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Is your paper here?
2,673 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
Yao S.
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Trpchevska N,
Freidin MB,
Broer L,
Oosterloo BC,
Yao S,
Zhou Y,
Vona B,
Bishop C,
Bizaki-Vallaskangas A,
Canlon B,
Castellana F,
Chasman DI
and 54 more — show all
Cherny S,
Christensen K,
Concas MP,
Correa A,
Elkon R,
Mengel-From J,
Gao Y,
Giersch ABS,
Girotto G,
Gudjonsson A,
Gudnason V,
Heard-Costa NL,
Hertzano R,
Hjelmborg JVB,
Hjerling-Leffler J,
Hoffman HJ,
Kaprio J,
Kettunen J,
Krebs K,
Kähler AK,
Lallemend F,
Launer LJ,
Lee IM,
Leonard H,
Li CM,
Lowenheim H,
Magnusson PKE,
van Meurs J,
Milani L,
Morton CC,
Mäkitie A,
Nalls MA,
Nardone GG,
Nygaard M,
Palviainen T,
Pratt S,
Quaranta N,
Rämö J,
Saarentaus E,
Sardone R,
Satizabal CL,
Schweinfurth JM,
Seshadri S,
Shiroma E,
Shulman E,
Simonsick E,
Spankovich C,
Tropitzsch A,
Lauschke VM,
Sullivan PF,
Goedegebure A,
Cederroth CR,
Williams FMK,
Nagtegaal AP
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction
Jia G,
Ping J,
Guo X,
Yang Y,
Tao R,
Li B,
Ambs S,
Barnard ME,
Chen Y,
Garcia-Closas M,
Gu J,
Hu JJ
and 35 more — show all
Huo D,
John EM,
Li CI,
Li JL,
Nathanson KL,
Nemesure B,
Olopade OI,
Pal T,
Press MF,
Sanderson M,
Sandler DP,
Shu XO,
Troester MA,
Yao S,
Adejumo PO,
Ahearn T,
Brewster AM,
Hennis AJM,
Makumbi T,
Ndom P,
O'Brien KM,
Olshan AF,
Oluwasanu MM,
Reid S,
Butler EN,
Huang M,
Ntekim A,
Qian H,
Zhang H,
Ambrosone CB,
Cai Q,
Long J,
Palmer JR,
Haiman CA,
Zheng W
Nature genetics · 2024 · PMID 38741014
5 pages
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC
Quan C,
Ren YQ,
Xiang LH,
Sun LD,
Xu AE,
Gao XH,
Chen HD,
Pu XM,
Wu RN,
Liang CZ,
Li JB,
Gao TW
and 55 more — show all
Zhang JZ,
Wang XL,
Wang J,
Yang RY,
Liang L,
Yu JB,
Zuo XB,
Zhang SQ,
Zhang SM,
Chen G,
Zheng XD,
Li P,
Zhu J,
Li YW,
Wei XD,
Hong WS,
Ye Y,
Zhang Y,
Wu WS,
Cheng H,
Dong PL,
Hu DY,
Li Y,
Li M,
Zhang X,
Tang HY,
Tang XF,
Xu SX,
He SM,
Lv YM,
Shen M,
Jiang HQ,
Wang Y,
Li K,
Kang XJ,
Liu YQ,
Sun L,
Liu ZF,
Xie SQ,
Zhu CY,
Xu Q,
Gao JP,
Hu WL,
Ni C,
Pan TM,
Li Y,
Yao S,
He CF,
Liu YS,
Yu ZY,
Yin XY,
Zhang FY,
Yang S,
Zhou Y,
Zhang XJ
Nature genetics · 2010 · PMID 20526339
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
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Watson HJ,
Yilmaz Z,
Thornton LM,
Hübel C,
Coleman JRI,
Gaspar HA,
Bryois J,
Hinney A,
Leppä VM,
Mattheisen M,
Medland SE,
Ripke S
and 198 more — show all
Yao S,
Giusti-Rodríguez P,
Hanscombe KB,
Purves KL,
Adan RAH,
Alfredsson L,
Ando T,
Andreassen OA,
Baker JH,
Berrettini WH,
Boehm I,
Boni C,
Perica VB,
Buehren K,
Burghardt R,
Cassina M,
Cichon S,
Clementi M,
Cone RD,
Courtet P,
Crow S,
Crowley JJ,
Danner UN,
Davis OSP,
de Zwaan M,
Dedoussis G,
Degortes D,
DeSocio JE,
Dick DM,
Dikeos D,
Dina C,
Dmitrzak-Weglarz M,
Docampo E,
Duncan LE,
Egberts K,
Ehrlich S,
Escaramís G,
Esko T,
Estivill X,
Farmer A,
Favaro A,
Fernández-Aranda F,
Fichter MM,
Fischer K,
Föcker M,
Foretova L,
Forstner AJ,
Forzan M,
Franklin CS,
Gallinger S,
Giegling I,
Giuranna J,
Gonidakis F,
Gorwood P,
Mayora MG,
Guillaume S,
Guo Y,
Hakonarson H,
Hatzikotoulas K,
Hauser J,
Hebebrand J,
Helder SG,
Herms S,
Herpertz-Dahlmann B,
Herzog W,
Huckins LM,
Hudson JI,
Imgart H,
Inoko H,
Janout V,
Jiménez-Murcia S,
Julià A,
Kalsi G,
Kaminská D,
Kaprio J,
Karhunen L,
Karwautz A,
Kas MJH,
Kennedy JL,
Keski-Rahkonen A,
Kiezebrink K,
Kim YR,
Klareskog L,
Klump KL,
Knudsen GPS,
La Via MC,
Le Hellard S,
Levitan RD,
Li D,
Lilenfeld L,
Lin BD,
Lissowska J,
Luykx J,
Magistretti PJ,
Maj M,
Mannik K,
Marsal S,
Marshall CR,
Mattingsdal M,
McDevitt S,
McGuffin P,
Metspalu A,
Meulenbelt I,
Micali N,
Mitchell K,
Monteleone AM,
Monteleone P,
Munn-Chernoff MA,
Nacmias B,
Navratilova M,
Ntalla I,
O'Toole JK,
Ophoff RA,
Padyukov L,
Palotie A,
Pantel J,
Papezova H,
Pinto D,
Rabionet R,
Raevuori A,
Ramoz N,
Reichborn-Kjennerud T,
Ricca V,
Ripatti S,
Ritschel F,
Roberts M,
Rotondo A,
Rujescu D,
Rybakowski F,
Santonastaso P,
Scherag A,
Scherer SW,
Schmidt U,
Schork NJ,
Schosser A,
Seitz J,
Slachtova L,
Slagboom PE,
Slof-Op 't Landt MCT,
Slopien A,
Sorbi S,
Świątkowska B,
Szatkiewicz JP,
Tachmazidou I,
Tenconi E,
Tortorella A,
Tozzi F,
Treasure J,
Tsitsika A,
Tyszkiewicz-Nwafor M,
Tziouvas K,
van Elburg AA,
van Furth EF,
Wagner G,
Walton E,
Widen E,
Zeggini E,
Zerwas S,
Zipfel S,
Bergen AW,
Boden JM,
Brandt H,
Crawford S,
Halmi KA,
Horwood LJ,
Johnson C,
Kaplan AS,
Kaye WH,
Mitchell JE,
Olsen CM,
Pearson JF,
Pedersen NL,
Strober M,
Werge T,
Whiteman DC,
Woodside DB,
Stuber GD,
Gordon S,
Grove J,
Henders AK,
Juréus A,
Kirk KM,
Larsen JT,
Parker R,
Petersen L,
Jordan J,
Kennedy M,
Montgomery GW,
Wade TD,
Birgegård A,
Lichtenstein P,
Norring C,
Landén M,
Martin NG,
Mortensen PB,
Sullivan PF,
Breen G,
Bulik CM
Anorexia Nervosa Genetics Initiative · Eating Disorders Working Group of the Psychiatric Genomics Consortium
Nature genetics · 2019 · PMID 31308545
1 page
UACA locus is associated with breast cancer chemoresistance and survival
Zhu Q,
Schultz E,
Long J,
Roh JM,
Valice E,
Laurent CA,
Radimer KH,
Yan L,
Ergas IJ,
Davis W,
Ranatunga D,
Gandhi S
and 7 more — show all
NPJ breast cancer · 2022 · PMID 35322040 · 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.