Ngā hua rapu - Pluzhnikov, Anna 

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

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Rational Inferences about Departures from Hardy-Weinberg Equilibrium mā 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 mā 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 mā Pluzhnikov, Anna , Nolan, Daniel K. , Tan, Zhiqiang , McPeek, Mary Sara , Ober, Carole 

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Genomewide Significant Linkage to Stuttering on Chromosome 12 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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 mā 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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