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2,657 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.
7 matches for
Dermitzakis E.
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
Houlston RS,
Cheadle J,
Dobbins SE,
Tenesa A,
Jones AM,
Howarth K,
Spain SL,
Broderick P,
Domingo E,
Farrington S,
Prendergast JG,
Pittman AM
and 33 more — show all
Theodoratou E,
Smith CG,
Olver B,
Walther A,
Barnetson RA,
Churchman M,
Jaeger EE,
Penegar S,
Barclay E,
Martin L,
Gorman M,
Mager R,
Johnstone E,
Midgley R,
Niittymäki I,
Tuupanen S,
Colley J,
Idziaszczyk S,
Thomas HJ,
Lucassen AM,
Evans DG,
Maher ER,
Maughan T,
Dimas A,
Dermitzakis E,
Cazier JB,
Aaltonen LA,
Pharoah P,
Kerr DJ,
Carvajal-Carmona LG,
Campbell H,
Dunlop MG,
Tomlinson IP
COGENT Consortium · CORGI Consortium and 2 more consortia
Nature genetics · 2010 · PMID 20972440 · open access
4 pages
A genome-wide association study of testicular germ cell tumor
Rapley EA,
Turnbull C,
Al Olama AA,
Dermitzakis ET,
Linger R,
Huddart RA,
Renwick A,
Hughes D,
Hines S,
Seal S,
Morrison J,
Nsengimana J
and 5 more — show all
UK Testicular Cancer Collaboration
Nature genetics · 2009 · PMID 19483681
3 pages
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
Strawbridge RJ,
Dupuis J,
Prokopenko I,
Barker A,
Ahlqvist E,
Rybin D,
Petrie JR,
Travers ME,
Bouatia-Naji N,
Dimas AS,
Nica A,
Wheeler E
and 91 more — show all
Chen H,
Voight BF,
Taneera J,
Kanoni S,
Peden JF,
Turrini F,
Gustafsson S,
Zabena C,
Almgren P,
Barker DJ,
Barnes D,
Dennison EM,
Eriksson JG,
Eriksson P,
Eury E,
Folkersen L,
Fox CS,
Frayling TM,
Goel A,
Gu HF,
Horikoshi M,
Isomaa B,
Jackson AU,
Jameson KA,
Kajantie E,
Kerr-Conte J,
Kuulasmaa T,
Kuusisto J,
Loos RJ,
Luan J,
Makrilakis K,
Manning AK,
Martínez-Larrad MT,
Narisu N,
Nastase Mannila M,
Ohrvik J,
Osmond C,
Pascoe L,
Payne F,
Sayer AA,
Sennblad B,
Silveira A,
Stancáková A,
Stirrups K,
Swift AJ,
Syvänen AC,
Tuomi T,
van 't Hooft FM,
Walker M,
Weedon MN,
Xie W,
Zethelius B,
Ongen H,
Mälarstig A,
Hopewell JC,
Saleheen D,
Chambers J,
Parish S,
Danesh J,
Kooner J,
Ostenson CG,
Lind L,
Cooper CC,
Serrano-Ríos M,
Ferrannini E,
Forsen TJ,
Clarke R,
Franzosi MG,
Seedorf U,
Watkins H,
Froguel P,
Johnson P,
Deloukas P,
Collins FS,
Laakso M,
Dermitzakis ET,
Boehnke M,
McCarthy MI,
Wareham NJ,
Groop L,
Pattou F,
Gloyn AL,
Dedoussis GV,
Lyssenko V,
Meigs JB,
Barroso I,
Watanabe RM,
Ingelsson E,
Langenberg C,
Hamsten A,
Florez JC
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Diabetes · 2011 · PMID 21873549 · open access
3 pages
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Lagou V,
Mägi R,
Hottenga JJ,
Grallert H,
Perry JRB,
Bouatia-Naji N,
Marullo L,
Rybin D,
Jansen R,
Min JL,
Dimas AS,
Ulrich A
and 192 more — show all
Zudina L,
Gådin JR,
Jiang L,
Faggian A,
Bonnefond A,
Fadista J,
Stathopoulou MG,
Isaacs A,
Willems SM,
Navarro P,
Tanaka T,
Jackson AU,
Montasser ME,
O'Connell JR,
Bielak LF,
Webster RJ,
Saxena R,
Stafford JM,
Pourcain BS,
Timpson NJ,
Salo P,
Shin SY,
Amin N,
Smith AV,
Li G,
Verweij N,
Goel A,
Ford I,
Johnson PCD,
Johnson T,
Kapur K,
Thorleifsson G,
Strawbridge RJ,
Rasmussen-Torvik LJ,
Esko T,
Mihailov E,
Fall T,
Fraser RM,
Mahajan A,
Kanoni S,
Giedraitis V,
Kleber ME,
Silbernagel G,
Meyer J,
Müller-Nurasyid M,
Ganna A,
Sarin AP,
Yengo L,
Shungin D,
Luan J,
Horikoshi M,
An P,
Sanna S,
Boettcher Y,
Rayner NW,
Nolte IM,
Zemunik T,
Iperen EV,
Kovacs P,
Hastie ND,
Wild SH,
McLachlan S,
Campbell S,
Polasek O,
Carlson O,
Egan J,
Kiess W,
Willemsen G,
Kuusisto J,
Laakso M,
Dimitriou M,
Hicks AA,
Rauramaa R,
Bandinelli S,
Thorand B,
Liu Y,
Miljkovic I,
Lind L,
Doney A,
Perola M,
Hingorani A,
Kivimaki M,
Kumari M,
Bennett AJ,
Groves CJ,
Herder C,
Koistinen HA,
Kinnunen L,
Faire U,
Bakker SJL,
Uusitupa M,
Palmer CNA,
Jukema JW,
Sattar N,
Pouta A,
Snieder H,
Boerwinkle E,
Pankow JS,
Magnusson PK,
Krus U,
Scapoli C,
de Geus EJCN,
Blüher M,
Wolffenbuttel BHR,
Province MA,
Abecasis GR,
Meigs JB,
Hovingh GK,
Lindström J,
Wilson JF,
Wright AF,
Dedoussis GV,
Bornstein SR,
Schwarz PEH,
Tönjes A,
Winkelmann BR,
Boehm BO,
März W,
Metspalu A,
Price JF,
Deloukas P,
Körner A,
Lakka TA,
Keinanen-Kiukaanniemi SM,
Saaristo TE,
Bergman RN,
Tuomilehto J,
Wareham NJ,
Langenberg C,
Männistö S,
Franks PW,
Hayward C,
Vitart V,
Kaprio J,
Visvikis-Siest S,
Balkau B,
Altshuler D,
Rudan I,
Stumvoll M,
Campbell H,
van Duijn CM,
Gieger C,
Illig T,
Ferrucci L,
Pedersen NL,
Pramstaller PP,
Boehnke M,
Frayling TM,
Shuldiner AR,
Peyser PA,
Kardia SLR,
Palmer LJ,
Penninx BW,
Meneton P,
Harris TB,
Navis G,
Harst PV,
Smith GD,
Forouhi NG,
Loos RJF,
Salomaa V,
Soranzo N,
Boomsma DI,
Groop L,
Tuomi T,
Hofman A,
Munroe PB,
Gudnason V,
Siscovick DS,
Watkins H,
Lecoeur C,
Vollenweider P,
Franco-Cereceda A,
Eriksson P,
Jarvelin MR,
Stefansson K,
Hamsten A,
Nicholson G,
Karpe F,
Dermitzakis ET,
Lindgren CM,
McCarthy MI,
Froguel P,
Kaakinen MA,
Lyssenko V,
Watanabe RM,
Ingelsson E,
Florez JC,
Dupuis J,
Barroso I,
Morris AP,
Prokopenko I
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC)
Nature communications · 2021 · PMID 33402679 · open access
3 pages
Genetic determinants of zinc homeostasis and its role in cardiometabolic diseases
Sadler MC,
Ghobril JP,
Borisov O,
Perrais M,
Schiano G,
Petrovic D,
Ha E,
Ponte B,
Li Y,
Rodriguez-Hernandez Z,
Pruijm M,
Ackermann D
and 20 more — show all
Guessous I,
Stringhini S,
Ehret G,
Corre T,
Vogt B,
Martin PY,
Ongen H,
Dermitzakis E,
Williams JE,
Murdoch BM,
McGuire MK,
Meehan CL,
Lenglet S,
Susztak K,
Vaucher J,
Thomas A,
Devuyst O,
Köttgen A,
Bochud M,
Kutalik Z
INSPIRE Consortium
PLoS genetics · 2025 · PMID 41325371 · open access
3 pages
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis
Hinds DA,
Buil A,
Ziemek D,
Martinez-Perez A,
Malik R,
Folkersen L,
Germain M,
Mälarstig A,
Brown A,
Soria JM,
Dichgans M,
Bing N
and 7 more — show all
METASTROKE Consortium, INVENT Consortium
Human molecular genetics · 2016 · PMID 26908601
2 pages
Genetic Landscape of the ACE2 Coronavirus Receptor
Yang Z,
Macdonald-Dunlop E,
Chen J,
Zhai R,
Li T,
Richmond A,
Klarić L,
Pirastu N,
Ning Z,
Zheng C,
Wang Y,
Huang T
and 57 more — show all
He Y,
Guo H,
Ying K,
Gustafsson S,
Prins B,
Ramisch A,
Dermitzakis ET,
Png G,
Eriksson N,
Haessler J,
Hu X,
Zanetti D,
Boutin T,
Hwang SJ,
Wheeler E,
Pietzner M,
Raffield LM,
Kalnapenkis A,
Peters JE,
Viñuela A,
Gilly A,
Elmståhl S,
Dedoussis G,
Petrie JR,
Polašek O,
Folkersen L,
Chen Y,
Yao C,
Võsa U,
Pairo-Castineira E,
Clohisey S,
Bretherick AD,
Rawlik K,
Esko T,
Enroth S,
Johansson Å,
Gyllensten U,
Langenberg C,
Levy D,
Hayward C,
Assimes TL,
Kooperberg C,
Manichaikul AW,
Siegbahn A,
Wallentin L,
Lind L,
Zeggini E,
Schwenk JM,
Butterworth AS,
Michaëlsson K,
Pawitan Y,
Joshi PK,
Baillie JK,
Mälarstig A,
Reiner AP,
Wilson JF,
Shen X
GenOMICC Consortium† · IMI-DIRECT Consortium†
Circulation · 2022 · PMID 35387486 · open access
2 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.