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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.
32 matches for
Lin L,
showing the first 12.
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic
Han F,
Faraco J,
Dong XS,
Ollila HM,
Lin L,
Li J,
An P,
Wang S,
Jiang KW,
Gao ZC,
Zhao L,
Yan H
and 13 more — show all
Liu YN,
Li QH,
Zhang XZ,
Hu Y,
Wang JY,
Lu YH,
Lu CJ,
Zhou W,
Hallmayer J,
Huang YS,
Strohl KP,
Pollmächer T,
Mignot E
PLoS genetics · 2013 · PMID 24204295 · open access
2 pages
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis
Olden M,
Corre T,
Hayward C,
Toniolo D,
Ulivi S,
Gasparini P,
Pistis G,
Hwang SJ,
Bergmann S,
Campbell H,
Cocca M,
Gandin I
and 18 more — show all
Girotto G,
Glaudemans B,
Hastie ND,
Loffing J,
Polasek O,
Rampoldi L,
Rudan I,
Sala C,
Traglia M,
Vollenweider P,
Vuckovic D,
Youhanna S,
Weber J,
Wright AF,
Kutalik Z,
Bochud M,
Fox CS,
Devuyst O
Journal of the American Society of Nephrology : JASN · 2014 · PMID 24578125
2 pages
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Jiang L,
Yin J,
Ye L,
Yang J,
Hemani G,
Liu AJ,
Zou H,
He D,
Sun L,
Zeng X,
Li Z,
Zheng Y
and 61 more — show all
Lin Y,
Liu Y,
Fang Y,
Xu J,
Li Y,
Dai S,
Guan J,
Jiang L,
Wei Q,
Wang Y,
Li Y,
Huang C,
Zuo X,
Liu Y,
Wu X,
Zhang L,
Zhou L,
Zhang Q,
Li T,
Chen L,
Xu Z,
Yang X,
Qian F,
Xie W,
Liu W,
Guo Q,
Huang S,
Zhao J,
Li M,
Jin Y,
Gao J,
Lv Y,
Wang Y,
Lin L,
Guo A,
Danoy P,
Willner D,
Cremin C,
Hadler J,
Zhang F,
Zhao Y,
Li M,
Yue T,
Fan X,
Guo J,
Mu R,
Li J,
Wu C,
Zeng M,
Wang J,
Li S,
Jin L,
Wang B,
Wang J,
Ma X,
Sun L,
Zhang X,
Brown MA,
Visscher PM,
Su DF,
Xu H
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Ollila HM,
Sharon E,
Lin L,
Sinnott-Armstrong N,
Ambati A,
Yogeshwar SM,
Hillary RP,
Jolanki O,
Faraco J,
Einen M,
Luo G,
Zhang J
and 78 more — show all
Han F,
Yan H,
Dong XS,
Li J,
Zhang J,
Hong SC,
Kim TW,
Dauvilliers Y,
Barateau L,
Lammers GJ,
Fronczek R,
Mayer G,
Santamaria J,
Arnulf I,
Knudsen-Heier S,
Bredahl MKL,
Thorsby PM,
Plazzi G,
Pizza F,
Moresco M,
Crowe C,
Van den Eeden SK,
Lecendreux M,
Bourgin P,
Kanbayashi T,
Martínez-Orozco FJ,
Peraita-Adrados R,
Benetó A,
Montplaisir J,
Desautels A,
Huang YS,
Jennum P,
Nevsimalova S,
Kemlink D,
Iranzo A,
Overeem S,
Wierzbicka A,
Geisler P,
Sonka K,
Honda M,
Högl B,
Stefani A,
Coelho FM,
Mantovani V,
Feketeova E,
Wadelius M,
Eriksson N,
Smedje H,
Hallberg P,
Hesla PE,
Rye D,
Pelin Z,
Ferini-Strambi L,
Bassetti CL,
Mathis J,
Khatami R,
Aran A,
Nampoothiri S,
Olsson T,
Kockum I,
Partinen M,
Perola M,
Kornum BR,
Rueger S,
Winkelmann J,
Miyagawa T,
Toyoda H,
Khor SS,
Shimada M,
Tokunaga K,
Rivas M,
Pritchard JK,
Risch N,
Kutalik Z,
O'Hara R,
Hallmayer J,
Ye CJ,
Mignot EJ
FinnGen
Nature communications · 2023 · PMID 37188663 · open access
2 pages
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
and 74 more — show all
Cousminer DL,
Kerkhof M,
Timpson NJ,
Ikram MA,
Beilin LJ,
Bønnelykke K,
Buxton JL,
Charoen P,
Chawes BLK,
Eriksson J,
Evans DM,
Hofman A,
Kemp JP,
Kim CE,
Klopp N,
Lahti J,
Lye SJ,
McMahon G,
Mentch FD,
Müller M,
O'Reilly PF,
Prokopenko I,
Rivadeneira F,
Steegers EAP,
Sunyer J,
Tiesler C,
Yaghootkar H,
Breteler MMB,
Debette S,
Fornage M,
Gudnason V,
Launer LJ,
van der Lugt A,
Mosley TH,
Seshadri S,
Smith AV,
Vernooij MW,
Blakemore AI,
Chiavacci RM,
Feenstra B,
Fernandez-Benet J,
Grant SFA,
Hartikainen AL,
van der Heijden AJ,
Iñiguez C,
Lathrop M,
McArdle WL,
Mølgaard A,
Newnham JP,
Palmer LJ,
Palotie A,
Palotie A,
Pouta A,
Ring SM,
Sovio U,
Standl M,
Uitterlinden AG,
Wichmann HE,
Vissing NH,
DeCarli C,
van Duijn CM,
McCarthy MI,
Koppelman GH,
Estivill X,
Hattersley AT,
Melbye M,
Bisgaard H,
Pennell CE,
Widen E,
Hakonarson H,
Smith GD,
Heinrich J,
Jarvelin MR,
Jaddoe VWV
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma
Swaminathan B,
Thorleifsson G,
Jöud M,
Ali M,
Johnsson E,
Ajore R,
Sulem P,
Halvarsson BM,
Eyjolfsson G,
Haraldsdottir V,
Hultman C,
Ingelsson E
and 22 more — show all
Kristinsson SY,
Kähler AK,
Lenhoff S,
Masson G,
Mellqvist UH,
Månsson R,
Nelander S,
Olafsson I,
Sigurðardottir O,
Steingrimsdóttir H,
Vangsted A,
Vogel U,
Waage A,
Nahi H,
Gudbjartsson DF,
Rafnar T,
Turesson I,
Gullberg U,
Stefánsson K,
Hansson M,
Thorsteinsdóttir U,
Nilsson B
Nature communications · 2015 · PMID 26007630 · open access
1 page
A Multinational Arab Genome-Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis
Saxena R,
Plenge RM,
Bjonnes AC,
Dashti HS,
Okada Y,
Gad El Haq W,
Hammoudeh M,
Al Emadi S,
Masri BK,
Halabi H,
Badsha H,
Uthman IW
and 8 more — show all
Arthritis & rheumatology (Hoboken, N.J.) · 2017 · PMID 28118524
1 page
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
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3
Nolan J,
Campbell PJ,
Brown SJ,
Zhu G,
Gordon S,
Lim EM,
Joseph J,
Cross SM,
Panicker V,
Medland SE,
Melton PE,
Beilin LJ
and 8 more — show all
European journal of endocrinology · 2021 · PMID 34524976
1 page
Genetic Variants Associated With Hidradenitis Suppurativa
Sun Q,
Broadaway KA,
Edmiston SN,
Fajgenbaum K,
Miller-Fleming T,
Westerkam LL,
Melendez-Gonzalez M,
Bui H,
Blum FR,
Levitt B,
Lin L,
Hao H
and 7 more — show all
JAMA dermatology · 2023 · PMID 37494057
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.