For researchers
Is your paper here?
2,671 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.
9 matches for
Mirel DB.
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 identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels
He M,
Cornelis MC,
Kraft P,
van Dam RM,
Sun Q,
Laurie CC,
Mirel DB,
Chasman DI,
Ridker PM,
Hunter DJ,
Hu FB,
Qi L
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20150558
2 pages
Genome-wide association study of Tourette's syndrome
Scharf JM,
Yu D,
Mathews CA,
Neale BM,
Stewart SE,
Fagerness JA,
Evans P,
Gamazon E,
Edlund CK,
Service SK,
Tikhomirov A,
Osiecki L
and 86 more — show all
Illmann C,
Pluzhnikov A,
Konkashbaev A,
Davis LK,
Han B,
Crane J,
Moorjani P,
Crenshaw AT,
Parkin MA,
Reus VI,
Lowe TL,
Rangel-Lugo M,
Chouinard S,
Dion Y,
Girard S,
Cath DC,
Smit JH,
King RA,
Fernandez TV,
Leckman JF,
Kidd KK,
Kidd JR,
Pakstis AJ,
State MW,
Herrera LD,
Romero R,
Fournier E,
Sandor P,
Barr CL,
Phan N,
Gross-Tsur V,
Benarroch F,
Pollak Y,
Budman CL,
Bruun RD,
Erenberg G,
Naarden AL,
Lee PC,
Weiss N,
Kremeyer B,
Berrío GB,
Campbell DD,
Cardona Silgado JC,
Ochoa WC,
Mesa Restrepo SC,
Muller H,
Valencia Duarte AV,
Lyon GJ,
Leppert M,
Morgan J,
Weiss R,
Grados MA,
Anderson K,
Davarya S,
Singer H,
Walkup J,
Jankovic J,
Tischfield JA,
Heiman GA,
Gilbert DL,
Hoekstra PJ,
Robertson MM,
Kurlan R,
Liu C,
Gibbs JR,
Singleton A,
Hardy J,
Strengman E,
Ophoff RA,
Wagner M,
Moessner R,
Mirel DB,
Posthuma D,
Sabatti C,
Eskin E,
Conti DV,
Knowles JA,
Ruiz-Linares A,
Rouleau GA,
Purcell S,
Heutink P,
Oostra BA,
McMahon WM,
Freimer NB,
Cox NJ,
Pauls DL
North American Brain Expression Consortium · UK Human Brain Expression Database
Molecular psychiatry · 2013 · PMID 22889924 · open access
2 pages
Evaluating genetic risk for prostate cancer among Japanese and Latinos
Cheng I,
Chen GK,
Nakagawa H,
He J,
Wan P,
Laurie CC,
Shen J,
Sheng X,
Pooler LC,
Crenshaw AT,
Mirel DB,
Takahashi A
and 19 more — show all
Kubo M,
Nakamura Y,
Al Olama AA,
Benlloch S,
Donovan JL,
Guy M,
Hamdy FC,
Kote-Jarai Z,
Neal DE,
Wilkens LR,
Monroe KR,
Stram DO,
Muir K,
Eeles RA,
Easton DF,
Kolonel LN,
Henderson BE,
Le Marchand L,
Haiman CA
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2012 · PMID 22923026
2 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
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
Hancock DB,
Soler Artigas M,
Gharib SA,
Henry A,
Manichaikul A,
Ramasamy A,
Loth DW,
Imboden M,
Koch B,
McArdle WL,
Smith AV,
Smolonska J
and 78 more — show all
Sood A,
Tang W,
Wilk JB,
Zhai G,
Zhao JH,
Aschard H,
Burkart KM,
Curjuric I,
Eijgelsheim M,
Elliott P,
Gu X,
Harris TB,
Janson C,
Homuth G,
Hysi PG,
Liu JZ,
Loehr LR,
Lohman K,
Loos RJ,
Manning AK,
Marciante KD,
Obeidat M,
Postma DS,
Aldrich MC,
Brusselle GG,
Chen TH,
Eiriksdottir G,
Franceschini N,
Heinrich J,
Rotter JI,
Wijmenga C,
Williams OD,
Bentley AR,
Hofman A,
Laurie CC,
Lumley T,
Morrison AC,
Joubert BR,
Rivadeneira F,
Couper DJ,
Kritchevsky SB,
Liu Y,
Wjst M,
Wain LV,
Vonk JM,
Uitterlinden AG,
Rochat T,
Rich SS,
Psaty BM,
O'Connor GT,
North KE,
Mirel DB,
Meibohm B,
Launer LJ,
Khaw KT,
Hartikainen AL,
Hammond CJ,
Gläser S,
Marchini J,
Kraft P,
Wareham NJ,
Völzke H,
Stricker BH,
Spector TD,
Probst-Hensch NM,
Jarvis D,
Jarvelin MR,
Heckbert SR,
Gudnason V,
Boezen HM,
Barr RG,
Cassano PA,
Strachan DP,
Fornage M,
Hall IP,
Dupuis J,
Tobin MD,
London SJ
PLoS genetics · 2012 · PMID 23284291 · open access
2 pages
Genetic variation associated with circulating monocyte count in the eMERGE Network
Crosslin DR,
McDavid A,
Weston N,
Zheng X,
Hart E,
de Andrade M,
Kullo IJ,
McCarty CA,
Doheny KF,
Pugh E,
Kho A,
Hayes MG
and 52 more — show all
Ritchie MD,
Saip A,
Crawford DC,
Crane PK,
Newton K,
Carrell DS,
Gallego CJ,
Nalls MA,
Li R,
Mirel DB,
Crenshaw A,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Zakai NA,
Yango Q,
Garcia M,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Felix JF,
Dehghan A,
Wilson JG,
Bis JC,
Fox CS,
Glazer NL,
Cupples LA,
Coresh J,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Larson EB,
Carlson CS,
Jarvik GP
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
2 pages
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Desch KC,
Ozel AB,
Siemieniak D,
Kalish Y,
Shavit JA,
Thornburg CD,
Sharathkumar AA,
McHugh CP,
Laurie CC,
Crenshaw A,
Mirel DB,
Kim Y
and 10 more — show all
Proceedings of the National Academy of Sciences of the United States of America · 2013 · PMID 23267103
1 page
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study
Urbanek M,
Hayes MG,
Armstrong LL,
Morrison J,
Lowe LP,
Badon SE,
Scheftner D,
Pluzhnikov A,
Levine D,
Laurie CC,
McHugh C,
Ackerman CM
and 9 more — show all
HAPO Study Cooperative Research Group
Human molecular genetics · 2013 · PMID 23575227
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.