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9 matches for
Streeten E.
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+
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Elks CE,
Perry JR,
Sulem P,
Chasman DI,
Franceschini N,
He C,
Lunetta KL,
Visser JA,
Byrne EM,
Cousminer DL,
Gudbjartsson DF,
Esko T
and 162 more — show all
Feenstra B,
Hottenga JJ,
Koller DL,
Kutalik Z,
Lin P,
Mangino M,
Marongiu M,
McArdle PF,
Smith AV,
Stolk L,
van Wingerden SH,
Zhao JH,
Albrecht E,
Corre T,
Ingelsson E,
Hayward C,
Magnusson PK,
Smith EN,
Ulivi S,
Warrington NM,
Zgaga L,
Alavere H,
Amin N,
Aspelund T,
Bandinelli S,
Barroso I,
Berenson GS,
Bergmann S,
Blackburn H,
Boerwinkle E,
Buring JE,
Busonero F,
Campbell H,
Chanock SJ,
Chen W,
Cornelis MC,
Couper D,
Coviello AD,
d'Adamo P,
de Faire U,
de Geus EJ,
Deloukas P,
Döring A,
Smith GD,
Easton DF,
Eiriksdottir G,
Emilsson V,
Eriksson J,
Ferrucci L,
Folsom AR,
Foroud T,
Garcia M,
Gasparini P,
Geller F,
Gieger C,
Gudnason V,
Hall P,
Hankinson SE,
Ferreli L,
Heath AC,
Hernandez DG,
Hofman A,
Hu FB,
Illig T,
Järvelin MR,
Johnson AD,
Karasik D,
Khaw KT,
Kiel DP,
Kilpeläinen TO,
Kolcic I,
Kraft P,
Launer LJ,
Laven JS,
Li S,
Liu J,
Levy D,
Martin NG,
McArdle WL,
Melbye M,
Mooser V,
Murray JC,
Murray SS,
Nalls MA,
Navarro P,
Nelis M,
Ness AR,
Northstone K,
Oostra BA,
Peacock M,
Palmer LJ,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peltonen L,
Pennell CE,
Pharoah P,
Polasek O,
Plump AS,
Pouta A,
Porcu E,
Rafnar T,
Rice JP,
Ring SM,
Rivadeneira F,
Rudan I,
Sala C,
Salomaa V,
Sanna S,
Schlessinger D,
Schork NJ,
Scuteri A,
Segrè AV,
Shuldiner AR,
Soranzo N,
Sovio U,
Srinivasan SR,
Strachan DP,
Tammesoo ML,
Tikkanen E,
Toniolo D,
Tsui K,
Tryggvadottir L,
Tyrer J,
Uda M,
van Dam RM,
van Meurs JB,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Weedon MN,
Wichmann HE,
Willemsen G,
Wilson JF,
Wright AF,
Young L,
Zhai G,
Zhuang WV,
Bierut LJ,
Boomsma DI,
Boyd HA,
Crisponi L,
Demerath EW,
van Duijn CM,
Econs MJ,
Harris TB,
Hunter DJ,
Loos RJ,
Metspalu A,
Montgomery GW,
Ridker PM,
Spector TD,
Streeten EA,
Stefansson K,
Thorsteinsdottir U,
Uitterlinden AG,
Widen E,
Murabito JM,
Ong KK,
Murray A
GIANT Consortium
Nature genetics · 2010 · PMID 21102462
11 pages
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
Stolk L,
Perry JR,
Chasman DI,
He C,
Mangino M,
Sulem P,
Barbalic M,
Broer L,
Byrne EM,
Ernst F,
Esko T,
Franceschini N
and 167 more — show all
Gudbjartsson DF,
Hottenga JJ,
Kraft P,
McArdle PF,
Porcu E,
Shin SY,
Smith AV,
van Wingerden S,
Zhai G,
Zhuang WV,
Albrecht E,
Alizadeh BZ,
Aspelund T,
Bandinelli S,
Lauc LB,
Beckmann JS,
Boban M,
Boerwinkle E,
Broekmans FJ,
Burri A,
Campbell H,
Chanock SJ,
Chen C,
Cornelis MC,
Corre T,
Coviello AD,
d'Adamo P,
Davies G,
de Faire U,
de Geus EJ,
Deary IJ,
Dedoussis GV,
Deloukas P,
Ebrahim S,
Eiriksdottir G,
Emilsson V,
Eriksson JG,
Fauser BC,
Ferreli L,
Ferrucci L,
Fischer K,
Folsom AR,
Garcia ME,
Gasparini P,
Gieger C,
Glazer N,
Grobbee DE,
Hall P,
Haller T,
Hankinson SE,
Hass M,
Hayward C,
Heath AC,
Hofman A,
Ingelsson E,
Janssens AC,
Johnson AD,
Karasik D,
Kardia SL,
Keyzer J,
Kiel DP,
Kolcic I,
Kutalik Z,
Lahti J,
Lai S,
Laisk T,
Laven JS,
Lawlor DA,
Liu J,
Lopez LM,
Louwers YV,
Magnusson PK,
Marongiu M,
Martin NG,
Klaric IM,
Masciullo C,
McKnight B,
Medland SE,
Melzer D,
Mooser V,
Navarro P,
Newman AB,
Nyholt DR,
Onland-Moret NC,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peeters PH,
Pistis G,
Plump AS,
Polasek O,
Pop VJ,
Psaty BM,
Räikkönen K,
Rehnberg E,
Rotter JI,
Rudan I,
Sala C,
Salumets A,
Scuteri A,
Singleton A,
Smith JA,
Snieder H,
Soranzo N,
Stacey SN,
Starr JM,
Stathopoulou MG,
Stirrups K,
Stolk RP,
Styrkarsdottir U,
Sun YV,
Tenesa A,
Thorand B,
Toniolo D,
Tryggvadottir L,
Tsui K,
Ulivi S,
van Dam RM,
van der Schouw YT,
van Gils CH,
van Nierop P,
Vink JM,
Visscher PM,
Voorhuis M,
Waeber G,
Wallaschofski H,
Wichmann HE,
Widen E,
Wijnands-van Gent CJ,
Willemsen G,
Wilson JF,
Wolffenbuttel BH,
Wright AF,
Yerges-Armstrong LM,
Zemunik T,
Zgaga L,
Zillikens MC,
Zygmunt M,
Arnold AM,
Boomsma DI,
Buring JE,
Crisponi L,
Demerath EW,
Gudnason V,
Harris TB,
Hu FB,
Hunter DJ,
Launer LJ,
Metspalu A,
Montgomery GW,
Oostra BA,
Ridker PM,
Sanna S,
Schlessinger D,
Spector TD,
Stefansson K,
Streeten EA,
Thorsteinsdottir U,
Uda M,
Uitterlinden AG,
van Duijn CM,
Völzke H,
Murray A,
Murabito JM,
Visser JA,
Lunetta KL
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Estrada K,
Styrkarsdottir U,
Evangelou E,
Hsu YH,
Duncan EL,
Ntzani EE,
Oei L,
Albagha OM,
Amin N,
Kemp JP,
Koller DL,
Li G
and 170 more — show all
Liu CT,
Minster RL,
Moayyeri A,
Vandenput L,
Willner D,
Xiao SM,
Yerges-Armstrong LM,
Zheng HF,
Alonso N,
Eriksson J,
Kammerer CM,
Kaptoge SK,
Leo PJ,
Thorleifsson G,
Wilson SG,
Wilson JF,
Aalto V,
Alen M,
Aragaki AK,
Aspelund T,
Center JR,
Dailiana Z,
Duggan DJ,
Garcia M,
Garcia-Giralt N,
Giroux S,
Hallmans G,
Hocking LJ,
Husted LB,
Jameson KA,
Khusainova R,
Kim GS,
Kooperberg C,
Koromila T,
Kruk M,
Laaksonen M,
Lacroix AZ,
Lee SH,
Leung PC,
Lewis JR,
Masi L,
Mencej-Bedrac S,
Nguyen TV,
Nogues X,
Nogues X,
Patel MS,
Prezelj J,
Rose LM,
Scollen S,
Siggeirsdottir K,
Smith AV,
Svensson O,
Trompet S,
Trummer O,
van Schoor NM,
Woo J,
Zhu K,
Balcells S,
Brandi ML,
Buckley BM,
Cheng S,
Christiansen C,
Cooper C,
Dedoussis G,
Ford I,
Frost M,
Goltzman D,
González-Macías J,
Kähönen M,
Karlsson M,
Khusnutdinova E,
Koh JM,
Kollia P,
Langdahl BL,
Leslie WD,
Lips P,
Ljunggren Ö,
Lorenc RS,
Marc J,
Mellström D,
Obermayer-Pietsch B,
Olmos JM,
Pettersson-Kymmer U,
Reid DM,
Riancho JA,
Ridker PM,
Rousseau F,
Slagboom PE,
Tang NL,
Urreizti R,
Van Hul W,
Viikari J,
Zarrabeitia MT,
Aulchenko YS,
Castano-Betancourt M,
Grundberg E,
Herrera L,
Ingvarsson T,
Johannsdottir H,
Kwan T,
Li R,
Luben R,
Medina-Gómez C,
Palsson ST,
Reppe S,
Rotter JI,
Sigurdsson G,
van Meurs JB,
Verlaan D,
Williams FM,
Wood AR,
Zhou Y,
Gautvik KM,
Pastinen T,
Raychaudhuri S,
Cauley JA,
Chasman DI,
Clark GR,
Cummings SR,
Danoy P,
Dennison EM,
Eastell R,
Eisman JA,
Gudnason V,
Hofman A,
Jackson RD,
Jones G,
Jukema JW,
Khaw KT,
Lehtimäki T,
Liu Y,
Lorentzon M,
McCloskey E,
Mitchell BD,
Nandakumar K,
Nicholson GC,
Oostra BA,
Peacock M,
Pols HA,
Prince RL,
Raitakari O,
Reid IR,
Robbins J,
Sambrook PN,
Sham PC,
Shuldiner AR,
Tylavsky FA,
van Duijn CM,
Wareham NJ,
Cupples LA,
Econs MJ,
Evans DM,
Harris TB,
Kung AW,
Psaty BM,
Reeve J,
Spector TD,
Streeten EA,
Zillikens MC,
Thorsteinsdottir U,
Ohlsson C,
Karasik D,
Richards JB,
Brown MA,
Stefansson K,
Uitterlinden AG,
Ralston SH,
Ioannidis JP,
Kiel DP,
Rivadeneira F
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Barban N,
Jansen R,
de Vlaming R,
Vaez A,
Mandemakers JJ,
Tropf FC,
Shen X,
Wilson JF,
Chasman DI,
Nolte IM,
Tragante V,
van der Laan SW
and 241 more — show all
Perry JR,
Kong A,
Ahluwalia TS,
Albrecht E,
Yerges-Armstrong L,
Atzmon G,
Auro K,
Ayers K,
Bakshi A,
Ben-Avraham D,
Berger K,
Bergman A,
Bertram L,
Bielak LF,
Bjornsdottir G,
Bonder MJ,
Broer L,
Bui M,
Barbieri C,
Cavadino A,
Chavarro JE,
Turman C,
Concas MP,
Cordell HJ,
Davies G,
Eibich P,
Eriksson N,
Esko T,
Eriksson J,
Falahi F,
Felix JF,
Fontana MA,
Franke L,
Gandin I,
Gaskins AJ,
Gieger C,
Gunderson EP,
Guo X,
Hayward C,
He C,
Hofer E,
Huang H,
Joshi PK,
Kanoni S,
Karlsson R,
Kiechl S,
Kifley A,
Kluttig A,
Kraft P,
Lagou V,
Lecoeur C,
Lahti J,
Li-Gao R,
Lind PA,
Liu T,
Makalic E,
Mamasoula C,
Matteson L,
Mbarek H,
McArdle PF,
McMahon G,
Meddens SF,
Mihailov E,
Miller M,
Missmer SA,
Monnereau C,
van der Most PJ,
Myhre R,
Nalls MA,
Nutile T,
Kalafati IP,
Porcu E,
Prokopenko I,
Rajan KB,
Rich-Edwards J,
Rietveld CA,
Robino A,
Rose LM,
Rueedi R,
Ryan KA,
Saba Y,
Schmidt D,
Smith JA,
Stolk L,
Streeten E,
Tönjes A,
Thorleifsson G,
Ulivi S,
Wedenoja J,
Wellmann J,
Willeit P,
Yao J,
Yengo L,
Zhao JH,
Zhao W,
Zhernakova DV,
Amin N,
Andrews H,
Balkau B,
Barzilai N,
Bergmann S,
Biino G,
Bisgaard H,
Bønnelykke K,
Boomsma DI,
Buring JE,
Campbell H,
Cappellani S,
Ciullo M,
Cox SR,
Cucca F,
Toniolo D,
Davey-Smith G,
Deary IJ,
Dedoussis G,
Deloukas P,
van Duijn CM,
de Geus EJ,
Eriksson JG,
Evans DA,
Faul JD,
Sala CF,
Froguel P,
Gasparini P,
Girotto G,
Grabe HJ,
Greiser KH,
Groenen PJ,
de Haan HG,
Haerting J,
Harris TB,
Heath AC,
Heikkilä K,
Hofman A,
Homuth G,
Holliday EG,
Hopper J,
Hyppönen E,
Jacobsson B,
Jaddoe VW,
Johannesson M,
Jugessur A,
Kähönen M,
Kajantie E,
Kardia SL,
Keavney B,
Kolcic I,
Koponen P,
Kovacs P,
Kronenberg F,
Kutalik Z,
La Bianca M,
Lachance G,
Iacono WG,
Lai S,
Lehtimäki T,
Liewald DC,
Lindgren CM,
Liu Y,
Luben R,
Lucht M,
Luoto R,
Magnus P,
Magnusson PK,
Martin NG,
McGue M,
McQuillan R,
Medland SE,
Meisinger C,
Mellström D,
Metspalu A,
Traglia M,
Milani L,
Mitchell P,
Montgomery GW,
Mook-Kanamori D,
de Mutsert R,
Nohr EA,
Ohlsson C,
Olsen J,
Ong KK,
Paternoster L,
Pattie A,
Penninx BW,
Perola M,
Peyser PA,
Pirastu M,
Polasek O,
Power C,
Kaprio J,
Raffel LJ,
Räikkönen K,
Raitakari O,
Ridker PM,
Ring SM,
Roll K,
Rudan I,
Ruggiero D,
Rujescu D,
Salomaa V,
Schlessinger D,
Schmidt H,
Schmidt R,
Schupf N,
Smit J,
Sorice R,
Spector TD,
Starr JM,
Stöckl D,
Strauch K,
Stumvoll M,
Swertz MA,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tung JY,
Uitterlinden AG,
Vaccargiu S,
Viikari J,
Vitart V,
Völzke H,
Vollenweider P,
Vuckovic D,
Waage J,
Wagner GG,
Wang JJ,
Wareham NJ,
Weir DR,
Willemsen G,
Willeit J,
Wright AF,
Zondervan KT,
Stefansson K,
Krueger RF,
Lee JJ,
Benjamin DJ,
Cesarini D,
Koellinger PD,
den Hoed M,
Snieder H,
Mills MC
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Wang TJ,
Zhang F,
Richards JB,
Kestenbaum B,
van Meurs JB,
Berry D,
Kiel DP,
Streeten EA,
Ohlsson C,
Koller DL,
Peltonen L,
Cooper JD
and 64 more — show all
O'Reilly PF,
Houston DK,
Glazer NL,
Vandenput L,
Peacock M,
Shi J,
Rivadeneira F,
McCarthy MI,
Anneli P,
de Boer IH,
Mangino M,
Kato B,
Smyth DJ,
Booth SL,
Jacques PF,
Burke GL,
Goodarzi M,
Cheung CL,
Wolf M,
Rice K,
Goltzman D,
Hidiroglou N,
Ladouceur M,
Wareham NJ,
Hocking LJ,
Hart D,
Arden NK,
Cooper C,
Malik S,
Fraser WD,
Hartikainen AL,
Zhai G,
Macdonald HM,
Forouhi NG,
Loos RJ,
Reid DM,
Hakim A,
Dennison E,
Liu Y,
Power C,
Stevens HE,
Jaana L,
Vasan RS,
Soranzo N,
Bojunga J,
Psaty BM,
Lorentzon M,
Foroud T,
Harris TB,
Hofman A,
Jansson JO,
Cauley JA,
Uitterlinden AG,
Gibson Q,
Järvelin MR,
Karasik D,
Siscovick DS,
Econs MJ,
Kritchevsky SB,
Florez JC,
Todd JA,
Dupuis J,
Hyppönen E,
Spector TD
Lancet (London, England) · 2010 · PMID 20541252
3 pages
Genetic Variants Associated with Circulating Parathyroid Hormone
Robinson-Cohen C,
Lutsey PL,
Kleber ME,
Nielson CM,
Mitchell BD,
Bis JC,
Eny KM,
Portas L,
Eriksson J,
Lorentzon M,
Koller DL,
Milaneschi Y
and 37 more — show all
Teumer A,
Pilz S,
Nethander M,
Selvin E,
Tang W,
Weng LC,
Wong HS,
Lai D,
Peacock M,
Hannemann A,
Völker U,
Homuth G,
Nauk M,
Murgia F,
Pattee JW,
Orwoll E,
Zmuda JM,
Riancho JA,
Wolf M,
Williams F,
Penninx B,
Econs MJ,
Ryan KA,
Ohlsson C,
Paterson AD,
Psaty BM,
Siscovick DS,
Rotter JI,
Pirastu M,
Streeten E,
März W,
Fox C,
Coresh J,
Wallaschofski H,
Pankow JS,
de Boer IH,
Kestenbaum B
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
3 pages
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
Jiang X,
O'Reilly PF,
Aschard H,
Aschard H,
Hsu YH,
Richards JB,
Dupuis J,
Ingelsson E,
Karasik D,
Pilz S,
Berry D,
Kestenbaum B
and 93 more — show all
Zheng J,
Luan J,
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Zhou A,
Power C,
McCarthy MI,
Michos ED,
Boerwinkle E,
Weinstein SJ,
Freedman ND,
Huang WY,
Van Schoor NM,
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Liu CT,
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Nature communications · 2018 · PMID 29343764 · open access
2 pages
Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm
Zheng HF,
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Goltzman D,
Blangero J,
Hanley DA,
Carless MA,
Streeten EA
and 7 more — show all
Journal of medical genetics · 2013 · PMID 23572186
1 page
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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
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My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
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My paper is not here. Does that mean you rejected it?
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