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Is your paper here?
2,661 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.
9 matches for
Lee JS.
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Klarin D,
Damrauer SM,
Cho K,
Sun YV,
Teslovich TM,
Honerlaw J,
Gagnon DR,
DuVall SL,
Li J,
Peloso GM,
Chaffin M,
Small AM
and 33 more — show all
Huang J,
Tang H,
Lynch JA,
Ho YL,
Liu DJ,
Emdin CA,
Li AH,
Huffman JE,
Lee JS,
Natarajan P,
Chowdhury R,
Saleheen D,
Vujkovic M,
Baras A,
Pyarajan S,
Di Angelantonio E,
Neale BM,
Naheed A,
Khera AV,
Danesh J,
Chang KM,
Abecasis G,
Willer C,
Dewey FE,
Carey DJ,
Concato J,
Gaziano JM,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Rader DJ,
Wilson PWF,
Assimes TL
Global Lipids Genetics Consortium · Myocardial Infarction Genetics (MIGen) Consortium and 2 more consortia
Nature genetics · 2018 · PMID 30275531 · open access
12 pages+
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
Vujkovic M,
Keaton JM,
Lynch JA,
Miller DR,
Zhou J,
Tcheandjieu C,
Huffman JE,
Assimes TL,
Lorenz K,
Zhu X,
Hilliard AT,
Judy RL
and 35 more — show all
Huang J,
Lee KM,
Klarin D,
Pyarajan S,
Danesh J,
Melander O,
Rasheed A,
Mallick NH,
Hameed S,
Qureshi IH,
Afzal MN,
Malik U,
Jalal A,
Abbas S,
Sheng X,
Gao L,
Kaestner KH,
Susztak K,
Sun YV,
DuVall SL,
Cho K,
Lee JS,
Gaziano JM,
Phillips LS,
Meigs JB,
Reaven PD,
Wilson PW,
Edwards TL,
Rader DJ,
Damrauer SM,
O'Donnell CJ,
Tsao PS,
Chang KM,
Voight BF,
Saleheen D
HPAP Consortium · Regeneron Genetics Center and 1 more consortia
Nature genetics · 2020 · PMID 32541925 · open access
12 pages+
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
and 78 more — show all
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 and 2 more consortia
Nature genetics · 2022 · PMID 35654975
8 pages
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures
Styrkarsdottir U,
Stefansson OA,
Gunnarsdottir K,
Thorleifsson G,
Lund SH,
Stefansdottir L,
Juliusson K,
Agustsdottir AB,
Zink F,
Halldorsson GH,
Ivarsdottir EV,
Benonisdottir S
and 40 more — show all
Jonsson H,
Gylfason A,
Norland K,
Trajanoska K,
Boer CG,
Southam L,
Leung JCS,
Tang NLS,
Kwok TCY,
Lee JSW,
Ho SC,
Byrjalsen I,
Center JR,
Lee SH,
Koh JM,
Lohmander LS,
Ho-Pham LT,
Nguyen TV,
Eisman JA,
Woo J,
Leung PC,
Loughlin J,
Zeggini E,
Christiansen C,
Rivadeneira F,
van Meurs J,
Uitterlinden AG,
Mogensen B,
Jonsson H,
Ingvarsson T,
Sigurdsson G,
Benediktsson R,
Sulem P,
Jonsdottir I,
Masson G,
Holm H,
Norddahl GL,
Thorsteinsdottir U,
Gudbjartsson DF,
Stefansson K
Nature communications · 2019 · PMID 31053729 · open access
7 pages
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Tcheandjieu C,
Zhu X,
Hilliard AT,
Clarke SL,
Napolioni V,
Ma S,
Lee KM,
Fang H,
Chen F,
Lu Y,
Tsao NL,
Raghavan S
and 70 more — show all
Koyama S,
Gorman BR,
Vujkovic M,
Klarin D,
Levin MG,
Sinnott-Armstrong N,
Wojcik GL,
Plomondon ME,
Maddox TM,
Waldo SW,
Bick AG,
Pyarajan S,
Huang J,
Song R,
Ho YL,
Buyske S,
Kooperberg C,
Haessler J,
Loos RJF,
Do R,
Verbanck M,
Chaudhary K,
North KE,
Avery CL,
Graff M,
Haiman CA,
Le Marchand L,
Wilkens LR,
Bis JC,
Leonard H,
Shen B,
Lange LA,
Giri A,
Dikilitas O,
Kullo IJ,
Stanaway IB,
Jarvik GP,
Gordon AS,
Hebbring S,
Namjou B,
Kaufman KM,
Ito K,
Ishigaki K,
Kamatani Y,
Verma SS,
Ritchie MD,
Kember RL,
Baras A,
Lotta LA,
Kathiresan S,
Hauser ER,
Miller DR,
Lee JS,
Saleheen D,
Reaven PD,
Cho K,
Gaziano JM,
Natarajan P,
Huffman JE,
Voight BF,
Rader DJ,
Chang KM,
Lynch JA,
Damrauer SM,
Wilson PWF,
Tang H,
Sun YV,
Tsao PS,
O'Donnell CJ,
Assimes TL
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
6 pages
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures
Styrkarsdottir U,
Thorleifsson G,
Gudjonsson SA,
Sigurdsson A,
Center JR,
Lee SH,
Nguyen TV,
Kwok TCY,
Lee JSW,
Ho SC,
Woo J,
Leung PC
and 11 more — show all
Kim BJ,
Rafnar T,
Kiemeney LA,
Ingvarsson T,
Koh JM,
Tang NLS,
Eisman JA,
Christiansen C,
Sigurdsson G,
Thorsteinsdottir U,
Stefansson K
Nature communications · 2016 · PMID 26733130 · open access
3 pages
Genome-wide association study of peripheral artery disease in the Million Veteran Program
Klarin D,
Lynch J,
Aragam K,
Chaffin M,
Assimes TL,
Huang J,
Lee KM,
Shao Q,
Huffman JE,
Natarajan P,
Arya S,
Small A
and 24 more — show all
Sun YV,
Vujkovic M,
Freiberg MS,
Wang L,
Chen J,
Saleheen D,
Lee JS,
Miller DR,
Reaven P,
Alba PR,
Patterson OV,
DuVall SL,
Boden WE,
Beckman JA,
Gaziano JM,
Concato J,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Tsao PS,
Damrauer SM
VA Million Veteran Program
Nature medicine · 2019 · PMID 31285632 · open access
3 pages
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations
Miki D,
Kubo M,
Takahashi A,
Yoon KA,
Kim J,
Lee GK,
Zo JI,
Lee JS,
Hosono N,
Morizono T,
Tsunoda T,
Kamatani N
and 5 more — show all
Nature genetics · 2010 · PMID 20871597
1 page
A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population
Yoon KA,
Park JH,
Han J,
Park S,
Lee GK,
Han JY,
Zo JI,
Kim J,
Lee JE,
Takahashi A,
Kubo M,
Nakamura Y
and 1 more — show all
Human molecular genetics · 2010 · PMID 20876614
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.