetic DisorderGeneticsPsychiatric Genetics	2007	357

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