Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Rosalind J Neuman"'
Autor:
Rosalind J Neuman, Jon Wasson, Gil Atzmon, Julio Wainstein, Yair Yerushalmi, Joseph Cohen, Nir Barzilai, Ilana Blech, Benjamin Glaser, M Alan Permutt
Publikováno v:
PLoS ONE, Vol 5, Iss 3, p e9903 (2010)
Evidence has accumulated that multiple genetic and environmental factors play important roles in determining susceptibility to type 2 diabetes (T2D). Although variants from candidate genes have become prime targets for genetic analysis, few studies h
Externí odkaz:
https://doaj.org/article/84510053daea43179543b6cbb29dbe9a
Publikováno v:
Journal of Lipid Research, Vol 48, Iss 12, Pp 2632-2639 (2007)
High plasma apolipoprotein B (apoB) and LDL cholesterol levels increase cardiovascular disease risk. These highly correlated measures may be partially controlled by common genetic polymorphisms. To identify chromosomal regions that contain genes caus
Externí odkaz:
https://doaj.org/article/59a995e5523d452d8730b5af7098b9b4
Autor:
Rosalind J. Neuman, Bo Yuan, Daniela S. Gerhard, Kuang-Yu Liu, Pin Yue, Shenghui Duan, Maurizio Averna, Gustav Schonfeld
Publikováno v:
Journal of Lipid Research, Vol 43, Iss 3, Pp 407-415 (2002)
Familial hypobetalipoproteinemia (FHBL) is a genetically heterogeneous condition characterized by very low apolipoprotein B (apoB) concentrations in plasma and/or low levels of LDL-cholesterol (LDL-C) with a propensity to developing fatty liver. In a
Externí odkaz:
https://doaj.org/article/9a84884995b4407ab9081d6950baee9c
Autor:
Erin M. Ramos, Arpana Agrawal, Laura J. Bierut, Elizabeth W. Pugh, Kathleen K. Bucholz, William Howells, Samuel Kuperman, Rosalind J. Neuman, Siiri N. Bennett, Robert F. Krueger, Marc A. Schuckit, John P. Rice, Naomi Breslau, Teri A. Manolio, Howard J. Edenberg, Nancy L. Saccone, Cathy C. Laurie, Bernice Porjesz, Alison Goate, John I. Nurnberger, John Kramer, Kimberly F. Doheny, Scott F. Saccone, Victor Hesselbrock, Sarah M. Hartz, Laura Almasy, Eric O. Johnson
Publikováno v:
Addiction. 107:2019-2028
Aims Nicotine dependence is a highly heritable disorder associated with severe medical morbidity and mortality. Recent meta-analyses have found novel genetic loci associated with cigarettes per day (CPD), a proxy for nicotine dependence. The aim of t
Autor:
Sherri L. Fisher, Laura J. Bierut, William Howells, Elizabeth W. Pugh, Louis Fox, Rosalind J. Neuman, Marc A. Schuckit, Robert C. Cloninger, John Kramer, Kimberly F. Doheny, Jay A. Tischfield, Kathleen K. Bucholz, Anthony L. Hinrichs, Howard J. Edenberg, Alison Goate, Michael T. Lynskey, Arpana Agrawal, Danielle M. Dick, Robert F. Krueger, Richard A. Grucza, Samuel Kuperman, John I. Nurnberger, Scott F. Saccone, Eric O. Johnson, John P. Rice, Victor Hesselbrock
Publikováno v:
Addiction Biology. 16:514-518
Cannabis dependence is the third leading contributor to admissions to chemical dependency treatment settings (Treatment Episode Data Set, 2003) and rates of past year cannabis dependence in the U.S. population have increased by 18% since 1991–1992
Autor:
Howard J. Edenberg, Alison Goate, Richard A. Grucza, Nancy L. Saccone, Sherri L. Fisher, John I. Nurnberger, Scott F. Saccone, Samuel Kuperman, Victor Hesselbrock, Elizabeth W. Pugh, John Kramer, Anthony L. Hinrichs, William Howells, Arpana Agrawal, Karl Mann, Laura Almasy, Kimberly F. Doheny, Robert Culverhouse, Monika Ridinger, Louis Fox, Robert F. Krueger, Michael T. Lynskey, Marcella Rietschel, Dorothy K. Hatsukami, Eric O. Johnson, Tatiana Foroud, Markus M. Nöthen, Cathy C. Laurie, Marc A. Schuckit, Danielle M. Dick, Rosalind J. Neuman, Naomi Breslau, Bernice Porjesz, Jen C. Wang, Jay A. Tischfield, Kathleen K. Bucholz, Laura J. Bierut, John P. Rice, Sarah Bertelsen
Publikováno v:
Proceedings of the National Academy of Sciences. 107:5082-5087
Excessive alcohol consumption is one of the leading causes of preventable death in the United States. Approximately 14% of those who use alcohol meet criteria during their lifetime for alcohol dependence, which is characterized by tolerance, withdraw
Autor:
Rosalind J. Neuman, Yun Ju Sung
Publikováno v:
Genetic Epidemiology. 33:S19-S23
This contribution summarizes the work done by six independent teams of investigators to identify the genetic and non-genetic variants that work together or independently to predispose to disease. The theme addressed in these studies is multistage str
Autor:
Benjamin Glaser, Andrew T. Hattersley, Jing Hua Zhao, Mark I. McCarthy, Nicholas J. Wareham, Graham A. Hitman, Ranganath Venkatesh, Eleftheria Zeggini, Panagiotis Deloukas, Michael N. Weedon, Sarah E. Hunt, Eleanor Wheeler, M. Alan Permutt, Richard Sherva, Marcos Delgado, Pamela Whittaker, Jian'an Luan, Timothy M. Frayling, Rosalind J. Neuman, Jon Wasson, Inês Barroso, Mark Walker
Publikováno v:
Diabetes
OBJECTIVE—Single nucleotide polymorphisms (SNPs) in the P2 promoter region of HNF4A were originally shown to be associated with predisposition for type 2 diabetes in Finnish, Ashkenazi, and, more recently, Scandinavian populations, but they generat
Publikováno v:
Journal of Lipid Research, Vol 48, Iss 12, Pp 2632-2639 (2007)
High plasma apolipoprotein B (apoB) and LDL cholesterol levels increase cardiovascular disease risk. These highly correlated measures may be partially controlled by common genetic polymorphisms. To identify chromosomal regionsthatcontain genes causin
Autor:
Richard D. Todd, Rosalind J. Neuman
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :971-975
To determine the mechanism of interaction of prenatal smoking exposure and child genotype in the development of attention deficit/hyperactivity disorder (ADHD), polymorphisms in the CHRNA4 gene were tested for interactions with prenatal smoking expos