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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.
11 matches for
Lee AT.
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
Harley JB,
Alarcón-Riquelme ME,
Criswell LA,
Jacob CO,
Kimberly RP,
Moser KL,
Tsao BP,
Vyse TJ,
Langefeld CD,
Nath SK,
Guthridge JM,
Cobb BL
and 29 more — show all
Mirel DB,
Marion MC,
Williams AH,
Divers J,
Wang W,
Frank SG,
Namjou B,
Gabriel SB,
Lee AT,
Gregersen PK,
Behrens TW,
Taylor KE,
Fernando M,
Zidovetzki R,
Gaffney PM,
Edberg JC,
Rioux JD,
Ojwang JO,
James JA,
Merrill JT,
Gilkeson GS,
Seldin MF,
Yin H,
Baechler EC,
Li QZ,
Wakeland EK,
Bruner GR,
Kaufman KM,
Kelly JA
International Consortium for Systemic Lupus Erythematosus Genetics (SLEGEN)
Nature genetics · 2008 · PMID 18204446
3 pages
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
Radstake TR,
Gorlova O,
Rueda B,
Martin JE,
Alizadeh BZ,
Palomino-Morales R,
Coenen MJ,
Vonk MC,
Voskuyl AE,
Schuerwegh AJ,
Broen JC,
van Riel PL
and 51 more — show all
van 't Slot R,
Italiaander A,
Ophoff RA,
Riemekasten G,
Hunzelmann N,
Simeon CP,
Ortego-Centeno N,
González-Gay MA,
González-Escribano MF,
Airo P,
van Laar J,
Herrick A,
Worthington J,
Hesselstrand R,
Smith V,
de Keyser F,
Houssiau F,
Chee MM,
Madhok R,
Shiels P,
Westhovens R,
Kreuter A,
Kiener H,
de Baere E,
Witte T,
Padykov L,
Klareskog L,
Beretta L,
Scorza R,
Lie BA,
Hoffmann-Vold AM,
Carreira P,
Varga J,
Hinchcliff M,
Gregersen PK,
Lee AT,
Ying J,
Han Y,
Weng SF,
Amos CI,
Wigley FM,
Hummers L,
Nelson JL,
Agarwal SK,
Assassi S,
Gourh P,
Tan FK,
Koeleman BP,
Arnett FC,
Martin J,
Mayes MD
Spanish Scleroderma Group
Nature genetics · 2010 · PMID 20383147
3 pages
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
Plenge RM,
Cotsapas C,
Davies L,
Price AL,
de Bakker PI,
Maller J,
Pe'er I,
Burtt NP,
Blumenstiel B,
DeFelice M,
Parkin M,
Barry R
and 26 more — show all
Winslow W,
Healy C,
Graham RR,
Neale BM,
Izmailova E,
Roubenoff R,
Parker AN,
Glass R,
Karlson EW,
Maher N,
Hafler DA,
Lee DM,
Seldin MF,
Remmers EF,
Lee AT,
Padyukov L,
Alfredsson L,
Coblyn J,
Weinblatt ME,
Gabriel SB,
Purcell S,
Klareskog L,
Gregersen PK,
Shadick NA,
Daly MJ,
Altshuler D
Nature genetics · 2007 · PMID 17982456
2 pages
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
Stahl EA,
Raychaudhuri S,
Remmers EF,
Xie G,
Eyre S,
Thomson BP,
Li Y,
Kurreeman FA,
Zhernakova A,
Hinks A,
Guiducci C,
Chen R
and 56 more — show all
Alfredsson L,
Amos CI,
Ardlie KG,
Barton A,
Bowes J,
Brouwer E,
Burtt NP,
Catanese JJ,
Coblyn J,
Coenen MJ,
Costenbader KH,
Criswell LA,
Crusius JB,
Cui J,
de Bakker PI,
De Jager PL,
Ding B,
Emery P,
Flynn E,
Harrison P,
Hocking LJ,
Huizinga TW,
Kastner DL,
Ke X,
Lee AT,
Liu X,
Martin P,
Morgan AW,
Padyukov L,
Posthumus MD,
Radstake TR,
Reid DM,
Seielstad M,
Seldin MF,
Shadick NA,
Steer S,
Tak PP,
Thomson W,
van der Helm-van Mil AH,
van der Horst-Bruinsma IE,
van der Schoot CE,
van Riel PL,
Weinblatt ME,
Wilson AG,
Wolbink GJ,
Wordsworth BP,
Wijmenga C,
Karlson EW,
Toes RE,
de Vries N,
Begovich AB,
Worthington J,
Siminovitch KA,
Gregersen PK,
Klareskog L,
Plenge RM
BIRAC Consortium · YEAR Consortium
Nature genetics · 2010 · PMID 20453842
2 pages
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis
Liu X,
Invernizzi P,
Lu Y,
Kosoy R,
Lu Y,
Bianchi I,
Podda M,
Xu C,
Xie G,
Macciardi F,
Selmi C,
Lupoli S
and 61 more — show all
Shigeta R,
Ransom M,
Lleo A,
Lee AT,
Mason AL,
Myers RP,
Peltekian KM,
Ghent CN,
Bernuzzi F,
Zuin M,
Rosina F,
Borghesio E,
Floreani A,
Lazzari R,
Niro G,
Andriulli A,
Muratori L,
Muratori P,
Almasio PL,
Andreone P,
Margotti M,
Brunetto M,
Coco B,
Alvaro D,
Bragazzi MC,
Marra F,
Pisano A,
Rigamonti C,
Colombo M,
Marzioni M,
Benedetti A,
Fabris L,
Strazzabosco M,
Portincasa P,
Palmieri VO,
Tiribelli C,
Croce L,
Bruno S,
Rossi S,
Vinci M,
Prisco C,
Mattalia A,
Toniutto P,
Picciotto A,
Galli A,
Ferrari C,
Ferrari C,
Colombo S,
Casella G,
Morini L,
Caporaso N,
Colli A,
Spinzi G,
Montanari R,
Gregersen PK,
Heathcote EJ,
Hirschfield GM,
Siminovitch KA,
Amos CI,
Gershwin ME,
Seldin MF
Nature genetics · 2010 · PMID 20639880
2 pages
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
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 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
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.