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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.
4 matches for
Generation Scotland.
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Day FR,
Ruth KS,
Thompson DJ,
Lunetta KL,
Pervjakova N,
Chasman DI,
Stolk L,
Finucane HK,
Sulem P,
Bulik-Sullivan B,
Esko T,
Johnson AD
and 230 more — show all
Elks CE,
Franceschini N,
He C,
Altmaier E,
Brody JA,
Franke LL,
Huffman JE,
Keller MF,
McArdle PF,
Nutile T,
Porcu E,
Robino A,
Rose LM,
Schick UM,
Smith JA,
Teumer A,
Traglia M,
Vuckovic D,
Yao J,
Zhao W,
Albrecht E,
Amin N,
Corre T,
Hottenga JJ,
Mangino M,
Smith AV,
Tanaka T,
Abecasis G,
Andrulis IL,
Anton-Culver H,
Antoniou AC,
Arndt V,
Arnold AM,
Barbieri C,
Beckmann MW,
Beeghly-Fadiel A,
Benitez J,
Bernstein L,
Bielinski SJ,
Blomqvist C,
Boerwinkle E,
Bogdanova NV,
Bojesen SE,
Bolla MK,
Borresen-Dale AL,
Boutin TS,
Brauch H,
Brenner H,
Brüning T,
Burwinkel B,
Campbell A,
Campbell H,
Chanock SJ,
Chapman JR,
Chen YI,
Chenevix-Trench G,
Couch FJ,
Coviello AD,
Cox A,
Czene K,
Darabi H,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dörk T,
Dos-Santos-Silva I,
Dunning AM,
Eicher JD,
Fasching PA,
Faul JD,
Figueroa J,
Flesch-Janys D,
Gandin I,
Garcia ME,
García-Closas M,
Giles GG,
Girotto GG,
Goldberg MS,
González-Neira A,
Goodarzi MO,
Grove ML,
Gudbjartsson DF,
Guénel P,
Guo X,
Haiman CA,
Hall P,
Hamann U,
Henderson BE,
Hocking LJ,
Hofman A,
Homuth G,
Hooning MJ,
Hopper JL,
Hu FB,
Huang J,
Humphreys K,
Hunter DJ,
Jakubowska A,
Jones SE,
Kabisch M,
Karasik D,
Knight JA,
Kolcic I,
Kooperberg C,
Kosma VM,
Kriebel J,
Kristensen V,
Lambrechts D,
Langenberg C,
Li J,
Li X,
Lindström S,
Liu Y,
Luan J,
Lubinski J,
Mägi R,
Mannermaa A,
Manz J,
Margolin S,
Marten J,
Martin NG,
Masciullo C,
Meindl A,
Michailidou K,
Mihailov E,
Milani L,
Milne RL,
Müller-Nurasyid M,
Nalls M,
Neale BM,
Nevanlinna H,
Neven P,
Newman AB,
Nordestgaard BG,
Olson JE,
Padmanabhan S,
Peterlongo P,
Peters U,
Petersmann A,
Peto J,
Pharoah PDP,
Pirastu NN,
Pirie A,
Pistis G,
Polasek O,
Porteous D,
Psaty BM,
Pylkäs K,
Radice P,
Raffel LJ,
Rivadeneira F,
Rudan I,
Rudolph A,
Ruggiero D,
Sala CF,
Sanna S,
Sawyer EJ,
Schlessinger D,
Schmidt MK,
Schmidt F,
Schmutzler RK,
Schoemaker MJ,
Scott RA,
Seynaeve CM,
Simard J,
Sorice R,
Southey MC,
Stöckl D,
Strauch K,
Swerdlow A,
Taylor KD,
Thorsteinsdottir U,
Toland AE,
Tomlinson I,
Truong T,
Tryggvadottir L,
Turner ST,
Vozzi D,
Wang Q,
Wellons M,
Willemsen G,
Wilson JF,
Winqvist R,
Wolffenbuttel BBHR,
Wright AF,
Yannoukakos D,
Zemunik T,
Zheng W,
Zheng W,
Zygmunt M,
Bergmann S,
Boomsma DI,
Buring JE,
Ferrucci L,
Montgomery GW,
Gudnason V,
Spector TD,
van Duijn CM,
Alizadeh BZ,
Ciullo M,
Crisponi L,
Easton DF,
Gasparini PP,
Gieger C,
Harris TB,
Hayward C,
Kardia SLR,
Kraft P,
McKnight B,
Metspalu A,
Morrison AC,
Reiner AP,
Ridker PM,
Rotter JI,
Toniolo D,
Uitterlinden AG,
Ulivi S,
Völzke H,
Wareham NJ,
Weir DR,
Yerges-Armstrong LM,
Price AL,
Stefansson K,
Visser JA,
Ong KK,
Chang-Claude J,
Murabito JM,
Perry JRB,
Murray A
PRACTICAL consortium · kConFab Investigators and 4 more consortia
Nature genetics · 2015 · PMID 26414677 · open access
12 pages+
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants
Nagy R,
Boutin TS,
Marten J,
Huffman JE,
Kerr SM,
Campbell A,
Evenden L,
Gibson J,
Amador C,
Howard DM,
Navarro P,
Morris A
and 13 more — show all
Deary IJ,
Hocking LJ,
Padmanabhan S,
Smith BH,
Joshi P,
Wilson JF,
Hastie ND,
Wright AF,
McIntosh AM,
Porteous DJ,
Haley CS,
Vitart V,
Hayward C
Genome medicine · 2017 · PMID 28270201 · open access
12 pages+
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Zhou W,
Kanai M,
Wu KH,
Rasheed H,
Tsuo K,
Hirbo JB,
Wang Y,
Bhattacharya A,
Zhao H,
Namba S,
Surakka I,
Wolford BN
and 140 more — show all
Lo Faro V,
Lopera-Maya EA,
Läll K,
Favé MJ,
Partanen JJ,
Chapman SB,
Karjalainen J,
Kurki M,
Maasha M,
Brumpton BM,
Chavan S,
Chen TT,
Daya M,
Ding Y,
Feng YA,
Guare LA,
Gignoux CR,
Graham SE,
Hornsby WE,
Ingold N,
Ismail SI,
Johnson R,
Laisk T,
Lin K,
Lv J,
Millwood IY,
Moreno-Grau S,
Nam K,
Palta P,
Pandit A,
Preuss MH,
Saad C,
Setia-Verma S,
Thorsteinsdottir U,
Uzunovic J,
Verma A,
Zawistowski M,
Zhong X,
Afifi N,
Al-Dabhani KM,
Al Thani A,
Bradford Y,
Campbell A,
Crooks K,
de Bock GH,
Damrauer SM,
Douville NJ,
Finer S,
Fritsche LG,
Fthenou E,
Gonzalez-Arroyo G,
Griffiths CJ,
Guo Y,
Hunt KA,
Ioannidis A,
Jansonius NM,
Konuma T,
Lee MTM,
Lopez-Pineda A,
Matsuda Y,
Marioni RE,
Moatamed B,
Nava-Aguilar MA,
Numakura K,
Patil S,
Rafaels N,
Richmond A,
Rojas-Muñoz A,
Shortt JA,
Straub P,
Tao R,
Vanderwerff B,
Vernekar M,
Veturi Y,
Barnes KC,
Boezen M,
Chen Z,
Chen CY,
Cho J,
Smith GD,
Finucane HK,
Franke L,
Gamazon ER,
Ganna A,
Gaunt TR,
Ge T,
Huang H,
Huffman J,
Katsanis N,
Koskela JT,
Lajonchere C,
Law MH,
Li L,
Lindgren CM,
Loos RJF,
MacGregor S,
Matsuda K,
Olsen CM,
Porteous DJ,
Shavit JA,
Snieder H,
Takano T,
Trembath RC,
Vonk JM,
Whiteman DC,
Wicks SJ,
Wijmenga C,
Wright J,
Zheng J,
Zhou X,
Awadalla P,
Boehnke M,
Bustamante CD,
Cox NJ,
Fatumo S,
Geschwind DH,
Hayward C,
Hveem K,
Kenny EE,
Lee S,
Lin YF,
Mbarek H,
Mägi R,
Martin HC,
Medland SE,
Okada Y,
Palotie AV,
Pasaniuc B,
Rader DJ,
Ritchie MD,
Sanna S,
Smoller JW,
Stefansson K,
van Heel DA,
Walters RG,
Zöllner S,
Martin AR,
Willer CJ,
Daly MJ,
Neale BM
Biobank of the Americas · Biobank Japan Project and 22 more consortia
Cell genomics · 2022 · PMID 36777996 · open access
12 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.