Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study by Buyske, Steven, Wu, Ying, Carty, Cara L, Cheng, Iona, Assimes, Themistocles L, Dumitrescu, Logan, Hindorff, Lucia A, Mitchell, Sabrina, Ambite, Jose Luis, Boerwinkle, Eric, Buzkova, Petra, Carlson, Chris S, Cochran, Barbara, Duggan, David, Eaton, Charles B, Fesinmeyer, Megan D, Franceschini, Nora, Haessler, Jeffrey, Jenny, Nancy, Kang, Hyun Min, Kooperberg, Charles, Lin, Yi, Le Marchand, Loic, Matise, Tara C, Robinson, Jennifer G, Rodriguez, Carlos, Schumacher, Fredrick R, Voight, Benjamin F, Young, Alicia, Manolio, Teri A, Mohlke, Karen L, Haiman, Christopher A, Peters, Ulrike, Crawford, Dana C, North, Kari E

Get full text

Macrophage Tropism of Human Immunodeficiency Virus Type 1 Isolates from Brain and Lymphoid Tissues Predicts Neurotropism Independent of Coreceptor Specificity by Gorry, P R, Bristol, G, Zack, J A, Ritola, K, Swanstrom, R, Birch, C J, Bell, J E, Bannert, N, Crawford, K, Wang, H, Schols, D, De Clercq, E, Kunstman, K, Wolinsky, S M, Gabuzda, D

Get full text

Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study by Perera, Minoli A, PharmD, Cavallari, Larisa H, PharmD, Limdi, Nita A, PharmD, Gamazon, Eric R, MS, Konkashbaev, Anuar, MS, Daneshjou, Roxana, BS, Pluzhnikov, Anna, PhD, Crawford, Dana C, PhD, Wang, Jelai, BS, Liu, Nianjun, PhD, Tatonetti, Nicholas, PhD, Bourgeois, Stephane, MS, Takahashi, Harumi, Prof, Bradford, Yukiko, MS, Burkley, Benjamin M, MS, Desnick, Robert J, Prof, Halperin, Jonathan L, Prof, Khalifa, Sherief I, Prof, Langaee, Taimour Y, PhD, Lubitz, Steven A, MD, Nutescu, Edith A, Prof, Oetjens, Matthew, BS, Shahin, Mohamed H, MS, Patel, Shitalben R, MS, Sagreiya, Hersh, MD, Tector, Matthew, PhD, Weck, Karen E, Prof, Rieder, Mark J, PhD, Scott, Stuart A, PhD, Wu, Alan HB, PhD, Burmester, James K, PhD, Wadelius, Mia, MD, Deloukas, Panos, PhD, Wagner, Michael J, PhD, Mushiroda, Taisei, PhD, Kubo, Michiaki, MD, Roden, Dan M, Prof, Cox, Nancy J, Prof, Altman, Russ B, Prof, Klein, Teri E, PhD, Nakamura, Yusuke, Prof, Johnson, Julie A, Prof

Get full text

KL-VS heterozygosity is associated with lower amyloid-dependent tau accumulation and memory impairment in Alzheimer’s disease by Neitzel, Julia, Franzmeier, Nicolai, Rubinski, Anna, Dichgans, Martin, Brendel, Matthias, Malik, Rainer, Ewers, Michael

Get full text

Genetic risk factors for BMI and obesity in an ethnically diverse population: Results from the population architecture using genomics and epidemiology (PAGE) study by Fesinmeyer, Megan D., North, Kari E., Ritchie, Marylyn D., Lim, Unhee, Franceschini, Nora, Wilkens, Lynne R., Gross, Myron D., Bůžková, Petra, Glenn, Kimberly, Quibrera, P. Miguel, Fernández‐Rhodes, Lindsay, Li, Qiong, Fowke, Jay H., Li, Rongling, Carlson, Christopher S., Prentice, Ross L., Kuller, Lewis H., Manson, JoAnn E., Matise, Tara C., Cole, Shelley A., Chen, Christina T.L., Howard, Barbara V., Kolonel, Laurence N., Henderson, Brian E., Monroe, Kristine R., Crawford, Dana C., Hindorff, Lucia A., Buyske, Steven, Haiman, Christopher A., Le Marchand, Loic, Peters, Ulrike

Get full text

The BIN1 rs744373 SNP is associated with increased tau-PET levels and impaired memory by Franzmeier, Nicolai, Rubinski, Anna, Neitzel, Julia, Ewers, Michael

Get full text

Correlation between Alzheimer’s disease and type 2 diabetes using non-negative matrix factorization by Chung, Yeonwoo, Lee, Hyunju

Get full text

Germline Genetic Variants and Lung Cancer Survival in African Americans by Jones, Carissa C, Bush, William S, Crawford, Dana C, Wenzlaff, Angela S, Schwartz, Ann G, Wiencke, John K, Wrensch, Margaret R, Blot, William J, Chanock, Stephen J, Grogan, Eric L, Aldrich, Melinda C

Get full text

Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity by Jahanshad, Neda, Rajagopalan, Priya, Hua, Xue, Hibar, Derrek P., Nir, Talia M., Toga, Arthur W., Jack, Clifford R., Saykin, Andrew J., Green, Robert C., Weiner, Michael W., Medland, Sarah E., Montgomery, Grant W., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Thompson, Paul M.

Get full text

Hi-MC: a novel method for high-throughput mitochondrial haplogroup classification by Smieszek, Sandra, Mitchell, Sabrina L, Farber-Eger, Eric H, Veatch, Olivia J, Wheeler, Nicholas R, Goodloe, Robert J, Wells, Quinn S, Murdock, Deborah G, Crawford, Dana C

Get full text

Association of cancer susceptibility variants with risk of multiple primary cancers: The population architecture using genomics and epidemiology study by Park, S Lani, Caberto, Christian P, Lin, Yi, Goodloe, Robert J, Dumitrescu, Logan, Love, Shelly-Ann, Matise, Tara C, Hindorff, Lucia A, Fowke, Jay H, Schumacher, Fredrick R, Beebe-Dimmer, Jennifer, Chen, Chu, Hou, Lifang, Thomas, Fridtjof, Deelman, Ewa, Han, Ying, Peters, Ulrike, North, Kari E, Heiss, Gerardo, Crawford, Dana C, Haiman, Christopher A, Wilkens, Lynne R, Bush, William S, Kooperberg, Charles, Cheng, Iona, Le Marchand, Loïc

Get full text

Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer’s disease pathogenesis by Zhou, Xiaopu, Chen, Yu, Mok, Kin Y., Zhao, Qianhua, Chen, Keliang, Chen, Yuewen, Hardy, John, Li, Yun, Fu, Amy K. Y., Guo, Qihao, Ip, Nancy Y.

Get full text

Serum vitamin D levels and severe asthma exacerbations in the Childhood Asthma Management Program study by Brehm, John M., MD, MPH, Schuemann, Brooke, BS, Fuhlbrigge, Anne L., MD, Hollis, Bruce W., PhD, Strunk, Robert C., MD, Zeiger, Robert S., MD, PhD, Weiss, Scott T., MD, MS, Litonjua, Augusto A., MD, MPH

Get full text

PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity by van Setten, Jessica, Brody, Jennifer A., Jamshidi, Yalda, Butler, Anne M., Campbell, Harry, Evans, Daniel S., Gibson, Quince, Gudbjartsson, Daniel F., Kerr, Kathleen F., Krijthe, Bouwe P., Lyytikäinen, Leo-Pekka, Müller, Christian, Müller-Nurasyid, Martina, Nolte, Ilja M., Padmanabhan, Sandosh, Ritchie, Marylyn D., Robino, Antonietta, Smith, Albert V., Tanaka, Toshiko, Teumer, Alexander, Trompet, Stella, Ulivi, Sheila, Verweij, Niek, Yin, Xiaoyan, Asselbergs, Folkert W., Bader, Joel S., Barnard, John, Bis, Josh, Blankenberg, Stefan, Boerwinkle, Eric, Bradford, Yuki, Buckley, Brendan M., Chung, Mina K., Crawford, Dana, den Hoed, Marcel, Denny, Josh C., Ellinor, Patrick T., Felix, Stephan B., Franco, Oscar H., Franke, Lude, Harris, Tamara B., Holm, Hilma, Ilaria, Gandin, Kolcic, Ivana, Kors, Jan A., Lin, Honghuang, Lin, Henry J., Macfarlane, Peter W., Magnani, Jared W., Meitinger, Thomas, Mitchell, Braxton D., Munzel, Thomas, Papanicolaou, George J., Peters, Annette, Pfeufer, Arne, Pramstaller, Peter P., Rudan, Igor, Samani, Nilesh J., Silva Aldana, Claudia T., Sinner, Moritz F., Smith, Jonathan D., Snieder, Harold, Soliman, Elsayed Z., Spector, Timothy D., Stott, David J., Strauch, Konstantin, Tarasov, Kirill V., Thorsteinsdottir, Unnur, Uitterlinden, Andre G., Van Wagoner, David R., Völzke, Henry, Waldenberger, Melanie, Wild, Philipp S., Zeller, Tanja, Alonso, Alvaro, Bandinelli, Stefania, Cucca, Francesco, Dörr, Marcus, Ferrucci, Luigi, Gasparini, Paolo, Gudnason, Vilmundur, Hayward, Caroline, Jukema, J. Wouter, Kääb, Stefan, Lehtimäki, Terho, Liu, Yongmei, Parsa, Afshin, Polasek, Ozren, Psaty, Bruce M., Schnabel, Renate B., Sinagra, Gianfranco, Stefansson, Kari, Stricker, Bruno H., van der Harst, Pim, van Duijn, Cornelia M., Wilson, James F., Gharib, Sina A., de Bakker, Paul I. W., Arking, Dan E., Sotoodehnia, Nona

Get full text

Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin by Xu, Hua, Jiang, Min, Oetjens, Matt, Bowton, Erica A, Ramirez, Andrea H, Jeff, Janina M, Basford, Melissa A, Pulley, Jill M, Cowan, James D, Wang, Xiaoming, Ritchie, Marylyn D, Masys, Daniel R, Roden, Dan M, Crawford, Dana C, Denny, Joshua C

Get full text

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project by Duan, Qing, Liu, Eric Yi, Auer, Paul L, Zhang, Guosheng, Lange, Ethan M, Jun, Goo, Bizon, Chris, Jiao, Shuo, Buyske, Steven, Franceschini, Nora, Carlson, Chris S, Hsu, Li, Reiner, Alex P, Peters, Ulrike, Haessler, Jeffrey, Curtis, Keith, Wassel, Christina L, Robinson, Jennifer G, Martin, Lisa W, Haiman, Christopher A, Le Marchand, Loic, Matise, Tara C, Hindorff, Lucia A, Crawford, Dana C, Assimes, Themistocles L, Kang, Hyun Min, Heiss, Gerardo, Jackson, Rebecca D, Kooperberg, Charles, Wilson, James G, Abecasis, Gonçalo R, North, Kari E, Nickerson, Deborah A, Lange, Leslie A, Li, Yun

Get full text

Pattern of sequence variation across 213 environmental response genes by Livingston, Robert J, von Niederhausern, Andrew, Jegga, Anil G, Crawford, Dana C, Carlson, Christopher S, Rieder, Mark J, Gowrisankar, Sivakumar, Aronow, Bruce J, Weiss, Robert B, Nickerson, Deborah A

Get full text

Tau‐Atrophy Variability Reveals Phenotypic Heterogeneity in Alzheimer's Disease by McCollum, Lauren, Jack, Clifford R., Thomas, Ronald G., Walter, Sarah, Sather, Tamie, Donohue, Michael, Bernstein, Matthew, Borowski, Bret, Kantarci, Kejal, Ward, Chad, Koeppe, Robert A., Mathis, Chet, Cairns, Nigel J., Korecka, Magdalena, Figurski, Michal, Crawford, Karen, Snyder, Peter J., Molchan, Susan, Lind, Betty, Dolen, Sara, Spann, Bryan M., Vanderswag, Helen, Fleisher, Adam, Rountree, Susan, Dang, Mimi, Honig, Lawrence S., Leon, Sue, Mintun, Mark A., Schneider, Stacy, Clark, David, Brockington, John, Roberson, Erik, Albert, Marilyn, Kielb, Stephanie, Michel, Christina A., Leon, Mony J, De Santi, Susan, Wolk, David, Smith, Charles D., Jicha, Greg, Oates, Elizabeth, Conrad, Gary, Lopez, Oscar L., Oakley, MaryAnn, Goldstein, Bonnie S., Martin, Kim, Makino, Kelly M., Mulnard, Ruth A., Ortiz, Catherine Mc Adams, Womack, Kyle, Quiceno, Mary, Arrastia, Ramon Diaz, Weiner, Myron, DeVous, Michael, Cellar, Janet S., Bums, Jeffrey M., Anderson, Heather S., Woo, Ellen, Parfitt, Francine, Kendall, Tracy, Johnson, Heather, Hake, Ann Marie, Hunt, Cynthia, Carson, Richard E., MacAvoy, Martha G., Bergman, Howard, Stefanovic, Bojana, Feldman, Howard, Assaly, Michele, Kertesz, Andrew, Rogers, John, Trost, Dick, Wu, Chuang Kuo, Johnson, Keith A., Marshall, Gad, Taylor, Joy L., Lane, Barton, Rosen, Allison, Belden, Christine M., Kowall, Neil, Norbash, Alexan, Hudson, Leon, Olichney, John, Lee, T Y, Bartha, Rob, Johnson, Sterling, Asthana, Sanjay, Capote, Horacio, Williamson, Jeff D., Watkins, Franklin, Salloway, Stephen, Malloy, Paul, Rosen, Howard J., Miller, Bruce L., Mintzer, Jacobo, Bachman, David, Finger, Elizabether, Rogers, John, Kertesz, Andrew, Fargher, Kristin

Get full text

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants by Verma, Anurag, Verma, Shefali S, Pendergrass, Sarah A, Crawford, Dana C, Crosslin, David R, Kuivaniemi, Helena, Bush, William S, Bradford, Yuki, Kullo, Iftikhar, Bielinski, Suzette J, Li, Rongling, Denny, Joshua C, Peissig, Peggy, Hebbring, Scott, De Andrade, Mariza, Ritchie, Marylyn D, Tromp, Gerard

Get full text

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index by Cronin, Robert M, Field, Julie R, Bradford, Yuki, Shaffer, Christian M, Carroll, Robert J, Mosley, Jonathan D, Bastarache, Lisa, Edwards, Todd L, Hebbring, Scott J, Lin, Simon, Hindorff, Lucia A, Crane, Paul K, Pendergrass, Sarah A, Ritchie, Marylyn D, Crawford, Dana C, Pathak, Jyotishman, Bielinski, Suzette J, Carrell, David S, Crosslin, David R, Ledbetter, David H, Carey, David J, Tromp, Gerard, Williams, Marc S, Larson, Eric B, Jarvik, Gail P, Peissig, Peggy L, Brilliant, Murray H, McCarty, Catherine A, Chute, Christopher G, Kullo, Iftikhar J, Bottinger, Erwin, Chisholm, Rex, Smith, Maureen E, Roden, Dan M, Denny, Joshua C

Get full text