Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Go, Rodney CP"'
Autor:
Ding Lili, Wiener Howard, Abebe Tilahun, Altaye Mekbib, Go Rodney CP, Kercsmar Carolyn, Grabowski Greg, Martin Lisa J, Khurana Hershey Gurjit K, Chakorborty Ranajit, Baye Tesfaye M
Publikováno v:
BMC Genomics, Vol 12, Iss 1, p 622 (2011)
Abstract Background Admixture mapping is a powerful gene mapping approach for an admixed population formed from ancestral populations with different allele frequencies. The power of this method relies on the ability of ancestry informative markers (A
Externí odkaz:
https://doaj.org/article/173181069cc2453e9e92b49e9c6abb98
Autor:
Hollowell William W, Barton Ellen H, Acton Ronald T, Dreibelbis Amy L, Go Rodney CP, Barton James C
Publikováno v:
BMC Cancer, Vol 4, Iss 1, p 47 (2004)
Abstract Background We sought to evaluate the hypothesis that the high incidence of cutaneous melanoma in white persons in central Alabama is associated with a predominance of Irish and Scots descent. Methods Frequencies of country of ancestry report
Externí odkaz:
https://doaj.org/article/5b4d7b8ea7054f198e97f59c09f6a2ed
Autor:
Ghani, Mahdi, Reitz, Christiane, Cheng, Rong, Vardarajan, Badri Narayan, Jun, Gyungah, Sato, Christine, Naj, Adam, Rajbhandary, Ruchita, Wang, Li-San, Valladares, Otto, Lin, Chiao-Feng, Larson, Eric B, Graff-Radford, Neill R, Evans, Denis, De Jager, Philip L, Crane, Paul K, Buxbaum, Joseph D, Murrell, Jill R, Raj, Towfique, Ertekin-Taner, Nilufer, Logue, Mark, Baldwin, Clinton T, Green, Robert C, Barnes, Lisa L, Cantwell, Laura B, Fallin, M Daniele, Go, Rodney CP, Griffith, Patrick A, Obisesan, Thomas O, Manly, Jennifer J, Lunetta, Kathryn L, Kamboh, M Ilyas, Lopez, Oscar L, Bennett, David A, Hendrie, Hugh, Hall, Kathleen S, Goate, Alison M, Byrd, Goldie S, Kukull, Walter A, Foroud, Tatiana M, Haines, Jonathan L, Farrer, Lindsay A, Pericak-Vance, Margaret A, Lee, Joseph H, Schellenberg, Gerard D, St George-Hyslop, Peter, Mayeux, Richard, Rogaeva, Ekaterina, Alzheimer’s Disease Genetics Consortium
Publikováno v:
JAMA neurology, vol 72, iss 11
ImportanceMutations in known causal Alzheimer disease (AD) genes account for only 1% to 3% of patients and almost all are dominantly inherited. Recessive inheritance of complex phenotypes can be linked to long (>1-megabase [Mb]) runs of homozygosity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::ed12894312b1b2132c5082c0d58b801b
https://escholarship.org/uc/item/9tk0m9t2
https://escholarship.org/uc/item/9tk0m9t2
Autor:
Barton JC; Southern Iron Disorders Center, Birmingham, Alabama, USA.; Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA., Wiener HW; Department of Epidemiology and International Health, University of Alabama at Birmingham, Birmingham, Alabama, USA., Acton RT; Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.; Department of Epidemiology and International Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.; Immunogenetics Program, Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama, USA., Go RC; Department of Epidemiology and International Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Publikováno v:
BMC blood disorders [BMC Blood Disord] 2005 Jul 25; Vol. 5, pp. 5. Date of Electronic Publication: 2005 Jul 25.