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2,681 papers hold this site up. Every variant and condition page names
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Search your name, your journal, or a PMID.
145 matches for
He G,
showing the first 20.
The genetic architecture of fibromyalgia across 2.5 million individuals
Kerrebijn I,
Bjornsdottir G,
Arbabi K,
Urpa L,
Haapaniemi H,
Thorleifsson G,
Stefansdottir L,
Frangakis S,
Valliere J,
Kunorozva L,
Abner E,
Ji C
and 41 more — show all
Kangur M,
Aagaard B,
Bliddal H,
Brunak S,
Bruun MT,
Didriksen M,
Erikstrup C,
Finer S,
Geirsson AJ,
Gudbjartsson DF,
Hansen TF,
van Heel D,
Jonsdottir I,
Knight S,
Knowlton KU,
Mikkelsen C,
Nadauld LD,
Olafsdottir TA,
Ostrowski SR,
Pedersen OBV,
Saevarsdottir S,
Skuladottir AT,
Sørensen E,
Stefansson H,
Sulem P,
Sveinsson OA,
Thorlacius GE,
Thorsteinsdottir U,
Ullum H,
Vikingsson A,
Werge TM,
Saxena R,
Stefansson K,
Brummett CM,
Glintborg B,
Clauw DJ,
Thorgeirsson TE,
Williams FMK,
Sinnott-Armstrong N,
Ollila HM,
Wainberg M
Chronic Pain Genomics Consortium · FinnGen and 3 more consortia
Nature medicine · 2026 · PMID 42521817 · open access
4 pages
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Wang TJ,
Zhang F,
Richards JB,
Kestenbaum B,
van Meurs JB,
Berry D,
Kiel DP,
Streeten EA,
Ohlsson C,
Koller DL,
Peltonen L,
Cooper JD
and 64 more — show all
O'Reilly PF,
Houston DK,
Glazer NL,
Vandenput L,
Peacock M,
Shi J,
Rivadeneira F,
McCarthy MI,
Anneli P,
de Boer IH,
Mangino M,
Kato B,
Smyth DJ,
Booth SL,
Jacques PF,
Burke GL,
Goodarzi M,
Cheung CL,
Wolf M,
Rice K,
Goltzman D,
Hidiroglou N,
Ladouceur M,
Wareham NJ,
Hocking LJ,
Hart D,
Arden NK,
Cooper C,
Malik S,
Fraser WD,
Hartikainen AL,
Zhai G,
Macdonald HM,
Forouhi NG,
Loos RJ,
Reid DM,
Hakim A,
Dennison E,
Liu Y,
Power C,
Stevens HE,
Jaana L,
Vasan RS,
Soranzo N,
Bojunga J,
Psaty BM,
Lorentzon M,
Foroud T,
Harris TB,
Hofman A,
Jansson JO,
Cauley JA,
Uitterlinden AG,
Gibson Q,
Järvelin MR,
Karasik D,
Siscovick DS,
Econs MJ,
Kritchevsky SB,
Florez JC,
Todd JA,
Dupuis J,
Hyppönen E,
Spector TD
Lancet (London, England) · 2010 · PMID 20541252
3 pages
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Heid IM,
Jackson AU,
Randall JC,
Winkler TW,
Qi L,
Steinthorsdottir V,
Thorleifsson G,
Zillikens MC,
Speliotes EK,
Mägi R,
Workalemahu T,
White CC
and 290 more — show all
Bouatia-Naji N,
Harris TB,
Berndt SI,
Ingelsson E,
Willer CJ,
Weedon MN,
Luan J,
Vedantam S,
Esko T,
Kilpeläinen TO,
Kutalik Z,
Li S,
Monda KL,
Dixon AL,
Holmes CC,
Kaplan LM,
Liang L,
Min JL,
Moffatt MF,
Molony C,
Nicholson G,
Schadt EE,
Zondervan KT,
Feitosa MF,
Ferreira T,
Lango Allen H,
Weyant RJ,
Wheeler E,
Wood AR,
Estrada K,
Goddard ME,
Lettre G,
Mangino M,
Nyholt DR,
Purcell S,
Smith AV,
Visscher PM,
Yang J,
McCarroll SA,
Nemesh J,
Voight BF,
Absher D,
Amin N,
Aspelund T,
Coin L,
Glazer NL,
Hayward C,
Heard-Costa NL,
Hottenga JJ,
Johansson A,
Johnson T,
Kaakinen M,
Kapur K,
Ketkar S,
Knowles JW,
Kraft P,
Kraja AT,
Lamina C,
Leitzmann MF,
McKnight B,
Morris AP,
Ong KK,
Perry JR,
Peters MJ,
Polasek O,
Prokopenko I,
Rayner NW,
Ripatti S,
Rivadeneira F,
Robertson NR,
Sanna S,
Sovio U,
Surakka I,
Teumer A,
van Wingerden S,
Vitart V,
Zhao JH,
Cavalcanti-Proença C,
Chines PS,
Fisher E,
Kulzer JR,
Lecoeur C,
Narisu N,
Sandholt C,
Scott LJ,
Silander K,
Stark K,
Tammesoo ML,
Teslovich TM,
Timpson NJ,
Watanabe RM,
Welch R,
Chasman DI,
Cooper MN,
Jansson JO,
Kettunen J,
Lawrence RW,
Pellikka N,
Perola M,
Vandenput L,
Alavere H,
Almgren P,
Atwood LD,
Bennett AJ,
Biffar R,
Bonnycastle LL,
Bornstein SR,
Buchanan TA,
Campbell H,
Day IN,
Dei M,
Dörr M,
Elliott P,
Erdos MR,
Eriksson JG,
Freimer NB,
Fu M,
Gaget S,
Geus EJ,
Gjesing AP,
Grallert H,
Grässler J,
Groves CJ,
Guiducci C,
Hartikainen AL,
Hassanali N,
Havulinna AS,
Herzig KH,
Hicks AA,
Hui J,
Igl W,
Jousilahti P,
Jula A,
Kajantie E,
Kinnunen L,
Kolcic I,
Koskinen S,
Kovacs P,
Kroemer HK,
Krzelj V,
Kuusisto J,
Kvaloy K,
Laitinen J,
Lantieri O,
Lathrop GM,
Lokki ML,
Luben RN,
Ludwig B,
McArdle WL,
McCarthy A,
Morken MA,
Nelis M,
Neville MJ,
Paré G,
Parker AN,
Peden JF,
Pichler I,
Pietiläinen KH,
Platou CG,
Pouta A,
Ridderstråle M,
Samani NJ,
Saramies J,
Sinisalo J,
Smit JH,
Strawbridge RJ,
Stringham HM,
Swift AJ,
Teder-Laving M,
Thomson B,
Usala G,
van Meurs JB,
van Ommen GJ,
Vatin V,
Volpato CB,
Wallaschofski H,
Walters GB,
Widen E,
Wild SH,
Willemsen G,
Witte DR,
Zgaga L,
Zitting P,
Beilby JP,
James AL,
James AL,
Kähönen M,
Lehtimäki T,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Raitakari O,
Ridker PM,
Stumvoll M,
Tönjes A,
Viikari J,
Balkau B,
Ben-Shlomo Y,
Bergman RN,
Boeing H,
Smith GD,
Ebrahim S,
Froguel P,
Hansen T,
Hengstenberg C,
Hveem K,
Isomaa B,
Jørgensen T,
Karpe F,
Khaw KT,
Laakso M,
Lawlor DA,
Marre M,
Meitinger T,
Metspalu A,
Midthjell K,
Pedersen O,
Salomaa V,
Schwarz PE,
Schwarz PE,
Tuomi T,
Tuomilehto J,
Valle TT,
Wareham NJ,
Arnold AM,
Beckmann JS,
Bergmann S,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Collins FS,
Eiriksdottir G,
Gudnason V,
Gyllensten U,
Hamsten A,
Hattersley AT,
Hofman A,
Hu FB,
Illig T,
Iribarren C,
Jarvelin MR,
Kao WH,
Kaprio J,
Launer LJ,
Munroe PB,
Oostra B,
Penninx BW,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rissanen A,
Rudan I,
Shuldiner AR,
Soranzo N,
Spector TD,
Syvanen AC,
Uda M,
Uitterlinden A,
Völzke H,
Vollenweider P,
Wilson JF,
Witteman JC,
Wright AF,
Abecasis GR,
Boehnke M,
Borecki IB,
Deloukas P,
Frayling TM,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
North KE,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
Hirschhorn JN,
Assimes TL,
Wichmann HE,
Thorsteinsdottir U,
van Duijn CM,
Stefansson K,
Cupples LA,
Loos RJ,
Barroso I,
McCarthy MI,
Fox CS,
Mohlke KL,
Lindgren CM
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations
Lona-Durazo F,
Hernandez-Pacheco N,
Fan S,
Zhang T,
Choi J,
Kovacs MA,
Loftus SK,
Le P,
Edwards M,
Fortes-Lima CA,
Fortes-Lima CA,
Eng C
and 15 more — show all
Huntsman S,
Hu D,
Gómez-Cabezas EJ,
Marín-Padrón LC,
Grauholm J,
Mors O,
Burchard EG,
Norton HL,
Pavan WJ,
Brown KM,
Tishkoff S,
Pino-Yanes M,
Beleza S,
Marcheco-Teruel B,
Parra EJ
BMC genetics · 2019 · PMID 31315583 · open access
3 pages
The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages
Li S,
Weinstein G,
Zare H,
Teumer A,
Völker U,
Friedrich N,
Knol MJ,
Satizabal CL,
Petyuk VA,
Adams HHH,
Launer LJ,
Bennett DA
and 6 more — show all
Brain communications · 2020 · PMID 33345186 · open access
3 pages
Discovery of 42 genome-wide significant loci associated with dyslexia
Doust C,
Fontanillas P,
Eising E,
Gordon SD,
Wang Z,
Alagöz G,
Molz B,
Pourcain BS,
Francks C,
Marioni RE,
Zhao J,
Paracchini S
and 15 more — show all
Talcott JB,
Monaco AP,
Stein JF,
Gruen JR,
Olson RK,
Willcutt EG,
DeFries JC,
Pennington BF,
Smith SD,
Wright MJ,
Martin NG,
Auton A,
Bates TC,
Fisher SE,
Luciano M
23andMe Research Team · Quantitative Trait Working Group of the GenLang Consortium
Nature genetics · 2022 · PMID 36266505 · open access
3 pages
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts
Li S,
Sanna S,
Maschio A,
Busonero F,
Usala G,
Mulas A,
Lai S,
Dei M,
Orrù M,
Albai G,
Bandinelli S,
Schlessinger D
and 12 more — show all
Lakatta E,
Scuteri A,
Najjar SS,
Guralnik J,
Naitza S,
Crisponi L,
Cao A,
Abecasis G,
Ferrucci L,
Uda M,
Chen WM,
Nagaraja R
PLoS genetics · 2007 · PMID 17997608 · open access
2 pages
A scan for genetic determinants of human hair morphology: EDAR is associated with Asian hair thickness
Fujimoto A,
Kimura R,
Ohashi J,
Omi K,
Yuliwulandari R,
Batubara L,
Mustofa MS,
Samakkarn U,
Settheetham-Ishida W,
Ishida T,
Morishita Y,
Furusawa T
and 3 more — show all
Human molecular genetics · 2008 · PMID 18065779
2 pages
A genome-wide association study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that affects disease progression of chronic HBV infection
Liu L,
Li J,
Yao J,
Yu J,
Zhang J,
Ning Q,
Wen Z,
Yang D,
He Y,
Kong X,
Song Q,
Chen M
and 4 more — show all
Viral immunology · 2011 · PMID 22004137
2 pages
Genome-wide association analysis identifies susceptibility loci for migraine without aura
Freilinger T,
Anttila V,
de Vries B,
Malik R,
Kallela M,
Terwindt GM,
Pozo-Rosich P,
Winsvold B,
Nyholt DR,
van Oosterhout WP,
Artto V,
Todt U
and 31 more — show all
Hämäläinen E,
Fernández-Morales J,
Louter MA,
Kaunisto MA,
Schoenen J,
Raitakari O,
Lehtimäki T,
Vila-Pueyo M,
Göbel H,
Wichmann E,
Sintas C,
Uitterlinden AG,
Hofman A,
Rivadeneira F,
Heinze A,
Tronvik E,
van Duijn CM,
Kaprio J,
Cormand B,
Wessman M,
Frants RR,
Meitinger T,
Müller-Myhsok B,
Zwart JA,
Färkkilä M,
Macaya A,
Ferrari MD,
Kubisch C,
Palotie A,
Dichgans M,
van den Maagdenberg AM
International Headache Genetics Consortium
Nature genetics · 2012 · PMID 22683712
2 pages
T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection
Lee RJ,
Xiong G,
Kofonow JM,
Chen B,
Lysenko A,
Jiang P,
Abraham V,
Doghramji L,
Adappa ND,
Palmer JN,
Kennedy DW,
Beauchamp GK
and 5 more — show all
The Journal of clinical investigation · 2012 · PMID 23041624
2 pages
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study
Manichaikul A,
Hoffman EA,
Smolonska J,
Gao W,
Cho MH,
Baumhauer H,
Budoff M,
Austin JH,
Washko GR,
Carr JJ,
Kaufman JD,
Pottinger T
and 22 more — show all
Powell CA,
Wijmenga C,
Zanen P,
Groen HJ,
Postma DS,
Wanner A,
Rouhani FN,
Brantly ML,
Powell R,
Smith BM,
Rabinowitz D,
Raffel LJ,
Hinckley Stukovsky KD,
Crapo JD,
Beaty TH,
Hokanson JE,
Silverman EK,
Dupuis J,
O'Connor GT,
Boezen HM,
Rich SS,
Barr RG
American journal of respiratory and critical care medicine · 2014 · PMID 24383474
2 pages
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Springelkamp H,
Höhn R,
Mishra A,
Hysi PG,
Khor CC,
Loomis SJ,
Bailey JN,
Gibson J,
Thorleifsson G,
Janssen SF,
Luo X,
Ramdas WD
and 66 more — show all
Vithana E,
Nongpiur ME,
Montgomery GW,
Xu L,
Mountain JE,
Gharahkhani P,
Lu Y,
Amin N,
Karssen LC,
Sim KS,
van Leeuwen EM,
Iglesias AI,
Verhoeven VJ,
Hauser MA,
Loon SC,
Despriet DD,
Nag A,
Venturini C,
Sanfilippo PG,
Schillert A,
Kang JH,
Landers J,
Jonasson F,
Cree AJ,
van Koolwijk LM,
Rivadeneira F,
Souzeau E,
Jonsson V,
Menon G,
Weinreb RN,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Ennis S,
Thorsteinsdottir U,
Burdon KP,
Spector TD,
Mirshahi A,
Saw SM,
Vingerling JR,
Teo YY,
Haines JL,
Wolfs RC,
Lemij HG,
Tai ES,
Jansonius NM,
Jonas JB,
Cheng CY,
Aung T,
Viswanathan AC,
Klaver CC,
Craig JE,
Macgregor S,
Mackey DA,
Lotery AJ,
Stefansson K,
Bergen AA,
Young TL,
Wiggs JL,
Pfeiffer N,
Wong TY,
Pasquale LR,
Hewitt AW,
van Duijn CM,
Hammond CJ
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium and 1 more consortia
Nature communications · 2014 · PMID 25241763 · 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.