Search Results - Service, Susan K.

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

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