Výsledky vyhledávání - Service, Susan K.

Cost-Effective Designs for Linkage Disequilibrium Mapping of Complex Traits Autor Service, Susan K., Sandkuijl, Lodewijk A., Freimer, Nelson B.

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Familial Aggregation of Absolute Pitch Autor Baharloo, Siamak, Service, Susan K., Risch, Neil, Gitschier, Jane, Freimer, Nelson B.

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Linkage Analysis of a Complex Pedigree with Severe Bipolar Disorder, Using a Markov Chain Monte Carlo Method Autor Garner, Chad, McInnes, L. Alison, Service, Susan K., Spesny, Mitzi, Fournier, Eduardo, Leon, Pedro, Freimer, Nelson B.

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Variance component model to account for sample structure in genome-wide association studies Autor Kang, Hyun Min, Sul, Jae Hoon, Service, Susan K, Zaitlen, Noah A, Kong, Sit-yee, Freimer, Nelson B, Sabatti, Chiara, Eskin, Eleazar

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Anatomic Brain Asymmetry in Vervet Monkeys Autor Fears, Scott C., Scheibel, Kevin, Abaryan, Zvart, Lee, Chris, Service, Susan K., Jorgensen, Matthew J., Fairbanks, Lynn A., Cantor, Rita M., Freimer, Nelson B., Woods, Roger P.

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Identifying Heritable Brain Phenotypes in an Extended Pedigree of Vervet Monkeys Autor Fears, Scott C., Melega, William P., Service, Susan K., Lee, Chris, Chen, Kelly, Tu, Zhuowen, Jorgensen, Matthew J., Fairbanks, Lynn A., Cantor, Rita M., Freimer, Nelson B., Woods, Roger P.

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Systems Biology of the Vervet Monkey Autor Jasinska, Anna J., Schmitt, Christopher A., Service, Susan K., Cantor, Rita M., Dewar, Ken, Jentsch, James D., Kaplan, Jay R., Turner, Trudy R., Warren, Wesley C., Weinstock, George M., Woods, Roger P., Freimer, Nelson B.

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A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using reference sequences from related species Autor Freimer, Nelson B., Service, Susan K., Ophoff, Roel A., Jasinska, Anna J., McKee, Kevin, Villeneuve, Amelie, Belisle, Alexandre, Bailey, Julia N., Breidenthal, Sherry E., Jorgensen, Matthew J., Mann, J. John, Cantor, Rita M., Dewar, Ken, Fairbanks, Lynn A.

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Phenotype mining in CNV carriers from a population cohort(†) Autor Pietiläinen, Olli P. H., Rehnström, Karola, Jakkula, Eveliina, Service, Susan K., Congdon, Eliza, Tilgmann, Carola, Hartikainen, Anna-Liisa, Taanila, Anja, Heikura, Ulla, Paunio, Tiina, Ripatti, Samuli, Jarvelin, Marjo-Riitta, Isohanni, Matti, Sabatti, Chiara, Palotie, Aarno, Freimer, Nelson B., Peltonen, Leena

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The Contribution of GWAS Loci in Familial Dyslipidemias Autor Ripatti, Pietari, Rämö, Joel T., Söderlund, Sanni, Surakka, Ida, Matikainen, Niina, Pirinen, Matti, Pajukanta, Päivi, Sarin, Antti-Pekka, Service, Susan K., Laurila, Pirkka-Pekka, Ehnholm, Christian, Salomaa, Veikko, Wilson, Richard K., Palotie, Aarno, Freimer, Nelson B., Taskinen, Marja-Riitta, Ripatti, Samuli

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Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder Autor Peterson, Christine B., Service, Susan K., Jasinska, Anna J., Gao, Fuying, Zelaya, Ivette, Teshiba, Terri M., Bearden, Carrie E., Cantor, Rita M., Reus, Victor I., Macaya, Gabriel, López-Jaramillo, Carlos, Bogomolov, Marina, Benjamini, Yoav, Eskin, Eleazar, Coppola, Giovanni, Freimer, Nelson B., Sabatti, Chiara

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Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits Autor Huang, Yu S., Ramensky, Vasily, Service, Susan K., Jasinska, Anna J., Jung, Yoon, Choi, Oi-Wa, Cantor, Rita M., Juretic, Nikoleta, Wasserscheid, Jessica, Kaplan, Jay R., Jorgensen, Matthew J., Dyer, Thomas D., Dewar, Ken, Blangero, John, Wilson, Richard K., Warren, Wesley, Weinstock, George M., Freimer, Nelson B.

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Genomewide Linkage Disequilibrium Mapping of Severe Bipolar Disorder in a Population Isolate Autor Ophoff, Roel A., Escamilla, Michael A., Service, Susan K., Spesny, Mitzi, Meshi, Dar B., Poon, Wingman, Molina, Julio, Fournier, Eduardo, Gallegos, Alvaro, Mathews, Carol, Neylan, Thomas, Batki, Steven L., Roche, Erin, Ramirez, Margarita, Silva, Sandra, De Mille, Melissa C., Dong, Penny, Leon, Pedro E., Reus, Victor I., Sandkuijl, Lodewijk A., Freimer, Nelson B.

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Hereditary Vascular Retinopathy, Cerebroretinal Vasculopathy, and Hereditary Endotheliopathy with Retinopathy, Nephropathy, and Stroke Map to a Single Locus on Chromosome 3p21.1-p2... Autor Ophoff, Roel A., DeYoung, Joseph, Service, Susan K., Joosse, Marijke, Caffo, Nathan A., Sandkuijl, Lodewijk A., Terwindt, Gisela M., Haan, Joost, van den Maagdenberg, Arn M. J. M., Jen, Joanna, Baloh, Robert W., Barilla-LaBarca, Maria-Louise, Saccone, Nancy L., Atkinson, John P., Ferrari, Michel D., Freimer, Nelson B., Frants, Rune R.

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A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees Autor McInnes, L. Alison, Escamilla, Michael A., Service, Susan K., Reus, Victor I., Leon, Pedro, Silva, Sandra, Rojas, Eugenia, Spesny, Mitzi, Baharloo, Siamak, Blankenship, Kathleen, Peterson, Amy, Tyler, David, Shimayoshi, Norito, Tobey, Christa, Batki, Steven, Vinogradov, Sophia, Meza, Luis, Gallegos, Alvaro, Fournier, Eduardo, Smith, Lauren B., Barondes, Samuel H., Sandkuijl, Lodewijk A., Freimer, Nelson B.

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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Autor Sabatti, Chiara, Service, Susan K, Hartikainen, Anna-Liisa, Pouta, Anneli, Ripatti, Samuli, Brodsky, Jae, Jones, Chris G, Zaitlen, Noah A, Varilo, Teppo, Kaakinen, Marika, Sovio, Ulla, Ruokonen, Aimo, Laitinen, Jaana, Jakkula, Eveliina, Coin, Lachlan, Hoggart, Clive, Collins, Andrew, Turunen, Hannu, Gabriel, Stacey, Elliot, Paul, McCarthy, Mark I, Daly, Mark J, Järvelin, Marjo-Riitta, Freimer, Nelson B, Peltonen, Leena

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Genetic architecture of human plasma lipidome and its link to cardiovascular disease Autor Tabassum, Rubina, Rämö, Joel T., Ripatti, Pietari, Koskela, Jukka T., Kurki, Mitja, Karjalainen, Juha, Palta, Priit, Hassan, Shabbeer, Nunez-Fontarnau, Javier, Kiiskinen, Tuomo T. J., Söderlund, Sanni, Matikainen, Niina, Gerl, Mathias J., Surma, Michal A., Klose, Christian, Stitziel, Nathan O., Laivuori, Hannele, Havulinna, Aki S., Service, Susan K., Salomaa, Veikko, Pirinen, Matti, Jauhiainen, Matti, Daly, Mark J., Freimer, Nelson B., Palotie, Aarno, Taskinen, Marja-Riitta, Simons, Kai, Ripatti, Samuli

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Association of structural variation with cardiometabolic traits in Finns Autor Chen, Lei, Abel, Haley J., Das, Indraniel, Larson, David E., Ganel, Liron, Kanchi, Krishna L., Regier, Allison A., Young, Erica P., Kang, Chul Joo, Scott, Alexandra J., Chiang, Colby, Wang, Xinxin, Lu, Shuangjia, Christ, Ryan, Service, Susan K., Chiang, Charleston W.K., Havulinna, Aki S., Kuusisto, Johanna, Boehnke, Michael, Laakso, Markku, Palotie, Aarno, Ripatti, Samuli, Freimer, Nelson B., Locke, Adam E., Stitziel, Nathan O., Hall, Ira M.

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Maintenance of genetic variation in human personality: Testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant... Autor Verweij, Karin J.H., Yang, Jian, Lahti, Jari, Veijola, Juha, Hintsanen, Mirka, Pulkki-Råback, Laura, Heinonen, Kati, Pouta, Anneli, Pesonen, Anu-Katriina, Widen, Elisabeth, Taanila, Anja, Isohanni, Matti, Miettunen, Jouko, Palotie, Aarno, Penke, Lars, Service, Susan K., Heath, Andrew C., Montgomery, Grant W., Raitakari, Olli, Kähönen, Mika, Viikari, Jorma, Räikkönen, Katri, Eriksson, Johan G, Keltikangas-Järvinen, Liisa, Lehtimäki, Terho, Martin, Nicholas G., Järvelin, Marjo-Riitta, Visscher, Peter M., Keller, Matthew C., Zietsch, Brendan P.

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Brain structure–function associations in multi-generational families genetically enriched for bipolar disorder Autor Fears, Scott C., Schür, Remmelt, Sjouwerman, Rachel, Service, Susan K., Araya, Carmen, Araya, Xinia, Bejarano, Julio, Knowles, Emma, Gomez-Makhinson, Juliana, Lopez, Maria C., Aldana, Ileana, Teshiba, Terri M., Abaryan, Zvart, Al-Sharif, Noor B., Navarro, Linda, Tishler, Todd A., Altshuler, Lori, Bartzokis, George, Escobar, Javier I., Glahn, David C., Thompson, Paul M., Lopez-Jaramillo, Carlos, Macaya, Gabriel, Molina, Julio, Reus, Victor I., Sabatti, Chiara, Cantor, Rita M., Freimer, Nelson B., Bearden, Carrie E.

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