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2,671 papers hold this site up. Every variant and condition page names
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Search your name, your journal, or a PMID.
11 matches for
Smith S.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
Graff M,
Justice AE,
Young KL,
Marouli E,
Zhang X,
Fine RS,
Lim E,
Buchanan V,
Rand K,
Feitosa MF,
Wojczynski MK,
Yanek LR
and 213 more — show all
Shao Y,
Rohde R,
Adeyemo AA,
Aldrich MC,
Allison MA,
Ambrosone CB,
Ambs S,
Amos C,
Arnett DK,
Atwood L,
Bandera EV,
Bartz T,
Becker DM,
Berndt SI,
Bernstein L,
Bielak LF,
Blot WJ,
Bottinger EP,
Bowden DW,
Bradfield JP,
Brody JA,
Broeckel U,
Burke G,
Cade BE,
Cai Q,
Caporaso N,
Carlson C,
Carpten J,
Casey G,
Chanock SJ,
Chen G,
Chen M,
Chen YI,
Chen WM,
Chesi A,
Chiang CWK,
Chu L,
Coetzee GA,
Conti DV,
Cooper RS,
Cushman M,
Demerath E,
Deming SL,
Dimitrov L,
Ding J,
Diver WR,
Duan Q,
Evans MK,
Falusi AG,
Faul JD,
Fornage M,
Fox C,
Freedman BI,
Garcia M,
Gillanders EM,
Goodman P,
Gottesman O,
Grant SFA,
Guo X,
Hakonarson H,
Haritunians T,
Harris TB,
Harris CC,
Henderson BE,
Hennis A,
Hernandez DG,
Hirschhorn JN,
McNeill LH,
Howard TD,
Howard B,
Hsing AW,
Hsu YH,
Hu JJ,
Huff CD,
Huo D,
Ingles SA,
Irvin MR,
John EM,
Johnson KC,
Jordan JM,
Kabagambe EK,
Kang SJ,
Kardia SL,
Keating BJ,
Kittles RA,
Klein EA,
Kolb S,
Kolonel LN,
Kooperberg C,
Kuller L,
Kutlar A,
Lange L,
Langefeld CD,
Le Marchand L,
Leonard H,
Lettre G,
Levin AM,
Li Y,
Li J,
Liu Y,
Liu Y,
Liu S,
Lohman K,
Lotay V,
Lu Y,
Maixner W,
Manson JE,
McKnight B,
Meng Y,
Monda KL,
Monroe K,
Moore JH,
Mosley TH,
Mudgal P,
Murphy AB,
Nadukuru R,
Nalls MA,
Nathanson KL,
Nayak U,
N'Diaye A,
Nemesure B,
Neslund-Dudas C,
Neuhouser ML,
Nyante S,
Ochs-Balcom H,
Ogundiran TO,
Ogunniyi A,
Ojengbede O,
Okut H,
Olopade OI,
Olshan A,
Padhukasahasram B,
Palmer J,
Palmer CD,
Palmer ND,
Papanicolaou G,
Patel SR,
Pettaway CA,
Peyser PA,
Press MF,
Rao DC,
Rasmussen-Torvik LJ,
Redline S,
Reiner AP,
Rhie SK,
Rodriguez-Gil JL,
Rotimi CN,
Rotter JI,
Ruiz-Narvaez EA,
Rybicki BA,
Salako B,
Sale MM,
Sanderson M,
Schadt E,
Schreiner PJ,
Schurmann C,
Schwartz AG,
Shriner DA,
Signorello LB,
Singleton AB,
Siscovick DS,
Smith JA,
Smith S,
Speliotes E,
Spitz M,
Stanford JL,
Stevens VL,
Stram A,
Strom SS,
Sucheston L,
Sun YV,
Tajuddin SM,
Taylor H,
Taylor K,
Tayo BO,
Thun MJ,
Tucker MA,
Vaidya D,
Van Den Berg DJ,
Vedantam S,
Vitolins M,
Wang Z,
Ware EB,
Wassertheil-Smoller S,
Weir DR,
Wiencke JK,
Williams SM,
Williams LK,
Wilson JG,
Witte JS,
Wrensch M,
Wu X,
Yao J,
Zakai N,
Zanetti K,
Zemel BS,
Zhao W,
Zhao JH,
Zheng W,
Zhi D,
Zhou J,
Zhu X,
Ziegler RG,
Zmuda J,
Zonderman AB,
Psaty BM,
Borecki IB,
Cupples LA,
Liu CT,
Haiman CA,
Loos R,
Ng MCY,
North KE
American journal of human genetics · 2021 · PMID 33713608
12 pages+
Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms
López-Isac E,
Smith SL,
Marion MC,
Wood A,
Sudman M,
Yarwood A,
Shi C,
Gaddi VP,
Martin P,
Prahalad S,
Eyre S,
Orozco G
and 5 more — show all
Annals of the rheumatic diseases · 2021 · PMID 33106285 · open access
6 pages
GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association
Rentería ME,
Coolen MW,
Statham AL,
Choi RS,
Qu W,
Campbell MJ,
Smith S,
Henders AK,
Montgomery GW,
Clark SJ,
Martin NG,
Medland SE
Twin research and human genetics : the official journal of the International Society for Twin Studies · 2013 · PMID 23725790
4 pages
GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos
Sanders AE,
Jain D,
Sofer T,
Kerr KF,
Laurie CC,
Shaffer JR,
Marazita ML,
Kaste LM,
Slade GD,
Fillingim RB,
Ohrbach R,
Maixner W
and 15 more — show all
Kocher T,
Bernhardt O,
Teumer A,
Schwahn C,
Sipilä K,
Lähdesmäki R,
Männikkö M,
Pesonen P,
Järvelin M,
Rizzatti-Barbosa CM,
Meloto CB,
Ribeiro-Dasilva M,
Diatchenko L,
Serrano P,
Smith SB
Journal of dental research · 2017 · PMID 28081371
3 pages
Discovery of 42 genome-wide significant loci associated with dyslexia
Doust C,
Fontanillas P,
Eising E,
Gordon SD,
Wang Z,
Alagöz G,
Molz B,
Pourcain BS,
Francks C,
Marioni RE,
Zhao J,
Paracchini S
and 15 more — show all
Talcott JB,
Monaco AP,
Stein JF,
Gruen JR,
Olson RK,
Willcutt EG,
DeFries JC,
Pennington BF,
Smith SD,
Wright MJ,
Martin NG,
Auton A,
Bates TC,
Fisher SE,
Luciano M
23andMe Research Team · Quantitative Trait Working Group of the GenLang Consortium
Nature genetics · 2022 · PMID 36266505 · open access
3 pages
Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties
Lee S,
Bijsterbosch JD,
Almagro FA,
Elliott L,
McCarthy P,
Taschler B,
Sala-Llonch R,
Beckmann CF,
Duff EP,
Smith SM,
Douaud G
NeuroImage · 2023 · PMID 36462729 · open access
3 pages
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Monda KL,
Chen GK,
Taylor KC,
Palmer C,
Edwards TL,
Lange LA,
Ng MC,
Adeyemo AA,
Allison MA,
Bielak LF,
Chen G,
Graff M
and 196 more — show all
Irvin MR,
Rhie SK,
Li G,
Liu Y,
Liu Y,
Lu Y,
Nalls MA,
Sun YV,
Wojczynski MK,
Yanek LR,
Aldrich MC,
Ademola A,
Amos CI,
Bandera EV,
Bock CH,
Britton A,
Broeckel U,
Cai Q,
Caporaso NE,
Carlson CS,
Carpten J,
Casey G,
Chen WM,
Chen F,
Chen YD,
Chiang CW,
Coetzee GA,
Demerath E,
Deming-Halverson SL,
Driver RW,
Dubbert P,
Feitosa MF,
Feng Y,
Freedman BI,
Gillanders EM,
Gottesman O,
Guo X,
Haritunians T,
Harris T,
Harris CC,
Hennis AJ,
Hernandez DG,
McNeill LH,
Howard TD,
Howard BV,
Howard VJ,
Johnson KC,
Kang SJ,
Keating BJ,
Kolb S,
Kuller LH,
Kutlar A,
Langefeld CD,
Lettre G,
Lohman K,
Lotay V,
Lyon H,
Manson JE,
Maixner W,
Meng YA,
Monroe KR,
Morhason-Bello I,
Murphy AB,
Mychaleckyj JC,
Nadukuru R,
Nathanson KL,
Nayak U,
N'diaye A,
Nemesure B,
Wu SY,
Leske MC,
Neslund-Dudas C,
Neuhouser M,
Nyante S,
Ochs-Balcom H,
Ogunniyi A,
Ogundiran TO,
Ojengbede O,
Olopade OI,
Palmer JR,
Ruiz-Narvaez EA,
Palmer ND,
Press MF,
Rampersaud E,
Rasmussen-Torvik LJ,
Rodriguez-Gil JL,
Salako B,
Schadt EE,
Schwartz AG,
Shriner DA,
Siscovick D,
Smith SB,
Wassertheil-Smoller S,
Speliotes EK,
Spitz MR,
Sucheston L,
Taylor H,
Tayo BO,
Tucker MA,
Van Den Berg DJ,
Edwards DR,
Wang Z,
Wiencke JK,
Winkler TW,
Witte JS,
Wrensch M,
Wu X,
Yang JJ,
Levin AM,
Young TR,
Zakai NA,
Cushman M,
Zanetti KA,
Zhao JH,
Zhao W,
Zheng Y,
Zhou J,
Ziegler RG,
Zmuda JM,
Fernandes JK,
Gilkeson GS,
Kamen DL,
Hunt KJ,
Spruill IJ,
Ambrosone CB,
Ambs S,
Arnett DK,
Atwood L,
Becker DM,
Berndt SI,
Bernstein L,
Blot WJ,
Borecki IB,
Bottinger EP,
Bowden DW,
Burke G,
Chanock SJ,
Cooper RS,
Ding J,
Duggan D,
Evans MK,
Fox C,
Garvey WT,
Bradfield JP,
Hakonarson H,
Grant SF,
Hsing A,
Chu L,
Hu JJ,
Huo D,
Ingles SA,
John EM,
Jordan JM,
Kabagambe EK,
Kardia SL,
Kittles RA,
Goodman PJ,
Klein EA,
Kolonel LN,
Le Marchand L,
Liu S,
McKnight B,
Millikan RC,
Mosley TH,
Padhukasahasram B,
Williams LK,
Patel SR,
Peters U,
Pettaway CA,
Peyser PA,
Psaty BM,
Redline S,
Rotimi CN,
Rybicki BA,
Sale MM,
Schreiner PJ,
Signorello LB,
Singleton AB,
Stanford JL,
Strom SS,
Thun MJ,
Vitolins M,
Zheng W,
Moore JH,
Williams SM,
Ketkar S,
Zhu X,
Zonderman AB,
Kooperberg C,
Papanicolaou GJ,
Henderson BE,
Reiner AP,
Hirschhorn JN,
Loos RJ,
North KE,
Haiman CA
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Armstrong NJ,
Mather KA,
Sargurupremraj M,
Knol MJ,
Malik R,
Satizabal CL,
Yanek LR,
Wen W,
Gudnason VG,
Dueker ND,
Elliott LT,
Hofer E
and 74 more — show all
Bis J,
Jahanshad N,
Li S,
Logue MA,
Luciano M,
Scholz M,
Smith AV,
Trompet S,
Vojinovic D,
Xia R,
Alfaro-Almagro F,
Ames D,
Amin N,
Amouyel P,
Beiser AS,
Brodaty H,
Deary IJ,
Fennema-Notestine C,
Gampawar PG,
Gottesman R,
Griffanti L,
Jack CR Jr,
Jenkinson M,
Jiang J,
Kral BG,
Kwok JB,
Lampe L,
C M Liewald D,
Maillard P,
Marchini J,
Bastin ME,
Mazoyer B,
Pirpamer L,
Rafael Romero J,
Roshchupkin GV,
Schofield PR,
Schroeter ML,
Stott DJ,
Thalamuthu A,
Trollor J,
Tzourio C,
van der Grond J,
Vernooij MW,
Witte VA,
Wright MJ,
Yang Q,
Morris Z,
Siggurdsson S,
Psaty B,
Villringer A,
Schmidt H,
Haberg AK,
van Duijn CM,
Jukema JW,
Dichgans M,
Sacco RL,
Wright CB,
Kremen WS,
Becker LC,
Thompson PM,
Mosley TH,
Wardlaw JM,
Ikram MA,
Adams HHH,
Seshadri S,
Sachdev PS,
Smith SM,
Launer L,
Longstreth W,
DeCarli C,
Schmidt R,
Fornage M,
Debette S,
Nyquist PA
Stroke · 2020 · PMID 32517579
2 pages
Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
Jin G,
Sun J,
Kim ST,
Feng J,
Wang Z,
Tao S,
Chen Z,
Purcell L,
Smith S,
Isaacs WB,
Rittmaster RS,
Zheng SL
and 2 more — show all
Human molecular genetics · 2012 · PMID 22936694
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.