A gene regulatory network explains RET-EDNRB epistasis in Hirschsprung disease von Chatterjee, Sumantra, Chakravarti, Aravinda

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Molecular Genetic Anatomy and Risk Profile of Hirschsprung’s Disease von Tilghman, Joseph M, Ling, Albee Y, Turner, Tychele N, Sosa, Maria X, Krumm, Niklas, Chatterjee, Sumantra, Kapoor, Ashish, Coe, Bradley P, Nguyen, Khanh-Dung H, Gupta, Namrata, Gabriel, Stacey, Eichler, Evan E, Berrios, Courtney, Chakravarti, Aravinda

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Profile of Mary-Claire King, 2014 Lasker-Koshland Special Achievement in Medical Science Awardee von Chakravarti, Aravinda

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The road ahead in genetics and genomics von McGuire, Amy L., Gabriel, Stacey, Tishkoff, Sarah A., Wonkam, Ambroise, Chakravarti, Aravinda, Furlong, Eileen E. M., Treutlein, Barbara, Meissner, Alexander, Chang, Howard Y., López-Bigas, Núria, Segal, Eran, Kim, Jin-Soo

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Population genetics--making sense out of sequence von Chakravarti, A

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Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease von Chatterjee, Sumantra, Kapoor, Ashish, Akiyama, Jennifer A., Auer, Dallas R., Lee, Dongwon, Gabriel, Stacey, Berrios, Courtney, Pennacchio, Len A., Chakravarti, Aravinda

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The Genome Project–Write von Boeke, Jef D., Church, George, Hessel, Andrew, Kelley, Nancy J., Arkin, Adam, Cai, Yizhi, Carlson, Rob, Chakravarti, Aravinda, Cornish, Virginia W., Holt, Liam, Isaacs, Farren J., Kuiken, Todd, Lajoie, Marc, Lessor, Tracy, Lunshof, Jeantine, Maurano, Matthew T., Mitchell, Leslie A., Rine, Jasper, Rosser, Susan, Sanjana, Neville E., Silver, Pamela A., Valle, David, Wang, Harris, Way, Jeffrey C., Yang, Luhan

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MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension von Nandakumar, Priyanka, Tin, Adrienne, Grove, Megan L, Ma, Jianzhong, Boerwinkle, Eric, Coresh, Josef, Chakravarti, Aravinda

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Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer von Meyer, Kerstin B, Maia, Ana-Teresa, O'Reilly, Martin, Teschendorff, Andrew E, Chin, Suet-Feung, Caldas, Carlos, Ponder, Bruce A J

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Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms von Kapoor, Ashish, Jiang, Qian, Chatterjee, Sumantra, Chakraborty, Prakash, Sosa, Maria X, Berrios, Courtney, Chakravarti, Aravinda

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Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung disease von Chatterjee, Sumantra, Nandakumar, Priyanka, Auer, Dallas R., Gabriel, Stacey B., Chakravarti, Aravinda

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Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure von Lee, Dongwon, Han, Seong Kyu, Yaacov, Or, Berk-Rauch, Hanna, Mathiyalagan, Prabhu, Ganesh, Santhi K., Chakravarti, Aravinda

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RET enhancer haplotype-dependent remodeling of the human fetal gut development program von Chatterjee, Sumantra, Fries, Lauren E, Yaacov, Or, Hu, Nan, Berk-Rauch, Hanna E, Chakravarti, Aravinda

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A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism von 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

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Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC) von Salfati, Elias, Morrison, Alanna C, Boerwinkle, Eric, Chakravarti, Aravinda

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Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits von Scuteri, Angelo, Sanna, Serena, Chen, Wei-Min, Uda, Manuela, Albai, Giuseppe, Strait, James, Najjar, Samer, Nagaraja, Ramaiah, Orrú, Marco, Usala, Gianluca, Dei, Mariano, Lai, Sandra, Maschio, Andrea, Busonero, Fabio, Mulas, Antonella, Ehret, Georg B, Fink, Ashley A, Weder, Alan B, Cooper, Richard S, Galan, Pilar, Chakravarti, Aravinda, Schlessinger, David, Cao, Antonio, Lakatta, Edward, Abecasis, Gonçalo R

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Magnitude of Mendelian versus complex inheritance of rare disorders von Chakravarti, Aravinda

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Association between Microdeletion and Microduplication at 16p11.2 and Autism von Weiss, Lauren A, Shen, Yiping, Korn, Joshua M, Arking, Dan E, Miller, David T, Fossdal, Ragnheidur, Saemundsen, Evald, Stefansson, Hreinn, Stefansson, Kari, Ferreira, Manuel A.R, Green, Todd, Platt, Orah S, Ruderfer, Douglas M, Walsh, Christopher A, Altshuler, David, Chakravarti, Aravinda, Tanzi, Rudolph E, Santangelo, Susan L, Gusella, James F, Sklar, Pamela, Wu, Bai-Lin, Daly, Mark J

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Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases von Lu, Xinyan, Shaw, Chad A, Patel, Ankita, Li, Jiangzhen, Cooper, M Lance, Wells, William R, Sullivan, Cathy M, Sahoo, Trilochan, Yatsenko, Svetlana A, Bacino, Carlos A, Stankiewicz, Pawel, Ou, Zhishu, Chinault, A Craig, Beaudet, Arthur L, Lupski, James R, Cheung, Sau W, Ward, Patricia A

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Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model von Alves, Maria M., Sribudiani, Yunia, Brouwer, Rutger W.W., Amiel, Jeanne, Antiñolo, Guillermo, Borrego, Salud, Ceccherini, Isabella, Chakravarti, Aravinda, Fernández, Raquel M., Garcia-Barcelo, Maria-Mercè, Griseri, Paola, Lyonnet, Stanislas, Tam, Paul K., van IJcken, Wilfred F.J., Eggen, Bart J.L., te Meerman, Gerard J., Hofstra, Robert M.W.

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