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14 matches for
Jiang L.
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Okada Y,
Wu D,
Trynka G,
Raj T,
Terao C,
Ikari K,
Kochi Y,
Ohmura K,
Suzuki A,
Yoshida S,
Graham RR,
Manoharan A
and 83 more — show all
Ortmann W,
Bhangale T,
Denny JC,
Carroll RJ,
Eyler AE,
Greenberg JD,
Kremer JM,
Pappas DA,
Jiang L,
Yin J,
Ye L,
Su DF,
Yang J,
Xie G,
Keystone E,
Westra HJ,
Esko T,
Metspalu A,
Zhou X,
Gupta N,
Mirel D,
Stahl EA,
Diogo D,
Cui J,
Liao K,
Guo MH,
Myouzen K,
Kawaguchi T,
Coenen MJ,
van Riel PL,
van de Laar MA,
Guchelaar HJ,
Huizinga TW,
Dieudé P,
Mariette X,
Bridges SL Jr,
Zhernakova A,
Toes RE,
Tak PP,
Miceli-Richard C,
Bang SY,
Lee HS,
Martin J,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Rantapää-Dahlqvist S,
Arlestig L,
Choi HK,
Kamatani Y,
Galan P,
Lathrop M,
Eyre S,
Bowes J,
Barton A,
de Vries N,
Moreland LW,
Criswell LA,
Karlson EW,
Taniguchi A,
Yamada R,
Kubo M,
Liu JS,
Bae SC,
Worthington J,
Padyukov L,
Klareskog L,
Gregersen PK,
Raychaudhuri S,
Stranger BE,
De Jager PL,
Franke L,
Visscher PM,
Brown MA,
Yamanaka H,
Mimori T,
Takahashi A,
Xu H,
Behrens TW,
Siminovitch KA,
Momohara S,
Matsuda F,
Yamamoto K,
Plenge RM
RACI consortium · GARNET consortium
Nature · 2014 · PMID 24390342 · open access
12 pages+
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
Lagou V,
Jiang L,
Ulrich A,
Zudina L,
González KSG,
Balkhiyarova Z,
Faggian A,
Maina JG,
Chen S,
Todorov PV,
Sharapov S,
David A
and 84 more — show all
Marullo L,
Mägi R,
Rujan RM,
Ahlqvist E,
Thorleifsson G,
Gao Η,
Εvangelou Ε,
Benyamin B,
Scott RA,
Isaacs A,
Zhao JH,
Willems SM,
Johnson T,
Gieger C,
Grallert H,
Meisinger C,
Müller-Nurasyid M,
Strawbridge RJ,
Goel A,
Rybin D,
Albrecht E,
Jackson AU,
Stringham HM,
Corrêa IR Jr,
Farber-Eger E,
Steinthorsdottir V,
Uitterlinden AG,
Munroe PB,
Brown MJ,
Schmidberger J,
Holmen O,
Thorand B,
Hveem K,
Wilsgaard T,
Mohlke KL,
Wang Z,
Shmeliov A,
den Hoed M,
Loos RJF,
Kratzer W,
Haenle M,
Koenig W,
Boehm BO,
Tan TM,
Tomas A,
Salem V,
Barroso I,
Tuomilehto J,
Boehnke M,
Florez JC,
Hamsten A,
Watkins H,
Njølstad I,
Wichmann HE,
Caulfield MJ,
Khaw KT,
van Duijn CM,
Hofman A,
Wareham NJ,
Langenberg C,
Whitfield JB,
Martin NG,
Montgomery G,
Scapoli C,
Tzoulaki I,
Elliott P,
Thorsteinsdottir U,
Stefansson K,
Brittain EL,
McCarthy MI,
Froguel P,
Sexton PM,
Wootten D,
Groop L,
Dupuis J,
Meigs JB,
Deganutti G,
Demirkan A,
Pers TH,
Reynolds CA,
Aulchenko YS,
Kaakinen MA,
Jones B,
Prokopenko I
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
12 pages+
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study
Ortiz-Fernández L,
Saruhan-Direskeneli G,
Alibaz-Oner F,
Kaymaz-Tahra S,
Coit P,
Kong X,
Kiprianos AP,
Maughan RT,
Aydin SZ,
Aksu K,
Keser G,
Kamali S
and 59 more — show all
Inanc M,
Springer J,
Akar S,
Onen F,
Akkoc N,
Khalidi NA,
Koening C,
Karadag O,
Kiraz S,
Forbess L,
Langford CA,
McAlear CA,
Ozbalkan Z,
Yavuz S,
Çetin GY,
Alpay-Kanitez N,
Chung S,
Ates A,
Karaaslan Y,
McKinnon-Maksimowicz K,
Monach PA,
Ozer HTE,
Seyahi E,
Fresko I,
Cefle A,
Seo P,
Warrington KJ,
Ozturk MA,
Ytterberg SR,
Cobankara V,
Onat AM,
Duzgun N,
Bıcakcıgil M,
Yentür SP,
Lally L,
Manfredi AA,
Baldissera E,
Erken E,
Yazici A,
Kısacık B,
Kaşifoğlu T,
Dalkilic E,
Cuthbertson D,
Pagnoux C,
Sreih A,
Reales G,
Wallace C,
Wren JD,
Cunninghame-Graham DS,
Vyse TJ,
Sun Y,
Chen H,
Grayson PC,
Tombetti E,
Jiang L,
Mason JC,
Merkel PA,
Direskeneli H,
Sawalha AH
American journal of human genetics · 2021 · PMID 33308445
6 pages
Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci
Cortes A,
Hadler J,
Pointon JP,
Robinson PC,
Karaderi T,
Leo P,
Cremin K,
Pryce K,
Harris J,
Lee S,
Joo KB,
Shim SC
and 53 more — show all
Weisman M,
Ward M,
Zhou X,
Garchon HJ,
Chiocchia G,
Nossent J,
Lie BA,
Førre Ø,
Tuomilehto J,
Laiho K,
Jiang L,
Liu Y,
Wu X,
Bradbury LA,
Elewaut D,
Burgos-Vargas R,
Stebbings S,
Appleton L,
Farrah C,
Lau J,
Kenna TJ,
Haroon N,
Ferreira MA,
Yang J,
Mulero J,
Fernandez-Sueiro JL,
Gonzalez-Gay MA,
Lopez-Larrea C,
Deloukas P,
Donnelly P,
Bowness P,
Gafney K,
Gaston H,
Gladman DD,
Rahman P,
Maksymowych WP,
Xu H,
Crusius JB,
van der Horst-Bruinsma IE,
Chou CT,
Valle-Oñate R,
Romero-Sánchez C,
Hansen IM,
Pimentel-Santos FM,
Inman RD,
Videm V,
Martin J,
Breban M,
Reveille JD,
Evans DM,
Kim TH,
Wordsworth BP,
Brown MA
International Genetics of Ankylosing Spondylitis Consortium (IGAS) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) and 4 more consortia
Nature genetics · 2013 · PMID 23749187
4 pages
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
Evans DM,
Spencer CC,
Pointon JJ,
Su Z,
Harvey D,
Kochan G,
Oppermann U,
Dilthey A,
Pirinen M,
Stone MA,
Appleton L,
Moutsianas L
and 81 more — show all
Leslie S,
Wordsworth T,
Kenna TJ,
Karaderi T,
Thomas GP,
Ward MM,
Weisman MH,
Farrar C,
Bradbury LA,
Danoy P,
Inman RD,
Maksymowych W,
Gladman D,
Rahman P,
Morgan A,
Marzo-Ortega H,
Bowness P,
Gaffney K,
Gaston JS,
Smith M,
Bruges-Armas J,
Couto AR,
Sorrentino R,
Paladini F,
Ferreira MA,
Xu H,
Liu Y,
Jiang L,
Lopez-Larrea C,
Díaz-Peña R,
López-Vázquez A,
Zayats T,
Band G,
Bellenguez C,
Blackburn H,
Blackwell JM,
Bramon E,
Bumpstead SJ,
Casas JP,
Corvin A,
Craddock N,
Deloukas P,
Dronov S,
Duncanson A,
Edkins S,
Freeman C,
Gillman M,
Gray E,
Gwilliam R,
Hammond N,
Hunt SE,
Jankowski J,
Jayakumar A,
Langford C,
Liddle J,
Markus HS,
Mathew CG,
McCann OT,
McCarthy MI,
Palmer CN,
Peltonen L,
Plomin R,
Potter SC,
Rautanen A,
Ravindrarajah R,
Ricketts M,
Samani N,
Sawcer SJ,
Strange A,
Trembath RC,
Viswanathan AC,
Waller M,
Weston P,
Whittaker P,
Widaa S,
Wood NW,
McVean G,
Reveille JD,
Wordsworth BP,
Brown MA,
Donnelly P
Spondyloarthritis Research Consortium of Canada (SPARCC) · Australo-Anglo-American Spondyloarthritis Consortium (TASC) and 1 more consortia
Nature genetics · 2011 · PMID 21743469
3 pages
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Lagou V,
Mägi R,
Hottenga JJ,
Grallert H,
Perry JRB,
Bouatia-Naji N,
Marullo L,
Rybin D,
Jansen R,
Min JL,
Dimas AS,
Ulrich A
and 192 more — show all
Zudina L,
Gådin JR,
Jiang L,
Faggian A,
Bonnefond A,
Fadista J,
Stathopoulou MG,
Isaacs A,
Willems SM,
Navarro P,
Tanaka T,
Jackson AU,
Montasser ME,
O'Connell JR,
Bielak LF,
Webster RJ,
Saxena R,
Stafford JM,
Pourcain BS,
Timpson NJ,
Salo P,
Shin SY,
Amin N,
Smith AV,
Li G,
Verweij N,
Goel A,
Ford I,
Johnson PCD,
Johnson T,
Kapur K,
Thorleifsson G,
Strawbridge RJ,
Rasmussen-Torvik LJ,
Esko T,
Mihailov E,
Fall T,
Fraser RM,
Mahajan A,
Kanoni S,
Giedraitis V,
Kleber ME,
Silbernagel G,
Meyer J,
Müller-Nurasyid M,
Ganna A,
Sarin AP,
Yengo L,
Shungin D,
Luan J,
Horikoshi M,
An P,
Sanna S,
Boettcher Y,
Rayner NW,
Nolte IM,
Zemunik T,
Iperen EV,
Kovacs P,
Hastie ND,
Wild SH,
McLachlan S,
Campbell S,
Polasek O,
Carlson O,
Egan J,
Kiess W,
Willemsen G,
Kuusisto J,
Laakso M,
Dimitriou M,
Hicks AA,
Rauramaa R,
Bandinelli S,
Thorand B,
Liu Y,
Miljkovic I,
Lind L,
Doney A,
Perola M,
Hingorani A,
Kivimaki M,
Kumari M,
Bennett AJ,
Groves CJ,
Herder C,
Koistinen HA,
Kinnunen L,
Faire U,
Bakker SJL,
Uusitupa M,
Palmer CNA,
Jukema JW,
Sattar N,
Pouta A,
Snieder H,
Boerwinkle E,
Pankow JS,
Magnusson PK,
Krus U,
Scapoli C,
de Geus EJCN,
Blüher M,
Wolffenbuttel BHR,
Province MA,
Abecasis GR,
Meigs JB,
Hovingh GK,
Lindström J,
Wilson JF,
Wright AF,
Dedoussis GV,
Bornstein SR,
Schwarz PEH,
Tönjes A,
Winkelmann BR,
Boehm BO,
März W,
Metspalu A,
Price JF,
Deloukas P,
Körner A,
Lakka TA,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Bergman RN,
Tuomilehto J,
Wareham NJ,
Langenberg C,
Männistö S,
Franks PW,
Hayward C,
Vitart V,
Kaprio J,
Visvikis-Siest S,
Balkau B,
Altshuler D,
Rudan I,
Stumvoll M,
Campbell H,
van Duijn CM,
Gieger C,
Illig T,
Ferrucci L,
Pedersen NL,
Pramstaller PP,
Boehnke M,
Frayling TM,
Shuldiner AR,
Peyser PA,
Kardia SLR,
Palmer LJ,
Penninx BW,
Meneton P,
Harris TB,
Navis G,
Harst PV,
Smith GD,
Forouhi NG,
Loos RJF,
Salomaa V,
Soranzo N,
Boomsma DI,
Groop L,
Tuomi T,
Hofman A,
Munroe PB,
Gudnason V,
Siscovick DS,
Watkins H,
Lecoeur C,
Vollenweider P,
Franco-Cereceda A,
Eriksson P,
Jarvelin MR,
Stefansson K,
Hamsten A,
Nicholson G,
Karpe F,
Dermitzakis ET,
Lindgren CM,
McCarthy MI,
Froguel P,
Kaakinen MA,
Lyssenko V,
Watanabe RM,
Ingelsson E,
Florez JC,
Dupuis J,
Barroso I,
Morris AP,
Prokopenko I
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Jiang L,
Yin J,
Ye L,
Yang J,
Hemani G,
Liu AJ,
Zou H,
He D,
Sun L,
Zeng X,
Li Z,
Zheng Y
and 61 more — show all
Lin Y,
Liu Y,
Fang Y,
Xu J,
Li Y,
Dai S,
Guan J,
Jiang L,
Wei Q,
Wang Y,
Li Y,
Huang C,
Zuo X,
Liu Y,
Wu X,
Zhang L,
Zhou L,
Zhang Q,
Li T,
Chen L,
Xu Z,
Yang X,
Qian F,
Xie W,
Liu W,
Guo Q,
Huang S,
Zhao J,
Li M,
Jin Y,
Gao J,
Lv Y,
Wang Y,
Lin L,
Guo A,
Danoy P,
Willner D,
Cremin C,
Hadler J,
Zhang F,
Zhao Y,
Li M,
Yue T,
Fan X,
Guo J,
Mu R,
Li J,
Wu C,
Zeng M,
Wang J,
Li S,
Jin L,
Wang B,
Wang J,
Ma X,
Sun L,
Zhang X,
Brown MA,
Visscher PM,
Su DF,
Xu H
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls
Zhu Z,
Tang NL,
Xu L,
Qin X,
Mao S,
Song Y,
Liu L,
Li F,
Liu P,
Yi L,
Chang J,
Jiang L
and 25 more — show all
Ng BK,
Shi B,
Zhang W,
Qiao J,
Sun X,
Qiu X,
Wang Z,
Wang F,
Xie D,
Chen L,
Chen Z,
Jin M,
Han X,
Hu Z,
Zhang Z,
Liu Z,
Zhu F,
Qian BP,
Yu Y,
Wang B,
Lee KM,
Lee WYW,
Lam TP,
Qiu Y,
Cheng JC
Nature communications · 2015 · PMID 26394188 · open access
2 pages
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Qiu F,
Tang R,
Zuo X,
Shi X,
Wei Y,
Zheng X,
Dai Y,
Gong Y,
Wang L,
Xu P,
Zhu X,
Wu J
and 78 more — show all
Han C,
Gao Y,
Zhang K,
Jiang Y,
Zhou J,
Shao Y,
Hu Z,
Tian Y,
Zhang H,
Dai N,
Liu L,
Wu X,
Zhao W,
Zhang X,
Zang Z,
Nie J,
Sun W,
Zhao Y,
Mao Y,
Jiang P,
Ji H,
Dong Q,
Li J,
Li Z,
Bai X,
Li L,
Lin M,
Dong M,
Li J,
Zhu P,
Wang C,
Zhang Y,
Jiang P,
Wang Y,
Jawed R,
Xu J,
Zhang Y,
Wang Q,
Yang Y,
Yang F,
Lian M,
Jiang X,
Xiao X,
Li Y,
Fang J,
Qiu D,
Zhu Z,
Qiu H,
Zhang J,
Tian W,
Chen S,
Jiang L,
Ji B,
Li P,
Chen G,
Wu T,
Sun Y,
Yu J,
Tang H,
He M,
Xia M,
Pei H,
Huang L,
Qing Z,
Wu J,
Huang Q,
Han J,
Xie W,
Sun Z,
Guo J,
He G,
Eric Gershwin M,
Lian Z,
Liu X,
Seldin MF,
Liu X,
Chen W,
Ma X
Nature communications · 2017 · PMID 28425483 · open access
2 pages
A genetic variant in IL-6 lowering its expression is protective for critical patients with COVID-19
Gong B,
Huang L,
He Y,
Xie W,
Yin Y,
Shi Y,
Xiao J,
Zhong L,
Zhang Y,
Jiang Z,
Hao F,
Zhou Y
and 11 more — show all
Li H,
Jiang L,
Yang X,
Song X,
Kang Y,
Tuo L,
Huang Y,
Shuai P,
Liu Y,
Zheng F,
Yang Z
Signal transduction and targeted therapy · 2022 · PMID 35368020 · open access
2 pages
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
Scott RA,
Scott LJ,
Mägi R,
Marullo L,
Gaulton KJ,
Kaakinen M,
Pervjakova N,
Pers TH,
Johnson AD,
Eicher JD,
Jackson AU,
Ferreira T
and 163 more — show all
Lee Y,
Ma C,
Steinthorsdottir V,
Thorleifsson G,
Qi L,
Van Zuydam NR,
Mahajan A,
Chen H,
Almgren P,
Voight BF,
Grallert H,
Müller-Nurasyid M,
Ried JS,
Rayner NW,
Robertson N,
Karssen LC,
van Leeuwen EM,
Willems SM,
Fuchsberger C,
Kwan P,
Teslovich TM,
Chanda P,
Li M,
Lu Y,
Dina C,
Thuillier D,
Yengo L,
Jiang L,
Sparso T,
Kestler HA,
Chheda H,
Eisele L,
Gustafsson S,
Frånberg M,
Strawbridge RJ,
Benediktsson R,
Hreidarsson AB,
Kong A,
Sigurðsson G,
Kerrison ND,
Luan J,
Liang L,
Meitinger T,
Roden M,
Thorand B,
Esko T,
Mihailov E,
Fox C,
Liu CT,
Rybin D,
Isomaa B,
Lyssenko V,
Tuomi T,
Couper DJ,
Pankow JS,
Grarup N,
Have CT,
Jørgensen ME,
Jørgensen T,
Linneberg A,
Cornelis MC,
van Dam RM,
Hunter DJ,
Kraft P,
Sun Q,
Edkins S,
Owen KR,
Perry JRB,
Wood AR,
Zeggini E,
Tajes-Fernandes J,
Abecasis GR,
Bonnycastle LL,
Chines PS,
Stringham HM,
Koistinen HA,
Kinnunen L,
Sennblad B,
Mühleisen TW,
Nöthen MM,
Pechlivanis S,
Baldassarre D,
Gertow K,
Humphries SE,
Tremoli E,
Klopp N,
Meyer J,
Steinbach G,
Wennauer R,
Eriksson JG,
Mӓnnistö S,
Peltonen L,
Tikkanen E,
Charpentier G,
Eury E,
Lobbens S,
Gigante B,
Leander K,
McLeod O,
Bottinger EP,
Gottesman O,
Ruderfer D,
Blüher M,
Kovacs P,
Tonjes A,
Maruthur NM,
Scapoli C,
Erbel R,
Jöckel KH,
Moebus S,
de Faire U,
Hamsten A,
Stumvoll M,
Deloukas P,
Donnelly PJ,
Frayling TM,
Hattersley AT,
Ripatti S,
Salomaa V,
Pedersen NL,
Boehm BO,
Bergman RN,
Collins FS,
Mohlke KL,
Tuomilehto J,
Hansen T,
Pedersen O,
Barroso I,
Lannfelt L,
Ingelsson E,
Lind L,
Lindgren CM,
Cauchi S,
Froguel P,
Loos RJF,
Balkau B,
Boeing H,
Franks PW,
Barricarte Gurrea A,
Palli D,
van der Schouw YT,
Altshuler D,
Groop LC,
Langenberg C,
Wareham NJ,
Sijbrands E,
van Duijn CM,
Florez JC,
Meigs JB,
Boerwinkle E,
Gieger C,
Strauch K,
Metspalu A,
Morris AD,
Palmer CNA,
Hu FB,
Thorsteinsdottir U,
Stefansson K,
Dupuis J,
Morris AP,
Boehnke M,
McCarthy MI,
Prokopenko I
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium
Diabetes · 2017 · PMID 28566273
1 page
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study
Foo JN,
Chew EGY,
Chung SJ,
Peng R,
Blauwendraat C,
Nalls MA,
Mok KY,
Satake W,
Toda T,
Chao Y,
Tan LCS,
Tandiono M
and 33 more — show all
Lian MM,
Ng EY,
Prakash KM,
Au WL,
Meah WY,
Mok SQ,
Annuar AA,
Chan AYY,
Chen L,
Chen Y,
Jeon BS,
Jiang L,
Lim JL,
Lin JJ,
Liu C,
Mao C,
Mok V,
Pei Z,
Shang HF,
Shi CH,
Song K,
Tan AH,
Wu YR,
Xu YM,
Xu R,
Yan Y,
Yang J,
Zhang B,
Koh WP,
Lim SY,
Khor CC,
Liu J,
Tan EK
JAMA neurology · 2020 · PMID 32310270
1 page
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My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.