Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Rebecca T Levinson"'
Publikováno v:
JMIR Cardio, Vol 8, p e54994 (2024)
BackgroundPatients with heart failure (HF) are the most commonly readmitted group of adult patients in Germany. Most patients with HF are readmitted for noncardiovascular reasons. Understanding the relevance of HF management outside the hospital sett
Externí odkaz:
https://doaj.org/article/4e41f75bc04a4625b86a2d3ce0e49ca2
Autor:
QiPing Feng, Wei-Qi Wei, Cecilia P Chung, Rebecca T Levinson, Alexandra C Sundermann, Jonathan D Mosley, Lisa Bastarache, Jane F Ferguson, Nancy J Cox, Dan M Roden, Joshua C Denny, MacRae F Linton, Digna R Velez Edwards, C Michael Stein
Publikováno v:
PLoS Medicine, Vol 15, Iss 8, p e1002642 (2018)
BACKGROUND:Observations from statin clinical trials and from Mendelian randomization studies suggest that low low-density lipoprotein cholesterol (LDL-C) concentrations may be associated with increased risk of type 2 diabetes mellitus (T2DM). Despite
Externí odkaz:
https://doaj.org/article/bbb947f0461d4dfcbc0c34e59c03d106
Autor:
Gabriella D Cozzi, Rebecca T Levinson, Hilary Toole, Malcolm-Robert Snyder, Angie Deng, Marta A Crispens, Dineo Khabele, Alicia Beeghly-Fadiel
Publikováno v:
PLoS ONE, Vol 12, Iss 4, p e0175119 (2017)
Blood type A and the A1 allele have been associated with increased ovarian cancer risk. With only two small studies published to date, evidence for an association between ABO blood type and ovarian cancer survival is limited.We conducted a retrospect
Externí odkaz:
https://doaj.org/article/0ca3f37cc6f74b5eaba23aa8fe4bdd46
Autor:
Ricardo O. Ramirez Flores, Jan D. Lanzer, Christian H. Holland, Florian Leuschner, Patrick Most, Jobst‐Hendrik Schultz, Rebecca T. Levinson, Julio Saez‐Rodriguez
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 7 (2021)
Background Transcriptomic studies have contributed to fundamental knowledge of myocardial remodeling in human heart failure (HF). However, the key HF genes reported are often inconsistent between studies, and systematic efforts to integrate evidence
Externí odkaz:
https://doaj.org/article/250c56dc64da4a23a16a360e0b547ec2
Autor:
Megan M Shuey, Giovanni E Davogustto, Shi Huang, Eric Farber-Eger, Rebecca T Levinson, Frank Harrell, Nancy Cox, Quinn Wells
Publikováno v:
Circulation. 145
Background: One in three Americans will have atrial fibrillation (AF) during their lifetime. Obesity and metabolic derangements are key risk factors for AF. It is unclear, however, which subset of patients would benefit most from targeted interventio
Autor:
Eric Farber-Eger, Nataraja Sarma Vaitinidin, Jonathan D. Mosley, Quinn S. Wells, Dan M. Roden, Rebecca T. Levinson, Thomas A. Lasko
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Heart failure (HF) has no cure and, for HF with preserved ejection fraction (HFpEF), no life-extending treatments. Defining the clinical epidemiology of HF could facilitate earlier identification of high-risk individuals. We define the clinical epide
Autor:
Christian H. Holland, Florian Leuschner, Jan D. Lanzer, Ricardo O. Ramirez Flores, Julio Saez-Rodriguez, Rebecca T. Levinson, Jobst-Hendrik Schultz, Patrick Most
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Transcriptomic studies have contributed to fundamental knowledge of myocardial remodeling in human heart failure (HF). However, the key HF genes reported are often inconsistent between studies, and systematic efforts to integrate evidence
Autor:
Rebecca T. Levinson, Jennifer R. Malinowski, Suzette J. Bielinski, Luke V. Rasmussen, Melissa P. Wilson, Sheila M. Manemann, Quinn S. Wells, Veronique L. Roger, Laura K. Wiley
BackgroundHeart failure (HF) is a complex syndrome associated with significant morbidity, mortality, and healthcare costs. Electronic health records (EHRs) are widely used to identify patients with HF. Despite the development of many HF phenotyping a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0c9da83918b56abb2279f79da8df793
https://doi.org/10.1101/2021.02.01.21250933
https://doi.org/10.1101/2021.02.01.21250933
Autor:
Quinn S. Wells, Julia M. Sealock, Nancy J. Cox, Abraham A. Palmer, Rebecca T. Levinson, Eric Farber-Eger, Peter Straub, Abdel Abdellaoui, Sarah L. Elson, Pierre Fontanillas, Dorret I. Boomsma, Jacob Franco, Guanhua Chen, Jessica Dennis, Jonathan D. Mosley, Donald Hucks, Sarah Fong, Lea K. Davis, Sandra Sanchez-Roige, Douglas M. Ruderfer, Wen-Liang Song, MacRae F. Linton
Publikováno v:
Molecular psychiatry, 26, 4254-4264. Nature Publishing Group
Dennis, J, Sealock, J, Levinson, R T, Farber-Eger, E, Franco, J, Fong, S, Straub, P, Hucks, D, Song, W-L, Linton, M F, Fontanillas, P, Elson, S L, Ruderfer, D, Abdellaoui, A, Sanchez-Roige, S, Palmer, A A, Boomsma, D I, Cox, N J, Chen, G, Mosley, J D, Wells, Q S & Davis, L K 2021, ' Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease ', Molecular Psychiatry, vol. 26, no. 8, pp. 4254-4264 . https://doi.org/10.1038/s41380-019-0614-y
Molecular psychiatry
Molecular Psychiatry, 26(8), 4254-4264. Nature Publishing Group
Molecular psychiatry, vol 26, iss 8
Dennis, J, Sealock, J, Levinson, R T, Farber-Eger, E, Franco, J, Fong, S, Straub, P, Hucks, D, Song, W-L, Linton, M F, Fontanillas, P, Elson, S L, Ruderfer, D, Abdellaoui, A, Sanchez-Roige, S, Palmer, A A, Boomsma, D I, Cox, N J, Chen, G, Mosley, J D, Wells, Q S & Davis, L K 2021, ' Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease ', Molecular Psychiatry, vol. 26, no. 8, pp. 4254-4264 . https://doi.org/10.1038/s41380-019-0614-y
Molecular psychiatry
Molecular Psychiatry, 26(8), 4254-4264. Nature Publishing Group
Molecular psychiatry, vol 26, iss 8
Major depressive disorder (MDD) and loneliness are phenotypically and genetically correlated with coronary artery disease (CAD), but whether these associations are explained by pleiotropic genetic variants or shared comorbidities is unclear. To tease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38f0eb04f544f3bbc28723e365d917d1
https://pure.amc.nl/en/publications/genetic-risk-for-major-depressive-disorder-and-loneliness-in-sexspecific-associations-with-coronary-artery-disease(351850a8-1555-4196-8b5e-1c7235cbfc78).html
https://pure.amc.nl/en/publications/genetic-risk-for-major-depressive-disorder-and-loneliness-in-sexspecific-associations-with-coronary-artery-disease(351850a8-1555-4196-8b5e-1c7235cbfc78).html
Autor:
Shi Huang, Heidi J. Silver, Nancy J. Cox, Katherine N. Cahill, Eric Farber-Eger, Frank E. Harrell, John R. Koethe, Rebecca T. Levinson, Joshua A. Beckman, Quinn S. Wells, Megan M. Shuey, Kevin D. Niswender
ObjectiveBody mass index (BMI) is the most commonly used predictor of weight-related comorbidities and outcomes. However, the presumed relationship between height and weight intrinsic to BMI may introduce bias with respect to prediction of clinical o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dba5e1994561aa31ed7f518bef4e8d5
https://doi.org/10.1101/2020.12.22.20248739
https://doi.org/10.1101/2020.12.22.20248739