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Is your paper here?
2,676 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.
31 matches for
Gregersen P,
showing the first 11.
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08
Gregersen PK,
Kosoy R,
Lee AT,
Lamb J,
Sussman J,
McKee D,
Simpfendorfer KR,
Pirskanen-Matell R,
Piehl F,
Pan-Hammarstrom Q,
Verschuuren JJ,
Titulaer MJ
and 17 more — show all
Niks EH,
Marx A,
Ströbel P,
Tackenberg B,
Pütz M,
Maniaol A,
Elsais A,
Tallaksen C,
Harbo HF,
Lie BA,
Raychaudhuri S,
de Bakker PI,
Melms A,
Garchon HJ,
Willcox N,
Hammarstrom L,
Seldin MF
Annals of neurology · 2012 · PMID 23055271
2 pages
Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of <i>TNFRSF11A</i> and Identification of <i>ZBTB10</i> and Three Distinct HLA Associations
Seldin MF,
Alkhairy OK,
Lee AT,
Lamb JA,
Sussman J,
Pirskanen-Matell R,
Piehl F,
Verschuuren JJGM,
Kostera-Pruszczyk A,
Szczudlik P,
McKee D,
Maniaol AH
and 7 more — show all
Molecular medicine (Cambridge, Mass.) · 2016 · PMID 26562150
2 pages
Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction
Braun A,
Shekhar S,
Levey DF,
Straub P,
Kraft J,
Panagiotaropoulou GM,
Heilbron K,
Awasthi S,
Meleka Hanna R,
Hoffmann S,
Stein M,
Lehnerer S
and 28 more — show all
Mergenthaler P,
Elnahas AG,
Topaloudi A,
Koromina M,
Palviainen T,
Asbjornsdottir B,
Stefansson H,
Skuladóttir AT,
Jónsdóttir I,
Stefansson K,
Reis K,
Esko T,
Palotie A,
Leypoldt F,
Stein MB,
Fontanillas P,
Kaprio J,
Gelernter J,
Davis LK,
Paschou P,
Tannemaat MR,
Verschuuren JJGM,
Kuhlenbäumer G,
Gregersen PK,
Huijbers MG,
Stascheit F,
Meisel A,
Ripke S
Estonian Biobank Research Team · 23andMe Research Team
Nature communications · 2024 · PMID 39537604 · open access
2 pages
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX
Hom G,
Graham RR,
Modrek B,
Taylor KE,
Ortmann W,
Garnier S,
Lee AT,
Chung SA,
Ferreira RC,
Pant PV,
Ballinger DG,
Kosoy R
and 15 more — show all
Demirci FY,
Kamboh MI,
Kao AH,
Tian C,
Gunnarsson I,
Bengtsson AA,
Rantapää-Dahlqvist S,
Petri M,
Manzi S,
Seldin MF,
Rönnblom L,
Syvänen AC,
Criswell LA,
Gregersen PK,
Behrens TW
The New England journal of medicine · 2008 · PMID 18204098
1 page
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study
Silverberg MS,
Cho JH,
Rioux JD,
McGovern DP,
Wu J,
Annese V,
Achkar JP,
Goyette P,
Scott R,
Xu W,
Barmada MM,
Klei L
and 22 more — show all
Daly MJ,
Abraham C,
Bayless TM,
Bossa F,
Griffiths AM,
Ippoliti AF,
Lahaie RG,
Latiano A,
Paré P,
Proctor DD,
Regueiro MD,
Steinhart AH,
Targan SR,
Schumm LP,
Kistner EO,
Lee AT,
Gregersen PK,
Rotter JI,
Brant SR,
Taylor KD,
Roeder K,
Duerr RH
Nature genetics · 2009 · PMID 19122664 · open access
1 page
REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis
Gregersen PK,
Amos CI,
Lee AT,
Lu Y,
Remmers EF,
Kastner DL,
Seldin MF,
Criswell LA,
Plenge RM,
Holers VM,
Mikuls TR,
Sokka T
and 5 more — show all
Nature genetics · 2009 · PMID 19503088 · open access
1 page
Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
Petukhova L,
Duvic M,
Hordinsky M,
Norris D,
Price V,
Shimomura Y,
Kim H,
Singh P,
Lee A,
Chen WV,
Meyer KC,
Paus R
and 4 more — show all
Nature · 2010 · PMID 20596022
1 page
Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
Juran BD,
Hirschfield GM,
Invernizzi P,
Atkinson EJ,
Li Y,
Xie G,
Kosoy R,
Ransom M,
Sun Y,
Bianchi I,
Schlicht EM,
Lleo A
and 29 more — show all
Coltescu C,
Bernuzzi F,
Podda M,
Lammert C,
Shigeta R,
Chan LL,
Balschun T,
Marconi M,
Cusi D,
Heathcote EJ,
Mason AL,
Myers RP,
Milkiewicz P,
Odin JA,
Luketic VA,
Bacon BR,
Bodenheimer HC Jr,
Liakina V,
Vincent C,
Levy C,
Franke A,
Gregersen PK,
Bossa F,
Gershwin ME,
deAndrade M,
Amos CI,
Lazaridis KN,
Seldin MF,
Siminovitch KA
Italian PBC Genetics Study Group
Human molecular genetics · 2012 · PMID 22936693
1 page
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder
Lencz T,
Guha S,
Liu C,
Rosenfeld J,
Mukherjee S,
DeRosse P,
John M,
Cheng L,
Zhang C,
Badner JA,
Ikeda M,
Iwata N
and 14 more — show all
Cichon S,
Rietschel M,
Nöthen MM,
Cheng AT,
Hodgkinson C,
Yuan Q,
Kane JM,
Lee AT,
Pisanté A,
Gregersen PK,
Pe'er I,
Malhotra AK,
Goldman D,
Darvasi A
Nature communications · 2013 · PMID 24253340 · open access
1 page
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
Rothwell S,
Cooper RG,
Lundberg IE,
Miller FW,
Gregersen PK,
Bowes J,
Vencovsky J,
Danko K,
Limaye V,
Selva-O'Callaghan A,
Hanna MG,
Machado PM
and 24 more — show all
Pachman LM,
Reed AM,
Rider LG,
Cobb J,
Platt H,
Molberg Ø,
Benveniste O,
Mathiesen P,
Radstake T,
Doria A,
De Bleecker J,
De Paepe B,
Maurer B,
Ollier WE,
Padyukov L,
O'Hanlon TP,
Lee A,
Amos CI,
Gieger C,
Meitinger T,
Winkelmann J,
Wedderburn LR,
Chinoy H,
Lamb JA
Myositis Genetics Consortium
Annals of the rheumatic diseases · 2016 · PMID 26362759
1 page
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture
Stuart PE,
Nair RP,
Tsoi LC,
Tejasvi T,
Das S,
Kang HM,
Ellinghaus E,
Chandran V,
Callis-Duffin K,
Ike R,
Li Y,
Wen X
and 28 more — show all
Enerbäck C,
Gudjonsson JE,
Kõks S,
Kingo K,
Esko T,
Mrowietz U,
Reis A,
Wichmann HE,
Gieger C,
Hoffmann P,
Nöthen MM,
Winkelmann J,
Kunz M,
Moreta EG,
Mease PJ,
Ritchlin CT,
Bowcock AM,
Krueger GG,
Lim HW,
Weidinger S,
Weichenthal M,
Voorhees JJ,
Rahman P,
Gregersen PK,
Franke A,
Gladman DD,
Abecasis GR,
Elder JT
American journal of human genetics · 2015 · PMID 26626624
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.