De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects
Priest, James R, Osoegawa, Kazutoyo, Mohammed, Nebil, Nanda, Vivek, Kundu, Ramendra, Schultz, Kathleen, Lammer, Edward J, Girirajan, Santhosh, Scheetz, Todd, Waggott, Daryl, Haddad, Francois, Reddy, Sushma, Bernstein, Daniel, Burns, Trudy, Steimle, Jeffrey D, Yang, Xinan H, Moskowitz, Ivan P, Hurles, Matthew, Lifton, Richard P, Nickerson, Debbie, Bamshad, Michael, Eichler, Evan E, Mital, Seema, Sheffield, Val, Quertermous, Thomas, Gelb, Bruce D, Portman, Michael, Ashley, Euan A
Published in PLoS genetics (08.04.2016)
Published in PLoS genetics (08.04.2016)
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Diacylglycerol Kinase K Variants Impact Hypospadias in a California Study Population
Carmichael, Suzan L, Mohammed, Nebil, Ma, Chen, Iovannisci, Dave, Choudhry, Shweta, Baskin, Larry S, Witte, John S, Shaw, Gary M, Lammer, Edward J
Published in The Journal of urology (01.01.2013)
Published in The Journal of urology (01.01.2013)
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Apolipoprotein E Epsilon 4 Genotype, Mild Traumatic Brain Injury, and the Development of Chronic Traumatic Encephalopathy
Deng, Hansen, Ordaz, Angel, Upadhyayula, Pavan S, Gillis-Buck, Eva M, Suen, Catherine G, Melhado, Caroline G, Mohammed, Nebil, Lam, Troy, Yue, John K
Published in Medical sciences (Basel) (14.09.2018)
Published in Medical sciences (Basel) (14.09.2018)
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Haploinsufficiency of insulin gene enhancer protein 1 (ISL1) is associated with d‐transposition of the great arteries
Osoegawa, Kazutoyo, Schultz, Kathleen, Yun, Kenneth, Mohammed, Nebil, Shaw, Gary M., Lammer, Edward J.
Published in Molecular genetics & genomic medicine (01.07.2014)
Published in Molecular genetics & genomic medicine (01.07.2014)
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