For researchers
Is your paper here?
2,675 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 JE.
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Landi MT,
Bishop DT,
MacGregor S,
Machiela MJ,
Stratigos AJ,
Ghiorzo P,
Brossard M,
Calista D,
Choi J,
Fargnoli MC,
Zhang T,
Rodolfo M
and 140 more — show all
Trower AJ,
Menin C,
Martinez J,
Hadjisavvas A,
Song L,
Stefanaki I,
Scolyer R,
Yang R,
Goldstein AM,
Potrony M,
Kypreou KP,
Pastorino L,
Queirolo P,
Pellegrini C,
Cattaneo L,
Zawistowski M,
Gimenez-Xavier P,
Rodriguez A,
Elefanti L,
Manoukian S,
Rivoltini L,
Smith BH,
Loizidou MA,
Del Regno L,
Massi D,
Mandala M,
Khosrotehrani K,
Akslen LA,
Amos CI,
Andresen PA,
Avril MF,
Azizi E,
Soyer HP,
Bataille V,
Dalmasso B,
Bowdler LM,
Burdon KP,
Chen WV,
Codd V,
Craig JE,
Dębniak T,
Falchi M,
Fang S,
Friedman E,
Simi S,
Galan P,
Garcia-Casado Z,
Gillanders EM,
Gordon S,
Green A,
Gruis NA,
Hansson J,
Harland M,
Harris J,
Helsing P,
Henders A,
Hočevar M,
Höiom V,
Hunter D,
Ingvar C,
Kumar R,
Lang J,
Lathrop GM,
Lee JE,
Li X,
Lubiński J,
Mackie RM,
Malt M,
Malvehy J,
McAloney K,
Mohamdi H,
Molven A,
Moses EK,
Neale RE,
Novaković S,
Nyholt DR,
Olsson H,
Orr N,
Fritsche LG,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
Randerson-Moor J,
Requena C,
Rowe C,
Samani NJ,
Sanna M,
Schadendorf D,
Schulze HJ,
Simms LA,
Smithers M,
Song F,
Swerdlow AJ,
van der Stoep N,
Kukutsch NA,
Visconti A,
Wallace L,
Ward SV,
Wheeler L,
Sturm RA,
Hutchinson A,
Jones K,
Malasky M,
Vogt A,
Zhou W,
Pooley KA,
Elder DE,
Han J,
Hicks B,
Hayward NK,
Kanetsky PA,
Brummett C,
Montgomery GW,
Olsen CM,
Hayward C,
Dunning AM,
Martin NG,
Evangelou E,
Mann GJ,
Long G,
Pharoah PDP,
Easton DF,
Barrett JH,
Cust AE,
Abecasis G,
Duffy DL,
Whiteman DC,
Gogas H,
De Nicolo A,
Tucker MA,
Newton-Bishop JA,
Peris K,
Chanock SJ,
Demenais F,
Brown KM,
Puig S,
Nagore E,
Shi J,
Iles MM,
Law MH
GenoMEL Consortium · Q-MEGA and QTWIN Investigators and 7 more consortia
Nature genetics · 2020 · PMID 32341527 · open access
12 pages+
The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians
Kim YJ,
Moon S,
Hwang MY,
Han S,
Jang HM,
Kong J,
Shin DM,
Yoon K,
Kim SM,
Lee JE,
Mahajan A,
Park HY
and 3 more — show all
Nature communications · 2022 · PMID 36333282 · open access
12 pages+
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits
Moon S,
Kim YJ,
Han S,
Hwang MY,
Shin DM,
Park MY,
Lu Y,
Yoon K,
Jang HM,
Kim YK,
Park TJ,
Song DS
and 3 more — show all
Scientific reports · 2019 · PMID 30718733 · open access
6 pages
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
Cho YS,
Go MJ,
Kim YJ,
Heo JY,
Oh JH,
Ban HJ,
Yoon D,
Lee MH,
Kim DJ,
Park M,
Cha SH,
Kim JW
and 20 more — show all
Han BG,
Min H,
Ahn Y,
Park MS,
Han HR,
Jang HY,
Cho EY,
Lee JE,
Cho NH,
Shin C,
Park T,
Park JW,
Lee JK,
Cardon L,
Clarke G,
McCarthy MI,
Lee JY,
Lee JK,
Oh B,
Kim HL
Nature genetics · 2009 · PMID 19396169
3 pages
Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma
Nan H,
Xu M,
Kraft P,
Qureshi AA,
Chen C,
Guo Q,
Hu FB,
Curhan G,
Amos CI,
Wang LE,
Lee JE,
Wei Q
and 2 more — show all
Human molecular genetics · 2011 · PMID 21700618
2 pages
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Law MH,
Bishop DT,
Lee JE,
Brossard M,
Martin NG,
Moses EK,
Song F,
Barrett JH,
Kumar R,
Easton DF,
Pharoah PDP,
Swerdlow AJ
and 63 more — show all
Kypreou KP,
Taylor JC,
Harland M,
Randerson-Moor J,
Akslen LA,
Andresen PA,
Avril MF,
Azizi E,
Scarrà GB,
Brown KM,
Dębniak T,
Duffy DL,
Elder DE,
Fang S,
Friedman E,
Galan P,
Ghiorzo P,
Gillanders EM,
Goldstein AM,
Gruis NA,
Hansson J,
Helsing P,
Hočevar M,
Höiom V,
Ingvar C,
Kanetsky PA,
Chen WV,
Landi MT,
Lang J,
Lathrop GM,
Lubiński J,
Mackie RM,
Mann GJ,
Molven A,
Montgomery GW,
Novaković S,
Olsson H,
Puig S,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
van der Stoep N,
van Doorn R,
Whiteman DC,
Craig JE,
Schadendorf D,
Simms LA,
Burdon KP,
Nyholt DR,
Pooley KA,
Orr N,
Stratigos AJ,
Cust AE,
Ward SV,
Hayward NK,
Han J,
Schulze HJ,
Dunning AM,
Bishop JAN,
Demenais F,
Amos CI,
MacGregor S,
Iles MM
GenoMEL Consortium · Essen-Heidelberg Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26237428 · open access
2 pages
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
Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans
Zhang M,
Song F,
Liang L,
Nan H,
Zhang J,
Liu H,
Wang LE,
Wei Q,
Lee JE,
Amos CI,
Kraft P,
Qureshi AA
and 1 more — show all
Human molecular genetics · 2013 · PMID 23548203
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.