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收藏分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 A missense variant in human perilipin 2 (PLIN2 Ser251Pro) reduces hepatic steatosis in mice
Scorletti, Eleonora; Saiman, Yedidya; Jeon, Sookyoung; Schneider, Carolin V.; Buyco, Delfin G.; Lin, Chelsea; Himes, Blanca E.; Mesaros, Clementina A.; Vujkovic, Marijana; Creasy, Kate Townsend; Furth, Emma E.; Billheimer, Jeffrey T.; Hand, Nicholas J.; Kaplan, David E.; Chang, Kyong-Mi; Tsao, Philip S.; Lynch, Julie A.; Dempsey, Joseph L.; Harkin, Julia; Bayen, Susovon; Conlon, Donna; Guerraty, Marie; Phillips, Michael C.; Rader, Daniel J.; Carr, Rotonya M. 分享 收藏 分享 收藏 分享 收藏 Large-scale genome-wide association study of coronary artery disease in genetically diverse populations遗传多样性人群冠状动脉疾病的大规模全基因组关联研究Tcheandjieu, Catherine; Zhu, Xiang; Hilliard, Austin T.; Clarke, Shoa L.; Napolioni, Valerio; Ma, Shining; Lee, Kyung Min; Fang, Huaying; Chen, Fei; Lu, Yingchang; Tsao, Noah L.; Raghavan, Sridharan; Koyama, Satoshi; Gorman, Bryan R.; Vujkovic, Marijana; Klarin, Derek; Levin, Michael G.; Sinnott-Armstrong, Nasa; Wojcik, Genevieve L.; Plomondon, Mary E.; Maddox, Thomas M.; Waldo, Stephen W.; Bick, Alexander G.; Pyarajan, Saiju; Huang, Jie; Song, Rebecca; Ho, Yuk-Lam; Buyske, Steven; Kooperberg, Charles; Haessler, Jeffrey; Loos, Ruth J. F.; Do, Ron; Verbanck, Marie; Chaudhary, Kumardeep; North, Kari E.; Avery, Christy L.; Graff, Mariaelisa; Haiman, Christopher A.; Le Marchand, Loic; Wilkens, Lynne R.; Bis, Joshua C.; Leonard, Hampton; Shen, Botong; Lange, Leslie A.; Giri, Ayush; Dikilitas, Ozan; Kullo, Iftikhar J.; Stanaway, Ian B.; Jarvik, Gail P.; Gordon, Adam S.; Hebbring, Scott; Namjou, Bahram; Kaufman, Kenneth M.; Ito, Kaoru; Ishigaki, Kazuyoshi; Kamatani, Yoichiro; Verma, Shefali S.; Ritchie, Marylyn D.; Kember, Rachel L.; Baras, Aris; Lotta, Luca A.; Kathiresan, Sekar; Hauser, Elizabeth R.; Miller, Donald R.; Lee, Jennifer S.; Saleheen, Danish; Reaven, Peter D.; Cho, Kelly; Gaziano, J. Michael; Natarajan, Pradeep; Huffman, Jennifer E.; Voight, Benjamin F.; Rader, Daniel J.; Chang, Kyong-Mi; Lynch, Julie A.; Damrauer, Scott M.; Wilson, Peter W. F.; Tang, Hua; Sun, Yan, V; Tsao, Philip S.; O'Donnell, Christopher J.; Assimes, Themistocles L. 分享 收藏 分享 收藏 Increased expression of ZFPM2 bypasses SRY to drive 46,XX testicular development: A new mechanism of 46,XX DSDRagno, Leah; Yang, Daphne; Bhatti, Trisha; Bradfield, Jonathan; Bowen, Diane; Grand, Katheryn; Hakonarson, Hakon; Kolon, Thomas; Glessner, Joseph; Simon, M. Celeste; Skuli, Nicolas; Vogiatzi, Maria; Guerraty, Marie; Deardorff, Matthew; Pyle, Louisa 分享 收藏 分享 收藏 分享 收藏 Diagnostic accuracy of SPECT and PET myocardial perfusion imaging in patients with left bundle branch block or ventricular-paced rhythmVidula, Mahesh K.; Wiener, Philip; Selvaraj, Senthil; Khan, Muhammad Shoaib; Salam, Usman Abdul; Rojulpote, Chaitanya; Metzler, Scott D.; Denduluri, Srinivas; Guerraty, Marie; Julien, Howard; Bravo, Paco E. 分享 收藏 Medical records-based chronic kidney disease phenotype for clinical care and big data observational and genetic studiesShang, Ning; Khan, Atlas; Polubriaginof, Fernanda; Zanoni, Francesca; Mehl, Karla; Fasel, David; Drawz, Paul E.; Carrol, Robert J.; Denny, Joshua C.; Hathcock, Matthew A.; Arruda-Olson, Adelaide M.; Peissig, Peggy L.; Dart, Richard A.; Brilliant, Murray H.; Larson, Eric B.; Carrell, David S.; Pendergrass, Sarah; Verma, Shefali Setia; Ritchie, Marylyn D.; Benoit, Barbara; Gainer, Vivian S.; Karlson, Elizabeth W.; Gordon, Adam S.; Jarvik, Gail P.; Stanaway, Ian B.; Crosslin, David R.; Mohan, Sumit; Ionita-Laza, Iuliana; Tatonetti, Nicholas P.; Gharavi, Ali G.; Hripcsak, George; Weng, Chunhua; Kiryluk, Krzysztof 分享 收藏 分享 收藏 分享 收藏 Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseases人类血管细胞的基因组分析将TWIST1鉴定为常见血管疾病的致病基因Nurnberg, Sylvia T.; Guerraty, Marie A.; Wirka, Robert C.; Rao, H. Shanker; Pjanic, Milos; Norton, Scott; Serrano, Felipe; Perisic, Ljubica; Elwyn, Susannah; Pluta, John; Zhao, Wei; Testa, Stephanie; Park, YoSon; Nguyen, Trieu; Ko, Yi-An; Wang, Ting; Hedin, Ulf; Sinha, Sanjay; Barash, Yoseph; Brown, Christopher D.; Quertermous, Thomas; Rader, Daniel J. 分享 收藏 Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino AncestryDamrauer, Scott M.; Chaudhary, Kumardeep; Cho, Judy H.; Liang, Lusha W.; Argulian, Edgar; Chan, Lili; Dobbyn, Amanda; Guerraty, Marie A.; Judy, Renae; Kay, Jenna; Kember, Rachel L.; Levin, Michael G.; Saha, Aparna; Van Vleck, Tielman; Verma, Shefali S.; Weaver, JoEllen; Abul-Husn, Noura S.; Baras, Aris; Chirinos, Julio A.; Drachman, Brian; Kenny, Eimear E.; Loos, Ruth J. F.; Narula, Jagat; Overton, John; Reid, Jeffrey; Ritchie, Marylyn; Sirugo, Giorgio; Nadkarni, Girish; Rader, Daniel J.; Do, Ron 分享 收藏 
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