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Is your paper here?
2,652 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.
4 matches for
Hamby SE.
Association analyses based on false discovery rate implicate new loci for coronary artery disease
Nelson CP,
Goel A,
Butterworth AS,
Kanoni S,
Webb TR,
Marouli E,
Zeng L,
Ntalla I,
Lai FY,
Hopewell JC,
Giannakopoulou O,
Jiang T
and 50 more — show all
Hamby SE,
Di Angelantonio E,
Assimes TL,
Bottinger EP,
Chambers JC,
Clarke R,
Palmer CNA,
Cubbon RM,
Ellinor P,
Ermel R,
Evangelou E,
Franks PW,
Grace C,
Gu D,
Hingorani AD,
Howson JMM,
Ingelsson E,
Kastrati A,
Kessler T,
Kyriakou T,
Lehtimäki T,
Lu X,
Lu Y,
März W,
McPherson R,
Metspalu A,
Pujades-Rodriguez M,
Ruusalepp A,
Schadt EE,
Schmidt AF,
Sweeting MJ,
Zalloua PA,
AlGhalayini K,
Keavney BD,
Kooner JS,
Loos RJF,
Patel RS,
Rutter MK,
Tomaszewski M,
Tzoulaki I,
Zeggini E,
Erdmann J,
Dedoussis G,
Björkegren JLM,
Schunkert H,
Farrall M,
Danesh J,
Samani NJ,
Watkins H,
Deloukas P
EPIC-CVD Consortium · CARDIoGRAMplusC4D and 1 more consortia
Nature genetics · 2017 · PMID 28714975
12 pages+
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Li C,
Stoma S,
Lotta LA,
Warner S,
Albrecht E,
Allione A,
Arp PP,
Broer L,
Buxton JL,
Da Silva Couto Alves A,
Deelen J,
Fedko IO
and 84 more — show all
Gordon SD,
Jiang T,
Karlsson R,
Kerrison N,
Loe TK,
Mangino M,
Milaneschi Y,
Miraglio B,
Pervjakova N,
Russo A,
Surakka I,
van der Spek A,
Verhoeven JE,
Amin N,
Beekman M,
Blakemore AI,
Canzian F,
Hamby SE,
Hottenga JJ,
Jones PD,
Jousilahti P,
Mägi R,
Medland SE,
Montgomery GW,
Nyholt DR,
Perola M,
Pietiläinen KH,
Salomaa V,
Sillanpää E,
Suchiman HE,
van Heemst D,
Willemsen G,
Agudo A,
Boeing H,
Boomsma DI,
Chirlaque MD,
Fagherazzi G,
Ferrari P,
Franks P,
Gieger C,
Eriksson JG,
Gunter M,
Hägg S,
Hovatta I,
Imaz L,
Kaprio J,
Kaaks R,
Key T,
Krogh V,
Martin NG,
Melander O,
Metspalu A,
Moreno C,
Onland-Moret NC,
Nilsson P,
Ong KK,
Overvad K,
Palli D,
Panico S,
Pedersen NL,
Penninx BWJH,
Quirós JR,
Jarvelin MR,
Rodríguez-Barranco M,
Scott RA,
Severi G,
Slagboom PE,
Spector TD,
Tjonneland A,
Trichopoulou A,
Tumino R,
Uitterlinden AG,
van der Schouw YT,
van Duijn CM,
Weiderpass E,
Denchi EL,
Matullo G,
Butterworth AS,
Danesh J,
Samani NJ,
Wareham NJ,
Nelson CP,
Langenberg C,
Codd V
American journal of human genetics · 2020 · PMID 32109421 · open access
4 pages
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
Jones GT,
Tromp G,
Kuivaniemi H,
Gretarsdottir S,
Baas AF,
Giusti B,
Strauss E,
Van't Hof FN,
Webb TR,
Erdman R,
Ritchie MD,
Elmore JR
and 105 more — show all
Verma A,
Pendergrass S,
Kullo IJ,
Ye Z,
Peissig PL,
Gottesman O,
Verma SS,
Malinowski J,
Rasmussen-Torvik LJ,
Borthwick KM,
Smelser DT,
Crosslin DR,
de Andrade M,
Ryer EJ,
McCarty CA,
Böttinger EP,
Pacheco JA,
Crawford DC,
Carrell DS,
Gerhard GS,
Franklin DP,
Carey DJ,
Phillips VL,
Williams MJ,
Wei W,
Blair R,
Hill AA,
Vasudevan TM,
Lewis DR,
Thomson IA,
Krysa J,
Hill GB,
Roake J,
Merriman TR,
Oszkinis G,
Galora S,
Saracini C,
Abbate R,
Pulli R,
Pratesi C,
Saratzis A,
Verissimo AR,
Bumpstead S,
Badger SA,
Clough RE,
Cockerill G,
Hafez H,
Scott DJ,
Futers TS,
Romaine SP,
Bridge K,
Griffin KJ,
Bailey MA,
Smith A,
Thompson MM,
van Bockxmeer FM,
Matthiasson SE,
Thorleifsson G,
Thorsteinsdottir U,
Blankensteijn JD,
Teijink JA,
Wijmenga C,
de Graaf J,
Kiemeney LA,
Lindholt JS,
Hughes A,
Bradley DT,
Stirrups K,
Golledge J,
Norman PE,
Powell JT,
Humphries SE,
Hamby SE,
Goodall AH,
Nelson CP,
Sakalihasan N,
Courtois A,
Ferrell RE,
Eriksson P,
Folkersen L,
Franco-Cereceda A,
Eicher JD,
Johnson AD,
Betsholtz C,
Ruusalepp A,
Franzén O,
Schadt EE,
Björkegren JL,
Lipovich L,
Drolet AM,
Verhoeven EL,
Zeebregts CJ,
Geelkerken RH,
van Sambeek MR,
van Sterkenburg SM,
de Vries JP,
Stefansson K,
Thompson JR,
de Bakker PI,
Deloukas P,
Sayers RD,
Harrison SC,
van Rij AM,
Samani NJ,
Bown MJ
Circulation research · 2017 · PMID 27899403 · open access
3 pages
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation
Adlam D,
Berrandou TE,
Georges A,
Nelson CP,
Giannoulatou E,
Henry J,
Ma L,
Blencowe M,
Turley TN,
Yang ML,
Chopade S,
Finan C
and 40 more — show all
Braund PS,
Sadeg-Sayoud I,
Iismaa SE,
Kosel ML,
Zhou X,
Hamby SE,
Cheng J,
Liu L,
Tarr I,
Muller DWM,
d'Escamard V,
King A,
Brunham LR,
Baranowska-Clarke AA,
Debette S,
Amouyel P,
Olin JW,
Patil S,
Hesselson SE,
Junday K,
Kanoni S,
Aragam KG,
Butterworth AS,
Tweet MS,
Gulati R,
Combaret N,
Kadian-Dodov D,
Kalman JM,
Fatkin D,
Hingorani AD,
Saw J,
Webb TR,
Hayes SN,
Yang X,
Ganesh SK,
Olson TM,
Kovacic JC,
Graham RM,
Samani NJ,
Bouatia-Naji N
CARDIoGRAMPlusC4D · MEGASTROKE and 2 more consortia
Nature genetics · 2023 · PMID 37248441 · 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.