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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.
10 matches for
Gamazon E.
Mapping the proteo-genomic convergence of human diseases
Pietzner M,
Wheeler E,
Carrasco-Zanini J,
Cortes A,
Koprulu M,
Wörheide MA,
Oerton E,
Cook J,
Stewart ID,
Kerrison ND,
Luan J,
Raffler J
and 9 more — show all
Science (New York, N.Y.) · 2021 · PMID 34648354
12 pages+
Rare and common genetic determinants of metabolic individuality and their effects on human health
Surendran P,
Stewart ID,
Au Yeung VPW,
Pietzner M,
Raffler J,
Wörheide MA,
Li C,
Smith RF,
Wittemans LBL,
Bomba L,
Menni C,
Zierer J
and 24 more — show all
Rossi N,
Sheridan PA,
Watkins NA,
Mangino M,
Hysi PG,
Di Angelantonio E,
Falchi M,
Spector TD,
Soranzo N,
Michelotti GA,
Arlt W,
Lotta LA,
Denaxas S,
Hemingway H,
Gamazon ER,
Howson JMM,
Wood AM,
Danesh J,
Wareham NJ,
Kastenmüller G,
Fauman EB,
Suhre K,
Butterworth AS,
Langenberg C
Nature medicine · 2022 · PMID 36357675 · open access
12 pages+
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Zhou W,
Kanai M,
Wu KH,
Rasheed H,
Tsuo K,
Hirbo JB,
Wang Y,
Bhattacharya A,
Zhao H,
Namba S,
Surakka I,
Wolford BN
and 140 more — show all
Lo Faro V,
Lopera-Maya EA,
Läll K,
Favé MJ,
Partanen JJ,
Chapman SB,
Karjalainen J,
Kurki M,
Maasha M,
Brumpton BM,
Chavan S,
Chen TT,
Daya M,
Ding Y,
Feng YA,
Guare LA,
Gignoux CR,
Graham SE,
Hornsby WE,
Ingold N,
Ismail SI,
Johnson R,
Laisk T,
Lin K,
Lv J,
Millwood IY,
Moreno-Grau S,
Nam K,
Palta P,
Pandit A,
Preuss MH,
Saad C,
Setia-Verma S,
Thorsteinsdottir U,
Uzunovic J,
Verma A,
Zawistowski M,
Zhong X,
Afifi N,
Al-Dabhani KM,
Al Thani A,
Bradford Y,
Campbell A,
Crooks K,
de Bock GH,
Damrauer SM,
Douville NJ,
Finer S,
Fritsche LG,
Fthenou E,
Gonzalez-Arroyo G,
Griffiths CJ,
Guo Y,
Hunt KA,
Ioannidis A,
Jansonius NM,
Konuma T,
Lee MTM,
Lopez-Pineda A,
Matsuda Y,
Marioni RE,
Moatamed B,
Nava-Aguilar MA,
Numakura K,
Patil S,
Rafaels N,
Richmond A,
Rojas-Muñoz A,
Shortt JA,
Straub P,
Tao R,
Vanderwerff B,
Vernekar M,
Veturi Y,
Barnes KC,
Boezen M,
Chen Z,
Chen CY,
Cho J,
Smith GD,
Finucane HK,
Franke L,
Gamazon ER,
Ganna A,
Gaunt TR,
Ge T,
Huang H,
Huffman J,
Katsanis N,
Koskela JT,
Lajonchere C,
Law MH,
Li L,
Lindgren CM,
Loos RJF,
MacGregor S,
Matsuda K,
Olsen CM,
Porteous DJ,
Shavit JA,
Snieder H,
Takano T,
Trembath RC,
Vonk JM,
Whiteman DC,
Wicks SJ,
Wijmenga C,
Wright J,
Zheng J,
Zhou X,
Awadalla P,
Boehnke M,
Bustamante CD,
Cox NJ,
Fatumo S,
Geschwind DH,
Hayward C,
Hveem K,
Kenny EE,
Lee S,
Lin YF,
Mbarek H,
Mägi R,
Martin HC,
Medland SE,
Okada Y,
Palotie AV,
Pasaniuc B,
Rader DJ,
Ritchie MD,
Sanna S,
Smoller JW,
Stefansson K,
van Heel DA,
Walters RG,
Zöllner S,
Martin AR,
Willer CJ,
Daly MJ,
Neale BM
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 pages+
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits
Petty LE,
Chen HH,
Frankel EG,
Zhu W,
Downie CG,
Graff M,
Lin P,
Sharma P,
Zhang X,
Scartozzi AC,
Roshani R,
Landman JM
and 80 more — show all
Boehnke M,
Bowden DW,
Chambers JC,
Mahajan A,
McCarthy MI,
Ng MCY,
Sim X,
Spracklen CN,
Zhang W,
Preuss M,
Bottinger EP,
Nadkarni GN,
Loos RJF,
Chen YI,
Tan J,
Ipp E,
Genter P,
Emery LS,
Louie T,
Sofer T,
Stilp AM,
Taylor KD,
Xiang AH,
Buchanan TA,
Roll K,
Gao C,
Palmer ND,
Norris JM,
Wagenknecht LE,
Nousome D,
Varma R,
McKean-Cowdin R,
Guo X,
Hai Y,
Hsueh W,
Sandow K,
Parra EJ,
Cruz M,
Valladares-Salgado A,
Wacher-Rodarte N,
Rotter JI,
Goodarzi MO,
Rich SS,
Bertoni A,
Raffel LJ,
Nadler JL,
Kandeel FR,
Duggirala R,
Blangero J,
Lehman DM,
DeFronzo RA,
Thameem F,
Wang Y,
Gahagan S,
Blanco E,
Burrows R,
Huerta-Chagoya A,
Florez JC,
Tusie-Luna T,
González-Villalpando C,
Orozco L,
Haiman CA,
Hanis CL,
Rohde R,
Whitsel EA,
Reiner AP,
Kooperberg C,
Li Y,
Duan Q,
Lee M,
Correa-Burrows P,
Fried SK,
North KE,
McCormick JB,
Fisher-Hoch SP,
Gamazon ER,
Morris AP,
Mercader JM,
Highland HM,
Below JE
DIAMANTE Hispanic/Latino Consortium · Global Hispanic Lipids Consortium
Nature communications · 2025 · PMID 40210677 · open access
12 pages+
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs
Below JE,
Parra EJ,
Gamazon ER,
Torres J,
Krithika S,
Candille S,
Lu Y,
Manichakul A,
Peralta-Romero J,
Duan Q,
Li Y,
Morris AP
and 13 more — show all
Gottesman O,
Bottinger E,
Wang XQ,
Taylor KD,
Ida Chen YD,
Rotter JI,
Rich SS,
Loos RJ,
Tang H,
Cox NJ,
Cruz M,
Hanis CL,
Valladares-Salgado A
Scientific reports · 2016 · PMID 26780889 · open access
3 pages
Genome-wide association study of Tourette's syndrome
Scharf JM,
Yu D,
Mathews CA,
Neale BM,
Stewart SE,
Fagerness JA,
Evans P,
Gamazon E,
Edlund CK,
Service SK,
Tikhomirov A,
Osiecki L
and 86 more — show all
Illmann C,
Pluzhnikov A,
Konkashbaev A,
Davis LK,
Han B,
Crane J,
Moorjani P,
Crenshaw AT,
Parkin MA,
Reus VI,
Lowe TL,
Rangel-Lugo M,
Chouinard S,
Dion Y,
Girard S,
Cath DC,
Smit JH,
King RA,
Fernandez TV,
Leckman JF,
Kidd KK,
Kidd JR,
Pakstis AJ,
State MW,
Herrera LD,
Romero R,
Fournier E,
Sandor P,
Barr CL,
Phan N,
Gross-Tsur V,
Benarroch F,
Pollak Y,
Budman CL,
Bruun RD,
Erenberg G,
Naarden AL,
Lee PC,
Weiss N,
Kremeyer B,
Berrío GB,
Campbell DD,
Cardona Silgado JC,
Ochoa WC,
Mesa Restrepo SC,
Muller H,
Valencia Duarte AV,
Lyon GJ,
Leppert M,
Morgan J,
Weiss R,
Grados MA,
Anderson K,
Davarya S,
Singer H,
Walkup J,
Jankovic J,
Tischfield JA,
Heiman GA,
Gilbert DL,
Hoekstra PJ,
Robertson MM,
Kurlan R,
Liu C,
Gibbs JR,
Singleton A,
Hardy J,
Strengman E,
Ophoff RA,
Wagner M,
Moessner R,
Mirel DB,
Posthuma D,
Sabatti C,
Eskin E,
Conti DV,
Knowles JA,
Ruiz-Linares A,
Rouleau GA,
Purcell S,
Heutink P,
Oostra BA,
McMahon WM,
Freimer NB,
Cox NJ,
Pauls DL
North American Brain Expression Consortium · UK Human Brain Expression Database
Molecular psychiatry · 2013 · PMID 22889924 · open access
2 pages
Genetic analysis in African ancestry populations reveals genetic contributors to lung cancer susceptibility
Betti MJ,
Jaworski J,
Zhao S,
Rao JS,
Ryan BM,
Schwartz AG,
Lusk CM,
McCoy L,
Wiencke JK,
Bruce MA,
Chanock S,
Gamazon ER
and 2 more — show all
American journal of human genetics · 2025 · PMID 40829600
2 pages
Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer
Huo D,
Feng Y,
Haddad S,
Zheng Y,
Yao S,
Han YJ,
Ogundiran TO,
Adebamowo C,
Ojengbede O,
Falusi AG,
Zheng W,
Blot W
and 35 more — show all
Cai Q,
Signorello L,
John EM,
Bernstein L,
Hu JJ,
Ziegler RG,
Nyante S,
Bandera EV,
Ingles SA,
Press MF,
Deming SL,
Rodriguez-Gil JL,
Nathanson KL,
Domchek SM,
Rebbeck TR,
Ruiz-Narváez EA,
Sucheston-Campbell LE,
Bensen JT,
Simon MS,
Hennis A,
Nemesure B,
Leske MC,
Ambs S,
Chen LS,
Qian F,
Gamazon ER,
Lunetta KL,
Cox NJ,
Chanock SJ,
Kolonel LN,
Olshan AF,
Ambrosone CB,
Olopade OI,
Palmer JR,
Haiman CA
Human molecular genetics · 2016 · PMID 28171663
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.