연구자에게
내 논문이 여기 있나요?
논문 2,673편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Peltonen L에 대해
49건, 그중 20건 표시.
Genome-wide association study identifies eight loci associated with blood pressure
Newton-Cheh C,
Johnson T,
Gateva V,
Tobin MD,
Bochud M,
Coin L,
Najjar SS,
Zhao JH,
Heath SC,
Eyheramendy S,
Papadakis K,
Voight BF
외 147명 — 모두 보기
Scott LJ,
Zhang F,
Farrall M,
Tanaka T,
Wallace C,
Chambers JC,
Khaw KT,
Nilsson P,
van der Harst P,
Polidoro S,
Grobbee DE,
Onland-Moret NC,
Bots ML,
Wain LV,
Elliott KS,
Teumer A,
Luan J,
Lucas G,
Kuusisto J,
Burton PR,
Hadley D,
McArdle WL,
Brown M,
Dominiczak A,
Newhouse SJ,
Samani NJ,
Webster J,
Zeggini E,
Beckmann JS,
Bergmann S,
Lim N,
Song K,
Vollenweider P,
Waeber G,
Waterworth DM,
Yuan X,
Groop L,
Orho-Melander M,
Allione A,
Di Gregorio A,
Guarrera S,
Panico S,
Ricceri F,
Romanazzi V,
Sacerdote C,
Vineis P,
Barroso I,
Sandhu MS,
Luben RN,
Crawford GJ,
Jousilahti P,
Perola M,
Boehnke M,
Bonnycastle LL,
Collins FS,
Jackson AU,
Mohlke KL,
Stringham HM,
Valle TT,
Willer CJ,
Bergman RN,
Morken MA,
Döring A,
Gieger C,
Illig T,
Meitinger T,
Org E,
Org E,
Pfeufer A,
Wichmann HE,
Kathiresan S,
Marrugat J,
O'Donnell CJ,
Schwartz SM,
Siscovick DS,
Subirana I,
Freimer NB,
Hartikainen AL,
McCarthy MI,
O'Reilly PF,
Peltonen L,
Pouta A,
de Jong PE,
Snieder H,
van Gilst WH,
Clarke R,
Goel A,
Hamsten A,
Peden JF,
Seedorf U,
Syvänen AC,
Tognoni G,
Lakatta EG,
Sanna S,
Scheet P,
Schlessinger D,
Scuteri A,
Dörr M,
Ernst F,
Felix SB,
Homuth G,
Lorbeer R,
Reffelmann T,
Rettig R,
Völker U,
Galan P,
Gut IG,
Hercberg S,
Lathrop GM,
Zelenika D,
Deloukas P,
Soranzo N,
Williams FM,
Zhai G,
Salomaa V,
Laakso M,
Elosua R,
Forouhi NG,
Völzke H,
Uiterwaal CS,
van der Schouw YT,
Numans ME,
Matullo G,
Navis G,
Berglund G,
Bingham SA,
Kooner JS,
Connell JM,
Bandinelli S,
Ferrucci L,
Watkins H,
Spector TD,
Tuomilehto J,
Altshuler D,
Strachan DP,
Laan M,
Meneton P,
Wareham NJ,
Uda M,
Jarvelin MR,
Mooser V,
Melander O,
Loos RJ,
Elliott P,
Abecasis GR,
Caulfield M,
Munroe PB
Wellcome Trust Case Control Consortium
Nature genetics · 2009 · PMID 19430483 · open access
페이지 4개
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Dupuis J,
Langenberg C,
Prokopenko I,
Saxena R,
Soranzo N,
Jackson AU,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Gloyn AL,
Lindgren CM,
Mägi R
외 292명 — 모두 보기
Morris AP,
Randall J,
Johnson T,
Elliott P,
Rybin D,
Thorleifsson G,
Steinthorsdottir V,
Henneman P,
Grallert H,
Dehghan A,
Hottenga JJ,
Franklin CS,
Navarro P,
Song K,
Goel A,
Perry JR,
Egan JM,
Lajunen T,
Grarup N,
Sparsø T,
Doney A,
Voight BF,
Stringham HM,
Li M,
Kanoni S,
Shrader P,
Cavalcanti-Proença C,
Kumari M,
Qi L,
Timpson NJ,
Gieger C,
Zabena C,
Rocheleau G,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Payne F,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ardlie K,
Ariyurek Y,
Balkau B,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Benediktsson R,
Bennett AJ,
Bergmann S,
Bochud M,
Boerwinkle E,
Bonnefond A,
Bonnycastle LL,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Charpentier G,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
Cooper MN,
Cornelis M,
Crawford G,
Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Dina C,
Erdos MR,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Fox CS,
Frants R,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Groves CJ,
Grundy S,
Gwilliam R,
Gyllensten U,
Hadjadj S,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hassanali N,
Hayward C,
Heath SC,
Hercberg S,
Herder C,
Hicks AA,
Hillman DR,
Hingorani AD,
Hofman A,
Hui J,
Hung J,
Isomaa B,
Johnson PR,
Jørgensen T,
Jula A,
Kaakinen M,
Kaprio J,
Kesaniemi YA,
Kivimaki M,
Knight B,
Koskinen S,
Kovacs P,
Kyvik KO,
Lathrop GM,
Lawlor DA,
Le Bacquer O,
Lecoeur C,
Li Y,
Lyssenko V,
Mahley R,
Mangino M,
Manning AK,
Martínez-Larrad MT,
McAteer JB,
McCulloch LJ,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Morken MA,
Mukherjee S,
Naitza S,
Narisu N,
Neville MJ,
Oostra BA,
Orrù M,
Pakyz R,
Palmer CN,
Paolisso G,
Pattaro C,
Pearson D,
Peden JF,
Pedersen NL,
Perola M,
Pfeiffer AF,
Pichler I,
Polasek O,
Posthuma D,
Potter SC,
Pouta A,
Province MA,
Psaty BM,
Rathmann W,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Roden M,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Scott LJ,
Seedorf U,
Sharp SJ,
Shields B,
Sigurethsson G,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tanaka T,
Thorand B,
Tichet J,
Tönjes A,
Tuomi T,
Uitterlinden AG,
van Dijk KW,
van Hoek M,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Walters GB,
Ward KL,
Watkins H,
Weedon MN,
Wild SH,
Willemsen G,
Willemsen G,
Witteman JC,
Yarnell JW,
Zeggini E,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Loos RJ,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Hattersley AT,
Silander K,
Salomaa V,
Smith GD,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Dedoussis GV,
Serrano-Ríos M,
Morris AD,
Lind L,
Palmer LJ,
Hu FB,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pankow JS,
Sampson MJ,
Kuusisto J,
Laakso M,
Hansen T,
Pedersen O,
Pramstaller PP,
Wichmann HE,
Illig T,
Rudan I,
Wright AF,
Stumvoll M,
Campbell H,
Wilson JF,
Bergman RN,
Buchanan TA,
Collins FS,
Mohlke KL,
Tuomilehto J,
Valle TT,
Altshuler D,
Rotter JI,
Siscovick DS,
Penninx BW,
Boomsma DI,
Deloukas P,
Spector TD,
Frayling TM,
Ferrucci L,
Kong A,
Thorsteinsdottir U,
Stefansson K,
van Duijn CM,
Aulchenko YS,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Waterworth DM,
Vollenweider P,
Peltonen L,
Mooser V,
Abecasis GR,
Wareham NJ,
Sladek R,
Froguel P,
Watanabe RM,
Meigs JB,
Groop L,
Boehnke M,
McCarthy MI,
Florez JC,
Barroso I
DIAGRAM Consortium · GIANT Consortium 외 컨소시엄 3곳
Nature genetics · 2010 · PMID 20081858 · open access
페이지 4개
Identification of ten loci associated with height highlights new biological pathways in human growth
Lettre G,
Jackson AU,
Gieger C,
Schumacher FR,
Berndt SI,
Sanna S,
Eyheramendy S,
Voight BF,
Butler JL,
Guiducci C,
Illig T,
Hackett R
외 19명 — 모두 보기
Heid IM,
Jacobs KB,
Lyssenko V,
Uda M,
Boehnke M,
Chanock SJ,
Groop LC,
Hu FB,
Isomaa B,
Kraft P,
Peltonen L,
Salomaa V,
Schlessinger D,
Hunter DJ,
Hayes RB,
Abecasis GR,
Wichmann HE,
Mohlke KL,
Hirschhorn JN
Diabetes Genetics Initiative · FUSION 외 컨소시엄 4곳
Nature genetics · 2008 · PMID 18391950
페이지 3개
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations
Kolz M,
Johnson T,
Sanna S,
Teumer A,
Vitart V,
Perola M,
Mangino M,
Albrecht E,
Wallace C,
Farrall M,
Johansson A,
Nyholt DR
외 44명 — 모두 보기
Aulchenko Y,
Beckmann JS,
Bergmann S,
Bochud M,
Brown M,
Campbell H,
Connell J,
Dominiczak A,
Homuth G,
Lamina C,
McCarthy MI,
Meitinger T,
Mooser V,
Munroe P,
Nauck M,
Peden J,
Prokisch H,
Salo P,
Salomaa V,
Samani NJ,
Schlessinger D,
Uda M,
Völker U,
Waeber G,
Waterworth D,
Wang-Sattler R,
Wright AF,
Adamski J,
Whitfield JB,
Gyllensten U,
Wilson JF,
Rudan I,
Pramstaller P,
Watkins H,
Doering A,
Wichmann HE,
Spector TD,
Peltonen L,
Völzke H,
Nagaraja R,
Vollenweider P,
Caulfield M,
Illig T,
Gieger C
EUROSPAN Consortium · ENGAGE Consortium 외 컨소시엄 3곳
PLoS genetics · 2009 · PMID 19503597 · open access
페이지 3개
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Lindgren CM,
Heid IM,
Randall JC,
Lamina C,
Steinthorsdottir V,
Qi L,
Speliotes EK,
Thorleifsson G,
Willer CJ,
Herrera BM,
Jackson AU,
Lim N
외 131명 — 모두 보기
Scheet P,
Soranzo N,
Amin N,
Aulchenko YS,
Chambers JC,
Drong A,
Luan J,
Lyon HN,
Rivadeneira F,
Sanna S,
Timpson NJ,
Zillikens MC,
Zhao JH,
Almgren P,
Bandinelli S,
Bennett AJ,
Bergman RN,
Bonnycastle LL,
Bumpstead SJ,
Chanock SJ,
Cherkas L,
Chines P,
Coin L,
Cooper C,
Crawford G,
Doering A,
Dominiczak A,
Doney AS,
Ebrahim S,
Elliott P,
Erdos MR,
Estrada K,
Ferrucci L,
Fischer G,
Forouhi NG,
Gieger C,
Grallert H,
Groves CJ,
Grundy S,
Guiducci C,
Hadley D,
Hamsten A,
Havulinna AS,
Hofman A,
Holle R,
Holloway JW,
Illig T,
Isomaa B,
Jacobs LC,
Jameson K,
Jousilahti P,
Karpe F,
Kuusisto J,
Laitinen J,
Lathrop GM,
Lawlor DA,
Mangino M,
McArdle WL,
Meitinger T,
Morken MA,
Morris AP,
Munroe P,
Narisu N,
Nordström A,
Nordström P,
Oostra BA,
Palmer CN,
Payne F,
Peden JF,
Prokopenko I,
Renström F,
Ruokonen A,
Salomaa V,
Sandhu MS,
Scott LJ,
Scuteri A,
Silander K,
Song K,
Yuan X,
Stringham HM,
Swift AJ,
Tuomi T,
Uda M,
Vollenweider P,
Waeber G,
Wallace C,
Walters GB,
Weedon MN,
Witteman JC,
Zhang C,
Zhang W,
Caulfield MJ,
Collins FS,
Davey Smith G,
Day IN,
Franks PW,
Hattersley AT,
Hu FB,
Jarvelin MR,
Kong A,
Kooner JS,
Laakso M,
Lakatta E,
Mooser V,
Morris AD,
Peltonen L,
Samani NJ,
Spector TD,
Strachan DP,
Tanaka T,
Tuomilehto J,
Uitterlinden AG,
van Duijn CM,
Wareham NJ,
Hugh Watkins,
Waterworth DM,
Boehnke M,
Deloukas P,
Groop L,
Hunter DJ,
Thorsteinsdottir U,
Schlessinger D,
Wichmann HE,
Frayling TM,
Abecasis GR,
Hirschhorn JN,
Loos RJ,
Stefansson K,
Mohlke KL,
Barroso I,
McCarthy MI
Wellcome Trust Case Control Consortium · Procardis Consortia 외 컨소시엄 1곳
PLoS genetics · 2009 · PMID 19557161 · open access
페이지 3개
Genome-wide association study identifies five loci associated with lung function
Repapi E,
Sayers I,
Wain LV,
Burton PR,
Johnson T,
Obeidat M,
Zhao JH,
Ramasamy A,
Zhai G,
Vitart V,
Huffman JE,
Igl W
외 83명 — 모두 보기
Albrecht E,
Deloukas P,
Henderson J,
Granell R,
McArdle WL,
Rudnicka AR,
Barroso I,
Loos RJ,
Wareham NJ,
Mustelin L,
Rantanen T,
Surakka I,
Imboden M,
Wichmann HE,
Grkovic I,
Jankovic S,
Zgaga L,
Hartikainen AL,
Peltonen L,
Gyllensten U,
Johansson A,
Zaboli G,
Campbell H,
Wild SH,
Wilson JF,
Gläser S,
Homuth G,
Völzke H,
Mangino M,
Soranzo N,
Spector TD,
Polasek O,
Rudan I,
Wright AF,
Heliövaara M,
Ripatti S,
Pouta A,
Naluai AT,
Olin AC,
Torén K,
Cooper MN,
James AL,
James AL,
Palmer LJ,
Hingorani AD,
Wannamethee SG,
Whincup PH,
Smith GD,
Ebrahim S,
McKeever TM,
Pavord ID,
MacLeod AK,
Morris AD,
Porteous DJ,
Cooper C,
Dennison E,
Shaheen S,
Karrasch S,
Schnabel E,
Schulz H,
Grallert H,
Bouatia-Naji N,
Delplanque J,
Froguel P,
Blakey JD,
Britton JR,
Morris RW,
Holloway JW,
Lawlor DA,
Hui J,
Nyberg F,
Jarvelin MR,
Jackson C,
Kähönen M,
Kaprio J,
Probst-Hensch NM,
Koch B,
Hayward C,
Evans DM,
Elliott P,
Strachan DP,
Hall IP,
Tobin MD
Wellcome Trust Case Control Consortium · NSHD Respiratory Study Team
Nature genetics · 2010 · PMID 20010834
페이지 3개
Multiple common variants for celiac disease influencing immune gene expression
Dubois PC,
Trynka G,
Franke L,
Hunt KA,
Romanos J,
Curtotti A,
Zhernakova A,
Heap GA,
Adány R,
Aromaa A,
Bardella MT,
van den Berg LH
외 55명 — 모두 보기
Bockett NA,
de la Concha EG,
Dema B,
Fehrmann RS,
Fernández-Arquero M,
Fiatal S,
Grandone E,
Green PM,
Groen HJ,
Gwilliam R,
Houwen RH,
Hunt SE,
Kaukinen K,
Kelleher D,
Korponay-Szabo I,
Kurppa K,
MacMathuna P,
Mäki M,
Mazzilli MC,
McCann OT,
Mearin ML,
Mein CA,
Mirza MM,
Mistry V,
Mora B,
Morley KI,
Mulder CJ,
Murray JA,
Núñez C,
Oosterom E,
Ophoff RA,
Polanco I,
Peltonen L,
Platteel M,
Rybak A,
Salomaa V,
Schweizer JJ,
Sperandeo MP,
Tack GJ,
Turner G,
Veldink JH,
Verbeek WH,
Weersma RK,
Wolters VM,
Urcelay E,
Cukrowska B,
Greco L,
Neuhausen SL,
McManus R,
Barisani D,
Deloukas P,
Barrett JC,
Saavalainen P,
Wijmenga C,
van Heel DA
Nature genetics · 2010 · PMID 20190752 · open access
페이지 3개
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Wang TJ,
Zhang F,
Richards JB,
Kestenbaum B,
van Meurs JB,
Berry D,
Kiel DP,
Streeten EA,
Ohlsson C,
Koller DL,
Peltonen L,
Cooper JD
외 64명 — 모두 보기
O'Reilly PF,
Houston DK,
Glazer NL,
Vandenput L,
Peacock M,
Shi J,
Rivadeneira F,
McCarthy MI,
Anneli P,
de Boer IH,
Mangino M,
Kato B,
Smyth DJ,
Booth SL,
Jacques PF,
Burke GL,
Goodarzi M,
Cheung CL,
Wolf M,
Rice K,
Goltzman D,
Hidiroglou N,
Ladouceur M,
Wareham NJ,
Hocking LJ,
Hart D,
Arden NK,
Cooper C,
Malik S,
Fraser WD,
Hartikainen AL,
Zhai G,
Macdonald HM,
Forouhi NG,
Loos RJ,
Reid DM,
Hakim A,
Dennison E,
Liu Y,
Power C,
Stevens HE,
Jaana L,
Vasan RS,
Soranzo N,
Bojunga J,
Psaty BM,
Lorentzon M,
Foroud T,
Harris TB,
Hofman A,
Jansson JO,
Cauley JA,
Uitterlinden AG,
Gibson Q,
Järvelin MR,
Karasik D,
Siscovick DS,
Econs MJ,
Kritchevsky SB,
Florez JC,
Todd JA,
Dupuis J,
Hyppönen E,
Spector TD
Lancet (London, England) · 2010 · PMID 20541252
페이지 3개
Genetic variants influencing circulating lipid levels and risk of coronary artery disease
Waterworth DM,
Ricketts SL,
Song K,
Chen L,
Zhao JH,
Ripatti S,
Aulchenko YS,
Zhang W,
Yuan X,
Lim N,
Luan J,
Ashford S
외 54명 — 모두 보기
Wheeler E,
Young EH,
Hadley D,
Thompson JR,
Braund PS,
Johnson T,
Struchalin M,
Surakka I,
Luben R,
Khaw KT,
Rodwell SA,
Loos RJ,
Boekholdt SM,
Inouye M,
Deloukas P,
Elliott P,
Schlessinger D,
Sanna S,
Scuteri A,
Jackson A,
Mohlke KL,
Tuomilehto J,
Roberts R,
Stewart A,
Kesäniemi YA,
Mahley RW,
Grundy SM,
McArdle W,
Cardon L,
Waeber G,
Vollenweider P,
Chambers JC,
Boehnke M,
Abecasis GR,
Salomaa V,
Järvelin MR,
Ruokonen A,
Barroso I,
Epstein SE,
Hakonarson HH,
Rader DJ,
Reilly MP,
Witteman JC,
Hall AS,
Samani NJ,
Strachan DP,
Barter P,
van Duijn CM,
Kooner JS,
Peltonen L,
Wareham NJ,
McPherson R,
Mooser V,
Sandhu MS
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
페이지 3개
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Heid IM,
Jackson AU,
Randall JC,
Winkler TW,
Qi L,
Steinthorsdottir V,
Thorleifsson G,
Zillikens MC,
Speliotes EK,
Mägi R,
Workalemahu T,
White CC
외 290명 — 모두 보기
Bouatia-Naji N,
Harris TB,
Berndt SI,
Ingelsson E,
Willer CJ,
Weedon MN,
Luan J,
Vedantam S,
Esko T,
Kilpeläinen TO,
Kutalik Z,
Li S,
Monda KL,
Dixon AL,
Holmes CC,
Kaplan LM,
Liang L,
Min JL,
Moffatt MF,
Molony C,
Nicholson G,
Schadt EE,
Zondervan KT,
Feitosa MF,
Ferreira T,
Lango Allen H,
Weyant RJ,
Wheeler E,
Wood AR,
Estrada K,
Goddard ME,
Lettre G,
Mangino M,
Nyholt DR,
Purcell S,
Smith AV,
Visscher PM,
Yang J,
McCarroll SA,
Nemesh J,
Voight BF,
Absher D,
Amin N,
Aspelund T,
Coin L,
Glazer NL,
Hayward C,
Heard-Costa NL,
Hottenga JJ,
Johansson A,
Johnson T,
Kaakinen M,
Kapur K,
Ketkar S,
Knowles JW,
Kraft P,
Kraja AT,
Lamina C,
Leitzmann MF,
McKnight B,
Morris AP,
Ong KK,
Perry JR,
Peters MJ,
Polasek O,
Prokopenko I,
Rayner NW,
Ripatti S,
Rivadeneira F,
Robertson NR,
Sanna S,
Sovio U,
Surakka I,
Teumer A,
van Wingerden S,
Vitart V,
Zhao JH,
Cavalcanti-Proença C,
Chines PS,
Fisher E,
Kulzer JR,
Lecoeur C,
Narisu N,
Sandholt C,
Scott LJ,
Silander K,
Stark K,
Tammesoo ML,
Teslovich TM,
Timpson NJ,
Watanabe RM,
Welch R,
Chasman DI,
Cooper MN,
Jansson JO,
Kettunen J,
Lawrence RW,
Pellikka N,
Perola M,
Vandenput L,
Alavere H,
Almgren P,
Atwood LD,
Bennett AJ,
Biffar R,
Bonnycastle LL,
Bornstein SR,
Buchanan TA,
Campbell H,
Day IN,
Dei M,
Dörr M,
Elliott P,
Erdos MR,
Eriksson JG,
Freimer NB,
Fu M,
Gaget S,
Geus EJ,
Gjesing AP,
Grallert H,
Grässler J,
Groves CJ,
Guiducci C,
Hartikainen AL,
Hassanali N,
Havulinna AS,
Herzig KH,
Hicks AA,
Hui J,
Igl W,
Jousilahti P,
Jula A,
Kajantie E,
Kinnunen L,
Kolcic I,
Koskinen S,
Kovacs P,
Kroemer HK,
Krzelj V,
Kuusisto J,
Kvaloy K,
Laitinen J,
Lantieri O,
Lathrop GM,
Lokki ML,
Luben RN,
Ludwig B,
McArdle WL,
McCarthy A,
Morken MA,
Nelis M,
Neville MJ,
Paré G,
Parker AN,
Peden JF,
Pichler I,
Pietiläinen KH,
Platou CG,
Pouta A,
Ridderstråle M,
Samani NJ,
Saramies J,
Sinisalo J,
Smit JH,
Strawbridge RJ,
Stringham HM,
Swift AJ,
Teder-Laving M,
Thomson B,
Usala G,
van Meurs JB,
van Ommen GJ,
Vatin V,
Volpato CB,
Wallaschofski H,
Walters GB,
Widen E,
Wild SH,
Willemsen G,
Witte DR,
Zgaga L,
Zitting P,
Beilby JP,
James AL,
James AL,
Kähönen M,
Lehtimäki T,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Raitakari O,
Ridker PM,
Stumvoll M,
Tönjes A,
Viikari J,
Balkau B,
Ben-Shlomo Y,
Bergman RN,
Boeing H,
Smith GD,
Ebrahim S,
Froguel P,
Hansen T,
Hengstenberg C,
Hveem K,
Isomaa B,
Jørgensen T,
Karpe F,
Khaw KT,
Laakso M,
Lawlor DA,
Marre M,
Meitinger T,
Metspalu A,
Midthjell K,
Pedersen O,
Salomaa V,
Schwarz PE,
Schwarz PE,
Tuomi T,
Tuomilehto J,
Valle TT,
Wareham NJ,
Arnold AM,
Beckmann JS,
Bergmann S,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Collins FS,
Eiriksdottir G,
Gudnason V,
Gyllensten U,
Hamsten A,
Hattersley AT,
Hofman A,
Hu FB,
Illig T,
Iribarren C,
Jarvelin MR,
Kao WH,
Kaprio J,
Launer LJ,
Munroe PB,
Oostra B,
Penninx BW,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rissanen A,
Rudan I,
Shuldiner AR,
Soranzo N,
Spector TD,
Syvanen AC,
Uda M,
Uitterlinden A,
Völzke H,
Vollenweider P,
Wilson JF,
Witteman JC,
Wright AF,
Abecasis GR,
Boehnke M,
Borecki IB,
Deloukas P,
Frayling TM,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
North KE,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
Hirschhorn JN,
Assimes TL,
Wichmann HE,
Thorsteinsdottir U,
van Duijn CM,
Stefansson K,
Cupples LA,
Loos RJ,
Barroso I,
McCarthy MI,
Fox CS,
Mohlke KL,
Lindgren CM
MAGIC
Nature genetics · 2010 · PMID 20935629
페이지 3개
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
Evans DM,
Spencer CC,
Pointon JJ,
Su Z,
Harvey D,
Kochan G,
Oppermann U,
Dilthey A,
Pirinen M,
Stone MA,
Appleton L,
Moutsianas L
외 81명 — 모두 보기
Leslie S,
Wordsworth T,
Kenna TJ,
Karaderi T,
Thomas GP,
Ward MM,
Weisman MH,
Farrar C,
Bradbury LA,
Danoy P,
Inman RD,
Maksymowych W,
Gladman D,
Rahman P,
Morgan A,
Marzo-Ortega H,
Bowness P,
Gaffney K,
Gaston JS,
Smith M,
Bruges-Armas J,
Couto AR,
Sorrentino R,
Paladini F,
Ferreira MA,
Xu H,
Liu Y,
Jiang L,
Lopez-Larrea C,
Díaz-Peña R,
López-Vázquez A,
Zayats T,
Band G,
Bellenguez C,
Blackburn H,
Blackwell JM,
Bramon E,
Bumpstead SJ,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Freeman C,
Gillman M,
Gray E,
Gwilliam R,
Hammond N,
Hunt SE,
Jankowski J,
Jayakumar A,
Langford C,
Liddle J,
Markus HS,
Mathew CG,
McCann OT,
McCarthy MI,
Palmer CN,
Peltonen L,
Plomin R,
Potter SC,
Rautanen A,
Ravindrarajah R,
Ricketts M,
Samani N,
Sawcer SJ,
Strange A,
Trembath RC,
Viswanathan AC,
Waller M,
Weston P,
Whittaker P,
Widaa S,
Wood NW,
McVean G,
Reveille JD,
Wordsworth BP,
Brown MA,
Donnelly P
Spondyloarthritis Research Consortium of Canada (SPARCC) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) 외 컨소시엄 1곳
Nature genetics · 2011 · PMID 21743469
페이지 3개
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits
Kristiansson K,
Perola M,
Tikkanen E,
Kettunen J,
Surakka I,
Havulinna AS,
Stancáková A,
Barnes C,
Widen E,
Kajantie E,
Eriksson JG,
Viikari J
외 22명 — 모두 보기
Kähönen M,
Lehtimäki T,
Raitakari OT,
Hartikainen AL,
Ruokonen A,
Pouta A,
Jula A,
Kangas AJ,
Soininen P,
Ala-Korpela M,
Männistö S,
Jousilahti P,
Bonnycastle LL,
Järvelin MR,
Kuusisto J,
Collins FS,
Laakso M,
Hurles ME,
Palotie A,
Peltonen L,
Ripatti S,
Salomaa V
Circulation. Cardiovascular genetics · 2012 · PMID 22399527
페이지 3개
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Sabatti C,
Service SK,
Hartikainen AL,
Pouta A,
Ripatti S,
Brodsky J,
Jones CG,
Zaitlen NA,
Varilo T,
Kaakinen M,
Sovio U,
Ruokonen A
외 13명 — 모두 보기
Laitinen J,
Jakkula E,
Coin L,
Hoggart C,
Collins A,
Turunen H,
Gabriel S,
Elliot P,
McCarthy MI,
Daly MJ,
Järvelin MR,
Freimer NB,
Peltonen L
Nature genetics · 2009 · PMID 19060910
페이지 2개
Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease
Elliott P,
Chambers JC,
Zhang W,
Clarke R,
Hopewell JC,
Peden JF,
Erdmann J,
Braund P,
Engert JC,
Bennett D,
Coin L,
Ashby D
외 24명 — 모두 보기
Tzoulaki I,
Brown IJ,
Mt-Isa S,
McCarthy MI,
Peltonen L,
Freimer NB,
Farrall M,
Ruokonen A,
Hamsten A,
Lim N,
Froguel P,
Waterworth DM,
Vollenweider P,
Waeber G,
Jarvelin MR,
Mooser V,
Scott J,
Hall AS,
Schunkert H,
Anand SS,
Collins R,
Samani NJ,
Watkins H,
Kooner JS
JAMA · 2009 · PMID 19567438
페이지 2개
Common variants conferring risk of schizophrenia
Stefansson H,
Ophoff RA,
Steinberg S,
Andreassen OA,
Cichon S,
Rujescu D,
Werge T,
Pietiläinen OP,
Mors O,
Mortensen PB,
Sigurdsson E,
Gustafsson O
외 75명 — 모두 보기
Nyegaard M,
Tuulio-Henriksson A,
Ingason A,
Hansen T,
Suvisaari J,
Lonnqvist J,
Paunio T,
Børglum AD,
Hartmann A,
Fink-Jensen A,
Nordentoft M,
Hougaard D,
Norgaard-Pedersen B,
Böttcher Y,
Olesen J,
Breuer R,
Möller HJ,
Giegling I,
Rasmussen HB,
Timm S,
Mattheisen M,
Bitter I,
Réthelyi JM,
Magnusdottir BB,
Sigmundsson T,
Olason P,
Masson G,
Gulcher JR,
Haraldsson M,
Fossdal R,
Thorgeirsson TE,
Thorsteinsdottir U,
Ruggeri M,
Tosato S,
Franke B,
Strengman E,
Kiemeney LA,
Melle I,
Djurovic S,
Abramova L,
Kaleda V,
Sanjuan J,
de Frutos R,
Bramon E,
Vassos E,
Fraser G,
Ettinger U,
Picchioni M,
Walker N,
Toulopoulou T,
Need AC,
Ge D,
Yoon JL,
Shianna KV,
Freimer NB,
Cantor RM,
Murray R,
Kong A,
Golimbet V,
Carracedo A,
Arango C,
Costas J,
Jönsson EG,
Terenius L,
Agartz I,
Petursson H,
Nöthen MM,
Rietschel M,
Matthews PM,
Muglia P,
Peltonen L,
St Clair D,
Goldstein DB,
Stefansson K,
Collier DA
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
페이지 2개
Genome-wide association study reveals multiple loci associated with primary tooth development during infancy
Pillas D,
Hoggart CJ,
Evans DM,
O'Reilly PF,
Sipilä K,
Lähdesmäki R,
Millwood IY,
Kaakinen M,
Netuveli G,
Blane D,
Charoen P,
Sovio U
외 18명 — 모두 보기
Pouta A,
Freimer N,
Hartikainen AL,
Laitinen J,
Vaara S,
Glaser B,
Crawford P,
Timpson NJ,
Ring SM,
Deng G,
Zhang W,
McCarthy MI,
Deloukas P,
Peltonen L,
Elliott P,
Coin LJ,
Smith GD,
Jarvelin MR
PLoS genetics · 2010 · PMID 20195514 · open access
페이지 2개
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
Zhou K,
Bellenguez C,
Spencer CC,
Bennett AJ,
Coleman RL,
Tavendale R,
Hawley SA,
Donnelly LA,
Schofield C,
Groves CJ,
Burch L,
Carr F
외 38명 — 모두 보기
Strange A,
Freeman C,
Blackwell JM,
Bramon E,
Brown MA,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Gray E,
Hunt S,
Jankowski J,
Langford C,
Markus HS,
Mathew CG,
Plomin R,
Rautanen A,
Sawcer SJ,
Samani NJ,
Trembath R,
Viswanathan AC,
Wood NW,
Harries LW,
Hattersley AT,
Doney AS,
Colhoun H,
Morris AD,
Sutherland C,
Hardie DG,
Peltonen L,
McCarthy MI,
Holman RR,
Palmer CN,
Donnelly P,
Pearson ER
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group · Wellcome Trust Case Control Consortium 2 외 컨소시엄 1곳
Nature genetics · 2011 · PMID 21186350 · open access
페이지 2개
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Schumann G,
Coin LJ,
Lourdusamy A,
Charoen P,
Berger KH,
Stacey D,
Desrivières S,
Aliev FA,
Khan AA,
Amin N,
Aulchenko YS,
Bakalkin G
외 104명 — 모두 보기
Bakker SJ,
Balkau B,
Beulens JW,
Bilbao A,
de Boer RA,
Beury D,
Bots ML,
Breetvelt EJ,
Cauchi S,
Cavalcanti-Proença C,
Chambers JC,
Clarke TK,
Dahmen N,
de Geus EJ,
Dick D,
Ducci F,
Easton A,
Edenberg HJ,
Esko T,
Fernández-Medarde A,
Foroud T,
Freimer NB,
Girault JA,
Grobbee DE,
Guarrera S,
Gudbjartsson DF,
Hartikainen AL,
Heath AC,
Hesselbrock V,
Hofman A,
Hottenga JJ,
Isohanni MK,
Kaprio J,
Khaw KT,
Kuehnel B,
Laitinen J,
Lobbens S,
Luan J,
Mangino M,
Maroteaux M,
Matullo G,
McCarthy MI,
Mueller C,
Navis G,
Numans ME,
Núñez A,
Nyholt DR,
Onland-Moret CN,
Oostra BA,
O'Reilly PF,
Palkovits M,
Penninx BW,
Polidoro S,
Pouta A,
Prokopenko I,
Ricceri F,
Santos E,
Smit JH,
Soranzo N,
Song K,
Sovio U,
Stumvoll M,
Surakk I,
Thorgeirsson TE,
Thorsteinsdottir U,
Troakes C,
Tyrfingsson T,
Tönjes A,
Uiterwaal CS,
Uitterlinden AG,
van der Harst P,
van der Schouw YT,
Staehlin O,
Vogelzangs N,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Whitfield JB,
Wichmann EH,
Willemsen G,
Witteman JC,
Yuan X,
Zhai G,
Zhao JH,
Zhang W,
Martin NG,
Metspalu A,
Doering A,
Scott J,
Spector TD,
Loos RJ,
Boomsma DI,
Mooser V,
Peltonen L,
Stefansson K,
van Duijn CM,
Vineis P,
Sommer WH,
Kooner JS,
Spanagel R,
Heberlein UA,
Jarvelin MR,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
페이지 2개
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
Bis JC,
Kavousi M,
Franceschini N,
Isaacs A,
Abecasis GR,
Schminke U,
Post WS,
Smith AV,
Cupples LA,
Markus HS,
Schmidt R,
Huffman JE
외 81명 — 모두 보기
Lehtimäki T,
Baumert J,
Münzel T,
Heckbert SR,
Dehghan A,
North K,
Oostra B,
Bevan S,
Stoegerer EM,
Hayward C,
Raitakari O,
Meisinger C,
Schillert A,
Sanna S,
Völzke H,
Cheng YC,
Thorsson B,
Fox CS,
Rice K,
Rivadeneira F,
Nambi V,
Halperin E,
Petrovic KE,
Peltonen L,
Wichmann HE,
Schnabel RB,
Dörr M,
Parsa A,
Aspelund T,
Demissie S,
Kathiresan S,
Reilly MP,
Taylor K,
Uitterlinden A,
Couper DJ,
Sitzer M,
Kähönen M,
Illig T,
Wild PS,
Orru M,
Lüdemann J,
Shuldiner AR,
Eiriksdottir G,
White CC,
Rotter JI,
Hofman A,
Seissler J,
Zeller T,
Usala G,
Ernst F,
Launer LJ,
D'Agostino RB Sr,
O'Leary DH,
Ballantyne C,
Thiery J,
Ziegler A,
Lakatta EG,
Chilukoti RK,
Harris TB,
Wolf PA,
Psaty BM,
Polak JF,
Li X,
Rathmann W,
Uda M,
Boerwinkle E,
Klopp N,
Schmidt H,
Wilson JF,
Viikari J,
Koenig W,
Blankenberg S,
Newman AB,
Witteman J,
Heiss G,
Duijn Cv,
Scuteri A,
Homuth G,
Mitchell BD,
Gudnason V,
O'Donnell CJ
CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21909108 · open access
페이지 2개
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.