Zobrazeno 1 - 6
of 6
pro vyhledávání: '"P L, St Jean"'
Publikováno v:
Annals of Global Health, Vol 82, Iss 3, Pp 496-497 (2016)
Externí odkaz:
https://doaj.org/article/d0c59ede1e124b27ac537a7ba136a30f
Autor:
Anna C. Need, Dongliang Ge, Michael E. Weale, Jessica Maia, Sheng Feng, Erin L. Heinzen, Kevin V. Shianna, Woohyun Yoon, Dalia Kasperavičiūtė, Massimo Gennarelli, Warren J. Strittmatter, Cristian Bonvicini, Giuseppe Rossi, Karu Jayathilake, Philip A. Cola, Joseph P. McEvoy, Richard S. E. Keefe, Elizabeth M. C. Fisher, Pamela L. St. Jean, Ina Giegling, Annette M. Hartmann, Hans-Jürgen Möller, Andreas Ruppert, Gillian Fraser, Caroline Crombie, Lefkos T. Middleton, David St. Clair, Allen D. Roses, Pierandrea Muglia, Clyde Francks, Dan Rujescu, Herbert Y. Meltzer, David B. Goldstein
Publikováno v:
PLoS Genetics, Vol 5, Iss 3 (2009)
Externí odkaz:
https://doaj.org/article/ee8f2989272a41b5b3a23afc4eef806e
Autor:
Anna C Need, Dongliang Ge, Michael E Weale, Jessica Maia, Sheng Feng, Erin L Heinzen, Kevin V Shianna, Woohyun Yoon, Dalia Kasperaviciūte, Massimo Gennarelli, Warren J Strittmatter, Cristian Bonvicini, Giuseppe Rossi, Karu Jayathilake, Philip A Cola, Joseph P McEvoy, Richard S E Keefe, Elizabeth M C Fisher, Pamela L St Jean, Ina Giegling, Annette M Hartmann, Hans-Jürgen Möller, Andreas Ruppert, Gillian Fraser, Caroline Crombie, Lefkos T Middleton, David St Clair, Allen D Roses, Pierandrea Muglia, Clyde Francks, Dan Rujescu, Herbert Y Meltzer, David B Goldstein
Publikováno v:
PLoS Genetics, Vol 5, Iss 2, p e1000373 (2009)
We report a genome-wide assessment of single nucleotide polymorphisms (SNPs) and copy number variants (CNVs) in schizophrenia. We investigated SNPs using 871 patients and 863 controls, following up the top hits in four independent cohorts comprising
Externí odkaz:
https://doaj.org/article/c19e84d31375449d8e0177d2a66e2fc4
Autor:
W C, Hsueh, B D, Mitchell, J L, Schneider, P L, St Jean, T I, Pollin, M G, Ehm, M J, Wagner, D K, Burns, H, Sakul, C J, Bell, A R, Shuldiner
Publikováno v:
The Journal of clinical endocrinology and metabolism. 86(3)
To identify the genetic determinants of typical obesity, we performed a genome-wide scan of obesity-related traits using data from the Amish. Multipoint linkage analysis was performed using a variance components procedure on body mass index (BMI), wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::17acf6deb63dfaa04883c47f5a0f3054
https://pubmed.ncbi.nlm.nih.gov/11238509
https://pubmed.ncbi.nlm.nih.gov/11238509
Autor:
Callum J. Bell, B K Michelsen, Braxton D. Mitchell, Hakan Sakul, P L St Jean, M Gelder Ehm, W. C. Knowler, T.I. Pollin, R Aburomia, Michael J. Wagner, Alan R. Shuldiner, Daniel K. Burns, Wen-Chi Hsueh
Publikováno v:
Diabetes care. 23(5)
OBJECTIVE: The Old Order Amish (OOA) are a genetically well-defined closed Caucasian founder population. The Amish Family Diabetes Study was initiated to identify susceptibility genes for type 2 diabetes. This article describes the genetic epidemiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b13d3e6127687f587a8bbd6f0c1d3ee
https://pubmed.ncbi.nlm.nih.gov/10834415
https://pubmed.ncbi.nlm.nih.gov/10834415
Publikováno v:
Human molecular genetics. 3(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87fc9254580259f82e02d3f3d8e1d1bc
https://pubmed.ncbi.nlm.nih.gov/7874138
https://pubmed.ncbi.nlm.nih.gov/7874138