The Distribution of Human Genetic Diversity: A Comparison of Mitochondrial, Autosomal, and Y-Chromosome Data von Jorde, L.B., Watkins, W.S., Bamshad, M.J., Dixon, M.E., Ricker, C.E., Seielstad, M.T., Batzer, M.A.

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A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family von Khan, S., Ansar, M., Khan, A. K., Shah, K., Muhammad, N., Shahzad, S., Nickerson, D.A., Bamshad, M.J., Santos‐Cortez, R.L.P., Leal, S.M., Ahmad, W.

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Patterns of Ancestral Human Diversity: An Analysis of Alu-Insertion and Restriction-Site Polymorphisms von Watkins, W.S., Ricker, C.E., Bamshad, M.J., Carroll, M.L., Nguyen, S.V., Batzer, M.A., Harpending, H.C., Rogers, A.R., Jorde, L.B.

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Population genomics : a bridge from evolutionary history to genetic medicine von JORDE, L. B, WATKINS, W. S, BAMSHAD, M. J

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DNA Sequence Variation in a 3.7-kb Noncoding Sequence 5′ of the CYP1A2 Gene: Implications for Human Population History and Natural Selection von Wooding, S.P., Watkins, W.S., Bamshad, M.J., Dunn, D.M., Weiss, R.B., Jorde, L.B.

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Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome von Przylepa, Kelly A, Paznekas, William, Zhang, Minghuang, Golabi, Mahin, Bias, Wilma, Bamshad, Michael J, Carey, John C, Hall, Bryan D, Stevenson, Roger, Orlow, Seth J, Cohen Jr, M. Michael, Jabs, Ethylin Wang

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Origins and affinities of modern humans : a comparison of mitochondrial and nuclear genetic data von JORDE, L. B, BAMSHAD, M. J, WATKINS, W. S, ZENGER, R, FRALEY, A. E, KRAKOWIAK, P. A, CARPENTER, K. D, SOODYALL, H, JENKINS, T, ROGERS, A. R

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Variants regulating ZBTB4 are associated with age‐at‐onset of Alzheimer's disease von Blue, E. E., Yu, C.‐E., Thornton, T. A., Chapman, N. H., Kernfeld, E., Jiang, N., Shively, K. M., Buckingham, K. J., Marvin, C. T., Bamshad, M. J., Bird, T. D., Wijsman, E. M.

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Crohn's Disease and Genetic Hitchhiking at IBD5 von Huff, Chad D., Witherspoon, David J., Zhang, Yuhua, Gatenbee, Chandler, Denson, Lee A., Kugathasan, Subra, Hakonarson, Hakon, Whiting, April, Davis, Chadwick T., Wu, Wilfred, Xing, Jinchuan, Watkins, W. Scott, Bamshad, Michael J., Bradfield, Jonathan P., Bulayeva, Kazima, Simonson, Tatum S., Jorde, Lynn B., Guthery, Stephen L.

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A Novel Skeletal Dysplasia with Developmental Delay and Acanthosis Nigricans Is Caused by a Lys650Met Mutation in the Fibroblast Growth Factor Receptor 3 Gene von Tavormina, Patricia L., Bellus, Gary A., Webster, Melanie K., Bamshad, Michael J., Fraley, Alexander E., McIntosh, Iain, Szabo, Jinny, Jiang, Wen, Jabs, Ethylin W., Wilcox, William R., Wasmuth, John J., Donoghue, Daniel J., Thompson, Leslie M., Francomano, Clair A.

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The role of CDHR3 in susceptibility to otitis media von Hirsch, Scott D., Elling, Christina L., Bootpetch, Tori C., Scholes, Melissa A., Hafrén, Lena, Streubel, Sven-Olrik, Pine, Harold S., Wine, Todd M., Szeremeta, Wasyl, Prager, Jeremy D., Einarsdottir, Elisabet, Yousaf, Ayesha, Baschal, Erin E., Rehman, Sakina, Bamshad, Michael J., Nickerson, Deborah A., Riazuddin, Saima, Leal, Suzanne M., Ahmed, Zubair M., Yoon, Patricia J., Kere, Juha, Chan, Kenny H., Mattila, Petri S., Friedman, Norman R., Chonmaitree, Tasnee, Frank, Daniel N., Ryan, Allen F., Santos-Cortez, Regie Lyn P.

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Association of two functional polymorphisms in the CCR5 gene with juvenile rheumatoid arthritis von Prahalad, S, Bohnsack, J F, Jorde, L B, Whiting, A, Clifford, B, Dunn, D, Weiss, R, Moroldo, M, Thompson, S D, Glass, D N, Bamshad, M J

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Female gene flow stratifies Hindu castes von Bamshad, Michael J, Watkins, W. Scott, Dixon, Mary E, Jorde, Lynn B, Rao, B. Bhaskara, Naidu, J. M, Prasad, B. V. Ravi, Rasanayagam, Arani, Hammer, Mike F

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Novel NKX2.1 mutation associated with hypothyroidism and lethal respiratory failure in a full-term neonate von Gillett, E S, Deutsch, G H, Bamshad, M J, McAdams, R M, Mann, P C

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A novel missense variant in the PNPLA1 gene underlies congenital ichthyosis in three consanguineous families von Ahmad, F., Ansar, M., Mehmood, S., Izoduwa, A., Lee, K., Nasir, A., Abrar, M., Ullah, A., Aziz, A., Smith, J.D., Shendure, J., Bamshad, M.J., Nicekrson, D.A., Santos-Cortez, R.L.P., Leal, S.M., Ahmad, W.

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Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages von Kivisild, T., Bamshad, M.J., Kaldma, K., Metspalu, M., Metspalu, E., Reidla, M., Laos, S., Parik, J., Watkins, W.S., Dixon, M.E., Papiha, S.S., Mastana, S.S., Mir, M.R., Ferak, V., Villems, R.

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Diversity and Divergence Among the Tribal Populations of India von Watkins, W.S., Prasad, B. V. R., Naidu, J. M., Rao, B. B., Bhanu, B. A., Ramachandran, B., Das, P. K., Gai, P. B., Reddy, P. C., Reddy, P. G., Sethuraman, M., Bamshad, M. J., Jorde, L. B.

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Massively parallel sequencing and rare disease von Ng, Sarah B., Nickerson, Deborah A., Bamshad, Michael J., Shendure, Jay

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Exome sequencing as a tool for Mendelian disease gene discovery von Bamshad, Michael J, Shendure, Jay, Ng, Sarah B, Bigham, Abigail W, Tabor, Holly K, Emond, Mary J, Nickerson, Deborah A

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De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay von Chong, Jessica X., McMillin, Margaret J., Shively, Kathryn M., Beck, Anita E., Marvin, Colby T., Armenteros, Jose R., Buckingham, Kati J., Nkinsi, Naomi T., Boyle, Evan A., Berry, Margaret N., Bocian, Maureen, Foulds, Nicola, Uzielli, Maria Luisa Giovannucci, Haldeman-Englert, Chad, Hennekam, Raoul C.M., Kaplan, Paige, Kline, Antonie D., Mercer, Catherine L., Nowaczyk, Malgorzata J.M., Klein Wassink-Ruiter, Jolien S., McPherson, Elizabeth W., Moreno, Regina A., Scheuerle, Angela E., Shashi, Vandana, Stevens, Cathy A., Carey, John C., Monteil, Arnaud, Lory, Philippe, Tabor, Holly K., Smith, Joshua D., Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., Shendure, Jay, Nickerson, Deborah A., Abecasis, Gonçalo R., Anderson, Peter, Blue, Elizabeth Marchani, Annable, Marcus, Browning, Brian L., Buckingham, Kati J., Chen, Christina, Chin, Jennifer, Chong, Jessica X., Cooper, Gregory M., Davis, Colleen P., Frazar, Christopher, Harrell, Tanya M., He, Zongxiao, Jain, Preti, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Jun, Goo, Kircher, Martin, Kolar, Tom, Krauter, Stephanie A., Krumm, Niklas, Leal, Suzanne M., Luksic, Daniel, Marvin, Colby T., McMillin, Margaret J., McGee, Sean, O’Reilly, Patrick, Paeper, Bryan, Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Poel, Christa, Reinier, Frederic, Robertson, Peggy D., Santos-Cortez, Regie, Shaffer, Tristan, Shephard, Cindy, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Staples, Jeffrey C., Tabor, Holly K., Tackett, Monica, Underwood, Jason G., Wegener, Marc, Wang, Gao, Wheeler, Marsha M., Yi, Qian, Bamshad, Michael J.

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