For researchers
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.
25 matches for
Zhang M,
showing the first 5.
ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma
Nongpiur ME,
Khor CC,
Jia H,
Cornes BK,
Chen LJ,
Qiao C,
Nair KS,
Cheng CY,
Xu L,
George R,
Tan D,
Abu-Amero K
and 61 more — show all
Perera SA,
Ozaki M,
Mizoguchi T,
Kurimoto Y,
Low S,
Tajudin LS,
Ho CL,
Tham CC,
Soto I,
Chew PT,
Wong HT,
Shantha B,
Kuroda M,
Osman EA,
Tang G,
Fan S,
Meng H,
Wang H,
Feng B,
Yong VH,
Ting SM,
Li Y,
Wang YX,
Li Z,
Lavanya R,
Wu RY,
Zheng YF,
Su DH,
Loon SC,
Yong VK,
Allingham RR,
Hauser MA,
Soumittra N,
Ramprasad VL,
Waseem N,
Yaakub A,
Chia KS,
Kumaramanickavel G,
Wong TT,
How AC,
Chau TN,
Simmons CP,
Bei JX,
Zeng YX,
Bhattacharya SS,
Zhang M,
Tan DT,
Teo YY,
Al-Obeidan SA,
Hon DN,
Tai ES,
Saw SM,
Foster PJ,
Vijaya L,
Jonas JB,
Wong TY,
John SW,
Pang CP,
Vithana EN,
Wang N,
Aung T
PLoS genetics · 2014 · PMID 24603532 · open access
1 page
Genome-wide Association Studies of Specific Antinuclear Autoantibody Subphenotypes in Primary Biliary Cholangitis
Wang C,
Zheng X,
Jiang P,
Tang R,
Gong Y,
Dai Y,
Wang L,
Xu P,
Sun W,
Wang L,
Han C,
Jiang Y
and 39 more — show all
Wei Y,
Zhang K,
Wu J,
Shao Y,
Gao Y,
Yu J,
Hu Z,
Zang Z,
Zhao Y,
Wu X,
Dai N,
Liu L,
Nie J,
Jiang B,
Lin M,
Li L,
Li Y,
Chen S,
Shu L,
Qiu F,
Wu Q,
Zhang M,
Chen R,
Jawed R,
Zhang Y,
Shi X,
Zhu Z,
Pei H,
Huang L,
Zhao W,
Tian Y,
Zhu X,
Qiu H,
Gershwin ME,
Chen W,
Seldin MF,
Liu X,
Sun L,
Ma X
Hepatology (Baltimore, Md.) · 2019 · PMID 30854688 · open access
1 page
Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study
Zhu M,
Xu K,
Chen Y,
Gu Y,
Zhang M,
Luo F,
Liu Y,
Gu W,
Hu J,
Xu H,
Xie Z,
Sun C
and 42 more — show all
Li Y,
Sun M,
Xu X,
Hsu HT,
Chen H,
Fu Q,
Shi Y,
Xu J,
Ji L,
Liu J,
Bian L,
Zhu J,
Chen S,
Xiao L,
Li X,
Jiang H,
Shen M,
Huang Q,
Fang C,
Li X,
Huang G,
Fan J,
Jiang Z,
Jiang Y,
Dai J,
Ma H,
Zheng S,
Cai Y,
Dai H,
Zheng X,
Zhou H,
Ni S,
Jin G,
She JX,
Yu L,
Polychronakos C,
Hu Z,
Zhou Z,
Weng J,
Weng J,
Shen H,
Yang T
Diabetes care · 2019 · PMID 31152121
1 page
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
Cade BE,
Lee J,
Sofer T,
Wang H,
Zhang M,
Chen H,
Gharib SA,
Gottlieb DJ,
Guo X,
Lane JM,
Liang J,
Lin X
and 27 more — show all
Mei H,
Patel SR,
Purcell SM,
Saxena R,
Shah NA,
Evans DS,
Hanis CL,
Hillman DR,
Mukherjee S,
Palmer LJ,
Stone KL,
Tranah GJ,
Abecasis GR,
Boerwinkle EA,
Correa A,
Cupples LA,
Kaplan RC,
Nickerson DA,
North KE,
Psaty BM,
Rotter JI,
Rich SS,
Tracy RP,
Vasan RS,
Wilson JG,
Zhu X,
Redline S
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Sleep Working Group
Genome medicine · 2021 · PMID 34446064 · open access
1 page
Genetic risk factors for COVID-19 and influenza are largely distinct
Kosmicki JA,
Marcketta A,
Sharma D,
Di Gioia SA,
Batista S,
Yang XM,
Tzoneva G,
Martinez H,
Sidore C,
Kessler MD,
Horowitz JE,
Roberts GHL
and 43 more — show all
Justice AE,
Banerjee N,
Coignet MV,
Leader JB,
Park DS,
Lanche R,
Maxwell E,
Knight SC,
Bai X,
Guturu H,
Baltzell A,
Girshick AR,
McCurdy SR,
Partha R,
Mansfield AJ,
Turissini DA,
Zhang M,
Mbatchou J,
Watanabe K,
Verma A,
Sirugo G,
Ritchie MD,
Salerno WJ,
Shuldiner AR,
Rader DJ,
Mirshahi T,
Marchini J,
Overton JD,
Carey DJ,
Habegger L,
Reid JG,
Economides A,
Kyratsous C,
Karalis K,
Baum A,
Cantor MN,
Rand KA,
Hong EL,
Ball CA,
Siminovitch K,
Baras A,
Abecasis GR,
Ferreira MAR
Colorado Center for Precision Medicine · Mayo Clinic Project Generation and 2 more consortia
Nature genetics · 2024 · PMID 39103650 · 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.