For researchers
Is your paper here?
2,662 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
Byun J.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
McKay JD,
Hung RJ,
Han Y,
Zong X,
Carreras-Torres R,
Christiani DC,
Caporaso NE,
Johansson M,
Xiao X,
Li Y,
Byun J,
Dunning A
and 128 more — show all
Pooley KA,
Qian DC,
Ji X,
Liu G,
Timofeeva MN,
Bojesen SE,
Wu X,
Le Marchand L,
Albanes D,
Bickeböller H,
Aldrich MC,
Bush WS,
Tardon A,
Rennert G,
Teare MD,
Field JK,
Kiemeney LA,
Lazarus P,
Haugen A,
Lam S,
Schabath MB,
Andrew AS,
Shen H,
Hong YC,
Yuan JM,
Bertazzi PA,
Pesatori AC,
Ye Y,
Diao N,
Su L,
Zhang R,
Brhane Y,
Leighl N,
Johansen JS,
Mellemgaard A,
Saliba W,
Haiman CA,
Wilkens LR,
Fernandez-Somoano A,
Fernandez-Tardon G,
van der Heijden HFM,
Kim JH,
Dai J,
Hu Z,
Davies MPA,
Marcus MW,
Brunnström H,
Manjer J,
Melander O,
Muller DC,
Overvad K,
Trichopoulou A,
Tumino R,
Doherty JA,
Barnett MP,
Chen C,
Goodman GE,
Cox A,
Taylor F,
Woll P,
Brüske I,
Wichmann HE,
Manz J,
Muley TR,
Risch A,
Rosenberger A,
Grankvist K,
Johansson M,
Shepherd FA,
Tsao MS,
Arnold SM,
Haura EB,
Bolca C,
Holcatova I,
Janout V,
Kontic M,
Lissowska J,
Mukeria A,
Ognjanovic S,
Orlowski TM,
Scelo G,
Swiatkowska B,
Zaridze D,
Bakke P,
Skaug V,
Zienolddiny S,
Duell EJ,
Butler LM,
Koh WP,
Gao YT,
Houlston RS,
McLaughlin J,
Stevens VL,
Joubert P,
Lamontagne M,
Nickle DC,
Obeidat M,
Timens W,
Zhu B,
Song L,
Kachuri L,
Artigas MS,
Tobin MD,
Wain LV,
Rafnar T,
Thorgeirsson TE,
Reginsson GW,
Stefansson K,
Hancock DB,
Bierut LJ,
Spitz MR,
Gaddis NC,
Lutz SM,
Gu F,
Johnson EO,
Kamal A,
Pikielny C,
Zhu D,
Lindströem S,
Jiang X,
Tyndale RF,
Chenevix-Trench G,
Beesley J,
Bossé Y,
Chanock S,
Brennan P,
Landi MT,
Amos CI
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
Multi-ancestry GWAS meta-analyses of lung cancer reveal susceptibility loci and elucidate smoking-independent genetic risk
Gorman BR,
Ji SG,
Francis M,
Sendamarai AK,
Shi Y,
Devineni P,
Saxena U,
Partan E,
DeVito AK,
Byun J,
Han Y,
Xiao X
and 11 more — show all
Sin DD,
Timens W,
Moser J,
Muralidhar S,
Ramoni R,
Hung RJ,
McKay JD,
Bossé Y,
Sun R,
Amos CI,
Pyarajan S
VA Million Veteran Program
Nature communications · 2024 · PMID 39366959 · open access
12 pages+
Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction
He Y,
Lu W,
Jee YH,
Shih MY,
Wang Y,
Tsuo K,
Qian DC,
Diao JA,
Huang H,
Patel CJ,
Byun J,
Pasaniuc B
and 6 more — show all
Nature genetics · 2026 · PMID 41565855
12 pages+
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes
Miller FW,
Chen W,
O'Hanlon TP,
Cooper RG,
Vencovsky J,
Rider LG,
Danko K,
Wedderburn LR,
Lundberg IE,
Pachman LM,
Reed AM,
Ytterberg SR
and 13 more — show all
Padyukov L,
Selva-O'Callaghan A,
Radstake TR,
Isenberg DA,
Chinoy H,
Ollier WE,
Scheet P,
Peng B,
Lee A,
Byun J,
Lamb JA,
Gregersen PK,
Amos CI
Myositis Genetics Consortium
Genes and immunity · 2015 · PMID 26291516
9 pages
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
Milne RL,
Kuchenbaecker KB,
Michailidou K,
Beesley J,
Kar S,
Lindström S,
Hui S,
Lemaçon A,
Soucy P,
Dennis J,
Jiang X,
Rostamianfar A
and 458 more — show all
Finucane H,
Bolla MK,
McGuffog L,
Wang Q,
Aalfs CM,
Adams M,
Adlard J,
Agata S,
Ahmed S,
Ahsan H,
Aittomäki K,
Al-Ejeh F,
Allen J,
Ambrosone CB,
Amos CI,
Andrulis IL,
Anton-Culver H,
Antonenkova NN,
Arndt V,
Arnold N,
Aronson KJ,
Auber B,
Auer PL,
Ausems MGEM,
Azzollini J,
Bacot F,
Balmaña J,
Barile M,
Barjhoux L,
Barkardottir RB,
Barrdahl M,
Barnes D,
Barrowdale D,
Baynes C,
Beckmann MW,
Benitez J,
Bermisheva M,
Bernstein L,
Bignon YJ,
Blazer KR,
Blok MJ,
Blomqvist C,
Blot W,
Bobolis K,
Boeckx B,
Bogdanova NV,
Bojesen A,
Bojesen SE,
Bonanni B,
Børresen-Dale AL,
Bozsik A,
Bradbury AR,
Brand JS,
Brauch H,
Brenner H,
Bressac-de Paillerets B,
Brewer C,
Brinton L,
Broberg P,
Brooks-Wilson A,
Brunet J,
Brüning T,
Burwinkel B,
Buys SS,
Byun J,
Cai Q,
Caldés T,
Caligo MA,
Campbell I,
Canzian F,
Caron O,
Carracedo A,
Carter BD,
Castelao JE,
Castera L,
Caux-Moncoutier V,
Chan SB,
Chang-Claude J,
Chanock SJ,
Chen X,
Cheng TD,
Chiquette J,
Christiansen H,
Claes KBM,
Clarke CL,
Conner T,
Conroy DM,
Cook J,
Cordina-Duverger E,
Cornelissen S,
Coupier I,
Cox A,
Cox DG,
Cross SS,
Cuk K,
Cunningham JM,
Czene K,
Daly MB,
Damiola F,
Darabi H,
Davidson R,
De Leeneer K,
Devilee P,
Dicks E,
Diez O,
Ding YC,
Ditsch N,
Doheny KF,
Domchek SM,
Dorfling CM,
Dörk T,
Dos-Santos-Silva I,
Dubois S,
Dugué PA,
Dumont M,
Dunning AM,
Durcan L,
Dwek M,
Dworniczak B,
Eccles D,
Eeles R,
Ehrencrona H,
Eilber U,
Ejlertsen B,
Ekici AB,
Eliassen AH,
Engel C,
Eriksson M,
Fachal L,
Faivre L,
Fasching PA,
Faust U,
Figueroa J,
Flesch-Janys D,
Fletcher O,
Flyger H,
Foulkes WD,
Friedman E,
Fritschi L,
Frost D,
Gabrielson M,
Gaddam P,
Gammon MD,
Ganz PA,
Gapstur SM,
Garber J,
Garcia-Barberan V,
García-Sáenz JA,
Gaudet MM,
Gauthier-Villars M,
Gehrig A,
Georgoulias V,
Gerdes AM,
Giles GG,
Glendon G,
Godwin AK,
Goldberg MS,
Goldgar DE,
González-Neira A,
Goodfellow P,
Greene MH,
Alnæs GIG,
Grip M,
Gronwald J,
Grundy A,
Gschwantler-Kaulich D,
Guénel P,
Guo Q,
Haeberle L,
Hahnen E,
Haiman CA,
Håkansson N,
Hallberg E,
Hamann U,
Hamel N,
Hankinson S,
Hansen TVO,
Harrington P,
Hart SN,
Hartikainen JM,
Healey CS,
Hein A,
Helbig S,
Henderson A,
Heyworth J,
Hicks B,
Hillemanns P,
Hodgson S,
Hogervorst FB,
Hollestelle A,
Hooning MJ,
Hoover B,
Hopper JL,
Hu C,
Huang G,
Hulick PJ,
Humphreys K,
Hunter DJ,
Imyanitov EN,
Isaacs C,
Iwasaki M,
Izatt L,
Jakubowska A,
James P,
Janavicius R,
Janni W,
Jensen UB,
John EM,
Johnson N,
Jones K,
Jones M,
Jukkola-Vuorinen A,
Kaaks R,
Kabisch M,
Kaczmarek K,
Kang D,
Kast K,
Keeman R,
Kerin MJ,
Kets CM,
Keupers M,
Khan S,
Khusnutdinova E,
Kiiski JI,
Kim SW,
Knight JA,
Konstantopoulou I,
Kosma VM,
Kristensen VN,
Kruse TA,
Kwong A,
Lænkholm AV,
Laitman Y,
Lalloo F,
Lambrechts D,
Landsman K,
Lasset C,
Lazaro C,
Le Marchand L,
Lecarpentier J,
Lee A,
Lee E,
Lee JW,
Lee MH,
Lejbkowicz F,
Lesueur F,
Li J,
Lilyquist J,
Lincoln A,
Lindblom A,
Lissowska J,
Lo WY,
Loibl S,
Long J,
Loud JT,
Lubinski J,
Luccarini C,
Lush M,
MacInnis RJ,
Maishman T,
Makalic E,
Kostovska IM,
Malone KE,
Manoukian S,
Manson JE,
Margolin S,
Martens JWM,
Martinez ME,
Matsuo K,
Mavroudis D,
Mazoyer S,
McLean C,
Meijers-Heijboer H,
Menéndez P,
Meyer J,
Miao H,
Miller A,
Miller N,
Mitchell G,
Montagna M,
Muir K,
Mulligan AM,
Mulot C,
Nadesan S,
Nathanson KL,
Neuhausen SL,
Nevanlinna H,
Nevelsteen I,
Niederacher D,
Nielsen SF,
Nordestgaard BG,
Norman A,
Nussbaum RL,
Olah E,
Olopade OI,
Olson JE,
Olswold C,
Ong KR,
Oosterwijk JC,
Orr N,
Osorio A,
Pankratz VS,
Papi L,
Park-Simon TW,
Paulsson-Karlsson Y,
Lloyd R,
Pedersen IS,
Peissel B,
Peixoto A,
Perez JIA,
Peterlongo P,
Peto J,
Pfeiler G,
Phelan CM,
Pinchev M,
Plaseska-Karanfilska D,
Poppe B,
Porteous ME,
Prentice R,
Presneau N,
Prokofieva D,
Pugh E,
Pujana MA,
Pylkäs K,
Rack B,
Radice P,
Rahman N,
Rantala J,
Rappaport-Fuerhauser C,
Rennert G,
Rennert HS,
Rhenius V,
Rhiem K,
Richardson A,
Rodriguez GC,
Romero A,
Romm J,
Rookus MA,
Rudolph A,
Ruediger T,
Saloustros E,
Sanders J,
Sandler DP,
Sangrajrang S,
Sawyer EJ,
Schmidt DF,
Schoemaker MJ,
Schumacher F,
Schürmann P,
Schwentner L,
Scott C,
Scott RJ,
Seal S,
Senter L,
Seynaeve C,
Shah M,
Sharma P,
Shen CY,
Sheng X,
Shimelis H,
Shrubsole MJ,
Shu XO,
Side LE,
Singer CF,
Sohn C,
Southey MC,
Spinelli JJ,
Spurdle AB,
Stegmaier C,
Stoppa-Lyonnet D,
Sukiennicki G,
Surowy H,
Sutter C,
Swerdlow A,
Szabo CI,
Tamimi RM,
Tan YY,
Taylor JA,
Tejada MI,
Tengström M,
Teo SH,
Terry MB,
Tessier DC,
Teulé A,
Thöne K,
Thull DL,
Tibiletti MG,
Tihomirova L,
Tischkowitz M,
Toland AE,
Tollenaar RAEM,
Tomlinson I,
Tong L,
Torres D,
Tranchant M,
Truong T,
Tucker K,
Tung N,
Tyrer J,
Ulmer HU,
Vachon C,
van Asperen CJ,
Van Den Berg D,
van den Ouweland AMW,
van Rensburg EJ,
Varesco L,
Varon-Mateeva R,
Vega A,
Viel A,
Vijai J,
Vincent D,
Vollenweider J,
Walker L,
Wang Z,
Wang-Gohrke S,
Wappenschmidt B,
Weinberg CR,
Weitzel JN,
Wendt C,
Wesseling J,
Whittemore AS,
Wijnen JT,
Willett W,
Winqvist R,
Wolk A,
Wu AH,
Xia L,
Yang XR,
Yannoukakos D,
Zaffaroni D,
Zheng W,
Zhu B,
Ziogas A,
Ziv E,
Zorn KK,
Gago-Dominguez M,
Mannermaa A,
Olsson H,
Teixeira MR,
Stone J,
Offit K,
Ottini L,
Park SK,
Thomassen M,
Hall P,
Meindl A,
Schmutzler RK,
Droit A,
Bader GD,
Pharoah PDP,
Couch FJ,
Easton DF,
Kraft P,
Chenevix-Trench G,
García-Closas M,
Schmidt MK,
Antoniou AC,
Simard J
ABCTB Investigators · EMBRACE and 4 more consortia
Nature genetics · 2017 · PMID 29058716
5 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
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Byun J,
Han Y,
Li Y,
Xia J,
Long E,
Choi J,
Xiao X,
Zhu M,
Zhou W,
Sun R,
Bossé Y,
Song Z
and 73 more — show all
Schwartz A,
Lusk C,
Rafnar T,
Stefansson K,
Zhang T,
Zhao W,
Pettit RW,
Liu Y,
Li X,
Zhou H,
Walsh KM,
Gorlov I,
Gorlova O,
Zhu D,
Rosenberg SM,
Pinney S,
Bailey-Wilson JE,
Mandal D,
de Andrade M,
Gaba C,
Willey JC,
You M,
Anderson M,
Wiencke JK,
Albanes D,
Lam S,
Tardon A,
Chen C,
Goodman G,
Bojeson S,
Brenner H,
Landi MT,
Chanock SJ,
Johansson M,
Muley T,
Risch A,
Wichmann HE,
Bickeböller H,
Christiani DC,
Rennert G,
Arnold S,
Field JK,
Shete S,
Le Marchand L,
Melander O,
Brunnstrom H,
Liu G,
Andrew AS,
Kiemeney LA,
Shen H,
Zienolddiny S,
Grankvist K,
Johansson M,
Caporaso N,
Cox A,
Hong YC,
Yuan JM,
Lazarus P,
Schabath MB,
Aldrich MC,
Patel A,
Lan Q,
Rothman N,
Taylor F,
Kachuri L,
Witte JS,
Sakoda LC,
Spitz M,
Brennan P,
Lin X,
McKay J,
Hung RJ,
Amos CI
Nature genetics · 2022 · PMID 35915169
3 pages
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis
Han Y,
Byun J,
Zhu C,
Sun R,
Roh JY,
Cordell HJ,
Lee HS,
Shaw VR,
Kang SW,
Razjouyan J,
Cooley MA,
Hassan MM
and 11 more — show all
Siminovitch KA,
Folseraas T,
Ellinghaus D,
Bergquist A,
Rushbrook SM,
Franke A,
Karlsen TH,
Lazaridis KN,
McGlynn KA,
Roberts LR,
Amos CI
International PSC Study Group
Nature communications · 2023 · PMID 36828809 · open access
3 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.