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33 matches for
Pers TH,
showing the first 13.
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
Felix JF,
Bradfield JP,
Monnereau C,
van der Valk RJ,
Stergiakouli E,
Chesi A,
Gaillard R,
Feenstra B,
Thiering E,
Kreiner-Møller E,
Mahajan A,
Pitkänen N
and 99 more — show all
Joro R,
Cavadino A,
Huikari V,
Franks S,
Groen-Blokhuis MM,
Cousminer DL,
Marsh JA,
Lehtimäki T,
Curtin JA,
Vioque J,
Ahluwalia TS,
Myhre R,
Price TS,
Vilor-Tejedor N,
Yengo L,
Grarup N,
Ntalla I,
Ang W,
Atalay M,
Bisgaard H,
Blakemore AI,
Bonnefond A,
Carstensen L,
Eriksson J,
Flexeder C,
Franke L,
Geller F,
Geserick M,
Hartikainen AL,
Haworth CM,
Hirschhorn JN,
Hofman A,
Holm JC,
Horikoshi M,
Hottenga JJ,
Huang J,
Kadarmideen HN,
Kähönen M,
Kiess W,
Lakka HM,
Lakka TA,
Lewin AM,
Liang L,
Lyytikäinen LP,
Ma B,
Magnus P,
McCormack SE,
McMahon G,
Mentch FD,
Middeldorp CM,
Murray CS,
Pahkala K,
Pers TH,
Pfäffle R,
Postma DS,
Power C,
Simpson A,
Sengpiel V,
Tiesler CM,
Torrent M,
Uitterlinden AG,
van Meurs JB,
Vinding R,
Waage J,
Wardle J,
Zeggini E,
Zemel BS,
Dedoussis GV,
Pedersen O,
Froguel P,
Sunyer J,
Plomin R,
Jacobsson B,
Hansen T,
Gonzalez JR,
Custovic A,
Raitakari OT,
Pennell CE,
Widén E,
Boomsma DI,
Koppelman GH,
Sebert S,
Järvelin MR,
Hyppönen E,
McCarthy MI,
Lindi V,
Harri N,
Körner A,
Bønnelykke K,
Heinrich J,
Melbye M,
Rivadeneira F,
Hakonarson H,
Ring SM,
Smith GD,
Sørensen TI,
Timpson NJ,
Grant SF,
Jaddoe VW
Bone Mineral Density in Childhood Study (BMDCS) · Early Genetics and Lifecourse Epidemiology (EAGLE) consortium and 2 more consortia
Human molecular genetics · 2016 · PMID 26604143
8 pages
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization
Bønnelykke K,
Matheson MC,
Pers TH,
Granell R,
Strachan DP,
Alves AC,
Linneberg A,
Curtin JA,
Warrington NM,
Standl M,
Kerkhof M,
Jonsdottir I
and 58 more — show all
Bukvic BK,
Kaakinen M,
Sleimann P,
Thorleifsson G,
Thorsteinsdottir U,
Schramm K,
Baltic S,
Kreiner-Møller E,
Simpson A,
St Pourcain B,
Coin L,
Hui J,
Walters EH,
Tiesler CMT,
Duffy DL,
Jones G,
Ring SM,
McArdle WL,
Price L,
Robertson CF,
Pekkanen J,
Pekkanen J,
Tang CS,
Thiering E,
Montgomery GW,
Hartikainen AL,
Dharmage SC,
Husemoen LL,
Herder C,
Kemp JP,
Elliot P,
James A,
Waldenberger M,
Abramson MJ,
Fairfax BP,
Knight JC,
Knight JC,
Gupta R,
Thompson PJ,
Holt P,
Sly P,
Hirschhorn JN,
Blekic M,
Weidinger S,
Hakonarsson H,
Stefansson K,
Heinrich J,
Postma DS,
Custovic A,
Pennell CE,
Pennell CE,
Jarvelin MR,
Koppelman GH,
Timpson N,
Ferreira MA,
Ferreira MA,
Bisgaard H,
Henderson AJ
AAGC
Nature genetics · 2013 · PMID 23817571
7 pages
Genome-wide association study identifies 30 loci associated with bipolar disorder
Stahl EA,
Breen G,
Forstner AJ,
McQuillin A,
Ripke S,
Trubetskoy V,
Mattheisen M,
Wang Y,
Coleman JRI,
Gaspar HA,
de Leeuw CA,
Steinberg S
and 265 more — show all
Pavlides JMW,
Trzaskowski M,
Byrne EM,
Pers TH,
Holmans PA,
Richards AL,
Abbott L,
Agerbo E,
Akil H,
Albani D,
Alliey-Rodriguez N,
Als TD,
Anjorin A,
Antilla V,
Awasthi S,
Badner JA,
Bækvad-Hansen M,
Barchas JD,
Bass N,
Bauer M,
Belliveau R,
Bergen SE,
Pedersen CB,
Bøen E,
Boks MP,
Boocock J,
Budde M,
Bunney W,
Burmeister M,
Bybjerg-Grauholm J,
Byerley W,
Casas M,
Cerrato F,
Cervantes P,
Chambert K,
Charney AW,
Chen D,
Churchhouse C,
Clarke TK,
Coryell W,
Craig DW,
Cruceanu C,
Curtis D,
Czerski PM,
Dale AM,
de Jong S,
Degenhardt F,
Del-Favero J,
DePaulo JR,
Djurovic S,
Dobbyn AL,
Dumont A,
Elvsåshagen T,
Escott-Price V,
Fan CC,
Fischer SB,
Flickinger M,
Foroud TM,
Forty L,
Frank J,
Fraser C,
Freimer NB,
Frisén L,
Gade K,
Gage D,
Garnham J,
Giambartolomei C,
Pedersen MG,
Goldstein J,
Gordon SD,
Gordon-Smith K,
Green EK,
Green MJ,
Greenwood TA,
Grove J,
Guan W,
Guzman-Parra J,
Hamshere ML,
Hautzinger M,
Heilbronner U,
Herms S,
Hipolito M,
Hoffmann P,
Holland D,
Huckins L,
Jamain S,
Johnson JS,
Juréus A,
Kandaswamy R,
Karlsson R,
Kennedy JL,
Kittel-Schneider S,
Knowles JA,
Kogevinas M,
Koller AC,
Kupka R,
Lavebratt C,
Lawrence J,
Lawson WB,
Leber M,
Lee PH,
Levy SE,
Li JZ,
Liu C,
Lucae S,
Maaser A,
MacIntyre DJ,
Mahon PB,
Maier W,
Martinsson L,
McCarroll S,
McGuffin P,
McInnis MG,
McKay JD,
Medeiros H,
Medland SE,
Meng F,
Milani L,
Montgomery GW,
Morris DW,
Mühleisen TW,
Mullins N,
Nguyen H,
Nievergelt CM,
Adolfsson AN,
Nwulia EA,
O'Donovan C,
Loohuis LMO,
Ori APS,
Oruc L,
Ösby U,
Perlis RH,
Perry A,
Pfennig A,
Potash JB,
Purcell SM,
Regeer EJ,
Reif A,
Reinbold CS,
Rice JP,
Rivas F,
Rivera M,
Roussos P,
Ruderfer DM,
Ryu E,
Sánchez-Mora C,
Schatzberg AF,
Scheftner WA,
Schork NJ,
Shannon Weickert C,
Shehktman T,
Shilling PD,
Sigurdsson E,
Slaney C,
Smeland OB,
Sobell JL,
Søholm Hansen C,
Spijker AT,
St Clair D,
Steffens M,
Strauss JS,
Streit F,
Strohmaier J,
Szelinger S,
Thompson RC,
Thorgeirsson TE,
Treutlein J,
Vedder H,
Wang W,
Watson SJ,
Weickert TW,
Witt SH,
Xi S,
Xu W,
Young AH,
Zandi P,
Zhang P,
Zöllner S,
Adolfsson R,
Agartz I,
Alda M,
Backlund L,
Baune BT,
Bellivier F,
Berrettini WH,
Biernacka JM,
Blackwood DHR,
Boehnke M,
Børglum AD,
Corvin A,
Craddock N,
Daly MJ,
Dannlowski U,
Esko T,
Etain B,
Frye M,
Fullerton JM,
Gershon ES,
Gill M,
Goes F,
Grigoroiu-Serbanescu M,
Hauser J,
Hougaard DM,
Hultman CM,
Jones I,
Jones LA,
Kahn RS,
Kirov G,
Landén M,
Leboyer M,
Lewis CM,
Li QS,
Lissowska J,
Martin NG,
Mayoral F,
McElroy SL,
McIntosh AM,
McMahon FJ,
Melle I,
Metspalu A,
Mitchell PB,
Morken G,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Myers RM,
Neale BM,
Nimgaonkar V,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Oedegaard KJ,
Owen MJ,
Paciga SA,
Pato C,
Pato MT,
Posthuma D,
Ramos-Quiroga JA,
Ribasés M,
Rietschel M,
Rouleau GA,
Schalling M,
Schofield PR,
Schulze TG,
Serretti A,
Smoller JW,
Stefansson H,
Stefansson K,
Stordal E,
Sullivan PF,
Turecki G,
Vaaler AE,
Vieta E,
Vincent JB,
Werge T,
Nurnberger JI,
Wray NR,
Di Florio A,
Edenberg HJ,
Cichon S,
Ophoff RA,
Scott LJ,
Andreassen OA,
Kelsoe J,
Sklar P
eQTLGen Consortium · BIOS Consortium and 1 more consortia
Nature genetics · 2019 · PMID 31043756 · open access
6 pages
Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function
Wild PS,
Felix JF,
Schillert A,
Teumer A,
Chen MH,
Leening MJG,
Völker U,
Großmann V,
Brody JA,
Irvin MR,
Shah SJ,
Pramana S
and 112 more — show all
Lieb W,
Schmidt R,
Stanton AV,
Malzahn D,
Smith AV,
Sundström J,
Minelli C,
Ruggiero D,
Lyytikäinen LP,
Tiller D,
Smith JG,
Monnereau C,
Di Tullio MR,
Musani SK,
Morrison AC,
Pers TH,
Morley M,
Kleber ME,
Aragam J,
Benjamin EJ,
Bis JC,
Bisping E,
Broeckel U,
Cheng S,
Deckers JW,
Del Greco M F,
Edelmann F,
Fornage M,
Franke L,
Friedrich N,
Harris TB,
Hofer E,
Hofman A,
Huang J,
Hughes AD,
Kähönen M,
Investigators K,
Kruppa J,
Lackner KJ,
Lannfelt L,
Laskowski R,
Launer LJ,
Leosdottir M,
Lin H,
Lindgren CM,
Loley C,
MacRae CA,
Mascalzoni D,
Mayet J,
Medenwald D,
Morris AP,
Müller C,
Müller-Nurasyid M,
Nappo S,
Nilsson PM,
Nuding S,
Nutile T,
Peters A,
Pfeufer A,
Pietzner D,
Pramstaller PP,
Raitakari OT,
Rice KM,
Rivadeneira F,
Rotter JI,
Ruohonen ST,
Sacco RL,
Samdarshi TE,
Schmidt H,
Sharp ASP,
Shields DC,
Sorice R,
Sotoodehnia N,
Stricker BH,
Surendran P,
Thom S,
Töglhofer AM,
Uitterlinden AG,
Wachter R,
Völzke H,
Ziegler A,
Münzel T,
März W,
Cappola TP,
Hirschhorn JN,
Mitchell GF,
Smith NL,
Fox ER,
Dueker ND,
Jaddoe VWV,
Melander O,
Russ M,
Lehtimäki T,
Ciullo M,
Hicks AA,
Lind L,
Gudnason V,
Pieske B,
Barron AJ,
Zweiker R,
Schunkert H,
Ingelsson E,
Liu K,
Arnett DK,
Psaty BM,
Blankenberg S,
Larson MG,
Felix SB,
Franco OH,
Zeller T,
Vasan RS,
Dörr M
The Journal of clinical investigation · 2017 · PMID 28394258
5 pages
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
Skotte L,
Fadista J,
Bybjerg-Grauholm J,
Appadurai V,
Hildebrand MS,
Hansen TF,
Banasik K,
Grove J,
Albiñana C,
Geller F,
Bjurström CF,
Vilhjálmsson BJ
and 27 more — show all
Coleman M,
Damiano JA,
Burgess R,
Scheffer IE,
Pedersen OBV,
Erikstrup C,
Westergaard D,
Nielsen KR,
Sørensen E,
Bruun MT,
Liu X,
Hjalgrim H,
Pers TH,
Mortensen PB,
Mors O,
Nordentoft M,
Dreier JW,
Børglum AD,
Christensen J,
Hougaard DM,
Buil A,
Hviid A,
Melbye M,
Ullum H,
Berkovic SF,
Werge T,
Feenstra B
Brain : a journal of neurology · 2022 · PMID 35022648 · open access
5 pages
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
Rietveld CA,
Esko T,
Davies G,
Pers TH,
Turley P,
Benyamin B,
Chabris CF,
Emilsson V,
Johnson AD,
Lee JJ,
de Leeuw C,
Marioni RE
and 48 more — show all
Medland SE,
Miller MB,
Rostapshova O,
van der Lee SJ,
Vinkhuyzen AA,
Amin N,
Conley D,
Derringer J,
van Duijn CM,
Fehrmann R,
Franke L,
Glaeser EL,
Hansell NK,
Hayward C,
Iacono WG,
Ibrahim-Verbaas C,
Jaddoe V,
Karjalainen J,
Laibson D,
Lichtenstein P,
Liewald DC,
Magnusson PK,
Martin NG,
McGue M,
McMahon G,
Pedersen NL,
Pinker S,
Porteous DJ,
Posthuma D,
Rivadeneira F,
Smith BH,
Smith BH,
Starr JM,
Tiemeier H,
Timpson NJ,
Trzaskowski M,
Uitterlinden AG,
Verhulst FC,
Ward ME,
Wright MJ,
Davey Smith G,
Deary IJ,
Johannesson M,
Plomin R,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
Proceedings of the National Academy of Sciences of the United States of America · 2014 · PMID 25201988
4 pages
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes
Bonàs-Guarch S,
Guindo-Martínez M,
Miguel-Escalada I,
Grarup N,
Sebastian D,
Rodriguez-Fos E,
Sánchez F,
Planas-Fèlix M,
Cortes-Sánchez P,
González S,
Timshel P,
Pers TH
and 31 more — show all
Morgan CC,
Moran I,
Atla G,
González JR,
Puiggros M,
Martí J,
Andersson EA,
Díaz C,
Badia RM,
Udler M,
Leong A,
Kaur V,
Flannick J,
Jørgensen T,
Linneberg A,
Jørgensen ME,
Witte DR,
Christensen C,
Brandslund I,
Appel EV,
Scott RA,
Luan J,
Langenberg C,
Wareham NJ,
Pedersen O,
Zorzano A,
Florez JC,
Hansen T,
Ferrer J,
Mercader JM,
Torrents D
Nature communications · 2018 · PMID 29358691 · open access
4 pages
Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits
Merino J,
Dashti HS,
Sarnowski C,
Lane JM,
Todorov PV,
Udler MS,
Song Y,
Wang H,
Kim J,
Tucker C,
Campbell J,
Tanaka T
and 8 more — show all
Nature human behaviour · 2022 · PMID 34426670
4 pages
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu Y,
Day FR,
Gustafsson S,
Buchkovich ML,
Na J,
Bataille V,
Cousminer DL,
Dastani Z,
Drong AW,
Esko T,
Evans DM,
Falchi M
and 247 more — show all
Feitosa MF,
Ferreira T,
Hedman ÅK,
Haring R,
Hysi PG,
Iles MM,
Justice AE,
Kanoni S,
Lagou V,
Li R,
Li X,
Locke A,
Lu C,
Mägi R,
Perry JR,
Pers TH,
Qi Q,
Sanna M,
Schmidt EM,
Scott WR,
Shungin D,
Teumer A,
Vinkhuyzen AA,
Walker RW,
Westra HJ,
Zhang M,
Zhang W,
Zhao JH,
Zhu Z,
Afzal U,
Ahluwalia TS,
Bakker SJ,
Bellis C,
Bonnefond A,
Borodulin K,
Buchman AS,
Cederholm T,
Choh AC,
Choi HJ,
Curran JE,
de Groot LC,
De Jager PL,
Dhonukshe-Rutten RA,
Enneman AW,
Eury E,
Evans DS,
Forsen T,
Friedrich N,
Fumeron F,
Garcia ME,
Gärtner S,
Han BG,
Havulinna AS,
Hayward C,
Hernandez D,
Hillege H,
Ittermann T,
Kent JW,
Kolcic I,
Laatikainen T,
Lahti J,
Mateo Leach I,
Lee CG,
Lee JY,
Liu T,
Liu Y,
Lobbens S,
Loh M,
Lyytikäinen LP,
Medina-Gomez C,
Michaëlsson K,
Nalls MA,
Nielson CM,
Oozageer L,
Pascoe L,
Paternoster L,
Polašek O,
Ripatti S,
Sarzynski MA,
Shin CS,
Narančić NS,
Spira D,
Srikanth P,
Steinhagen-Thiessen E,
Sung YJ,
Swart KM,
Taittonen L,
Tanaka T,
Tikkanen E,
van der Velde N,
van Schoor NM,
Verweij N,
Wright AF,
Yu L,
Zmuda JM,
Eklund N,
Forrester T,
Grarup N,
Jackson AU,
Kristiansson K,
Kuulasmaa T,
Kuusisto J,
Lichtner P,
Luan J,
Mahajan A,
Männistö S,
Palmer CD,
Ried JS,
Scott RA,
Stancáková A,
Wagner PJ,
Demirkan A,
Döring A,
Gudnason V,
Kiel DP,
Kühnel B,
Mangino M,
Mcknight B,
Menni C,
O'Connell JR,
Oostra BA,
Shuldiner AR,
Song K,
Vandenput L,
van Duijn CM,
Vollenweider P,
White CC,
Boehnke M,
Boettcher Y,
Cooper RS,
Forouhi NG,
Gieger C,
Grallert H,
Hingorani A,
Jørgensen T,
Jousilahti P,
Kivimaki M,
Kumari M,
Laakso M,
Langenberg C,
Linneberg A,
Luke A,
Mckenzie CA,
Palotie A,
Pedersen O,
Peters A,
Strauch K,
Tayo BO,
Wareham NJ,
Bennett DA,
Bertram L,
Blangero J,
Blüher M,
Bouchard C,
Campbell H,
Cho NH,
Cummings SR,
Czerwinski SA,
Demuth I,
Eckardt R,
Eriksson JG,
Ferrucci L,
Franco OH,
Froguel P,
Gansevoort RT,
Hansen T,
Harris TB,
Hastie N,
Heliövaara M,
Hofman A,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Knekt PB,
Koskinen S,
Kovacs P,
Lehtimäki T,
Lind L,
Liu Y,
Orwoll ES,
Osmond C,
Perola M,
Pérusse L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Rivadeneira F,
Rudan I,
Salomaa V,
Sørensen TI,
Stumvoll M,
Tönjes A,
Towne B,
Tranah GJ,
Tremblay A,
Uitterlinden AG,
van der Harst P,
Vartiainen E,
Viikari JS,
Vitart V,
Vohl MC,
Völzke H,
Walker M,
Wallaschofski H,
Wild S,
Wilson JF,
Yengo L,
Bishop DT,
Borecki IB,
Chambers JC,
Cupples LA,
Dehghan A,
Deloukas P,
Fatemifar G,
Fox C,
Furey TS,
Franke L,
Han J,
Hunter DJ,
Karjalainen J,
Karpe F,
Kaplan RC,
Kooner JS,
McCarthy MI,
Murabito JM,
Morris AP,
Bishop JA,
North KE,
Ohlsson C,
Ong KK,
Prokopenko I,
Richards JB,
Schadt EE,
Spector TD,
Widén E,
Willer CJ,
Yang J,
Ingelsson E,
Mohlke KL,
Hirschhorn JN,
Pospisilik JA,
Zillikens MC,
Lindgren C,
Kilpeläinen TO,
Loos RJ
Nature communications · 2016 · PMID 26833246 · open access
3 pages
A novel common variant in DCST2 is associated with length in early life and height in adulthood
van der Valk RJ,
Kreiner-Møller E,
Kooijman MN,
Guxens M,
Stergiakouli E,
Sääf A,
Bradfield JP,
Geller F,
Hayes MG,
Cousminer DL,
Körner A,
Thiering E
and 105 more — show all
Curtin JA,
Myhre R,
Huikari V,
Joro R,
Kerkhof M,
Warrington NM,
Pitkänen N,
Ntalla I,
Horikoshi M,
Veijola R,
Freathy RM,
Teo YY,
Barton SJ,
Evans DM,
Kemp JP,
St Pourcain B,
Ring SM,
Davey Smith G,
Bergström A,
Kull I,
Hakonarson H,
Mentch FD,
Bisgaard H,
Chawes B,
Stokholm J,
Waage J,
Eriksen P,
Sevelsted A,
Melbye M,
van Duijn CM,
Medina-Gomez C,
Hofman A,
de Jongste JC,
Taal HR,
Uitterlinden AG,
Armstrong LL,
Eriksson J,
Palotie A,
Bustamante M,
Estivill X,
Gonzalez JR,
Llop S,
Kiess W,
Mahajan A,
Flexeder C,
Tiesler CM,
Murray CS,
Simpson A,
Magnus P,
Sengpiel V,
Hartikainen AL,
Keinanen-Kiukaanniemi S,
Lewin A,
Da Silva Couto Alves A,
Blakemore AI,
Buxton JL,
Kaakinen M,
Rodriguez A,
Sebert S,
Vaarasmaki M,
Lakka T,
Lindi V,
Gehring U,
Postma DS,
Ang W,
Newnham JP,
Lyytikäinen LP,
Pahkala K,
Raitakari OT,
Panoutsopoulou K,
Zeggini E,
Boomsma DI,
Groen-Blokhuis M,
Ilonen J,
Franke L,
Hirschhorn JN,
Pers TH,
Liang L,
Huang J,
Hocher B,
Knip M,
Saw SM,
Holloway JW,
Melén E,
Grant SF,
Feenstra B,
Lowe WL,
Widén E,
Sergeyev E,
Grallert H,
Custovic A,
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Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium and 1 more consortia
Human molecular genetics · 2015 · PMID 25281659 · open access
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LifeLines Cohort Study · ADIPOGen Consortium and 12 more consortia
Nature · 2015 · PMID 25673413
2 pages
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GIANT Consortium
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