未登录 Rare predicted loss-of-function and damaging missense variants in CFHR5 associate with protection from age-related macular degeneration CFHR5基因中罕见的预测失活和破坏性错义变异与年龄相关性黄斑变性的保护作用相关联 Holleman, AM; Deaton, AM; Hoffing, RA; Krohn, L; LoGerfo, P; Nioi, P; Plekan, ME; Serrano, SA; Ticau, S; Walshe, TE; Borodovsky, A; Ward, LD 分享 收藏
Impact of Long-Term Blood Pressure Variability on Adverse Cardiovascular Outcomes in High- and Low-Risk Populations 长期血压变异性对高、低风险人群不良心血管结局的影响 Krohn, Lynne; Zappe, Dion; Hoffing, Rachel; Holleman, Aaron; LoGerfo, Philip; Plekan, Mollie; Serrano, Sebastian Akle; Ward, Lucas; Nioi, Paul; Williams, Bryan; Deaton, Aimee; Ho-Chou Tu 分享 收藏
Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity hepatokine基因中罕见的功能变体丧失INHBE可预防腹部肥胖 Deaton, Aimee M.; Dubey, Aditi; Ward, Lucas D.; Dornbos, Peter; Flannick, Jason; Yee, Elaine; Ticau, Simina; Noetzli, Leila; Parker, Margaret M.; Hoffing, Rachel A.; Willis, Carissa; Plekan, Mollie E.; Holleman, Aaron M.; Hinkle, Gregory; Fitzgerald, Kevin; Vaishnaw, Akshay K.; Nioi, Paul 分享 收藏
Epidemiology beyond its limits McCullough, Lauren E.; Maliniak, Maret L.; Amin, Avnika B.; Baker, Julia M.; Baliashvili, Davit; Barberio, Julie; Barrera, Chloe M.; Brown, Carolyn A.; Collin, Lindsay J.; Freedman, Alexa A.; Gibbs, David C.; Haddad, Maryam B.; Hall, Eric W.; Hamid, Sarah; Harrington, Kristin R., V; Holleman, Aaron M.; Kaufman, John A.; Khan, Mohammed A.; Labgold, Katie; Lee, Veronica C.; Malik, Amyn A.; Mann, Laura M.; Marks, Kristin J.; Nelson, Kristin N.; Quader, Zerleen S.; Ross-Driscoll, Katherine; Sarkar, Supriya; Shah, Monica P.; Shao, Iris Y.; Smith, Jonathan P.; Stanhope, Kaitlyn K.; Valenzuela-Lara, Marisol; Van Dyke, Miriam E.; Vyas, Kartavya J.; Lash, Timothy L. 分享 收藏
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (vol 10, 18051, 2020) Trevino, Cristina E.; Holleman, Aaron M.; Corbitt, Holly; Maslen, Cheryl L.; Rosser, Tracie C.; Cutler, David J.; Johnston, H. Richard; Rambo-Martin, Benjamin L.; Oberoi, Jai; Dooley, Kenneth J.; Capone, George T.; Reeves, Roger H.; Cordell, Heather J.; Keavney, Bernard D.; Agopian, A. J.; Goldmuntz, Elizabeth; Gruber, Peter J.; O'Brien, James E.; Bittel, Douglas C.; Wadhwa, Lalita; Cua, Clifford L.; Moskowitz, Ivan P.; Mulle, Jennifer G.; Epstein, Michael P.; Sherman, Stephanie L.; Zwick, Michael E. 分享 收藏
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome Trevino, Cristina E.; Holleman, Aaron M.; Corbitt, Holly; Maslen, Cheryl L.; Rosser, Tracie C.; Cutler, David J.; Johnston, H. Richard; Rambo-Martin, Benjamin L.; Oberoi, Jai; Dooley, Kenneth J.; Capone, George T.; Reeves, Roger H.; Cordell, Heather J.; Keavney, Bernard D.; Agopian, A. J.; Goldmuntz, Elizabeth; Gruber, Peter J.; O'Brien, James E., Jr.; Bittel, Douglas C.; Wadhwa, Lalita; Cua, Clifford L.; Mulle, Jennifer G.; Epstein, Michael P.; Sherman, Stephanie L.; Zwick, Michael E. 分享 收藏
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S.; Heung, Tracy; Holleman, Aaron M.; Johnston, H. Richard; Monfeuga, Thomas; McDonald-McGinn, Donna M.; Gur, Raquel E.; Morrow, Bernice E.; Swillen, Ann; Vorstman, Jacob A. S.; Bearden, Carrie E.; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; Warren, Stephen T.; Owen, Michael J.; Chopra, Pankaj; Cutler, David J.; Duncan, Richard; Kotlar, Alex, V; Mulle, Jennifer G.; Voss, Anna J.; Zwick, Michael E.; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih-Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold, I; Oanh Tran; Holmans, Peter; Pardinas, Antonio; Walters, James T. R.; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J.; Costain, Gregory A.; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A. M. J.; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T. Blaine; McGinn, Daniel E.; Moss, Edward M.; Sharkus, Robert J.; Unolt, Marta; Zackai, Elaine H.; Calkins, Monica E.; Gallagher, Robert S.; Gur, Ruben C.; Tang, Sunny X.; Fritsch, Rosemarie; Ornstein, Claudia; Repetto, Gabriela M.; Breetvelt, Elemi; Duijff, Sasja N.; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C.; Prasad, Sarah E.; Daly, Eileen M.; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan G.; Buzzanca, Antonio; Di Fabio, Fabio; Digilio, Maria C.; Pontillo, Maria; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F.; Ousley, Opal Y.; Carmel, Miri; Gothelf, Doron; Mekori-Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Weizman, Abraham; Kushan, Leila; Jalbrzikowski, Maria; Armando, Marco; Eliez, Stephan; Sandini, Corrado; Schneider, Maude; Bena, Frederique Sloan; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.; Belzeaux, Raoul; Busa, Tiffany; Philip, Nicole; Campbell, Linda E.; McCabe, Kathryn L.; Hooper, Stephen R.; Schoch, Kelly; Shashi, Vandana; Simon, Tony J.; Tassone, Flora; Arango, Celso; Fraguas, David; Garcia-Minaur, Sixto; Morey-Canyelles, Jaume; Rosell, Jordi; Suner, Damia H.; Raventos-Simic, Jasna; Epstein, Michael P.; Williams, Nigel M.; Bassett, Anne S. 分享 收藏
Powerful and Efficient Strategies for Genetic Association Testing of Symptom and Questionnaire Data in Psychiatric Genetic Studies Holleman, Aaron M.; Broadaway, K. Alaine; Duncan, Richard; Todor, Andrei; Almli, Lynn M.; Bradley, Bekh; Ressler, Kerry J.; Ghosh, Debashis; Mulle, Jennifer G.; Epstein, Michael P. 分享 收藏
SCHIZOPHRENIA POLYGENIC RISK SCORE ANALYSIS IN 22Q11.2 DELETION SYNDROME Monfeuga, Thomas; Epstein, Michael P.; Holleman, Aaron M.; Cleynen, Isabelle; Johnston, Henry; Zhao, Yingjie; McDonald-McGinn, Donna M.; Gur, Raquel E.; Warren, Stephen T.; Vermeesch, Joris; Emanuel, Beverly S.; Morrow, Bernice E.; Bassett, Anne S.; Williams, Nigel 分享 收藏
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