Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Karen Y, He"'
Autor:
Karen Y. He, Ekaterina A. Khramtsova, Alfredo Cabrera-Socorro, Yanfei Zhang, Shuwei Li, Brice A. J. Sarver, Bart Smets, Qingqin S. Li, Louis De Muynck, Antonio R. Parrado, Simon Lovestone, Mary Helen Black
Publikováno v:
Molecular Neurodegeneration, Vol 18, Iss 1, Pp 1-4 (2023)
Externí odkaz:
https://doaj.org/article/963aba3c0f6644fe9e74f893f8ec0328
Autor:
Karen Y. He, Tanika N. Kelly, Heming Wang, Jingjing Liang, Luke Zhu, Brian E. Cade, Themistocles L. Assimes, Lewis C. Becker, Amber L. Beitelshees, Lawrence F. Bielak, Adam P. Bress, Jennifer A. Brody, Yen-Pei Christy Chang, Yi-Cheng Chang, Paul S. de Vries, Ravindranath Duggirala, Ervin R. Fox, Nora Franceschini, Anna L. Furniss, Yan Gao, Xiuqing Guo, Jeffrey Haessler, Yi-Jen Hung, Shih-Jen Hwang, Marguerite Ryan Irvin, Rita R. Kalyani, Ching-Ti Liu, Chunyu Liu, Lisa Warsinger Martin, May E. Montasser, Paul M. Muntner, Stanford Mwasongwe, Take Naseri, Walter Palmas, Muagututi’a Sefuiva Reupena, Kenneth M. Rice, Wayne H.-H. Sheu, Daichi Shimbo, Jennifer A. Smith, Beverly M. Snively, Lisa R. Yanek, Wei Zhao, John Blangero, Eric Boerwinkle, Yii-Der Ida Chen, Adolfo Correa, L. Adrienne Cupples, Joanne E. Curran, Myriam Fornage, Jiang He, Lifang Hou, Robert C. Kaplan, Sharon L. R. Kardia, Eimear E. Kenny, Charles Kooperberg, Donald Lloyd-Jones, Ruth J. F. Loos, Rasika A. Mathias, Stephen T. McGarvey, Braxton D. Mitchell, Kari E. North, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, D. C. Rao, Susan Redline, Alex P. Reiner, Stephen S. Rich, Jerome I. Rotter, Kent D. Taylor, Russell Tracy, Ramachandran S. Vasan, The Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Alanna C. Morrison, Daniel Levy, Aravinda Chakravarti, Donna K. Arnett, Xiaofeng Zhu
Publikováno v:
BMC Genomics, Vol 23, Iss 1, Pp 1-18 (2022)
Abstract Background While large genome-wide association studies have identified nearly one thousand loci associated with variation in blood pressure, rare variant identification is still a challenge. In family-based cohorts, genome-wide linkage scans
Externí odkaz:
https://doaj.org/article/ef3227d670ad41388d430a8ee8f9216c
Autor:
Xumin Ni, Mengshi Zhou, Heming Wang, Karen Y. He, Uli Broeckel, Craig Hanis, Sharon Kardia, Susan Redline, Richard S. Cooper, Hua Tang, Xiaofeng Zhu
Publikováno v:
BMC Genomics, Vol 21, Iss 1, Pp 1-13 (2020)
Abstract Background Fitness epistasis, the interaction effect of genes at different loci on fitness, makes an important contribution to adaptive evolution. Although fitness interaction evidence has been observed in model organisms, it is more difficu
Externí odkaz:
https://doaj.org/article/4fffa5d374cb4d5db36d098968891e2c
Autor:
Ekaterina A. Khramtsova, Melissa A. Wilson, Joanna Martin, Stacey J. Winham, Karen Y. He, Lea K. Davis, Barbara E. Stranger
Publikováno v:
Cell. 186:2044-2061
Autor:
Max M. He, Quan Li, Muqing Yan, Hui Cao, Yue Hu, Karen Y. He, Kajia Cao, Marilyn M. Li, Kai Wang
Publikováno v:
Genome Medicine, Vol 11, Iss 1, Pp 1-14 (2019)
Abstract Background Clinical laboratories implement a variety of measures to classify somatic sequence variants and identify clinically significant variants to facilitate the implementation of precision medicine. To standardize the interpretation pro
Externí odkaz:
https://doaj.org/article/94a906bdd778478a8c51ec01049109a6
Autor:
Tanika N, Kelly, Xiao, Sun, Karen Y, He, Michael R, Brown, Sarah A Gagliano, Taliun, Jacklyn N, Hellwege, Marguerite R, Irvin, Xuenan, Mi, Jennifer A, Brody, Nora, Franceschini, Xiuqing, Guo, Shih-Jen, Hwang, Paul S, de Vries, Yan, Gao, Arden, Moscati, Girish N, Nadkarni, Lisa R, Yanek, Tali, Elfassy, Jennifer A, Smith, Ren-Hua, Chung, Amber L, Beitelshees, Amit, Patki, Stella, Aslibekyan, Brandon M, Blobner, Juan M, Peralta, Themistocles L, Assimes, Walter R, Palmas, Chunyu, Liu, Adam P, Bress, Zhijie, Huang, Lewis C, Becker, Chii-Min, Hwa, Jeffrey R, O'Connell, Jenna C, Carlson, Helen R, Warren, Sayantan, Das, Ayush, Giri, Lisa W, Martin, W, Craig Johnson, Ervin R, Fox, Erwin P, Bottinger, Alexander C, Razavi, Dhananjay, Vaidya, Lee-Ming, Chuang, Yen-Pei C, Chang, Take, Naseri, Deepti, Jain, Hyun Min, Kang, Adriana M, Hung, Vinodh, Srinivasasainagendra, Beverly M, Snively, Dongfeng, Gu, May E, Montasser, Muagututi'a Sefuiva, Reupena, Benjamin D, Heavner, Jonathon, LeFaive, James E, Hixson, Kenneth M, Rice, Fei Fei, Wang, Jonas B, Nielsen, Jianfeng, Huang, Alyna T, Khan, Wei, Zhou, Jovia L, Nierenberg, Cathy C, Laurie, Nicole D, Armstrong, Mengyao, Shi, Yang, Pan, Adrienne M, Stilp, Leslie, Emery, Quenna, Wong, Nicola L, Hawley, Ryan L, Minster, Joanne E, Curran, Patricia B, Munroe, Daniel E, Weeks, Kari E, North, Russell P, Tracy, Eimear E, Kenny, Daichi, Shimbo, Aravinda, Chakravarti, Stephen S, Rich, Alex P, Reiner, John, Blangero, Susan, Redline, Braxton D, Mitchell, Dabeeru C, Rao, Yii-Der, Ida Chen, Sharon L R, Kardia, Robert C, Kaplan, Rasika A, Mathias, Jiang, He, Bruce M, Psaty, Myriam, Fornage, Ruth J F, Loos, Adolfo, Correa, Eric, Boerwinkle, Jerome I, Rotter, Charles, Kooperberg, Todd L, Edwards, Gonçalo R, Abecasis, Xiaofeng, Zhu, Daniel, Levy, Donna K, Arnett, Alanna C, Morrison
Publikováno v:
Hypertension (Dallas, Tex. : 1979). 79(8)
Background: The availability of whole-genome sequencing data in large studies has enabled the assessment of coding and noncoding variants across the allele frequency spectrum for their associations with blood pressure. Methods: We conducted a multian
Autor:
William Sproviero, Upamanyu Ghose, Laura M Winchester, Marco Fernandes, Danielle Newby, Daisy Sproviero, Najaf Amin, Bart Smets, Karen Y. He, Ekaterina A. Khramtsova, Parth Patel, Brice A. J. Sarver, Trevor Howe, Mary Helen Black, Cornelia van Duijn, Alejo Nevado-Holgado
We performed a genome-wide association study of 143,067 highly polymorphic short tandem repeats (STRs) with MRI brain grey matter volumes (GMVs) on 10,702 UK Biobank (UKB) participants, including 8,751 in the discovery stage and 1,701 in the replicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da95e9c8fe334221e199023944908ba3
https://doi.org/10.1101/2023.02.27.23286496
https://doi.org/10.1101/2023.02.27.23286496
Autor:
Karen Y. He, Ekaterina A. Khramtsova, Alfredo Cabrera-Socorro, Yanfei Zhang, Shuwei Li, Brice A. J. Sarver, Bart Smets, Qingqin S. Li, Louis De Muynck, Antonio R. Parrado, Simon Lovestone, Mary Helen Black
ImportanceA few case studies have reported the APOE Christchurch (APOECh) variant to confer protective effects for Alzheimer’s disease (AD) and a higher risk of premature cardiovascular disease (CVD). However, these studies primarily focused on a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8150e221f6b14586af35050c753501b0
https://doi.org/10.1101/2022.12.05.22283048
https://doi.org/10.1101/2022.12.05.22283048
Autor:
Karen Y He, Heming Wang, Brian E Cade, Priyanka Nandakumar, Ayush Giri, Erin B Ware, Jeffrey Haessler, Jingjing Liang, Jennifer A Smith, Nora Franceschini, Thu H Le, Charles Kooperberg, Todd L Edwards, Sharon L R Kardia, Xihong Lin, Aravinda Chakravarti, Susan Redline, Xiaofeng Zhu
Publikováno v:
PLoS Genetics, Vol 13, Iss 3, p e1006678 (2017)
Many large genome-wide association studies (GWAS) have identified common blood pressure (BP) variants. However, most of the identified BP variants do not overlap with the linkage evidence observed from family studies. We thus hypothesize that multipl
Externí odkaz:
https://doaj.org/article/15c8b3456ef145f7bb11e50c058424f3
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0163912 (2016)
Meta-analysis of single trait for multiple cohorts has been used for increasing statistical power in genome-wide association studies (GWASs). Although hundreds of variants have been identified by GWAS, these variants only explain a small fraction of
Externí odkaz:
https://doaj.org/article/57f4da01430d4cf19056d70b2696807d