المؤلفون: Jie Jin Wang, Robert P. Igo, Barry I. Freedman, Jerome I. Rotter, Kathyrn P. Burdon, Alan D. Penman, Albert V. Smith, Xiaohui Li, Jamie E. Craig, Paul Mitchell, Brian L. Yaspan, Mary Frances Cotch, John M. Rouhana, Ayellet V. Segrè, Barbara E.K. Klein, Ashley Li, Richard A. Jensen, Gayatri Susarla, Lynn K. Stanwyck, Sudha K. Iyengar, Maggie C.Y. Ng, Ching J. Chen, Kent D. Taylor, Donald W. Bowden, Lucia Sobrin, Tien Yin Wong, Emily Y. Chew, Sharon G. Adler, Samuela Pollack, Jane Z. Kuo

المصدر: Am J Ophthalmol

مصطلحات موضوعية: Lipid catabolic process, Clinical Sciences, Genome-wide association study, Type 2 diabetes, Biology, Ophthalmology & Optometry, Polymorphism, Single Nucleotide, Article, Opthalmology and Optometry, Risk Factors, Diabetes Mellitus, Genetics, medicine, 2.1 Biological and endogenous factors, Humans, Interferon gamma, Polymorphism, Aetiology, Eye Disease and Disorders of Vision, Gene, Metabolic and endocrine, Lipid Transport, Diabetic Retinopathy, Catabolism, Diabetes, Human Genome, Single Nucleotide, medicine.disease, Ophthalmology, Diabetes Mellitus, Type 2, Public Health and Health Services, Lipid digestion, Type 2, Biotechnology, Genome-Wide Association Study, medicine.drug

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ad6e49bb0953ea357e7561f1b3b1a6Test
https://doi.org/10.1016/j.ajo.2021.06.014Test

المؤلفون: Shabnam Salimi, Laura M. Raffield, Steve T. Turner, Margaret R Irvin, Tanika N. Kelly, Xiaoming Liu, Chao A Hsiung, Yoichiro Kamatani, L. Adrienne Cupples, James P. Lash, Leslie J. Baier, James A. Perry, Wei Zhao, Sharon R. Browning, Robert L. Hanson, Betsi A Young, Daniel Levy, Sharon L.R. Kardia, Donna K. Arnett, Jiang He, Timothy A. Thornton, Josyf C. Mychaleckyj, Leslie A. Lange, Dhananjay Vaidya, Charles Kooperberg, Shih-Jen Hwang, Danyu Lin, Eric Boerwinkle, Lisa R. Yanek, Yukihide Momozawa, Koichi Matsuda, Ramachandran S. Vasan, Yun Li, Jerome I. Rotter, George J. Papanicolaou, Solomon K. Musani, Braxton D. Mitchell, Saori Sakaue, Lisa de las Fuentes, Bridget M Lin, Charles E Breeze, Stephen S. Rich, Jennifer A. Smith, Yukinori Okada, Rasika A. Mathias, Bruce M. Psaty, Afshin Parsa, Benjamin D. Heavner, Sayuko Kobes, Jennifer A. Brody, Adrienne Tin, Kelsey Grinde, Huijun Qian, Wayne H-H Sheu, Yi-Jen Hung, Adolfo Correa, Deepti Jain, Anna Köttgen, Deborah A. Nickerson, Gonzalo Abecasis, Xuenan Mi, Xiuqing Guo, Alexander P. Reiner, Kent D. Taylor, Robert B. Wallace, Kenichi Yamamoto, Holly Kramer, Jianwen Cai, Albert V. Smith, Alan R. Shuldiner, Ida Yii-Der Chen, Nora Franceschini

المصدر: EBioMedicine
EBioMedicine, Vol 63, Iss, Pp 103157-(2021)

مصطلحات موضوعية: Male, 0301 basic medicine, lcsh:Medicine, Ancestry-specific variants, 0302 clinical medicine, Gene Frequency, and Blood Institute (U.S.), 2.1 Biological and endogenous factors, Public Health Surveillance, Aetiology, Precision Medicine, Lung, Genetics, lcsh:R5-920, Single Nucleotide, Genomics, General Medicine, 030220 oncology & carcinogenesis, Public Health and Health Services, lcsh:Medicine (General), Biotechnology, Glomerular Filtration Rate, Research Paper, Clinical Sciences, Genetic relationship, Biology, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Quantitative Trait, 03 medical and health sciences, Quantitative Trait, Heritable, Humans, Genetic Predisposition to Disease, Polymorphism, Heritable, Gene, Alleles, Kidney traits, Whole genome sequencing, Whole Genome Sequencing, Human Genome, lcsh:R, Rare variants, National Heart, Omics, Precision medicine, United States, Minor allele frequency, Good Health and Well Being, 030104 developmental biology, National Heart, Lung, and Blood Institute (U.S.), Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb723cd342a3bdb50de0ce4e9d0bc72Test
https://doi.org/10.1016/j.ebiom.2020.103157Test