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2,660 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.
10 matches for
Lee D.
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Barry A,
McNulty MT,
Jia X,
Gupta Y,
Debiec H,
Luo Y,
Nagano C,
Horinouchi T,
Jung S,
Colucci M,
Ahram DF,
Mitrotti A
and 58 more — show all
Sinha A,
Teeninga N,
Jin G,
Shril S,
Caridi G,
Bodria M,
Lim TY,
Westland R,
Zanoni F,
Marasa M,
Turudic D,
Giordano M,
Gesualdo L,
Magistroni R,
Pisani I,
Fiaccadori E,
Reiterova J,
Maringhini S,
Morello W,
Montini G,
Weng PL,
Scolari F,
Saraga M,
Tasic V,
Santoro D,
van Wijk JAE,
Milošević D,
Kawai Y,
Kiryluk K,
Pollak MR,
Gharavi A,
Lin F,
Simœs E Silva AC,
Loos RJF,
Kenny EE,
Schreuder MF,
Zurowska A,
Dossier C,
Ariceta G,
Drozynska-Duklas M,
Hogan J,
Jankauskiene A,
Hildebrandt F,
Prikhodina L,
Song K,
Bagga A,
Cheong H 2nd,
Ghiggeri GM,
Vachvanichsanong P,
Nozu K,
Lee D,
Vivarelli M,
Raychaudhuri S,
Tokunaga K,
Sanna-Cherchi S,
Ronco P,
Iijima K,
Sampson MG
Nature communications · 2023 · PMID 37120605 · open access
12 pages+
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
Lee DSM,
Cardone KM,
Zhang DY,
Tsao NL,
Abramowitz S,
Sharma P,
DePaolo JS,
Conery M,
Aragam KG,
Biddinger K,
Dikilitas O,
Hoffman-Andrews L
and 23 more — show all
Judy RL,
Khan A,
Kullo IJ,
Puckelwartz MJ,
Reza N,
Satterfield BA,
Singhal P,
Arany Z,
Cappola TP,
Carruth ED,
Day SM,
Do R,
Haggerty CM,
Joseph J,
McNally EM,
Nadkarni G,
Owens AT,
Rader DJ,
Ritchie MD,
Sun YV,
Voight BF,
Levin MG,
Damrauer SM
Penn Medicine Biobank
Nature genetics · 2025 · PMID 40195560
12 pages+
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation
Pereyra F,
Jia X,
McLaren PJ,
Telenti A,
de Bakker PI,
Walker BD,
Ripke S,
Brumme CJ,
Pulit SL,
Carrington M,
Kadie CM,
Carlson JM
and 326 more — show all
Heckerman D,
Graham RR,
Plenge RM,
Deeks SG,
Gianniny L,
Crawford G,
Sullivan J,
Gonzalez E,
Davies L,
Camargo A,
Moore JM,
Beattie N,
Gupta S,
Crenshaw A,
Burtt NP,
Guiducci C,
Gupta N,
Gao X,
Qi Y,
Yuki Y,
Piechocka-Trocha A,
Cutrell E,
Rosenberg R,
Moss KL,
Lemay P,
O'Leary J,
Schaefer T,
Verma P,
Toth I,
Block B,
Baker B,
Rothchild A,
Lian J,
Proudfoot J,
Alvino DM,
Vine S,
Addo MM,
Allen TM,
Altfeld M,
Henn MR,
Le Gall S,
Streeck H,
Haas DW,
Kuritzkes DR,
Robbins GK,
Shafer RW,
Gulick RM,
Shikuma CM,
Haubrich R,
Riddler S,
Sax PE,
Daar ES,
Ribaudo HJ,
Agan B,
Agarwal S,
Ahern RL,
Allen BL,
Altidor S,
Altschuler EL,
Ambardar S,
Anastos K,
Anderson B,
Anderson V,
Andrady U,
Antoniskis D,
Bangsberg D,
Barbaro D,
Barrie W,
Bartczak J,
Barton S,
Basden P,
Basgoz N,
Bazner S,
Bellos NC,
Benson AM,
Berger J,
Bernard NF,
Bernard AM,
Birch C,
Bodner SJ,
Bolan RK,
Boudreaux ET,
Bradley M,
Braun JF,
Brndjar JE,
Brown SJ,
Brown K,
Brown ST,
Burack J,
Bush LM,
Cafaro V,
Campbell O,
Campbell J,
Carlson RH,
Carmichael JK,
Casey KK,
Cavacuiti C,
Celestin G,
Chambers ST,
Chez N,
Chirch LM,
Cimoch PJ,
Cohen D,
Cohn LE,
Conway B,
Cooper DA,
Cornelson B,
Cox DT,
Cristofano MV,
Cuchural G Jr,
Czartoski JL,
Dahman JM,
Daly JS,
Davis BT,
Davis K,
Davod SM,
DeJesus E,
Dietz CA,
Dunham E,
Dunn ME,
Ellerin TB,
Eron JJ,
Fangman JJ,
Farel CE,
Ferlazzo H,
Fidler S,
Fleenor-Ford A,
Frankel R,
Freedberg KA,
French NK,
Fuchs JD,
Fuller JD,
Gaberman J,
Gallant JE,
Gandhi RT,
Garcia E,
Garmon D,
Gathe JC Jr,
Gaultier CR,
Gebre W,
Gilman FD,
Gilson I,
Goepfert PA,
Gottlieb MS,
Goulston C,
Groger RK,
Gurley TD,
Haber S,
Hardwicke R,
Hardy WD,
Harrigan PR,
Hawkins TN,
Heath S,
Hecht FM,
Henry WK,
Hladek M,
Hoffman RP,
Horton JM,
Hsu RK,
Huhn GD,
Hunt P,
Hupert MJ,
Illeman ML,
Jaeger H,
Jellinger RM,
John M,
Johnson JA,
Johnson KL,
Johnson H,
Johnson K,
Joly J,
Jordan WC,
Kauffman CA,
Khanlou H,
Killian RK,
Kim AY,
Kim DD,
Kinder CA,
Kirchner JT,
Kogelman L,
Kojic EM,
Korthuis PT,
Kurisu W,
Kwon DS,
LaMar M,
Lampiris H,
Lanzafame M,
Lederman MM,
Lee DM,
Lee JM,
Lee MJ,
Lee ET,
Lemoine J,
Levy JA,
Llibre JM,
Liguori MA,
Little SJ,
Liu AY,
Lopez AJ,
Loutfy MR,
Loy D,
Mohammed DY,
Man A,
Mansour MK,
Marconi VC,
Markowitz M,
Marques R,
Martin JN,
Martin HL Jr,
Mayer KH,
McElrath MJ,
McGhee TA,
McGovern BH,
McGowan K,
McIntyre D,
Mcleod GX,
Menezes P,
Mesa G,
Metroka CE,
Meyer-Olson D,
Miller AO,
Montgomery K,
Mounzer KC,
Nagami EH,
Nagin I,
Nahass RG,
Nelson MO,
Nielsen C,
Norene DL,
O'Connor DH,
Ojikutu BO,
Okulicz J,
Oladehin OO,
Oldfield EC 3rd,
Olender SA,
Ostrowski M,
Owen WF Jr,
Pae E,
Parsonnet J,
Pavlatos AM,
Perlmutter AM,
Pierce MN,
Pincus JM,
Pisani L,
Price LJ,
Proia L,
Prokesch RC,
Pujet HC,
Ramgopal M,
Rathod A,
Rausch M,
Ravishankar J,
Rhame FS,
Richards CS,
Richman DD,
Rodes B,
Rodriguez M,
Rose RC 3rd,
Rosenberg ES,
Rosenthal D,
Ross PE,
Rubin DS,
Rumbaugh E,
Saenz L,
Salvaggio MR,
Sanchez WC,
Sanjana VM,
Santiago S,
Schmidt W,
Schuitemaker H,
Sestak PM,
Shalit P,
Shay W,
Shirvani VN,
Silebi VI,
Sizemore JM Jr,
Skolnik PR,
Sokol-Anderson M,
Sosman JM,
Stabile P,
Stapleton JT,
Starrett S,
Stein F,
Stellbrink HJ,
Sterman FL,
Stone VE,
Stone DR,
Tambussi G,
Taplitz RA,
Tedaldi EM,
Telenti A,
Theisen W,
Torres R,
Tosiello L,
Tremblay C,
Tribble MA,
Trinh PD,
Tsao A,
Ueda P,
Vaccaro A,
Valadas E,
Vanig TJ,
Vecino I,
Vega VM,
Veikley W,
Wade BH,
Walworth C,
Wanidworanun C,
Ward DJ,
Warner DA,
Weber RD,
Webster D,
Weis S,
Wheeler DA,
White DJ,
Wilkins E,
Winston A,
Wlodaver CG,
van't Wout A,
Wright DP,
Yang OO,
Yurdin DL,
Zabukovic BW,
Zachary KC,
Zeeman B,
Zhao M
International HIV Controllers Study
Science (New York, N.Y.) · 2010 · PMID 21051598
6 pages
Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Huang L,
Chen Y,
Lin Y,
Tam POS,
Cheng Y,
Shi Y,
Gong B,
Lu F,
Yang J,
Wang H,
Yin Y,
Cao Y
and 9 more — show all
Science China. Life sciences · 2019 · PMID 30591961
5 pages
Gene discovery and biological insights into anxiety disorders from a large-scale multi-ancestry genome-wide association study
Friligkou E,
Løkhammer S,
Cabrera-Mendoza B,
Shen J,
He J,
Deiana G,
Zanoaga MD,
Asgel Z,
Pilcher A,
Di Lascio L,
Makharashvili A,
Koller D
and 3 more — show all
Nature genetics · 2024 · PMID 39294497
5 pages
Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders
Kim H,
Ahn Y,
Yoon J,
Jung K,
Kim S,
Shim I,
Park TH,
Ko H,
Jung SH,
Kim J,
Park S,
Lee DJ
and 15 more — show all
Choi S,
Cha S,
Kim B,
Cho MY,
Cho H,
Kim DS,
Jang Y,
Ihm HK,
Park WY,
Bakhshi H,
O Connell KS,
Andreassen OA,
Kendler KS,
Myung W,
Won HH
Psychiatry research · 2024 · PMID 38335777
3 pages
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
Plenge RM,
Cotsapas C,
Davies L,
Price AL,
de Bakker PI,
Maller J,
Pe'er I,
Burtt NP,
Blumenstiel B,
DeFelice M,
Parkin M,
Barry R
and 26 more — show all
Winslow W,
Healy C,
Graham RR,
Neale BM,
Izmailova E,
Roubenoff R,
Parker AN,
Glass R,
Karlson EW,
Maher N,
Hafler DA,
Lee DM,
Seldin MF,
Remmers EF,
Lee AT,
Padyukov L,
Alfredsson L,
Coblyn J,
Weinblatt ME,
Gabriel SB,
Purcell S,
Klareskog L,
Gregersen PK,
Shadick NA,
Daly MJ,
Altshuler D
Nature genetics · 2007 · PMID 17982456
2 pages
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome
Jia X,
Yamamura T,
Gbadegesin R,
McNulty MT,
Song K,
Nagano C,
Hitomi Y,
Lee D,
Aiba Y,
Khor SS,
Ueno K,
Kawai Y
and 33 more — show all
Nagasaki M,
Noiri E,
Horinouchi T,
Kaito H,
Hamada R,
Okamoto T,
Kamei K,
Kaku Y,
Fujimaru R,
Tanaka R,
Shima Y,
Baek J,
Kang HG,
Ha IS,
Han KH,
Yang EM,
Abeyagunawardena A,
Lane B,
Chryst-Stangl M,
Esezobor C,
Solarin A,
Dossier C,
Deschênes G,
Vivarelli M,
Debiec H,
Ishikura K,
Matsuo M,
Nozu K,
Ronco P,
Cheong HI,
Sampson MG,
Tokunaga K,
Iijima K
Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan · Korean Consortium of Hereditary Renal Diseases in Children and 2 more consortia
Kidney international · 2020 · PMID 32554042
1 page
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages
Park JY,
Lee D,
Lee JJ,
Gim J,
Gunasekaran TI,
Choi KY,
Kang S,
Do AR,
Jo J,
Park J,
Park K,
Li D
and 21 more — show all
Lee S,
Kim H,
Dhanasingh I,
Ghosh S,
Keum S,
Choi JH,
Song GJ,
Sael L,
Rhee S,
Lovestone S,
Kim E,
Moon SH,
Kim BC,
Kim S,
Saykin AJ,
Nho K,
Lee SH,
Farrer LA,
Jun GR,
Won S,
Lee KH
Alzheimer’s Disease Neuroimaging Initiative
Translational psychiatry · 2021 · PMID 34785643 · 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.