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2,661 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.
3 matches for
Scotland G.
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
Sim X,
Barnes DR,
Witkowska K,
Staley JR,
Tragante V
and 198 more — show all
Tukiainen T,
Yaghootkar H,
Masca N,
Freitag DF,
Ferreira T,
Giannakopoulou O,
Tinker A,
Harakalova M,
Mihailov E,
Liu C,
Kraja AT,
Fallgaard Nielsen S,
Rasheed A,
Samuel M,
Zhao W,
Bonnycastle LL,
Jackson AU,
Narisu N,
Swift AJ,
Southam L,
Marten J,
Huyghe JR,
Stančáková A,
Fava C,
Ohlsson T,
Matchan A,
Stirrups KE,
Bork-Jensen J,
Gjesing AP,
Kontto J,
Perola M,
Shaw-Hawkins S,
Havulinna AS,
Zhang H,
Donnelly LA,
Groves CJ,
Rayner NW,
Neville MJ,
Robertson NR,
Yiorkas AM,
Herzig KH,
Kajantie E,
Zhang W,
Willems SM,
Lannfelt L,
Malerba G,
Soranzo N,
Trabetti E,
Verweij N,
Evangelou E,
Moayyeri A,
Vergnaud AC,
Nelson CP,
Poveda A,
Varga TV,
Caslake M,
de Craen AJ,
Trompet S,
Luan J,
Scott RA,
Harris SE,
Liewald DC,
Marioni R,
Menni C,
Farmaki AE,
Hallmans G,
Renström F,
Huffman JE,
Hassinen M,
Burgess S,
Vasan RS,
Felix JF,
Uria-Nickelsen M,
Malarstig A,
Reily DF,
Hoek M,
Vogt T,
Lin H,
Lieb W,
Traylor M,
Markus HF,
Highland HM,
Justice AE,
Marouli E,
Lindström J,
Uusitupa M,
Komulainen P,
Lakka TA,
Rauramaa R,
Polasek O,
Rudan I,
Rolandsson O,
Franks PW,
Dedoussis G,
Spector TD,
Jousilahti P,
Männistö S,
Deary IJ,
Starr JM,
Langenberg C,
Wareham NJ,
Brown MJ,
Dominiczak AF,
Connell JM,
Jukema JW,
Sattar N,
Ford I,
Packard CJ,
Esko T,
Mägi R,
Metspalu A,
de Boer RA,
van der Meer P,
van der Harst P,
Gambaro G,
Ingelsson E,
Lind L,
de Bakker PI,
Numans ME,
Brandslund I,
Christensen C,
Petersen ER,
Korpi-Hyövälti E,
Oksa H,
Chambers JC,
Kooner JS,
Blakemore AI,
Franks S,
Jarvelin MR,
Husemoen LL,
Linneberg A,
Skaaby T,
Thuesen B,
Karpe F,
Tuomilehto J,
Doney AS,
Morris AD,
Palmer CN,
Holmen OL,
Hveem K,
Willer CJ,
Tuomi T,
Groop L,
Käräjämäki A,
Palotie A,
Ripatti S,
Salomaa V,
Alam DS,
Shafi Majumder AA,
Di Angelantonio E,
Chowdhury R,
McCarthy MI,
Poulter N,
Stanton AV,
Sever P,
Amouyel P,
Arveiler D,
Blankenberg S,
Ferrières J,
Kee F,
Kuulasmaa K,
Müller-Nurasyid M,
Veronesi G,
Virtamo J,
Deloukas P,
Elliott P,
Zeggini E,
Kathiresan S,
Melander O,
Kuusisto J,
Laakso M,
Padmanabhan S,
Porteous D,
Hayward C,
Scotland G,
Collins FS,
Mohlke KL,
Hansen T,
Pedersen O,
Boehnke M,
Stringham HM,
Frossard P,
Newton-Cheh C,
Tobin MD,
Nordestgaard BG,
Caulfield MJ,
Mahajan A,
Morris AP,
Tomaszewski M,
Samani NJ,
Saleheen D,
Asselbergs FW,
Lindgren CM,
Danesh J,
Wain LV,
Butterworth AS,
Howson JM,
Munroe PB
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Loth DW,
Soler Artigas M,
Gharib SA,
Wain LV,
Franceschini N,
Koch B,
Pottinger TD,
Smith AV,
Duan Q,
Oldmeadow C,
Lee MK,
Strachan DP
and 148 more — show all
James AL,
Huffman JE,
Vitart V,
Ramasamy A,
Wareham NJ,
Kaprio J,
Wang XQ,
Trochet H,
Kähönen M,
Flexeder C,
Albrecht E,
Lopez LM,
de Jong K,
Thyagarajan B,
Alves AC,
Enroth S,
Omenaas E,
Joshi PK,
Fall T,
Viñuela A,
Launer LJ,
Loehr LR,
Fornage M,
Li G,
Wilk JB,
Tang W,
Manichaikul A,
Lahousse L,
Harris TB,
North KE,
Rudnicka AR,
Hui J,
Gu X,
Lumley T,
Wright AF,
Hastie ND,
Campbell S,
Kumar R,
Pin I,
Scott RA,
Pietiläinen KH,
Surakka I,
Liu Y,
Holliday EG,
Schulz H,
Heinrich J,
Davies G,
Vonk JM,
Wojczynski M,
Pouta A,
Johansson A,
Wild SH,
Ingelsson E,
Rivadeneira F,
Völzke H,
Hysi PG,
Eiriksdottir G,
Morrison AC,
Rotter JI,
Gao W,
Postma DS,
White WB,
Rich SS,
Hofman A,
Aspelund T,
Couper D,
Smith LJ,
Psaty BM,
Lohman K,
Burchard EG,
Uitterlinden AG,
Garcia M,
Joubert BR,
McArdle WL,
Musk AB,
Hansel N,
Heckbert SR,
Zgaga L,
van Meurs JB,
Navarro P,
Rudan I,
Oh YM,
Redline S,
Jarvis DL,
Zhao JH,
Rantanen T,
O'Connor GT,
Ripatti S,
Scott RJ,
Karrasch S,
Grallert H,
Gaddis NC,
Starr JM,
Wijmenga C,
Minster RL,
Lederer DJ,
Pekkanen J,
Gyllensten U,
Campbell H,
Morris AP,
Gläser S,
Hammond CJ,
Burkart KM,
Beilby J,
Kritchevsky SB,
Gudnason V,
Hancock DB,
Williams OD,
Polasek O,
Zemunik T,
Kolcic I,
Petrini MF,
Wjst M,
Kim WJ,
Porteous DJ,
Scotland G,
Smith BH,
Viljanen A,
Heliövaara M,
Attia JR,
Sayers I,
Hampel R,
Gieger C,
Deary IJ,
Boezen HM,
Newman A,
Jarvelin MR,
Wilson JF,
Lind L,
Stricker BH,
Teumer A,
Spector TD,
Melén E,
Peters MJ,
Lange LA,
Barr RG,
Bracke KR,
Verhamme FM,
Sung J,
Hiemstra PS,
Cassano PA,
Sood A,
Hayward C,
Dupuis J,
Hall IP,
Brusselle GG,
Tobin MD,
London SJ
Nature genetics · 2014 · PMID 24929828
4 pages
Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank
Hall LS,
Adams MJ,
Arnau-Soler A,
Clarke TK,
Howard DM,
Zeng Y,
Davies G,
Hagenaars SP,
Maria Fernandez-Pujals A,
Gibson J,
Wigmore EM,
Boutin TS
and 7 more — show all
Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Translational psychiatry · 2018 · PMID 29317602 · 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.