A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
Arking, Dan E., Cutler, David J., Brune, Camille W., Teslovich, Tanya M., West, Kristen, Ikeda, Morna, Rea, Alexis, Guy, Moltu, Lin, Shin, Cook, Edwin H., Chakravarti, Aravinda
Published in American journal of human genetics (01.01.2008)
Published in American journal of human genetics (01.01.2008)
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A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
Chakravarti, Aravinda, Arking, Dan E, Pfeufer, Arne, Post, Wendy, Kao, W H Linda, Newton-Cheh, Christopher, Ikeda, Morna, West, Kristen, Kashuk, Carl, Akyol, Mahmut, Perz, Siegfried, Jalilzadeh, Shapour, Illig, Thomas, Gieger, Christian, Guo, Chao-Yu, Larson, Martin G, Wichmann, H Erich, Marbán, Eduardo, O'Donnell, Christopher J, Hirschhorn, Joel N, Kääb, Stefan, Spooner, Peter M, Meitinger, Thomas
Published in Nature genetics (01.06.2006)
Published in Nature genetics (01.06.2006)
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Genomic alterations in cultured human embryonic stem cells
Rao, Mahendra, Chakravarti, Aravinda, Maitra, Anirban, Arking, Dan E, Shivapurkar, Narayan, Ikeda, Morna, Stastny, Victor, Kassauei, Keyaunoosh, Sui, Guoping, Cutler, David J, Liu, Ying, Brimble, Sandii N, Noaksson, Karin, Hyllner, Johan, Schulz, Thomas C, Zeng, Xianmin, Freed, William J, Crook, Jeremy, Abraham, Suman, Colman, Alan, Sartipy, Peter, Matsui, Sei-Ichi, Carpenter, Melissa, Gazdar, Adi F
Published in Nature genetics (01.10.2005)
Published in Nature genetics (01.10.2005)
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Multiple Genes for Essential-Hypertension Susceptibility on Chromosome 1q
Chang, Yen-Pei Christy, Liu, Xin, Kim, James Dae Ok, Ikeda, Morna A., Layton, Marnie R., Weder, Alan B., Cooper, Richard S., Kardia, Sharon L.R., Rao, D.C., Hunt, Steve C., Luke, Amy, Boerwinkle, Eric, Chakravarti, Aravinda
Published in American journal of human genetics (01.02.2007)
Published in American journal of human genetics (01.02.2007)
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Robust regression analysis of copy number variation data based on a univariate score
Satten, Glen A, Allen, Andrew S, Ikeda, Morna, Mulle, Jennifer G, Warren, Stephen T
Published in PloS one (07.02.2014)
Published in PloS one (07.02.2014)
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Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program
Zhu, Xiaofeng, Yan, Denise, Cooper, Richard S, Luke, Amy, Ikeda, Morna A, Chang, Yen-Pei C, Weder, Alan, Chakravarti, Aravinda
Published in Genome research (01.02.2003)
Published in Genome research (01.02.2003)
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Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: A case report and review of the literature
Coffee, Bradford, Ikeda, Morna, Budimirovic, Dejan B., Hjelm, Lawrence N., Kaufmann, Walter E., Warren, Stephen T.
Published in American journal of medical genetics. Part A (15.05.2008)
Published in American journal of medical genetics. Part A (15.05.2008)
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Multiple Genes for Essential-Hypertension Susceptibility on Chromosome lq
Yen-Pei, Christy Chang, Liu, Xin, Kim, James Dae Ok, Ikeda, Morna A
Published in American journal of human genetics (01.02.2007)
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Published in American journal of human genetics (01.02.2007)
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A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism. Commentary
STEPHAN, Dietrich A, ARKING, Dan E, COOK, Edwin H, CHAKRAVARTI, Aravinda, CUTLER, David J, BRUNE, Camille W, TESLOVICH, Tanya M, WEST, Kristen, IKEDA, Morna, REA, Alexis, GUY, Moltu, LIN, Shin
Published in American journal of human genetics (2008)
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Published in American journal of human genetics (2008)
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