Rare variants in previously identified linkage regions associated with carotid plaque in Dominican Republic families von Dueker, Nicole D, Beecham, Ashley, Wang, Liyong, Dong, Chuanhui, Sacco, Ralph L, Blanton, Susan H, Rundek, Tatjana

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Rare Variants in NOD1 Associated with Carotid Bifurcation Intima-Media Thickness in Dominican Republic Families von Dueker, Nicole D, Beecham, Ashley, Wang, Liyong, Blanton, Susan H, Guo, Shengru, Rundek, Tatjana, Sacco, Ralph L

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Extreme Phenotype Approach Suggests Taste Transduction Pathway for Carotid Plaque in a Multi-Ethnic Cohort von Dueker, Nicole D., Doliner, Brett, Gardener, Hannah, Dong, Chuanhui, Beecham, Ashley, Della-Morte, David, Sacco, Ralph L., Blanton, Susan H., Wang, Liyong, Rundek, Tatjana

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Genetic determinants of intracranial large artery stenosis in the northern Manhattan study von Liu, Minghua, Sariya, Sanjeev, Khasiyev, Farid, Tosto, Giuseppe, Dueker, Nicole D., Cheung, Ying Kuen, Wright, Clinton B., Sacco, Ralph L., Rundek, Tatjana, Elkind, Mitchell S.V., Gutierrez, Jose

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Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders von Cukier, Holly N, Dueker, Nicole D, Slifer, Susan H, Lee, Joycelyn M, Whitehead, Patrice L, Lalanne, Eminisha, Leyva, Natalia, Konidari, Ioanna, Gentry, Ryan C, Hulme, William F, Booven, Derek Van, Mayo, Vera, Hofmann, Natalia K, Schmidt, Michael A, Martin, Eden R, Haines, Jonathan L, Cuccaro, Michael L, Gilbert, John R, Pericak-Vance, Margaret A

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Rare variants in previously identified linkage regions associated with carotid plaque in Dominican Republic families von Nicole D Dueker, Ashley Beecham, Liyong Wang, Chuanhui Dong, Ralph L Sacco, Susan H Blanton, Tatjana Rundek

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Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants von Griswold, Anthony J, Dueker, Nicole D, Van Booven, Derek, Rantus, Joseph A, Jaworski, James M, Slifer, Susan H, Schmidt, Michael A, Hulme, William, Konidari, Ioanna, Whitehead, Patrice L, Cuccaro, Michael L, Martin, Eden R, Haines, Jonathan L, Gilbert, John R, Hussman, John P, Pericak-Vance, Margaret A

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Sickle Cell Trait and Renal Function in Hispanics in the United States: The Northern Manhattan Study von Dueker, Nicole D., Della-Morte, David, Rundek, Tatjana, Sacco, Ralph L., Blanton, Susan H.

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Family History of Eating Disorder and the Broad Autism Phenotype in Autism von Barrionuevo, Bianca A., Chowdhury, Aneesa R., Lee, Joycelyn M., Dueker, Nicole D., Martin, Eden R., Pericak‐Vance, Margaret A., Cuccaro, Michael

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Sequencing of Linkage Region on Chromosome 12p11 Identifies PKP2 as a Candidate Gene for Left Ventricular Mass in Dominican Families von Dueker, Nicole D, Guo, Shengru, Beecham, Ashley, Wang, Liyong, Blanton, Susan H, Di Tullio, Marco R, Rundek, Tatjana, Sacco, Ralph L

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Rare variants in ischemic stroke: an exome pilot study von Cole, John W, Stine, O Colin, Liu, Xinyue, Pratap, Abhishek, Cheng, Yuching, Tallon, Luke J, Sadzewicz, Lisa K, Dueker, Nicole, Wozniak, Marcella A, Stern, Barney J, Meschia, James F, Mitchell, Braxton D, Kittner, Steven J, O'Connell, Jeffrey R

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Analysis of Genetic Linkage Data for Mendelian Traits von Dueker, Nicole D., Pericak‐Vance, Margaret A.

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Recruitment and maintenance of tendon progenitors by TGFβ signaling are essential for tendon formation von Pryce, Brian A., Watson, Spencer S., Murchison, Nicholas D., Staverosky, Julia A., Dünker, Nicole, Schweitzer, Ronen

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The role of sirtuins and uncoupling proteins on vascular aging: The Northern Manhattan Study experience von Della-Morte, David, Pacifici, Francesca, Simonetto, Marialaura, Dong, Chuanhui, Dueker, Nicole, Blanton, Susan H., Wang, Liyong, Rundek, Tatjana

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Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection von Debette, Stéphanie, Kamatani, Yoichiro, Metso, Tiina M, Kloss, Manja, Chauhan, Ganesh, Engelter, Stefan T, Pezzini, Alessandro, Thijs, Vincent, Markus, Hugh S, Dichgans, Martin, Wolf, Christiane, Dittrich, Ralf, Touzé, Emmanuel, Southerland, Andrew M, Samson, Yves, Abboud, Shérine, Béjot, Yannick, Caso, Valeria, Bersano, Anna, Gschwendtner, Andreas, Sessa, Maria, Cole, John, Lamy, Chantal, Medeiros, Elisabeth, Beretta, Simone, Bonati, Leo H, Grau, Armin J, Michel, Patrik, Majersik, Jennifer J, Sharma, Pankaj, Kalashnikova, Ludmila, Nazarova, Maria, Dobrynina, Larisa, Bartels, Eva, Guillon, Benoit, van den Herik, Evita G, Fernandez-Cadenas, Israel, Jood, Katarina, Nalls, Michael A, De Leeuw, Frank-Erik, Jern, Christina, Cheng, Yu-Ching, Werner, Inge, Metso, Antti J, Lichy, Christoph, Lyrer, Philippe A, Brandt, Tobias, Boncoraglio, Giorgio B, Wichmann, Heinz-Erich, Gieger, Christian, Johnson, Andrew D, Böttcher, Thomas, Castellano, Maurizio, Arveiler, Dominique, Ikram, M Arfan, Breteler, Monique M B, Padovani, Alessandro, Meschia, James F, Kuhlenbäumer, Gregor, Rolfs, Arndt, Worrall, Bradford B, Ringelstein, Erich-Bernd, Zelenika, Diana, Tatlisumak, Turgut, Lathrop, Mark, Leys, Didier, Amouyel, Philippe, Dallongeville, Jean

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Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies von Morris, Andrew P., Le, Thu H., Wu, Haojia, Akbarov, Artur, van der Most, Peter J., Hemani, Gibran, Smith, George Davey, Mahajan, Anubha, Gaulton, Kyle J., Nadkarni, Girish N., Valladares-Salgado, Adan, Wacher-Rodarte, Niels, Mychaleckyj, Josyf C., Dueker, Nicole D., Guo, Xiuqing, Hai, Yang, Haessler, Jeffrey, Kamatani, Yoichiro, Stilp, Adrienne M., Zhu, Gu, Cook, James P., Ärnlöv, Johan, Blanton, Susan H., de Borst, Martin H., Bottinger, Erwin P., Buchanan, Thomas A., Cechova, Sylvia, Charchar, Fadi J., Chu, Pei-Lun, Damman, Jeffrey, Eales, James, Gharavi, Ali G., Giedraitis, Vilmantas, Heath, Andrew C., Ipp, Eli, Kiryluk, Krzysztof, Kramer, Holly J., Kubo, Michiaki, Larsson, Anders, Lindgren, Cecilia M., Lu, Yingchang, Madden, Pamela A. F., Montgomery, Grant W., Papanicolaou, George J., Raffel, Leslie J., Sacco, Ralph L., Sanchez, Elena, Stark, Holger, Sundstrom, Johan, Taylor, Kent D., Xiang, Anny H., Zivkovic, Aleksandra, Lind, Lars, Ingelsson, Erik, Martin, Nicholas G., Whitfield, John B., Cai, Jianwen, Laurie, Cathy C., Okada, Yukinori, Matsuda, Koichi, Kooperberg, Charles, Chen, Yii-Der Ida, Rundek, Tatjana, Rich, Stephen S., Loos, Ruth J. F., Parra, Esteban J., Cruz, Miguel, Rotter, Jerome I., Snieder, Harold, Tomaszewski, Maciej, Humphreys, Benjamin D., Franceschini, Nora

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Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities von Armstrong, Nicola J., Mather, Karen A., Sargurupremraj, Muralidharan, Knol, Maria J., Malik, Rainer, Satizabal, Claudia L., Yanek, Lisa R., Wen, Wei, Gudnason, Vilmundur G., Dueker, Nicole D., Elliott, Lloyd T., Hofer, Edith, Bis, Joshua, Jahanshad, Neda, Li, Shuo, Logue, Mark A., Luciano, Michelle, Scholz, Markus, Smith, Albert V., Trompet, Stella, Vojinovic, Dina, Xia, Rui, Alfaro-Almagro, Fidel, Ames, David, Amin, Najaf, Amouyel, Philippe, Beiser, Alexa S., Brodaty, Henry, Deary, Ian J., Fennema-Notestine, Christine, Gampawar, Piyush G., Gottesman, Rebecca, Griffanti, Ludovica, Jack, Clifford R., Jenkinson, Mark, Jiang, Jiyang, Kral, Brian G., Kwok, John B., Lampe, Leonie, C.M. Liewald, David, Maillard, Pauline, Marchini, Jonathan, Bastin, Mark E., Mazoyer, Bernard, Pirpamer, Lukas, Rafael Romero, José, Roshchupkin, Gennady V., Schofield, Peter R., Schroeter, Matthias L., Stott, David J., Thalamuthu, Anbupalam, Trollor, Julian, Tzourio, Christophe, van der Grond, Jeroen, Vernooij, Meike W., Witte, Veronica A., Wright, Margaret J., Yang, Qiong, Morris, Zoe, Siggurdsson, Siggi, Psaty, Bruce, Villringer, Arno, Schmidt, Helena, Haberg, Asta K., van Duijn, Cornelia M., Jukema, J. Wouter, Dichgans, Martin, Sacco, Ralph L., Wright, Clinton B., Kremen, William S., Becker, Lewis C., Thompson, Paul M., Mosley, Thomas H., Wardlaw, Joanna M., Ikram, M. Arfan, Adams, Hieab H.H., Seshadri, Sudha, Sachdev, Perminder S., Smith, Stephen M., Launer, Lenore, Longstreth, William, DeCarli, Charles, Schmidt, Reinhold, Fornage, Myriam, Debette, Stephanie, Nyquist, Paul A.

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Abstract WMP60: Adiponutrin Gene Polymorphism is Associated With Unexplained Embolic Covert Brain Infarction in the Northern Manhattan Study von Parikh, Neal S, Dueker, Nicole, Varela, Dalila, Rundek, Tatjana, Wright, Clinton B, Sacco, Ralph, Elkind, Mitchell S, Gutierrez, Jose

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Polymorphisms in migraine-associated gene, atp1a2, and ischemic stroke risk in a biracial population: the genetics of early onset stroke study von Harriott, Andrea M, Dueker, Nicole, Cheng, Yu-Ching, Ryan, Kathleen A, O’Connell, Jeffrey R, Stine, O Colin, McArdle, Patrick F, Wozniak, Marcella A, Stern, Barney J, Mitchell, Braxton D, Kittner, Steven J, Cole, John W

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Genome-wide association study of executive function in a multi-ethnic cohort implicates LINC01362: Results from the northern Manhattan study von Dueker, Nicole, Wang, Liyong, Gardener, Hannah, Gomez, Lissette, Kaur, Sonya, Beecham, Ashley, Blanton, Susan H., Dong, Chuanhui, Gutierrez, Jose, Cheung, Ying Kuen, Moon, Yeseon P., Levin, Bonnie, Wright, Clinton B., Elkind, Mitchell S.V., Sacco, Ralph L., Rundek, Tatjana

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