检索结果 - Pluzhnikov, Anna

Inferences about human demography based on multilocus analyses of noncoding sequences. 由 Pluzhnikov, Anna, Di Rienzo, Anna, Hudson, Richard R

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Rational Inferences about Departures from Hardy-Weinberg Equilibrium 由 Wittke-Thompson, Jacqueline K., Pluzhnikov, Anna, Cox, Nancy J.

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Identifying Plausible Genetic Models Based on Association and Linkage Results: Application to Type 2 Diabetes 由 Guan, Weihua, Boehnke, Michael, Pluzhnikov, Anna, Cox, Nancy J., Scott, Laura J.

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Correlation of Intergenerational Family Sizes Suggests a Genetic Component of Reproductive Fitness 由 Pluzhnikov, Anna , Nolan, Daniel K. , Tan, Zhiqiang , McPeek, Mary Sara , Ober, Carole 

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Genomewide Significant Linkage to Stuttering on Chromosome 12 由 Riaz, Naveeda, Steinberg, Stacy, Ahmad, Jamil, Pluzhnikov, Anna, Riazuddin, Sheikh, Cox, Nancy J., Drayna, Dennis

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Meta-Analysis of 23 Type 2 Diabetes Linkage Studies from the International Type 2 Diabetes Linkage Analysis Consortium 由 Guan, Weihua, Pluzhnikov, Anna, Cox, Nancy J., Boehnke, Michael, for the International Type 2 Diabetes Linkage Analysis Consortium

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Spoiling the Whole Bunch: Quality Control Aimed at Preserving the Integrity of High-Throughput Genotyping 由 Pluzhnikov, Anna, Below, Jennifer E., Konkashbaev, Anuar, Tikhomirov, Anna, Kistner-Griffin, Emily, Roe, Cheryl A., Nicolae, Dan L., Cox, Nancy J.

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Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues 由 Nekhaeva, Ekaterina, Bodyak, Natalya D., Kraytsberg, Yevgenya, McGrath, Sean B., Van Orsouw, Nathalie J., Pluzhnikov, Anna, Wei, Jeanne Y., Vijg, Jan, Khrapko, Konstantin

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New Complexities in the Genetics of Stuttering: Significant Sex-Specific Linkage Signals 由 Suresh, Rathi, Ambrose, Nicoline, Roe, Cheryl, Pluzhnikov, Anna, Wittke-Thompson, Jacqueline K., Ng, Maggie C.-Y., Wu, Xiaolin, Cook, Edwin H., Lundstrom, Cecilia, Garsten, Marie, Ezrati, Ruth, Yairi, Ehud, Cox, Nancy J.

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A Novel Mechanism of Inherited TBG Deficiency: Mutation in a Liver-Specific Enhancer 由 Ferrara, Alfonso Massimiliano, Pappa, Theodora, Fu, Jiao, Brown, Christopher D., Peterson, April, Moeller, Lars C., Wyne, Kathleen, White, Kevin P., Pluzhnikov, Anna, Trubetskoy, Vassily, Nobrega, Marcelo, Weiss, Roy E., Dumitrescu, Alexandra M., Refetoff, Samuel

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Insulin gene mutations as a cause of permanent neonatal diabetes 由 Støy, Julie, Edghill, Emma L., Flanagan, Sarah E., Ye, Honggang, Paz, Veronica P., Pluzhnikov, Anna, Below, Jennifer E., Hayes, M. Geoffrey, Cox, Nancy J., Lipkind, Gregory M., Lipton, Rebecca B., Greeley, Siri Atma W., Patch, Ann-Marie, Ellard, Sian, Steiner, Donald F., Hattersley, Andrew T., Philipson, Louis H., Bell, Graeme I.

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The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study 由 Urbanek, Margrit, Hayes, M. Geoffrey, Armstrong, Loren L., Morrison, Jean, Lowe, Lynn P., Badon, Sylvia E., Scheftner, Doug, Pluzhnikov, Anna, Levine, David, Laurie, Cathy C., McHugh, Caitlin, Ackerman, Christine M., Mirel, Daniel B., Doheny, Kimberly F., Guo, Cong, Scholtens, Denise M., Dyer, Alan R., Metzger, Boyd E., Reddy, Timothy E., Cox, Nancy J., Lowe, William L.

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Identification of HKDC1 and BACE2 as Genes Influencing Glycemic Traits During Pregnancy Through Genome-Wide Association Studies 由 Hayes, M. Geoffrey, Urbanek, Margrit, Hivert, Marie-France, Armstrong, Loren L., Morrison, Jean, Guo, Cong, Lowe, Lynn P., Scheftner, Douglas A., Pluzhnikov, Anna, Levine, David M., McHugh, Caitlin P., Ackerman, Christine M., Bouchard, Luigi, Brisson, Diane, Layden, Brian T., Mirel, Daniel, Doheny, Kimberly F., Leya, Marysa V., Lown-Hecht, Rachel N., Dyer, Alan R., Metzger, Boyd E., Reddy, Timothy E., Cox, Nancy J., Lowe, William L.

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

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Genome-wide association study of Tourette Syndrome 由 Scharf, Jeremiah M., Yu, Dongmei, Mathews, Carol A., Neale, Benjamin M., Stewart, S. Evelyn, Fagerness, Jesen A, Evans, Patrick, Gamazon, Eric, Edlund, Christopher K., Service, Susan, Tikhomirov, Anna, Osiecki, Lisa, Illmann, Cornelia, Pluzhnikov, Anna, Konkashbaev, Anuar, Davis, Lea K, Han, Buhm, Crane, Jacquelyn, Moorjani, Priya, Crenshaw, Andrew T., Parkin, Melissa A., Reus, Victor I., Lowe, Thomas L., Rangel-Lugo, Martha, Chouinard, Sylvain, Dion, Yves, Girard, Simon, Cath, Danielle C, Smit, Jan H, King, Robert A., Fernandez, Thomas, Leckman, James F., Kidd, Kenneth K., Kidd, Judith R., Pakstis, Andrew J., State, Matthew, Herrera, Luis Diego, Romero, Roxana, Fournier, Eduardo, Sandor, Paul, Barr, Cathy L, Phan, Nam, Gross-Tsur, Varda, Benarroch, Fortu, Pollak, Yehuda, Budman, Cathy L., Bruun, Ruth D., Erenberg, Gerald, Naarden, Allan L, Lee, Paul C, Weiss, Nicholas, Kremeyer, Barbara, Berrío, Gabriel Bedoya, Campbell, Desmond, Silgado, Julio C. Cardona, Ochoa, William Cornejo, Restrepo, Sandra C. Mesa, Muller, Heike, Duarte, Ana V. Valencia, Lyon, Gholson J, Leppert, Mark, Morgan, Jubel, Weiss, Robert, Grados, Marco A., Anderson, Kelley, Davarya, Sarah, Singer, Harvey, Walkup, John, Jankovic, Joseph, Tischfield, Jay A., Heiman, Gary A., Gilbert, Donald L., Hoekstra, Pieter J., Robertson, Mary M., Kurlan, Roger, Liu, Chunyu, Gibbs, J. Raphael, Singleton, Andrew, Hardy, John, Strengman, Eric, Ophoff, Roel, Wagner, Michael, Moessner, Rainald, Mirel, Daniel B., Posthuma, Danielle, Sabatti, Chiara, Eskin, Eleazar, Conti, David V., Knowles, James A., Ruiz-Linares, Andres, Rouleau, Guy A., Purcell, Shaun, Heutink, Peter, Oostra, Ben A., McMahon, William, Freimer, Nelson, Cox, Nancy J., Pauls, David L.

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Genome-wide Association Study of Obsessive-Compulsive Disorder 由 Stewart, S Evelyn, Yu, Dongmei, Scharf, Jeremiah M, Neale, Benjamin M, Fagerness, Jesen A, Mathews, Carol A, Arnold, Paul D, Evans, Patrick D, Gamazon, Eric R, Osiecki, Lisa, McGrath, Lauren, Haddad, Stephen, Crane, Jacquelyn, Hezel, Dianne, Illman, Cornelia, Mayerfeld, Catherine, Konkashbaev, Anuar, Liu, Chunyu, Pluzhnikov, Anna, Tikhomirov, Anna, Edlund, Christopher K, Rauch, Scott L, Moessner, Rainald, Falkai, Peter, Maier, Wolfgang, Ruhrmann, Stephan, Grabe, Hans-Jörgen, Lennertz, Leonard, Wagner, Michael, Bellodi, Laura, Cavallini, Maria Cristina, Richter, Margaret A, Cook, Edwin H, Kennedy, James L, Rosenberg, David, Stein, Dan J, Hemmings, Sian MJ, Lochner, Christine, Azzam, Amin, Chavira, Denise A, Fournier, Eduardo, Garrido, Helena, Sheppard, Brooke, Umaña, Paul, Murphy, Dennis L, Wendland, Jens R, Veenstra-VanderWeele, Jeremy, Denys, Damiaan, Blom, Rianne, Deforce, Dieter, Van Nieuwerburgh, Filip, Westenberg, Herman GM, Walitza, Susanne, Egberts, Karin, Renner, Tobias, Miguel, Euripedes Constantino, Cappi, Carolina, Hounie, Ana G, Conceição do Rosário, Maria, Sampaio, Aline S, Vallada, Homero, Nicolini, Humberto, Lanzagorta, Nuria, Camarena, Beatriz, Delorme, Richard, Leboyer, Marion, Pato, Carlos N, Pato, Michele T, Voyiaziakis, Emanuel, Heutink, Peter, Cath, Danielle C, Posthuma, Danielle, Smit, Jan H, Samuels, Jack, Bienvenu, O Joseph, Cullen, Bernadette, Fyer, Abby J, Grados, Marco A, Greenberg, Benjamin D, McCracken, James T, Riddle, Mark A, Wang, Ying, Coric, Vladimir, Leckman, James F, Bloch, Michael, Pittenger, Christopher, Eapen, Valsamma, Black, Donald W, Ophoff, Roel A, Strengman, Eric, Cusi, Daniele, Turiel, Maurizio, Frau, Francesca, Macciardi, Fabio, Gibbs, J Raphael, Cookson, Mark R, Singleton, Andrew, Hardy, John, Crenshaw, Andrew T, Parkin, Melissa A, Mirel, Daniel B, Conti, David V, Purcell, Shaun, Nestadt, Gerald, Hanna, Gregory L, Jenike, Michael A, Knowles, James A, Cox, Nancy, Pauls, David L

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