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2,665 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
Gu H.
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
Yin X,
Kim K,
Suetsugu H,
Bang SY,
Wen L,
Koido M,
Ha E,
Liu L,
Sakamoto Y,
Jo S,
Leng RX,
Otomo N
and 76 more — show all
Laurynenka V,
Kwon YC,
Sheng Y,
Sugano N,
Sugano N,
Hwang MY,
Li W,
Mukai M,
Yoon K,
Cai M,
Ishigaki K,
Chung WT,
Huang H,
Takahashi D,
Lee SS,
Wang M,
Karino K,
Shim SC,
Zheng X,
Miyamura T,
Kang YM,
Ye D,
Nakamura J,
Suh CH,
Tang Y,
Motomura G,
Park YB,
Ding H,
Kuroda T,
Choe JY,
Li C,
Niiro H,
Park Y,
Shen C,
Miyamoto T,
Ahn GY,
Fei W,
Takeuchi T,
Shin JM,
Li K,
Kawaguchi Y,
Lee YK,
Wang Y,
Amano K,
Park DJ,
Yang W,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Suzuki A,
Sumida T,
Okada Y,
Matsuda K,
Matsuo K,
Kochi Y,
Kottyan LC,
Weirauch MT,
Parameswaran S,
Eswar S,
Salim H,
Chen X,
Yamamoto K,
Harley JB,
Ohmura K,
Kim TH,
Yang S,
Yamamoto T,
Kim BJ,
Shen N,
Ikegawa S,
Lee HS,
Zhang X,
Terao C,
Cui Y,
Bae SC
Japanese Research Committee on Idiopathic Osteonecrosis of the Femoral Head
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
12 pages+
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Ishikawa Y,
Tanaka N,
Asano Y,
Kodera M,
Shirai Y,
Akahoshi M,
Hasegawa M,
Matsushita T,
Saito K,
Motegi SI,
Yoshifuji H,
Yoshizaki A
and 60 more — show all
Kohmoto T,
Takagi K,
Oka A,
Kanda M,
Tanaka Y,
Ito Y,
Nakano K,
Kasamatsu H,
Utsunomiya A,
Sekiguchi A,
Niiro H,
Jinnin M,
Makino K,
Makino T,
Ihn H,
Yamamoto M,
Suzuki C,
Takahashi H,
Nishida E,
Morita A,
Yamamoto T,
Fujimoto M,
Kondo Y,
Goto D,
Sumida T,
Ayuzawa N,
Yanagida H,
Horita T,
Atsumi T,
Endo H,
Shima Y,
Kumanogoh A,
Hirata J,
Otomo N,
Suetsugu H,
Koike Y,
Tomizuka K,
Yoshino S,
Liu X,
Ito S,
Hikino K,
Suzuki A,
Momozawa Y,
Ikegawa S,
Tanaka Y,
Ishikawa O,
Takehara K,
Torii T,
Sato S,
Okada Y,
Mimori T,
Matsuda F,
Matsuda K,
Amariuta T,
Imoto I,
Matsuo K,
Kuwana M,
Kawaguchi Y,
Ohmura K,
Terao C
Nature communications · 2024 · PMID 38296975 · open access
7 pages
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
Salem RM,
Todd JN,
Sandholm N,
Cole JB,
Chen WM,
Andrews D,
Pezzolesi MG,
McKeigue PM,
Hiraki LT,
Qiu C,
Nair V,
Di Liao C
and 76 more — show all
Cao JJ,
Valo E,
Onengut-Gumuscu S,
Smiles AM,
McGurnaghan SJ,
Haukka JK,
Harjutsalo V,
Brennan EP,
van Zuydam N,
Ahlqvist E,
Doyle R,
Ahluwalia TS,
Lajer M,
Hughes MF,
Park J,
Skupien J,
Spiliopoulou A,
Liu A,
Menon R,
Boustany-Kari CM,
Kang HM,
Nelson RG,
Klein R,
Klein BE,
Lee KE,
Gao X,
Mauer M,
Maestroni S,
Caramori ML,
de Boer IH,
Miller RG,
Guo J,
Boright AP,
Tregouet D,
Gyorgy B,
Snell-Bergeon JK,
Maahs DM,
Bull SB,
Canty AJ,
Palmer CNA,
Stechemesser L,
Paulweber B,
Weitgasser R,
Sokolovska J,
Rovīte V,
Pīrāgs V,
Prakapiene E,
Radzeviciene L,
Verkauskiene R,
Panduru NM,
Groop LC,
McCarthy MI,
Gu HF,
Möllsten A,
Falhammar H,
Brismar K,
Martin F,
Rossing P,
Costacou T,
Zerbini G,
Marre M,
Hadjadj S,
McKnight AJ,
Forsblom C,
McKay G,
Godson C,
Maxwell AP,
Kretzler M,
Susztak K,
Colhoun HM,
Krolewski A,
Paterson AD,
Groop PH,
Rich SS,
Hirschhorn JN,
Florez JC
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2019 · PMID 31537649
5 pages
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes
Strawbridge RJ,
Dupuis J,
Prokopenko I,
Barker A,
Ahlqvist E,
Rybin D,
Petrie JR,
Travers ME,
Bouatia-Naji N,
Dimas AS,
Nica A,
Wheeler E
and 91 more — show all
Chen H,
Voight BF,
Taneera J,
Kanoni S,
Peden JF,
Turrini F,
Gustafsson S,
Zabena C,
Almgren P,
Barker DJ,
Barnes D,
Dennison EM,
Eriksson JG,
Eriksson P,
Eury E,
Folkersen L,
Fox CS,
Frayling TM,
Goel A,
Gu HF,
Horikoshi M,
Isomaa B,
Jackson AU,
Jameson KA,
Kajantie E,
Kerr-Conte J,
Kuulasmaa T,
Kuusisto J,
Loos RJ,
Luan J,
Makrilakis K,
Manning AK,
Martínez-Larrad MT,
Narisu N,
Nastase Mannila M,
Ohrvik J,
Osmond C,
Pascoe L,
Payne F,
Sayer AA,
Sennblad B,
Silveira A,
Stancáková A,
Stirrups K,
Swift AJ,
Syvänen AC,
Tuomi T,
van 't Hooft FM,
Walker M,
Weedon MN,
Xie W,
Zethelius B,
Ongen H,
Mälarstig A,
Hopewell JC,
Saleheen D,
Chambers J,
Parish S,
Danesh J,
Kooner J,
Ostenson CG,
Lind L,
Cooper CC,
Serrano-Ríos M,
Ferrannini E,
Forsen TJ,
Clarke R,
Franzosi MG,
Seedorf U,
Watkins H,
Froguel P,
Johnson P,
Deloukas P,
Collins FS,
Laakso M,
Dermitzakis ET,
Boehnke M,
McCarthy MI,
Wareham NJ,
Groop L,
Pattou F,
Gloyn AL,
Dedoussis GV,
Lyssenko V,
Meigs JB,
Barroso I,
Watanabe RM,
Ingelsson E,
Langenberg C,
Hamsten A,
Florez JC
DIAGRAM Consortium · GIANT Consortium and 3 more consortia
Diabetes · 2011 · PMID 21873549 · open access
3 pages
New susceptibility loci associated with kidney disease in type 1 diabetes
Sandholm N,
Salem RM,
McKnight AJ,
Brennan EP,
Forsblom C,
Isakova T,
McKay GJ,
Williams WW,
Sadlier DM,
Mäkinen VP,
Swan EJ,
Palmer C
and 80 more — show all
Boright AP,
Ahlqvist E,
Deshmukh HA,
Keller BJ,
Huang H,
Ahola AJ,
Fagerholm E,
Gordin D,
Harjutsalo V,
He B,
Heikkilä O,
Hietala K,
Kytö J,
Lahermo P,
Lehto M,
Lithovius R,
Osterholm AM,
Parkkonen M,
Pitkäniemi J,
Rosengård-Bärlund M,
Saraheimo M,
Sarti C,
Söderlund J,
Soro-Paavonen A,
Syreeni A,
Thorn LM,
Tikkanen H,
Tolonen N,
Tryggvason K,
Tuomilehto J,
Wadén J,
Gill GV,
Prior S,
Guiducci C,
Mirel DB,
Taylor A,
Hosseini SM,
Parving HH,
Rossing P,
Tarnow L,
Ladenvall C,
Alhenc-Gelas F,
Lefebvre P,
Rigalleau V,
Roussel R,
Tregouet DA,
Maestroni A,
Maestroni S,
Falhammar H,
Gu T,
Möllsten A,
Cimponeriu D,
Ioana M,
Mota M,
Mota E,
Serafinceanu C,
Stavarachi M,
Hanson RL,
Nelson RG,
Kretzler M,
Colhoun HM,
Panduru NM,
Gu HF,
Brismar K,
Zerbini G,
Hadjadj S,
Marre M,
Groop L,
Lajer M,
Bull SB,
Waggott D,
Paterson AD,
Savage DA,
Bain SC,
Martin F,
Hirschhorn JN,
Godson C,
Florez JC,
Groop PH,
Maxwell AP
DCCT/EDIC Research Group
PLoS genetics · 2012 · PMID 23028342 · open access
2 pages
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
Suetsugu H,
Kim K,
Yamamoto T,
Bang SY,
Sakamoto Y,
Shin JM,
Sugano N,
Kim JS,
Mukai M,
Lee YK,
Ohmura K,
Park DJ
and 43 more — show all
Takahashi D,
Ahn GY,
Karino K,
Kwon YC,
Miyamura T,
Kim J,
Nakamura J,
Motomura G,
Kuroda T,
Niiro H,
Miyamoto T,
Takeuchi T,
Ikari K,
Amano K,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Seki T,
Tanaka Y,
Kubo T,
Hisada R,
Yoshioka T,
Yamazaki M,
Kabata T,
Kajino T,
Ohta Y,
Okawa T,
Naito Y,
Kaneuji A,
Yasunaga Y,
Ohzono K,
Tomizuka K,
Koido M,
Matsuda K,
Okada Y,
Suzuki A,
Kim BJ,
Kochi Y,
Lee HS,
Ikegawa S,
Bae SC,
Terao C
Human molecular genetics · 2022 · PMID 34850884
2 pages
Identification of the BTN3A3 Gene as a Molecule Implicated in Generalized Pustular Psoriasis in a Chinese Population
Zhang Q,
Shi P,
Wang Z,
Sun L,
Li W,
Zhao Q,
Liu T,
Pan Q,
Sun Y,
Jia F,
Chen W,
Fu X
and 10 more — show all
The Journal of investigative dermatology · 2023 · PMID 36804966
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.