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Is your paper here?
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.
2 matches for
Rissanen H.
Association analyses identify 31 new risk loci for colorectal cancer susceptibility
Law PJ,
Timofeeva M,
Fernandez-Rozadilla C,
Broderick P,
Studd J,
Fernandez-Tajes J,
Farrington S,
Svinti V,
Palles C,
Orlando G,
Sud A,
Holroyd A
and 86 more — show all
Penegar S,
Theodoratou E,
Vaughan-Shaw P,
Campbell H,
Zgaga L,
Hayward C,
Campbell A,
Harris S,
Deary IJ,
Starr J,
Gatcombe L,
Pinna M,
Briggs S,
Martin L,
Jaeger E,
Sharma-Oates A,
East J,
Leedham S,
Arnold R,
Johnstone E,
Wang H,
Kerr D,
Kerr R,
Maughan T,
Kaplan R,
Al-Tassan N,
Palin K,
Hänninen UA,
Cajuso T,
Tanskanen T,
Kondelin J,
Kaasinen E,
Sarin AP,
Eriksson JG,
Rissanen H,
Knekt P,
Pukkala E,
Jousilahti P,
Salomaa V,
Ripatti S,
Palotie A,
Renkonen-Sinisalo L,
Lepistö A,
Böhm J,
Mecklin JP,
Buchanan DD,
Win AK,
Hopper J,
Jenkins ME,
Lindor NM,
Newcomb PA,
Gallinger S,
Duggan D,
Casey G,
Hoffmann P,
Nöthen MM,
Jöckel KH,
Easton DF,
Pharoah PDP,
Peto J,
Canzian F,
Swerdlow A,
Eeles RA,
Kote-Jarai Z,
Muir K,
Pashayan N,
Harkin A,
Allan K,
McQueen J,
Paul J,
Iveson T,
Saunders M,
Butterbach K,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Kirac I,
Matošević P,
Hofer P,
Brezina S,
Gsur A,
Cheadle JP,
Aaltonen LA,
Tomlinson I,
Houlston RS,
Dunlop MG
PRACTICAL consortium
Nature communications · 2019 · PMID 31089142 · open access
12 pages+
Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries
Fernandez-Rozadilla C,
Timofeeva M,
Chen Z,
Law P,
Thomas M,
Schmit S,
Díez-Obrero V,
Hsu L,
Fernandez-Tajes J,
Palles C,
Sherwood K,
Briggs S
and 198 more — show all
Svinti V,
Donnelly K,
Farrington S,
Blackmur J,
Vaughan-Shaw P,
Shu XO,
Long J,
Cai Q,
Guo X,
Lu Y,
Broderick P,
Studd J,
Huyghe J,
Harrison T,
Conti D,
Dampier C,
Devall M,
Schumacher F,
Melas M,
Rennert G,
Obón-Santacana M,
Martín-Sánchez V,
Moratalla-Navarro F,
Oh JH,
Kim J,
Jee SH,
Jung KJ,
Kweon SS,
Shin MH,
Shin A,
Ahn YO,
Kim DH,
Oze I,
Wen W,
Matsuo K,
Matsuda K,
Tanikawa C,
Ren Z,
Gao YT,
Jia WH,
Hopper J,
Jenkins M,
Win AK,
Pai R,
Figueiredo J,
Haile R,
Gallinger S,
Woods M,
Newcomb P,
Duggan D,
Cheadle J,
Kaplan R,
Maughan T,
Kerr R,
Kerr D,
Kirac I,
Böhm J,
Mecklin LP,
Jousilahti P,
Knekt P,
Aaltonen L,
Rissanen H,
Pukkala E,
Eriksson J,
Cajuso T,
Hänninen U,
Kondelin J,
Palin K,
Tanskanen T,
Renkonen-Sinisalo L,
Zanke B,
Männistö S,
Albanes D,
Weinstein S,
Ruiz-Narvaez E,
Palmer J,
Buchanan D,
Platz E,
Visvanathan K,
Ulrich C,
Siegel E,
Brezina S,
Gsur A,
Campbell P,
Chang-Claude J,
Hoffmeister M,
Brenner H,
Slattery M,
Potter J,
Tsilidis K,
Schulze M,
Gunter M,
Murphy N,
Castells A,
Castellví-Bel S,
Moreira L,
Arndt V,
Shcherbina A,
Stern M,
Pardamean B,
Bishop T,
Giles G,
Southey M,
Idos G,
McDonnell K,
Abu-Ful Z,
Greenson J,
Shulman K,
Lejbkowicz F,
Offit K,
Su YR,
Steinfelder R,
Keku T,
van Guelpen B,
Hudson T,
Hampel H,
Pearlman R,
Berndt S,
Hayes R,
Martinez ME,
Thomas S,
Corley D,
Pharoah P,
Larsson S,
Yen Y,
Lenz HJ,
White E,
Li L,
Doheny K,
Pugh E,
Shelford T,
Chan A,
Cruz-Correa M,
Lindblom A,
Hunter D,
Joshi A,
Schafmayer C,
Scacheri P,
Kundaje A,
Nickerson D,
Schoen R,
Hampe J,
Stadler Z,
Vodicka P,
Vodickova L,
Vymetalkova V,
Papadopoulos N,
Edlund C,
Gauderman W,
Thomas D,
Shibata D,
Toland A,
Markowitz S,
Kim A,
Chanock S,
van Duijnhoven F,
Feskens E,
Sakoda L,
Gago-Dominguez M,
Wolk A,
Naccarati A,
Pardini B,
FitzGerald L,
Lee SC,
Ogino S,
Bien S,
Kooperberg C,
Li C,
Lin Y,
Prentice R,
Qu C,
Bézieau S,
Tangen C,
Mardis E,
Yamaji T,
Sawada N,
Iwasaki M,
Haiman C,
Le Marchand L,
Wu A,
Qu C,
McNeil C,
Coetzee G,
Hayward C,
Deary I,
Harris S,
Theodoratou E,
Reid S,
Walker M,
Ooi LY,
Moreno V,
Casey G,
Gruber S,
Tomlinson I,
Zheng W,
Dunlop M,
Houlston R,
Peters U
Nature genetics · 2023 · PMID 36539618
12 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.