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Is your paper here?
2,663 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
Xu M.
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci
He M,
Xu M,
Zhang B,
Liang J,
Chen P,
Lee JY,
Johnson TA,
Li H,
Yang X,
Dai J,
Liang L,
Gui L
and 79 more — show all
Qi Q,
Huang J,
Li Y,
Adair LS,
Aung T,
Cai Q,
Cheng CY,
Cho MC,
Cho YS,
Chu M,
Cui B,
Gao YT,
Go MJ,
Gu D,
Gu W,
Guo H,
Hao Y,
Hong J,
Hu Z,
Hu Y,
Huang J,
Hwang JY,
Ikram MK,
Jin G,
Kang DH,
Khor CC,
Kim BJ,
Kim HT,
Kubo M,
Lee J,
Lee J,
Lee NR,
Li R,
Li J,
Liu J,
Longe J,
Lu W,
Lu X,
Miao X,
Okada Y,
Ong RT,
Qiu G,
Seielstad M,
Sim X,
Song H,
Takeuchi F,
Tanaka T,
Taylor PR,
Wang L,
Wang W,
Wang Y,
Wu C,
Wu Y,
Xiang YB,
Yamamoto K,
Yang H,
Liao M,
Yokota M,
Young T,
Zhang X,
Kato N,
Wang QK,
Zheng W,
Zheng W,
Hu FB,
Lin D,
Shen H,
Teo YY,
Mo Z,
Wong TY,
Lin X,
Mohlke KL,
Ning G,
Tsunoda T,
Han BG,
Shu XO,
Tai ES,
Wu T,
Qi L
Human molecular genetics · 2015 · PMID 25429064
12 pages+
Exome-wide association study of plasma lipids in >300,000 individuals
Liu DJ,
Peloso GM,
Yu H,
Butterworth AS,
Wang X,
Mahajan A,
Saleheen D,
Emdin C,
Alam D,
Alves AC,
Amouyel P,
Di Angelantonio E
and 215 more — show all
Arveiler D,
Assimes TL,
Auer PL,
Baber U,
Ballantyne CM,
Bang LE,
Benn M,
Bis JC,
Boehnke M,
Boerwinkle E,
Bork-Jensen J,
Bottinger EP,
Brandslund I,
Brown M,
Busonero F,
Caulfield MJ,
Chambers JC,
Chasman DI,
Chen YE,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Connell JM,
Cucca F,
Cupples LA,
Damrauer SM,
Davies G,
Deary IJ,
Dedoussis G,
Denny JC,
Dominiczak A,
Dubé MP,
Ebeling T,
Eiriksdottir G,
Esko T,
Farmaki AE,
Feitosa MF,
Ferrario M,
Ferrieres J,
Ford I,
Fornage M,
Franks PW,
Frayling TM,
Frikke-Schmidt R,
Fritsche LG,
Frossard P,
Fuster V,
Ganesh SK,
Gao W,
Garcia ME,
Gieger C,
Giulianini F,
Goodarzi MO,
Grallert H,
Grarup N,
Groop L,
Grove ML,
Gudnason V,
Hansen T,
Harris TB,
Hayward C,
Hirschhorn JN,
Holmen OL,
Huffman J,
Huo Y,
Hveem K,
Jabeen S,
Jackson AU,
Jakobsdottir J,
Jarvelin MR,
Jensen GB,
Jørgensen ME,
Jukema JW,
Justesen JM,
Kamstrup PR,
Kanoni S,
Karpe F,
Kee F,
Khera AV,
Klarin D,
Koistinen HA,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka T,
Langenberg C,
Langsted A,
Launer LJ,
Lauritzen T,
Liewald DCM,
Lin LA,
Linneberg A,
Loos RJF,
Lu Y,
Lu X,
Mägi R,
Malarstig A,
Manichaikul A,
Manning AK,
Mäntyselkä P,
Marouli E,
Masca NGD,
Maschio A,
Meigs JB,
Melander O,
Metspalu A,
Morris AP,
Morrison AC,
Mulas A,
Müller-Nurasyid M,
Munroe PB,
Neville MJ,
Nielsen JB,
Nielsen SF,
Nordestgaard BG,
Ordovas JM,
Mehran R,
O'Donnell CJ,
Orho-Melander M,
Molony CM,
Muntendam P,
Padmanabhan S,
Palmer CNA,
Pasko D,
Patel AP,
Pedersen O,
Perola M,
Peters A,
Pisinger C,
Pistis G,
Polasek O,
Poulter N,
Psaty BM,
Rader DJ,
Rasheed A,
Rauramaa R,
Reilly DF,
Reiner AP,
Renström F,
Rich SS,
Ridker PM,
Rioux JD,
Robertson NR,
Roden DM,
Rotter JI,
Rudan I,
Salomaa V,
Samani NJ,
Sanna S,
Sattar N,
Schmidt EM,
Scott RA,
Sever P,
Sevilla RS,
Shaffer CM,
Sim X,
Sivapalaratnam S,
Small KS,
Smith AV,
Smith BH,
Somayajula S,
Southam L,
Spector TD,
Speliotes EK,
Starr JM,
Stirrups KE,
Stitziel N,
Strauch K,
Stringham HM,
Surendran P,
Tada H,
Tall AR,
Tang H,
Tardif JC,
Taylor KD,
Trompet S,
Tsao PS,
Tuomilehto J,
Tybjaerg-Hansen A,
van Zuydam NR,
Varbo A,
Varga TV,
Virtamo J,
Waldenberger M,
Wang N,
Wareham NJ,
Warren HR,
Weeke PE,
Weinstock J,
Wessel J,
Wilson JG,
Wilson PWF,
Xu M,
Yaghootkar H,
Young R,
Zeggini E,
Zhang H,
Zheng NS,
Zhang W,
Zhang Y,
Zhou W,
Zhou Y,
Zoledziewska M,
Howson JMM,
Danesh J,
McCarthy MI,
Cowan CA,
Abecasis G,
Deloukas P,
Musunuru K,
Willer CJ,
Kathiresan S
Charge Diabetes Working Group · EPIC-InterAct Consortium and 3 more consortia
Nature genetics · 2017 · PMID 29083408 · open access
11 pages
Genome-wide association study identifies 48 common genetic variants associated with handedness
Cuellar-Partida G,
Tung JY,
Eriksson N,
Albrecht E,
Aliev F,
Andreassen OA,
Barroso I,
Beckmann JS,
Boks MP,
Boomsma DI,
Boyd HA,
Breteler MMB
and 106 more — show all
Campbell H,
Chasman DI,
Cherkas LF,
Davies G,
de Geus EJC,
Deary IJ,
Deloukas P,
Dick DM,
Duffy DL,
Eriksson JG,
Esko T,
Feenstra B,
Geller F,
Gieger C,
Giegling I,
Gordon SD,
Han J,
Hansen TF,
Hartmann AM,
Hayward C,
Heikkilä K,
Hicks AA,
Hirschhorn JN,
Hottenga JJ,
Huffman JE,
Hwang LD,
Ikram MA,
Kaprio J,
Kemp JP,
Khaw KT,
Klopp N,
Konte B,
Kutalik Z,
Lahti J,
Li X,
Loos RJF,
Luciano M,
Magnusson SH,
Mangino M,
Marques-Vidal P,
Martin NG,
McArdle WL,
McCarthy MI,
Medina-Gomez C,
Melbye M,
Melville SA,
Metspalu A,
Milani L,
Mooser V,
Nelis M,
Nyholt DR,
O'Connell KS,
Ophoff RA,
Palmer C,
Palotie A,
Palviainen T,
Pare G,
Paternoster L,
Peltonen L,
Penninx BWJH,
Polasek O,
Pramstaller PP,
Prokopenko I,
Raikkonen K,
Ripatti S,
Rivadeneira F,
Rudan I,
Rujescu D,
Smit JH,
Smith GD,
Smoller JW,
Soranzo N,
Spector TD,
Pourcain BS,
Starr JM,
Stefánsson H,
Steinberg S,
Teder-Laving M,
Thorleifsson G,
Stefánsson K,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
van Rooij FJA,
Vink JM,
Vollenweider P,
Vuoksimaa E,
Waeber G,
Wareham NJ,
Warrington N,
Waterworth D,
Werge T,
Wichmann HE,
Widen E,
Willemsen G,
Wright AF,
Wright MJ,
Xu M,
Zhao JH,
Kraft P,
Hinds DA,
Lindgren CM,
Mägi R,
Neale BM,
Evans DM,
Medland SE
Nature human behaviour · 2021 · PMID 32989287
7 pages
Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma
Nan H,
Xu M,
Kraft P,
Qureshi AA,
Chen C,
Guo Q,
Hu FB,
Curhan G,
Amos CI,
Wang LE,
Lee JE,
Wei Q
and 2 more — show all
Human molecular genetics · 2011 · PMID 21700618
2 pages
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Lin Z,
Bei JX,
Shen M,
Li Q,
Liao Z,
Zhang Y,
Lv Q,
Wei Q,
Low HQ,
Guo YM,
Cao S,
Yang M
and 39 more — show all
Hu Z,
Xu M,
Wang X,
Wei Y,
Li L,
Li C,
Li T,
Huang J,
Pan Y,
Jin O,
Wu Y,
Wu J,
Guo Z,
He P,
Hu S,
Wu H,
Song H,
Zhan F,
Liu S,
Gao G,
Liu Z,
Li Y,
Xiao C,
Li J,
Ye Z,
He W,
Liu D,
Shen L,
Huang A,
Wu H,
Tao Y,
Pan X,
Yu B,
Tai ES,
Zeng YX,
Ren EC,
Shen Y,
Liu J,
Gu J
Nature genetics · 2011 · PMID 22138694
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.