Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Christopher L. Sanders"'
Autor:
Friedrich Kueppers, Mark D. Andrake, Qifang Xu, Roland L. Dunbrack, Joannah Kim, Christopher L. Sanders
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-19 (2019)
Abstract Background Alpha 1 Antitrypsin (AAT) is a key serum proteinase inhibitor encoded by SERPINA1. Sequence variants of the gene can cause Alpha 1 Antitrypsin Deficiency (AATD), a condition associated with lung and liver disease. The majority of
Externí odkaz:
https://doaj.org/article/d32b605cb01a47899ade581892491c43
Autor:
Sekar Kathiresan, Noël P. Burtt, Candace Guiducci, Christopher L. Sanders, Mary E. Keebler, Aarti Surti
Publikováno v:
Circulation: Cardiovascular Genetics. 2:238-243
Background— Using the genome-wide association approach in individuals of European ancestry, we and others recently identified single-nucleotide polymorphisms (SNPs) at 19 loci as associated with blood lipids; 8 of these loci were novel. Whether the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6055907c22e1ebe1792292023dcc878
https://doi.org/10.1161/circgenetics.108.829473
https://doi.org/10.1161/circgenetics.108.829473
Autor:
Margaret Gallagher, Robert Welch, Cynthia A. Moore, Nicole F. Dowling, Mary Lou Lindegren, Christopher L. Sanders, Stephen J. Chanock, Ramal Moonesinghe, Ajay Yesupriya, Renée M. Ned, Man Huei Chang, Muin J. Khoury, Mary R. Reichler, Mary Ann Butler
Publikováno v:
American Journal of Epidemiology. 169:54-66
Population-based allele frequencies and genotype prevalence are important for measuring the contribution of genetic variation to human disease susceptibility, progression, and outcomes. Population-based prevalence estimates also provide the basis for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a8c89e8364b5d64fdbcd9e797ed4e05
https://doi.org/10.1093/aje/kwn286
https://doi.org/10.1093/aje/kwn286
Publikováno v:
Journal of the American Statistical Association. 105(490)
Developing, targeting, and evaluating genomic strategies for population-based disease prevention require population-based data. In response to this urgent need, genotyping has been conducted within the Third National Health and Nutrition Examination
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::086387b76f8805af4fd4b401fa8803f2
https://pubmed.ncbi.nlm.nih.gov/20664713
https://pubmed.ncbi.nlm.nih.gov/20664713
Autor:
Lorenzo D. Botto, J. David Erickson, Karen K. Steinberg, Deborah Koontz, Christopher L. Sanders, Quan He Yang, Jan M. Friedman, Stanimila Nikolova, Margaret Gallagher
Publikováno v:
The American journal of clinical nutrition. 88(1)
Background Abnormalities of folate and homocysteine metabolism are associated with a number of pediatric and adult disorders. Folate intake and genetic polymorphisms encoding folate-metabolizing enzymes influence blood folate and homocysteine concent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1453a9ee809ac207d36efa9a31640953
https://pubmed.ncbi.nlm.nih.gov/18614746
https://pubmed.ncbi.nlm.nih.gov/18614746
Autor:
Cynthia Shephard, Laura Witrak, Christopher L. Sanders, Joshua D. Smith, Michelle Wong, Xiaoting Qin, Mark J. Rieder, Deborah A. Nickerson, Dana C. Crawford
Publikováno v:
Circulation. 114(23)
Background— Increased serum C-reactive protein (CRP) is an independent risk factor for cardiovascular disease. Previous studies have suggested that genetic variation within the CRP gene is associated with serum CRP. Methods and Results— We genoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81ee72b93201b12c3d585fe0928febd4
https://pubmed.ncbi.nlm.nih.gov/17101857
https://pubmed.ncbi.nlm.nih.gov/17101857
Autor:
Man-huei Chang, Mary Lou Lindegren, Mary A. Butler, Stephen J. Chanock, Nicole F. Dowling, Margaret Gallagher, Ramal Moonesinghe, Cynthia A. Moore, Renée M. Ned, Mary R. Reichler, Christopher L. Sanders, Robert Welch, Ajay Yesupriya, Muin J. Khoury, for the CDC/NCI NHANES III Genomics Working Group
Publikováno v:
American Journal of Epidemiology; Jan2009, Vol. 169 Issue 1, p54-54, 1p
Autor:
Sanders, Christopher L.1 (AUTHOR) CSanders@Biocerna.com, Ponte, Amy1 (AUTHOR), Kueppers, Friedrich2 (AUTHOR)
Publikováno v:
COPD: Journal of Chronic Obstructive Pulmonary Disease. Feb2018, Vol. 15 Issue 1, p10-16. 7p.
Autor:
Crawford, Dana C.1,2 crawford@chgr.mc.vanderbilt.edu, Brown-Gentry, Kristin1, Rieder, Mark J.3
Publikováno v:
PLoS ONE. 2010, Vol. 5 Issue 12, p1-7. 7p.
Publikováno v:
BMC Medical Genetics. 2009, Vol. 10, p108-117. 10p.