For researchers
Is your paper here?
2,671 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.
90 matches for
Hansen T,
showing the first 20.
Many sequence variants affecting diversity of adult human height
Gudbjartsson DF,
Walters GB,
Thorleifsson G,
Stefansson H,
Halldorsson BV,
Zusmanovich P,
Sulem P,
Thorlacius S,
Gylfason A,
Steinberg S,
Helgadottir A,
Ingason A
and 25 more — show all
Steinthorsdottir V,
Olafsdottir EJ,
Olafsdottir GH,
Jonsson T,
Borch-Johnsen K,
Hansen T,
Andersen G,
Jorgensen T,
Pedersen O,
Aben KK,
Witjes JA,
Swinkels DW,
den Heijer M,
Franke B,
Verbeek AL,
Becker DM,
Yanek LR,
Becker LC,
Tryggvadottir L,
Rafnar T,
Gulcher J,
Kiemeney LA,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2008 · PMID 18391951
3 pages
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations
Unoki H,
Takahashi A,
Kawaguchi T,
Hara K,
Horikoshi M,
Andersen G,
Ng DP,
Holmkvist J,
Borch-Johnsen K,
Jørgensen T,
Sandbaek A,
Lauritzen T
and 18 more — show all
Hansen T,
Nurbaya S,
Tsunoda T,
Kubo M,
Babazono T,
Hirose H,
Hayashi M,
Iwamoto Y,
Kashiwagi A,
Kaku K,
Kawamori R,
Tai ES,
Pedersen O,
Kamatani N,
Kadowaki T,
Kikkawa R,
Nakamura Y,
Maeda S
Nature genetics · 2008 · PMID 18711366
3 pages
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Heid IM,
Jackson AU,
Randall JC,
Winkler TW,
Qi L,
Steinthorsdottir V,
Thorleifsson G,
Zillikens MC,
Speliotes EK,
Mägi R,
Workalemahu T,
White CC
and 290 more — show all
Bouatia-Naji N,
Harris TB,
Berndt SI,
Ingelsson E,
Willer CJ,
Weedon MN,
Luan J,
Vedantam S,
Esko T,
Kilpeläinen TO,
Kutalik Z,
Li S,
Monda KL,
Dixon AL,
Holmes CC,
Kaplan LM,
Liang L,
Min JL,
Moffatt MF,
Molony C,
Nicholson G,
Schadt EE,
Zondervan KT,
Feitosa MF,
Ferreira T,
Lango Allen H,
Weyant RJ,
Wheeler E,
Wood AR,
Estrada K,
Goddard ME,
Lettre G,
Mangino M,
Nyholt DR,
Purcell S,
Smith AV,
Visscher PM,
Yang J,
McCarroll SA,
Nemesh J,
Voight BF,
Absher D,
Amin N,
Aspelund T,
Coin L,
Glazer NL,
Hayward C,
Heard-Costa NL,
Hottenga JJ,
Johansson A,
Johnson T,
Kaakinen M,
Kapur K,
Ketkar S,
Knowles JW,
Kraft P,
Kraja AT,
Lamina C,
Leitzmann MF,
McKnight B,
Morris AP,
Ong KK,
Perry JR,
Peters MJ,
Polasek O,
Prokopenko I,
Rayner NW,
Ripatti S,
Rivadeneira F,
Robertson NR,
Sanna S,
Sovio U,
Surakka I,
Teumer A,
van Wingerden S,
Vitart V,
Zhao JH,
Cavalcanti-Proença C,
Chines PS,
Fisher E,
Kulzer JR,
Lecoeur C,
Narisu N,
Sandholt C,
Scott LJ,
Silander K,
Stark K,
Tammesoo ML,
Teslovich TM,
Timpson NJ,
Watanabe RM,
Welch R,
Chasman DI,
Cooper MN,
Jansson JO,
Kettunen J,
Lawrence RW,
Pellikka N,
Perola M,
Vandenput L,
Alavere H,
Almgren P,
Atwood LD,
Bennett AJ,
Biffar R,
Bonnycastle LL,
Bornstein SR,
Buchanan TA,
Campbell H,
Day IN,
Dei M,
Dörr M,
Elliott P,
Erdos MR,
Eriksson JG,
Freimer NB,
Fu M,
Gaget S,
Geus EJ,
Gjesing AP,
Grallert H,
Grässler J,
Groves CJ,
Guiducci C,
Hartikainen AL,
Hassanali N,
Havulinna AS,
Herzig KH,
Hicks AA,
Hui J,
Igl W,
Jousilahti P,
Jula A,
Kajantie E,
Kinnunen L,
Kolcic I,
Koskinen S,
Kovacs P,
Kroemer HK,
Krzelj V,
Kuusisto J,
Kvaloy K,
Laitinen J,
Lantieri O,
Lathrop GM,
Lokki ML,
Luben RN,
Ludwig B,
McArdle WL,
McCarthy A,
Morken MA,
Nelis M,
Neville MJ,
Paré G,
Parker AN,
Peden JF,
Pichler I,
Pietiläinen KH,
Platou CG,
Pouta A,
Ridderstråle M,
Samani NJ,
Saramies J,
Sinisalo J,
Smit JH,
Strawbridge RJ,
Stringham HM,
Swift AJ,
Teder-Laving M,
Thomson B,
Usala G,
van Meurs JB,
van Ommen GJ,
Vatin V,
Volpato CB,
Wallaschofski H,
Walters GB,
Widen E,
Wild SH,
Willemsen G,
Witte DR,
Zgaga L,
Zitting P,
Beilby JP,
James AL,
James AL,
Kähönen M,
Lehtimäki T,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Raitakari O,
Ridker PM,
Stumvoll M,
Tönjes A,
Viikari J,
Balkau B,
Ben-Shlomo Y,
Bergman RN,
Boeing H,
Smith GD,
Ebrahim S,
Froguel P,
Hansen T,
Hengstenberg C,
Hveem K,
Isomaa B,
Jørgensen T,
Karpe F,
Khaw KT,
Laakso M,
Lawlor DA,
Marre M,
Meitinger T,
Metspalu A,
Midthjell K,
Pedersen O,
Salomaa V,
Schwarz PE,
Schwarz PE,
Tuomi T,
Tuomilehto J,
Valle TT,
Wareham NJ,
Arnold AM,
Beckmann JS,
Bergmann S,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Collins FS,
Eiriksdottir G,
Gudnason V,
Gyllensten U,
Hamsten A,
Hattersley AT,
Hofman A,
Hu FB,
Illig T,
Iribarren C,
Jarvelin MR,
Kao WH,
Kaprio J,
Launer LJ,
Munroe PB,
Oostra B,
Penninx BW,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rissanen A,
Rudan I,
Shuldiner AR,
Soranzo N,
Spector TD,
Syvanen AC,
Uda M,
Uitterlinden A,
Völzke H,
Vollenweider P,
Wilson JF,
Witteman JC,
Wright AF,
Abecasis GR,
Boehnke M,
Borecki IB,
Deloukas P,
Frayling TM,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
North KE,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
Hirschhorn JN,
Assimes TL,
Wichmann HE,
Thorsteinsdottir U,
van Duijn CM,
Stefansson K,
Cupples LA,
Loos RJ,
Barroso I,
McCarthy MI,
Fox CS,
Mohlke KL,
Lindgren CM
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Kuchenbaecker KB,
Ramus SJ,
Tyrer J,
Lee A,
Shen HC,
Beesley J,
Lawrenson K,
McGuffog L,
Healey S,
Lee JM,
Spindler TJ,
Lin YG
and 277 more — show all
Pejovic T,
Bean Y,
Li Q,
Coetzee S,
Hazelett D,
Miron A,
Southey M,
Terry MB,
Goldgar DE,
Buys SS,
Janavicius R,
Dorfling CM,
van Rensburg EJ,
Neuhausen SL,
Ding YC,
Hansen TV,
Jønson L,
Gerdes AM,
Ejlertsen B,
Barrowdale D,
Dennis J,
Benitez J,
Osorio A,
Garcia MJ,
Komenaka I,
Weitzel JN,
Ganschow P,
Peterlongo P,
Bernard L,
Viel A,
Bonanni B,
Peissel B,
Manoukian S,
Radice P,
Papi L,
Ottini L,
Fostira F,
Konstantopoulou I,
Garber J,
Frost D,
Perkins J,
Platte R,
Ellis S,
Godwin AK,
Schmutzler RK,
Meindl A,
Engel C,
Sutter C,
Sinilnikova OM,
Damiola F,
Mazoyer S,
Stoppa-Lyonnet D,
Claes K,
De Leeneer K,
Kirk J,
Rodriguez GC,
Piedmonte M,
O'Malley DM,
de la Hoya M,
Caldes T,
Aittomäki K,
Nevanlinna H,
Collée JM,
Rookus MA,
Oosterwijk JC,
Tihomirova L,
Tung N,
Hamann U,
Isaccs C,
Tischkowitz M,
Imyanitov EN,
Caligo MA,
Campbell IG,
Hogervorst FB,
Olah E,
Diez O,
Blanco I,
Brunet J,
Lazaro C,
Pujana MA,
Jakubowska A,
Gronwald J,
Lubinski J,
Sukiennicki G,
Barkardottir RB,
Plante M,
Simard J,
Soucy P,
Montagna M,
Tognazzo S,
Teixeira MR,
Pankratz VS,
Wang X,
Lindor N,
Szabo CI,
Kauff N,
Vijai J,
Aghajanian CA,
Pfeiler G,
Berger A,
Singer CF,
Tea MK,
Phelan CM,
Greene MH,
Mai PL,
Rennert G,
Mulligan AM,
Tchatchou S,
Andrulis IL,
Glendon G,
Toland AE,
Jensen UB,
Kruse TA,
Thomassen M,
Bojesen A,
Zidan J,
Friedman E,
Laitman Y,
Soller M,
Liljegren A,
Arver B,
Einbeigi Z,
Stenmark-Askmalm M,
Olopade OI,
Nussbaum RL,
Rebbeck TR,
Nathanson KL,
Domchek SM,
Lu KH,
Karlan BY,
Walsh C,
Lester J,
Hein A,
Ekici AB,
Beckmann MW,
Fasching PA,
Lambrechts D,
Van Nieuwenhuysen E,
Vergote I,
Lambrechts S,
Dicks E,
Doherty JA,
Wicklund KG,
Rossing MA,
Rudolph A,
Chang-Claude J,
Wang-Gohrke S,
Eilber U,
Moysich KB,
Odunsi K,
Sucheston L,
Lele S,
Wilkens LR,
Goodman MT,
Thompson PJ,
Shvetsov YB,
Runnebaum IB,
Dürst M,
Hillemanns P,
Dörk T,
Antonenkova N,
Bogdanova N,
Leminen A,
Pelttari LM,
Butzow R,
Modugno F,
Kelley JL,
Edwards RP,
Ness RB,
du Bois A,
Heitz F,
Schwaab I,
Harter P,
Matsuo K,
Hosono S,
Orsulic S,
Jensen A,
Kjaer SK,
Hogdall E,
Hasmad HN,
Azmi MA,
Teo SH,
Woo YL,
Fridley BL,
Goode EL,
Cunningham JM,
Vierkant RA,
Bruinsma F,
Giles GG,
Liang D,
Hildebrandt MA,
Wu X,
Levine DA,
Bisogna M,
Berchuck A,
Iversen ES,
Schildkraut JM,
Concannon P,
Weber RP,
Cramer DW,
Terry KL,
Poole EM,
Tworoger SS,
Bandera EV,
Orlow I,
Olson SH,
Krakstad C,
Salvesen HB,
Tangen IL,
Bjorge L,
van Altena AM,
Aben KK,
Kiemeney LA,
Massuger LF,
Kellar M,
Brooks-Wilson A,
Kelemen LE,
Cook LS,
Le ND,
Cybulski C,
Yang H,
Lissowska J,
Brinton LA,
Wentzensen N,
Hogdall C,
Lundvall L,
Nedergaard L,
Baker H,
Song H,
Eccles D,
McNeish I,
Paul J,
Carty K,
Siddiqui N,
Glasspool R,
Whittemore AS,
Rothstein JH,
McGuire V,
Sieh W,
Ji BT,
Zheng W,
Shu XO,
Gao YT,
Rosen B,
Risch HA,
McLaughlin JR,
Narod SA,
Monteiro AN,
Chen A,
Lin HY,
Permuth-Wey J,
Sellers TA,
Tsai YY,
Chen Z,
Ziogas A,
Anton-Culver H,
Gentry-Maharaj A,
Menon U,
Harrington P,
Lee AW,
Wu AH,
Pearce CL,
Coetzee G,
Pike MC,
Dansonka-Mieszkowska A,
Timorek A,
Rzepecka IK,
Kupryjanczyk J,
Freedman M,
Noushmehr H,
Easton DF,
Offit K,
Couch FJ,
Gayther S,
Pharoah PP,
Antoniou AC,
Chenevix-Trench G
EMBRACE · GEMO Study Collaborators and 6 more consortia
Nature genetics · 2015 · PMID 25581431 · open access
3 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
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Joshi PK,
Pirastu N,
Kentistou KA,
Fischer K,
Hofer E,
Schraut KE,
Clark DW,
Nutile T,
Barnes CLK,
Timmers PRHJ,
Shen X,
Gandin I
and 101 more — show all
McDaid AF,
Hansen TF,
Gordon SD,
Giulianini F,
Boutin TS,
Abdellaoui A,
Zhao W,
Medina-Gomez C,
Bartz TM,
Trompet S,
Lange LA,
Raffield L,
van der Spek A,
Galesloot TE,
Proitsi P,
Yanek LR,
Bielak LF,
Payton A,
Murgia F,
Concas MP,
Biino G,
Tajuddin SM,
Seppälä I,
Amin N,
Boerwinkle E,
Børglum AD,
Campbell A,
Demerath EW,
Demuth I,
Faul JD,
Ford I,
Gialluisi A,
Gögele M,
Graff M,
Hingorani A,
Hottenga JJ,
Hougaard DM,
Hurme MA,
Ikram MA,
Jylhä M,
Kuh D,
Ligthart L,
Lill CM,
Lindenberger U,
Lumley T,
Mägi R,
Marques-Vidal P,
Medland SE,
Milani L,
Nagy R,
Ollier WER,
Peyser PA,
Pramstaller PP,
Ridker PM,
Rivadeneira F,
Ruggiero D,
Saba Y,
Schmidt R,
Schmidt H,
Slagboom PE,
Smith BH,
Smith JA,
Sotoodehnia N,
Steinhagen-Thiessen E,
van Rooij FJA,
Verbeek AL,
Vermeulen SH,
Vollenweider P,
Wang Y,
Werge T,
Whitfield JB,
Zonderman AB,
Lehtimäki T,
Evans MK,
Pirastu M,
Fuchsberger C,
Bertram L,
Pendleton N,
Kardia SLR,
Ciullo M,
Becker DM,
Wong A,
Psaty BM,
van Duijn CM,
Wilson JG,
Jukema JW,
Kiemeney L,
Uitterlinden AG,
Franceschini N,
North KE,
Weir DR,
Metspalu A,
Boomsma DI,
Hayward C,
Chasman D,
Martin NG,
Sattar N,
Campbell H,
Esko T,
Kutalik Z,
Wilson JF
Nature communications · 2017 · PMID 29030599 · open access
3 pages
Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth
Wang Y,
Nudel R,
Benros ME,
Skogstrand K,
Fishilevich S,
Lancet D,
Sun J,
Hougaard DM,
Andreassen OA,
Mortensen PB,
Buil A,
Hansen TF
and 2 more — show all
iPSYCH-BROAD
PLoS genetics · 2020 · PMID 33227023 · open access
3 pages
FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses
Ahluwalia TS,
Eliasen AU,
Sevelsted A,
Pedersen CT,
Stokholm J,
Chawes B,
Bork-Jensen J,
Grarup N,
Pedersen O,
Hansen T,
Linneberg A,
Sharma A
and 21 more — show all
Weiss ST,
Evans MD,
Jackson DJ,
Morin A,
Krogfelt KA,
Schjørring S,
Mortensen PB,
Hougaard DM,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Mors O,
Nordentoft M,
Børglum AD,
Werge T,
Agerbo E,
Gern JE,
Lemanske RF Jr,
Ober C,
Pedersen AG,
Bisgaard H,
Bønnelykke K
Nature communications · 2020 · PMID 33328473 · open access
3 pages
Genome-wide association study of preserved ratio impaired spirometry (PRISm)
Higbee DH,
Lirio A,
Hamilton F,
Granell R,
Wyss AB,
London SJ,
Bartz TM,
Gharib SA,
Cho MH,
Wan E,
Silverman E,
Crapo JD
and 33 more — show all
Lominchar JVT,
Hansen T,
Grarup N,
Dantoft T,
Kårhus L,
Linneberg A,
O'Connor GT,
Dupuis J,
Xu H,
De Vries MM,
Hu X,
Rich SS,
Barr RG,
Manichaikul A,
Wijnant SRA,
Brusselle GG,
Lahousse L,
Li X,
Hernández Cordero AI,
Obeidat M,
Sin DD,
Harris SE,
Redmond P,
Taylor AM,
Cox SR,
Williams AT,
Shrine N,
John C,
Guyatt AL,
Hall IP,
Davey Smith G,
Tobin MD,
Dodd JW
The European respiratory journal · 2024 · PMID 38097206 · open access
3 pages
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
Thorleifsson G,
Walters GB,
Gudbjartsson DF,
Steinthorsdottir V,
Sulem P,
Helgadottir A,
Styrkarsdottir U,
Gretarsdottir S,
Thorlacius S,
Jonsdottir I,
Jonsdottir T,
Olafsdottir EJ
and 23 more — show all
Olafsdottir GH,
Jonsson T,
Jonsson F,
Borch-Johnsen K,
Hansen T,
Andersen G,
Jorgensen T,
Lauritzen T,
Aben KK,
Verbeek AL,
Roeleveld N,
Kampman E,
Yanek LR,
Becker LC,
Tryggvadottir L,
Rafnar T,
Becker DM,
Gulcher J,
Kiemeney LA,
Pedersen O,
Kong A,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2009 · PMID 19079260
2 pages
Common variants conferring risk of schizophrenia
Stefansson H,
Ophoff RA,
Steinberg S,
Andreassen OA,
Cichon S,
Rujescu D,
Werge T,
Pietiläinen OP,
Mors O,
Mortensen PB,
Sigurdsson E,
Gustafsson O
and 75 more — show all
Nyegaard M,
Tuulio-Henriksson A,
Ingason A,
Hansen T,
Suvisaari J,
Lonnqvist J,
Paunio T,
Børglum AD,
Hartmann A,
Fink-Jensen A,
Nordentoft M,
Hougaard D,
Norgaard-Pedersen B,
Böttcher Y,
Olesen J,
Breuer R,
Möller HJ,
Giegling I,
Rasmussen HB,
Timm S,
Mattheisen M,
Bitter I,
Réthelyi JM,
Magnusdottir BB,
Sigmundsson T,
Olason P,
Masson G,
Gulcher JR,
Haraldsson M,
Fossdal R,
Thorgeirsson TE,
Thorsteinsdottir U,
Ruggeri M,
Tosato S,
Franke B,
Strengman E,
Kiemeney LA,
Melle I,
Djurovic S,
Abramova L,
Kaleda V,
Sanjuan J,
de Frutos R,
Bramon E,
Vassos E,
Fraser G,
Ettinger U,
Picchioni M,
Walker N,
Toulopoulou T,
Need AC,
Ge D,
Yoon JL,
Shianna KV,
Freimer NB,
Cantor RM,
Murray R,
Kong A,
Golimbet V,
Carracedo A,
Arango C,
Costas J,
Jönsson EG,
Terenius L,
Agartz I,
Petursson H,
Nöthen MM,
Rietschel M,
Matthews PM,
Muglia P,
Peltonen L,
St Clair D,
Goldstein DB,
Stefansson K,
Collier DA
Genetic Risk and Outcome in Psychosis (GROUP)
Nature · 2009 · PMID 19571808
2 pages
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Gretarsdottir S,
Baas AF,
Thorleifsson G,
Holm H,
den Heijer M,
de Vries JP,
Kranendonk SE,
Zeebregts CJ,
van Sterkenburg SM,
Geelkerken RH,
van Rij AM,
Williams MJ
and 90 more — show all
Boll AP,
Kostic JP,
Jonasdottir A,
Jonasdottir A,
Walters GB,
Masson G,
Sulem P,
Saemundsdottir J,
Mouy M,
Magnusson KP,
Tromp G,
Elmore JR,
Sakalihasan N,
Limet R,
Defraigne JO,
Ferrell RE,
Ronkainen A,
Ruigrok YM,
Wijmenga C,
Grobbee DE,
Shah SH,
Granger CB,
Quyyumi AA,
Vaccarino V,
Patel RS,
Zafari AM,
Levey AI,
Austin H,
Girelli D,
Pignatti PF,
Olivieri O,
Martinelli N,
Malerba G,
Trabetti E,
Becker LC,
Becker DM,
Reilly MP,
Rader DJ,
Mueller T,
Dieplinger B,
Haltmayer M,
Urbonavicius S,
Lindblad B,
Gottsäter A,
Gaetani E,
Pola R,
Wells P,
Rodger M,
Forgie M,
Langlois N,
Corral J,
Vicente V,
Fontcuberta J,
España F,
Grarup N,
Jørgensen T,
Witte DR,
Hansen T,
Pedersen O,
Aben KK,
de Graaf J,
Holewijn S,
Folkersen L,
Franco-Cereceda A,
Eriksson P,
Collier DA,
Stefansson H,
Steinthorsdottir V,
Rafnar T,
Valdimarsson EM,
Magnadottir HB,
Sveinbjornsdottir S,
Olafsson I,
Magnusson MK,
Palmason R,
Haraldsdottir V,
Andersen K,
Onundarson PT,
Thorgeirsson G,
Kiemeney LA,
Powell JT,
Carey DJ,
Kuivaniemi H,
Lindholt JS,
Jones GT,
Kong A,
Blankensteijn JD,
Matthiasson SE,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2010 · PMID 20622881
2 pages
Genome-wide association study identifies four loci associated with eruption of permanent teeth
Geller F,
Feenstra B,
Zhang H,
Shaffer JR,
Hansen T,
Esserlind AL,
Boyd HA,
Nohr EA,
Timpson NJ,
Fatemifar G,
Paternoster L,
Evans DM
and 10 more — show all
PLoS genetics · 2011 · PMID 21931568 · open access
2 pages
Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes
Xie W,
Wood AR,
Lyssenko V,
Weedon MN,
Knowles JW,
Alkayyali S,
Assimes TL,
Quertermous T,
Abbasi F,
Paananen J,
Häring H,
Hansen T
and 11 more — show all
Pedersen O,
Smith U,
Laakso M,
Dekker JM,
Nolan JJ,
Groop L,
Ferrannini E,
Adam KP,
Gall WE,
Frayling TM,
Walker M
MAGIC Investigators · DIAGRAM Consortium and 2 more consortia
Diabetes · 2013 · PMID 23378610 · open access
2 pages
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
and 233 more — show all
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
Müller-Nurasyid M,
Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
Ohnaka K,
Parish S,
Paternoster L,
Peng H,
Peters A,
Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
Viikari JS,
Waldenberger M,
Wang Y,
Wang A,
Wilson R,
Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
Franks S,
Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
Pedersen O,
Samani NJ,
Sørensen TIA,
Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
Danesh J,
Deary IJ,
Franco OH,
Franke L,
Heijman BT,
Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
Mohlke KL,
Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
Wickremasinghe AR,
Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
Zheng W,
Zhu D,
Vineis P,
Kyrtopoulos SA,
Kleinjans JCS,
McCarthy MI,
Soong R,
Gieger C,
Scott J,
Teo YY,
He J,
Elliott P,
Tai ES,
van der Harst P,
Kooner JS,
Chambers JC
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents
Nielsen TR,
Nielsen TR,
Appel EV,
Svendstrup M,
Ohrt JD,
Dahl M,
Fonvig CE,
Hollensted M,
Have CT,
Kadarmideen HN,
Pedersen O,
Hansen T
and 2 more — show all
PloS one · 2017 · PMID 28333968 · open access
2 pages
A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants
Wood AR,
Jonsson A,
Jackson AU,
Wang N,
van Leewen N,
Palmer ND,
Kobes S,
Deelen J,
Boquete-Vilarino L,
Paananen J,
Stančáková A,
Boomsma DI
and 40 more — show all
de Geus EJC,
Eekhoff EMW,
Fritsche A,
Kramer M,
Nijpels G,
Simonis-Bik A,
van Haeften TW,
Mahajan A,
Boehnke M,
Bergman RN,
Tuomilehto J,
Collins FS,
Mohlke KL,
Banasik K,
Groves CJ,
McCarthy MI,
Pearson ER,
Natali A,
Mari A,
Buchanan TA,
Taylor KD,
Xiang AH,
Xiang AH,
Gjesing AP,
Grarup N,
Eiberg H,
Pedersen O,
Chen YD,
Laakso M,
Norris JM,
Smith U,
Wagenknecht LE,
Baier L,
Bowden DW,
Hansen T,
Walker M,
Watanabe RM,
't Hart LM,
Hanson RL,
Frayling TM
Diabetes Research on Patient Stratification (DIRECT)
Diabetes · 2017 · PMID 28490609 · open access
2 pages
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
Cousminer DL,
Ahlqvist E,
Mishra R,
Andersen MK,
Chesi A,
Hawa MI,
Davis A,
Hodge KM,
Bradfield JP,
Zhou K,
Guy VC,
Åkerlund M
and 41 more — show all
Wod M,
Fritsche LG,
Vestergaard H,
Snyder J,
Højlund K,
Linneberg A,
Käräjämäki A,
Brandslund I,
Kim CE,
Witte D,
Sørgjerd EP,
Brillon DJ,
Pedersen O,
Beck-Nielsen H,
Grarup N,
Pratley RE,
Rickels MR,
Vella A,
Ovalle F,
Melander O,
Harris RI,
Varvel S,
Grill VER,
Hakonarson H,
Froguel P,
Lonsdale JT,
Mauricio D,
Schloot NC,
Khunti K,
Greenbaum CJ,
Åsvold BO,
Yderstræde KB,
Pearson ER,
Schwartz S,
Voight BF,
Hansen T,
Tuomi T,
Boehm BO,
Groop L,
Leslie RD,
Grant SFA
Bone Mineral Density in Childhood Study
Diabetes care · 2018 · PMID 30254083 · open access
2 pages
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Flannick J,
Mercader JM,
Fuchsberger C,
Udler MS,
Mahajan A,
Wessel J,
Teslovich TM,
Caulkins L,
Koesterer R,
Barajas-Olmos F,
Blackwell TW,
Boerwinkle E
and 152 more — show all
Brody JA,
Centeno-Cruz F,
Chen L,
Chen S,
Contreras-Cubas C,
Córdova E,
Correa A,
Cortes M,
DeFronzo RA,
Dolan L,
Drews KL,
Elliott A,
Floyd JS,
Gabriel S,
Garay-Sevilla ME,
García-Ortiz H,
Gross M,
Han S,
Heard-Costa NL,
Jackson AU,
Jørgensen ME,
Kang HM,
Kelsey M,
Kim BJ,
Koistinen HA,
Kuusisto J,
Leader JB,
Linneberg A,
Liu CT,
Liu J,
Lyssenko V,
Manning AK,
Marcketta A,
Malacara-Hernandez JM,
Martínez-Hernández A,
Matsuo K,
Mayer-Davis E,
Mendoza-Caamal E,
Mohlke KL,
Morrison AC,
Ndungu A,
Ng MCY,
O'Dushlaine C,
Payne AJ,
Pihoker C,
Post WS,
Preuss M,
Psaty BM,
Vasan RS,
Rayner NW,
Reiner AP,
Revilla-Monsalve C,
Robertson NR,
Santoro N,
Schurmann C,
So WY,
Soberón X,
Stringham HM,
Strom TM,
Tam CHT,
Thameem F,
Tomlinson B,
Torres JM,
Tracy RP,
van Dam RM,
Vujkovic M,
Wang S,
Welch RP,
Witte DR,
Wong TY,
Atzmon G,
Barzilai N,
Blangero J,
Bonnycastle LL,
Bowden DW,
Chambers JC,
Chan E,
Cheng CY,
Cho YS,
Collins FS,
de Vries PS,
Duggirala R,
Glaser B,
Gonzalez C,
Gonzalez ME,
Groop L,
Kooner JS,
Kwak SH,
Laakso M,
Lehman DM,
Nilsson P,
Spector TD,
Tai ES,
Tuomi T,
Tuomilehto J,
Wilson JG,
Aguilar-Salinas CA,
Bottinger E,
Burke B,
Carey DJ,
Chan JCN,
Dupuis J,
Frossard P,
Heckbert SR,
Hwang MY,
Kim YJ,
Kirchner HL,
Lee JY,
Lee J,
Loos RJF,
Ma RCW,
Morris AD,
O'Donnell CJ,
Palmer CNA,
Pankow J,
Park KS,
Rasheed A,
Saleheen D,
Sim X,
Small KS,
Teo YY,
Haiman C,
Hanis CL,
Henderson BE,
Orozco L,
Tusié-Luna T,
Dewey FE,
Baras A,
Gieger C,
Meitinger T,
Strauch K,
Lange L,
Grarup N,
Hansen T,
Pedersen O,
Zeitler P,
Dabelea D,
Abecasis G,
Bell GI,
Cox NJ,
Seielstad M,
Sladek R,
Meigs JB,
Rich SS,
Rotter JI,
Altshuler D,
Burtt NP,
Scott LJ,
Morris AP,
Florez JC,
McCarthy MI,
Boehnke M
Broad Genomics Platform · DiscovEHR Collaboration and 8 more consortia
Nature · 2019 · PMID 31118516 · open access
2 pages
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
Spracklen CN,
Karaderi T,
Yaghootkar H,
Schurmann C,
Fine RS,
Kutalik Z,
Preuss MH,
Lu Y,
Wittemans LBL,
Adair LS,
Allison M,
Amin N
and 92 more — show all
Auer PL,
Bartz TM,
Blüher M,
Boehnke M,
Borja JB,
Bork-Jensen J,
Broer L,
Chasman DI,
Chen YI,
Chirstofidou P,
Demirkan A,
van Duijn CM,
Feitosa MF,
Garcia ME,
Graff M,
Grallert H,
Grarup N,
Guo X,
Haesser J,
Hansen T,
Harris TB,
Highland HM,
Hong J,
Ikram MA,
Ingelsson E,
Jackson R,
Jousilahti P,
Kähönen M,
Kizer JR,
Kovacs P,
Kriebel J,
Laakso M,
Lange LA,
Lehtimäki T,
Li J,
Li-Gao R,
Lind L,
Luan J,
Lyytikäinen LP,
MacGregor S,
Mackey DA,
Mahajan A,
Mangino M,
Männistö S,
McCarthy MI,
McKnight B,
Medina-Gomez C,
Meigs JB,
Molnos S,
Mook-Kanamori D,
Morris AP,
de Mutsert R,
Nalls MA,
Nedeljkovic I,
North KE,
Pennell CE,
Pradhan AD,
Province MA,
Raitakari OT,
Raulerson CK,
Reiner AP,
Ridker PM,
Ripatti S,
Roberston N,
Rotter JI,
Salomaa V,
Sandoval-Zárate AA,
Sitlani CM,
Spector TD,
Strauch K,
Stumvoll M,
Taylor KD,
Thuesen B,
Tönjes A,
Uitterlinden AG,
Venturini C,
Walker M,
Wang CA,
Wang S,
Wareham NJ,
Willems SM,
Willems van Dijk K,
Wilson JG,
Wu Y,
Yao J,
Young KL,
Langenberg C,
Frayling TM,
Kilpeläinen TO,
Lindgren CM,
Loos RJF,
Mohlke KL
American journal of human genetics · 2019 · PMID 31178129
2 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.