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.
6 matches for
Walter S.
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling
Ho JE,
Chen WY,
Chen MH,
Larson MG,
McCabe EL,
Cheng S,
Ghorbani A,
Coglianese E,
Emilsson V,
Johnson AD,
Walter S,
Franceschini N
and 12 more — show all
O'Donnell CJ,
Dehghan A,
Lu C,
Levy D,
Newton-Cheh C,
Lin H,
Felix JF,
Schreiter ER,
Vasan RS,
Januzzi JL,
Lee RT,
Wang TJ
CARDIoGRAM Consortium · CHARGE Inflammation Working Group and 1 more consortia
The Journal of clinical investigation · 2013 · PMID 23999434
9 pages
Large-scale association analyses identify host factors influencing human gut microbiome composition
Kurilshikov A,
Medina-Gomez C,
Bacigalupe R,
Radjabzadeh D,
Wang J,
Demirkan A,
Le Roy CI,
Raygoza Garay JA,
Finnicum CT,
Liu X,
Zhernakova DV,
Bonder MJ
and 92 more — show all
Hansen TH,
Frost F,
Rühlemann MC,
Turpin W,
Moon JY,
Kim HN,
Lüll K,
Barkan E,
Shah SA,
Fornage M,
Szopinska-Tokov J,
Wallen ZD,
Borisevich D,
Agreus L,
Andreasson A,
Bang C,
Bedrani L,
Bell JT,
Bisgaard H,
Boehnke M,
Boomsma DI,
Burk RD,
Claringbould A,
Croitoru K,
Davies GE,
van Duijn CM,
Duijts L,
Falony G,
Fu J,
van der Graaf A,
Hansen T,
Homuth G,
Hughes DA,
Ijzerman RG,
Jackson MA,
Jaddoe VWV,
Joossens M,
Jørgensen T,
Keszthelyi D,
Knight R,
Laakso M,
Laudes M,
Launer LJ,
Lieb W,
Lusis AJ,
Masclee AAM,
Moll HA,
Mujagic Z,
Qibin Q,
Rothschild D,
Shin H,
Sørensen SJ,
Steves CJ,
Thorsen J,
Timpson NJ,
Tito RY,
Vieira-Silva S,
Völker U,
Völzke H,
Võsa U,
Wade KH,
Walter S,
Watanabe K,
Weiss S,
Weiss FU,
Weissbrod O,
Westra HJ,
Willemsen G,
Payami H,
Jonkers DMAE,
Arias Vasquez A,
de Geus EJC,
Meyer KA,
Stokholm J,
Segal E,
Org E,
Wijmenga C,
Kim HL,
Kaplan RC,
Spector TD,
Uitterlinden AG,
Rivadeneira F,
Franke A,
Lerch MM,
Franke L,
Sanna S,
D'Amato M,
Pedersen O,
Paterson AD,
Kraaij R,
Raes J,
Zhernakova A
Nature genetics · 2021 · PMID 33462485
5 pages
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women
Jones G,
Trajanoska K,
Santanasto AJ,
Stringa N,
Kuo CL,
Atkins JL,
Lewis JR,
Duong T,
Hong S,
Biggs ML,
Luan J,
Sarnowski C
and 54 more — show all
Lunetta KL,
Tanaka T,
Wojczynski MK,
Cvejkus R,
Nethander M,
Ghasemi S,
Yang J,
Zillikens MC,
Walter S,
Sicinski K,
Kague E,
Ackert-Bicknell CL,
Arking DE,
Windham BG,
Boerwinkle E,
Grove ML,
Graff M,
Spira D,
Demuth I,
van der Velde N,
de Groot LCPGM,
Psaty BM,
Odden MC,
Fohner AE,
Langenberg C,
Wareham NJ,
Bandinelli S,
van Schoor NM,
Huisman M,
Tan Q,
Zmuda J,
Mellström D,
Karlsson M,
Bennett DA,
Buchman AS,
De Jager PL,
Uitterlinden AG,
Völker U,
Kocher T,
Teumer A,
Rodriguéz-Mañas L,
García FJ,
Carnicero JA,
Herd P,
Bertram L,
Ohlsson C,
Murabito JM,
Melzer D,
Kuchel GA,
Ferrucci L,
Karasik D,
Rivadeneira F,
Kiel DP,
Pilling LC
Nature communications · 2021 · PMID 33510174 · open access
3 pages
Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome
Bonfiglio F,
Zheng T,
Garcia-Etxebarria K,
Hadizadeh F,
Bujanda L,
Bresso F,
Agreus L,
Andreasson A,
Dlugosz A,
Lindberg G,
Schmidt PT,
Karling P
and 24 more — show all
Ohlsson B,
Simren M,
Walter S,
Nardone G,
Cuomo R,
Usai-Satta P,
Galeazzi F,
Neri M,
Portincasa P,
Bellini M,
Barbara G,
Latiano A,
Hübenthal M,
Thijs V,
Netea MG,
Jonkers D,
Chang L,
Mayer EA,
Wouters MM,
Boeckxstaens G,
Camilleri M,
Franke A,
Zhernakova A,
D'Amato M
Gastroenterology · 2018 · PMID 29626450
2 pages
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeirsson TE,
Gudbjartsson DF,
Surakka I,
Vink JM,
Amin N,
Geller F,
Sulem P,
Rafnar T,
Esko T,
Walter S,
Gieger C,
Rawal R
and 82 more — show all
Mangino M,
Prokopenko I,
Mägi R,
Keskitalo K,
Gudjonsdottir IH,
Gretarsdottir S,
Stefansson H,
Thompson JR,
Aulchenko YS,
Nelis M,
Aben KK,
den Heijer M,
Dirksen A,
Ashraf H,
Soranzo N,
Valdes AM,
Steves C,
Uitterlinden AG,
Hofman A,
Tönjes A,
Kovacs P,
Hottenga JJ,
Willemsen G,
Vogelzangs N,
Döring A,
Dahmen N,
Nitz B,
Pergadia ML,
Saez B,
De Diego V,
Lezcano V,
Garcia-Prats MD,
Ripatti S,
Perola M,
Kettunen J,
Hartikainen AL,
Pouta A,
Laitinen J,
Isohanni M,
Huei-Yi S,
Allen M,
Krestyaninova M,
Hall AS,
Jones GT,
van Rij AM,
Mueller T,
Dieplinger B,
Haltmayer M,
Jonsson S,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Kiemeney LA,
Mayordomo JI,
Lindholt JS,
Pedersen JH,
Franklin WA,
Wolf H,
Montgomery GW,
Heath AC,
Martin NG,
Madden PA,
Giegling I,
Rujescu D,
Järvelin MR,
Salomaa V,
Stumvoll M,
Spector TD,
Wichmann HE,
Metspalu A,
Samani NJ,
Penninx BW,
Oostra BA,
Boomsma DI,
Tiemeier H,
van Duijn CM,
Kaprio J,
Gulcher JR,
McCarthy MI,
Peltonen L,
Thorsteinsdottir U,
Stefansson K
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome
Bonfiglio F,
Liu X,
Smillie C,
Pandit A,
Kurilshikov A,
Bacigalupe R,
Zheng T,
Nim H,
Garcia-Etxebarria K,
Bujanda L,
Andreasson A,
Agreus L
and 15 more — show all
Walter S,
Abecasis G,
Eijsbouts C,
Jostins L,
Parkes M,
Hughes DA,
Timpson N,
Raes J,
Franke A,
Kennedy NA,
Regev A,
Zhernakova A,
Simren M,
Camilleri M,
D'Amato M
Cell genomics · 2021 · PMID 34957435 · open access
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.