For researchers
Is your paper here?
2,677 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.
44 matches for
Park J,
showing the first 4.
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Xie J,
Liu L,
Mladkova N,
Li Y,
Ren H,
Wang W,
Cui Z,
Lin L,
Hu X,
Yu X,
Xu J,
Liu G
and 108 more — show all
Caliskan Y,
Sidore C,
Balderes O,
Rosen RJ,
Bodria M,
Zanoni F,
Zhang JY,
Krithivasan P,
Mehl K,
Marasa M,
Khan A,
Ozay F,
Canetta PA,
Bomback AS,
Appel GB,
Sanna-Cherchi S,
Sampson MG,
Mariani LH,
Perkowska-Ptasinska A,
Durlik M,
Mucha K,
Moszczuk B,
Foroncewicz B,
Pączek L,
Habura I,
Ars E,
Ballarin J,
Mani LY,
Vogt B,
Ozturk S,
Yildiz A,
Seyahi N,
Arikan H,
Koc M,
Basturk T,
Karahan G,
Akgul SU,
Sever MS,
Zhang D,
Santoro D,
Bonomini M,
Londrino F,
Gesualdo L,
Reiterova J,
Tesar V,
Izzi C,
Savoldi S,
Spotti D,
Marcantoni C,
Messa P,
Galliani M,
Roccatello D,
Granata S,
Zaza G,
Lugani F,
Ghiggeri G,
Pisani I,
Allegri L,
Sprangers B,
Park JH,
Cho B,
Kim YS,
Kim DK,
Suzuki H,
Amoroso A,
Cattran DC,
Fervenza FC,
Pani A,
Hamilton P,
Harris S,
Gupta S,
Cheshire C,
Dufek S,
Issler N,
Pepper RJ,
Connolly J,
Powis S,
Bockenhauer D,
Stanescu HC,
Ashman N,
Loos RJF,
Kenny EE,
Wuttke M,
Eckardt KU,
Köttgen A,
Hofstra JM,
Coenen MJH,
Kiemeney LA,
Akilesh S,
Kretzler M,
Beck LH,
Stengel B,
Debiec H,
Ronco P,
Wetzels JFM,
Zoledziewska M,
Cucca F,
Ionita-Laza I,
Lee H,
Hoxha E,
Stahl RAK,
Brenchley P,
Scolari F,
Zhao MH,
Gharavi AG,
Kleta R,
Chen N,
Kiryluk K
Nature communications · 2020 · PMID 32231244 · open access
1 page
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages
Park JY,
Lee D,
Lee JJ,
Gim J,
Gunasekaran TI,
Choi KY,
Kang S,
Do AR,
Jo J,
Park J,
Park K,
Li D
and 21 more — show all
Lee S,
Kim H,
Dhanasingh I,
Ghosh S,
Keum S,
Choi JH,
Song GJ,
Sael L,
Rhee S,
Lovestone S,
Kim E,
Moon SH,
Kim BC,
Kim S,
Saykin AJ,
Nho K,
Lee SH,
Farrer LA,
Jun GR,
Won S,
Lee KH
Alzheimer’s Disease Neuroimaging Initiative
Translational psychiatry · 2021 · PMID 34785643 · open access
1 page
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci
Bellomo TR,
Bone WP,
Chen BY,
Gawronski KAB,
Zhang D,
Park J,
Levin M,
Tsao N,
Klarin D,
Lynch J,
Assimes TL,
Gaziano JM
and 10 more — show all
Frontiers in genetics · 2021 · PMID 35186008 · open access
1 page
Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry
Chen F,
Madduri RK,
Rodriguez AA,
Darst BF,
Chou A,
Sheng X,
Wang A,
Shen J,
Saunders EJ,
Rhie SK,
Bensen JT,
Ingles SA
and 106 more — show all
Kittles RA,
Strom SS,
Rybicki BA,
Nemesure B,
Isaacs WB,
Stanford JL,
Zheng W,
Sanderson M,
John EM,
Park JY,
Xu J,
Wang Y,
Berndt SI,
Huff CD,
Yeboah ED,
Tettey Y,
Lachance J,
Tang W,
Rentsch CT,
Cho K,
Mcmahon BH,
Biritwum RB,
Adjei AA,
Tay E,
Truelove A,
Niwa S,
Sellers TA,
Yamoah K,
Murphy AB,
Crawford DC,
Patel AV,
Bush WS,
Aldrich MC,
Cussenot O,
Petrovics G,
Cullen J,
Neslund-Dudas CM,
Stern MC,
Kote-Jarai Z,
Govindasami K,
Cook MB,
Chokkalingam AP,
Hsing AW,
Goodman PJ,
Hoffmann TJ,
Drake BF,
Hu JJ,
Keaton JM,
Hellwege JN,
Clark PE,
Jalloh M,
Gueye SM,
Niang L,
Ogunbiyi O,
Idowu MO,
Popoola O,
Adebiyi AO,
Aisuodionoe-Shadrach OI,
Ajibola HO,
Jamda MA,
Oluwole OP,
Nwegbu M,
Adusei B,
Mante S,
Darkwa-Abrahams A,
Mensah JE,
Diop H,
Van Den Eeden SK,
Blanchet P,
Fowke JH,
Casey G,
Hennis AJ,
Lubwama A,
Thompson IM Jr,
Leach R,
Easton DF,
Preuss MH,
Loos RJ,
Gundell SM,
Wan P,
Mohler JL,
Fontham ET,
Smith GJ,
Taylor JA,
Srivastava S,
Eeles RA,
Carpten JD,
Kibel AS,
Multigner L,
Parent MÉ,
Menegaux F,
Cancel-Tassin G,
Klein EA,
Andrews C,
Rebbeck TR,
Brureau L,
Ambs S,
Edwards TL,
Watya S,
Chanock SJ,
Witte JS,
Blot WJ,
Michael Gaziano J,
Justice AC,
Conti DV,
Haiman CA
European urology · 2023 · PMID 36872133
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.