检索结果 - Service, Susan K.

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

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Familial Aggregation of Absolute Pitch 由 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 由 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 由 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 由 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 由 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 由 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 由 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(†) 由 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 由 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 由 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 由 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 由 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... 由 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 由 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 由 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 由 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 由 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... 由 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 由 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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