For researchers
Is your paper here?
2,665 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.
7 matches for
Kottyan LC.
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
Yin X,
Kim K,
Suetsugu H,
Bang SY,
Wen L,
Koido M,
Ha E,
Liu L,
Sakamoto Y,
Jo S,
Leng RX,
Otomo N
and 76 more — show all
Laurynenka V,
Kwon YC,
Sheng Y,
Sugano N,
Sugano N,
Hwang MY,
Li W,
Mukai M,
Yoon K,
Cai M,
Ishigaki K,
Chung WT,
Huang H,
Takahashi D,
Lee SS,
Wang M,
Karino K,
Shim SC,
Zheng X,
Miyamura T,
Kang YM,
Ye D,
Nakamura J,
Suh CH,
Tang Y,
Motomura G,
Park YB,
Ding H,
Kuroda T,
Choe JY,
Li C,
Niiro H,
Park Y,
Shen C,
Miyamoto T,
Ahn GY,
Fei W,
Takeuchi T,
Shin JM,
Li K,
Kawaguchi Y,
Lee YK,
Wang Y,
Amano K,
Park DJ,
Yang W,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Suzuki A,
Sumida T,
Okada Y,
Matsuda K,
Matsuo K,
Kochi Y,
Kottyan LC,
Weirauch MT,
Parameswaran S,
Eswar S,
Salim H,
Chen X,
Yamamoto K,
Harley JB,
Ohmura K,
Kim TH,
Yang S,
Yamamoto T,
Kim BJ,
Shen N,
Ikegawa S,
Lee HS,
Zhang X,
Terao C,
Cui Y,
Bae SC
Japanese Research Committee on Idiopathic Osteonecrosis of the Femoral Head
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
12 pages+
Genome-wide meta-analysis identifies novel risk loci for uterine fibroids within and across multiple ancestry groups
Kim J,
Williams A,
Noh H,
Jasper EA,
Jones SH,
Jaworski JA,
Shuey MM,
Ruiz-Narváez EA,
Wise LA,
Palmer JR,
Connolly J,
Keaton JM
and 11 more — show all
Denny JC,
Khan A,
Abbass MA,
Rasmussen-Torvik LJ,
Kottyan LC,
Madhivanan P,
Krupp K,
Wei WQ,
Edwards TL,
Velez Edwards DR,
Hellwege JN
Nature communications · 2025 · PMID 40050615 · open access
12 pages+
Genetic influences on susceptibility to rheumatoid arthritis in African-Americans
Laufer VA,
Tiwari HK,
Reynolds RJ,
Danila MI,
Wang J,
Edberg JC,
Kimberly RP,
Kottyan LC,
Harley JB,
Mikuls TR,
Gregersen PK,
Absher DM
and 3 more — show all
Human molecular genetics · 2019 · PMID 30423114
4 pages
Medical Records-Based Genetic Studies of the Complement System
Khan A,
Shang N,
Petukhova L,
Zhang J,
Shen Y,
Hebbring SJ,
Moncrieffe H,
Kottyan LC,
Namjou-Khales B,
Knevel R,
Raychaudhuri S,
Karlson EW
and 9 more — show all
Journal of the American Society of Nephrology : JASN · 2021 · PMID 33941608
3 pages
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Levin MG,
Tsao NL,
Singhal P,
Liu C,
Vy HMT,
Paranjpe I,
Backman JD,
Bellomo TR,
Bone WP,
Biddinger KJ,
Hui Q,
Dikilitas O
and 31 more — show all
Satterfield BA,
Yang Y,
Morley MP,
Bradford Y,
Burke M,
Reza N,
Charest B,
Judy RL,
Puckelwartz MJ,
Hakonarson H,
Khan A,
Kottyan LC,
Kullo I,
Luo Y,
McNally EM,
Rasmussen-Torvik LJ,
Day SM,
Do R,
Phillips LS,
Ellinor PT,
Nadkarni GN,
Ritchie MD,
Arany Z,
Cappola TP,
Margulies KB,
Aragam KG,
Haggerty CM,
Joseph J,
Sun YV,
Voight BF,
Damrauer SM
Regeneron Genetics Center
Nature communications · 2022 · PMID 36376295 · open access
3 pages
Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease
Kottyan LC,
Davis BP,
Sherrill JD,
Liu K,
Rochman M,
Kaufman K,
Weirauch MT,
Vaughn S,
Lazaro S,
Rupert AM,
Kohram M,
Stucke EM
and 17 more — show all
Kemme KA,
Magnusen A,
He H,
Dexheimer P,
Chehade M,
Wood RA,
Pesek RD,
Vickery BP,
Fleischer DM,
Lindbad R,
Sampson HA,
Mukkada VA,
Putnam PE,
Abonia JP,
Martin LJ,
Harley JB,
Rothenberg ME
Nature genetics · 2014 · PMID 25017104 · open access
2 pages
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
Zhang G,
Feenstra B,
Bacelis J,
Liu X,
Muglia LM,
Juodakis J,
Miller DE,
Litterman N,
Jiang PP,
Russell L,
Hinds DA,
Hu Y
and 26 more — show all
Weirauch MT,
Chen X,
Chavan AR,
Wagner GP,
Pavličev M,
Nnamani MC,
Maziarz J,
Karjalainen MK,
Rämet M,
Sengpiel V,
Geller F,
Boyd HA,
Palotie A,
Momany A,
Bedell B,
Ryckman KK,
Huusko JM,
Forney CR,
Kottyan LC,
Hallman M,
Teramo K,
Nohr EA,
Davey Smith G,
Melbye M,
Jacobsson B,
Muglia LJ
The New England journal of medicine · 2017 · PMID 28877031 · open access
2 pages
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.