Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity von 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

Volltext

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome von 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.

Volltext

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome von 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.

Volltext

Powerful and Efficient Strategies for Genetic Association Testing of Symptom and Questionnaire Data in Psychiatric Genetic Studies von 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.

Volltext

Epidemiology beyond its limits von 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

Volltext

Abstract 4140003: Impact of Long-Term Blood Pressure Variability on Adverse Cardiovascular Outcomes in High- and Low-Risk Populations von Krohn, Lynne, Zappe, Dion, Hoffing, Rachel, Holleman, Aaron, LoGerfo, Philip, Plekan, Mollie, Akle Serrano, Sebastian, Ward, Lucas, Nioi, Paul, Williams, Bryan, Deaton, Aimee, Tu, Ho-Chou

Volltext

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion von Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A. S., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Warren, Stephen T., Chopra, Pankaj, Cutler, David J., Duncan, Richard, Mulle, Jennifer G., Voss, Anna J., Zwick, Michael E., Diacou, Alexander, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Jin, Andrea, Lilley, Brenna, Salmons, Harold I., Tran, Oanh, Pardinas, Antonio, Walters, James T. R., Demaerel, Wolfram, Boot, Erik, Butcher, Nancy J., Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese A. M. J., van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koen, Vogels, Annick, Moss, Edward M., Sharkus, Robert J., 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, Niarchou, Maria, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Declan G., Buzzanca, Antonio, Digilio, Maria C., Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F., Ousley, Opal Y., Carmel, Miri, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stéphan, Sandini, Corrado, Béna, Frédérique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Philip, Nicole, Campbell, Linda E., McCabe, Kathryn L., Hooper, Stephen R., Schoch, Kelly, Shashi, Vandana, Simon, Tony J., Tassone, Flora, Arango, Celso, García-Miñaúr, Sixto, Suñer, Damià H., Raventos-Simic, Jasna, Epstein, Michael P., Williams, Nigel M., Bassett, Anne S.

Volltext

7SCHIZOPHRENIA POLYGENIC RISK SCORE ANALYSIS IN 22Q11.2 DELETION SYNDROME von 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

Volltext