অনুসন্ধান ফলাফলগুলি - "genetic architecture"

CAS-viewer: web-based tool for splicing-guided integrative analysis of multi-omics cancer data অনুযায়ী Seonggyun Han, Dongwook Kim, Youngjun Kim, Kanghoon Choi, Jason E. Miller, Dokyoon Kim, Younghee Lee

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GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome অনুযায়ী Ferdinando Bonfiglio, Xingrong Liu, Christopher Smillie, Anita Pandit, Alexander Kurilshikov, Rodrigo Bacigalupe, Tenghao Zheng, Hieu Nim, Koldo Garcia-Etxebarria, Luis Bujanda, Anna Andreasson, Lars Agreus, Susanna Walter, Gonçalo Abecasis, Chris Eijsbouts, Luke Jostins, Miles Parkes, David A. Hughes, Nicholas Timpson, Jeroen Raes, Andre Franke, Nicholas A. Kennedy, Aviv Regev, Alexandra Zhernakova, Magnus Simren, Michael Camilleri, Mauro D'Amato

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Pharmacogenomic landscape of Indian population using whole genomes অনুযায়ী S. Sahana, Rahul C. Bhoyar, Ambily Sivadas, Abhinav Jain, Mohamed Imran, Mercy Rophina, Vigneshwar Senthivel, Mohit Kumar Diwakar, Disha Sharma, Anushree Mishra, Sridhar Sivasubbu, Vinod Scaria

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Genome-wide association study and trans-ethnic meta-analysis identify novel susceptibility loci for type 2 diabetes mellitus অনুযায়ী Asma A Elashi, Salman M Toor, Umm-Kulthum Ismail Umlai, Yasser A Al-Sarraj, Shahrad Taheri, Karsten Suhre, Abdul Badi Abou-Samra, Omar M E Albagha

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A severe atherosclerosis mouse model on the resistant NOD background অনুযায়ী Xugang Wang, Rong Huang, Lichen Zhang, Saichao Li, Jing Luo, Yanrong Gu, Zhijun Chen, Qianqian Zheng, Tianzhu Chao, Wenping Zheng, Xinhui Qi, Li Wang, Yinhang Wen, Yinming Liang, Liaoxun Lu

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Use of preclinical models to identify markers of type 2 diabetes susceptibility and novel regulators of insulin secretion - A step towards precision medicine অনুযায়ী Bernard Thorens, Ana Rodriguez, Céline Cruciani-Guglielmacci, Leonore Wigger, Mark Ibberson, Christophe Magnan

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Aedes Mosquito Dynamics: Unravelling Behavior, Genetics, and Arbovirus Risks in India অনুযায়ী Preeti Acharya, Showkat Ahmad Mir, Binata Nayak

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Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk অনুযায়ী Wills Amanda G, Simonson Matthew A, Keller Matthew C, McQueen Matthew B

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Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants অনুযায়ী Wei Luo, Hanni Ke, Shuyan Tang, Xue Jiao, Zhuqing Li, Shidou Zhao, Feng Zhang, Ting Guo, Yingying Qin

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A rare functional variant of SHARPIN attenuates the inflammatory response and associates with increased risk of late-onset Alzheimer's disease অনুযায়ী Yuya Asanomi, Daichi Shigemizu, Akinori Miyashita, Risa Mitsumori, Taiki Mori, Norikazu Hara, Kaoru Ito, Shumpei Niida, Takeshi Ikeuchi, Kouichi Ozaki

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Gene-gene interaction and association of Wnt/Β-catenin signalling pathway gene polymorphisms with ankylosing spondylitis susceptibility in the Chinese Han population অনুযায়ী Rui Liu, Xu Zhang, Guangming Jiang, Yubo Ma, Jiajia Yang, Meng Wu, Renfang Han, Mengya Chen, Yaping Yuan, Xingxing Hu, Meijuan Pan, Shengqian Xu, Jianhua Xu, Zongwen Shuai, Yanfeng Zou, Guixia Pan, Faming Pan

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Epoxygenase inactivation exacerbates diet and aging-associated metabolic dysfunction resulting from impaired adipogenesis অনুযায়ী Antoni Olona, Ximena Terra, Jeong-Hun Ko, Carme Grau-Bové, Montserrat Pinent, Anna Ardevol, Ana Garcia Diaz, Aida Moreno-Moral, Matthew Edin, David Bishop-Bailey, Darryl C. Zeldin, Timothy J. Aitman, Enrico Petretto, Mayte Blay, Jacques Behmoaras

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Genetic background modifies phenotypic severity and longevity in a mouse model of Niemann-Pick disease type C1 অনুযায়ী Jorge L. Rodriguez-Gil, Dawn E. Watkins-Chow, Laura L. Baxter, Gene Elliot, Ursula L. Harper, Stephen M. Wincovitch, Julia C. Wedel, Arturo A. Incao, Mylene Huebecker, Frederick J. Boehm, William S. Garver, Forbes D. Porter, Karl W. Broman, Frances M. Platt, William J. Pavan

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Association of integrin-β2 polymorphism and expression with the risk of rheumatoid arthritis and osteoarthritis in Egyptian patients অনুযায়ী Aliaa M. Selim, Yumn A. Elsabagh, Maha M. El-Sawalhi, Nabila A. Ismail, Mahmoud A. Senousy

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Gene-based whole genome sequencing meta-analysis of 250 circulating proteins in three isolated European populations অনুযায়ী Arthur Gilly, Lucija Klaric, Young-Chan Park, Grace Png, Andrei Barysenka, Joseph A. Marsh, Emmanouil Tsafantakis, Maria Karaleftheri, George Dedoussis, James F. Wilson, Eleftheria Zeggini

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Association of the ADORA2A receptor and CD73 polymorphisms with epilepsy অনুযায়ী Nan-Rui Shi, Qi Wang, Jie Liu, Ji-Zhou Zhang, Bin-Lu Deng, Xiu-Min Hu, Jie Yang, Xin Wang, Xiang Chen, Yan-Qin Zuo, Ting-Ting Liu, Jia-Ling Zheng, Xin Yang, Peter Illes, Peter Illes, Yong Tang, Yong Tang

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Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes অনুযায়ী Morag A. Lewis, Lisa S. Nolan, Barbara A. Cadge, Lois J. Matthews, Bradley A. Schulte, Judy R. Dubno, Karen P. Steel, Sally J. Dawson

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Statistical driver genes as a means to uncover missing heritability for age-related macular degeneration অনুযায়ী Andrea R. Waksmunski, Michelle Grunin, Tyler G. Kinzy, Robert P. Igo, Jonathan L. Haines, Jessica N. Cooke Bailey

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Whole-exome sequencing reveals ANO8 as a genetic risk factor for intrahepatic cholestasis of pregnancy অনুযায়ী Xianxian Liu, Hua Lai, Xiaoming Zeng, Siming Xin, Liju Nie, Zhenyi Liang, Meiling Wu, Yu Chen, Jiusheng Zheng, Yang Zou

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Whole-exome sequencing identifies novel mutations in ABC transporter genes associated with intrahepatic cholestasis of pregnancy disease: a case-control study অনুযায়ী Xianxian Liu, Hua Lai, Siming Xin, Zengming Li, Xiaoming Zeng, Liju Nie, Zhengyi Liang, Meiling Wu, Jiusheng Zheng, Yang Zou

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