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Almajano J, Bragin A, Trachtenberg JT, Peles E, Geschwind DH. (2011). Absence of CNTNAP2 in mice leads to epileptic seizures, ASD-related behavior and atypical neuronal network functioning. Cell. 147(1):235-46. [PMID: 21962519]
The Autism Genome Project Consortium. (2011). A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics. Oct 14. [PMID: 21996756]
Abrahams BS. (2011). Syndromic vs. Idiopathic ASCs. Autism Spectrum Conditions: International Experts answer your Questions on Autism, Asperger syndrome and PDD-NOS. Eds. Hallmayer and Boelte. Hogrefe Press.
Abrahams BS. (2011). Many roads to the Autism Spectrum Disorders. Neuropsychology of Autism. Ed. D. Fein. Oxford Univ Press. ISBN13: 9780195378313
The Autism Genome Project Consortium. (2011). Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders. Eur J Hum Genet. 19(10):1082-9. [PMID: 21522181]
Scott AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie J, Ghahremani D, Mumford J, Poldrack RA, Dapretto M, Geschwind DH, Bookheimer SY. (2010). Altered Functional Connectivity within the frontal lobe of brain associated with Variation in CNTNAP2. Science Translational Medicine. 3;2(56):56ra80. [PMID: 21048216]
The Autism Genome Project Consortium. (2010). A genomewide scan for common alleles affecting risk for autism. Hum Mol Genet. 19(20):4072-82. [PMID: 20663923]
The Autism Genome Project Consortium. (2010). Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 15;466(7304):368-72. [PMID: 20531469]
Panaitof SC, Abrahams BS, Dong H, Geschwind DH, White SA. (2010). Language-related Cntnap2 gene is differentially expressed in sexually dimorphic song nuclei essential for vocal learning in songbirds. Journal of Comparative Neurology. 518(11):1995-2018. [PMID: 20394055]
Abrahams BS, & Geschwind DH, (2010). Connecting genes to brain in the autisms. Arch. Neurol. 67(4): 395-399. [PMID: 20385903]
Abrahams BS, & Geschwind DH. (2010). Genetics of Autism. Human Genetics: Problems & Approaches. Eds. Speicher, Antonarakiso, and Motulsky. 4th Ed. Springer-Verlag. [ISBN: 9783540376538]
Bucan M*, Abrahams BS*, Wang K*,, thirty-one additional authors, Geschwind DH, and Hakonarson H. (2009). Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. *Contributed Equally. PLoS Genetics. 5(6): e1000536. [PMID: 19557195]
Wang K*, Zhang H*, Ma DQ*, Bucan M, Glessner JT, Abrahams BS, thirty-nine additional authors, Geschwind DH, Pericak-Vance MA, Schellenberg GD, and Hakonarson H. (2009). Common genetic variation is associated with susceptibility to autism spectrum disorders. *Contributed Equally. Nature. 459(7246):528-33 [PMID: 19404256]
Abrahams BS, and Geschwind DH. (2008). Advances in autism genetics: on the threshold of a new neurobiology. Nature Reviews Genetics. 9:341-355 [PMID: 18414403]
Vernes SC, Newbury DF, Abrahams BS, Winchester L, Nicod J, Groszer M, Alarcón M, Oliver PL, Davies KE, Geschwind DH, Monaco AP, Fisher, SE. (2008). A functional genetic link between distinct developmental language disorders. New England Journal of Medicine. 359(22):2337-2345 [PMID: 18987363].
Alarcón, M,*, Abrahams BS*, Stone SL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH. (2008). Linkage, association and gene expression analyses identify CNTNAP2 as an autism susceptibility gene. *Contributed Equally. American Journal of Human Genetics. 82:150-159. [PMID: 18179893].
Bakkaloglu B*, O’Roak BJ*, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek G, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW (2008). Molecular cytogenetic analysis and re-sequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorder. *Contributed Equally. American Journal of Human Genetics. 82:165-173. [PMID: 18179895].
Kumar R.A, McGhee KA, Leach S, Bonaguro R, Maclean A, Aguirre-Hennandez R, Abrahams BS, Coccarro EF, Hodgins S, Turecki G, Condon, A, Muir W, Brooks-Wilson AR, Blackwood D, Simpson EM. (2008). Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing. American Journal of Medical Genetics. 5;147B(6):880-9. [PMID: 18205168].
Abrahams BS, Tentler D*, Perederiy JV*, Oldham MC, Coppola G, Geschwind DH. (2007). Genomewide analyses of human peri-sylvian cerebral cortical patterning. *Contributed Equally. Proceedings of the National Academy of Sciences. 104:17849-54. [PMID: 17978184].