연구자에게
내 논문이 여기 있나요?
논문 2,682편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
An P에 대해
373건, 그중 20건 표시.
Discovery of novel ancestry specific genes for androgens and hypogonadism in Million Veteran Program Men
Pagadala MS,
Teerlink CC,
Jasuja GK,
Palnati M,
Anglin-Foote T,
Chang NN,
Deka R,
Lee KM,
Agiri FY,
Amariuta T,
Seibert TM,
Rose BS
외 5명 — 모두 보기
Nature communications · 2025 · PMID 40316537 · open access
페이지 12개+
Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population
Enzan N,
Miyazawa K,
Koyama S,
Kurosawa R,
Ieki H,
Yoshida H,
Takechi F,
Fukuyama M,
Osako R,
Tomizuka K,
Liu X,
Ozaki K
외 18명 — 모두 보기
Onouchi Y,
Matsuda K,
Momozawa Y,
Aburatani H,
Kamatani Y,
Yamaguchi T,
Akazawa H,
Node K,
Ellinor PT,
Levin MG,
Damrauer SM,
Voight BF,
Joseph J,
Sun YV,
Terao C,
Ninomiya T,
Komuro I,
Ito K
BioBank Japan Project
Nature communications · 2025 · PMID 41184235 · open access
페이지 12개+
Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction
Small AM,
Yang TY,
Itoh S,
Thériault S,
Dufresne L,
Kurosawa R,
Komuro I,
Matsuda K,
Vy HMT,
Farber-Eger EH,
Shaffer LL,
Boulier KM
외 89명 — 모두 보기
Corey KM,
Ramaker ME,
Laporte F,
Schott JJ,
Le Scouarnec S,
Singh SA,
Sonawane AR,
Smith HA,
Rafaels N,
Ghouse J,
Raja AA,
Ostrowski SR,
Sørensen E,
Mikkelsen C,
Pedersen OB,
Erikstrup C,
Ullum H,
Sveinbjornsson G,
Gudbjartsson DF,
Abner E,
Lee J,
Ganna A,
Nowak-Göttl U,
Finer S,
Schumacher J,
Maj C,
Al-Kassou B,
Nickenig G,
Trenkwalder T,
Dreβen M,
Krane M,
Nöthen MM,
Moksnes MR,
Brumpton BM,
Knight S,
Knowlton KU,
Nadauld L,
Debiec R,
Musameh MD,
Braund PS,
Nelson CP,
Czuba T,
Melander O,
Selvaraj MS,
Koyama S,
Bhukar R,
Ruan Y,
Ljungberg J,
Damrauer SM,
Levin MG,
Franke A,
Berger K,
Ruff CT,
Melloni GEM,
Kamanu FK,
Ito K,
Do R,
Loos RJF,
Schunkert H,
Wells QS,
Shah SH,
Le Tourneau T,
Messika-Zeitoun D,
Gignoux C,
Bundgaard H,
Larsson SC,
Michaëlsson K,
Holm H,
Helgadottir A,
Esko T,
van Heel DA,
Mathieu P,
Samani NJ,
Smith JG,
Söderberg S,
Rader DJ,
Marston NA,
Sabatine MS,
Pasaniuc B,
Cho K,
Wilson PWF,
O'Donnell CJ,
Stefansson K,
Bossé Y,
Aikawa E,
Engert JC,
Peloso GM,
Natarajan P,
Thanassoulis G
Colorado Center for Personalized Medicine · DBDS Genomic Consortium 외 컨소시엄 2곳
Nature genetics · 2026 · PMID 41419686 · open access
페이지 12개+
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL,
Brasher MS,
Pattee J,
Zhou W,
Chapman S,
Jee YH,
Bell CC,
Jamil TL,
Barrio M,
Arehart CH,
Evans LM,
Hirbo J
외 73명 — 모두 보기
Cox NJ,
Straub P,
Namba S,
Bertucci-Richter E,
Guare L,
Edris A,
Morris S,
Mulford AJ,
Zhang H,
Fennessy B,
Tobin MD,
Chen J,
Williams AT,
John C,
van Heel DA,
Mathur R,
Finer S,
Moksnes MR,
Brumpton BM,
Åsvold BO,
Peculis R,
Rovite V,
Konrade I,
Wang Y,
Crooks K,
Chavan S,
Fisher MJ,
Rafaels N,
Lin M,
Shortt JA,
Sanders AR,
Whiteman DC,
MacGregor S,
Medland SE,
Thorsteinsdóttir U,
Stefánsson K,
Karaderi T,
Egan KM,
Bocklage T,
McCrary HC,
Riedlinger G,
Salhia B,
Shriver C,
Phan MD,
Farlow JL,
Edge S,
Kaur V,
Churchman ML,
Rounbehler RJ,
Brock PL,
Ringel MD,
Pividori M,
Schweppe R,
Raeburn CD,
Walters RG,
Chen Z,
Li L,
Matsuda K,
Okada Y,
Zöllner S,
Verma A,
Preuss MH,
Kenny E,
Hendricks AE,
Fishbein L,
Kraft P,
Daly MJ,
Neale BM,
Martin AR,
Cole JB,
Haugen BR,
Gignoux CR,
Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium 외 컨소시엄 4곳
Nature genetics · 2026 · PMID 41644669 · open access
페이지 12개+
Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis
Bujnis MN,
Sterenborg RBTM,
Li Y,
Åsvold BO,
Brčić L,
Boraska Perica V,
Babbar A,
Denny JC,
Fritsche LG,
Kanai M,
Konrade I,
Leese G
외 22명 — 모두 보기
Marouli E,
Metspalu A,
Moksnes MR,
Mukherjee B,
Okada Y,
Palmer CNA,
Papadopoulou A,
Peculis R,
Rovite V,
Sauer PJ,
Soto-Pedre E,
Srinivasan S,
Steinbrenner I,
Teder-Laving M,
Wang B,
Weihs A,
Zeng C,
Zhou J,
Song X,
Jorde LB,
Medici M,
Teumer A
Biobank Japan Project
Nature genetics · 2026 · PMID 42527560 · open access
페이지 12개+
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Speliotes EK,
Willer CJ,
Berndt SI,
Monda KL,
Thorleifsson G,
Jackson AU,
Lango Allen H,
Lindgren CM,
Luan J,
Mägi R,
Randall JC,
Vedantam S
외 366명 — 모두 보기
Winkler TW,
Qi L,
Workalemahu T,
Heid IM,
Steinthorsdottir V,
Stringham HM,
Weedon MN,
Wheeler E,
Wood AR,
Ferreira T,
Weyant RJ,
Segrè AV,
Estrada K,
Liang L,
Nemesh J,
Park JH,
Gustafsson S,
Kilpeläinen TO,
Yang J,
Bouatia-Naji N,
Esko T,
Feitosa MF,
Kutalik Z,
Mangino M,
Raychaudhuri S,
Scherag A,
Smith AV,
Welch R,
Zhao JH,
Aben KK,
Absher DM,
Amin N,
Dixon AL,
Fisher E,
Glazer NL,
Goddard ME,
Heard-Costa NL,
Hoesel V,
Hottenga JJ,
Johansson A,
Johnson T,
Ketkar S,
Lamina C,
Li S,
Moffatt MF,
Myers RH,
Narisu N,
Perry JR,
Peters MJ,
Preuss M,
Ripatti S,
Rivadeneira F,
Sandholt C,
Scott LJ,
Timpson NJ,
Tyrer JP,
van Wingerden S,
Watanabe RM,
White CC,
Wiklund F,
Barlassina C,
Chasman DI,
Cooper MN,
Jansson JO,
Lawrence RW,
Pellikka N,
Prokopenko I,
Shi J,
Thiering E,
Alavere H,
Alibrandi MT,
Almgren P,
Arnold AM,
Aspelund T,
Atwood LD,
Balkau B,
Balmforth AJ,
Bennett AJ,
Ben-Shlomo Y,
Bergman RN,
Bergmann S,
Biebermann H,
Blakemore AI,
Boes T,
Bonnycastle LL,
Bornstein SR,
Brown MJ,
Buchanan TA,
Busonero F,
Campbell H,
Cappuccio FP,
Cavalcanti-Proença C,
Chen YD,
Chen CM,
Chines PS,
Clarke R,
Coin L,
Connell J,
Day IN,
den Heijer M,
Duan J,
Ebrahim S,
Elliott P,
Elliott P,
Elosua R,
Eiriksdottir G,
Erdos MR,
Eriksson JG,
Facheris MF,
Felix SB,
Fischer-Posovszky P,
Folsom AR,
Friedrich N,
Freimer NB,
Fu M,
Gaget S,
Gejman PV,
Geus EJ,
Gieger C,
Gjesing AP,
Goel A,
Goyette P,
Grallert H,
Grässler J,
Greenawalt DM,
Groves CJ,
Gudnason V,
Guiducci C,
Hartikainen AL,
Hassanali N,
Hall AS,
Havulinna AS,
Hayward C,
Heath AC,
Hengstenberg C,
Hicks AA,
Hinney A,
Hofman A,
Homuth G,
Hui J,
Igl W,
Iribarren C,
Isomaa B,
Jacobs KB,
Jarick I,
Jewell E,
John U,
Jørgensen T,
Jousilahti P,
Jula A,
Kaakinen M,
Kajantie E,
Kaplan LM,
Kathiresan S,
Kettunen J,
Kinnunen L,
Knowles JW,
Kolcic I,
König IR,
Koskinen S,
Kovacs P,
Kuusisto J,
Kraft P,
Kvaløy K,
Laitinen J,
Lantieri O,
Lanzani C,
Launer LJ,
Lecoeur C,
Lehtimäki T,
Lettre G,
Liu J,
Lokki ML,
Lorentzon M,
Luben RN,
Ludwig B,
Manunta P,
Marek D,
Marre M,
Martin NG,
McArdle WL,
McCarthy A,
McKnight B,
Meitinger T,
Melander O,
Meyre D,
Midthjell K,
Montgomery GW,
Morken MA,
Morris AP,
Mulic R,
Ngwa JS,
Nelis M,
Neville MJ,
Nyholt DR,
O'Donnell CJ,
O'Rahilly S,
Ong KK,
Oostra B,
Paré G,
Parker AN,
Perola M,
Pichler I,
Pietiläinen KH,
Platou CG,
Polasek O,
Pouta A,
Rafelt S,
Raitakari O,
Rayner NW,
Ridderstråle M,
Rief W,
Ruokonen A,
Robertson NR,
Rzehak P,
Salomaa V,
Sanders AR,
Sandhu MS,
Sanna S,
Saramies J,
Savolainen MJ,
Scherag S,
Schipf S,
Schreiber S,
Schunkert H,
Silander K,
Sinisalo J,
Siscovick DS,
Smit JH,
Soranzo N,
Sovio U,
Stephens J,
Surakka I,
Swift AJ,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teslovich TM,
Thompson JR,
Thomson B,
Tönjes A,
Tuomi T,
van Meurs JB,
van Ommen GJ,
Vatin V,
Viikari J,
Visvikis-Siest S,
Vitart V,
Vogel CI,
Voight BF,
Waite LL,
Wallaschofski H,
Walters GB,
Widen E,
Wiegand S,
Wild SH,
Willemsen G,
Witte DR,
Witteman JC,
Xu J,
Zhang Q,
Zgaga L,
Ziegler A,
Zitting P,
Beilby JP,
Farooqi IS,
Hebebrand J,
Huikuri HV,
James AL,
James AL,
Kähönen M,
Levinson DF,
Macciardi F,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Ridker PM,
Stumvoll M,
Beckmann JS,
Boeing H,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Chanock SJ,
Collins FS,
Cupples LA,
Smith GD,
Erdmann J,
Froguel P,
Grönberg H,
Gyllensten U,
Hall P,
Hansen T,
Harris TB,
Hattersley AT,
Hayes RB,
Heinrich J,
Hu FB,
Hveem K,
Illig T,
Jarvelin MR,
Kaprio J,
Karpe F,
Khaw KT,
Kiemeney LA,
Krude H,
Laakso M,
Lawlor DA,
Metspalu A,
Munroe PB,
Ouwehand WH,
Pedersen O,
Penninx BW,
Peters A,
Pramstaller PP,
Quertermous T,
Reinehr T,
Rissanen A,
Rudan I,
Samani NJ,
Schwarz PE,
Schwarz PE,
Shuldiner AR,
Spector TD,
Tuomilehto J,
Uda M,
Uitterlinden A,
Valle TT,
Wabitsch M,
Waeber G,
Wareham NJ,
Watkins H,
Wilson JF,
Wright AF,
Zillikens MC,
Chatterjee N,
McCarroll SA,
Purcell S,
Schadt EE,
Visscher PM,
Assimes TL,
Borecki IB,
Deloukas P,
Fox CS,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
Mohlke KL,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
van Duijn CM,
Wichmann HE,
Frayling TM,
Thorsteinsdottir U,
Abecasis GR,
Barroso I,
Boehnke M,
Stefansson K,
North KE,
McCarthy MI,
Hirschhorn JN,
Ingelsson E,
Loos RJ
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
페이지 11개
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Sawcer S,
Hellenthal G,
Pirinen M,
Spencer CC,
Patsopoulos NA,
Moutsianas L,
Dilthey A,
Su Z,
Freeman C,
Hunt SE,
Edkins S,
Gray E
외 230명 — 모두 보기
Booth DR,
Potter SC,
Goris A,
Band G,
Oturai AB,
Strange A,
Saarela J,
Bellenguez C,
Fontaine B,
Gillman M,
Hemmer B,
Gwilliam R,
Zipp F,
Jayakumar A,
Martin R,
Leslie S,
Hawkins S,
Giannoulatou E,
D'alfonso S,
Blackburn H,
Martinelli Boneschi F,
Liddle J,
Harbo HF,
Perez ML,
Spurkland A,
Waller MJ,
Mycko MP,
Ricketts M,
Comabella M,
Hammond N,
Kockum I,
McCann OT,
Ban M,
Whittaker P,
Kemppinen A,
Weston P,
Hawkins C,
Widaa S,
Zajicek J,
Dronov S,
Robertson N,
Bumpstead SJ,
Barcellos LF,
Ravindrarajah R,
Abraham R,
Alfredsson L,
Ardlie K,
Aubin C,
Baker A,
Baker K,
Baranzini SE,
Bergamaschi L,
Bergamaschi R,
Bernstein A,
Berthele A,
Boggild M,
Bradfield JP,
Brassat D,
Broadley SA,
Buck D,
Butzkueven H,
Capra R,
Carroll WM,
Cavalla P,
Celius EG,
Cepok S,
Chiavacci R,
Clerget-Darpoux F,
Clysters K,
Comi G,
Cossburn M,
Cournu-Rebeix I,
Cox MB,
Cozen W,
Cree BA,
Cross AH,
Cusi D,
Daly MJ,
Davis E,
de Bakker PI,
Debouverie M,
D'hooghe MB,
Dixon K,
Dobosi R,
Dubois B,
Ellinghaus D,
Elovaara I,
Esposito F,
Fontenille C,
Foote S,
Franke A,
Galimberti D,
Ghezzi A,
Glessner J,
Gomez R,
Gout O,
Graham C,
Grant SF,
Guerini FR,
Hakonarson H,
Hall P,
Hamsten A,
Hartung HP,
Heard RN,
Heath S,
Hobart J,
Hoshi M,
Infante-Duarte C,
Ingram G,
Ingram W,
Islam T,
Jagodic M,
Kabesch M,
Kermode AG,
Kilpatrick TJ,
Kim C,
Klopp N,
Koivisto K,
Larsson M,
Lathrop M,
Lechner-Scott JS,
Leone MA,
Leppä V,
Liljedahl U,
Bomfim IL,
Lincoln RR,
Link J,
Liu J,
Lorentzen AR,
Lupoli S,
Macciardi F,
Mack T,
Marriott M,
Martinelli V,
Mason D,
McCauley JL,
Mentch F,
Mero IL,
Mihalova T,
Montalban X,
Mottershead J,
Myhr KM,
Naldi P,
Ollier W,
Page A,
Palotie A,
Pelletier J,
Piccio L,
Pickersgill T,
Piehl F,
Pobywajlo S,
Quach HL,
Ramsay PP,
Reunanen M,
Reynolds R,
Rioux JD,
Rodegher M,
Roesner S,
Rubio JP,
Rückert IM,
Salvetti M,
Salvi E,
Santaniello A,
Schaefer CA,
Schreiber S,
Schulze C,
Scott RJ,
Sellebjerg F,
Selmaj KW,
Sexton D,
Shen L,
Simms-Acuna B,
Skidmore S,
Sleiman PM,
Smestad C,
Sørensen PS,
Søndergaard HB,
Stankovich J,
Strange RC,
Sulonen AM,
Sundqvist E,
Syvänen AC,
Taddeo F,
Taylor B,
Blackwell JM,
Tienari P,
Bramon E,
Tourbah A,
Brown MA,
Tronczynska E,
Casas JP,
Tubridy N,
Corvin A,
Vickery J,
Jankowski J,
Villoslada P,
Markus HS,
Wang K,
Mathew CG,
Wason J,
Palmer CN,
Wichmann HE,
Plomin R,
Willoughby E,
Rautanen A,
Winkelmann J,
Wittig M,
Trembath RC,
Yaouanq J,
Viswanathan AC,
Zhang H,
Wood NW,
Zuvich R,
Deloukas P,
Langford C,
Duncanson A,
Oksenberg JR,
Pericak-Vance MA,
Haines JL,
Olsson T,
Hillert J,
Ivinson AJ,
De Jager PL,
Peltonen L,
Stewart GJ,
Hafler DA,
Hauser SL,
McVean G,
Donnelly P,
Compston A
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium 2
Nature · 2011 · PMID 21833088 · open access
페이지 11개
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Paternoster L,
Standl M,
Waage J,
Baurecht H,
Hotze M,
Strachan DP,
Curtin JA,
Bønnelykke K,
Tian C,
Takahashi A,
Esparza-Gordillo J,
Alves AC
외 140명 — 모두 보기
Thyssen JP,
den Dekker HT,
Ferreira MA,
Altmaier E,
Sleiman PM,
Xiao FL,
Gonzalez JR,
Marenholz I,
Kalb B,
Yanes MP,
Xu CJ,
Carstensen L,
Groen-Blokhuis MM,
Venturini C,
Pennell CE,
Barton SJ,
Levin AM,
Curjuric I,
Bustamante M,
Kreiner-Møller E,
Lockett GA,
Bacelis J,
Bacelis J,
Bunyavanich S,
Myers RA,
Matanovic A,
Kumar A,
Tung JY,
Hirota T,
Kubo M,
McArdle WL,
Henderson AJ,
Kemp JP,
Zheng J,
Smith GD,
Rüschendorf F,
Bauerfeind A,
Lee-Kirsch MA,
Arnold A,
Homuth G,
Schmidt CO,
Mangold E,
Cichon S,
Keil T,
Rodríguez E,
Peters A,
Peters A,
Franke A,
Lieb W,
Novak N,
Fölster-Holst R,
Horikoshi M,
Pekkanen J,
Sebert S,
Husemoen LL,
Grarup N,
de Jongste JC,
Rivadeneira F,
Hofman A,
Jaddoe VW,
Pasmans SG,
Elbert NJ,
Uitterlinden AG,
Marks GB,
Thompson PJ,
Matheson MC,
Robertson CF,
Ried JS,
Li J,
Zuo XB,
Zheng XD,
Yin XY,
Sun LD,
McAleer MA,
O'Regan GM,
Fahy CM,
Campbell LE,
Macek M,
Kurek M,
Hu D,
Eng C,
Postma DS,
Feenstra B,
Geller F,
Hottenga JJ,
Middeldorp CM,
Hysi P,
Bataille V,
Spector T,
Tiesler CM,
Thiering E,
Pahukasahasram B,
Yang JJ,
Imboden M,
Huntsman S,
Vilor-Tejedor N,
Relton CL,
Myhre R,
Nystad W,
Custovic A,
Weiss ST,
Meyers DA,
Söderhäll C,
Melén E,
Ober C,
Raby BA,
Simpson A,
Jacobsson B,
Holloway JW,
Bisgaard H,
Sunyer J,
Hensch NMP,
Williams LK,
Godfrey KM,
Wang CA,
Boomsma DI,
Melbye M,
Koppelman GH,
Jarvis D,
McLean WI,
Irvine AD,
Zhang XJ,
Hakonarson H,
Gieger C,
Burchard EG,
Martin NG,
Duijts L,
Linneberg A,
Jarvelin MR,
Noethen MM,
Lau S,
Hübner N,
Lee YA,
Tamari M,
Hinds DA,
Glass D,
Brown SJ,
Heinrich J,
Evans DM,
Weidinger S
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
페이지 11개
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
Sim X,
Barnes DR,
Witkowska K,
Staley JR,
Tragante V
외 198명 — 모두 보기
Tukiainen T,
Yaghootkar H,
Masca N,
Freitag DF,
Ferreira T,
Giannakopoulou O,
Tinker A,
Harakalova M,
Mihailov E,
Liu C,
Kraja AT,
Fallgaard Nielsen S,
Rasheed A,
Samuel M,
Zhao W,
Bonnycastle LL,
Jackson AU,
Narisu N,
Swift AJ,
Southam L,
Marten J,
Huyghe JR,
Stančáková A,
Fava C,
Ohlsson T,
Matchan A,
Stirrups KE,
Bork-Jensen J,
Gjesing AP,
Kontto J,
Perola M,
Shaw-Hawkins S,
Havulinna AS,
Zhang H,
Donnelly LA,
Groves CJ,
Rayner NW,
Neville MJ,
Robertson NR,
Yiorkas AM,
Herzig KH,
Kajantie E,
Zhang W,
Willems SM,
Lannfelt L,
Malerba G,
Soranzo N,
Trabetti E,
Verweij N,
Evangelou E,
Moayyeri A,
Vergnaud AC,
Nelson CP,
Poveda A,
Varga TV,
Caslake M,
de Craen AJ,
Trompet S,
Luan J,
Scott RA,
Harris SE,
Liewald DC,
Marioni R,
Menni C,
Farmaki AE,
Hallmans G,
Renström F,
Huffman JE,
Hassinen M,
Burgess S,
Vasan RS,
Felix JF,
Uria-Nickelsen M,
Malarstig A,
Reily DF,
Hoek M,
Vogt T,
Lin H,
Lieb W,
Traylor M,
Markus HF,
Highland HM,
Justice AE,
Marouli E,
Lindström J,
Uusitupa M,
Komulainen P,
Lakka TA,
Rauramaa R,
Polasek O,
Rudan I,
Rolandsson O,
Franks PW,
Dedoussis G,
Spector TD,
Jousilahti P,
Männistö S,
Deary IJ,
Starr JM,
Langenberg C,
Wareham NJ,
Brown MJ,
Dominiczak AF,
Connell JM,
Jukema JW,
Sattar N,
Ford I,
Packard CJ,
Esko T,
Mägi R,
Metspalu A,
de Boer RA,
van der Meer P,
van der Harst P,
Gambaro G,
Ingelsson E,
Lind L,
de Bakker PI,
Numans ME,
Brandslund I,
Christensen C,
Petersen ER,
Korpi-Hyövälti E,
Oksa H,
Chambers JC,
Kooner JS,
Blakemore AI,
Franks S,
Jarvelin MR,
Husemoen LL,
Linneberg A,
Skaaby T,
Thuesen B,
Karpe F,
Tuomilehto J,
Doney AS,
Morris AD,
Palmer CN,
Holmen OL,
Hveem K,
Willer CJ,
Tuomi T,
Groop L,
Käräjämäki A,
Palotie A,
Ripatti S,
Salomaa V,
Alam DS,
Shafi Majumder AA,
Di Angelantonio E,
Chowdhury R,
McCarthy MI,
Poulter N,
Stanton AV,
Sever P,
Amouyel P,
Arveiler D,
Blankenberg S,
Ferrières J,
Kee F,
Kuulasmaa K,
Müller-Nurasyid M,
Veronesi G,
Virtamo J,
Deloukas P,
Elliott P,
Zeggini E,
Kathiresan S,
Melander O,
Kuusisto J,
Laakso M,
Padmanabhan S,
Porteous D,
Hayward C,
Scotland G,
Collins FS,
Mohlke KL,
Hansen T,
Pedersen O,
Boehnke M,
Stringham HM,
Frossard P,
Newton-Cheh C,
Tobin MD,
Nordestgaard BG,
Caulfield MJ,
Mahajan A,
Morris AP,
Tomaszewski M,
Samani NJ,
Saleheen D,
Asselbergs FW,
Lindgren CM,
Danesh J,
Wain LV,
Butterworth AS,
Howson JM,
Munroe PB
CHARGE-Heart Failure Consortium · EchoGen Consortium 외 컨소시엄 12곳
Nature genetics · 2016 · PMID 27618447 · open access
페이지 11개
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium
Ng MCY,
Graff M,
Lu Y,
Justice AE,
Mudgal P,
Liu CT,
Young K,
Yanek LR,
Feitosa MF,
Wojczynski MK,
Rand K,
Brody JA
외 101명 — 모두 보기
Cade BE,
Dimitrov L,
Duan Q,
Guo X,
Lange LA,
Nalls MA,
Okut H,
Tajuddin SM,
Tayo BO,
Vedantam S,
Bradfield JP,
Chen G,
Chen WM,
Chesi A,
Irvin MR,
Padhukasahasram B,
Smith JA,
Zheng W,
Zheng W,
Allison MA,
Ambrosone CB,
Bandera EV,
Bartz TM,
Berndt SI,
Bernstein L,
Blot WJ,
Bottinger EP,
Carpten J,
Chanock SJ,
Chen YI,
Conti DV,
Cooper RS,
Fornage M,
Freedman BI,
Garcia M,
Goodman PJ,
Hsu YH,
Hu J,
Huff CD,
Ingles SA,
John EM,
Kittles R,
Klein E,
Li J,
McKnight B,
Nayak U,
Nemesure B,
Ogunniyi A,
Olshan A,
Press MF,
Rohde R,
Rybicki BA,
Salako B,
Sanderson M,
Shao Y,
Siscovick DS,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Vaidya D,
Witte JS,
Yao J,
Zhu X,
Ziegler RG,
Zonderman AB,
Adeyemo A,
Ambs S,
Cushman M,
Faul JD,
Hakonarson H,
Levin AM,
Nathanson KL,
Ware EB,
Weir DR,
Zhao W,
Zhi D,
Arnett DK,
Grant SFA,
Kardia SLR,
Oloapde OI,
Rao DC,
Rotimi CN,
Sale MM,
Williams LK,
Zemel BS,
Becker DM,
Borecki IB,
Evans MK,
Harris TB,
Hirschhorn JN,
Li Y,
Patel SR,
Psaty BM,
Rotter JI,
Wilson JG,
Bowden DW,
Cupples LA,
Haiman CA,
Loos RJF,
North KE
Bone Mineral Density in Childhood Study (BMDCS) Group
PLoS genetics · 2017 · PMID 28430825 · open access
페이지 11개
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
Zhao W,
Rasheed A,
Tikkanen E,
Lee JJ,
Butterworth AS,
Howson JMM,
Assimes TL,
Chowdhury R,
Orho-Melander M,
Damrauer S,
Small A,
Asma S
외 78명 — 모두 보기
Imamura M,
Yamauch T,
Chambers JC,
Chen P,
Sapkota BR,
Shah N,
Jabeen S,
Surendran P,
Lu Y,
Zhang W,
Imran A,
Abbas S,
Majeed F,
Trindade K,
Qamar N,
Mallick NH,
Yaqoob Z,
Saghir T,
Rizvi SNH,
Memon A,
Rasheed SZ,
Memon FU,
Mehmood K,
Ahmed N,
Qureshi IH,
Tanveer-Us-Salam,
Iqbal W,
Malik U,
Mehra N,
Kuo JZ,
Sheu WH,
Guo X,
Hsiung CA,
Juang JJ,
Taylor KD,
Hung YJ,
Lee WJ,
Quertermous T,
Lee IT,
Hsu CC,
Bottinger EP,
Ralhan S,
Teo YY,
Wang TD,
Alam DS,
Di Angelantonio E,
Epstein S,
Nielsen SF,
Nordestgaard BG,
Tybjaerg-Hansen A,
Young R,
Benn M,
Frikke-Schmidt R,
Kamstrup PR,
Jukema JW,
Sattar N,
Smit R,
Chung RH,
Liang KW,
Anand S,
Sanghera DK,
Ripatti S,
Loos RJF,
Kooner JS,
Tai ES,
Rotter JI,
Chen YI,
Frossard P,
Maeda S,
Kadowaki T,
Reilly M,
Pare G,
Melander O,
Salomaa V,
Rader DJ,
Danesh J,
Voight BF,
Saleheen D
CHD Exome+ Consortium · EPIC-CVD Consortium 외 컨소시엄 2곳
Nature genetics · 2017 · PMID 28869590 · open access
페이지 11개
Exome-wide association study of plasma lipids in >300,000 individuals
Liu DJ,
Peloso GM,
Yu H,
Butterworth AS,
Wang X,
Mahajan A,
Saleheen D,
Emdin C,
Alam D,
Alves AC,
Amouyel P,
Di Angelantonio E
외 215명 — 모두 보기
Arveiler D,
Assimes TL,
Auer PL,
Baber U,
Ballantyne CM,
Bang LE,
Benn M,
Bis JC,
Boehnke M,
Boerwinkle E,
Bork-Jensen J,
Bottinger EP,
Brandslund I,
Brown M,
Busonero F,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YE,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Connell JM,
Cucca F,
Cupples LA,
Damrauer SM,
Davies G,
Deary IJ,
Dedoussis G,
Denny JC,
Dominiczak A,
Dubé MP,
Ebeling T,
Eiriksdottir G,
Esko T,
Farmaki AE,
Feitosa MF,
Ferrario M,
Ferrieres J,
Ford I,
Fornage M,
Franks PW,
Frayling TM,
Frikke-Schmidt R,
Fritsche LG,
Frossard P,
Fuster V,
Ganesh SK,
Gao W,
Garcia ME,
Gieger C,
Giulianini F,
Goodarzi MO,
Grallert H,
Grarup N,
Groop L,
Grove ML,
Gudnason V,
Hansen T,
Harris TB,
Hayward C,
Hirschhorn JN,
Holmen OL,
Huffman J,
Huo Y,
Hveem K,
Jabeen S,
Jackson AU,
Jakobsdottir J,
Jarvelin MR,
Jensen GB,
Jørgensen ME,
Jukema JW,
Justesen JM,
Kamstrup PR,
Kanoni S,
Karpe F,
Kee F,
Khera AV,
Klarin D,
Koistinen HA,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka T,
Langenberg C,
Langsted A,
Launer LJ,
Lauritzen T,
Liewald DCM,
Lin LA,
Linneberg A,
Loos RJF,
Lu Y,
Lu X,
Mägi R,
Malarstig A,
Manichaikul A,
Manning AK,
Mäntyselkä P,
Marouli E,
Masca NGD,
Maschio A,
Meigs JB,
Melander O,
Metspalu A,
Morris AP,
Morrison AC,
Mulas A,
Müller-Nurasyid M,
Munroe PB,
Neville MJ,
Nielsen JB,
Nielsen SF,
Nordestgaard BG,
Ordovas JM,
Mehran R,
O'Donnell CJ,
Orho-Melander M,
Molony CM,
Muntendam P,
Padmanabhan S,
Palmer CNA,
Pasko D,
Patel AP,
Pedersen O,
Perola M,
Peters A,
Pisinger C,
Pistis G,
Polasek O,
Poulter N,
Psaty BM,
Rader DJ,
Rasheed A,
Rauramaa R,
Reilly DF,
Reiner AP,
Renström F,
Rich SS,
Ridker PM,
Rioux JD,
Robertson NR,
Roden DM,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sanna S,
Sattar N,
Schmidt EM,
Scott RA,
Sever P,
Sevilla RS,
Shaffer CM,
Sim X,
Sivapalaratnam S,
Small KS,
Smith AV,
Smith BH,
Somayajula S,
Southam L,
Spector TD,
Speliotes EK,
Starr JM,
Stirrups KE,
Stitziel N,
Strauch K,
Stringham HM,
Surendran P,
Tada H,
Tall AR,
Tang H,
Tardif JC,
Taylor KD,
Trompet S,
Tsao PS,
Tuomilehto J,
Tybjaerg-Hansen A,
van Zuydam NR,
Varbo A,
Varga TV,
Virtamo J,
Waldenberger M,
Wang N,
Wareham NJ,
Warren HR,
Weeke PE,
Weinstock J,
Wessel J,
Wilson JG,
Wilson PWF,
Xu M,
Yaghootkar H,
Young R,
Zeggini E,
Zhang H,
Zheng NS,
Zhang W,
Zhang Y,
Zhou W,
Zhou Y,
Zoledziewska M,
Howson JMM,
Danesh J,
McCarthy MI,
Cowan CA,
Abecasis G,
Deloukas P,
Musunuru K,
Willer CJ,
Kathiresan S
Charge Diabetes Working Group · EPIC-InterAct Consortium 외 컨소시엄 3곳
Nature genetics · 2017 · PMID 29083408 · open access
페이지 11개
An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs
Cordell HJ,
Fryett JJ,
Ueno K,
Darlay R,
Aiba Y,
Hitomi Y,
Kawashima M,
Nishida N,
Khor SS,
Gervais O,
Kawai Y,
Nagasaki M
외 31명 — 모두 보기
Tokunaga K,
Tang R,
Shi Y,
Li Z,
Juran BD,
Atkinson EJ,
Gerussi A,
Carbone M,
Asselta R,
Cheung A,
de Andrade M,
Baras A,
Horowitz J,
Ferreira MAR,
Sun D,
Jones DE,
Flack S,
Spicer A,
Mulcahy VL,
Byan J,
Han Y,
Sandford RN,
Lazaridis KN,
Amos CI,
Hirschfield GM,
Seldin MF,
Invernizzi P,
Siminovitch KA,
Ma X,
Nakamura M,
Mells GF
PBC Consortia · Canadian PBC Consortium 외 컨소시엄 5곳
Journal of hepatology · 2021 · PMID 34033851 · open access
페이지 11개
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Ripke S,
O'Dushlaine C,
Chambert K,
Moran JL,
Kähler AK,
Akterin S,
Bergen SE,
Collins AL,
Crowley JJ,
Fromer M,
Kim Y,
Lee SH
외 176명 — 모두 보기
Lee SH,
Magnusson PK,
Sanchez N,
Stahl EA,
Williams S,
Wray NR,
Xia K,
Bettella F,
Borglum AD,
Bulik-Sullivan BK,
Cormican P,
Craddock N,
de Leeuw C,
Durmishi N,
Gill M,
Golimbet V,
Hamshere ML,
Holmans P,
Hougaard DM,
Kendler KS,
Lin K,
Morris DW,
Mors O,
Mortensen PB,
Neale BM,
O'Neill FA,
Owen MJ,
Milovancevic MP,
Posthuma D,
Powell J,
Richards AL,
Riley BP,
Ruderfer D,
Rujescu D,
Sigurdsson E,
Silagadze T,
Smit AB,
Stefansson H,
Steinberg S,
Suvisaari J,
Tosato S,
Verhage M,
Walters JT,
Levinson DF,
Gejman PV,
Kendler KS,
Laurent C,
Mowry BJ,
O'Donovan MC,
Owen MJ,
Pulver AE,
Riley BP,
Schwab SG,
Wildenauer DB,
Dudbridge F,
Holmans P,
Shi J,
Albus M,
Alexander M,
Campion D,
Cohen D,
Dikeos D,
Duan J,
Eichhammer P,
Godard S,
Hansen M,
Lerer FB,
Liang KY,
Maier W,
Mallet J,
Nertney DA,
Nestadt G,
Norton N,
O'Neill FA,
Papadimitriou GN,
Ribble R,
Sanders AR,
Silverman JM,
Walsh D,
Williams NM,
Wormley B,
Arranz MJ,
Bakker S,
Bender S,
Bramon E,
Collier D,
Crespo-Facorro B,
Hall J,
Iyegbe C,
Jablensky A,
Kahn RS,
Kalaydjieva L,
Lawrie S,
Lewis CM,
Lin K,
Linszen DH,
Mata I,
McIntosh A,
Murray RM,
Ophoff RA,
Powell J,
Rujescu D,
Van Os J,
Walshe M,
Weisbrod M,
Wiersma D,
Donnelly P,
Barroso I,
Blackwell JM,
Bramon E,
Brown MA,
Casas JP,
Corvin AP,
Deloukas P,
Duncanson A,
Jankowski J,
Markus HS,
Mathew CG,
Palmer CN,
Plomin R,
Rautanen A,
Sawcer SJ,
Trembath RC,
Viswanathan AC,
Wood NW,
Spencer CC,
Band G,
Bellenguez C,
Freeman C,
Hellenthal G,
Giannoulatou E,
Pirinen M,
Pearson RD,
Strange A,
Su Z,
Vukcevic D,
Donnelly P,
Langford C,
Hunt SE,
Edkins S,
Gwilliam R,
Blackburn H,
Bumpstead SJ,
Dronov S,
Gillman M,
Gray E,
Hammond N,
Jayakumar A,
McCann OT,
Liddle J,
Potter SC,
Ravindrarajah R,
Ricketts M,
Tashakkori-Ghanbaria A,
Waller MJ,
Weston P,
Widaa S,
Whittaker P,
Barroso I,
Deloukas P,
Mathew CG,
Blackwell JM,
Brown MA,
Corvin AP,
McCarthy MI,
Spencer CC,
Bramon E,
Corvin AP,
O'Donovan MC,
Stefansson K,
Scolnick E,
Purcell S,
McCarroll SA,
Sklar P,
Hultman CM,
Sullivan PF
Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium 외 컨소시엄 1곳
Nature genetics · 2013 · PMID 23974872 · open access
페이지 10개
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
Al Olama AA,
Kote-Jarai Z,
Berndt SI,
Conti DV,
Schumacher F,
Han Y,
Benlloch S,
Hazelett DJ,
Wang Z,
Saunders E,
Leongamornlert D,
Lindstrom S
외 152명 — 모두 보기
Jugurnauth-Little S,
Dadaev T,
Tymrakiewicz M,
Stram DO,
Rand K,
Wan P,
Stram A,
Sheng X,
Pooler LC,
Park K,
Xia L,
Tyrer J,
Kolonel LN,
Le Marchand L,
Hoover RN,
Machiela MJ,
Yeager M,
Burdette L,
Chung CC,
Hutchinson A,
Yu K,
Goh C,
Ahmed M,
Govindasami K,
Guy M,
Tammela TL,
Auvinen A,
Wahlfors T,
Schleutker J,
Visakorpi T,
Leinonen KA,
Xu J,
Aly M,
Donovan J,
Travis RC,
Key TJ,
Siddiq A,
Canzian F,
Khaw KT,
Takahashi A,
Kubo M,
Pharoah P,
Pashayan N,
Weischer M,
Nordestgaard BG,
Nielsen SF,
Klarskov P,
Røder MA,
Iversen P,
Thibodeau SN,
McDonnell SK,
Schaid DJ,
Stanford JL,
Kolb S,
Holt S,
Knudsen B,
Coll AH,
Gapstur SM,
Diver WR,
Stevens VL,
Maier C,
Luedeke M,
Herkommer K,
Rinckleb AE,
Strom SS,
Pettaway C,
Yeboah ED,
Tettey Y,
Biritwum RB,
Adjei AA,
Tay E,
Truelove A,
Niwa S,
Chokkalingam AP,
Cannon-Albright L,
Cybulski C,
Wokołorczyk D,
Kluźniak W,
Park J,
Sellers T,
Lin HY,
Isaacs WB,
Partin AW,
Brenner H,
Dieffenbach AK,
Stegmaier C,
Chen C,
Giovannucci EL,
Ma J,
Stampfer M,
Penney KL,
Mucci L,
John EM,
Ingles SA,
Kittles RA,
Murphy AB,
Pandha H,
Michael A,
Kierzek AM,
Blot W,
Signorello LB,
Zheng W,
Albanes D,
Virtamo J,
Weinstein S,
Nemesure B,
Carpten J,
Leske C,
Wu SY,
Hennis A,
Kibel AS,
Rybicki BA,
Neslund-Dudas C,
Hsing AW,
Chu L,
Goodman PJ,
Klein EA,
Zheng SL,
Batra J,
Clements J,
Spurdle A,
Teixeira MR,
Paulo P,
Maia S,
Slavov C,
Kaneva R,
Mitev V,
Witte JS,
Casey G,
Gillanders EM,
Seminara D,
Riboli E,
Hamdy FC,
Coetzee GA,
Li Q,
Freedman ML,
Hunter DJ,
Muir K,
Gronberg H,
Neal DE,
Southey M,
Giles GG,
Severi G,
Cook MB,
Nakagawa H,
Wiklund F,
Kraft P,
Chanock SJ,
Henderson BE,
Easton DF,
Eeles RA,
Haiman CA
Breast and Prostate Cancer Cohort Consortium (BPC3) · PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium 외 컨소시엄 2곳
Nature genetics · 2014 · PMID 25217961 · open access
페이지 10개
Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk
Patel YM,
Park SL,
Han Y,
Wilkens LR,
Bickeböller H,
Rosenberger A,
Caporaso N,
Landi MT,
Brüske I,
Risch A,
Wei Y,
Christiani DC
외 9명 — 모두 보기
Cancer research · 2016 · PMID 27488534
페이지 10개
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
Melin BS,
Barnholtz-Sloan JS,
Wrensch MR,
Johansen C,
Il'yasova D,
Kinnersley B,
Ostrom QT,
Labreche K,
Chen Y,
Armstrong G,
Liu Y,
Eckel-Passow JE
외 51명 — 모두 보기
Decker PA,
Labussière M,
Idbaih A,
Hoang-Xuan K,
Di Stefano AL,
Mokhtari K,
Delattre JY,
Broderick P,
Galan P,
Gousias K,
Schramm J,
Schoemaker MJ,
Fleming SJ,
Herms S,
Heilmann S,
Nöthen MM,
Wichmann HE,
Schreiber S,
Swerdlow A,
Lathrop M,
Simon M,
Sanson M,
Andersson U,
Rajaraman P,
Chanock S,
Linet M,
Wang Z,
Yeager M,
Wiencke JK,
Hansen H,
McCoy L,
Rice T,
Kosel ML,
Sicotte H,
Amos CI,
Bernstein JL,
Davis F,
Lachance D,
Lau C,
Merrell RT,
Shildkraut J,
Ali-Osman F,
Sadetzki S,
Scheurer M,
Shete S,
Lai RK,
Claus EB,
Olson SH,
Jenkins RB,
Houlston RS,
Bondy ML
GliomaScan Consortium
Nature genetics · 2017 · PMID 28346443
페이지 10개
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Wray NR,
Ripke S,
Mattheisen M,
Trzaskowski M,
Byrne EM,
Abdellaoui A,
Adams MJ,
Agerbo E,
Air TM,
Andlauer TMF,
Bacanu SA,
Bækvad-Hansen M
외 205명 — 모두 보기
Beekman AFT,
Bigdeli TB,
Binder EB,
Blackwood DRH,
Bryois J,
Buttenschøn HN,
Bybjerg-Grauholm J,
Cai N,
Castelao E,
Christensen JH,
Clarke TK,
Coleman JIR,
Colodro-Conde L,
Couvy-Duchesne B,
Craddock N,
Crawford GE,
Crowley CA,
Dashti HS,
Davies G,
Deary IJ,
Degenhardt F,
Derks EM,
Direk N,
Dolan CV,
Dunn EC,
Eley TC,
Eriksson N,
Escott-Price V,
Kiadeh FHF,
Finucane HK,
Forstner AJ,
Frank J,
Gaspar HA,
Gill M,
Giusti-Rodríguez P,
Goes FS,
Gordon SD,
Grove J,
Hall LS,
Hannon E,
Hansen CS,
Hansen TF,
Herms S,
Hickie IB,
Hoffmann P,
Homuth G,
Horn C,
Hottenga JJ,
Hougaard DM,
Hu M,
Hyde CL,
Ising M,
Jansen R,
Jansen R,
Jin F,
Jorgenson E,
Knowles JA,
Kohane IS,
Kraft J,
Kretzschmar WW,
Krogh J,
Kutalik Z,
Lane JM,
Li Y,
Li Y,
Lind PA,
Liu X,
Lu L,
MacIntyre DJ,
MacKinnon DF,
Maier RM,
Maier W,
Marchini J,
Mbarek H,
McGrath P,
McGuffin P,
Medland SE,
Mehta D,
Middeldorp CM,
Mihailov E,
Milaneschi Y,
Milani L,
Mill J,
Mondimore FM,
Montgomery GW,
Mostafavi S,
Mullins N,
Nauck M,
Ng B,
Nivard MG,
Nyholt DR,
O'Reilly PF,
Oskarsson H,
Owen MJ,
Painter JN,
Pedersen CB,
Pedersen MG,
Peterson RE,
Pettersson E,
Peyrot WJ,
Pistis G,
Posthuma D,
Purcell SM,
Quiroz JA,
Qvist P,
Rice JP,
Riley BP,
Rivera M,
Saeed Mirza S,
Saxena R,
Schoevers R,
Schulte EC,
Shen L,
Shi J,
Shyn SI,
Sigurdsson E,
Sinnamon GBC,
Smit JH,
Smith DJ,
Stefansson H,
Steinberg S,
Stockmeier CA,
Streit F,
Strohmaier J,
Tansey KE,
Teismann H,
Teumer A,
Thompson W,
Thomson PA,
Thorgeirsson TE,
Tian C,
Traylor M,
Treutlein J,
Trubetskoy V,
Uitterlinden AG,
Umbricht D,
Van der Auwera S,
van Hemert AM,
Viktorin A,
Visscher PM,
Wang Y,
Webb BT,
Weinsheimer SM,
Wellmann J,
Willemsen G,
Witt SH,
Wu Y,
Xi HS,
Yang J,
Zhang F,
Arolt V,
Baune BT,
Berger K,
Boomsma DI,
Cichon S,
Dannlowski U,
de Geus ECJ,
DePaulo JR,
Domenici E,
Domschke K,
Esko T,
Grabe HJ,
Hamilton SP,
Hayward C,
Heath AC,
Hinds DA,
Kendler KS,
Kloiber S,
Lewis G,
Li QS,
Lucae S,
Madden PFA,
Magnusson PK,
Martin NG,
McIntosh AM,
Metspalu A,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Paciga SA,
Pedersen NL,
Penninx BWJH,
Perlis RH,
Porteous DJ,
Potash JB,
Preisig M,
Rietschel M,
Schaefer C,
Schulze TG,
Smoller JW,
Stefansson K,
Tiemeier H,
Uher R,
Völzke H,
Weissman MM,
Werge T,
Winslow AR,
Lewis CM,
Levinson DF,
Breen G,
Børglum AD,
Sullivan PF
eQTLGen · 23andMe 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29700475 · open access
페이지 10개
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
Bao EL,
Nandakumar SK,
Liao X,
Bick AG,
Karjalainen J,
Tabaka M,
Gan OI,
Havulinna AS,
Kiiskinen TTJ,
Lareau CA,
de Lapuente Portilla AL,
Li B
외 23명 — 모두 보기
Emdin C,
Codd V,
Nelson CP,
Walker CJ,
Churchhouse C,
de la Chapelle A,
Klein DE,
Nilsson B,
Wilson PWF,
Cho K,
Pyarajan S,
Gaziano JM,
Samani NJ,
Regev A,
Palotie A,
Neale BM,
Dick JE,
Natarajan P,
O'Donnell CJ,
Daly MJ,
Milyavsky M,
Kathiresan S,
Sankaran VG
FinnGen · 23andMe Research Team
Nature · 2020 · PMID 33057200 · open access
페이지 10개
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.