For researchers
Is your paper here?
2,660 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.
6 matches for
Price AL.
Defining the role of common variation in the genomic and biological architecture of adult human height
Wood AR,
Esko T,
Yang J,
Vedantam S,
Pers TH,
Gustafsson S,
Chu AY,
Estrada K,
Luan J,
Kutalik Z,
Amin N,
Buchkovich ML
and 433 more — show all
Croteau-Chonka DC,
Day FR,
Duan Y,
Fall T,
Fehrmann R,
Ferreira T,
Jackson AU,
Karjalainen J,
Lo KS,
Locke AE,
Mägi R,
Mihailov E,
Porcu E,
Randall JC,
Scherag A,
Vinkhuyzen AA,
Westra HJ,
Winkler TW,
Workalemahu T,
Zhao JH,
Absher D,
Albrecht E,
Anderson D,
Baron J,
Beekman M,
Demirkan A,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Fraser RM,
Goel A,
Gong J,
Justice AE,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Lui JC,
Mangino M,
Mateo Leach I,
Medina-Gomez C,
Nalls MA,
Nyholt DR,
Palmer CD,
Pasko D,
Pechlivanis S,
Prokopenko I,
Ried JS,
Ripke S,
Shungin D,
Stancáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Afzal U,
Arnlöv J,
Arscott GM,
Bandinelli S,
Barrett A,
Bellis C,
Bennett AJ,
Berne C,
Blüher M,
Bolton JL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Buckley BM,
Buyske S,
Caspersen IH,
Chines PS,
Clarke R,
Claudi-Boehm S,
Cooper M,
Daw EW,
De Jong PA,
Deelen J,
Delgado G,
Denny JC,
Dhonukshe-Rutten R,
Dimitriou M,
Doney AS,
Dörr M,
Eklund N,
Eury E,
Folkersen L,
Garcia ME,
Geller F,
Giedraitis V,
Go AS,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
de Groot LC,
Groves CJ,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hannemann A,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hemani G,
Henders AK,
Hillege HL,
Hlatky MA,
Hoffmann W,
Hoffmann P,
Holmen O,
Houwing-Duistermaat JJ,
Illig T,
Isaacs A,
James AL,
Jeff J,
Johansen B,
Johansson Å,
Jolley J,
Juliusdottir T,
Junttila J,
Kho AN,
Kinnunen L,
Klopp N,
Kocher T,
Kratzer W,
Lichtner P,
Lind L,
Lindström J,
Lobbens S,
Lorentzon M,
Lu Y,
Lyssenko V,
Magnusson PK,
Mahajan A,
Maillard M,
McArdle WL,
McKenzie CA,
McLachlan S,
McLaren PJ,
Menni C,
Merger S,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Müller G,
Müller-Nurasyid M,
Musk AW,
Narisu N,
Nauck M,
Nolte IM,
Nöthen MM,
Oozageer L,
Pilz S,
Rayner NW,
Renstrom F,
Robertson NR,
Rose LM,
Roussel R,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Schunkert H,
Scott RA,
Sehmi J,
Seufferlein T,
Shi J,
Silventoinen K,
Smit JH,
Smith AV,
Smolonska J,
Stanton AV,
Stirrups K,
Stott DJ,
Stringham HM,
Sundström J,
Swertz MA,
Syvänen AC,
Tayo BO,
Thorleifsson G,
Tyrer JP,
van Dijk S,
van Schoor NM,
van der Velde N,
van Heemst D,
van Oort FV,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Waldenberger M,
Wennauer R,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Arveiler D,
Bakker SJ,
Beilby J,
Bergman RN,
Bergmann S,
Biffar R,
Blangero J,
Boomsma DI,
Bornstein SR,
Bovet P,
Brambilla P,
Brown MJ,
Campbell H,
Caulfield MJ,
Chakravarti A,
Collins R,
Collins FS,
Crawford DC,
Cupples LA,
Danesh J,
de Faire U,
den Ruijter HM,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Gansevoort RT,
Gejman PV,
Gieger C,
Golay A,
Gottesman O,
Gudnason V,
Gyllensten U,
Haas DW,
Hall AS,
Harris TB,
Hattersley AT,
Heath AC,
Hengstenberg C,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Hovingh GK,
Humphries SE,
Hunt SC,
Hypponen E,
Jacobs KB,
Jarvelin MR,
Jousilahti P,
Jula AM,
Kaprio J,
Kastelein JJ,
Kayser M,
Kee F,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Kooner JS,
Kooperberg C,
Koskinen S,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Le Marchand L,
Lehtimäki T,
Lupoli S,
Madden PA,
Männistö S,
Manunta P,
Marette A,
Matise TC,
McKnight B,
Meitinger T,
Moll FL,
Montgomery GW,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Ouwehand WH,
Pasterkamp G,
Peters A,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ritchie M,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schwarz PE,
Sebert S,
Sever P,
Shuldiner AR,
Sinisalo J,
Steinthorsdottir V,
Stolk RP,
Tardif JC,
Tönjes A,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PI,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hayes MG,
Hui J,
Hunter DJ,
Hveem K,
Jukema JW,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CN,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Powell JE,
Power C,
Quertermous T,
Rauramaa R,
Reinmaa E,
Ridker PM,
Rivadeneira F,
Rotter JI,
Saaristo TE,
Saleheen D,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Strauch K,
Stumvoll M,
Tuomilehto J,
Uusitupa M,
van der Harst P,
Völzke H,
Walker M,
Wareham NJ,
Watkins H,
Wichmann HE,
Wilson JF,
Zanen P,
Deloukas P,
Heid IM,
Lindgren CM,
Mohlke KL,
Speliotes EK,
Thorsteinsdottir U,
Barroso I,
Fox CS,
North KE,
Strachan DP,
Beckmann JS,
Berndt SI,
Boehnke M,
Borecki IB,
McCarthy MI,
Metspalu A,
Stefansson K,
Uitterlinden AG,
van Duijn CM,
Franke L,
Willer CJ,
Price AL,
Lettre G,
Loos RJ,
Weedon MN,
Ingelsson E,
O'Connell JR,
Abecasis GR,
Chasman DI,
Goddard ME,
Visscher PM,
Hirschhorn JN,
Frayling TM
Electronic Medical Records and Genomics (eMEMERGEGE) Consortium · MIGen Consortium and 2 more consortia
Nature genetics · 2014 · PMID 25282103 · open access
12 pages+
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+
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
Plenge RM,
Cotsapas C,
Davies L,
Price AL,
de Bakker PI,
Maller J,
Pe'er I,
Burtt NP,
Blumenstiel B,
DeFelice M,
Parkin M,
Barry R
and 26 more — show all
Winslow W,
Healy C,
Graham RR,
Neale BM,
Izmailova E,
Roubenoff R,
Parker AN,
Glass R,
Karlson EW,
Maher N,
Hafler DA,
Lee DM,
Seldin MF,
Remmers EF,
Lee AT,
Padyukov L,
Alfredsson L,
Coblyn J,
Weinblatt ME,
Gabriel SB,
Purcell S,
Klareskog L,
Gregersen PK,
Shadick NA,
Daly MJ,
Altshuler D
Nature genetics · 2007 · PMID 17982456
2 pages
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
and 204 more — show all
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes
Meng W,
Shah KP,
Pollack S,
Toppila I,
Hebert HL,
McCarthy MI,
Groop L,
Ahlqvist E,
Lyssenko V,
Agardh E,
Daniell M,
Kaidonis G
and 28 more — show all
Craig JE,
Mitchell P,
Liew G,
Kifley A,
Wang JJ,
Christiansen MW,
Jensen RA,
Penman A,
Hancock HA,
Chen CJ,
Correa A,
Kuo JZ,
Li X,
Chen YI,
Rotter JI,
Klein R,
Klein B,
Wong TY,
Morris AD,
Doney ASF,
Colhoun HM,
Price AL,
Burdon KP,
Groop PH,
Sandholm N,
Grassi MA,
Sobrin L,
Palmer CNA
Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group
Acta ophthalmologica · 2018 · PMID 30178632 · 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.