연구자에게
내 논문이 여기 있나요?
논문 2,663편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
He L에 대해
83건, 그중 20건 표시.
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Vujkovic M,
Ramdas S,
Lorenz KM,
Guo X,
Darlay R,
Cordell HJ,
He J,
Gindin Y,
Chung C,
Myers RP,
Schneider CV,
Park J
외 78명 — 모두 보기
Lee KM,
Serper M,
Carr RM,
Kaplan DE,
Haas ME,
MacLean MT,
Witschey WR,
Zhu X,
Tcheandjieu C,
Kember RL,
Kranzler HR,
Verma A,
Giri A,
Klarin DM,
Sun YV,
Huang J,
Huffman JE,
Creasy KT,
Hand NJ,
Liu CT,
Long MT,
Yao J,
Budoff M,
Tan J,
Li X,
Lin HJ,
Chen YI,
Taylor KD,
Chang RK,
Krauss RM,
Vilarinho S,
Brancale J,
Nielsen JB,
Locke AE,
Jones MB,
Verweij N,
Baras A,
Reddy KR,
Neuschwander-Tetri BA,
Schwimmer JB,
Sanyal AJ,
Chalasani N,
Ryan KA,
Mitchell BD,
Gill D,
Wells AD,
Manduchi E,
Saiman Y,
Mahmud N,
Miller DR,
Reaven PD,
Phillips LS,
Muralidhar S,
DuVall SL,
Lee JS,
Assimes TL,
Pyarajan S,
Cho K,
Edwards TL,
Damrauer SM,
Wilson PW,
Gaziano JM,
O'Donnell CJ,
Khera AV,
Grant SFA,
Brown CD,
Tsao PS,
Saleheen D,
Lotta LA,
Bastarache L,
Anstee QM,
Daly AK,
Meigs JB,
Rotter JI,
Lynch JA,
Rader DJ,
Voight BF,
Chang KM
Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration 외 컨소시엄 2곳
Nature genetics · 2022 · PMID 35654975
페이지 8개
Seven new loci associated with age-related macular degeneration
Fritsche LG,
Chen W,
Schu M,
Yaspan BL,
Yu Y,
Thorleifsson G,
Zack DJ,
Arakawa S,
Cipriani V,
Ripke S,
Igo RP Jr,
Buitendijk GH
외 144명 — 모두 보기
Sim X,
Weeks DE,
Guymer RH,
Merriam JE,
Francis PJ,
Hannum G,
Agarwal A,
Armbrecht AM,
Audo I,
Aung T,
Barile GR,
Benchaboune M,
Bird AC,
Bishop PN,
Branham KE,
Brooks M,
Brucker AJ,
Cade WH,
Cain MS,
Campochiaro PA,
Chan CC,
Cheng CY,
Chew EY,
Chin KA,
Chowers I,
Clayton DG,
Cojocaru R,
Conley YP,
Cornes BK,
Daly MJ,
Dhillon B,
Edwards AO,
Evangelou E,
Fagerness J,
Ferreyra HA,
Friedman JS,
Geirsdottir A,
George RJ,
Gieger C,
Gupta N,
Hagstrom SA,
Harding SP,
Haritoglou C,
Heckenlively JR,
Holz FG,
Hughes G,
Ioannidis JP,
Ishibashi T,
Joseph P,
Jun G,
Kamatani Y,
Katsanis N,
N Keilhauer C,
Khan JC,
Kim IK,
Kiyohara Y,
Klein BE,
Klein R,
Kovach JL,
Kozak I,
Lee CJ,
Lee KE,
Lichtner P,
Lotery AJ,
Meitinger T,
Mitchell P,
Mohand-Saïd S,
Moore AT,
Morgan DJ,
Morrison MA,
Myers CE,
Naj AC,
Nakamura Y,
Okada Y,
Orlin A,
Ortube MC,
Othman MI,
Pappas C,
Park KH,
Pauer GJ,
Peachey NS,
Poch O,
Priya RR,
Reynolds R,
Richardson AJ,
Ripp R,
Rudolph G,
Ryu E,
Sahel JA,
Schaumberg DA,
Scholl HP,
Schwartz SG,
Scott WK,
Shahid H,
Sigurdsson H,
Silvestri G,
Sivakumaran TA,
Smith RT,
Sobrin L,
Souied EH,
Stambolian DE,
Stefansson H,
Sturgill-Short GM,
Takahashi A,
Tosakulwong N,
Truitt BJ,
Tsironi EE,
Uitterlinden AG,
van Duijn CM,
Vijaya L,
Vingerling JR,
Vithana EN,
Webster AR,
Wichmann HE,
Winkler TW,
Wong TY,
Wright AF,
Zelenika D,
Zhang M,
Zhao L,
Zhang K,
Klein ML,
Hageman GS,
Lathrop GM,
Stefansson K,
Allikmets R,
Baird PN,
Gorin MB,
Wang JJ,
Klaver CC,
Seddon JM,
Pericak-Vance MA,
Iyengar SK,
Yates JR,
Swaroop A,
Weber BH,
Kubo M,
Deangelis MM,
Léveillard T,
Thorsteinsdottir U,
Haines JL,
Farrer LA,
Heid IM,
Abecasis GR
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
페이지 7개
Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study
Shrine N,
Portelli MA,
John C,
Soler Artigas M,
Bennett N,
Hall R,
Lewis J,
Henry AP,
Billington CK,
Ahmad A,
Packer RJ,
Shaw D
외 31명 — 모두 보기
Pogson ZEK,
Fogarty A,
McKeever TM,
Singapuri A,
Heaney LG,
Mansur AH,
Chaudhuri R,
Thomson NC,
Holloway JW,
Lockett GA,
Howarth PH,
Djukanovic R,
Hankinson J,
Niven R,
Simpson A,
Chung KF,
Sterk PJ,
Blakey JD,
Adcock IM,
Hu S,
Guo Y,
Obeidat M,
Sin DD,
van den Berge M,
Nickle DC,
Bossé Y,
Tobin MD,
Hall IP,
Brightling CE,
Wain LV,
Sayers I
The Lancet. Respiratory medicine · 2019 · PMID 30552067 · open access
페이지 7개
Age-of-onset information helps identify 76 genetic variants associated with allergic disease
Ferreira MAR,
Vonk JM,
Baurecht H,
Marenholz I,
Tian C,
Hoffman JD,
Helmer Q,
Tillander A,
Ullemar V,
Lu Y,
Grosche S,
Rüschendorf F
외 28명 — 모두 보기
Granell R,
Brumpton BM,
Fritsche LG,
Bhatta L,
Gabrielsen ME,
Nielsen JB,
Zhou W,
Hveem K,
Langhammer A,
Holmen OL,
Løset M,
Abecasis GR,
Willer CJ,
Emami NC,
Cavazos TB,
Witte JS,
Szwajda A,
Hinds DA,
Hübner N,
Weidinger S,
Magnusson PK,
Jorgenson E,
Karlsson R,
Paternoster L,
Boomsma DI,
Almqvist C,
Lee YA,
Koppelman GH
23andMe Research Team · collaborators of the SHARE study
PLoS genetics · 2020 · PMID 32603359 · open access
페이지 7개
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
Wain LV,
Shrine N,
Miller S,
Jackson VE,
Ntalla I,
Soler Artigas M,
Billington CK,
Kheirallah AK,
Allen R,
Cook JP,
Probert K,
Obeidat M
외 27명 — 모두 보기
Bossé Y,
Hao K,
Postma DS,
Paré PD,
Ramasamy A,
Mägi R,
Mihailov E,
Reinmaa E,
Melén E,
O'Connell J,
Frangou E,
Delaneau O,
Freeman C,
Petkova D,
McCarthy M,
Sayers I,
Deloukas P,
Hubbard R,
Pavord I,
Hansell AL,
Thomson NC,
Zeggini E,
Morris AP,
Marchini J,
Strachan DP,
Tobin MD,
Hall IP
UK Brain Expression Consortium (UKBEC) · OxGSK Consortium
The Lancet. Respiratory medicine · 2015 · PMID 26423011 · open access
페이지 6개
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis
Gharahkhani P,
Fitzgerald RC,
Vaughan TL,
Palles C,
Gockel I,
Tomlinson I,
Buas MF,
May A,
Gerges C,
Anders M,
Becker J,
Kreuser N
외 57명 — 모두 보기
Noder T,
Venerito M,
Veits L,
Schmidt T,
Manner H,
Schmidt C,
Hess T,
Böhmer AC,
Izbicki JR,
Hölscher AH,
Lang H,
Lorenz D,
Schumacher B,
Hackelsberger A,
Mayershofer R,
Pech O,
Vashist Y,
Ott K,
Vieth M,
Weismüller J,
Nöthen MM,
Attwood S,
Barr H,
Chegwidden L,
de Caestecker J,
Harrison R,
Love SB,
MacDonald D,
Moayyedi P,
Prenen H,
Watson RGP,
Iyer PG,
Anderson LA,
Bernstein L,
Chow WH,
Hardie LJ,
Lagergren J,
Liu G,
Risch HA,
Wu AH,
Ye W,
Bird NC,
Shaheen NJ,
Gammon MD,
Corley DA,
Caldas C,
Moebus S,
Knapp M,
Peters WHM,
Neuhaus H,
Rösch T,
Ell C,
MacGregor S,
Pharoah P,
Whiteman DC,
Jankowski J,
Schumacher J
Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) · Esophageal Adenocarcinoma GenEtics Consortium (EAGLE) 외 컨소시엄 1곳
The Lancet. Oncology · 2016 · PMID 27527254 · open access
페이지 6개
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Klarin D,
Verma SS,
Judy R,
Dikilitas O,
Wolford BN,
Paranjpe I,
Levin MG,
Pan C,
Tcheandjieu C,
Spin JM,
Lynch J,
Assimes TL
외 41명 — 모두 보기
Åldstedt Nyrønning L,
Mattsson E,
Edwards TL,
Denny J,
Larson E,
Lee MTM,
Carrell D,
Zhang Y,
Jarvik GP,
Gharavi AG,
Harley J,
Mentch F,
Pacheco JA,
Hakonarson H,
Skogholt AH,
Thomas L,
Gabrielsen ME,
Hveem K,
Nielsen JB,
Zhou W,
Fritsche L,
Huang J,
Natarajan P,
Sun YV,
DuVall SL,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Scali ST,
Berceli SA,
Willer C,
Jones GT,
Bown MJ,
Nadkarni G,
Kullo IJ,
Ritchie M,
Damrauer SM,
Tsao PS
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
페이지 6개
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension
Lu X,
Wang L,
Lin X,
Huang J,
Charles Gu C,
He M,
Shen H,
He J,
Zhu J,
Li H,
Hixson JE,
Wu T
외 37명 — 모두 보기
Dai J,
Lu L,
Shen C,
Chen S,
He L,
Mo Z,
Hao Y,
Mo X,
Yang X,
Li J,
Cao J,
Chen J,
Fan Z,
Li Y,
Zhao L,
Li H,
Lu F,
Yao C,
Yu L,
Xu L,
Mu J,
Wu X,
Deng Y,
Hu D,
Zhang W,
Ji X,
Guo D,
Guo Z,
Zhou Z,
Yang Z,
Wang R,
Yang J,
Zhou X,
Yan W,
Sun N,
Gao P,
Gu D
Human molecular genetics · 2015 · PMID 25249183
페이지 5개
Stroke genetics informs drug discovery and risk prediction across ancestries
Mishra A,
Malik R,
Hachiya T,
Jürgenson T,
Namba S,
Posner DC,
Kamanu FK,
Koido M,
Le Grand Q,
Shi M,
He Y,
Georgakis MK
외 175명 — 모두 보기
Caro I,
Krebs K,
Liaw YC,
Vaura FC,
Lin K,
Winsvold BS,
Srinivasasainagendra V,
Parodi L,
Bae HJ,
Chauhan G,
Chong MR,
Tomppo L,
Akinyemi R,
Roshchupkin GV,
Habib N,
Jee YH,
Thomassen JQ,
Abedi V,
Cárcel-Márquez J,
Nygaard M,
Leonard HL,
Yang C,
Yonova-Doing E,
Knol MJ,
Lewis AJ,
Judy RL,
Ago T,
Amouyel P,
Armstrong ND,
Bakker MK,
Bartz TM,
Bennett DA,
Bis JC,
Bordes C,
Børte S,
Cain A,
Ridker PM,
Cho K,
Chen Z,
Cruchaga C,
Cole JW,
de Jager PL,
de Cid R,
Endres M,
Ferreira LE,
Geerlings MI,
Gasca NC,
Gudnason V,
Hata J,
He J,
Heath AK,
Ho YL,
Havulinna AS,
Hopewell JC,
Hyacinth HI,
Inouye M,
Jacob MA,
Jeon CE,
Jern C,
Kamouchi M,
Keene KL,
Kitazono T,
Kittner SJ,
Konuma T,
Kumar A,
Lacaze P,
Launer LJ,
Lee KJ,
Lepik K,
Li J,
Li L,
Manichaikul A,
Markus HS,
Marston NA,
Meitinger T,
Mitchell BD,
Montellano FA,
Morisaki T,
Mosley TH,
Nalls MA,
Nordestgaard BG,
O'Donnell MJ,
Okada Y,
Onland-Moret NC,
Ovbiagele B,
Peters A,
Psaty BM,
Rich SS,
Rosand J,
Sabatine MS,
Sacco RL,
Saleheen D,
Sandset EC,
Salomaa V,
Sargurupremraj M,
Sasaki M,
Satizabal CL,
Schmidt CO,
Shimizu A,
Smith NL,
Sloane KL,
Sutoh Y,
Sun YV,
Tanno K,
Tiedt S,
Tatlisumak T,
Torres-Aguila NP,
Tiwari HK,
Trégouët DA,
Trompet S,
Tuladhar AM,
Tybjærg-Hansen A,
van Vugt M,
Vibo R,
Verma SS,
Wiggins KL,
Wennberg P,
Woo D,
Wilson PWF,
Xu H,
Yang Q,
Yoon K,
Millwood IY,
Gieger C,
Ninomiya T,
Grabe HJ,
Jukema JW,
Rissanen IL,
Strbian D,
Kim YJ,
Chen PH,
Mayerhofer E,
Howson JMM,
Irvin MR,
Adams H,
Wassertheil-Smoller S,
Christensen K,
Ikram MA,
Rundek T,
Worrall BB,
Lathrop GM,
Riaz M,
Simonsick EM,
Kõrv J,
França PHC,
Zand R,
Prasad K,
Frikke-Schmidt R,
de Leeuw FE,
Liman T,
Haeusler KG,
Ruigrok YM,
Heuschmann PU,
Longstreth WT,
Jung KJ,
Bastarache L,
Paré G,
Damrauer SM,
Chasman DI,
Rotter JI,
Anderson CD,
Zwart JA,
Niiranen TJ,
Fornage M,
Liaw YP,
Seshadri S,
Fernández-Cadenas I,
Walters RG,
Ruff CT,
Owolabi MO,
Huffman JE,
Milani L,
Kamatani Y,
Dichgans M,
Debette S
COMPASS Consortium · INVENT Consortium 외 컨소시엄 13곳
Nature · 2022 · PMID 36180795 · open access
페이지 5개
Regulatory Variants on the Leukocyte Immunoglobulin-Like Receptor Gene Cluster are Associated with Crohn's Disease and Interact with Regulatory Variants for TAP2
Kim K,
Oh SJ,
Lee J,
Kwon A,
Yu CY,
Kim S,
Choi CH,
Kang SB,
Kim TO,
Park DI,
Lee CK
Journal of Crohn's & colitis · 2024 · PMID 37523193
페이지 5개
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Chen ZJ,
Zhao H,
He L,
Shi Y,
Qin Y,
Shi Y,
Li Z,
You L,
Zhao J,
Liu J,
Liang X,
Zhao X
외 22명 — 모두 보기
Zhao J,
Sun Y,
Zhang B,
Jiang H,
Zhao D,
Bian Y,
Gao X,
Geng L,
Li Y,
Zhu D,
Sun X,
Xu JE,
Hao C,
Ren CE,
Zhang Y,
Chen S,
Zhang W,
Yang A,
Yan J,
Li Y,
Ma J,
Zhao Y
Nature genetics · 2011 · PMID 21151128
페이지 4개
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Shi Y,
Zhao H,
Shi Y,
Cao Y,
Yang D,
Li Z,
Zhang B,
Liang X,
Li T,
Chen J,
Shen J,
Zhao J
외 41명 — 모두 보기
You L,
Gao X,
Zhu D,
Zhao X,
Yan Y,
Qin Y,
Li W,
Yan J,
Wang Q,
Zhao J,
Geng L,
Ma J,
Zhao Y,
He G,
Zhang A,
Zou S,
Yang A,
Liu J,
Li W,
Li B,
Wan C,
Qin Y,
Shi J,
Yang J,
Jiang H,
Xu JE,
Qi X,
Sun Y,
Zhang Y,
Hao C,
Ju X,
Zhao D,
Ren CE,
Li X,
Zhang W,
Zhang Y,
Zhang J,
Wu D,
Zhang C,
He L,
Chen ZJ
Nature genetics · 2012 · PMID 22885925
페이지 4개
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
외 70명 — 모두 보기
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
페이지 4개
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development
Nielsen JB,
Fritsche LG,
Zhou W,
Teslovich TM,
Holmen OL,
Gustafsson S,
Gabrielsen ME,
Schmidt EM,
Beaumont R,
Wolford BN,
Lin M,
Brummett CM
외 33명 — 모두 보기
Preuss MH,
Refsgaard L,
Bottinger EP,
Graham SE,
Surakka I,
Chu Y,
Skogholt AH,
Dalen H,
Boyle AP,
Oral H,
Herron TJ,
Kitzman J,
Jalife J,
Svendsen JH,
Olesen MS,
Njølstad I,
Løchen ML,
Baras A,
Gottesman O,
Marcketta A,
O'Dushlaine C,
Ritchie MD,
Wilsgaard T,
Loos RJF,
Frayling TM,
Boehnke M,
Ingelsson E,
Carey DJ,
Dewey FE,
Kang HM,
Abecasis GR,
Hveem K,
Willer CJ
American journal of human genetics · 2018 · PMID 29290336
페이지 4개
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study
Yu H,
Yan H,
Wang L,
Li J,
Tan L,
Deng W,
Chen Q,
Yang G,
Zhang F,
Lu T,
Yang J,
Li K
외 12명 — 모두 보기
Lv L,
Tan Q,
Zhang H,
Xiao X,
Li M,
Ma X,
Yang F,
Li L,
Wang C,
Li T,
Zhang D,
Yue W
Chinese Antipsychotics Pharmacogenomics Consortium
The lancet. Psychiatry · 2018 · PMID 29503163
페이지 4개
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis
Rhodes CJ,
Batai K,
Bleda M,
Haimel M,
Southgate L,
Germain M,
Pauciulo MW,
Hadinnapola C,
Aman J,
Girerd B,
Arora A,
Knight J
외 106명 — 모두 보기
Hanscombe KB,
Karnes JH,
Kaakinen M,
Gall H,
Ulrich A,
Harbaum L,
Cebola I,
Ferrer J,
Lutz K,
Swietlik EM,
Ahmad F,
Amouyel P,
Archer SL,
Argula R,
Austin ED,
Badesch D,
Bakshi S,
Barnett C,
Benza R,
Bhatt N,
Bogaard HJ,
Burger CD,
Chakinala M,
Church C,
Coghlan JG,
Condliffe R,
Corris PA,
Danesino C,
Debette S,
Elliott CG,
Elwing J,
Eyries M,
Fortin T,
Franke A,
Frantz RP,
Frost A,
Garcia JGN,
Ghio S,
Ghofrani HA,
Gibbs JSR,
Harley J,
He H,
Hill NS,
Hirsch R,
Houweling AC,
Howard LS,
Ivy D,
Kiely DG,
Klinger J,
Kovacs G,
Lahm T,
Laudes M,
Machado RD,
MacKenzie Ross RV,
Marsolo K,
Martin LJ,
Moledina S,
Montani D,
Nathan SD,
Newnham M,
Olschewski A,
Olschewski H,
Oudiz RJ,
Ouwehand WH,
Peacock AJ,
Pepke-Zaba J,
Rehman Z,
Robbins I,
Roden DM,
Rosenzweig EB,
Saydain G,
Scelsi L,
Schilz R,
Seeger W,
Shaffer CM,
Simms RW,
Simon M,
Sitbon O,
Suntharalingam J,
Tang H,
Tchourbanov AY,
Thenappan T,
Torres F,
Toshner MR,
Treacy CM,
Vonk Noordegraaf A,
Waisfisz Q,
Walsworth AK,
Walter RE,
Wharton J,
White RJ,
Wilt J,
Wort SJ,
Yung D,
Lawrie A,
Humbert M,
Soubrier F,
Trégouët DA,
Prokopenko I,
Kittles R,
Gräf S,
Nichols WC,
Trembath RC,
Desai AA,
Morrell NW,
Wilkins MR
UK NIHR BioResource Rare Diseases Consortium · UK PAH Cohort Study Consortium 외 컨소시엄 1곳
The Lancet. Respiratory medicine · 2019 · PMID 30527956 · open access
페이지 4개
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
Zheng T,
Ellinghaus D,
Juzenas S,
Cossais F,
Burmeister G,
Mayr G,
Jørgensen IF,
Teder-Laving M,
Skogholt AH,
Chen S,
Strege PR,
Ito G
외 73명 — 모두 보기
Banasik K,
Becker T,
Bokelmann F,
Brunak S,
Buch S,
Clausnitzer H,
Datz C,
Degenhardt F,
Doniec M,
Erikstrup C,
Esko T,
Forster M,
Frey N,
Fritsche LG,
Gabrielsen ME,
Gräßle T,
Gsur A,
Gross J,
Hampe J,
Hendricks A,
Hinz S,
Hveem K,
Jongen J,
Junker R,
Karlsen TH,
Hemmrich-Stanisak G,
Kruis W,
Kupcinskas J,
Laubert T,
Rosenstiel PC,
Röcken C,
Laudes M,
Leendertz FH,
Lieb W,
Limperger V,
Margetis N,
Mätz-Rensing K,
Németh CG,
Ness-Jensen E,
Nowak-Göttl U,
Pandit A,
Pedersen OB,
Peleikis HG,
Peuker K,
Rodriguez CL,
Rühlemann MC,
Schniewind B,
Schulzky M,
Skieceviciene J,
Tepel J,
Thomas L,
Uellendahl-Werth F,
Ullum H,
Vogel I,
Volzke H,
von Fersen L,
von Schönfels W,
Vanderwerff B,
Wilking J,
Wittig M,
Zeissig S,
Zobel M,
Zawistowski M,
Vacic V,
Sazonova O,
Noblin ES,
Farrugia G,
Beyder A,
Wedel T,
Kahlke V,
Schafmayer C,
D'Amato M,
Franke A
DBDS Consortium · 23andMe Research Team
Gut · 2021 · PMID 33888516 · open access
페이지 4개
GWAS of Chronic Spontaneous Urticaria Reveals Genetic Overlap with Autoimmune Diseases, Not Atopic Diseases
Zhang L,
Qiu L,
Wu J,
Qi Y,
Gao X,
He C,
Qi R,
Wang H,
Yao X,
Zhu H,
Li Y,
Hao S
외 33명 — 모두 보기
Lu Q,
Long H,
Lian S,
Zhu W,
Zhang H,
Lai W,
Su X,
Lu R,
Guo Z,
Li J,
Li M,
Liu Q,
Wang H,
He L,
Nong X,
Li F,
Li Y,
Yao C,
Xu J,
Tang H,
Wang D,
Li Z,
Yu H,
Xiao S,
An J,
Pu X,
Yu S,
Zhang J,
Chen X,
Wang H,
Huang W,
Chen H,
Xiao T
The Journal of investigative dermatology · 2023 · PMID 35933036
페이지 4개
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.