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Is your paper here?
2,665 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.
49 matches for
Rust C,
showing the first 9.
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Willer CJ,
Speliotes EK,
Loos RJ,
Li S,
Lindgren CM,
Heid IM,
Berndt SI,
Elliott AL,
Jackson AU,
Lamina C,
Lettre G,
Lim N
and 133 more — show all
Lyon HN,
McCarroll SA,
Papadakis K,
Qi L,
Randall JC,
Roccasecca RM,
Sanna S,
Scheet P,
Weedon MN,
Wheeler E,
Zhao JH,
Jacobs LC,
Prokopenko I,
Soranzo N,
Tanaka T,
Timpson NJ,
Almgren P,
Bennett A,
Bergman RN,
Bingham SA,
Bonnycastle LL,
Brown M,
Burtt NP,
Chines P,
Coin L,
Collins FS,
Connell JM,
Cooper C,
Smith GD,
Dennison EM,
Deodhar P,
Elliott P,
Erdos MR,
Estrada K,
Evans DM,
Gianniny L,
Gieger C,
Gillson CJ,
Guiducci C,
Hackett R,
Hadley D,
Hall AS,
Havulinna AS,
Hebebrand J,
Hofman A,
Isomaa B,
Jacobs KB,
Johnson T,
Jousilahti P,
Jovanovic Z,
Khaw KT,
Kraft P,
Kuokkanen M,
Kuusisto J,
Laitinen J,
Lakatta EG,
Luan J,
Luben RN,
Mangino M,
McArdle WL,
Meitinger T,
Mulas A,
Munroe PB,
Narisu N,
Ness AR,
Northstone K,
O'Rahilly S,
Purmann C,
Rees MG,
Ridderstråle M,
Ring SM,
Rivadeneira F,
Ruokonen A,
Sandhu MS,
Saramies J,
Scott LJ,
Scuteri A,
Silander K,
Sims MA,
Song K,
Stephens J,
Stevens S,
Stringham HM,
Tung YC,
Valle TT,
Van Duijn CM,
Vimaleswaran KS,
Vollenweider P,
Waeber G,
Wallace C,
Watanabe RM,
Waterworth DM,
Watkins N,
Witteman JC,
Zeggini E,
Zhai G,
Zillikens MC,
Altshuler D,
Caulfield MJ,
Chanock SJ,
Farooqi IS,
Ferrucci L,
Guralnik JM,
Hattersley AT,
Hu FB,
Jarvelin MR,
Laakso M,
Mooser V,
Ong KK,
Ouwehand WH,
Salomaa V,
Samani NJ,
Spector TD,
Tuomi T,
Tuomilehto J,
Uda M,
Uitterlinden AG,
Wareham NJ,
Deloukas P,
Frayling TM,
Groop LC,
Hayes RB,
Hunter DJ,
Mohlke KL,
Peltonen L,
Schlessinger D,
Strachan DP,
Wichmann HE,
McCarthy MI,
Boehnke M,
Barroso I,
Abecasis GR,
Hirschhorn JN
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
1 page
Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies
Nolte IM,
Wallace C,
Newhouse SJ,
Waggott D,
Fu J,
Soranzo N,
Gwilliam R,
Deloukas P,
Savelieva I,
Zheng D,
Dalageorgou C,
Farrall M
and 24 more — show all
Samani NJ,
Connell J,
Brown M,
Dominiczak A,
Lathrop M,
Zeggini E,
Wain LV,
Newton-Cheh C,
Eijgelsheim M,
Rice K,
de Bakker PI,
Pfeufer A,
Sanna S,
Arking DE,
Asselbergs FW,
Spector TD,
Carter ND,
Jeffery S,
Tobin M,
Caulfield M,
Snieder H,
Paterson AD,
Munroe PB,
Jamshidi Y
Wellcome Trust Case Control Consortium · DCCT/EDIC Research Group and 2 more consortia
PloS one · 2009 · PMID 19587794 · open access
1 page
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts
Dehghan A,
Yang Q,
Peters A,
Basu S,
Bis JC,
Rudnicka AR,
Kavousi M,
Chen MH,
Baumert J,
Lowe GD,
McKnight B,
Tang W
and 29 more — show all
de Maat M,
Larson MG,
Eyhermendy S,
McArdle WL,
Lumley T,
Pankow JS,
Hofman A,
Massaro JM,
Rivadeneira F,
Kolz M,
Taylor KD,
van Duijn CM,
Kathiresan S,
Illig T,
Aulchenko YS,
Volcik KA,
Johnson AD,
Uitterlinden AG,
Tofler GH,
Gieger C,
Psaty BM,
Couper DJ,
Boerwinkle E,
Koenig W,
O'Donnell CJ,
Witteman JC,
Strachan DP,
Smith NL,
Folsom AR
Wellcome Trust Case Control Consortium
Circulation. Cardiovascular genetics · 2009 · PMID 20031576
1 page
Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4
Ellinghaus D,
Folseraas T,
Holm K,
Ellinghaus E,
Melum E,
Balschun T,
Laerdahl JK,
Shiryaev A,
Gotthardt DN,
Weismüller TJ,
Schramm C,
Wittig M
and 25 more — show all
Bergquist A,
Björnsson E,
Marschall HU,
Vatn M,
Teufel A,
Rust C,
Gieger C,
Wichmann HE,
Runz H,
Sterneck M,
Rupp C,
Braun F,
Weersma RK,
Wijmenga C,
Ponsioen CY,
Mathew CG,
Rutgeerts P,
Vermeire S,
Schrumpf E,
Hov JR,
Manns MP,
Boberg KM,
Schreiber S,
Franke A,
Karlsen TH
Hepatology (Baltimore, Md.) · 2013 · PMID 22821403
1 page
Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis
Buck D,
Albrecht E,
Aslam M,
Goris A,
Hauenstein N,
Jochim A,
Cepok S,
Grummel V,
Dubois B,
Berthele A,
Lichtner P,
Gieger C
and 2 more — show all
International Multiple Sclerosis Genetics Consortium · Wellcome Trust Case Control Consortium
Annals of neurology · 2013 · PMID 23225573
1 page
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis
Fakiola M,
Strange A,
Cordell HJ,
Miller EN,
Pirinen M,
Su Z,
Mishra A,
Mehrotra S,
Monteiro GR,
Band G,
Bellenguez C,
Dronov S
and 39 more — show all
Edkins S,
Freeman C,
Giannoulatou E,
Gray E,
Hunt SE,
Lacerda HG,
Langford C,
Pearson R,
Pontes NN,
Rai M,
Singh SP,
Smith L,
Sousa O,
Vukcevic D,
Bramon E,
Brown MA,
Casas JP,
Corvin A,
Duncanson A,
Jankowski J,
Markus HS,
Mathew CG,
Palmer CN,
Plomin R,
Rautanen A,
Sawcer SJ,
Trembath RC,
Viswanathan AC,
Wood NW,
Wilson ME,
Deloukas P,
Peltonen L,
Christiansen F,
Witt C,
Jeronimo SM,
Sundar S,
Spencer CC,
Blackwell JM,
Donnelly P
LeishGEN Consortium · Wellcome Trust Case Control Consortium 2
Nature genetics · 2013 · PMID 23291585 · open access
1 page
Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis
Robinson PC,
Claushuis TA,
Cortes A,
Martin TM,
Evans DM,
Leo P,
Mukhopadhyay P,
Bradbury LA,
Cremin K,
Harris J,
Maksymowych WP,
Inman RD
and 19 more — show all
Rahman P,
Haroon N,
Gensler L,
Powell JE,
van der Horst-Bruinsma IE,
Hewitt AW,
Craig JE,
Lim LL,
Wakefield D,
McCluskey P,
Voigt V,
Fleming P,
Degli-Esposti M,
Pointon JJ,
Weisman MH,
Wordsworth BP,
Reveille JD,
Rosenbaum JT,
Brown MA
Spondyloarthritis Research Consortium of Canada, Australio-Anglo-American Spondylitis Consortium, International Genetics of Ankylosing Spondylitis Consortium, Wellcome Trust Case Control Study 2, Mariapia Degli-Esposti
Arthritis & rheumatology (Hoboken, N.J.) · 2015 · PMID 25200001
1 page
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes
Meng W,
Shah KP,
Pollack S,
Toppila I,
Hebert HL,
McCarthy MI,
Groop L,
Ahlqvist E,
Lyssenko V,
Agardh E,
Daniell M,
Kaidonis G
and 28 more — show all
Craig JE,
Mitchell P,
Liew G,
Kifley A,
Wang JJ,
Christiansen MW,
Jensen RA,
Penman A,
Hancock HA,
Chen CJ,
Correa A,
Kuo JZ,
Li X,
Chen YI,
Rotter JI,
Klein R,
Klein B,
Wong TY,
Morris AD,
Doney ASF,
Colhoun HM,
Price AL,
Burdon KP,
Groop PH,
Sandholm N,
Grassi MA,
Sobrin L,
Palmer CNA
Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group
Acta ophthalmologica · 2018 · PMID 30178632 · 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.