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34 matches for
Geller F,
showing the first 20.
Genome-wide association analyses identify variants in developmental genes associated with hypospadias
Geller F,
Feenstra B,
Carstensen L,
Pers TH,
van Rooij IA,
Körberg IB,
Choudhry S,
Karjalainen JM,
Schnack TH,
Hollegaard MV,
Feitz WF,
Roeleveld N
and 7 more — show all
Nature genetics · 2014 · PMID 25108383
12 pages+
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Perry JR,
Day F,
Elks CE,
Sulem P,
Thompson DJ,
Ferreira T,
He C,
Chasman DI,
Esko T,
Thorleifsson G,
Albrecht E,
Ang WQ
and 186 more — show all
Corre T,
Cousminer DL,
Feenstra B,
Franceschini N,
Ganna A,
Johnson AD,
Kjellqvist S,
Lunetta KL,
McMahon G,
Nolte IM,
Paternoster L,
Porcu E,
Smith AV,
Stolk L,
Teumer A,
Tšernikova N,
Tikkanen E,
Ulivi S,
Wagner EK,
Amin N,
Bierut LJ,
Byrne EM,
Hottenga JJ,
Koller DL,
Mangino M,
Pers TH,
Yerges-Armstrong LM,
Zhao JH,
Andrulis IL,
Anton-Culver H,
Atsma F,
Bandinelli S,
Beckmann MW,
Benitez J,
Blomqvist C,
Bojesen SE,
Bolla MK,
Bonanni B,
Brauch H,
Brenner H,
Buring JE,
Chang-Claude J,
Chanock S,
Chen J,
Chenevix-Trench G,
Collée JM,
Couch FJ,
Couper D,
Coveillo AD,
Cox A,
Czene K,
D'adamo AP,
Smith GD,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dieffenbach AK,
Dunning AM,
Eiriksdottir G,
Eriksson JG,
Fasching PA,
Ferrucci L,
Flesch-Janys D,
Flyger H,
Foroud T,
Franke L,
Garcia ME,
García-Closas M,
Geller F,
de Geus EE,
Giles GG,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Guo S,
Hall P,
Hamann U,
Haring R,
Hartman CA,
Heath AC,
Hofman A,
Hooning MJ,
Hopper JL,
Hu FB,
Hunter DJ,
Karasik D,
Kiel DP,
Knight JA,
Kosma VM,
Kutalik Z,
Lai S,
Lambrechts D,
Lindblom A,
Mägi R,
Magnusson PK,
Mannermaa A,
Martin NG,
Masson G,
McArdle PF,
McArdle WL,
Melbye M,
Michailidou K,
Mihailov E,
Milani L,
Milne RL,
Nevanlinna H,
Neven P,
Nohr EA,
Oldehinkel AJ,
Oostra BA,
Palotie A,
Peacock M,
Pedersen NL,
Peterlongo P,
Peto J,
Pharoah PD,
Postma DS,
Pouta A,
Pylkäs K,
Radice P,
Ring S,
Rivadeneira F,
Robino A,
Rose LM,
Rudolph A,
Salomaa V,
Sanna S,
Schlessinger D,
Schmidt MK,
Southey MC,
Sovio U,
Stampfer MJ,
Stöckl D,
Storniolo AM,
Timpson NJ,
Tyrer J,
Visser JA,
Vollenweider P,
Völzke H,
Waeber G,
Waldenberger M,
Wallaschofski H,
Wang Q,
Willemsen G,
Winqvist R,
Wolffenbuttel BH,
Wright MJ,
Boomsma DI,
Econs MJ,
Khaw KT,
Loos RJ,
McCarthy MI,
Montgomery GW,
Rice JP,
Streeten EA,
Thorsteinsdottir U,
van Duijn CM,
Alizadeh BZ,
Bergmann S,
Boerwinkle E,
Boyd HA,
Crisponi L,
Gasparini P,
Gieger C,
Harris TB,
Ingelsson E,
Järvelin MR,
Kraft P,
Lawlor D,
Metspalu A,
Pennell CE,
Ridker PM,
Snieder H,
Sørensen TI,
Spector TD,
Strachan DP,
Uitterlinden AG,
Wareham NJ,
Widen E,
Zygmunt M,
Murray A,
Easton DF,
Stefansson K,
Murabito JM,
Ong KK
Australian Ovarian Cancer Study · GENICA Network and 4 more consortia
Nature · 2014 · PMID 25231870 · open access
12 pages+
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+
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
Winkler TW,
Justice AE,
Graff M,
Barata L,
Feitosa MF,
Chu S,
Czajkowski J,
Esko T,
Fall T,
Kilpeläinen TO,
Lu Y,
Mägi R
and 427 more — show all
Mihailov E,
Pers TH,
Rüeger S,
Teumer A,
Ehret GB,
Ferreira T,
Heard-Costa NL,
Karjalainen J,
Lagou V,
Mahajan A,
Neinast MD,
Prokopenko I,
Simino J,
Teslovich TM,
Jansen R,
Westra HJ,
White CC,
Absher D,
Ahluwalia TS,
Ahmad S,
Albrecht E,
Alves AC,
Bragg-Gresham JL,
de Craen AJ,
Bis JC,
Bonnefond A,
Boucher G,
Cadby G,
Cheng YC,
Chiang CW,
Delgado G,
Demirkan A,
Dueker N,
Eklund N,
Eiriksdottir G,
Eriksson J,
Feenstra B,
Fischer K,
Frau F,
Galesloot TE,
Geller F,
Goel A,
Gorski M,
Grammer TB,
Gustafsson S,
Haitjema S,
Hottenga JJ,
Huffman JE,
Jackson AU,
Jacobs KB,
Johansson Å,
Kaakinen M,
Kleber ME,
Lahti J,
Mateo Leach I,
Lehne B,
Liu Y,
Lo KS,
Lorentzon M,
Luan J,
Madden PA,
Mangino M,
McKnight B,
Medina-Gomez C,
Monda KL,
Montasser ME,
Müller G,
Müller-Nurasyid M,
Nolte IM,
Panoutsopoulou K,
Pascoe L,
Paternoster L,
Rayner NW,
Renström F,
Rizzi F,
Rose LM,
Ryan KA,
Salo P,
Sanna S,
Scharnagl H,
Shi J,
Smith AV,
Southam L,
Stančáková A,
Steinthorsdottir V,
Strawbridge RJ,
Sung YJ,
Tachmazidou I,
Tanaka T,
Thorleifsson G,
Trompet S,
Pervjakova N,
Tyrer JP,
Vandenput L,
van der Laan SW,
van der Velde N,
van Setten J,
van Vliet-Ostaptchouk JV,
Verweij N,
Vlachopoulou E,
Waite LL,
Wang SR,
Wang Z,
Wild SH,
Willenborg C,
Wilson JF,
Wong A,
Yang J,
Yengo L,
Yerges-Armstrong LM,
Yu L,
Zhang W,
Zhao JH,
Andersson EA,
Bakker SJ,
Baldassarre D,
Banasik K,
Barcella M,
Barlassina C,
Bellis C,
Benaglio P,
Blangero J,
Blüher M,
Bonnet F,
Bonnycastle LL,
Boyd HA,
Bruinenberg M,
Buchman AS,
Campbell H,
Chen YD,
Chines PS,
Claudi-Boehm S,
Cole J,
Collins FS,
de Geus EJ,
de Groot LC,
Dimitriou M,
Duan J,
Enroth S,
Eury E,
Farmaki AE,
Forouhi NG,
Friedrich N,
Gejman PV,
Gigante B,
Glorioso N,
Go AS,
Gottesman O,
Gräßler J,
Grallert H,
Grarup N,
Gu YM,
Broer L,
Ham AC,
Hansen T,
Harris TB,
Hartman CA,
Hassinen M,
Hastie N,
Hattersley AT,
Heath AC,
Henders AK,
Hernandez D,
Hillege H,
Holmen O,
Hovingh KG,
Hui J,
Husemoen LL,
Hutri-Kähönen N,
Hysi PG,
Illig T,
De Jager PL,
Jalilzadeh S,
Jørgensen T,
Jukema JW,
Juonala M,
Kanoni S,
Karaleftheri M,
Khaw KT,
Kinnunen L,
Kittner SJ,
Koenig W,
Kolcic I,
Kovacs P,
Krarup NT,
Kratzer W,
Krüger J,
Kuh D,
Kumari M,
Kyriakou T,
Langenberg C,
Lannfelt L,
Lanzani C,
Lotay V,
Launer LJ,
Leander K,
Lindström J,
Linneberg A,
Liu YP,
Lobbens S,
Luben R,
Lyssenko V,
Männistö S,
Magnusson PK,
McArdle WL,
Menni C,
Merger S,
Milani L,
Montgomery GW,
Morris AP,
Narisu N,
Nelis M,
Ong KK,
Palotie A,
Pérusse L,
Pichler I,
Pilia MG,
Pouta A,
Rheinberger M,
Ribel-Madsen R,
Richards M,
Rice KM,
Rice TK,
Rivolta C,
Salomaa V,
Sanders AR,
Sarzynski MA,
Scholtens S,
Scott RA,
Scott WR,
Sebert S,
Sengupta S,
Sennblad B,
Seufferlein T,
Silveira A,
Slagboom PE,
Smit JH,
Sparsø TH,
Stirrups K,
Stolk RP,
Stringham HM,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Thorand B,
Tönjes A,
Tremblay A,
Tsafantakis E,
van der Most PJ,
Völker U,
Vohl MC,
Vonk JM,
Waldenberger M,
Walker RW,
Wennauer R,
Widén E,
Willemsen G,
Wilsgaard T,
Wright AF,
Zillikens MC,
van Dijk SC,
van Schoor NM,
Asselbergs FW,
de Bakker PI,
Beckmann JS,
Beilby J,
Bennett DA,
Bergman RN,
Bergmann S,
Böger CA,
Boehm BO,
Boerwinkle E,
Boomsma DI,
Bornstein SR,
Bottinger EP,
Bouchard C,
Chambers JC,
Chanock SJ,
Chasman DI,
Cucca F,
Cusi D,
Dedoussis G,
Erdmann J,
Eriksson JG,
Evans DA,
de Faire U,
Farrall M,
Ferrucci L,
Ford I,
Franke L,
Franks PW,
Froguel P,
Gansevoort RT,
Gieger C,
Grönberg H,
Gudnason V,
Gyllensten U,
Hall P,
Hamsten A,
van der Harst P,
Hayward C,
Heliövaara M,
Hengstenberg C,
Hicks AA,
Hingorani A,
Hofman A,
Hu F,
Huikuri HV,
Hveem K,
James AL,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Kathiresan S,
Kiemeney LA,
Kivimaki M,
Knekt PB,
Koistinen HA,
Kooner JS,
Koskinen S,
Kuusisto J,
Maerz W,
Martin NG,
Laakso M,
Lakka TA,
Lehtimäki T,
Lettre G,
Levinson DF,
Lind L,
Lokki ML,
Mäntyselkä P,
Melbye M,
Metspalu A,
Mitchell BD,
Moll FL,
Murray JC,
Musk AW,
Nieminen MS,
Njølstad I,
Ohlsson C,
Oldehinkel AJ,
Oostra BA,
Palmer LJ,
Pankow JS,
Pasterkamp G,
Pedersen NL,
Pedersen O,
Penninx BW,
Perola M,
Peters A,
Polašek O,
Pramstaller PP,
Psaty BM,
Qi L,
Quertermous T,
Raitakari OT,
Rankinen T,
Rauramaa R,
Ridker PM,
Rioux JD,
Rivadeneira F,
Rotter JI,
Rudan I,
den Ruijter HM,
Saltevo J,
Sattar N,
Schunkert H,
Schwarz PE,
Shuldiner AR,
Sinisalo J,
Snieder H,
Sørensen TI,
Spector TD,
Staessen JA,
Stefania B,
Thorsteinsdottir U,
Stumvoll M,
Tardif JC,
Tremoli E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
Verbeek AL,
Vermeulen SH,
Viikari JS,
Vitart V,
Völzke H,
Vollenweider P,
Waeber G,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Zeggini E,
Chakravarti A,
Clegg DJ,
Cupples LA,
Gordon-Larsen P,
Jaquish CE,
Rao DC,
Abecasis GR,
Assimes TL,
Barroso I,
Berndt SI,
Boehnke M,
Deloukas P,
Fox CS,
Groop LC,
Hunter DJ,
Ingelsson E,
Kaplan RC,
McCarthy MI,
Mohlke KL,
O'Connell JR,
Schlessinger D,
Strachan DP,
Stefansson K,
van Duijn CM,
Hirschhorn JN,
Lindgren CM,
Heid IM,
North KE,
Borecki IB,
Kutalik Z,
Loos RJ
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
and 157 more — show all
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
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Granström AL,
Wester T,
Salo P,
Virtanen V,
Carstensen L
and 8 more — show all
European journal of human genetics : EJHG · 2018 · PMID 29379196
3 pages
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.