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2,663 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.
4 matches for
Krogh V.
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 Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Li C,
Stoma S,
Lotta LA,
Warner S,
Albrecht E,
Allione A,
Arp PP,
Broer L,
Buxton JL,
Da Silva Couto Alves A,
Deelen J,
Fedko IO
and 84 more — show all
Gordon SD,
Jiang T,
Karlsson R,
Kerrison N,
Loe TK,
Mangino M,
Milaneschi Y,
Miraglio B,
Pervjakova N,
Russo A,
Surakka I,
van der Spek A,
Verhoeven JE,
Amin N,
Beekman M,
Blakemore AI,
Canzian F,
Hamby SE,
Hottenga JJ,
Jones PD,
Jousilahti P,
Mägi R,
Medland SE,
Montgomery GW,
Nyholt DR,
Perola M,
Pietiläinen KH,
Salomaa V,
Sillanpää E,
Suchiman HE,
van Heemst D,
Willemsen G,
Agudo A,
Boeing H,
Boomsma DI,
Chirlaque MD,
Fagherazzi G,
Ferrari P,
Franks P,
Gieger C,
Eriksson JG,
Gunter M,
Hägg S,
Hovatta I,
Imaz L,
Kaprio J,
Kaaks R,
Key T,
Krogh V,
Martin NG,
Melander O,
Metspalu A,
Moreno C,
Onland-Moret NC,
Nilsson P,
Ong KK,
Overvad K,
Palli D,
Panico S,
Pedersen NL,
Penninx BWJH,
Quirós JR,
Jarvelin MR,
Rodríguez-Barranco M,
Scott RA,
Severi G,
Slagboom PE,
Spector TD,
Tjonneland A,
Trichopoulou A,
Tumino R,
Uitterlinden AG,
van der Schouw YT,
van Duijn CM,
Weiderpass E,
Denchi EL,
Matullo G,
Butterworth AS,
Danesh J,
Samani NJ,
Wareham NJ,
Nelson CP,
Langenberg C,
Codd V
American journal of human genetics · 2020 · PMID 32109421 · 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
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Schmit SL,
Edlund CK,
Schumacher FR,
Gong J,
Harrison TA,
Huyghe JR,
Qu C,
Melas M,
Van Den Berg DJ,
Wang H,
Tring S,
Plummer SJ
and 171 more — show all
Albanes D,
Alonso MH,
Amos CI,
Anton K,
Aragaki AK,
Arndt V,
Barry EL,
Berndt SI,
Bezieau S,
Bien S,
Bloomer A,
Boehm J,
Boutron-Ruault MC,
Brenner H,
Brezina S,
Buchanan DD,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castelao JE,
Chan AT,
Chang-Claude J,
Chanock SJ,
Cheng I,
Cheng YW,
Chin LS,
Church JM,
Church T,
Coetzee GA,
Cotterchio M,
Cruz Correa M,
Curtis KR,
Duggan D,
Easton DF,
English D,
Feskens EJM,
Fischer R,
FitzGerald LM,
Fortini BK,
Fritsche LG,
Fuchs CS,
Gago-Dominguez M,
Gala M,
Gallinger SJ,
Gauderman WJ,
Giles GG,
Giovannucci EL,
Gogarten SM,
Gonzalez-Villalpando C,
Gonzalez-Villalpando EM,
Grady WM,
Greenson JK,
Gsur A,
Gunter M,
Haiman CA,
Hampe J,
Harlid S,
Harju JF,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Huang SC,
Huerta JM,
Hudson TJ,
Hunter DJ,
Idos GE,
Iwasaki M,
Jackson RD,
Jacobs EJ,
Jee SH,
Jenkins MA,
Jia WH,
Jiao S,
Joshi AD,
Kolonel LN,
Kono S,
Kooperberg C,
Krogh V,
Kuehn T,
Küry S,
LaCroix A,
Laurie CA,
Lejbkowicz F,
Lemire M,
Lenz HJ,
Levine D,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindor NM,
Liu YR,
Loupakis F,
Lu Y,
Luh F,
Ma J,
Mancao C,
Manion FJ,
Markowitz SD,
Martin V,
Matsuda K,
Matsuo K,
McDonnell KJ,
McNeil CE,
Milne R,
Molina AJ,
Mukherjee B,
Murphy N,
Newcomb PA,
Offit K,
Omichessan H,
Palli D,
Cotoré JPP,
Pérez-Mayoral J,
Pharoah PD,
Potter JD,
Qu C,
Raskin L,
Rennert G,
Rennert HS,
Riggs BM,
Schafmayer C,
Schoen RE,
Sellers TA,
Seminara D,
Severi G,
Shi W,
Shibata D,
Shu XO,
Siegel EM,
Slattery ML,
Southey M,
Stadler ZK,
Stern MC,
Stintzing S,
Taverna D,
Thibodeau SN,
Thomas DC,
Trichopoulou A,
Tsugane S,
Ulrich CM,
van Duijnhoven FJB,
van Guelpan B,
Vijai J,
Virtamo J,
Weinstein SJ,
White E,
Win AK,
Wolk A,
Woods M,
Wu AH,
Wu K,
Xiang YB,
Yen Y,
Zanke BW,
Zeng YX,
Zhang B,
Zubair N,
Kweon SS,
Figueiredo JC,
Zheng W,
Marchand LL,
Lindblom A,
Moreno V,
Peters U,
Casey G,
Hsu L,
Conti DV,
Gruber SB
Journal of the National Cancer Institute · 2019 · PMID 29917119
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.