Search Results - (Author, Cooperation:K. E. Samocha)
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1B. M. Neale ; Y. Kou ; L. Liu ; A. Ma'ayan ; K. E. Samocha ; A. Sabo ; C. F. Lin ; C. Stevens ; L. S. Wang ; V. Makarov ; P. Polak ; S. Yoon ; J. Maguire ; E. L. Crawford ; N. G. Campbell ; E. T. Geller ; O. Valladares ; C. Schafer ; H. Liu ; T. Zhao ; G. Cai ; J. Lihm ; R. Dannenfelser ; O. Jabado ; Z. Peralta ; U. Nagaswamy ; D. Muzny ; J. G. Reid ; I. Newsham ; Y. Wu ; L. Lewis ; Y. Han ; B. F. Voight ; E. Lim ; E. Rossin ; A. Kirby ; J. Flannick ; M. Fromer ; K. Shakir ; T. Fennell ; K. Garimella ; E. Banks ; R. Poplin ; S. Gabriel ; M. DePristo ; J. R. Wimbish ; B. E. Boone ; S. E. Levy ; C. Betancur ; S. Sunyaev ; E. Boerwinkle ; J. D. Buxbaum ; E. H. Cook, Jr. ; B. Devlin ; R. A. Gibbs ; K. Roeder ; G. D. Schellenberg ; J. S. Sutcliffe ; M. J. Daly
Nature Publishing Group (NPG)
Published 2012Staff ViewPublication Date: 2012-04-13Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: Autistic Disorder/*genetics ; Case-Control Studies ; DNA-Binding Proteins/*genetics ; Exome/genetics ; Exons/*genetics ; Family Health ; Genetic Predisposition to Disease/*genetics ; Humans ; Models, Genetic ; Multifactorial Inheritance/genetics ; Mutation/*genetics ; Phenotype ; Poisson Distribution ; Protein Interaction Maps ; Transcription Factors/*geneticsPublished by: -
2De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomaliesJ. Homsy ; S. Zaidi ; Y. Shen ; J. S. Ware ; K. E. Samocha ; K. J. Karczewski ; S. R. DePalma ; D. McKean ; H. Wakimoto ; J. Gorham ; S. C. Jin ; J. Deanfield ; A. Giardini ; G. A. Porter, Jr. ; R. Kim ; K. Bilguvar ; F. Lopez-Giraldez ; I. Tikhonova ; S. Mane ; A. Romano-Adesman ; H. Qi ; B. Vardarajan ; L. Ma ; M. Daly ; A. E. Roberts ; M. W. Russell ; S. Mital ; J. W. Newburger ; J. W. Gaynor ; R. E. Breitbart ; I. Iossifov ; M. Ronemus ; S. J. Sanders ; J. R. Kaltman ; J. G. Seidman ; M. Brueckner ; B. D. Gelb ; E. Goldmuntz ; R. P. Lifton ; C. E. Seidman ; W. K. Chung
American Association for the Advancement of Science (AAAS)
Published 2016Staff ViewPublication Date: 2016-01-20Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Brain/abnormalities/metabolism ; Child ; Congenital Abnormalities/genetics ; Exome/genetics ; Heart Defects, Congenital/*diagnosis/*genetics ; Humans ; Mutation ; Nervous System Malformations/*genetics ; Neurogenesis/*genetics ; Prognosis ; RNA Splicing/genetics ; RNA, Messenger/genetics ; RNA-Binding Proteins/genetics ; Repressor Proteins/genetics ; Transcription, GeneticPublished by: