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2,657 papers hold this site up. Every variant and condition page names
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5 matches for
Sesso HD.
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
Scelo G,
Purdue MP,
Brown KM,
Johansson M,
Wang Z,
Eckel-Passow JE,
Ye Y,
Hofmann JN,
Choi J,
Foll M,
Gaborieau V,
Machiela MJ
and 111 more — show all
Colli LM,
Li P,
Sampson JN,
Abedi-Ardekani B,
Besse C,
Blanche H,
Boland A,
Burdette L,
Chabrier A,
Durand G,
Le Calvez-Kelm F,
Prokhortchouk E,
Robinot N,
Skryabin KG,
Wozniak MB,
Yeager M,
Basta-Jovanovic G,
Dzamic Z,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Mukeriya A,
Rascu S,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Szeszenia-Dabrowska N,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Baglietto L,
Boeing H,
Khaw KT,
Weiderpass E,
Ljungberg B,
Sitaram RT,
Bruinsma F,
Jordan SJ,
Severi G,
Winship I,
Hveem K,
Vatten LJ,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Freeman LEB,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Gapstur SM,
Stevens VL,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Buring J,
Lee IM,
Chow WH,
Moore LE,
Wood C,
Eisen T,
Henrion M,
Larkin J,
Barman P,
Leibovich BC,
Choueiri TK,
Mark Lathrop G,
Rothman N,
Deleuze JF,
McKay JD,
Parker AS,
Wu X,
Houlston RS,
Brennan P,
Chanock SJ
Nature communications · 2017 · PMID 28598434 · open access
6 pages
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Wolpin BM,
Rizzato C,
Kraft P,
Kooperberg C,
Petersen GM,
Wang Z,
Arslan AA,
Beane-Freeman L,
Bracci PM,
Buring J,
Canzian F,
Duell EJ
and 106 more — show all
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Jacobs EJ,
Kamineni A,
Klein AP,
Kolonel LN,
Kulke MH,
Li D,
Malats N,
Olson SH,
Risch HA,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Austin MA,
Barfield R,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Brotzman M,
Büchler MW,
Bueno-de-Mesquita HB,
Bugert P,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Chung C,
Cotterchio M,
Costello E,
Elena J,
Funel N,
Gaziano JM,
Giese NA,
Giovannucci EL,
Goggins M,
Gorman MJ,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Henderson BE,
Holly EA,
Hu N,
Hunter DJ,
Innocenti F,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
LaCroix A,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Nakamura Y,
Oberg AL,
Owzar K,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Piepoli A,
Porta M,
Real FX,
Riboli E,
Rothman N,
Scarpa A,
Shu XO,
Silverman DT,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Taylor PR,
Theodoropoulos GE,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Wu C,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Hoover R,
Hartge P,
Fuchs C,
Chanock SJ,
Stolzenberg-Solomon RS,
Amundadottir LT
Nature genetics · 2014 · PMID 25086665 · open access
5 pages
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Klein AP,
Wolpin BM,
Risch HA,
Stolzenberg-Solomon RZ,
Mocci E,
Zhang M,
Canzian F,
Childs EJ,
Hoskins JW,
Jermusyk A,
Zhong J,
Chen F
and 112 more — show all
Albanes D,
Andreotti G,
Arslan AA,
Babic A,
Bamlet WR,
Beane-Freeman L,
Berndt SI,
Blackford A,
Borges M,
Borgida A,
Bracci PM,
Brais L,
Brennan P,
Brenner H,
Bueno-de-Mesquita B,
Buring J,
Campa D,
Capurso G,
Cavestro GM,
Chaffee KG,
Chung CC,
Cleary S,
Cotterchio M,
Dijk F,
Duell EJ,
Foretova L,
Fuchs C,
Funel N,
Gallinger S,
M Gaziano JM,
Gazouli M,
Giles GG,
Giovannucci E,
Goggins M,
Goodman GE,
Goodman PJ,
Hackert T,
Haiman C,
Hartge P,
Hasan M,
Hegyi P,
Helzlsouer KJ,
Herman J,
Holcatova I,
Holly EA,
Hoover R,
Hung RJ,
Jacobs EJ,
Jamroziak K,
Janout V,
Kaaks R,
Khaw KT,
Klein EA,
Kogevinas M,
Kooperberg C,
Kulke MH,
Kupcinskas J,
Kurtz RJ,
Laheru D,
Landi S,
Lawlor RT,
Lee IM,
LeMarchand L,
Lu L,
Malats N,
Mambrini A,
Mannisto S,
Milne RL,
Mohelníková-Duchoňová B,
Neale RE,
Neoptolemos JP,
Oberg AL,
Olson SH,
Orlow I,
Pasquali C,
Patel AV,
Peters U,
Pezzilli R,
Porta M,
Real FX,
Rothman N,
Scelo G,
Sesso HD,
Severi G,
Shu XO,
Silverman D,
Smith JP,
Soucek P,
Sund M,
Talar-Wojnarowska R,
Tavano F,
Thornquist MD,
Tobias GS,
Van Den Eeden SK,
Vashist Y,
Visvanathan K,
Vodicka P,
Wactawski-Wende J,
Wang Z,
Wentzensen N,
White E,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Zheng W,
Zheng W,
Kraft P,
Li D,
Chanock S,
Obazee O,
Petersen GM,
Amundadottir LT
Nature communications · 2018 · PMID 29422604 · open access
4 pages
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
Zhang M,
Wang Z,
Obazee O,
Jia J,
Childs EJ,
Hoskins J,
Figlioli G,
Mocci E,
Collins I,
Chung CC,
Hautman C,
Arslan AA
and 112 more — show all
Beane-Freeman L,
Bracci PM,
Buring J,
Duell EJ,
Gallinger S,
Giles GG,
Goodman GE,
Goodman PJ,
Kamineni A,
Kolonel LN,
Kulke MH,
Malats N,
Olson SH,
Sesso HD,
Visvanathan K,
White E,
Zheng W,
Zheng W,
Abnet CC,
Albanes D,
Andreotti G,
Brais L,
Bueno-de-Mesquita HB,
Basso D,
Berndt SI,
Boutron-Ruault MC,
Bijlsma MF,
Brenner H,
Burdette L,
Campa D,
Caporaso NE,
Capurso G,
Cavestro GM,
Cotterchio M,
Costello E,
Elena J,
Boggi U,
Gaziano JM,
Gazouli M,
Giovannucci EL,
Goggins M,
Gross M,
Haiman CA,
Hassan M,
Helzlsouer KJ,
Hu N,
Hunter DJ,
Iskierka-Jazdzewska E,
Jenab M,
Kaaks R,
Key TJ,
Khaw KT,
Klein EA,
Kogevinas M,
Krogh V,
Kupcinskas J,
Kurtz RC,
Landi MT,
Landi S,
Le Marchand L,
Mambrini A,
Mannisto S,
Milne RL,
Neale RE,
Oberg AL,
Panico S,
Patel AV,
Peeters PH,
Peters U,
Pezzilli R,
Porta M,
Purdue M,
Quiros JR,
Riboli E,
Rothman N,
Scarpa A,
Scelo G,
Shu XO,
Silverman DT,
Soucek P,
Strobel O,
Sund M,
Małecka-Panas E,
Taylor PR,
Tavano F,
Travis RC,
Thornquist M,
Tjønneland A,
Tobias GS,
Trichopoulos D,
Vashist Y,
Vodicka P,
Wactawski-Wende J,
Wentzensen N,
Yu H,
Yu K,
Zeleniuch-Jacquotte A,
Kooperberg C,
Risch HA,
Jacobs EJ,
Li D,
Fuchs C,
Hoover R,
Hartge P,
Chanock SJ,
Petersen GM,
Stolzenberg-Solomon RS,
Wolpin BM,
Kraft P,
Klein AP,
Canzian F,
Amundadottir LT
Oncotarget · 2016 · PMID 27579533 · open access
3 pages
Sex specific associations in genome wide association analysis of renal cell carcinoma
Laskar RS,
Muller DC,
Li P,
Machiela MJ,
Ye Y,
Gaborieau V,
Foll M,
Hofmann JN,
Colli L,
Sampson JN,
Wang Z,
Bacq-Daian D
and 96 more — show all
Boland A,
Abedi-Ardekani B,
Durand G,
Le Calvez-Kelm F,
Robinot N,
Blanche H,
Prokhortchouk E,
Skryabin KG,
Burdett L,
Yeager M,
Radojevic-Skodric S,
Savic S,
Foretova L,
Holcatova I,
Janout V,
Mates D,
Rascu S,
Mukeria A,
Zaridze D,
Bencko V,
Cybulski C,
Fabianova E,
Jinga V,
Lissowska J,
Lubinski J,
Navratilova M,
Rudnai P,
Świątkowska B,
Benhamou S,
Cancel-Tassin G,
Cussenot O,
Trichopoulou A,
Riboli E,
Overvad K,
Panico S,
Ljungberg B,
Sitaram RT,
Giles GG,
Milne RL,
Severi G,
Bruinsma F,
Fletcher T,
Koppova K,
Larsson SC,
Wolk A,
Banks RE,
Selby PJ,
Easton DF,
Pharoah P,
Andreotti G,
Beane Freeman LE,
Koutros S,
Albanes D,
Männistö S,
Weinstein S,
Clark PE,
Edwards TL,
Lipworth L,
Carol H,
Freedman ML,
Pomerantz MM,
Cho E,
Kraft P,
Preston MA,
Wilson KM,
Michael Gaziano J,
Sesso HD,
Black A,
Freedman ND,
Huang WY,
Anema JG,
Kahnoski RJ,
Lane BR,
Noyes SL,
Petillo D,
Teh BT,
Peters U,
White E,
Anderson GL,
Johnson L,
Luo J,
Chow WH,
Moore LE,
Choueiri TK,
Wood C,
Johansson M,
McKay JD,
Brown KM,
Rothman N,
Lathrop MG,
Deleuze JF,
Wu X,
Brennan P,
Chanock SJ,
Purdue MP,
Scelo G
European journal of human genetics : EJHG · 2019 · PMID 31231134
1 page
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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.