연구자에게
내 논문이 여기 있나요?
논문 2,676편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
He G에 대해
145건, 그중 20건 표시.
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+
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Morris AP,
Voight BF,
Teslovich TM,
Ferreira T,
Segrè AV,
Steinthorsdottir V,
Strawbridge RJ,
Khan H,
Grallert H,
Mahajan A,
Prokopenko I,
Kang HM
외 192명 — 모두 보기
Dina C,
Esko T,
Fraser RM,
Kanoni S,
Kumar A,
Lagou V,
Langenberg C,
Luan J,
Lindgren CM,
Müller-Nurasyid M,
Pechlivanis S,
Rayner NW,
Scott LJ,
Wiltshire S,
Yengo L,
Kinnunen L,
Rossin EJ,
Raychaudhuri S,
Johnson AD,
Dimas AS,
Loos RJ,
Vedantam S,
Chen H,
Florez JC,
Fox C,
Liu CT,
Rybin D,
Couper DJ,
Kao WH,
Li M,
Cornelis MC,
Kraft P,
Sun Q,
van Dam RM,
Stringham HM,
Chines PS,
Fischer K,
Fontanillas P,
Holmen OL,
Hunt SE,
Jackson AU,
Kong A,
Lawrence R,
Meyer J,
Perry JR,
Platou CG,
Potter S,
Rehnberg E,
Robertson N,
Sivapalaratnam S,
Stančáková A,
Stirrups K,
Thorleifsson G,
Tikkanen E,
Wood AR,
Almgren P,
Atalay M,
Benediktsson R,
Bonnycastle LL,
Burtt N,
Carey J,
Charpentier G,
Crenshaw AT,
Doney AS,
Dorkhan M,
Edkins S,
Emilsson V,
Eury E,
Forsen T,
Gertow K,
Gigante B,
Grant GB,
Groves CJ,
Guiducci C,
Herder C,
Hreidarsson AB,
Hui J,
James A,
Jonsson A,
Rathmann W,
Klopp N,
Kravic J,
Krjutškov K,
Langford C,
Leander K,
Lindholm E,
Lobbens S,
Männistö S,
Mirza G,
Mühleisen TW,
Musk B,
Parkin M,
Rallidis L,
Saramies J,
Sennblad B,
Shah S,
Sigurðsson G,
Silveira A,
Steinbach G,
Thorand B,
Trakalo J,
Veglia F,
Wennauer R,
Winckler W,
Zabaneh D,
Campbell H,
van Duijn C,
Uitterlinden AG,
Hofman A,
Sijbrands E,
Abecasis GR,
Owen KR,
Zeggini E,
Trip MD,
Forouhi NG,
Syvänen AC,
Eriksson JG,
Peltonen L,
Nöthen MM,
Balkau B,
Palmer CN,
Lyssenko V,
Tuomi T,
Isomaa B,
Hunter DJ,
Qi L,
Shuldiner AR,
Roden M,
Barroso I,
Wilsgaard T,
Beilby J,
Hovingh K,
Price JF,
Wilson JF,
Rauramaa R,
Lakka TA,
Lind L,
Dedoussis G,
Njølstad I,
Pedersen NL,
Khaw KT,
Wareham NJ,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Korpi-Hyövälti E,
Saltevo J,
Laakso M,
Kuusisto J,
Metspalu A,
Collins FS,
Mohlke KL,
Bergman RN,
Tuomilehto J,
Boehm BO,
Gieger C,
Hveem K,
Cauchi S,
Froguel P,
Baldassarre D,
Tremoli E,
Humphries SE,
Saleheen D,
Danesh J,
Ingelsson E,
Ripatti S,
Salomaa V,
Erbel R,
Jöckel KH,
Moebus S,
Peters A,
Illig T,
de Faire U,
Hamsten A,
Morris AD,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Boerwinkle E,
Melander O,
Kathiresan S,
Nilsson PM,
Deloukas P,
Thorsteinsdottir U,
Groop LC,
Stefansson K,
Hu F,
Pankow JS,
Dupuis J,
Meigs JB,
Altshuler D,
Boehnke M,
McCarthy MI
Wellcome Trust Case Control Consortium · Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC) Investigators 외 컨소시엄 4곳
Nature genetics · 2012 · PMID 22885922 · 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
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
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 association studies reveal new insights into the genetic basis of IgG4-related disease in the Chinese Han population
Yan S,
Peng Y,
Xu J,
Liu Y,
Li Z,
Yang Y,
Peng L,
Zhou J,
Li L,
Liu C,
Chen H,
Wang M
외 14명 — 모두 보기
Wu Z,
Zhang S,
Xu H,
Li H,
Feng F,
Fei Y,
Chen Y,
Dong L,
Li M,
Li Z,
Zhang F,
Zuo X,
Zhang W,
Li Y
Annals of the rheumatic diseases · 2026 · PMID 41298177
페이지 10개
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Mahajan A,
Go MJ,
Zhang W,
Below JE,
Gaulton KJ,
Ferreira T,
Horikoshi M,
Johnson AD,
Ng MC,
Prokopenko I,
Saleheen D,
Wang X
외 322명 — 모두 보기
Zeggini E,
Abecasis GR,
Adair LS,
Almgren P,
Atalay M,
Aung T,
Baldassarre D,
Balkau B,
Bao Y,
Barnett AH,
Barroso I,
Basit A,
Been LF,
Beilby J,
Bell GI,
Benediktsson R,
Bergman RN,
Boehm BO,
Boerwinkle E,
Bonnycastle LL,
Burtt N,
Cai Q,
Campbell H,
Carey J,
Cauchi S,
Caulfield M,
Chan JC,
Chang LC,
Chang TJ,
Chang YC,
Charpentier G,
Chen CH,
Chen H,
Chen YT,
Chia KS,
Chidambaram M,
Chines PS,
Cho NH,
Cho YM,
Chuang LM,
Chuang LM,
Collins FS,
Cornelis MC,
Couper DJ,
Crenshaw AT,
van Dam RM,
Danesh J,
Das D,
de Faire U,
Dedoussis G,
Deloukas P,
Dimas AS,
Dina C,
Doney AS,
Donnelly PJ,
Dorkhan M,
van Duijn C,
Dupuis J,
Edkins S,
Elliott P,
Emilsson V,
Erbel R,
Eriksson JG,
Escobedo J,
Esko T,
Eury E,
Florez JC,
Fontanillas P,
Forouhi NG,
Forsen T,
Fox C,
Fraser RM,
Frayling TM,
Froguel P,
Frossard P,
Gao Y,
Gertow K,
Gieger C,
Gigante B,
Grallert H,
Grant GB,
Grrop LC,
Groves CJ,
Grundberg E,
Guiducci C,
Hamsten A,
Han BG,
Hara K,
Hassanali N,
Hattersley AT,
Hayward C,
Hedman AK,
Herder C,
Hofman A,
Holmen OL,
Hovingh K,
Hreidarsson AB,
Hu C,
Hu FB,
Hui J,
Humphries SE,
Hunt SE,
Hunter DJ,
Hveem K,
Hydrie ZI,
Ikegami H,
Illig T,
Ingelsson E,
Islam M,
Isomaa B,
Jackson AU,
Jafar T,
James A,
Jia W,
Jöckel KH,
Jonsson A,
Jowett JB,
Kadowaki T,
Kang HM,
Kanoni S,
Kao WH,
Kathiresan S,
Kato N,
Katulanda P,
Keinanen-Kiukaanniemi KM,
Kelly AM,
Khan H,
Khaw KT,
Khor CC,
Kim HL,
Kim S,
Kim YJ,
Kinnunen L,
Klopp N,
Kong A,
Korpi-Hyövälti E,
Kowlessur S,
Kraft P,
Kravic J,
Kristensen MM,
Krithika S,
Kumar A,
Kumate J,
Kuusisto J,
Kwak SH,
Laakso M,
Lagou V,
Lakka TA,
Langenberg C,
Langford C,
Lawrence R,
Leander K,
Lee JM,
Lee NR,
Li M,
Li X,
Li Y,
Liang J,
Liju S,
Lim WY,
Lind L,
Lindgren CM,
Lindholm E,
Liu CT,
Liu JJ,
Lobbens S,
Long J,
Loos RJ,
Lu W,
Luan J,
Lyssenko V,
Ma RC,
Maeda S,
Mägi R,
Männisto S,
Matthews DR,
Meigs JB,
Melander O,
Metspalu A,
Meyer J,
Mirza G,
Mihailov E,
Moebus S,
Mohan V,
Mohlke KL,
Morris AD,
Mühleisen TW,
Müller-Nurasyid M,
Musk B,
Nakamura J,
Nakashima E,
Navarro P,
Ng PK,
Nica AC,
Nilsson PM,
Njølstad I,
Nöthen MM,
Ohnaka K,
Ong TH,
Owen KR,
Palmer CN,
Pankow JS,
Park KS,
Parkin M,
Pechlivanis S,
Pedersen NL,
Peltonen L,
Perry JR,
Peters A,
Pinidiyapathirage JM,
Platou CG,
Potter S,
Price JF,
Qi L,
Radha V,
Rallidis L,
Rasheed A,
Rathman W,
Rauramaa R,
Raychaudhuri S,
Rayner NW,
Rees SD,
Rehnberg E,
Ripatti S,
Robertson N,
Roden M,
Rossin EJ,
Rudan I,
Rybin D,
Saaristo TE,
Salomaa V,
Saltevo J,
Samuel M,
Sanghera DK,
Saramies J,
Scott J,
Scott LJ,
Scott RA,
Segrè AV,
Sehmi J,
Sennblad B,
Shah N,
Shah S,
Shera AS,
Shu XO,
Shuldiner AR,
Sigurđsson G,
Sijbrands E,
Silveira A,
Sim X,
Sivapalaratnam S,
Small KS,
So WY,
Stančáková A,
Stefansson K,
Steinbach G,
Steinthorsdottir V,
Stirrups K,
Strawbridge RJ,
Stringham HM,
Sun Q,
Suo C,
Syvänen AC,
Takayanagi R,
Takeuchi F,
Tay WT,
Teslovich TM,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tikkanen E,
Trakalo J,
Tremoli E,
Trip MD,
Tsai FJ,
Tuomi T,
Tuomilehto J,
Uitterlinden AG,
Valladares-Salgado A,
Vedantam S,
Veglia F,
Voight BF,
Wang C,
Wareham NJ,
Wennauer R,
Wickremasinghe AR,
Wilsgaard T,
Wilson JF,
Wiltshire S,
Winckler W,
Wong TY,
Wood AR,
Wu JY,
Wu Y,
Yamamoto K,
Yamauchi T,
Yang M,
Yengo L,
Yokota M,
Young R,
Zabaneh D,
Zhang F,
Zhang R,
Zheng W,
Zheng W,
Zimmet PZ,
Altshuler D,
Bowden DW,
Cho YS,
Cox NJ,
Cruz M,
Hanis CL,
Kooner J,
Lee JY,
Seielstad M,
Teo YY,
Boehnke M,
Parra EJ,
Chambers JC,
Tai ES,
McCarthy MI,
Morris AP
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium 외 컨소시엄 3곳
Nature genetics · 2014 · PMID 24509480 · open access
페이지 9개
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Gormley P,
Anttila V,
Winsvold BS,
Palta P,
Esko T,
Pers TH,
Farh KH,
Cuenca-Leon E,
Muona M,
Furlotte NA,
Kurth T,
Ingason A
외 95명 — 모두 보기
McMahon G,
Ligthart L,
Terwindt GM,
Kallela M,
Freilinger TM,
Ran C,
Gordon SG,
Stam AH,
Steinberg S,
Borck G,
Koiranen M,
Quaye L,
Adams HH,
Lehtimäki T,
Sarin AP,
Wedenoja J,
Hinds DA,
Buring JE,
Schürks M,
Ridker PM,
Hrafnsdottir MG,
Stefansson H,
Ring SM,
Hottenga JJ,
Penninx BW,
Färkkilä M,
Artto V,
Kaunisto M,
Vepsäläinen S,
Malik R,
Heath AC,
Madden PA,
Martin NG,
Montgomery GW,
Kurki MI,
Kals M,
Mägi R,
Pärn K,
Hämäläinen E,
Huang H,
Byrnes AE,
Franke L,
Huang J,
Stergiakouli E,
Lee PH,
Sandor C,
Webber C,
Cader Z,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Eriksson JG,
Salomaa V,
Heikkilä K,
Loehrer E,
Uitterlinden AG,
Hofman A,
van Duijn CM,
Cherkas L,
Pedersen LM,
Stubhaug A,
Nielsen CS,
Männikkö M,
Mihailov E,
Milani L,
Göbel H,
Esserlind AL,
Christensen AF,
Hansen TF,
Werge T,
Kaprio J,
Aromaa AJ,
Raitakari O,
Ikram MA,
Spector T,
Järvelin MR,
Metspalu A,
Kubisch C,
Strachan DP,
Ferrari MD,
Belin AC,
Dichgans M,
Wessman M,
van den Maagdenberg AM,
Zwart JA,
Boomsma DI,
Smith GD,
Stefansson K,
Eriksson N,
Daly MJ,
Neale BM,
Olesen J,
Chasman DI,
Nyholt DR,
Palotie A
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
페이지 9개
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez C,
Küçükali F,
Jansen IE,
Kleineidam L,
Moreno-Grau S,
Amin N,
Naj AC,
Campos-Martin R,
Grenier-Boley B,
Andrade V,
Holmans PA,
Boland A
외 391명 — 모두 보기
Damotte V,
van der Lee SJ,
Costa MR,
Kuulasmaa T,
Yang Q,
de Rojas I,
Bis JC,
Yaqub A,
Prokic I,
Chapuis J,
Ahmad S,
Giedraitis V,
Aarsland D,
Garcia-Gonzalez P,
Abdelnour C,
Alarcón-Martín E,
Alcolea D,
Alegret M,
Alvarez I,
Álvarez V,
Armstrong NJ,
Tsolaki A,
Antúnez C,
Appollonio I,
Arcaro M,
Archetti S,
Pastor AA,
Arosio B,
Athanasiu L,
Bailly H,
Banaj N,
Baquero M,
Barral S,
Beiser A,
Pastor AB,
Below JE,
Benchek P,
Benussi L,
Berr C,
Besse C,
Bessi V,
Binetti G,
Bizarro A,
Blesa R,
Boada M,
Boerwinkle E,
Borroni B,
Boschi S,
Bossù P,
Bråthen G,
Bressler J,
Bresner C,
Brodaty H,
Brookes KJ,
Brusco LI,
Buiza-Rueda D,
Bûrger K,
Burholt V,
Bush WS,
Calero M,
Cantwell LB,
Chene G,
Chung J,
Cuccaro ML,
Carracedo Á,
Cecchetti R,
Cervera-Carles L,
Charbonnier C,
Chen HH,
Chillotti C,
Ciccone S,
Claassen JAHR,
Clark C,
Conti E,
Corma-Gómez A,
Costantini E,
Custodero C,
Daian D,
Dalmasso MC,
Daniele A,
Dardiotis E,
Dartigues JF,
de Deyn PP,
de Paiva Lopes K,
de Witte LD,
Debette S,
Deckert J,
Del Ser T,
Denning N,
DeStefano A,
Dichgans M,
Diehl-Schmid J,
Diez-Fairen M,
Rossi PD,
Djurovic S,
Duron E,
Düzel E,
Dufouil C,
Eiriksdottir G,
Engelborghs S,
Escott-Price V,
Espinosa A,
Ewers M,
Faber KM,
Fabrizio T,
Nielsen SF,
Fardo DW,
Farotti L,
Fenoglio C,
Fernández-Fuertes M,
Ferrari R,
Ferreira CB,
Ferri E,
Fin B,
Fischer P,
Fladby T,
Fließbach K,
Fongang B,
Fornage M,
Fortea J,
Foroud TM,
Fostinelli S,
Fox NC,
Franco-Macías E,
Bullido MJ,
Frank-García A,
Froelich L,
Fulton-Howard B,
Galimberti D,
García-Alberca JM,
García-González P,
Garcia-Madrona S,
Garcia-Ribas G,
Ghidoni R,
Giegling I,
Giorgio G,
Goate AM,
Goldhardt O,
Gomez-Fonseca D,
González-Pérez A,
Graff C,
Grande G,
Green E,
Grimmer T,
Grünblatt E,
Grunin M,
Gudnason V,
Guetta-Baranes T,
Haapasalo A,
Hadjigeorgiou G,
Haines JL,
Hamilton-Nelson KL,
Hampel H,
Hanon O,
Hardy J,
Hartmann AM,
Hausner L,
Harwood J,
Heilmann-Heimbach S,
Helisalmi S,
Heneka MT,
Hernández I,
Herrmann MJ,
Hoffmann P,
Holmes C,
Holstege H,
Vilas RH,
Hulsman M,
Humphrey J,
Biessels GJ,
Jian X,
Johansson C,
Jun GR,
Kastumata Y,
Kauwe J,
Kehoe PG,
Kilander L,
Ståhlbom AK,
Kivipelto M,
Koivisto A,
Kornhuber J,
Kosmidis MH,
Kukull WA,
Kuksa PP,
Kunkle BW,
Kuzma AB,
Lage C,
Laukka EJ,
Launer L,
Lauria A,
Lee CY,
Lehtisalo J,
Lerch O,
Lleó A,
Longstreth W Jr,
Lopez O,
de Munain AL,
Love S,
Löwemark M,
Luckcuck L,
Lunetta KL,
Ma Y,
Macías J,
MacLeod CA,
Maier W,
Mangialasche F,
Spallazzi M,
Marquié M,
Marshall R,
Martin ER,
Montes AM,
Rodríguez CM,
Masullo C,
Mayeux R,
Mead S,
Mecocci P,
Medina M,
Meggy A,
Mehrabian S,
Mendoza S,
Menéndez-González M,
Mir P,
Moebus S,
Mol M,
Molina-Porcel L,
Montrreal L,
Morelli L,
Moreno F,
Morgan K,
Mosley T,
Nöthen MM,
Muchnik C,
Mukherjee S,
Nacmias B,
Ngandu T,
Nicolas G,
Nordestgaard BG,
Olaso R,
Orellana A,
Orsini M,
Ortega G,
Padovani A,
Paolo C,
Papenberg G,
Parnetti L,
Pasquier F,
Pastor P,
Peloso G,
Pérez-Cordón A,
Pérez-Tur J,
Pericard P,
Peters O,
Pijnenburg YAL,
Pineda JA,
Piñol-Ripoll G,
Pisanu C,
Polak T,
Popp J,
Posthuma D,
Priller J,
Puerta R,
Quenez O,
Quintela I,
Thomassen JQ,
Rábano A,
Rainero I,
Rajabli F,
Ramakers I,
Real LM,
Reinders MJT,
Reitz C,
Reyes-Dumeyer D,
Ridge P,
Riedel-Heller S,
Riederer P,
Roberto N,
Rodriguez-Rodriguez E,
Rongve A,
Allende IR,
Rosende-Roca M,
Royo JL,
Rubino E,
Rujescu D,
Sáez ME,
Sakka P,
Saltvedt I,
Sanabria Á,
Sánchez-Arjona MB,
Sanchez-Garcia F,
Juan PS,
Sánchez-Valle R,
Sando SB,
Sarnowski C,
Satizabal CL,
Scamosci M,
Scarmeas N,
Scarpini E,
Scheltens P,
Scherbaum N,
Scherer M,
Schmid M,
Schneider A,
Schott JM,
Selbæk G,
Seripa D,
Serrano M,
Sha J,
Shadrin AA,
Skrobot O,
Slifer S,
Snijders GJL,
Soininen H,
Solfrizzi V,
Solomon A,
Song Y,
Sorbi S,
Sotolongo-Grau O,
Spalletta G,
Spottke A,
Squassina A,
Stordal E,
Tartan JP,
Tárraga L,
Tesí N,
Thalamuthu A,
Thomas T,
Tosto G,
Traykov L,
Tremolizzo L,
Tybjærg-Hansen A,
Uitterlinden A,
Ullgren A,
Ulstein I,
Valero S,
Valladares O,
Broeckhoven CV,
Vance J,
Vardarajan BN,
van der Lugt A,
Dongen JV,
van Rooij J,
van Swieten J,
Vandenberghe R,
Verhey F,
Vidal JS,
Vogelgsang J,
Vyhnalek M,
Wagner M,
Wallon D,
Wang LS,
Wang R,
Weinhold L,
Wiltfang J,
Windle G,
Woods B,
Yannakoulia M,
Zare H,
Zhao Y,
Zhang X,
Zhu C,
Zulaica M,
Farrer LA,
Psaty BM,
Ghanbari M,
Raj T,
Sachdev P,
Mather K,
Jessen F,
Ikram MA,
de Mendonça A,
Hort J,
Tsolaki M,
Pericak-Vance MA,
Amouyel P,
Williams J,
Frikke-Schmidt R,
Clarimon J,
Deleuze JF,
Rossi G,
Seshadri S,
Andreassen OA,
Ingelsson M,
Hiltunen M,
Sleegers K,
Schellenberg GD,
van Duijn CM,
Sims R,
van der Flier WM,
Ruiz A,
Ramirez A,
Lambert JC
EADB · GR@ACE 외 컨소시엄 7곳
Nature genetics · 2022 · PMID 35379992 · open access
페이지 9개
Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease
Ji SG,
Juran BD,
Mucha S,
Folseraas T,
Jostins L,
Melum E,
Kumasaka N,
Atkinson EJ,
Schlicht EM,
Liu JZ,
Shah T,
Gutierrez-Achury J
외 58명 — 모두 보기
Boberg KM,
Bergquist A,
Vermeire S,
Eksteen B,
Durie PR,
Farkkila M,
Müller T,
Schramm C,
Sterneck M,
Weismüller TJ,
Gotthardt DN,
Ellinghaus D,
Braun F,
Teufel A,
Laudes M,
Lieb W,
Jacobs G,
Beuers U,
Weersma RK,
Wijmenga C,
Marschall HU,
Milkiewicz P,
Pares A,
Kontula K,
Chazouillères O,
Invernizzi P,
Goode E,
Spiess K,
Moore C,
Sambrook J,
Ouwehand WH,
Roberts DJ,
Danesh J,
Floreani A,
Gulamhusein AF,
Eaton JE,
Schreiber S,
Coltescu C,
Bowlus CL,
Luketic VA,
Odin JA,
Chopra KB,
Kowdley KV,
Chalasani N,
Manns MP,
Srivastava B,
Mells G,
Sandford RN,
Alexander G,
Gaffney DJ,
Chapman RW,
Hirschfield GM,
de Andrade M,
Rushbrook SM,
Franke A,
Karlsen TH,
Lazaridis KN,
Anderson CA
UK-PSC Consortium · International IBD Genetics Consortium 외 컨소시엄 1곳
Nature genetics · 2017 · PMID 27992413 · open access
페이지 8개
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Rahmioglu N,
Mortlock S,
Ghiasi M,
Møller PL,
Stefansdottir L,
Galarneau G,
Turman C,
Danning R,
Law MH,
Sapkota Y,
Christofidou P,
Skarp S
외 121명 — 모두 보기
Giri A,
Banasik K,
Krassowski M,
Lepamets M,
Marciniak B,
Nõukas M,
Perro D,
Sliz E,
Sobalska-Kwapis M,
Thorleifsson G,
Topbas-Selcuki NF,
Vitonis A,
Westergaard D,
Arnadottir R,
Burgdorf KS,
Campbell A,
Cheuk CSK,
Clementi C,
Cook J,
De Vivo I,
DiVasta A,
Dorien O,
Donoghue JF,
Edwards T,
Fontanillas P,
Fung JN,
Geirsson RT,
Girling JE,
Harkki P,
Harris HR,
Healey M,
Heikinheimo O,
Holdsworth-Carson S,
Hostettler IC,
Houlden H,
Houshdaran S,
Irwin JC,
Jarvelin MR,
Kamatani Y,
Kennedy SH,
Kepka E,
Kettunen J,
Kubo M,
Kulig B,
Kurra V,
Laivuori H,
Laufer MR,
Lindgren CM,
MacGregor S,
Mangino M,
Martin NG,
Matalliotaki C,
Matalliotakis M,
Murray AD,
Ndungu A,
Nezhat C,
Olsen CM,
Opoku-Anane J,
Padmanabhan S,
Paranjpe M,
Peters M,
Polak G,
Porteous DJ,
Rabban J,
Rexrode KM,
Romanowicz H,
Saare M,
Saavalainen L,
Schork AJ,
Sen S,
Shafrir AL,
Siewierska-Górska A,
Słomka M,
Smith BH,
Smolarz B,
Szaflik T,
Szyłło K,
Takahashi A,
Terry KL,
Tomassetti C,
Treloar SA,
Vanhie A,
Vincent K,
Vo KC,
Werring DJ,
Zeggini E,
Zervou MI,
Adachi S,
Buring JE,
Ridker PM,
D'Hooghe T,
Goulielmos GN,
Hapangama DK,
Hayward C,
Horne AW,
Low SK,
Martikainen H,
Chasman DI,
Rogers PAW,
Saunders PT,
Sirota M,
Spector T,
Strapagiel D,
Tung JY,
Whiteman DC,
Giudice LC,
Velez-Edwards DR,
Uimari O,
Kraft P,
Salumets A,
Nyholt DR,
Mägi R,
Stefansson K,
Becker CM,
Yurttas-Beim P,
Steinthorsdottir V,
Nyegaard M,
Missmer SA,
Montgomery GW,
Morris AP,
Zondervan KT
DBDS Genomic Consortium · FinnGen Study 외 컨소시엄 3곳
Nature genetics · 2023 · PMID 36914876
페이지 8개
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Trynka G,
Hunt KA,
Bockett NA,
Romanos J,
Mistry V,
Szperl A,
Bakker SF,
Bardella MT,
Bhaw-Rosun L,
Castillejo G,
de la Concha EG,
de Almeida RC
외 52명 — 모두 보기
Dias KR,
van Diemen CC,
Dubois PC,
Duerr RH,
Edkins S,
Franke L,
Fransen K,
Gutierrez J,
Heap GA,
Hrdlickova B,
Hunt S,
Plaza Izurieta L,
Izzo V,
Joosten LA,
Langford C,
Mazzilli MC,
Mein CA,
Midah V,
Mitrovic M,
Mora B,
Morelli M,
Nutland S,
Núñez C,
Onengut-Gumuscu S,
Pearce K,
Platteel M,
Polanco I,
Potter S,
Ribes-Koninckx C,
Ricaño-Ponce I,
Rich SS,
Rybak A,
Santiago JL,
Senapati S,
Sood A,
Szajewska H,
Troncone R,
Varadé J,
Wallace C,
Wolters VM,
Zhernakova A,
Thelma BK,
Cukrowska B,
Urcelay E,
Bilbao JR,
Mearin ML,
Barisani D,
Barrett JC,
Plagnol V,
Deloukas P,
Wijmenga C,
van Heel DA
Spanish Consortium on the Genetics of Coeliac Disease (CEGEC) · PreventCD Study Group 외 컨소시엄 1곳
Nature genetics · 2011 · PMID 22057235 · open access
페이지 7개
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array
Eeles RA,
Olama AA,
Benlloch S,
Saunders EJ,
Leongamornlert DA,
Tymrakiewicz M,
Ghoussaini M,
Luccarini C,
Dennis J,
Jugurnauth-Little S,
Dadaev T,
Neal DE
외 132명 — 모두 보기
Hamdy FC,
Donovan JL,
Muir K,
Giles GG,
Severi G,
Wiklund F,
Gronberg H,
Haiman CA,
Schumacher F,
Henderson BE,
Le Marchand L,
Lindstrom S,
Kraft P,
Hunter DJ,
Gapstur S,
Chanock SJ,
Berndt SI,
Albanes D,
Andriole G,
Schleutker J,
Weischer M,
Canzian F,
Riboli E,
Key TJ,
Travis RC,
Campa D,
Ingles SA,
John EM,
Hayes RB,
Pharoah PD,
Pashayan N,
Khaw KT,
Stanford JL,
Ostrander EA,
Signorello LB,
Thibodeau SN,
Schaid D,
Maier C,
Vogel W,
Kibel AS,
Cybulski C,
Lubinski J,
Cannon-Albright L,
Brenner H,
Park JY,
Kaneva R,
Batra J,
Spurdle AB,
Clements JA,
Teixeira MR,
Dicks E,
Lee A,
Dunning AM,
Baynes C,
Conroy D,
Maranian MJ,
Ahmed S,
Govindasami K,
Guy M,
Wilkinson RA,
Sawyer EJ,
Morgan A,
Dearnaley DP,
Horwich A,
Huddart RA,
Khoo VS,
Parker CC,
Van As NJ,
Woodhouse CJ,
Thompson A,
Dudderidge T,
Ogden C,
Cooper CS,
Lophatananon A,
Cox A,
Southey MC,
Hopper JL,
English DR,
Aly M,
Adolfsson J,
Xu J,
Zheng SL,
Yeager M,
Kaaks R,
Diver WR,
Gaudet MM,
Stern MC,
Corral R,
Joshi AD,
Shahabi A,
Wahlfors T,
Tammela TL,
Auvinen A,
Virtamo J,
Klarskov P,
Nordestgaard BG,
Røder MA,
Nielsen SF,
Bojesen SE,
Siddiq A,
Fitzgerald LM,
Kolb S,
Kwon EM,
Karyadi DM,
Blot WJ,
Zheng W,
Cai Q,
McDonnell SK,
Rinckleb AE,
Drake B,
Colditz G,
Wokolorczyk D,
Stephenson RA,
Teerlink C,
Muller H,
Rothenbacher D,
Sellers TA,
Lin HY,
Slavov C,
Mitev V,
Lose F,
Srinivasan S,
Maia S,
Paulo P,
Lange E,
Cooney KA,
Antoniou AC,
Vincent D,
Bacot F,
Tessier DC,
Kote-Jarai Z,
Easton DF
COGS–Cancer Research UK GWAS–ELLIPSE (part of GAME-ON) Initiative · Australian Prostate Cancer Bioresource 외 컨소시엄 3곳
Nature genetics · 2013 · PMID 23535732
페이지 7개
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment
Kemp JP,
Medina-Gomez C,
Estrada K,
St Pourcain B,
Heppe DH,
Warrington NM,
Oei L,
Ring SM,
Kruithof CJ,
Timpson NJ,
Wolber LE,
Reppe S
외 21명 — 모두 보기
Gautvik K,
Grundberg E,
Ge B,
van der Eerden B,
van de Peppel J,
Hibbs MA,
Ackert-Bicknell CL,
Choi K,
Koller DL,
Econs MJ,
Williams FM,
Foroud T,
Zillikens MC,
Ohlsson C,
Hofman A,
Uitterlinden AG,
Davey Smith G,
Jaddoe VW,
Tobias JH,
Rivadeneira F,
Evans DM
PLoS genetics · 2014 · PMID 24945404 · open access
페이지 7개
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis
Ivarsdottir EV,
Holm H,
Benonisdottir S,
Olafsdottir T,
Sveinbjornsson G,
Thorleifsson G,
Eggertsson HP,
Halldorsson GH,
Hjorleifsson KE,
Melsted P,
Gylfason A,
Arnadottir GA
외 16명 — 모두 보기
Oddsson A,
Jensson BO,
Jonasdottir A,
Jonasdottir A,
Juliusdottir T,
Stefansdottir L,
Tragante V,
Halldorsson BV,
Petersen H,
Thorgeirsson G,
Thorsteinsdottir U,
Sulem P,
Hinriksdottir I,
Jonsdottir I,
Gudbjartsson DF,
Stefansson K
Communications biology · 2021 · PMID 34108613 · open access
페이지 7개
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden
Gabriel AAG,
Atkins JR,
Penha RCC,
Smith-Byrne K,
Gaborieau V,
Voegele C,
Abedi-Ardekani B,
Milojevic M,
Olaso R,
Meyer V,
Boland A,
Deleuze JF
외 21명 — 모두 보기
Zaridze D,
Mukeriya A,
Swiatkowska B,
Janout V,
Schejbalová M,
Mates D,
Stojšić J,
Ognjanovic M,
Witte JS,
Rashkin SR,
Kachuri L,
Hung RJ,
Kar S,
Brennan P,
Sertier AS,
Ferrari A,
Viari A,
Johansson M,
Amos CI,
Foll M,
McKay JD
ILCCO consortium
Journal of the National Cancer Institute · 2022 · PMID 35511172 · open access
페이지 7개
The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders
Ou YN,
Ge YJ,
Wu BS,
Zhang Y,
Jiang YC,
Kuo K,
Yang L,
Tan L,
Feng JF,
Cheng W,
Yu JT
Translational psychiatry · 2023 · PMID 37236919 · open access
페이지 7개
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.