Artikkelit - Selaus nimekkeen mukaan

Viitteet 2772-2791 / 16217

    • Common Genetic Variants, QT Interval, and Sudden Cardiac Death in a Finnish Population-Based Study 

      Noseworthy, Peter A.; Havulinna, Aki S.; Porthan, Kimmo; Lahtinen, Annukka M.; Jula, Antti; Karhunen, Pekka J.; Perola, Markus; Oikarinen, Lasse; Kontula, Kimmo K.; Salomaa, Veikko; Newton-Cheh, Christopher
      CIRCULATION-CARDIOVASCULAR GENETICS : 3 (2011)
    • Common Genetic Variation and Age of Onset of Anorexia Nervosa 

      Watson, Hunna J.; Thornton, Laura M.; Yilmaz, Zeynep; Baker, Jessica H.; Coleman, Johanthan R.I.; Adan, Roger A.H.; Alfredsson, Lars; Andreassen, Ole A.; Ask, Helga; Berrettini, Wade H.; Boehke, Michael; Boehm, Ilka; Boni, Claudette; Buehren, Katarina; Bulant, Josef; Burghardt, Roland; Chang, Xiao; Cichon, Sven; Cone, Roger D.; Courtet, Philippe; Eriksson, Johan G.; et al.
      Biological psychiatry: Global open science : 4 (10 / 2022)
    • Common genetic variation near MC4R is associated with eating behaviour patterns in European populations 

      Stutzmann F; Cauchi S; Durand E; Calvacanti-Proença C; Pigeyre M; Hartikainen AL; Sovio U; Tichet J; Marre M; Weill J; Balkau B; Potoczna N; Laitinen J; Elliott P; Järvelin MR; Horber F; Meyre D; Froguel P
      International Journal of Obesity (2009)
    • Common Genetic Variation Near Melatonin Receptor 1A Gene Linked to Job-Related Exhaustion in Shift Workers 

      Sulkava, Sonja; Ollila, Hanna M.; Alasaari, Jukka; Puttonen, Sampsa; Harma, Mikko; Viitasalo, Katriina; Lahtinen, Alexandra; Lindstrom, Jaana; Toivola, Auli; Sulkava, Raimo; Kivimaki, Mika; Vahtera, Jussi; Partonen, Timo; Silander, Kaisa; Porkka-Heiskanen, Tarja; Paunio, Tiina
      SLEEP : 1 (2017)
    • Common Genetic Variation Near Melatonin Receptor MTNR1B Contributes to Raised Plasma Glucose and Increased Risk of Type 2 Diabetes Among Indian Asians and European Caucasians 

      Chambers, John C.; Zhang, Weihua; Zabaneh, Delilah; Sehmi, Joban; Jain, Piyush; McCarthy, Mark I.; Froguel, Philippe; Ruokonen, Aimo; Balding, David; Jarvelin, Marjo-Riitta; Scott, James; Elliott, Paul; Kooner, Jaspal S.
      DIABETES : 11 (2009)
    • Common genetic variations of the renin-angiotensin-aldosterone system and response to acute angiotensin I-converting enzyme inhibition in essential hypertension 

      Hannila-Handelberg, Tuula; Kontula, Kimmo K.; Paukku, Kirsi; Lehtonen, Jukka Y.; Virtamo, Jarmo; Tikkanen, Ilkka; Hiltunen, Timo P.
      JOURNAL OF HYPERTENSION : 4 (2010)
    • Common mental and musculoskeletal disorders as predictors of disability retirement among Finns 

      Kaila-Kangas, Leena; Haukka, Eija; Miranda, Helena; Kivekas, Teija; Ahola, Kirsi; Luukkonen, Ritva; Shiri, Rahman; Kaaria, Sanna; Heliovaara, Markku; Leino-Arjas, Paivi
      JOURNAL OF AFFECTIVE DISORDERS (28.08.2014)
    • Common mental disorders and subsequent work disability : A population-based Health 2000 Study 

      Ahola, Kirsi; Virtanen, Marianna; Honkonen, Teija; Isometsa, Erkki; Aromaa, Arpo; Lonnqvist, Jouko
      JOURNAL OF AFFECTIVE DISORDERS : 1-3 (2011)
    • Common mental disorders in young adults born late-preterm 

      Heinonen, K.; Kajantie, E.; Pesonen, A. -K.; Lahti, M.; Pirkola, S.; Wolke, D.; Lano, A.; Sammallahti, S.; Lahti, J.; Andersson, S.; Eriksson, J. G.; Raikkonen, K.
      PSYCHOLOGICAL MEDICINE : 10 (2016)
    • Common Single Nucleotide Polymorphisms Associated with Sudden Cardiac Death: The FinSCDgen Study 

      Salomaa, Veikko; Noseworthy, Peter A.; Havulinna, Aki S.; Lahtinen, Annukka M.; Jula, Antti; Karhunen, Pekka J.; Perola, Markus; Kontula, Kimmo; Newton-Cheh, Christopher
      CIRCULATION : 21 (2012)
    • Common variant at 16p11.2 conferring risk of psychosis 

      Steinberg, S.; de Jong, S.; Mattheisen, M.; Costas, J.; Demontis, D.; Jamain, S.; Pietilainen, O. P. H.; Lin, K.; Papiol, S.; Huttenlocher, J.; Sigurdsson, E.; Vassos, E.; Giegling, I.; Breuer, R.; Fraser, G.; Walker, N.; Melle, I.; Djurovic, S.; Agartz, I.; Tuulio-Henriksson, A.; Suvisaari, J.; Lonnqvist, J.; Paunio, T.; Olsen, L.; Hansen, T.; Ingason, A.; Pirinen, M.; Strengman, E.; Hougaard, D. M.; Orntoft, T.; Didriksen, M.; Hollegaard, M. V.; Nordentoft, M.; Abramova, L.; Kaleda, V.; Arrojo, M.; Sanjuan, J.; Arango, C.; Etain, B.; Bellivier, F.; Meary, A.; Schuerhoff, F.; Szoke, A.; Ribolsi, M.; Magni, V.; Siracusano, A.; Sperling, S.; Rossner, M.; Christiansen, C.; Kiemeney, L. A.; Franke, B.; van den Berg, L. H.; Veldink, J.; Curran, S.; Bolton, P.; Poot, M.; Staal, W.; Rehnstrom, K.; Kilpinen, H.; Freitag, C. M.; Meyer, J.; Magnusson, P.; Saemundsen, E.; Martsenkovsky, I.; Bikshaieva, I.; Martsenkovska, I.; Vashchenko, O.; Raleva, M.; Paketchieva, K.; Stefanovski, B.; Durmishi, N.; Milovancevic, M. Pejovic; Tosevski, D. Lecic; Silagadze, T.; Naneishvili, N.; Mikeladze, N.; Surguladze, S.; Vincent, J. B.; Farmer, A.; Mitchell, P. B.; Wright, A.; Schofield, P. R.; Fullerton, J. M.; Montgomery, G. W.; Martin, N. G.; Rubino, I. A.; van Winkel, R.; Kenis, G.; De Hert, M.; Rethelyi, J. M.; Bitter, I.; Terenius, L.; Jonsson, E. G.; Bakker, S.; van Os, J.; Jablensky, A.; Leboyer, M.; Bramon, E.; Powell, J.; Murray, R.; Corvin, A.; Gill, M.; Morris, D.; O'Neill, F. A.; Kendler, K.; Riley, B.; Craddock, N.; Owen, M. J.; O'Donovan, M. C.; Thorsteinsdottir, U.; Kong, A.; Ehrenreich, H.; Carracedo, A.; Golimbet, V.; Andreassen, O. A.; Borglum, A. D.; Mors, O.; Mortensen, P. B.; Werge, T.; Ophoff, R. A.; Noethen, M. M.; Rietschel, M.; Cichon, S.; Ruggeri, M.; Tosato, S.; Palotie, A.; St Clair, D.; Rujescu, D.; Collier, D. A.; Stefansson, H.; Stefansson, K.
      MOLECULAR PSYCHIATRY : 1 (01.02.2014)
    • Common variant at 16p11.2 conferring risk of psychosis. 

      Steinberg S; de Jong S; Mattheisen M; Pietilainen OP; Tuulio-Henriksson A; Suvisaari J; Lonnqvist J; Paunio T; Rehnstrom K; Kilpinen H; Wellcome Trust Case Control Consortium; Palotie A; Stefansson K
      Molecular psychiatry : 101038 (2012)
    • Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families 

      Gormley, Padhraig; Kurki, Mitja I.; Hiekkala, Marjo Eveliina; Veerapen, Kumar; Happola, Paavo; Mitchell, Adele A.; Lal, Dennis; Palta, Priit; Surakka, Ida; Kaunisto, Mari Anneli; Hamalainen, Eija; Vepsalainen, Salli; Havanka, Hannele; Harno, Hanna; Ilmavirta, Matti; Nissila, Markku; Sako, Erkki; Sumelahti, Marja-Liisa; Liukkonen, Jarmo; Sillanpaa, Matti; Metsahonkala, Liisa; Koskinen, Seppo; Lehtimaki, Terho; Raitakari, Olli; Mannikko, Minna; Ran, Caroline; Belin, Andrea Carmine; Jousilahti, Pekka; Anttila, Verneri; Salomaa, Veikko; Artto, Ville; Farkkila, Markus; Runz, Heiko; Daly, Mark J.; Neale, Benjamin M.; Ripatti, Samuli; Kallela, Mikko; Wessman, Maija; Palotie, Aarno
      NEURON (2018)
    • Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion 

      Lyssenko V; Nagorny CLF; Erdos MR; Wierup N; Jonsson A; Spegel P; Bugliani M; Saxena R; Fex M; Pulizzi N; Isomaa B; Tuomi T; Nilsson P; Kuusisto J; Tuomilehto J; Boehnke M; Altshuler D; Sundler F; Eriksson JG; Jackson AU; Laakso M; Marchetti P; Watanabe RM; Mulder H; Groop L
      Nat Genet (2009)
    • Common variant in the FTO gene did not modify the effect of lifestyle changes on body weight: The Finnish Diabetes Prevention Study 

      Lappalainen TJ; Tolppanen AM; Kolehmainen M; Schwab U; Lindström J; Tuomilehto J; Pulkkinen L; Eriksson JG; Laakso M; Gylling H; Uusitupa M
      Obesity (2009)
    • Common variants associated with plasma triglycerides and risk for coronary artery disease 

      Do, Ron; Willer, Cristen J.; Schmidt, Ellen M.; Sengupta, Sebanti; Gao, Chi; Peloso, Gina M.; Gustafsson, Stefan; Kanoni, Stavroula; Ganna, Andrea; Chen, Jin; Buchkovich, Martin L.; Mora, Samia; Beckmann, Jacques S.; Bragg-Gresham, Jennifer L.; Chang, Hsing-Yi; Demirkan, Ayse; Den Hertog, Heleen M.; Donnelly, Louise A.; Ehret, Georg B.; Esko, Tonu; Feitosa, Mary F.; Ferreira, Teresa; Fischer, Krista; Fontanillas, Pierre; Fraser, Ross M.; Freitag, Daniel F.; Gurdasani, Deepti; Heikkila, Kauko; Hyppoenen, Elina; Isaacs, Aaron; Jackson, Anne U.; Johansson, Asa; Johnson, Toby; Kaakinen, Marika; Kettunen, Johannes; Kleber, Marcus E.; Li, Xiaohui; Luan, Jian'an; Lyytikainen, Leo-Pekka; Magnusson, Patrik K. E.; Mangino, Massimo; Mihailov, Evelin; Montasser, May E.; Mueller-Nurasyid, Martina; Nolte, Ilja M.; O'Connell, Jeffrey R.; Palmer, Cameron D.; Perola, Markus; Petersen, Ann-Kristin; Sanna, Serena; Saxena, Richa; Service, Susan K.; Shah, Sonia; Shungin, Dmitry; Sidore, Carlo; Song, Ci; Strawbridge, Rona J.; Surakka, Ida; Tanaka, Toshiko; Teslovich, Tanya M.; Thorleifsson, Gudmar; Van den Herik, Evita G.; Voight, Benjamin F.; Volcik, Kelly A.; Waite, Lindsay L.; Wong, Andrew; Wu, Ying; Zhang, Weihua; Absher, Devin; Asiki, Gershim; Barroso, Ines; Been, Latonya F.; Bolton, Jennifer L.; Bonnycastle, Lori L.; Brambilla, Paolo; Burnett, Mary S.; Cesana, Giancarlo; Dimitriou, Maria; Doney, Alex S. F.; Doering, Angela; Elliott, Paul; Epstein, Stephen E.; Eyjolfsson, Gudmundur Ingi; Gigante, Bruna; Goodarzi, Mark O.; Grallert, Harald; Gravito, Martha L.; Groves, Christopher J.; Hallmans, Goran; Hartikainen, Anna-Liisa; Hayward, Caroline; Hernandez, Dena; Hicks, Andrew A.; Holm, Hilma; Hung, Yi-Jen; Illig, Thomas; Jones, Michelle R.; Kaleebu, Pontiano; Kastelein, John J. P.; Khaw, Kay-Tee; Kim, Eric; Klopp, Norman; Komulainen, Pirjo; Kumari, Meena; Langenberg, Claudia; Lehtimaki, Terho; Lin, Shih-Yi; Lindstrom, Jaana; Loos, Ruth J. F.; Mach, Francois; McArdle, Wendy L.; Meisinger, Christa; Mitchell, Braxton D.; Mueller, Gabrielle; Nagaraja, Ramaiah; Narisu, Narisu; Nieminen, Tuomo V. M.; Nsubuga, Rebecca N.; Olafsson, Isleifur; Ong, Ken K.; Palotie, Aarno; Papamarkou, Theodore; Pomilla, Cristina; Pouta, Anneli; Rader, Daniel J.; Reilly, Muredach P.; Ridker, Paul M.; Rivadeneira, Fernando; Rudan, Igor; Ruokonen, Aimo; Samani, Nilesh; Scharnagl, Hubert; Seeley, Janet; Silander, Kaisa; Stancakova, Alena; Stirrups, Kathleen; Swift, Amy J.; Tiret, Laurence; Uitterlinden, Andre G.; van Pelt, L. Joost; Vedantam, Sailaja; Wainwright, Nicholas; Wijmenga, Cisca; Wild, Sarah H.; Willemsen, Gonneke; Wilsgaard, Tom; Wilson, James F.; Young, Elizabeth H.; Zhao, Jing Hua; Adair, Linda S.; Arveiler, Dominique; Assimes, Themistocles L.; Bandinelli, Stefania; Bennett, Franklyn; Bochud, Murielle; Boehm, Bernhard O.; Boomsma, Dorret I.; Borecki, Ingrid B.; Bornstein, Stefan R.; Bovet, Pascal; Burnier, Michel; Campbell, Harry; Chakravarti, Aravinda; Chambers, John C.; Chen, Yii-Der Ida; Collins, Francis S.; Cooper, Richard S.; Danesh, John; Dedoussis, George; de Faire, Ulf; Feranil, Alan B.; Ferrieres, Jean; Ferrucci, Luigi; Freimer, Nelson B.; Gieger, Christian; Groop, Leif C.; Gudnason, Vilmundur; Gyllensten, Ulf; Hamsten, Anders; Harris, Tamara B.; Hingorani, Aroon; Hirschhorn, Joel N.; Hofman, Albert; Hovingh, G. Kees; Hsiung, Chao Agnes; Humphries, Steve E.; Hunt, Steven C.; Hveem, Kristian; Iribarren, Carlos; Jarvelin, Marjo-Riitta; Jula, Antti; Kahonen, Mika; Kaprio, Jaakko; Kesaniemi, Antero; Kivimaki, Mika; Kooner, Jaspal S.; Koudstaal, Peter J.; Krauss, Ronald M.; Kuh, Diana; Kuusisto, Johanna; Kyvik, Kirsten O.; Laakso, Markku; Lakka, Timo A.; Lind, Lars; Lindgren, Cecilia M.; Martin, Nicholas G.; Maerz, Winfried; McCarthy, Mark I.; McKenzie, Colin A.; Meneton, Pierre; Metspalu, Andres; Moilanen, Leena; Morris, Andrew D.; Munroe, Patricia B.; Njolstad, Inger; Pedersen, Nancy L.; Power, Chris; Pramstaller, Peter P.; Price, Jackie F.; Psaty, Bruce M.; Quertermous, Thomas; Rauramaa, Rainer; Saleheen, Danish; Salomaa, Veikko; Sanghera, Dharambir K.; Saramies, Jouko; Schwarz, Peter E. H.; Sheu, Wayne H-H; Shuldiner, Alan R.; Siegbahn, Agneta; Spector, Tim D.; Stefansson, Kari; Strachan, David P.; Tayo, Bamidele O.; Tremoli, Elena; Tuomilehto, Jaakko; Uusitupa, Matti; van Duijn, Cornelia M.; Vollenweider, Peter; Wallentin, Lars; Wareham, Nicholas J.; Whitfield, John B.; Wolffenbuttel, Bruce H. R.; Altshuler, David; Ordovas, Jose M.; Boerwinkle, Eric; Palmer, Colin N. A.; Thorsteinsdottir, Unnur; Chasman, Daniel I.; Rotter, Jerome I.; Franks, Paul W.; Ripatti, Samuli; Cupples, L. Adrienne; Sandhu, Manjinder S.; Rich, Stephen S.; Boehnke, Michael; Deloukas, Panos; Mohlke, Karen L.; Ingelsson, Erik; Abecasis, Goncalo R.; Daly, Mark J.; Neale, Benjamin M.; Kathiresan, Sekar
      NATURE GENETICS : 11 (28.11.2013)
    • Common variants at 12q15 and 12q24 are associated with infant head circumference 

      Taal, H. Rob; St Pourcain, Beate; Thiering, Elisabeth; Das, Shikta; Mook-Kanamori, Dennis O.; Warrington, Nicole M.; Kaakinen, Marika; Kreiner-Moller, Eskil; Bradfield, Jonathan P.; Freathy, Rachel M.; Geller, Frank; Guxens, Monica; Cousminer, Diana L.; Kerkhof, Marjan; Timpson, Nicholas J.; Ikram, M. Arfan; Beilin, Lawrence J.; Bonnelykke, Klaus; Buxton, Jessica L.; Charoen, Pimphen; Chawes, Bo Lund Krogsgaard; Eriksson, Johan; Evans, David M.; Hofman, Albert; Kemp, John P.; Kim, Cecilia E.; Klopp, Norman; Lahti, Jari; Lye, Stephen J.; McMahon, George; Mentch, Frank D.; Mueller-Nurasyid, Martina; O'Reilly, Paul F.; Prokopenko, Inga; Rivadeneira, Fernando; Steegers, Eric A. P.; Sunyer, Jordi; Tiesler, Carla; Yaghootkar, Hanieh; Breteler, Monique M. B.; Debette, Stephanie; Fornage, Myriam; Gudnason, Vilmundur; Launer, Lenore J.; van der Lugt, Aad; Mosley, Thomas H., Jr.; Seshadri, Sudha; Smith, Albert V.; Vernooij, Meike W.; Blakemore, Alexandra I. F.; Chiavacci, Rosetta M.; Feenstra, Bjarke; Fernandez-Banet, Julio; Grant, Struan F. A.; Hartikainen, Anna-Liisa; van der Heijden, Albert J.; Iniguez, Carmen; Lathrop, Mark; McArdle, Wendy L.; Molgaard, Anne; Newnham, John P.; Palmer, Lyle J.; Palotie, Aarno; Pouta, Annneli; Ring, Susan M.; Sovio, Ulla; Standl, Marie; Uitterlinden, Andre G.; Wichmann, H-Erich; Vissing, Nadja Hawwa; DeCarli, Charles; van Duijn, Cornelia M.; McCarthy, Mark I.; Koppelman, Gerard H.; Estivill, Xavier; Hattersley, Andrew T.; Melbye, Mads; Bisgaard, Hans; Pennell, Craig E.; Widen, Elisabeth; Hakonarson, Hakon; Smith, George Davey; Heinrich, Joachim; Jarvelin, Marjo-Riitta; Jaddoe, Vincent W. V.; Adair, Linda S.; Ang, Wei; Atalay, Mustafa; van Beijsterveldt, Toos; Bergen, Nienke; Benke, Kelly; Berry, Diane; Bradfield, Jonathan P.; Charoen, Pimphen; Coin, Lachlan; Cousminer, Diana L.; Das, Shikta; Davis, Oliver S. P.; Elliott, Paul; Evans, David M.; Feenstra, Bjarke; Flexeder, Claudia; Frayling, Tim; Freathy, Rachel M.; Gaillard, Romy; Geller, Frank; Groen-Blokhuis, Maria; Goh, Liang-Kee; Guxens, Monica; Haworth, Claire M. A.; Hadley, Dexter; Hedebrand, Johannes; Hinney, Anke; Hirschhorn, Joel N.; Holloway, John W.; Holst, Claus; Hottenga, Jouke Jan; Horikoshi, Momoko; Huikari, Ville; Hypponen, Elina; Iniguez, Carmen; Kaakinen, Marika; Kilpelainen, Tuomas O.; Kirin, Mirna; Kowgier, Matthew; Lakka, Hanna-Maaria; Lange, Leslie A.; Lawlor, Debbie A.; Lehtimaki, Terho; Lewin, Alex; Lindgren, Cecilia; Lindi, Virpi; Maggi, Reedik; Marsh, Julie; Middeldorp, Christel; Millwood, Iona; Mook-Kanamori, Dennis O.; Murray, Jeffrey C.; Nivard, Michel; Nohr, Ellen Aagaard; Ntalla, Ioanna; Oken, Emily; O'Reilly, Paul F.; Palmer, Lyle J.; Panoutsopoulou, Kalliope; Pararajasingham, Jennifer; Prokopenko, Inga; Rodriguez, Alina; Salem, Rany M.; Sebert, Sylvain; Siitonen, Niina; Sovio, Ulla; St Pourcain, Beate; Strachan, David P.; Sunyer, Jordi; Taal, H. Rob; Teo, Yik-Ying; Thiering, Elisabeth; Tiesler, Carla; Uitterlinden, Andre G.; Valcarcel, Beatriz; Warrington, Nicole M.; White, Scott; Willemsen, Gonneke; Yaghootkar, Hanieh; Zeggini, Eleftheria; Boomsma, Dorret I.; Cooper, Cyrus; Estivill, Xavier; Gillman, Matthew; Grant, Struan F. A.; Hakonarson, Hakon; Hattersley, Andrew T.; Heinrich, Joachim; Hocher, Berthold; Jaddoe, Vincent W. V.; Jarvelin, Marjo-Riitta; Lakka, Timo A.; McCarthy, Mark I.; Melbye, Mads; Mohlke, Karen L.; Dedoussis, George V.; Ong, Ken K.; Pearson, Ewan R.; Pennell, Craig E.; Price, Thomas S.; Power, Chris; Raitakari, Olli T.; Saw, Seang-Mei; Scherag, Andre; Simell, Olli; Sorensen, Thorkild I. A.; Timpson, Nicholas J.; Widen, Elisabeth; Wilson, James F.; Ang, Wei; van Beijsterveldt, Toos; Bergen, Nienke; Benke, Kelly; Berry, Diane; Bradfield, Jonathan P.; Charoen, Pimphen; Coin, Lachlan; Cousminer, Diana L.; Das, Shikta; Elliott, Paul; Evans, David M.; Frayling, Tim; Freathy, Rachel M.; Gaillard, Romy; Groen-Blokhuis, Maria; Guxens, Monica; Hadley, Dexter; Hottenga, Jouke Jan; Huikari, Ville; Hypponen, Elina; Kaakinen, Marika; Kowgier, Matthew; Lawlor, Debbie A.; Lewin, Alex; Lindgren, Cecilia; Marsh, Julie; Middeldorp, Christel; Millwood, Iona; Mook-Kanamori, Dennis O.; Nivard, Michel; O'Reilly, Paul F.; Palmer, Lyle J.; Prokopenko, Inga; Rodriguez, Alina; Sebert, Sylvain; Sovio, Ulla; St Pourcain, Beate; Standl, Marie; Strachan, David P.; Sunyer, Jordi; Taal, H. Rob; Thiering, Elisabeth; Tiesler, Carla; Uitterlinden, Andre G.; Valcarcel, Beatriz; Warrington, Nicole M.; White, Scott; Willemsen, Gonneke; Yaghootkar, Hanieh; Boomsma, Dorret I.; Estivill, Xavier; Grant, Struan F. A.; Hakonarson, Hakon; Hattersley, Andrew T.; Heinrich, Joachim; Jaddoe, Vincent W. V.; Jarvelin, Marjo-Riitta; McCarthy, Mark I.; Pennell, Craig E.; Power, Chris; Timpson, Nicholas J.; Widen, Elisabeth; Ikram, M. Arfan; Fornage, Myriam; Smith, Albert V.; Seshadri, Sudha; Schmidt, Reinhold; Debette, Stephanie; Vrooman, Henri A.; Sigurdsson, Sigurdur; Ropele, Stefan; Coker, Laura H.; Longstreth, W. T., Jr.; Niessen, Wiro J.; DeStefano, Anita L.; Beiser, Alexa; Zijdenbos, Alex P.; Struchalin, Maksim; Jack, Clifford R., Jr.; Nalls, Mike A.; Au, Rhoda; Hofman, Albert; Gudnason, Haukur; van der Lugt, Aad; Harris, Tamara B.; Meeks, William M.; Vernooij, Meike W.; van Buchem, Mark A.; Catellier, Diane; Gudnason, Vilmundur; Windham, B. Gwen; Wolf, Philip A.; van Duijn, Cornelia M.; Mosley, Thomas H., Jr.; Schmidt, Helena; Launer, Lenore J.; Breteler, Monique M. B.; DeCarli, Charles
      NATURE GENETICS : 5 (2012)
    • Common variants at 30 loci contribute to polygenic dyslipidemia 

      Kathiresan S; Willer CJ; Peloso GM; Demissie S; Musunuru K; Schadt EE; Kaplan L; Bennett D; Li Y; Tanaka T; Voight BF; Bonnycastle LL; Jackson AU; Crawford G; Surti A; Guiducci C; Burtt NP; Parish S; Clarke R; Zelenika D; Kubalanza KA; Morken MA; Scott LJ; Stringham HM; Galan P; Swift AJ; Kuusisto J; Bergman RN; Sundvall J; Laakso M; Ferrucci L; Scheet P; Sanna S; Uda M; Yang Q; Lunetta KL; Dupuis J; de Bakker PIW; Chambers JC; Kooner JS; Hercberg S; Meneton P; Lakatta EG; Scuteri A; Schlessinger D; Tuomilehto J; Collins FS; Groop L; Altshuler D; Collins R; Lathrop GM; Melander O; Salomaa V; Peltonen L; Orho-Melander M; Ordovas JM; Boehnke M; Abecasis GR; Mohlke KL; Cupples LA
      Nat Genet (2009)
    • Common variants at 6q22 and 17q21 are associated with intracranial volume 

      Ikram, M. Arfan; Fornage, Myriam; Smith, Albert V.; Seshadri, Sudha; Schmidt, Reinhold; Debette, Stephanie; Vrooman, Henri A.; Sigurdsson, Sigurdur; Ropele, Stefan; Taal, H. Rob; Mook-Kanamori, Dennis O.; Coker, Laura H.; Longstreth, W. T., Jr.; Niessen, Wiro J.; DeStefano, Anita L.; Beiser, Alexa; Zijdenbos, Alex P.; Struchalin, Maksim; Jack, Clifford R., Jr.; Rivadeneira, Fernando; Uitterlinden, Andre G.; Knopman, David S.; Hartikainen, Anna-Liisa; Pennell, Craig E.; Thiering, Elisabeth; Steegers, Eric A. P.; Hakonarson, Hakon; Heinrich, Joachim; Palmer, Lyle J.; Jarvelin, Marjo-Riitta; McCarthy, Mark I.; Grant, Struan F. A.; St Pourcain, Beate; Timpson, Nicholas J.; Smith, George Davey; Sovio, Ulla; Nalls, Mike A.; Au, Rhoda; Hofman, Albert; Gudnason, Haukur; van der Lugt, Aad; Harris, Tamara B.; Meeks, William M.; Vernooij, Meike W.; van Buchem, Mark A.; Catellier, Diane; Jaddoe, Vincent W. V.; Gudnason, Vilmundur; Windham, B. Gwen; Wolf, Philip A.; van Duijn, Cornelia M.; Mosley, Thomas H., Jr.; Schmidt, Helena; Launer, Lenore J.; Breteler, Monique M. B.; DeCarli, Charles; Adair, Linda S.; Ang, Wei; Atalay, Mustafa; vanBeijsterveldt, Toos; Bergen, Nienke; Benke, Kelly; Berry, Diane; Coin, Lachlan; Davis, Oliver S. P.; Elliott, Paul; Flexeder, Claudia; Frayling, Tim; Gaillard, Romy; Groen-Blokhuis, Maria; Goh, Liang-Kee; Haworth, Claire M. A.; Hadley, Dexter; Hedebrand, Johannes; Hinney, Anke; Hirschhorn, Joel N.; Holloway, John W.; Holst, Claus; Hottenga, Jouke Jan; Horikoshi, Momoko; Huikari, Ville; Hypponen, Elina; Kilpelainen, Tuomas O.; Kirin, Mirna; Kowgier, Matthew; Lakka, Hanna-Maaria; Lange, Leslie A.; Lawlor, Debbie A.; Lehtimaki, Terho; Lewin, Alex; Lindgren, Cecilia; Lindi, Virpi; Maggi, Reedik; Marsh, Julie; Middeldorp, Christel; Millwood, Iona; Murray, Jeffrey C.; Nivard, Michel; Nohr, Ellen Aagaard; Ntalla, Ioanna; Oken, Emily; Panoutsopoulou, Kalliope; Pararajasingham, Jennifer; Rodriguez, Alina; Salem, Rany M.; Sebert, Sylvain; Siitonen, Niina; Strachan, David P.; Teo, Yik-Ying; Valcarcel, Beatriz; Willemsen, Gonneke; Zeggini, Eleftheria; Boomsma, Dorret I.; Cooper, Cyrus; Gillman, Matthew; Hocher, Berthold; Lakka, Timo A.; Mohlke, Karen L.; Dedoussis, George V.; Ong, Ken K.; Pearson, Ewan R.; Price, Thomas S.; Power, Chris; Raitakari, Olli T.; Saw, Seang-Mei; Scherag, Andre; Simell, Olli; Sorensen, Thorkild I. A.; Wilson, James F.
      NATURE GENETICS : 5 (2012)