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2,676 papers hold this site up. Every variant and condition page names
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Search your name, your journal, or a PMID.
7 matches for
Chang T.
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
and 322 more — show all
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 and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
9 pages
Genome-wide analysis links NFATC2 with asparaginase hypersensitivity
Fernandez CA,
Smith C,
Yang W,
Mullighan CG,
Qu C,
Larsen E,
Bowman WP,
Liu C,
Ramsey LB,
Chang T,
Karol SE,
Loh ML
and 9 more — show all
Blood · 2015 · PMID 25987655
2 pages
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study
Chen PL,
Shih SR,
Wang PW,
Lin YC,
Chu CC,
Lin JH,
Chen SC,
Chang CC,
Huang TS,
Tsai KS,
Tseng FY,
Wang CY
and 8 more — show all
Nature communications · 2015 · PMID 26151496 · open access
2 pages
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Wang H,
Chang TS,
Dombroski BA,
Cheng PL,
Patil V,
Valiente-Banuet L,
Farrell K,
Mclean C,
Molina-Porcel L,
Rajput A,
De Deyn PP,
Le Bastard N
and 49 more — show all
Gearing M,
Kaat LD,
Van Swieten JC,
Dopper E,
Ghetti BF,
Newell KL,
Troakes C,
de Yébenes JG,
Rábano-Gutierrez A,
Meller T,
Oertel WH,
Respondek G,
Stamelou M,
Arzberger T,
Roeber S,
Müller U,
Hopfner F,
Pastor P,
Brice A,
Durr A,
Le Ber I,
Beach TG,
Serrano GE,
Hazrati LN,
Litvan I,
Rademakers R,
Ross OA,
Galasko D,
Boxer AL,
Miller BL,
Seeley WW,
Van Deerlin VM,
Lee EB,
White CL 3rd,
Morris H,
de Silva R,
Crary JF,
Goate AM,
Friedman JS,
Leung YY,
Coppola G,
Naj AC,
Wang LS,
Dalgard C,
Dickson DW,
Höglinger GU,
Schellenberg GD,
Geschwind DH,
Lee WP
P. S. P. genetics study group
Molecular neurodegeneration · 2024 · PMID 39152475 · open access
2 pages
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians
Cho YS,
Chen CH,
Hu C,
Long J,
Ong RT,
Sim X,
Takeuchi F,
Wu Y,
Go MJ,
Yamauchi T,
Chang YC,
Kwak SH
and 56 more — show all
Ma RC,
Yamamoto K,
Adair LS,
Aung T,
Cai Q,
Chang LC,
Chen YT,
Gao Y,
Hu FB,
Kim HL,
Kim S,
Kim YJ,
Lee JJ,
Lee NR,
Li Y,
Liu JJ,
Lu W,
Nakamura J,
Nakashima E,
Ng DP,
Tay WT,
Tsai FJ,
Wong TY,
Yokota M,
Zheng W,
Zheng W,
Zhang R,
Wang C,
So WY,
Ohnaka K,
Ikegami H,
Hara K,
Cho YM,
Cho NH,
Chang TJ,
Bao Y,
Hedman ÅK,
Morris AP,
McCarthy MI,
Takayanagi R,
Park KS,
Jia W,
Chuang LM,
Chuang LM,
Chan JC,
Maeda S,
Kadowaki T,
Lee JY,
Wu JY,
Teo YY,
Tai ES,
Shu XO,
Mohlke KL,
Kato N,
Han BG,
Seielstad M
DIAGRAM Consortium · MuTHER Consortium
Nature genetics · 2011 · PMID 22158537
1 page
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia
Karol SE,
Yang W,
Van Driest SL,
Chang TY,
Kaste S,
Bowton E,
Basford M,
Bastarache L,
Roden DM,
Denny JC,
Larsen E,
Winick N
and 16 more — show all
Carroll WL,
Cheng C,
Pei D,
Fernandez CA,
Liu C,
Smith C,
Loh ML,
Raetz EA,
Hunger SP,
Scheet P,
Jeha S,
Pui CH,
Evans WE,
Devidas M,
Mattano LA Jr,
Relling MV
Blood · 2015 · PMID 26265699
1 page
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
Farrell K,
Humphrey J,
Chang T,
Zhao Y,
Leung YY,
Kuksa PP,
Patil V,
Lee WP,
Kuzma AB,
Valladares O,
Cantwell LB,
Wang H
and 37 more — show all
Ravi A,
De Sanctis C,
Han N,
Christie TD,
Afzal R,
Kandoi S,
Whitney K,
Krassner MM,
Ressler H,
Kim S,
Dangoor D,
Iida MA,
Casella A,
Walker RH,
Nirenberg MJ,
Renton AE,
Babrowicz B,
Coppola G,
Raj T,
Höglinger GU,
Müller U,
Golbe LI,
Morris HR,
Hardy J,
Revesz T,
Warner TT,
Jaunmuktane Z,
Mok KY,
Rademakers R,
Dickson DW,
Ross OA,
Wang LS,
Goate A,
Schellenberg G,
Geschwind DH,
Crary JF,
Naj A
PSP Genetics Study Group
Nature communications · 2024 · PMID 39251599 · open access
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
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.