Basic concepts of medical genetics. Formal genetics, part 4

Autor: Mohammad Saad Zaghloul Salem

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 15, Iss 4, Pp 409-415 (2014)

Externí odkaz: https://doaj.org/article/b15a46a5c228438a95e0ce20cbcfb4dd

Diametrical diseases reflect evolutionary-genetic tradeoffs

Autor: Crespi, Bernard J., Go, Matthew C.

Publikováno v: Evolution, Medicine, and Public Health

Tradeoffs centrally mediate the expression of human adaptations. We propose that tradeoffs also influence the prevalence and forms of human maladaptation manifest in disease. By this logic, increased risk for one set of diseases commonly engenders de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8b4ead3d6633277984b4205ac7add33c
http://europepmc.org/articles/PMC4600345

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome-wide association study of both common and rare variants

Autor: Yang, Li, Neale, Benjamin M., Liu, Lu, Lee, S. Hong, Wray, Naomi R., Ji, Ning, Li, Haimei, Qian, Qiujin, Wang, Dongliang, Li, Jun, Faraone, Stephen V., Wang, Yufeng, Doyle, Alysa, Reif, Andreas, Rothenberger, Aribert, Franke, Barbara, Sonuga-Barke, Edmund J.S., Steinhausen, Hans-Christoph, Buitelaar, Jan K, Kuntsi, Jonna, Biederman, Joseph, Lesch, Klaus Peter, Kent, Lindsey, Asherson, Philip, Oades, Robert D., Loo, Sandra K., Nelson, Stanley F., Smalley, Susan L., Banaschewski, Tobias, Vasquez, Alejandro Arias, Todorov, Alexandre, Charach, A., Miranda, Ana, Warnke, Andreas, Thapar, Anita, Cormand, B., Freitag, Christine, Mick, Eric, Mulas, Fernando, Middleton, Frank, Hakonarson, Hakon, Pálmason, Haukur, Schäfer, Helmut, Roeyers, Herbert, McGough, James J., Romanos, Jasmin, Crosbie, J., Meyer, Jobst, Ramos-Qiroga, J.A., Sergeant, Joseph A, Elia, Josephine, Langely, Kate, Nisenbaum, Laura, Romanos, Marcel, Daly, Mark, Ribases, M., Gill, Michael, O’Donovan, Michael, Owen, Michael, Casas, M., Bayes, M., Lambregts-Rommelse, Nanda, Williams, Nigel, Holmans, Peter, Anney, Richard J.L., Ebstein, Richard, Schachar, R., Medland, Sarah E., Ripke, Stephan, Walitza, Susanne, Nguyen, Thuy Trang, Renner, Tobias J., Hu, Xiaolan

Publikováno v: American Journal of Medical Genetics Part B-neuropsychiatric Genetics, 162B(5), 419-430. Wiley
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 162B, 419-30
American Journal of Medical Genetics. Part B : Neuropsychiatric Genetics, 162B, 5, pp. 419-30

Attention-deficit hyperactivity disorder (ADHD) is a complex polygenic disorder. This study aimed to discover common and rare DNA variants associated with ADHD in a large homogeneous Han Chinese ADHD case-control sample. The sample comprised 1,040 ca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8716900432f90604e2c87cec43f69b6
https://doi.org/10.1002/ajmg.b.32169

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