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45 matches for
Ost P,
showing the first 20.
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
Raghavan S,
Miao J,
Arias JD
and 610 more — show all
Graham SE,
Mukamel RE,
Spracklen CN,
Yin X,
Chen SH,
Ferreira T,
Highland HH,
Ji Y,
Karaderi T,
Lin K,
Lüll K,
Malden DE,
Medina-Gomez C,
Machado M,
Moore A,
Rüeger S,
Sim X,
Vrieze S,
Ahluwalia TS,
Akiyama M,
Allison MA,
Alvarez M,
Andersen MK,
Ani A,
Appadurai V,
Arbeeva L,
Bhaskar S,
Bielak LF,
Bollepalli S,
Bonnycastle LL,
Bork-Jensen J,
Bradfield JP,
Bradford Y,
Braund PS,
Brody JA,
Burgdorf KS,
Cade BE,
Cai H,
Cai Q,
Campbell A,
Cañadas-Garre M,
Catamo E,
Chai JF,
Chai X,
Chang LC,
Chang YC,
Chen CH,
Chesi A,
Choi SH,
Chung RH,
Cocca M,
Concas MP,
Couture C,
Cuellar-Partida G,
Danning R,
Daw EW,
Degenhard F,
Delgado GE,
Delitala A,
Demirkan A,
Deng X,
Devineni P,
Dietl A,
Dimitriou M,
Dimitrov L,
Dorajoo R,
Ekici AB,
Engmann JE,
Fairhurst-Hunter Z,
Farmaki AE,
Faul JD,
Fernandez-Lopez JC,
Forer L,
Francescatto M,
Freitag-Wolf S,
Fuchsberger C,
Galesloot TE,
Gao Y,
Gao Z,
Geller F,
Giannakopoulou O,
Giulianini F,
Gjesing AP,
Goel A,
Gordon SD,
Gorski M,
Grove J,
Guo X,
Gustafsson S,
Haessler J,
Hansen TF,
Havulinna AS,
Haworth SJ,
He J,
Heard-Costa N,
Hebbar P,
Hindy G,
Ho YA,
Hofer E,
Holliday E,
Horn K,
Hornsby WE,
Hottenga JJ,
Huang H,
Huang J,
Huerta-Chagoya A,
Huffman JE,
Hung YJ,
Huo S,
Hwang MY,
Iha H,
Ikeda DD,
Isono M,
Jackson AU,
Jäger S,
Jansen IE,
Johansson I,
Jonas JB,
Jonsson A,
Jørgensen T,
Kalafati IP,
Kanai M,
Kanoni S,
Kårhus LL,
Kasturiratne A,
Katsuya T,
Kawaguchi T,
Kember RL,
Kentistou KA,
Kim HN,
Kim YJ,
Kleber ME,
Knol MJ,
Kurbasic A,
Lauzon M,
Le P,
Lea R,
Lee JY,
Leonard HL,
Li SA,
Li X,
Li X,
Liang J,
Lin H,
Lin SY,
Liu J,
Liu X,
Lo KS,
Long J,
Lores-Motta L,
Luan J,
Lyssenko V,
Lyytikäinen LP,
Mahajan A,
Mamakou V,
Mangino M,
Manichaikul A,
Marten J,
Mattheisen M,
Mavarani L,
McDaid AF,
Meidtner K,
Melendez TL,
Mercader JM,
Milaneschi Y,
Miller JE,
Millwood IY,
Mishra PP,
Mitchell RE,
Møllehave LT,
Morgan A,
Mucha S,
Munz M,
Nakatochi M,
Nelson CP,
Nethander M,
Nho CW,
Nielsen AA,
Nolte IM,
Nongmaithem SS,
Noordam R,
Ntalla I,
Nutile T,
Pandit A,
Christofidou P,
Pärna K,
Pauper M,
Petersen ERB,
Petersen LV,
Pitkänen N,
Polašek O,
Poveda A,
Preuss MH,
Pyarajan S,
Raffield LM,
Rakugi H,
Ramirez J,
Rasheed A,
Raven D,
Rayner NW,
Riveros C,
Rohde R,
Ruggiero D,
Ruotsalainen SE,
Ryan KA,
Sabater-Lleal M,
Saxena R,
Scholz M,
Sendamarai A,
Shen B,
Shi J,
Shin JH,
Sidore C,
Sitlani CM,
Slieker RC,
Smit RAJ,
Smith AV,
Smith JA,
Smyth LJ,
Southam L,
Steinthorsdottir V,
Sun L,
Takeuchi F,
Tallapragada DSP,
Taylor KD,
Tayo BO,
Tcheandjieu C,
Terzikhan N,
Tesolin P,
Teumer A,
Theusch E,
Thompson DJ,
Thorleifsson G,
Timmers PRHJ,
Trompet S,
Turman C,
Vaccargiu S,
van der Laan SW,
van der Most PJ,
van Klinken JB,
van Setten J,
Verma SS,
Verweij N,
Veturi Y,
Wang CA,
Wang C,
Wang L,
Wang Z,
Warren HR,
Bin Wei W,
Wickremasinghe AR,
Wielscher M,
Wiggins KL,
Winsvold BS,
Wong A,
Wu Y,
Wuttke M,
Xia R,
Xie T,
Yamamoto K,
Yang J,
Yao J,
Young H,
Yousri NA,
Yu L,
Zeng L,
Zhang W,
Zhang X,
Zhao JH,
Zhao W,
Zhou W,
Zimmermann ME,
Zoledziewska M,
Adair LS,
Adams HHH,
Aguilar-Salinas CA,
Al-Mulla F,
Arnett DK,
Asselbergs FW,
Åsvold BO,
Attia J,
Banas B,
Bandinelli S,
Bennett DA,
Bergler T,
Bharadwaj D,
Biino G,
Bisgaard H,
Boerwinkle E,
Böger CA,
Bønnelykke K,
Boomsma DI,
Børglum AD,
Borja JB,
Bouchard C,
Bowden DW,
Brandslund I,
Brumpton B,
Buring JE,
Caulfield MJ,
Chambers JC,
Chandak GR,
Chanock SJ,
Chaturvedi N,
Chen YI,
Chen Z,
Cheng CY,
Christophersen IE,
Ciullo M,
Cole JW,
Collins FS,
Cooper RS,
Cruz M,
Cucca F,
Cupples LA,
Cutler MJ,
Damrauer SM,
Dantoft TM,
de Borst GJ,
de Groot LCPGM,
De Jager PL,
de Kleijn DPV,
Janaka de Silva H,
Dedoussis GV,
den Hollander AI,
Du S,
Easton DF,
Elders PJM,
Eliassen AH,
Ellinor PT,
Elmståhl S,
Erdmann J,
Evans MK,
Fatkin D,
Feenstra B,
Feitosa MF,
Ferrucci L,
Ford I,
Fornage M,
Franke A,
Franks PW,
Freedman BI,
Gasparini P,
Gieger C,
Girotto G,
Goddard ME,
Golightly YM,
Gonzalez-Villalpando C,
Gordon-Larsen P,
Grallert H,
Grant SFA,
Grarup N,
Griffiths L,
Gudnason V,
Haiman C,
Hakonarson H,
Hansen T,
Hartman CA,
Hattersley AT,
Hayward C,
Heckbert SR,
Heng CK,
Hengstenberg C,
Hewitt AW,
Hishigaki H,
Hoyng CB,
Huang PL,
Huang W,
Hunt SC,
Hveem K,
Hyppönen E,
Iacono WG,
Ichihara S,
Ikram MA,
Isasi CR,
Jackson RD,
Jarvelin MR,
Jin ZB,
Jöckel KH,
Joshi PK,
Jousilahti P,
Jukema JW,
Kähönen M,
Kamatani Y,
Kang KD,
Kaprio J,
Kardia SLR,
Karpe F,
Kato N,
Kee F,
Kessler T,
Khera AV,
Khor CC,
Kiemeney LALM,
Kim BJ,
Kim EK,
Kim HL,
Kirchhof P,
Kivimaki M,
Koh WP,
Koistinen HA,
Kolovou GD,
Kooner JS,
Kooperberg C,
Köttgen A,
Kovacs P,
Kraaijeveld A,
Kraft P,
Krauss RM,
Kumari M,
Kutalik Z,
Laakso M,
Lange LA,
Langenberg C,
Launer LJ,
Le Marchand L,
Lee H,
Lee NR,
Lehtimäki T,
Li H,
Li L,
Lieb W,
Lin X,
Lind L,
Linneberg A,
Liu CT,
Liu J,
Loeffler M,
London B,
Lubitz SA,
Lye SJ,
Mackey DA,
Mägi R,
Magnusson PKE,
Marcus GM,
Vidal PM,
Martin NG,
März W,
Matsuda F,
McGarrah RW,
McGue M,
McKnight AJ,
Medland SE,
Mellström D,
Metspalu A,
Mitchell BD,
Mitchell P,
Mook-Kanamori DO,
Morris AD,
Mucci LA,
Munroe PB,
Nalls MA,
Nazarian S,
Nelson AE,
Neville MJ,
Newton-Cheh C,
Nielsen CS,
Nöthen MM,
Ohlsson C,
Oldehinkel AJ,
Orozco L,
Pahkala K,
Pajukanta P,
Palmer CNA,
Parra EJ,
Pattaro C,
Pedersen O,
Pennell CE,
Penninx BWJH,
Perusse L,
Peters A,
Peyser PA,
Porteous DJ,
Posthuma D,
Power C,
Pramstaller PP,
Province MA,
Qi Q,
Qu J,
Rader DJ,
Raitakari OT,
Ralhan S,
Rallidis LS,
Rao DC,
Redline S,
Reilly DF,
Reiner AP,
Rhee SY,
Ridker PM,
Rienstra M,
Ripatti S,
Ritchie MD,
Roden DM,
Rosendaal FR,
Rotter JI,
Rudan I,
Rutters F,
Sabanayagam C,
Saleheen D,
Salomaa V,
Samani NJ,
Sanghera DK,
Sattar N,
Schmidt B,
Schmidt H,
Schmidt R,
Schulze MB,
Schunkert H,
Scott LJ,
Scott RJ,
Sever P,
Shiroma EJ,
Shoemaker MB,
Shu XO,
Simonsick EM,
Sims M,
Singh JR,
Singleton AB,
Sinner MF,
Smith JG,
Snieder H,
Spector TD,
Stampfer MJ,
Stark KJ,
Strachan DP,
't Hart LM,
Tabara Y,
Tang H,
Tardif JC,
Thanaraj TA,
Timpson NJ,
Tönjes A,
Tremblay A,
Tuomi T,
Tuomilehto J,
Tusié-Luna MT,
Uitterlinden AG,
van Dam RM,
van der Harst P,
Van der Velde N,
van Duijn CM,
van Schoor NM,
Vitart V,
Völker U,
Vollenweider P,
Völzke H,
Wacher-Rodarte NH,
Walker M,
Wang YX,
Wareham NJ,
Watanabe RM,
Watkins H,
Weir DR,
Werge TM,
Widen E,
Wilkens LR,
Willemsen G,
Willett WC,
Wilson JF,
Wong TY,
Woo JT,
Wright AF,
Wu JY,
Xu H,
Yajnik CS,
Yokota M,
Yuan JM,
Zeggini E,
Zemel BS,
Zheng W,
Zhu X,
Zmuda JM,
Zonderman AB,
Zwart JA,
Chasman DI,
Cho YS,
Heid IM,
McCarthy MI,
Ng MCY,
O'Donnell CJ,
Rivadeneira F,
Thorsteinsdottir U,
Sun YV,
Tai ES,
Boehnke M,
Deloukas P,
Justice AE,
Lindgren CM,
Loos RJF,
Mohlke KL,
North KE,
Stefansson K,
Walters RG,
Winkler TW,
Young KL,
Loh PR,
Yang J,
Esko T,
Assimes TL,
Auton A,
Abecasis GR,
Willer CJ,
Locke AE,
Berndt SI,
Lettre G,
Frayling TM,
Okada Y,
Wood AR,
Visscher PM,
Hirschhorn JN
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants
Wang A,
Shen J,
Rodriguez AA,
Saunders EJ,
Chen F,
Janivara R,
Darst BF,
Sheng X,
Xu Y,
Chou AJ,
Benlloch S,
Dadaev T
and 279 more — show all
Brook MN,
Plym A,
Sahimi A,
Hoffman TJ,
Takahashi A,
Matsuda K,
Momozawa Y,
Fujita M,
Laisk T,
Figuerêdo J,
Muir K,
Ito S,
Liu X,
Uchio Y,
Kubo M,
Kamatani Y,
Lophatananon A,
Wan P,
Andrews C,
Lori A,
Choudhury PP,
Schleutker J,
Tammela TLJ,
Sipeky C,
Auvinen A,
Giles GG,
Southey MC,
MacInnis RJ,
Cybulski C,
Wokolorczyk D,
Lubinski J,
Rentsch CT,
Cho K,
Mcmahon BH,
Neal DE,
Donovan JL,
Hamdy FC,
Martin RM,
Nordestgaard BG,
Nielsen SF,
Weischer M,
Bojesen SE,
Røder A,
Stroomberg HV,
Batra J,
Chambers S,
Horvath L,
Clements JA,
Tilly W,
Risbridger GP,
Gronberg H,
Aly M,
Szulkin R,
Eklund M,
Nordstrom T,
Pashayan N,
Dunning AM,
Ghoussaini M,
Travis RC,
Key TJ,
Riboli E,
Park JY,
Sellers TA,
Lin HY,
Albanes D,
Weinstein S,
Cook MB,
Mucci LA,
Giovannucci E,
Lindstrom S,
Kraft P,
Hunter DJ,
Penney KL,
Turman C,
Tangen CM,
Goodman PJ,
Thompson IM Jr,
Hamilton RJ,
Fleshner NE,
Finelli A,
Parent MÉ,
Stanford JL,
Ostrander EA,
Koutros S,
Beane Freeman LE,
Stampfer M,
Wolk A,
Håkansson N,
Andriole GL,
Hoover RN,
Machiela MJ,
Sørensen KD,
Borre M,
Blot WJ,
Zheng W,
Yeboah ED,
Mensah JE,
Lu YJ,
Zhang HW,
Feng N,
Mao X,
Wu Y,
Zhao SC,
Sun Z,
Thibodeau SN,
McDonnell SK,
Schaid DJ,
West CML,
Barnett G,
Maier C,
Schnoeller T,
Luedeke M,
Kibel AS,
Drake BF,
Cussenot O,
Cancel-Tassin G,
Menegaux F,
Truong T,
Koudou YA,
John EM,
Grindedal EM,
Maehle L,
Khaw KT,
Ingles SA,
Stern MC,
Vega A,
Gómez-Caamaño A,
Fachal L,
Rosenstein BS,
Kerns SL,
Ostrer H,
Teixeira MR,
Paulo P,
Brandão A,
Watya S,
Lubwama A,
Bensen JT,
Butler EN,
Mohler JL,
Taylor JA,
Kogevinas M,
Dierssen-Sotos T,
Castaño-Vinyals G,
Cannon-Albright L,
Teerlink CC,
Huff CD,
Pilie P,
Yu Y,
Bohlender RJ,
Gu J,
Strom SS,
Multigner L,
Blanchet P,
Brureau L,
Kaneva R,
Slavov C,
Mitev V,
Leach RJ,
Brenner H,
Chen X,
Holleczek B,
Schöttker B,
Klein EA,
Hsing AW,
Kittles RA,
Murphy AB,
Logothetis CJ,
Kim J,
Neuhausen SL,
Steele L,
Ding YC,
Isaacs WB,
Nemesure B,
Hennis AJM,
Carpten J,
Pandha H,
Michael A,
De Ruyck K,
De Meerleer G,
Ost P,
Xu J,
Razack A,
Lim J,
Teo SH,
Newcomb LF,
Lin DW,
Fowke JH,
Neslund-Dudas CM,
Rybicki BA,
Gamulin M,
Lessel D,
Kulis T,
Usmani N,
Abraham A,
Singhal S,
Parliament M,
Claessens F,
Joniau S,
Van den Broeck T,
Gago-Dominguez M,
Castelao JE,
Martinez ME,
Larkin S,
Townsend PA,
Aukim-Hastie C,
Bush WS,
Aldrich MC,
Crawford DC,
Srivastava S,
Cullen J,
Petrovics G,
Casey G,
Wang Y,
Tettey Y,
Lachance J,
Tang W,
Biritwum RB,
Adjei AA,
Tay E,
Truelove A,
Niwa S,
Yamoah K,
Govindasami K,
Chokkalingam AP,
Keaton JM,
Hellwege JN,
Clark PE,
Jalloh M,
Gueye SM,
Niang L,
Ogunbiyi O,
Shittu O,
Amodu O,
Adebiyi AO,
Aisuodionoe-Shadrach OI,
Ajibola HO,
Jamda MA,
Oluwole OP,
Nwegbu M,
Adusei B,
Mante S,
Darkwa-Abrahams A,
Diop H,
Gundell SM,
Roobol MJ,
Jenster G,
van Schaik RHN,
Hu JJ,
Sanderson M,
Kachuri L,
Varma R,
McKean-Cowdin R,
Torres M,
Preuss MH,
Loos RJF,
Zawistowski M,
Zöllner S,
Lu Z,
Van Den Eeden SK,
Easton DF,
Ambs S,
Edwards TL,
Mägi R,
Rebbeck TR,
Fritsche L,
Chanock SJ,
Berndt SI,
Wiklund F,
Nakagawa H,
Witte JS,
Gaziano JM,
Justice AC,
Mancuso N,
Terao C,
Eeles RA,
Kote-Jarai Z,
Madduri RK,
Conti DV,
Haiman CA
Biobank Japan Project
Nature genetics · 2023 · PMID 37945903
12 pages+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
and 135 more — show all
Giri A,
Zheng Z,
Zeng J,
Chasman DI,
Morris AP,
Caulfield MJ,
Hwang SJ,
Kooner JS,
Conen D,
Attia JR,
Morrison AC,
Loos RJF,
Kristiansson K,
Schmidt R,
Hicks AA,
Pramstaller PP,
Nelson CP,
Samani NJ,
Risch L,
Gyllensten U,
Melander O,
Riese H,
Wilson JF,
Campbell H,
Rich SS,
Psaty BM,
Lu Y,
Rotter JI,
Guo X,
Rice KM,
Vollenweider P,
Sundström J,
Langenberg C,
Tobin MD,
Giedraitis V,
Luan J,
Tuomilehto J,
Kutalik Z,
Ripatti S,
Salomaa V,
Girotto G,
Trompet S,
Jukema JW,
van der Harst P,
Ridker PM,
Giulianini F,
Vitart V,
Goel A,
Watkins H,
Harris SE,
Deary IJ,
van der Most PJ,
Oldehinkel AJ,
Keavney BD,
Hayward C,
Campbell A,
Boehnke M,
Scott LJ,
Boutin T,
Mamasoula C,
Järvelin MR,
Peters A,
Gieger C,
Lakatta EG,
Cucca F,
Hui J,
Knekt P,
Enroth S,
De Borst MH,
Polašek O,
Concas MP,
Catamo E,
Cocca M,
Li-Gao R,
Hofer E,
Schmidt H,
Spedicati B,
Waldenberger M,
Strachan DP,
Laan M,
Teumer A,
Dörr M,
Gudnason V,
Cook JP,
Ruggiero D,
Kolcic I,
Boerwinkle E,
Traglia M,
Lehtimäki T,
Raitakari OT,
Johnson AD,
Newton-Cheh C,
Brown MJ,
Dominiczak AF,
Sever PJ,
Poulter N,
Chambers JC,
Elosua R,
Siscovick D,
Esko T,
Metspalu A,
Strawbridge RJ,
Laakso M,
Hamsten A,
Hottenga JJ,
de Geus E,
Morris AD,
Palmer CNA,
Nolte IM,
Milaneschi Y,
Marten J,
Wright A,
Zeggini E,
Howson JMM,
O'Donnell CJ,
Spector T,
Nalls MA,
Simonsick EM,
Liu Y,
van Duijn CM,
Butterworth AS,
Danesh JN,
Menni C,
Wareham NJ,
Khaw KT,
Sun YV,
Wilson PWF,
Cho K,
Visscher PM,
Denny JC,
Levy D,
Edwards TL,
Munroe PB,
Snieder H,
Warren HR
Million Veteran Program · Lifelines Cohort Study and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Okbay A,
Baselmans BM,
De Neve JE,
Turley P,
Nivard MG,
Fontana MA,
Meddens SF,
Linnér RK,
Rietveld CA,
Derringer J,
Gratten J,
Lee JJ
and 180 more — show all
Liu JZ,
de Vlaming R,
Ahluwalia TS,
Buchwald J,
Cavadino A,
Frazier-Wood AC,
Furlotte NA,
Garfield V,
Geisel MH,
Gonzalez JR,
Haitjema S,
Karlsson R,
van der Laan SW,
Ladwig KH,
Lahti J,
van der Lee SJ,
Lind PA,
Liu T,
Matteson L,
Mihailov E,
Miller MB,
Minica CC,
Nolte IM,
Mook-Kanamori D,
van der Most PJ,
Oldmeadow C,
Qian Y,
Raitakari O,
Rawal R,
Realo A,
Rueedi R,
Schmidt B,
Smith AV,
Stergiakouli E,
Tanaka T,
Taylor K,
Thorleifsson G,
Wedenoja J,
Wellmann J,
Westra HJ,
Willems SM,
Zhao W,
Amin N,
Bakshi A,
Bergmann S,
Bjornsdottir G,
Boyle PA,
Cherney S,
Cox SR,
Davies G,
Davis OS,
Ding J,
Direk N,
Eibich P,
Eibich P,
Emeny RT,
Fatemifar G,
Faul JD,
Ferrucci L,
Ferrucci L,
Forstner AJ,
Gieger C,
Gupta R,
Harris TB,
Harris JM,
Holliday EG,
Hottenga JJ,
De Jager PL,
Kaakinen MA,
Kajantie E,
Karhunen V,
Kolcic I,
Kumari M,
Launer LJ,
Franke L,
Franke L,
Li-Gao R,
Liewald DC,
Koini M,
Loukola A,
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Hood MM,
Houghton SC,
Karvonen-Gutierrez CA,
Kawaguchi T,
Kilpeläinen TO,
Komulainen P,
Lin HJ,
Linchangco GV Jr,
Luik AI,
Ma J,
Meigs JB,
McCormick JB,
Menni C,
Nolte IM,
Norris JM,
Petty LE,
Polikowsky HG,
Raffield LM,
Rich SS,
Riha RL,
Russ TC,
Ruiz-Narvaez EA,
Sitlani CM,
Smith JA,
Snieder H,
Sofer T,
Shen B,
Tang J,
Taylor KD,
Teder-Laving M,
Triatin R,
Tsai MY,
Völzke H,
Westerman KE,
Xia R,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Zhu X,
Below JE,
Cox SR,
Evans M,
Fornage M,
Fox ER,
Franceschini N,
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Kelly T,
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Li C,
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Mägi R,
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Nauck M,
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Penninx BW,
Province MA,
Psaty BM,
Rotter JI,
Spector TD,
Wagenknecht LE,
van Dijk KW,
Jaquish CE,
Wilson PW,
Peyser PA,
Munroe PB,
de Vries PS,
Gauderman WJ,
Sun YV,
Chen H,
Miller CL,
Winkler TW,
Rao DC,
Redline S,
van Heemst D
Lifelines Cohort Study · Million Veteran Program
Atherosclerosis · 2026 · PMID 41325697
3 pages
A genome- and phenome-wide association study of plasma procalcitonin concentrations in individuals of European ancestry
Zhang W,
van der Most PJ,
Wang S,
Kamali Z,
Giontella A,
Enhörning S,
Gansevoort RT,
van der Harst P,
Bakker SJL,
Melander O,
Keus F,
Lunter G
and 1 more — show all
EBioMedicine · 2026 · PMID 41406505 · open access
3 pages
Meta-analysis of genome-wide association studies of anxiety disorders
Otowa T,
Hek K,
Lee M,
Byrne EM,
Mirza SS,
Nivard MG,
Bigdeli T,
Aggen SH,
Adkins D,
Wolen A,
Fanous A,
Keller MC
and 35 more — show all
Castelao E,
Kutalik Z,
Van der Auwera S,
Homuth G,
Nauck M,
Teumer A,
Milaneschi Y,
Hottenga JJ,
Direk N,
Hofman A,
Uitterlinden A,
Mulder CL,
Henders AK,
Medland SE,
Gordon S,
Heath AC,
Madden PA,
Pergadia ML,
van der Most PJ,
Nolte IM,
van Oort FV,
Hartman CA,
Oldehinkel AJ,
Preisig M,
Grabe HJ,
Middeldorp CM,
Penninx BW,
Boomsma D,
Martin NG,
Montgomery G,
Maher BS,
van den Oord EJ,
Wray NR,
Tiemeier H,
Hettema JM
Molecular psychiatry · 2016 · PMID 26754954 · open access
2 pages
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
van Leeuwen EM,
Sabo A,
Bis JC,
Huffman JE,
Manichaikul A,
Smith AV,
Feitosa MF,
Demissie S,
Joshi PK,
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van Klinken JB
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Surakka I,
Nolte IM,
Zhang W,
Mbarek H,
Li-Gao R,
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Verweij N,
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Lyytikäinen LP,
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Morrison A,
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LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
2 pages
Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci
Thio CHL,
Reznichenko A,
van der Most PJ,
Kamali Z,
Vaez A,
Smit JH,
Penninx BWJH,
Haller T,
Mihailov E,
Metspalu A,
Damman J,
de Borst MH
and 6 more — show all
Lifelines Cohort Study group
American journal of nephrology · 2019 · PMID 30808845
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.