For researchers
Is your paper here?
2,657 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
8 matches for
Chung S.
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 Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis
Merkel PA,
Xie G,
Monach PA,
Ji X,
Ciavatta DJ,
Byun J,
Pinder BD,
Zhao A,
Zhang J,
Tadesse Y,
Qian D,
Weirauch M
and 32 more — show all
Nair R,
Tsoi A,
Pagnoux C,
Carette S,
Chung S,
Cuthbertson D,
Davis JC Jr,
Dellaripa PF,
Forbess L,
Gewurz-Singer O,
Hoffman GS,
Khalidi N,
Koening C,
Langford CA,
Mahr AD,
McAlear C,
Moreland L,
Seo EP,
Specks U,
Spiera RF,
Sreih A,
St Clair EW,
Stone JH,
Ytterberg SR,
Elder JT,
Qu J,
Ochi T,
Hirano N,
Edberg JC,
Falk RJ,
Amos CI,
Siminovitch KA
Vasculitis Clinical Research Consortium
Arthritis & rheumatology (Hoboken, N.J.) · 2017 · PMID 28029757 · open access
4 pages
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus
Gateva V,
Sandling JK,
Hom G,
Taylor KE,
Chung SA,
Sun X,
Ortmann W,
Kosoy R,
Ferreira RC,
Nordmark G,
Gunnarsson I,
Svenungsson E
and 24 more — show all
Padyukov L,
Sturfelt G,
Jönsen A,
Bengtsson AA,
Rantapää-Dahlqvist S,
Baechler EC,
Brown EE,
Alarcón GS,
Edberg JC,
Ramsey-Goldman R,
McGwin G Jr,
Reveille JD,
Vilá LM,
Kimberly RP,
Manzi S,
Petri MA,
Lee A,
Gregersen PK,
Seldin MF,
Rönnblom L,
Criswell LA,
Syvänen AC,
Behrens TW,
Graham RR
Nature genetics · 2009 · PMID 19838195
3 pages
HLA-C*01 is a Risk Factor for Crohn's Disease
Jung ES,
Cheon JH,
Lee JH,
Park SJ,
Jang HW,
Chung SH,
Park MH,
Kim TG,
Oh HB,
Yang SK,
Park SH,
Han JY
and 4 more — show all
Inflammatory bowel diseases · 2016 · PMID 26891255
3 pages
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX
Hom G,
Graham RR,
Modrek B,
Taylor KE,
Ortmann W,
Garnier S,
Lee AT,
Chung SA,
Ferreira RC,
Pant PV,
Ballinger DG,
Kosoy R
and 15 more — show all
Demirci FY,
Kamboh MI,
Kao AH,
Tian C,
Gunnarsson I,
Bengtsson AA,
Rantapää-Dahlqvist S,
Petri M,
Manzi S,
Seldin MF,
Rönnblom L,
Syvänen AC,
Criswell LA,
Gregersen PK,
Behrens TW
The New England journal of medicine · 2008 · PMID 18204098
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
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.