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2,685 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.
27 matches for
Caporaso N,
showing the first 7.
Genome-wide meta-analyses of smoking behaviors in African Americans
David SP,
Hamidovic A,
Chen GK,
Bergen AW,
Wessel J,
Kasberger JL,
Brown WM,
Petruzella S,
Thacker EL,
Kim Y,
Nalls MA,
Tranah GJ
and 68 more — show all
Sung YJ,
Ambrosone CB,
Arnett D,
Bandera EV,
Becker DM,
Becker L,
Berndt SI,
Bernstein L,
Blot WJ,
Broeckel U,
Buxbaum SG,
Caporaso N,
Casey G,
Chanock SJ,
Deming SL,
Diver WR,
Eaton CB,
Evans DS,
Evans MK,
Fornage M,
Franceschini N,
Harris TB,
Henderson BE,
Hernandez DG,
Hitsman B,
Hu JJ,
Hunt SC,
Ingles SA,
John EM,
Kittles R,
Kolb S,
Kolonel LN,
Le Marchand L,
Liu Y,
Lohman KK,
McKnight B,
Millikan RC,
Murphy A,
Neslund-Dudas C,
Nyante S,
Press M,
Psaty BM,
Rao DC,
Redline S,
Rodriguez-Gil JL,
Rybicki BA,
Signorello LB,
Singleton AB,
Smoller J,
Snively B,
Spring B,
Stanford JL,
Strom SS,
Swan GE,
Taylor KD,
Thun MJ,
Wilson AF,
Witte JS,
Yamamura Y,
Yanek LR,
Yu K,
Zheng W,
Zheng W,
Ziegler RG,
Zonderman AB,
Jorgenson E,
Haiman CA,
Furberg H
Translational psychiatry · 2012 · PMID 22832964 · open access
1 page
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer
Wang Y,
McKay JD,
Rafnar T,
Wang Z,
Timofeeva MN,
Broderick P,
Zong X,
Laplana M,
Wei Y,
Han Y,
Lloyd A,
Delahaye-Sourdeix M
and 71 more — show all
Chubb D,
Gaborieau V,
Wheeler W,
Chatterjee N,
Thorleifsson G,
Sulem P,
Liu G,
Kaaks R,
Henrion M,
Kinnersley B,
Vallée M,
LeCalvez-Kelm F,
Stevens VL,
Gapstur SM,
Chen WV,
Zaridze D,
Szeszenia-Dabrowska N,
Lissowska J,
Rudnai P,
Fabianova E,
Mates D,
Bencko V,
Foretova L,
Janout V,
Krokan HE,
Gabrielsen ME,
Skorpen F,
Vatten L,
Njølstad I,
Chen C,
Goodman G,
Benhamou S,
Vooder T,
Välk K,
Nelis M,
Metspalu A,
Lener M,
Lubiński J,
Johansson M,
Vineis P,
Agudo A,
Clavel-Chapelon F,
Bueno-de-Mesquita HB,
Trichopoulos D,
Khaw KT,
Johansson M,
Weiderpass E,
Tjønneland A,
Riboli E,
Lathrop M,
Scelo G,
Albanes D,
Caporaso NE,
Ye Y,
Gu J,
Wu X,
Spitz MR,
Dienemann H,
Rosenberger A,
Su L,
Matakidou A,
Eisen T,
Stefansson K,
Risch A,
Chanock SJ,
Christiani DC,
Hung RJ,
Brennan P,
Landi MT,
Houlston RS,
Amos CI
Nature genetics · 2014 · PMID 24880342 · open access
1 page
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women
Wang Z,
Seow WJ,
Shiraishi K,
Hsiung CA,
Matsuo K,
Liu J,
Chen K,
Yamji T,
Yang Y,
Chang IS,
Wu C,
Hong YC
and 138 more — show all
Burdett L,
Wyatt K,
Chung CC,
Li SA,
Yeager M,
Hutchinson A,
Hu W,
Caporaso N,
Landi MT,
Chatterjee N,
Song M,
Fraumeni JF Jr,
Kohno T,
Yokota J,
Kunitoh H,
Ashikawa K,
Momozawa Y,
Daigo Y,
Mitsudomi T,
Yatabe Y,
Hida T,
Hu Z,
Dai J,
Ma H,
Jin G,
Song B,
Wang Z,
Cheng S,
Yin Z,
Li X,
Ren Y,
Guan P,
Chang J,
Tan W,
Chen CJ,
Chang GC,
Tsai YH,
Su WC,
Chen KY,
Huang MS,
Chen YM,
Zheng H,
Li H,
Cui P,
Guo H,
Xu P,
Liu L,
Iwasaki M,
Shimazu T,
Tsugane S,
Zhu J,
Jiang G,
Fei K,
Park JY,
Kim YH,
Sung JS,
Park KH,
Kim YT,
Jung YJ,
Kang CH,
Park IK,
Kim HN,
Jeon HS,
Choi JE,
Choi YY,
Kim JH,
Oh IJ,
Kim YC,
Sung SW,
Kim JS,
Yoon HI,
Kweon SS,
Shin MH,
Seow A,
Chen Y,
Lim WY,
Liu J,
Wong MP,
Lee VH,
Bassig BA,
Tucker M,
Berndt SI,
Chow WH,
Ji BT,
Wang J,
Xu J,
Sihoe AD,
Ho JC,
Chan JK,
Wang JC,
Lu D,
Zhao X,
Zhao Z,
Wu J,
Chen H,
Jin L,
Wei F,
Wu G,
An SJ,
Zhang XC,
Su J,
Wu YL,
Gao YT,
Xiang YB,
He X,
Li J,
Zheng W,
Shu XO,
Cai Q,
Klein R,
Pao W,
Lawrence C,
Hosgood HD 3rd,
Hsiao CF,
Chien LH,
Chen YH,
Chen CH,
Wang WC,
Chen CY,
Wang CL,
Yu CJ,
Chen HL,
Su YC,
Tsai FY,
Chen YS,
Li YJ,
Yang TY,
Lin CC,
Yang PC,
Wu T,
Lin D,
Zhou B,
Yu J,
Shen H,
Kubo M,
Chanock SJ,
Rothman N,
Lan Q
Human molecular genetics · 2016 · PMID 26732429
1 page
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia
McMaster ML,
Berndt SI,
Zhang J,
Slager SL,
Li SA,
Vajdic CM,
Smedby KE,
Yan H,
Birmann BM,
Brown EE,
Smith A,
Kleinstern G
and 69 more — show all
Fansler MM,
Mayr C,
Zhu B,
Chung CC,
Park JH,
Burdette L,
Hicks BD,
Hutchinson A,
Teras LR,
Adami HO,
Bracci PM,
McKay J,
Monnereau A,
Link BK,
Vermeulen RCH,
Ansell SM,
Maria A,
Diver WR,
Melbye M,
Ojesina AI,
Kraft P,
Boffetta P,
Clavel J,
Giovannucci E,
Besson CM,
Canzian F,
Travis RC,
Vineis P,
Weiderpass E,
Montalvan R,
Wang Z,
Yeager M,
Becker N,
Benavente Y,
Brennan P,
Foretova L,
Maynadie M,
Nieters A,
de Sanjose S,
Staines A,
Conde L,
Riby J,
Glimelius B,
Hjalgrim H,
Pradhan N,
Feldman AL,
Novak AJ,
Lawrence C,
Bassig BA,
Lan Q,
Zheng T,
North KE,
Tinker LF,
Cozen W,
Severson RK,
Hofmann JN,
Zhang Y,
Jackson RD,
Morton LM,
Purdue MP,
Chatterjee N,
Offit K,
Cerhan JR,
Chanock SJ,
Rothman N,
Vijai J,
Goldin LR,
Skibola CF,
Caporaso NE
Nature communications · 2018 · PMID 30305637 · open access
1 page
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes
Chen J,
Loukola A,
Gillespie NA,
Peterson R,
Jia P,
Riley B,
Maes H,
Dick DM,
Kendler KS,
Damaj MI,
Miles MF,
Zhao Z
and 34 more — show all
Li MD,
Vink JM,
Minica CC,
Willemsen G,
Boomsma DI,
Qaiser B,
Madden PAF,
Korhonen T,
Jousilahti P,
Hällfors J,
Gelernter J,
Kranzler HR,
Sherva R,
Farrer L,
Maher B,
Vanyukov M,
Taylor M,
Ware JJ,
Munafò MR,
Lutz SM,
Hokanson JE,
Gu F,
Landi MT,
Caporaso NE,
Hancock DB,
Gaddis NC,
Baker TB,
Bierut LJ,
Johnson EO,
Chenoweth M,
Lerman C,
Tyndale R,
Kaprio J,
Chen X
Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2020 · PMID 31294817
1 page
Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers
Lesseur C,
Ferreiro-Iglesias A,
McKay JD,
Bossé Y,
Johansson M,
Gaborieau V,
Landi MT,
Christiani DC,
Caporaso NC,
Bojesen SE,
Amos CI,
Shete S
and 41 more — show all
Liu G,
Rennert G,
Albanes D,
Aldrich MC,
Tardon A,
Chen C,
Triantafillos L,
Field JK,
Teare MD,
Kiemeney LA,
Diergaarde B,
Ferris RL,
Zienolddiny S,
Lam S,
Olshan AF,
Weissler MC,
Lacko M,
Risch A,
Bickeböller H,
Ness AR,
Thomas S,
Le Marchand L,
Schabath MB,
Wünsch-Filho V,
Tajara EH,
Andrew AS,
Clifford GM,
Lazarus P,
Grankvist K,
Johansson M,
Arnold S,
Melander O,
Brunnström H,
Boccia S,
Cadoni G,
Timens W,
Obeidat M,
Xiao X,
Houlston RS,
Hung RJ,
Brennan P
PLoS genetics · 2021 · PMID 33667223 · open access
1 page
Genome-wide association study for lung cancer in 6531 African Americans reveals new susceptibility loci
Byun J,
Han Y,
Choi J,
Sun R,
Shaw VR,
Zhu C,
Xiao X,
Lusk C,
Badr H,
Lee HS,
Jang HJ,
Li Y
and 44 more — show all
Lim H,
Long E,
Liu Y,
Kachuri L,
Walsh KM,
Wiencke JK,
Albanes D,
Lam S,
Tardon A,
Neuhouser ML,
Barnett MJ,
Chen C,
Bojesen S,
Brenner H,
Landi MT,
Johansson M,
Risch A,
Wichmann HE,
Bickeböller H,
Christiani DC,
Rennert G,
Arnold S,
Field JK,
Shete S,
Le Marchand L,
Liu G,
Andrew AS,
Zienolddiny S,
Grankvist K,
Johansson M,
Caporaso N,
Taylor F,
Lazarus P,
Schabath MB,
Aldrich MC,
Patel A,
Lin X,
Zanetti KA,
Harris CC,
Chanock S,
McKay J,
Schwartz AG,
Hung RJ,
Amos CI
INTEGRAL-ILCCO Consortium
Human molecular genetics · 2025 · PMID 40341939
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.