연구자에게
내 논문이 여기 있나요?
논문 2,681편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
Sulem P에 대해
73건, 그중 20건 표시.
Seventy-five genetic loci influencing the human red blood cell
van der Harst P,
Zhang W,
Mateo Leach I,
Rendon A,
Verweij N,
Sehmi J,
Paul DS,
Elling U,
Allayee H,
Li X,
Radhakrishnan A,
Tan ST
외 183명 — 모두 보기
Voss K,
Weichenberger CX,
Albers CA,
Al-Hussani A,
Asselbergs FW,
Ciullo M,
Danjou F,
Dina C,
Esko T,
Evans DM,
Franke L,
Gögele M,
Hartiala J,
Hersch M,
Holm H,
Hottenga JJ,
Kanoni S,
Kleber ME,
Lagou V,
Langenberg C,
Lopez LM,
Lyytikäinen LP,
Melander O,
Murgia F,
Nolte IM,
O'Reilly PF,
Padmanabhan S,
Parsa A,
Pirastu N,
Porcu E,
Portas L,
Prokopenko I,
Ried JS,
Shin SY,
Tang CS,
Teumer A,
Traglia M,
Ulivi S,
Westra HJ,
Yang J,
Zhao JH,
Anni F,
Abdellaoui A,
Attwood A,
Balkau B,
Bandinelli S,
Bastardot F,
Benyamin B,
Boehm BO,
Cookson WO,
Das D,
de Bakker PI,
de Boer RA,
de Geus EJ,
de Moor MH,
Dimitriou M,
Domingues FS,
Döring A,
Engström G,
Eyjolfsson GI,
Ferrucci L,
Fischer K,
Galanello R,
Garner SF,
Genser B,
Gibson QD,
Girotto G,
Gudbjartsson DF,
Harris SE,
Hartikainen AL,
Hastie CE,
Hedblad B,
Illig T,
Jolley J,
Kähönen M,
Kema IP,
Kemp JP,
Liang L,
Lloyd-Jones H,
Loos RJ,
Meacham S,
Medland SE,
Meisinger C,
Memari Y,
Mihailov E,
Miller K,
Moffatt MF,
Nauck M,
Novatchkova M,
Nutile T,
Olafsson I,
Onundarson PT,
Parracciani D,
Penninx BW,
Perseu L,
Piga A,
Pistis G,
Pouta A,
Puc U,
Raitakari O,
Ring SM,
Robino A,
Ruggiero D,
Ruokonen A,
Saint-Pierre A,
Sala C,
Salumets A,
Sambrook J,
Schepers H,
Schmidt CO,
Silljé HH,
Sladek R,
Smit JH,
Starr JM,
Stephens J,
Sulem P,
Tanaka T,
Thorsteinsdottir U,
Tragante V,
van Gilst WH,
van Pelt LJ,
van Veldhuisen DJ,
Völker U,
Whitfield JB,
Willemsen G,
Winkelmann BR,
Wirnsberger G,
Algra A,
Cucca F,
d'Adamo AP,
Danesh J,
Deary IJ,
Dominiczak AF,
Elliott P,
Fortina P,
Froguel P,
Gasparini P,
Greinacher A,
Hazen SL,
Jarvelin MR,
Khaw KT,
Lehtimäki T,
Maerz W,
Martin NG,
Metspalu A,
Mitchell BD,
Montgomery GW,
Moore C,
Navis G,
Pirastu M,
Pramstaller PP,
Ramirez-Solis R,
Schadt E,
Scott J,
Shuldiner AR,
Smith GD,
Smith JG,
Snieder H,
Sorice R,
Spector TD,
Stefansson K,
Stumvoll M,
Tang WH,
Toniolo D,
Tönjes A,
Visscher PM,
Vollenweider P,
Wareham NJ,
Wolffenbuttel BH,
Boomsma DI,
Beckmann JS,
Dedoussis GV,
Deloukas P,
Ferreira MA,
Sanna S,
Uda M,
Hicks AA,
Penninger JM,
Gieger C,
Kooner JS,
Ouwehand WH,
Soranzo N,
Chambers JC
Nature · 2012 · PMID 23222517
페이지 12개+
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Perry JR,
Day F,
Elks CE,
Sulem P,
Thompson DJ,
Ferreira T,
He C,
Chasman DI,
Esko T,
Thorleifsson G,
Albrecht E,
Ang WQ
외 186명 — 모두 보기
Corre T,
Cousminer DL,
Feenstra B,
Franceschini N,
Ganna A,
Johnson AD,
Kjellqvist S,
Lunetta KL,
McMahon G,
Nolte IM,
Paternoster L,
Porcu E,
Smith AV,
Stolk L,
Teumer A,
Tšernikova N,
Tikkanen E,
Ulivi S,
Wagner EK,
Amin N,
Bierut LJ,
Byrne EM,
Hottenga JJ,
Koller DL,
Mangino M,
Pers TH,
Yerges-Armstrong LM,
Zhao JH,
Andrulis IL,
Anton-Culver H,
Atsma F,
Bandinelli S,
Beckmann MW,
Benitez J,
Blomqvist C,
Bojesen SE,
Bolla MK,
Bonanni B,
Brauch H,
Brenner H,
Buring JE,
Chang-Claude J,
Chanock S,
Chen J,
Chenevix-Trench G,
Collée JM,
Couch FJ,
Couper D,
Coveillo AD,
Cox A,
Czene K,
D'adamo AP,
Smith GD,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dieffenbach AK,
Dunning AM,
Eiriksdottir G,
Eriksson JG,
Fasching PA,
Ferrucci L,
Flesch-Janys D,
Flyger H,
Foroud T,
Franke L,
Garcia ME,
García-Closas M,
Geller F,
de Geus EE,
Giles GG,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Guo S,
Hall P,
Hamann U,
Haring R,
Hartman CA,
Heath AC,
Hofman A,
Hooning MJ,
Hopper JL,
Hu FB,
Hunter DJ,
Karasik D,
Kiel DP,
Knight JA,
Kosma VM,
Kutalik Z,
Lai S,
Lambrechts D,
Lindblom A,
Mägi R,
Magnusson PK,
Mannermaa A,
Martin NG,
Masson G,
McArdle PF,
McArdle WL,
Melbye M,
Michailidou K,
Mihailov E,
Milani L,
Milne RL,
Nevanlinna H,
Neven P,
Nohr EA,
Oldehinkel AJ,
Oostra BA,
Palotie A,
Peacock M,
Pedersen NL,
Peterlongo P,
Peto J,
Pharoah PD,
Postma DS,
Pouta A,
Pylkäs K,
Radice P,
Ring S,
Rivadeneira F,
Robino A,
Rose LM,
Rudolph A,
Salomaa V,
Sanna S,
Schlessinger D,
Schmidt MK,
Southey MC,
Sovio U,
Stampfer MJ,
Stöckl D,
Storniolo AM,
Timpson NJ,
Tyrer J,
Visser JA,
Vollenweider P,
Völzke H,
Waeber G,
Waldenberger M,
Wallaschofski H,
Wang Q,
Willemsen G,
Winqvist R,
Wolffenbuttel BH,
Wright MJ,
Boomsma DI,
Econs MJ,
Khaw KT,
Loos RJ,
McCarthy MI,
Montgomery GW,
Rice JP,
Streeten EA,
Thorsteinsdottir U,
van Duijn CM,
Alizadeh BZ,
Bergmann S,
Boerwinkle E,
Boyd HA,
Crisponi L,
Gasparini P,
Gieger C,
Harris TB,
Ingelsson E,
Järvelin MR,
Kraft P,
Lawlor D,
Metspalu A,
Pennell CE,
Ridker PM,
Snieder H,
Sørensen TI,
Spector TD,
Strachan DP,
Uitterlinden AG,
Wareham NJ,
Widen E,
Zygmunt M,
Murray A,
Easton DF,
Stefansson K,
Murabito JM,
Ong KK
Australian Ovarian Cancer Study · GENICA Network 외 컨소시엄 4곳
Nature · 2014 · PMID 25231870 · open access
페이지 12개+
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Day FR,
Ruth KS,
Thompson DJ,
Lunetta KL,
Pervjakova N,
Chasman DI,
Stolk L,
Finucane HK,
Sulem P,
Bulik-Sullivan B,
Esko T,
Johnson AD
외 230명 — 모두 보기
Elks CE,
Franceschini N,
He C,
Altmaier E,
Brody JA,
Franke LL,
Huffman JE,
Keller MF,
McArdle PF,
Nutile T,
Porcu E,
Robino A,
Rose LM,
Schick UM,
Smith JA,
Teumer A,
Traglia M,
Vuckovic D,
Yao J,
Zhao W,
Albrecht E,
Amin N,
Corre T,
Hottenga JJ,
Mangino M,
Smith AV,
Tanaka T,
Abecasis G,
Andrulis IL,
Anton-Culver H,
Antoniou AC,
Arndt V,
Arnold AM,
Barbieri C,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bernstein L,
Bielinski SJ,
Blomqvist C,
Boerwinkle E,
Bogdanova NV,
Bojesen SE,
Bolla MK,
Borresen-Dale AL,
Boutin TS,
Brauch H,
Brenner H,
Brüning T,
Burwinkel B,
Campbell A,
Campbell H,
Chanock SJ,
Chapman JR,
Chen YI,
Chenevix-Trench G,
Couch FJ,
Coviello AD,
Cox A,
Czene K,
Darabi H,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dörk T,
Dos-Santos-Silva I,
Dunning AM,
Eicher JD,
Fasching PA,
Faul JD,
Figueroa J,
Flesch-Janys D,
Gandin I,
Garcia ME,
García-Closas M,
Giles GG,
Girotto GG,
Goldberg MS,
González-Neira A,
Goodarzi MO,
Grove ML,
Gudbjartsson DF,
Guénel P,
Guo X,
Haiman CA,
Hall P,
Hamann U,
Henderson BE,
Hocking LJ,
Hofman A,
Homuth G,
Hooning MJ,
Hopper JL,
Hu FB,
Huang J,
Humphreys K,
Hunter DJ,
Jakubowska A,
Jones SE,
Kabisch M,
Karasik D,
Knight JA,
Kolcic I,
Kooperberg C,
Kosma VM,
Kriebel J,
Kristensen V,
Lambrechts D,
Langenberg C,
Li J,
Li X,
Lindström S,
Liu Y,
Luan J,
Lubinski J,
Mägi R,
Mannermaa A,
Manz J,
Margolin S,
Marten J,
Martin NG,
Masciullo C,
Meindl A,
Michailidou K,
Mihailov E,
Milani L,
Milne RL,
Müller-Nurasyid M,
Nalls M,
Neale BM,
Nevanlinna H,
Neven P,
Newman AB,
Nordestgaard BG,
Olson JE,
Padmanabhan S,
Peterlongo P,
Peters U,
Petersmann A,
Peto J,
Pharoah PDP,
Pirastu NN,
Pirie A,
Pistis G,
Polasek O,
Porteous D,
Psaty BM,
Pylkäs K,
Radice P,
Raffel LJ,
Rivadeneira F,
Rudan I,
Rudolph A,
Ruggiero D,
Sala CF,
Sanna S,
Sawyer EJ,
Schlessinger D,
Schmidt MK,
Schmidt F,
Schmutzler RK,
Schoemaker MJ,
Scott RA,
Seynaeve CM,
Simard J,
Sorice R,
Southey MC,
Stöckl D,
Strauch K,
Swerdlow A,
Taylor KD,
Thorsteinsdottir U,
Toland AE,
Tomlinson I,
Truong T,
Tryggvadottir L,
Turner ST,
Vozzi D,
Wang Q,
Wellons M,
Willemsen G,
Wilson JF,
Winqvist R,
Wolffenbuttel BBHR,
Wright AF,
Yannoukakos D,
Zemunik T,
Zheng W,
Zheng W,
Zygmunt M,
Bergmann S,
Boomsma DI,
Buring JE,
Ferrucci L,
Montgomery GW,
Gudnason V,
Spector TD,
van Duijn CM,
Alizadeh BZ,
Ciullo M,
Crisponi L,
Easton DF,
Gasparini PP,
Gieger C,
Harris TB,
Hayward C,
Kardia SLR,
Kraft P,
McKnight B,
Metspalu A,
Morrison AC,
Reiner AP,
Ridker PM,
Rotter JI,
Toniolo D,
Uitterlinden AG,
Ulivi S,
Völzke H,
Wareham NJ,
Weir DR,
Yerges-Armstrong LM,
Price AL,
Stefansson K,
Visser JA,
Ong KK,
Chang-Claude J,
Murabito JM,
Perry JRB,
Murray A
PRACTICAL consortium · kConFab Investigators 외 컨소시엄 4곳
Nature genetics · 2015 · PMID 26414677 · open access
페이지 12개+
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
Nielsen JB,
Thorolfsdottir RB,
Fritsche LG,
Zhou W,
Skov MW,
Graham SE,
Herron TJ,
McCarthy S,
Schmidt EM,
Sveinbjornsson G,
Surakka I,
Mathis MR
외 37명 — 모두 보기
Yamazaki M,
Crawford RD,
Gabrielsen ME,
Skogholt AH,
Holmen OL,
Lin M,
Wolford BN,
Dey R,
Dalen H,
Sulem P,
Chung JH,
Backman JD,
Arnar DO,
Thorsteinsdottir U,
Baras A,
O'Dushlaine C,
Holst AG,
Wen X,
Hornsby W,
Dewey FE,
Boehnke M,
Kheterpal S,
Mukherjee B,
Lee S,
Kang HM,
Holm H,
Kitzman J,
Shavit JA,
Jalife J,
Brummett CM,
Teslovich TM,
Carey DJ,
Gudbjartsson DF,
Stefansson K,
Abecasis GR,
Hveem K,
Willer CJ
Nature genetics · 2018 · PMID 30061737
페이지 12개+
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
Rafnar T,
Gunnarsson B,
Stefansson OA,
Sulem P,
Ingason A,
Frigge ML,
Stefansdottir L,
Sigurdsson JK,
Tragante V,
Steinthorsdottir V,
Styrkarsdottir U,
Stacey SN
외 25명 — 모두 보기
Gudmundsson J,
Arnadottir GA,
Oddsson A,
Zink F,
Halldorsson G,
Sveinbjornsson G,
Kristjansson RP,
Davidsson OB,
Salvarsdottir A,
Thoroddsen A,
Helgadottir EA,
Kristjansdottir K,
Ingthorsson O,
Gudmundsson V,
Geirsson RT,
Arnadottir R,
Gudbjartsson DF,
Masson G,
Asselbergs FW,
Jonasson JG,
Olafsson K,
Thorsteinsdottir U,
Halldorsson BV,
Thorleifsson G,
Stefansson K
Nature communications · 2018 · PMID 30194396 · open access
페이지 12개+
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Tin A,
Marten J,
Halperin Kuhns VL,
Li Y,
Wuttke M,
Kirsten H,
Sieber KB,
Qiu C,
Gorski M,
Yu Z,
Giri A,
Sveinbjornsson G
외 213명 — 모두 보기
Li M,
Chu AY,
Hoppmann A,
O'Connor LJ,
Prins B,
Nutile T,
Noce D,
Akiyama M,
Cocca M,
Ghasemi S,
van der Most PJ,
Horn K,
Xu Y,
Fuchsberger C,
Sedaghat S,
Afaq S,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boerwinkle E,
Bottinger EP,
Boutin TS,
Brumat M,
Burkhardt R,
Campana E,
Campbell A,
Campbell H,
Carroll RJ,
Catamo E,
Chambers JC,
Ciullo M,
Concas MP,
Coresh J,
Corre T,
Cusi D,
Felicita SC,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Delgado G,
Demirkan A,
Devuyst O,
Dittrich K,
Eckardt KU,
Ehret G,
Endlich K,
Evans MK,
Gansevoort RT,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hayward C,
Hicks AA,
Hofer E,
Holm H,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Lewis RM,
Ingelsson E,
Jakobsdottir J,
Jonsdottir I,
Jonsson H,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kanai M,
Kerr SM,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
La Bianca M,
Lange LA,
Lehne B,
Lehtimäki T,
Liu J,
Loeffler M,
Loos RJF,
Lyytikäinen LP,
Magi R,
Mahajan A,
Martin NG,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Metspalu A,
Milaneschi Y,
O'Donnell CJ,
Wilson OD,
Gaziano JM,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Müller-Nurasyid M,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell JR,
Olafsson I,
Padmanabhan S,
Penninx BWJH,
Perls T,
Peters A,
Pirastu M,
Pirastu N,
Pistis G,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Preuss MH,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rizzi F,
Robino A,
Rudan I,
Krajcoviechova A,
Cifkova R,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Salvi E,
Schmidt H,
Schmidt R,
Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
Thiery J,
Thio CHL,
Thorsteinsdottir U,
Toniolo D,
Tönjes A,
Tremblay J,
Uitterlinden AG,
Vaccargiu S,
van der Harst P,
van Duijn CM,
Verweij N,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Whitfield JB,
Wild SH,
Wilson JF,
Yang Q,
Zhang W,
Zonderman AB,
Bochud M,
Wilson JG,
Pendergrass SA,
Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
Böger CA,
Snieder H,
Butterworth AS,
Okada Y,
Edwards TL,
Stefansson K,
Susztak K,
Scholz M,
Heid IM,
Hung AM,
Teumer A,
Pattaro C,
Woodward OM,
Vitart V,
Köttgen A
German Chronic Kidney Disease Study · Lifelines Cohort Study 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 31578528 · open access
페이지 12개+
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Oskarsson GR,
Oddsson A,
Magnusson MK,
Kristjansson RP,
Halldorsson GH,
Ferkingstad E,
Zink F,
Helgadottir A,
Ivarsdottir EV,
Arnadottir GA,
Jensson BO,
Katrinardottir H
외 26명 — 모두 보기
Sveinbjornsson G,
Kristinsdottir AM,
Lee AL,
Saemundsdottir J,
Stefansdottir L,
Sigurdsson JK,
Davidsson OB,
Benonisdottir S,
Jonasdottir A,
Jonasdottir A,
Jonsson S,
Gudmundsson RL,
Asselbergs FW,
Tragante V,
Gunnarsson B,
Masson G,
Thorleifsson G,
Rafnar T,
Holm H,
Olafsson I,
Onundarson PT,
Gudbjartsson DF,
Norddahl GL,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Communications biology · 2020 · PMID 32327693 · open access
페이지 12개+
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ntalla I,
Weng LC,
Cartwright JH,
Hall AW,
Sveinbjornsson G,
Tucker NR,
Choi SH,
Chaffin MD,
Roselli C,
Barnes MR,
Mifsud B,
Warren HR
외 175명 — 모두 보기
Hayward C,
Marten J,
Cranley JJ,
Concas MP,
Gasparini P,
Boutin T,
Kolcic I,
Polasek O,
Rudan I,
Araujo NM,
Lima-Costa MF,
Ribeiro ALP,
Souza RP,
Tarazona-Santos E,
Giedraitis V,
Ingelsson E,
Mahajan A,
Morris AP,
Del Greco M F,
Foco L,
Gögele M,
Hicks AA,
Cook JP,
Lind L,
Lindgren CM,
Sundström J,
Nelson CP,
Riaz MB,
Samani NJ,
Sinagra G,
Ulivi S,
Kähönen M,
Mishra PP,
Mononen N,
Nikus K,
Caulfield MJ,
Dominiczak A,
Padmanabhan S,
Montasser ME,
O'Connell JR,
Ryan K,
Shuldiner AR,
Aeschbacher S,
Conen D,
Risch L,
Thériault S,
Hutri-Kähönen N,
Lehtimäki T,
Lyytikäinen LP,
Raitakari OT,
Barnes CLK,
Campbell H,
Joshi PK,
Wilson JF,
Isaacs A,
Kors JA,
van Duijn CM,
Huang PL,
Gudnason V,
Harris TB,
Launer LJ,
Smith AV,
Bottinger EP,
Loos RJF,
Nadkarni GN,
Preuss MH,
Correa A,
Mei H,
Wilson J,
Meitinger T,
Müller-Nurasyid M,
Peters A,
Waldenberger M,
Mangino M,
Spector TD,
Rienstra M,
van de Vegte YJ,
van der Harst P,
Verweij N,
Kääb S,
Schramm K,
Sinner MF,
Strauch K,
Cutler MJ,
Fatkin D,
London B,
Olesen M,
Roden DM,
Benjamin Shoemaker M,
Gustav Smith J,
Biggs ML,
Bis JC,
Brody JA,
Psaty BM,
Rice K,
Sotoodehnia N,
De Grandi A,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Ford I,
Wouter Jukema J,
Macfarlane PW,
Trompet S,
Dörr M,
Felix SB,
Völker U,
Weiss S,
Havulinna AS,
Jula A,
Sääksjärvi K,
Salomaa V,
Guo X,
Heckbert SR,
Lin HJ,
Rotter JI,
Taylor KD,
Yao J,
de Mutsert R,
Maan AC,
Mook-Kanamori DO,
Noordam R,
Cucca F,
Ding J,
Lakatta EG,
Qian Y,
Tarasov KV,
Levy D,
Lin H,
Newton-Cheh CH,
Lunetta KL,
Murray AD,
Porteous DJ,
Smith BH,
Stricker BH,
Uitterlinden A,
van den Berg ME,
Haessler J,
Jackson RD,
Kooperberg C,
Peters U,
Reiner AP,
Whitsel EA,
Alonso A,
Arking DE,
Boerwinkle E,
Ehret GB,
Soliman EZ,
Avery CL,
Gogarten SM,
Kerr KF,
Laurie CC,
Seyerle AA,
Stilp A,
Assa S,
Abdullah Said M,
Yldau van der Ende M,
Lambiase PD,
Orini M,
Ramirez J,
Van Duijvenboden S,
Arnar DO,
Gudbjartsson DF,
Holm H,
Sulem P,
Thorleifsson G,
Thorolfsdottir RB,
Thorsteinsdottir U,
Benjamin EJ,
Tinker A,
Stefansson K,
Ellinor PT,
Jamshidi Y,
Lubitz SA,
Munroe PB
Nature communications · 2020 · PMID 32439900 · open access
페이지 12개+
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Saevarsdottir S,
Olafsdottir TA,
Ivarsdottir EV,
Halldorsson GH,
Gunnarsdottir K,
Sigurdsson A,
Johannesson A,
Sigurdsson JK,
Juliusdottir T,
Lund SH,
Arnthorsson AO,
Styrmisdottir EL
외 34명 — 모두 보기
Gudmundsson J,
Grondal GM,
Steinsson K,
Alfredsson L,
Askling J,
Benediktsson R,
Bjarnason R,
Geirsson AJ,
Gudbjornsson B,
Gudjonsson H,
Hjaltason H,
Hreidarsson AB,
Klareskog L,
Kockum I,
Kristjansdottir H,
Love TJ,
Ludviksson BR,
Olsson T,
Onundarson PT,
Orvar KB,
Padyukov L,
Sigurgeirsson B,
Tragante V,
Bjarnadottir K,
Rafnar T,
Masson G,
Sulem P,
Gudbjartsson DF,
Melsted P,
Thorleifsson G,
Norddahl GL,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Nature · 2020 · PMID 32581359
페이지 12개+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
Mifsud B,
Yao C,
Kraja AT,
Cartwright JH,
Hellwege JN
외 269명 — 모두 보기
Giri A,
Tragante V,
Thorleifsson G,
Liu DJ,
Prins BP,
Stewart ID,
Cabrera CP,
Eales JM,
Akbarov A,
Auer PL,
Bielak LF,
Bis JC,
Braithwaite VS,
Brody JA,
Daw EW,
Warren HR,
Drenos F,
Nielsen SF,
Faul JD,
Fauman EB,
Fava C,
Ferreira T,
Foley CN,
Franceschini N,
Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
Mei H,
Menni C,
Mook-Kanamori DO,
Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
Perola M,
Poveda A,
Rauramaa R,
Richard M,
Richardson TG,
Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
Staley JR,
Stanáková A,
Sulem P,
Thériault S,
Thorsteinsdottir U,
Trompet S,
Varga TV,
Velez Edwards DR,
Veronesi G,
Weiss S,
Willems SM,
Yao J,
Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
Aeschbacher S,
Asllanaj E,
Blankenberg S,
Bonnycastle LL,
Bork-Jensen J,
Brandslund I,
Braund PS,
Burgess S,
Cho K,
Christensen C,
Connell J,
Mutsert R,
Dominiczak AF,
Dörr M,
Eiriksdottir G,
Farmaki AE,
Gaziano JM,
Grarup N,
Grove ML,
Hallmans G,
Hansen T,
Have CT,
Heiss G,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Kamat M,
Käräjämäki A,
Karpe F,
Koistinen HA,
Kovesdy CP,
Kuulasmaa K,
Laatikainen T,
Lannfelt L,
Lee IT,
Lee WJ,
Linneberg A,
Martin LW,
Moitry M,
Nadkarni G,
Neville MJ,
Palmer CNA,
Papanicolaou GJ,
Pedersen O,
Peters J,
Poulter N,
Rasheed A,
Rasmussen KL,
Rayner NW,
Mägi R,
Renström F,
Rettig R,
Rossouw J,
Schreiner PJ,
Sever PS,
Sigurdsson EL,
Skaaby T,
Sun YV,
Sundstrom J,
Thorgeirsson G,
Esko T,
Trabetti E,
Tsao PS,
Tuomi T,
Turner ST,
Tzoulaki I,
Vaartjes I,
Vergnaud AC,
Willer CJ,
Wilson PWF,
Witte DR,
Yonova-Doing E,
Zhang H,
Aliya N,
Almgren P,
Amouyel P,
Asselbergs FW,
Barnes MR,
Blakemore AI,
Boehnke M,
Bots ML,
Bottinger EP,
Buring JE,
Chambers JC,
Chen YI,
Chowdhury R,
Conen D,
Correa A,
Davey Smith G,
Boer RA,
Deary IJ,
Dedoussis G,
Deloukas P,
Di Angelantonio E,
Elliott P,
Felix SB,
Ferrières J,
Ford I,
Fornage M,
Franks PW,
Franks S,
Frossard P,
Gambaro G,
Gaunt TR,
Groop L,
Gudnason V,
Harris TB,
Hayward C,
Hennig BJ,
Herzig KH,
Ingelsson E,
Tuomilehto J,
Järvelin MR,
Jukema JW,
Kardia SLR,
Kee F,
Kooner JS,
Kooperberg C,
Launer LJ,
Lind L,
Loos RJF,
Majumder AAS,
Laakso M,
McCarthy MI,
Melander O,
Mohlke KL,
Murray AD,
Nordestgaard BG,
Orho-Melander M,
Packard CJ,
Padmanabhan S,
Palmas W,
Polasek O,
Porteous DJ,
Prentice AM,
Province MA,
Relton CL,
Rice K,
Ridker PM,
Rolandsson O,
Rosendaal FR,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sattar N,
Sheu WH,
Smith BH,
Soranzo N,
Spector TD,
Starr JM,
Sebert S,
Taylor KD,
Lakka TA,
Timpson NJ,
Tobin MD,
van der Harst P,
van der Meer P,
Ramachandran VS,
Verweij N,
Virtamo J,
Völker U,
Weir DR,
Zeggini E,
Charchar FJ,
Wareham NJ,
Langenberg C,
Tomaszewski M,
Butterworth AS,
Caulfield MJ,
Danesh J,
Edwards TL,
Holm H,
Hung AM,
Lindgren CM,
Liu C,
Manning AK,
Morris AP,
Morrison AC,
O'Donnell CJ,
Psaty BM,
Saleheen D,
Stefansson K,
Boerwinkle E,
Chasman DI,
Levy D,
Newton-Cheh C,
Munroe PB,
Howson JMM
LifeLines Cohort Study · EPIC-CVD 외 컨소시엄 3곳
Nature genetics · 2020 · PMID 33230300 · open access
페이지 12개+
Genetic insights into biological mechanisms governing human ovarian ageing
Ruth KS,
Day FR,
Hussain J,
Martínez-Marchal A,
Aiken CE,
Azad A,
Thompson DJ,
Knoblochova L,
Abe H,
Tarry-Adkins JL,
Gonzalez JM,
Fontanillas P
외 256명 — 모두 보기
Claringbould A,
Bakker OB,
Sulem P,
Walters RG,
Terao C,
Turon S,
Horikoshi M,
Lin K,
Onland-Moret NC,
Sankar A,
Hertz EPT,
Timshel PN,
Shukla V,
Borup R,
Olsen KW,
Aguilera P,
Ferrer-Roda M,
Huang Y,
Stankovic S,
Timmers PRHJ,
Ahearn TU,
Alizadeh BZ,
Naderi E,
Andrulis IL,
Arnold AM,
Aronson KJ,
Augustinsson A,
Bandinelli S,
Barbieri CM,
Beaumont RN,
Becher H,
Beckmann MW,
Benonisdottir S,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Boomsma DI,
Bowker N,
Brody JA,
Broer L,
Buring JE,
Campbell A,
Campbell H,
Castelao JE,
Catamo E,
Chanock SJ,
Chenevix-Trench G,
Ciullo M,
Corre T,
Couch FJ,
Cox A,
Crisponi L,
Cross SS,
Cucca F,
Czene K,
Smith GD,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Demerath EW,
Dennis J,
Dunning AM,
Dwek M,
Eriksson M,
Esko T,
Fasching PA,
Faul JD,
Ferrucci L,
Franceschini N,
Frayling TM,
Gago-Dominguez M,
Mezzavilla M,
García-Closas M,
Gieger C,
Giles GG,
Grallert H,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Haiman CA,
Håkansson N,
Hall P,
Hayward C,
He C,
He W,
Heiss G,
Høffding MK,
Hopper JL,
Hottenga JJ,
Hu F,
Hunter D,
Ikram MA,
Jackson RD,
Joaquim MDR,
John EM,
Joshi PK,
Karasik D,
Kardia SLR,
Kartsonaki C,
Karlsson R,
Kitahara CM,
Kolcic I,
Kooperberg C,
Kraft P,
Kurian AW,
Kutalik Z,
La Bianca M,
LaChance G,
Langenberg C,
Launer LJ,
Laven JSE,
Lawlor DA,
Le Marchand L,
Li J,
Lindblom A,
Lindstrom S,
Lindstrom T,
Linet M,
Liu Y,
Liu S,
Luan J,
Mägi R,
Magnusson PKE,
Mangino M,
Mannermaa A,
Marco B,
Marten J,
Martin NG,
Mbarek H,
McKnight B,
Medland SE,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Milani L,
Milne RL,
Montgomery GW,
Mook-Kanamori DO,
Mulas A,
Mulligan AM,
Murray A,
Nalls MA,
Newman A,
Noordam R,
Nutile T,
Nyholt DR,
Olshan AF,
Olsson H,
Painter JN,
Patel AV,
Pedersen NL,
Perjakova N,
Peters A,
Peters U,
Pharoah PDP,
Polasek O,
Porcu E,
Psaty BM,
Rahman I,
Rennert G,
Rennert HS,
Ridker PM,
Ring SM,
Robino A,
Rose LM,
Rosendaal FR,
Rossouw J,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Saloustros E,
Sandler DP,
Sanna S,
Sawyer EJ,
Sarnowski C,
Schlessinger D,
Schmidt MK,
Schoemaker MJ,
Schraut KE,
Scott C,
Shekari S,
Shrikhande A,
Smith AV,
Smith BH,
Smith JA,
Sorice R,
Southey MC,
Spector TD,
Spinelli JJ,
Stampfer M,
Stöckl D,
van Meurs JBJ,
Strauch K,
Styrkarsdottir U,
Swerdlow AJ,
Tanaka T,
Teras LR,
Teumer A,
Þorsteinsdottir U,
Timpson NJ,
Toniolo D,
Traglia M,
Troester MA,
Truong T,
Tyrrell J,
Uitterlinden AG,
Ulivi S,
Vachon CM,
Vitart V,
Völker U,
Vollenweider P,
Völzke H,
Wang Q,
Wareham NJ,
Weinberg CR,
Weir DR,
Wilcox AN,
van Dijk KW,
Willemsen G,
Wilson JF,
Wolffenbuttel BHR,
Wolk A,
Wood AR,
Zhao W,
Zygmunt M,
Chen Z,
Li L,
Franke L,
Burgess S,
Deelen P,
Pers TH,
Grøndahl ML,
Andersen CY,
Pujol A,
Lopez-Contreras AJ,
Daniel JA,
Stefansson K,
Chang-Claude J,
van der Schouw YT,
Lunetta KL,
Chasman DI,
Easton DF,
Visser JA,
Ozanne SE,
Namekawa SH,
Solc P,
Murabito JM,
Ong KK,
Hoffmann ER,
Murray A,
Roig I,
Perry JRB
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium 외 컨소시엄 6곳
Nature · 2021 · PMID 34349265
페이지 12개+
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
Skuladottir AT,
Bjornsdottir G,
Ferkingstad E,
Einarsson G,
Stefansdottir L,
Nawaz MS,
Oddsson A,
Olafsdottir TA,
Saevarsdottir S,
Walters GB,
Magnusson SH,
Bjornsdottir A
외 18명 — 모두 보기
Sveinsson OA,
Vikingsson A,
Hansen TF,
Jacobsen RL,
Erikstrup C,
Schwinn M,
Brunak S,
Banasik K,
Ostrowski SR,
Troelsen A,
Henkel C,
Pedersen OB,
Jonsdottir I,
Gudbjartsson DF,
Sulem P,
Thorgeirsson TE,
Stefansson H,
Stefansson K
DBDS Genetic Consortium
Nature communications · 2022 · PMID 35332129 · open access
페이지 12개+
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
Ghouse J,
Sveinbjörnsson G,
Vujkovic M,
Seidelin AS,
Gellert-Kristensen H,
Ahlberg G,
Tragante V,
Rand SA,
Brancale J,
Vilarinho S,
Lundegaard PR,
Sørensen E
외 39명 — 모두 보기
Erikstrup C,
Bruun MT,
Jensen BA,
Brunak S,
Banasik K,
Ullum H,
Verweij N,
Lotta L,
Baras A,
Mirshahi T,
Carey DJ,
Kaplan DE,
Lynch J,
Morgan T,
Schwantes-An TH,
Dochtermann DR,
Pyarajan S,
Tsao PS,
Laisk T,
Mägi R,
Kozlitina J,
Tybjærg-Hansen A,
Jones D,
Knowlton KU,
Nadauld L,
Ferkingstad E,
Björnsson ES,
Ulfarsson MO,
Sturluson Á,
Sulem P,
Pedersen OB,
Ostrowski SR,
Gudbjartsson DF,
Stefansson K,
Olesen MS,
Chang KM,
Holm H,
Bundgaard H,
Stender S
DBDS Genomic Consortium · Regeneron Genetics Center 외 컨소시엄 3곳
Nature genetics · 2024 · PMID 38632349 · open access
페이지 12개+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
Smith R,
Keene SJ,
Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
Mason A,
Karthikeyan S,
Lumbers RT
외 60명 — 모두 보기
Bonglack E,
Ouwehand W,
Roberts DJ,
Dowsett J,
Ostrowski SR,
Larsen MH,
Ullum H,
Pedersen OB,
Brunak S,
Banasik K,
Erikstrup C,
Mitchell J,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Girelli D,
Arvas M,
Toivonen J,
Molnos S,
Peters A,
Polasek O,
Rudan I,
Hayward C,
McDonnell C,
Pirastu N,
Wilson JF,
van den Hurk K,
Quee F,
Ferrucci L,
Bandinelli S,
Tanaka T,
Girotto G,
Concas MP,
Pecori A,
Verweij N,
van der Harst P,
van de Vegte YJ,
Kiemeney LA,
Sweep FC,
Galesloot TE,
Sulem P,
Gudbjartsson D,
Ferkingstad E,
Djousse L,
Cho K,
Inouye M,
Burgess S,
Benyamin B,
Oexle K,
Swinkels D,
Stefansson K,
Magnusson M,
Ganna A,
Gaziano M,
Ivey K,
Danesh J,
Pereira A,
Wood AM,
Butterworth AS,
Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
페이지 12개+
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Elks CE,
Perry JR,
Sulem P,
Chasman DI,
Franceschini N,
He C,
Lunetta KL,
Visser JA,
Byrne EM,
Cousminer DL,
Gudbjartsson DF,
Esko T
외 162명 — 모두 보기
Feenstra B,
Hottenga JJ,
Koller DL,
Kutalik Z,
Lin P,
Mangino M,
Marongiu M,
McArdle PF,
Smith AV,
Stolk L,
van Wingerden SH,
Zhao JH,
Albrecht E,
Corre T,
Ingelsson E,
Hayward C,
Magnusson PK,
Smith EN,
Ulivi S,
Warrington NM,
Zgaga L,
Alavere H,
Amin N,
Aspelund T,
Bandinelli S,
Barroso I,
Berenson GS,
Bergmann S,
Blackburn H,
Boerwinkle E,
Buring JE,
Busonero F,
Campbell H,
Chanock SJ,
Chen W,
Cornelis MC,
Couper D,
Coviello AD,
d'Adamo P,
de Faire U,
de Geus EJ,
Deloukas P,
Döring A,
Smith GD,
Easton DF,
Eiriksdottir G,
Emilsson V,
Eriksson J,
Ferrucci L,
Folsom AR,
Foroud T,
Garcia M,
Gasparini P,
Geller F,
Gieger C,
Gudnason V,
Hall P,
Hankinson SE,
Ferreli L,
Heath AC,
Hernandez DG,
Hofman A,
Hu FB,
Illig T,
Järvelin MR,
Johnson AD,
Karasik D,
Khaw KT,
Kiel DP,
Kilpeläinen TO,
Kolcic I,
Kraft P,
Launer LJ,
Laven JS,
Li S,
Liu J,
Levy D,
Martin NG,
McArdle WL,
Melbye M,
Mooser V,
Murray JC,
Murray SS,
Nalls MA,
Navarro P,
Nelis M,
Ness AR,
Northstone K,
Oostra BA,
Peacock M,
Palmer LJ,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peltonen L,
Pennell CE,
Pharoah P,
Polasek O,
Plump AS,
Pouta A,
Porcu E,
Rafnar T,
Rice JP,
Ring SM,
Rivadeneira F,
Rudan I,
Sala C,
Salomaa V,
Sanna S,
Schlessinger D,
Schork NJ,
Scuteri A,
Segrè AV,
Shuldiner AR,
Soranzo N,
Sovio U,
Srinivasan SR,
Strachan DP,
Tammesoo ML,
Tikkanen E,
Toniolo D,
Tsui K,
Tryggvadottir L,
Tyrer J,
Uda M,
van Dam RM,
van Meurs JB,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Weedon MN,
Wichmann HE,
Willemsen G,
Wilson JF,
Wright AF,
Young L,
Zhai G,
Zhuang WV,
Bierut LJ,
Boomsma DI,
Boyd HA,
Crisponi L,
Demerath EW,
van Duijn CM,
Econs MJ,
Harris TB,
Hunter DJ,
Loos RJ,
Metspalu A,
Montgomery GW,
Ridker PM,
Spector TD,
Streeten EA,
Stefansson K,
Thorsteinsdottir U,
Uitterlinden AG,
Widen E,
Murabito JM,
Ong KK,
Murray A
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
페이지 11개
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density
Ivarsdottir EV,
Benonisdottir S,
Thorleifsson G,
Sulem P,
Oddsson A,
Styrkarsdottir U,
Kristmundsdottir S,
Arnadottir GA,
Thorgeirsson G,
Jonsdottir I,
Zoega GM,
Thorsteinsdottir U
외 4명 — 모두 보기
Nature communications · 2019 · PMID 30894546 · open access
페이지 11개
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
Olafsson S,
Alexandersson KF,
Gizurarson JGK,
Hauksdottir K,
Gunnarsson O,
Olafsson K,
Gudmundsson J,
Stacey SN,
Sveinbjornsson G,
Saemundsdottir J,
Bjornsson ES,
Olafsson S
외 22명 — 모두 보기
Bjornsson S,
Orvar KB,
Vikingsson A,
Geirsson AJ,
Arinbjarnarson S,
Bjornsdottir G,
Thorgeirsson TE,
Sigurdsson S,
Halldorsson GH,
Magnusson OT,
Masson G,
Holm H,
Jonsdottir I,
Sigurdardottir O,
Eyjolfsson GI,
Olafsson I,
Sulem P,
Thorsteinsdottir U,
Jonsson T,
Rafnar T,
Gudbjartsson DF,
Stefansson K
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
페이지 11개
Physical and neurobehavioral determinants of reproductive onset and success
Day FR,
Helgason H,
Chasman DI,
Rose LM,
Loh PR,
Scott RA,
Helgason A,
Kong A,
Masson G,
Magnusson OT,
Gudbjartsson D,
Thorsteinsdottir U
외 6명 — 모두 보기
Nature genetics · 2016 · PMID 27089180
페이지 10개
Deciphering the genetics and mechanisms of predisposition to multiple myeloma
Went M,
Duran-Lozano L,
Halldorsson GH,
Gunnell A,
Ugidos-Damboriena N,
Law P,
Ekdahl L,
Sud A,
Thorleifsson G,
Thodberg M,
Olafsdottir T,
Lamarca-Arrizabalaga A
외 38명 — 모두 보기
Cafaro C,
Niroula A,
Ajore R,
Lopez de Lapuente Portilla A,
Ali Z,
Pertesi M,
Goldschmidt H,
Stefansdottir L,
Kristinsson SY,
Stacey SN,
Love TJ,
Rognvaldsson S,
Hajek R,
Vodicka P,
Pettersson-Kymmer U,
Späth F,
Schinke C,
Van Rhee F,
Sulem P,
Ferkingstad E,
Hjorleifsson Eldjarn G,
Mellqvist UH,
Jonsdottir I,
Morgan G,
Sonneveld P,
Waage A,
Weinhold N,
Thomsen H,
Försti A,
Hansson M,
Juul-Vangsted A,
Thorsteinsdottir U,
Hemminki K,
Kaiser M,
Rafnar T,
Stefansson K,
Houlston R,
Nilsson B
Nature communications · 2024 · PMID 39103364 · open access
페이지 10개
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA
Gudmundsson J,
Sigurdsson JK,
Stefansdottir L,
Agnarsson BA,
Isaksson HJ,
Stefansson OA,
Gudjonsson SA,
Gudbjartsson DF,
Masson G,
Frigge ML,
Stacey SN,
Sulem P
외 16명 — 모두 보기
Halldorsson GH,
Tragante V,
Holm H,
Eyjolfsson GI,
Sigurdardottir O,
Olafsson I,
Jonsson T,
Jonsson E,
Barkardottir RB,
Hilmarsson R,
Asselbergs FW,
Geirsson G,
Thorsteinsdottir U,
Rafnar T,
Thorleifsson G,
Stefansson K
Nature communications · 2018 · PMID 30410027 · open access
페이지 9개
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.