Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Gerard D. O'Conner"'
Autor:
Chantal Depondt, Kenneth D. Cronin, Gerard D. O'Conner, Saurabh R. Sinha, James O. McNamara, Rodney A. Radtke, Jessica M. Maia, Krishna Chinthapalli, Sanjay M. Sisodiya, Ram S. Puranam, Nicole M. Walley, Norman Delanty, Erin L. Heinzen, Anna C. Need, Dongliang Ge, Kevin V. Shianna, Mark McCormack, Ruth Ottman, David Goldstein, Mohamad A. Mikati, Min He, William Gallentine, Elizabeth T. Cirulli, Elizabeth K. Ruzzo, Qian Zhao, Gianpiero L. Cavalleri, C. Ryan Campbell, Linda K. Hong, Aatif M. Husain, Curtis Gumbs
Publikováno v:
American journal of human genetics, 91 (2
Idiopathic generalized epilepsy (IGE) is a complex disease with high heritability, but little is known about its genetic architecture. Rare copy-number variants have been found to explain nearly 3% of individuals with IGE; however, it remains unclear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dddd2f81ce3476b8cf753817fc9930d6
https://europepmc.org/articles/PMC3415540/
https://europepmc.org/articles/PMC3415540/
Autor:
Erin L. Heinzen, Mark McCormack, Massimo Pandolfo, Gerard D. O'Conner, Kevin V. Shianna, Chantal Depondt, Gianpiero L. Cavalleri, Dalia Kasperavičiūtė, Elijah Chaila, Norman Delanty, Thomas J. Urban, Sanjay M. Sisodiya, Rodney A. Radtke, Nicole M. Walley
Publikováno v:
Pharmacogenomics. 13(4)
Aims: An association between carbamazepine-induced hypersensitivity and HLA-A*3101 has been reported in populations of both European and Asian descent. We aimed to investigate HLA-A*3101 and other common variants across the genome as markers for cuta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ee543503b42ab60874c39247b91b20d
https://pubmed.ncbi.nlm.nih.gov/22379998
https://pubmed.ncbi.nlm.nih.gov/22379998
