Artikkelit - Selaus tekijän mukaan "Wilson, Richard K."

Viitteet 1-5 / 5

    • Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation (vol 25, pg 1859, 2018) 

      Bis, Joshua C.; Jian, Xueqiu; Kunkle, Brian W.; Chen, Yuning; Hamilton-Nelson, Kara L.; Bush, William S.; Salerno, William J.; Lancour, Daniel; Ma, Yiyi; Renton, Alan E.; Marcora, Edoardo; Farrell, John J.; Zhao, Yi; Qu, Liming; Ahmad, Shahzad; Amin, Najaf; Amouyel, Philippe; Beecham, Gary W.; Below, Jennifer E.; Campion, Dominique; Cantwell, Laura; Charbonnier, Camille; Chung, Jaeyoon; Crane, Paul K.; Cruchaga, Carlos; Cupples, L. Adrienne; Dartigues, Jean-Francois; Debette, Stephanie; Deleuze, Jean-Francois; Fulton, Lucinda; Gabriel, Stacey B.; Genin, Emmanuelle; Gibbs, Richard A.; Goate, Alison; Grenier-Boley, Benjamin; Gupta, Namrata; Haines, Jonathan L.; Havulinna, Aki S.; Helisalmi, Seppo; Hiltunen, Mikko; Howrigan, Daniel P.; Ikram, M. Arfan; Kaprio, Jaakko; Konrad, Jan; Kuzma, Amanda; Lander, Eric S.; Lathrop, Mark; Lehtimaki, Terho; Lin, Honghuang; Mattila, Kari; Mayeux, Richard; Muzny, Donna M.; Nasser, Waleed; Neale, Benjamin; Nho, Kwangsik; Nicolas, Gael; Patel, Devanshi; Pericak-Vance, Margaret A.; Perola, Markus; Psaty, Bruce M.; Quenez, Olivier; Rajabli, Farid; Redon, Richard; Reitz, Christiane; Remes, Anne M.; Salomaa, Veikko; Sarnowski, Chloe; Schmidt, Helena; Schmidt, Michael; Schmidt, Reinhold; Soininen, Hilkka; Thornton, Timothy A.; Tosto, Giuseppe; Tzourio, Christophe; van der Lee, Sven J.; van Duijn, Cornelia M.; Valladares, Otto; Vardarajan, Badri; Wang, Li-San; Wang, Weixin; Wijsman, Ellen; Wilson, Richard K.; Witten, Daniela; Worley, Kim C.; Zhang, Xiaoling; Bellenguez, Celine; Lambert, Jean-Charles; Kurki, Mitja I.; Palotie, Aarno; Daly, Mark; Boerwinkle, Eric; Lunetta, Kathryn L.; Destefano, Anita L.; Dupuis, Josee; Martin, Eden R.; Schellenberg, Gerard D.; Seshadri, Sudha; Naj, Adam C.; Fornage, Myriam; Farrer, Lindsay A.
      MOLECULAR PSYCHIATRY (2020)

    • Exome sequencing of Finnish isolates enhances rare-variant association power 

      Locke, Adam E.; Steinberg, Karyn Meltz; Chiang, Charleston W. K.; Service, Susan K.; Havulinna, Aki S.; Stell, Laurel; Pirinen, Matti; Abel, Haley J.; Chiang, Colby C.; Fulton, Robert S.; Jackson, Anne U.; Kang, Chul Joo; Kanchi, Krishna L.; Koboldt, Daniel C.; Larson, David E.; Nelson, Joanne; Nicholas, Thomas J.; Pietila, Arto; Ramensky, Vasily; Ray, Debashree; Scott, Laura J.; Stringham, Heather M.; Vangipurapu, Jagadish; Welch, Ryan; Yajnik, Pranav; Yin, Xianyong; Eriksson, Johan G.; Ala-Korpela, Mika; Jarvelin, Marjo-Riitta; Mannikko, Minna; Laivuori, Hannele; Dutcher, Susan K.; Stitziel, Nathan O.; Wilson, Richard K.; Hall, Ira M.; Sabatti, Chiara; Palotie, Aarno; Salomaa, Veikko; Laakso, Markku; Ripatti, Samuli; Boehnke, Michael; Freimer, Nelson B.
      NATURE (2019)

    • Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci 

      Service, Susan K.; Teslovich, Tanya M.; Fuchsberger, Christian; Ramensky, Vasily; Yajnik, Pranav; Koboldt, Daniel C.; Larson, David E.; Zhang, Qunyuan; Lin, Ling; Welch, Ryan; Ding, Li; McLellan, Michael D.; O'Laughlin, Michele; Fronick, Catrina; Fulton, Lucinda L.; Magrini, Vincent; Swift, Amy; Elliott, Paul; Jarvelin, Marjo-Riitta; Kaakinen, Marika; McCarthy, Mark I.; Peltonen, Leena; Pouta, Anneli; Bonnycastle, Lori L.; Collins, Francis S.; Narisu, Narisu; Stringham, Heather M.; Tuomilehto, Jaakko; Ripatti, Samuli; Fulton, Robert S.; Sabatti, Chiara; Wilson, Richard K.; Boehnke, Michael; Freimer, Nelson B.
      PLOS GENETICS : 1 (28.08.2014)

    • The Contribution of GWAS Loci in Familial Dyslipidemias 

      Ripatti, Pietari; Ramo, Joel T.; Soderlund, Sanni; Surakka, Ida; Matikainen, Niina; Pirinen, Matti; Pajukanta, Paivi; 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
      PLOS GENETICS : 5 (2016)

    • Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation 

      Bis, Joshua C.; Jian, Xueqiu; Kunkle, Brian W.; Chen, Yuning; Hamilton-Nelson, Kara L.; Bush, William S.; Salerno, William J.; Lancour, Daniel; Ma, Yiyi; Renton, Alan E.; Marcora, Edoardo; Farrell, John J.; Zhao, Yi; Qu, Liming; Ahmad, Shahzad; Amin, Najaf; Amouyel, Philippe; Beecham, Gary W.; Below, Jennifer E.; Campion, Dominique; Charbonnier, Camille; Chung, Jaeyoon; Crane, Paul K.; Cruchaga, Carlos; Cupples, L. Adrienne; Dartigues, Jean-Francois; Debette, Stephanie; Deleuze, Jean-Francois; Fulton, Lucinda; Gabriel, Stacey B.; Genin, Emmanuelle; Gibbs, Richard A.; Goate, Alison; Grenier-Boley, Benjamin; Gupta, Namrata; Haines, Jonathan L.; Havulinna, Aki S.; Helisalmi, Seppo; Hiltunen, Mikko; Howrigan, Daniel P.; Ikram, M. Arfan; Kaprio, Jaakko; Konrad, Jan; Kuzma, Amanda; Lander, Eric S.; Lathrop, Mark; Lehtimaki, Terho; Lin, Honghuang; Mattila, Kari; Mayeux, Richard; Muzny, Donna M.; Nasser, Waleed; Neale, Benjamin; Nho, Kwangsik; Nicolas, Gael; Patel, Devanshi; Pericak-Vance, Margaret A.; Perola, Markus; Psaty, Bruce M.; Quenez, Olivier; Rajabli, Farid; Redon, Richard; Reitz, Christiane; Remes, Anne M.; Salomaa, Veikko; Sarnowski, Chloe; Schmidt, Helena; Schmidt, Michael; Schmidt, Reinhold; Soininen, Hilkka; Thornton, Timothy A.; Tosto, Giuseppe; Tzourio, Christophe; van der Lee, Sven J.; van Duijn, Cornelia M.; Vardarajan, Badri; Wang, Weixin; Wijsman, Ellen; Wilson, Richard K.; Witten, Daniela; Worley, Kim C.; Zhang, Xiaoling; Bellenguez, Celine; Lambert, Jean-Charles; Kurki, Mitja, I; Palotie, Aarno; Daly, Mark; Boerwinkle, Eric; Lunetta, Kathryn L.; Destefano, Anita L.; Dupuis, Josee; Martin, Eden R.; Schellenberg, Gerard D.; Seshadri, Sudha; Naj, Adam C.; Fornage, Myriam; Farrer, Lindsay A.
      MOLECULAR PSYCHIATRY (2020)