For researchers
Is your paper here?
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.
7 matches for
Lu H.
Combining genome-wide association studies highlight novel loci involved in human facial variation
Xiong Z,
Gao X,
Chen Y,
Feng Z,
Pan S,
Lu H,
Uitterlinden AG,
Nijsten T,
Ikram A,
Rivadeneira F,
Ghanbari M,
Wang Y
and 2 more — show all
Nature communications · 2022 · PMID 36539420 · open access
5 pages
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese
Kou I,
Otomo N,
Takeda K,
Momozawa Y,
Lu HF,
Kubo M,
Kamatani Y,
Ogura Y,
Takahashi Y,
Nakajima M,
Minami S,
Uno K
and 35 more — show all
Kawakami N,
Ito M,
Yonezawa I,
Watanabe K,
Kaito T,
Yanagida H,
Taneichi H,
Harimaya K,
Taniguchi Y,
Shigematsu H,
Iida T,
Demura S,
Sugawara R,
Fujita N,
Yagi M,
Okada E,
Hosogane N,
Kono K,
Nakamura M,
Chiba K,
Kotani T,
Sakuma T,
Akazawa T,
Suzuki T,
Nishida K,
Kakutani K,
Tsuji T,
Sudo H,
Iwata A,
Sato T,
Inami S,
Matsumoto M,
Terao C,
Watanabe K,
Ikegawa S
Nature communications · 2019 · PMID 31417091 · open access
3 pages
Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome
Liu X,
Tong X,
Zhu J,
Tian L,
Jie Z,
Zou Y,
Lin X,
Liang H,
Li W,
Ju Y,
Qin Y,
Zou L
and 11 more — show all
Lu H,
Zhu S,
Jin X,
Xu X,
Yang H,
Wang J,
Zong Y,
Liu W,
Hou Y,
Jia H,
Zhang T
Cell discovery · 2021 · PMID 34873157 · open access
3 pages
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Kavousi M,
Bos MM,
Barnes HJ,
Lino Cardenas CL,
Wong D,
Lu H,
Hodonsky CJ,
Landsmeer LPL,
Turner AW,
Kho M,
Hasbani NR,
de Vries PS
and 77 more — show all
Bowden DW,
Chopade S,
Deelen J,
Benavente ED,
Guo X,
Hofer E,
Hwang SJ,
Lutz SM,
Lyytikäinen LP,
Slenders L,
Smith AV,
Stanislawski MA,
van Setten J,
Wong Q,
Yanek LR,
Becker DM,
Beekman M,
Budoff MJ,
Feitosa MF,
Finan C,
Hilliard AT,
Kardia SLR,
Kovacic JC,
Kral BG,
Langefeld CD,
Launer LJ,
Malik S,
Hoesein FAAM,
Mokry M,
Schmidt R,
Smith JA,
Taylor KD,
Terry JG,
van der Grond J,
van Meurs J,
Vliegenthart R,
Xu J,
Young KA,
Zilhão NR,
Zweiker R,
Assimes TL,
Becker LC,
Bos D,
Carr JJ,
Cupples LA,
de Kleijn DPV,
de Winther M,
den Ruijter HM,
Fornage M,
Freedman BI,
Gudnason V,
Hingorani AD,
Hokanson JE,
Ikram MA,
Išgum I,
Jacobs DR Jr,
Kähönen M,
Lange LA,
Lehtimäki T,
Pasterkamp G,
Raitakari OT,
Schmidt H,
Slagboom PE,
Uitterlinden AG,
Vernooij MW,
Bis JC,
Franceschini N,
Psaty BM,
Post WS,
Rotter JI,
Björkegren JLM,
O'Donnell CJ,
Bielak LF,
Peyser PA,
Malhotra R,
van der Laan SW,
Miller CL
Nature genetics · 2023 · PMID 37770635
2 pages
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk
Surakka I,
Fritsche LG,
Zhou W,
Backman J,
Kosmicki JA,
Lu H,
Brumpton B,
Nielsen JB,
Gabrielsen ME,
Skogholt AH,
Wolford B,
Graham SE
and 14 more — show all
Chen YE,
Lee S,
Kang HM,
Langhammer A,
Forsmo S,
Åsvold BO,
Styrkarsdottir U,
Holm H,
Gudbjartsson D,
Stefansson K,
Baras A,
Abecasis GR,
Hveem K,
Willer CJ
Regeneron Genetics Center
Nature communications · 2020 · PMID 33097703 · 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.