For researchers
Is your paper here?
2,663 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.
40 matches for
Järvelin MR,
showing the first 20.
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
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
Nolte IM,
Munoz ML,
Tragante V,
Amare AT,
Jansen R,
Vaez A,
von der Heyde B,
Avery CL,
Bis JC,
Dierckx B,
van Dongen J,
Gogarten SM
and 153 more — show all
Goyette P,
Hernesniemi J,
Huikari V,
Hwang SJ,
Jaju D,
Kerr KF,
Kluttig A,
Krijthe BP,
Kumar J,
van der Laan SW,
Lyytikäinen LP,
Maihofer AX,
Minassian A,
van der Most PJ,
Müller-Nurasyid M,
Nivard M,
Salvi E,
Stewart JD,
Thayer JF,
Verweij N,
Wong A,
Zabaneh D,
Zafarmand MH,
Abdellaoui A,
Albarwani S,
Albert C,
Alonso A,
Ashar F,
Auvinen J,
Axelsson T,
Baker DG,
de Bakker PIW,
Barcella M,
Bayoumi R,
Bieringa RJ,
Boomsma D,
Boucher G,
Britton AR,
Christophersen I,
Dietrich A,
Ehret GB,
Ellinor PT,
Eskola M,
Felix JF,
Floras JS,
Franco OH,
Friberg P,
Gademan MGJ,
Geyer MA,
Giedraitis V,
Hartman CA,
Hemerich D,
Hofman A,
Hottenga JJ,
Huikuri H,
Hutri-Kähönen N,
Jouven X,
Junttila J,
Juonala M,
Kiviniemi AM,
Kors JA,
Kumari M,
Kuznetsova T,
Kuznetsova T,
Laurie CC,
Lefrandt JD,
Li Y,
Li Y,
Liao D,
Limacher MC,
Lin HJ,
Lindgren CM,
Lubitz SA,
Mahajan A,
McKnight B,
Zu Schwabedissen HM,
Milaneschi Y,
Mononen N,
Morris AP,
Nalls MA,
Navis G,
Neijts M,
Nikus K,
North KE,
O'Connor DT,
Ormel J,
Perz S,
Peters A,
Psaty BM,
Raitakari OT,
Risbrough VB,
Sinner MF,
Siscovick D,
Smit JH,
Smith NL,
Soliman EZ,
Sotoodehnia N,
Staessen JA,
Stein PK,
Stilp AM,
Stolarz-Skrzypek K,
Strauch K,
Sundström J,
Swenne CA,
Syvänen AC,
Tardif JC,
Taylor KD,
Teumer A,
Thornton TA,
Tinker LE,
Uitterlinden AG,
van Setten J,
Voss A,
Waldenberger M,
Wilhelmsen KC,
Willemsen G,
Wong Q,
Zhang ZM,
Zonderman AB,
Cusi D,
Evans MK,
Greiser HK,
van der Harst P,
Hassan M,
Ingelsson E,
Järvelin MR,
Kääb S,
Kähönen M,
Kivimaki M,
Kooperberg C,
Kuh D,
Lehtimäki T,
Lind L,
Nievergelt CM,
O'Donnell CJ,
Oldehinkel AJ,
Penninx B,
Reiner AP,
Riese H,
van Roon AM,
Rioux JD,
Rotter JI,
Sofer T,
Stricker BH,
Tiemeier H,
Vrijkotte TGM,
Asselbergs FW,
Brundel BJJM,
Heckbert SR,
Whitsel EA,
den Hoed M,
Snieder H,
de Geus EJC
Nature communications · 2017 · PMID 28613276 · open access
6 pages
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret GB,
Munroe PB,
Rice KM,
Bochud M,
Johnson AD,
Chasman DI,
Smith AV,
Tobin MD,
Verwoert GC,
Hwang SJ,
Pihur V,
Vollenweider P
and 336 more — show all
O'Reilly PF,
Amin N,
Bragg-Gresham JL,
Teumer A,
Glazer NL,
Launer L,
Zhao JH,
Aulchenko Y,
Heath S,
Sõber S,
Parsa A,
Luan J,
Arora P,
Dehghan A,
Zhang F,
Lucas G,
Hicks AA,
Jackson AU,
Peden JF,
Tanaka T,
Wild SH,
Rudan I,
Igl W,
Milaneschi Y,
Parker AN,
Fava C,
Chambers JC,
Fox ER,
Kumari M,
Go MJ,
van der Harst P,
Kao WH,
Sjögren M,
Vinay DG,
Alexander M,
Tabara Y,
Shaw-Hawkins S,
Whincup PH,
Liu Y,
Shi G,
Kuusisto J,
Tayo B,
Seielstad M,
Sim X,
Nguyen KD,
Lehtimäki T,
Matullo G,
Wu Y,
Gaunt TR,
Onland-Moret NC,
Cooper MN,
Platou CG,
Org E,
Org E,
Hardy R,
Dahgam S,
Palmen J,
Vitart V,
Braund PS,
Kuznetsova T,
Kuznetsova T,
Uiterwaal CS,
Adeyemo A,
Palmas W,
Campbell H,
Ludwig B,
Tomaszewski M,
Tzoulaki I,
Palmer ND,
Aspelund T,
Garcia M,
Chang YP,
O'Connell JR,
Steinle NI,
Grobbee DE,
Arking DE,
Kardia SL,
Morrison AC,
Hernandez D,
Najjar S,
McArdle WL,
Hadley D,
Brown MJ,
Connell JM,
Hingorani AD,
Day IN,
Lawlor DA,
Beilby JP,
Lawrence RW,
Clarke R,
Hopewell JC,
Ongen H,
Dreisbach AW,
Li Y,
Young JH,
Bis JC,
Kähönen M,
Viikari J,
Adair LS,
Lee NR,
Chen MH,
Olden M,
Pattaro C,
Bolton JA,
Köttgen A,
Bergmann S,
Mooser V,
Chaturvedi N,
Frayling TM,
Islam M,
Jafar TH,
Erdmann J,
Kulkarni SR,
Bornstein SR,
Grässler J,
Groop L,
Voight BF,
Kettunen J,
Howard P,
Taylor A,
Guarrera S,
Ricceri F,
Emilsson V,
Plump A,
Barroso I,
Khaw KT,
Weder AB,
Hunt SC,
Sun YV,
Bergman RN,
Collins FS,
Bonnycastle LL,
Scott LJ,
Stringham HM,
Peltonen L,
Perola M,
Vartiainen E,
Brand SM,
Staessen JA,
Wang TJ,
Burton PR,
Soler Artigas M,
Dong Y,
Snieder H,
Wang X,
Zhu H,
Lohman KK,
Rudock ME,
Heckbert SR,
Smith NL,
Wiggins KL,
Doumatey A,
Shriner D,
Veldre G,
Viigimaa M,
Kinra S,
Prabhakaran D,
Tripathy V,
Langefeld CD,
Rosengren A,
Thelle DS,
Corsi AM,
Singleton A,
Forrester T,
Hilton G,
McKenzie CA,
Salako T,
Iwai N,
Kita Y,
Ogihara T,
Ohkubo T,
Okamura T,
Ueshima H,
Umemura S,
Eyheramendy S,
Meitinger T,
Wichmann HE,
Cho YS,
Kim HL,
Lee JY,
Scott J,
Sehmi JS,
Zhang W,
Hedblad B,
Nilsson P,
Smith GD,
Wong A,
Narisu N,
Stančáková A,
Raffel LJ,
Yao J,
Kathiresan S,
O'Donnell CJ,
Schwartz SM,
Ikram MA,
Longstreth WT Jr,
Mosley TH,
Seshadri S,
Shrine NR,
Wain LV,
Morken MA,
Swift AJ,
Laitinen J,
Prokopenko I,
Zitting P,
Cooper JA,
Humphries SE,
Danesh J,
Rasheed A,
Goel A,
Hamsten A,
Watkins H,
Bakker SJ,
van Gilst WH,
Janipalli CS,
Mani KR,
Yajnik CS,
Hofman A,
Mattace-Raso FU,
Oostra BA,
Demirkan A,
Isaacs A,
Rivadeneira F,
Lakatta EG,
Orru M,
Scuteri A,
Ala-Korpela M,
Kangas AJ,
Lyytikäinen LP,
Soininen P,
Tukiainen T,
Würtz P,
Ong RT,
Dörr M,
Kroemer HK,
Völker U,
Völzke H,
Galan P,
Hercberg S,
Lathrop M,
Zelenika D,
Deloukas P,
Mangino M,
Spector TD,
Zhai G,
Meschia JF,
Nalls MA,
Sharma P,
Terzic J,
Kumar MV,
Denniff M,
Zukowska-Szczechowska E,
Wagenknecht LE,
Fowkes FG,
Charchar FJ,
Schwarz PE,
Hayward C,
Guo X,
Rotimi C,
Bots ML,
Brand E,
Samani NJ,
Polasek O,
Talmud PJ,
Nyberg F,
Kuh D,
Laan M,
Hveem K,
Palmer LJ,
van der Schouw YT,
Casas JP,
Mohlke KL,
Vineis P,
Raitakari O,
Ganesh SK,
Wong TY,
Tai ES,
Cooper RS,
Laakso M,
Rao DC,
Harris TB,
Morris RW,
Dominiczak AF,
Kivimaki M,
Marmot MG,
Miki T,
Saleheen D,
Chandak GR,
Coresh J,
Navis G,
Salomaa V,
Han BG,
Zhu X,
Kooner JS,
Melander O,
Ridker PM,
Bandinelli S,
Gyllensten UB,
Wright AF,
Wilson JF,
Ferrucci L,
Farrall M,
Tuomilehto J,
Pramstaller PP,
Elosua R,
Soranzo N,
Sijbrands EJ,
Altshuler D,
Loos RJ,
Shuldiner AR,
Gieger C,
Meneton P,
Uitterlinden AG,
Wareham NJ,
Gudnason V,
Rotter JI,
Rettig R,
Uda M,
Strachan DP,
Witteman JC,
Hartikainen AL,
Beckmann JS,
Boerwinkle E,
Vasan RS,
Boehnke M,
Larson MG,
Järvelin MR,
Psaty BM,
Abecasis GR,
Chakravarti A,
Elliott P,
van Duijn CM,
Newton-Cheh C,
Levy D,
Caulfield MJ,
Johnson T
International Consortium for Blood Pressure Genome-Wide Association Studies · CARDIoGRAM consortium and 4 more consortia
Nature · 2011 · PMID 21909115 · open access
5 pages
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease
Jia Q,
Han Y,
Huang P,
Woodward NC,
Gukasyan J,
Kettunen J,
Ala-Korpela M,
Anufrieva O,
Wang Q,
Perola M,
Raitakari O,
Lehtimäki T
and 11 more — show all
Viikari J,
Järvelin MR,
Boehnke M,
Laakso M,
Mohlke KL,
Fiehn O,
Wang Z,
Tang WHW,
Hazen SL,
Hartiala JA,
Allayee H
Journal of the American Heart Association · 2019 · PMID 31070104 · open access
5 pages
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity
Bradfield JP,
Vogelezang S,
Felix JF,
Chesi A,
Helgeland Ø,
Horikoshi M,
Karhunen V,
Lowry E,
Cousminer DL,
Ahluwalia TS,
Thiering E,
Boh ET
and 87 more — show all
Zafarmand MH,
Vilor-Tejedor N,
Wang CA,
Joro R,
Chen Z,
Gauderman WJ,
Pitkänen N,
Parra EJ,
Fernandez-Rhodes L,
Alyass A,
Monnereau C,
Curtin JA,
Have CT,
McCormack SE,
Hollensted M,
Frithioff-Bøjsøe C,
Valladares-Salgado A,
Peralta-Romero J,
Teo YY,
Standl M,
Leinonen JT,
Holm JC,
Peters T,
Vioque J,
Vrijheid M,
Simpson A,
Custovic A,
Vaudel M,
Canouil M,
Lindi V,
Atalay M,
Kähönen M,
Raitakari OT,
van Schaik BDC,
Berkowitz RI,
Cole SA,
Voruganti VS,
Wang Y,
Highland HM,
Comuzzie AG,
Butte NF,
Justice AE,
Gahagan S,
Blanco E,
Lehtimäki T,
Lakka TA,
Hebebrand J,
Bonnefond A,
Grarup N,
Froguel P,
Lyytikäinen LP,
Cruz M,
Kobes S,
Hanson RL,
Zemel BS,
Hinney A,
Teo KK,
Meyre D,
North KE,
Gilliland FD,
Bisgaard H,
Bustamante M,
Bonnelykke K,
Pennell CE,
Rivadeneira F,
Uitterlinden AG,
Baier LJ,
Vrijkotte TGM,
Heinrich J,
Sørensen TIA,
Saw SM,
Pedersen O,
Hansen T,
Eriksson J,
Widén E,
McCarthy MI,
Njølstad PR,
Power C,
Hyppönen E,
Sebert S,
Brown CD,
Järvelin MR,
Timpson NJ,
Johansson S,
Hakonarson H,
Jaddoe VWV,
Grant SFA
Early Growth Genetics Consortium
Human molecular genetics · 2019 · PMID 31504550
5 pages
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
Willems SM,
Ng NHJ,
Fernandez J,
Fine RS,
Wheeler E,
Wessel J,
Kitajima H,
Marenne G,
Sim X,
Yaghootkar H,
Wang S,
Chen S
and 228 more — show all
Chen Y,
Chen YI,
Grarup N,
Li-Gao R,
Varga TV,
Asimit JL,
Feng S,
Strawbridge RJ,
Kleinbrink EL,
Ahluwalia TS,
An P,
Appel EV,
Arking DE,
Auvinen J,
Bielak LF,
Bihlmeyer NA,
Bork-Jensen J,
Brody JA,
Campbell A,
Chu AY,
Davies G,
Demirkan A,
Floyd JS,
Giulianini F,
Guo X,
Gustafsson S,
Jackson AU,
Jakobsdottir J,
Järvelin MR,
Jensen RA,
Kanoni S,
Keinanen-Kiukaanniemi S,
Li M,
Lu Y,
Luan J,
Manning AK,
Marten J,
Meidtner K,
Mook-Kanamori DO,
Muka T,
Pistis G,
Prins B,
Rice KM,
Sanna S,
Smith AV,
Smith JA,
Southam L,
Stringham HM,
Tragante V,
van der Laan SW,
Warren HR,
Yao J,
Yiorkas AM,
Zhang W,
Zhao W,
Graff M,
Highland HM,
Justice AE,
Marouli E,
Medina-Gomez C,
Afaq S,
Alhejily WA,
Amin N,
Asselbergs FW,
Bonnycastle LL,
Bots ML,
Brandslund I,
Chen J,
Danesh J,
de Mutsert R,
Dehghan A,
Ebeling T,
Elliott P,
Farmaki AE,
Faul JD,
Franks PW,
Franks S,
Fritsche A,
Gjesing AP,
Goodarzi MO,
Gudnason V,
Hallmans G,
Harris TB,
Herzig KH,
Hivert MF,
Jørgensen T,
Jørgensen ME,
Jousilahti P,
Kajantie E,
Karaleftheri M,
Kardia SLR,
Kinnunen L,
Koistinen HA,
Komulainen P,
Kovacs P,
Kuusisto J,
Laakso M,
Lange LA,
Launer LJ,
Leong A,
Lindström J,
Manning Fox JE,
Männistö S,
Maruthur NM,
Moilanen L,
Mulas A,
Nalls MA,
Neville M,
Pankow JS,
Pattie A,
Petersen ERB,
Puolijoki H,
Rasheed A,
Redmond P,
Renström F,
Roden M,
Saleheen D,
Saltevo J,
Savonen K,
Sebert S,
Skaaby T,
Small KS,
Stančáková A,
Stokholm J,
Strauch K,
Tai ES,
Taylor KD,
Thuesen BH,
Tönjes A,
Tsafantakis E,
Tuomi T,
Tuomilehto J,
Uusitupa M,
Vääräsmäki M,
Vaartjes I,
Zoledziewska M,
Abecasis G,
Balkau B,
Bisgaard H,
Blakemore AI,
Blüher M,
Boeing H,
Boerwinkle E,
Bønnelykke K,
Bottinger EP,
Caulfield MJ,
Chambers JC,
Chasman DI,
Cheng CY,
Collins FS,
Coresh J,
Cucca F,
de Borst GJ,
Deary IJ,
Dedoussis G,
Deloukas P,
den Ruijter HM,
Dupuis J,
Evans MK,
Ferrannini E,
Franco OH,
Grallert H,
Hansen T,
Hattersley AT,
Hayward C,
Hirschhorn JN,
Ikram A,
Ingelsson E,
Karpe F,
Kaw KT,
Kiess W,
Kooner JS,
Körner A,
Lakka T,
Langenberg C,
Lind L,
Lindgren CM,
Linneberg A,
Lipovich L,
Liu CT,
Liu J,
Liu Y,
Loos RJF,
MacDonald PE,
Mohlke KL,
Morris AD,
Munroe PB,
Murray A,
Padmanabhan S,
Palmer CNA,
Pasterkamp G,
Pedersen O,
Peyser PA,
Polasek O,
Porteous D,
Province MA,
Psaty BM,
Rauramaa R,
Ridker PM,
Rolandsson O,
Rorsman P,
Rosendaal FR,
Rudan I,
Salomaa V,
Schulze MB,
Sladek R,
Smith BH,
Spector TD,
Starr JM,
Stumvoll M,
van Duijn CM,
Walker M,
Wareham NJ,
Weir DR,
Wilson JG,
Wong TY,
Zeggini E,
Zonderman AB,
Rotter JI,
Morris AP,
Boehnke M,
Florez JC,
McCarthy MI,
Meigs JB,
Mahajan A,
Scott RA,
Gloyn AL,
Barroso I
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
5 pages
Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects
Brito Nunes C,
Rukins V,
Cisse AH,
White F,
McBride N,
Kuang A,
Allard C,
Ronkainen J,
Hughes A,
Elliott A,
Thorleifsson G,
Vaudel M
and 67 more — show all
Laisk T,
Gu Y,
Lamri A,
Chen L,
Tuhkanen J,
Lahti J,
Calas L,
Muntaner M,
Karhunen V,
Choi J,
Heiskala A,
Hatem G,
Fragoso-Bargas N,
Rifas-Shiman SL,
Paz-Lopez G,
Stinson SE,
Bhowmik B,
Ahlqvist E,
Deleuze JF,
Eriksson JG,
Park J,
Teo K,
Räikkönen K,
Stefansson K,
Molina-Vega M,
Subbarao P,
Beaumont RN,
Johansson S,
Tuomi T,
Hansen T,
Engelbrechtsen L,
Morcillo S,
Oken E,
Quigstad E,
Birkeland KI,
Vääräsmäki M,
Hattersley AT,
Sebert S,
Hitman GA,
Kwak SH,
Järvelin MR,
Prasad RB,
Heude B,
Meirhaeghe A,
Bouchard L,
Jacques PÉ,
Laivuori H,
Tan KH,
Anand SS,
van Heel DA,
Liu S,
Njølstad PR,
Steinthorsdottir V,
Widén E,
Keikkala E,
Scholtens DM,
Lowe WL,
Finer S,
Morris AP,
Mägi R,
Zöllner J,
Borges MC,
Lawlor DA,
Hivert MF,
Freathy RM,
Evans DM,
Moen GH
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2026 · PMID 42225636 · open access
5 pages
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
Soler Artigas M,
Loth DW,
Wain LV,
Gharib SA,
Obeidat M,
Tang W,
Zhai G,
Zhao JH,
Smith AV,
Huffman JE,
Albrecht E,
Jackson CM
and 158 more — show all
Evans DM,
Cadby G,
Fornage M,
Manichaikul A,
Lopez LM,
Johnson T,
Aldrich MC,
Aspelund T,
Barroso I,
Campbell H,
Cassano PA,
Couper DJ,
Eiriksdottir G,
Franceschini N,
Garcia M,
Gieger C,
Gislason GK,
Grkovic I,
Hammond CJ,
Hancock DB,
Harris TB,
Ramasamy A,
Heckbert SR,
Heliövaara M,
Homuth G,
Hysi PG,
James AL,
James AL,
Jankovic S,
Joubert BR,
Karrasch S,
Klopp N,
Koch B,
Kritchevsky SB,
Launer LJ,
Liu Y,
Loehr LR,
Lohman K,
Loos RJ,
Lumley T,
Al Balushi KA,
Ang WQ,
Barr RG,
Beilby J,
Blakey JD,
Boban M,
Boraska V,
Brisman J,
Britton JR,
Brusselle GG,
Cooper C,
Curjuric I,
Dahgam S,
Deary IJ,
Ebrahim S,
Eijgelsheim M,
Francks C,
Gaysina D,
Granell R,
Gu X,
Hankinson JL,
Hardy R,
Harris SE,
Henderson J,
Henry A,
Hingorani AD,
Hofman A,
Holt PG,
Hui J,
Hunter ML,
Imboden M,
Jameson KA,
Kerr SM,
Kolcic I,
Kronenberg F,
Liu JZ,
Marchini J,
McKeever T,
Morris AD,
Olin AC,
Porteous DJ,
Postma DS,
Rich SS,
Ring SM,
Rivadeneira F,
Rochat T,
Sayer AA,
Sayers I,
Sly PD,
Smith GD,
Sood A,
Starr JM,
Uitterlinden AG,
Vonk JM,
Wannamethee SG,
Whincup PH,
Wijmenga C,
Williams OD,
Wong A,
Mangino M,
Marciante KD,
McArdle WL,
Meibohm B,
Morrison AC,
North KE,
Omenaas E,
Palmer LJ,
Pietiläinen KH,
Pin I,
Pola Sbreve Ek O,
Pouta A,
Psaty BM,
Hartikainen AL,
Rantanen T,
Ripatti S,
Rotter JI,
Rudan I,
Rudnicka AR,
Schulz H,
Shin SY,
Spector TD,
Surakka I,
Vitart V,
Völzke H,
Wareham NJ,
Warrington NM,
Wichmann HE,
Wild SH,
Wilk JB,
Wjst M,
Wright AF,
Zgaga L,
Zemunik T,
Pennell CE,
Nyberg F,
Kuh D,
Holloway JW,
Boezen HM,
Lawlor DA,
Morris RW,
Probst-Hensch N,
Kaprio J,
Wilson JF,
Hayward C,
Kähönen M,
Heinrich J,
Musk AW,
Jarvis DL,
Gläser S,
Järvelin MR,
Ch Stricker BH,
Elliott P,
O'Connor GT,
Strachan DP,
London SJ,
Hall IP,
Gudnason V,
Tobin MD
International Lung Cancer Consortium · GIANT consortium
Nature genetics · 2011 · PMID 21946350 · open access
4 pages
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns
Sliz E,
Kalaoja M,
Ahola-Olli A,
Raitakari O,
Perola M,
Salomaa V,
Lehtimäki T,
Karhu T,
Viinamäki H,
Salmi M,
Santalahti K,
Jalkanen S
and 7 more — show all
Journal of medical genetics · 2019 · PMID 31217265 · open access
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 influencing circulating lipid levels and risk of coronary artery disease
Waterworth DM,
Ricketts SL,
Song K,
Chen L,
Zhao JH,
Ripatti S,
Aulchenko YS,
Zhang W,
Yuan X,
Lim N,
Luan J,
Ashford S
and 54 more — show all
Wheeler E,
Young EH,
Hadley D,
Thompson JR,
Braund PS,
Johnson T,
Struchalin M,
Surakka I,
Luben R,
Khaw KT,
Rodwell SA,
Loos RJ,
Boekholdt SM,
Inouye M,
Deloukas P,
Elliott P,
Schlessinger D,
Sanna S,
Scuteri A,
Jackson A,
Mohlke KL,
Tuomilehto J,
Roberts R,
Stewart A,
Kesäniemi YA,
Mahley RW,
Grundy SM,
McArdle W,
Cardon L,
Waeber G,
Vollenweider P,
Chambers JC,
Boehnke M,
Abecasis GR,
Salomaa V,
Järvelin MR,
Ruokonen A,
Barroso I,
Epstein SE,
Hakonarson HH,
Rader DJ,
Reilly MP,
Witteman JC,
Hall AS,
Samani NJ,
Strachan DP,
Barter P,
van Duijn CM,
Kooner JS,
Peltonen L,
Wareham NJ,
McPherson R,
Mooser V,
Sandhu MS
Wellcome Trust Case Control Consortium
Arteriosclerosis, thrombosis, and vascular biology · 2010 · PMID 20864672
3 pages
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits
Kristiansson K,
Perola M,
Tikkanen E,
Kettunen J,
Surakka I,
Havulinna AS,
Stancáková A,
Barnes C,
Widen E,
Kajantie E,
Eriksson JG,
Viikari J
and 22 more — show all
Kähönen M,
Lehtimäki T,
Raitakari OT,
Hartikainen AL,
Ruokonen A,
Pouta A,
Jula A,
Kangas AJ,
Soininen P,
Ala-Korpela M,
Männistö S,
Jousilahti P,
Bonnycastle LL,
Järvelin MR,
Kuusisto J,
Collins FS,
Laakso M,
Hurles ME,
Palotie A,
Peltonen L,
Ripatti S,
Salomaa V
Circulation. Cardiovascular genetics · 2012 · PMID 22399527
3 pages
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
Rietveld CA,
Medland SE,
Derringer J,
Yang J,
Esko T,
Martin NW,
Westra HJ,
Shakhbazov K,
Abdellaoui A,
Agrawal A,
Albrecht E,
Alizadeh BZ
and 191 more — show all
Amin N,
Barnard J,
Baumeister SE,
Benke KS,
Bielak LF,
Boatman JA,
Boyle PA,
Davies G,
de Leeuw C,
Eklund N,
Evans DS,
Ferhmann R,
Fischer K,
Gieger C,
Gjessing HK,
Hägg S,
Harris JR,
Hayward C,
Holzapfel C,
Ibrahim-Verbaas CA,
Ingelsson E,
Jacobsson B,
Joshi PK,
Jugessur A,
Kaakinen M,
Kanoni S,
Karjalainen J,
Kolcic I,
Kristiansson K,
Kutalik Z,
Lahti J,
Lee SH,
Lin P,
Lind PA,
Liu Y,
Lohman K,
Loitfelder M,
McMahon G,
Vidal PM,
Meirelles O,
Milani L,
Myhre R,
Nuotio ML,
Oldmeadow CJ,
Petrovic KE,
Peyrot WJ,
Polasek O,
Quaye L,
Reinmaa E,
Rice JP,
Rizzi TS,
Schmidt H,
Schmidt R,
Smith AV,
Smith JA,
Tanaka T,
Terracciano A,
van der Loos MJ,
Vitart V,
Völzke H,
Wellmann J,
Yu L,
Zhao W,
Allik J,
Attia JR,
Bandinelli S,
Bastardot F,
Beauchamp J,
Bennett DA,
Berger K,
Bierut LJ,
Boomsma DI,
Bültmann U,
Campbell H,
Chabris CF,
Cherkas L,
Chung MK,
Cucca F,
de Andrade M,
De Jager PL,
De Neve JE,
Deary IJ,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Eiríksdóttir G,
Elderson MF,
Eriksson JG,
Evans DM,
Faul JD,
Ferrucci L,
Garcia ME,
Grönberg H,
Guðnason V,
Hall P,
Harris JM,
Harris TB,
Hastie ND,
Heath AC,
Hernandez DG,
Hoffmann W,
Hofman A,
Holle R,
Holliday EG,
Hottenga JJ,
Iacono WG,
Illig T,
Järvelin MR,
Kähönen M,
Kaprio J,
Kirkpatrick RM,
Kowgier M,
Latvala A,
Launer LJ,
Lawlor DA,
Lehtimäki T,
Li J,
Lichtenstein P,
Lichtner P,
Liewald DC,
Madden PA,
Magnusson PK,
Mäkinen TE,
Masala M,
McGue M,
Metspalu A,
Mielck A,
Miller MB,
Montgomery GW,
Mukherjee S,
Nyholt DR,
Oostra BA,
Palmer LJ,
Palotie A,
Penninx BW,
Perola M,
Peyser PA,
Preisig M,
Räikkönen K,
Raitakari OT,
Realo A,
Ring SM,
Ripatti S,
Rivadeneira F,
Rudan I,
Rustichini A,
Salomaa V,
Sarin AP,
Schlessinger D,
Scott RJ,
Snieder H,
St Pourcain B,
Starr JM,
Sul JH,
Surakka I,
Svento R,
Teumer A,
Tiemeier H,
van Rooij FJ,
Van Wagoner DR,
Vartiainen E,
Viikari J,
Vollenweider P,
Vonk JM,
Waeber G,
Weir DR,
Wichmann HE,
Widen E,
Willemsen G,
Wilson JF,
Wright AF,
Conley D,
Davey-Smith G,
Franke L,
Groenen PJ,
Hofman A,
Johannesson M,
Kardia SL,
Krueger RF,
Laibson D,
Martin NG,
Meyer MN,
Posthuma D,
Thurik AR,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Kettunen J,
Demirkan A,
Würtz P,
Draisma HH,
Haller T,
Rawal R,
Vaarhorst A,
Kangas AJ,
Lyytikäinen LP,
Pirinen M,
Pool R,
Sarin AP
and 38 more — show all
Soininen P,
Tukiainen T,
Wang Q,
Tiainen M,
Tynkkynen T,
Amin N,
Zeller T,
Beekman M,
Deelen J,
van Dijk KW,
Esko T,
Hottenga JJ,
van Leeuwen EM,
Lehtimäki T,
Mihailov E,
Rose RJ,
de Craen AJ,
Gieger C,
Kähönen M,
Perola M,
Blankenberg S,
Savolainen MJ,
Verhoeven A,
Viikari J,
Willemsen G,
Boomsma DI,
van Duijn CM,
Eriksson J,
Jula A,
Järvelin MR,
Kaprio J,
Metspalu A,
Raitakari O,
Salomaa V,
Slagboom PE,
Waldenberger M,
Ripatti S,
Ala-Korpela M
Nature communications · 2016 · PMID 27005778 · open access
3 pages
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
Sabatti C,
Service SK,
Hartikainen AL,
Pouta A,
Ripatti S,
Brodsky J,
Jones CG,
Zaitlen NA,
Varilo T,
Kaakinen M,
Sovio U,
Ruokonen A
and 13 more — show all
Laitinen J,
Jakkula E,
Coin L,
Hoggart C,
Collins A,
Turunen H,
Gabriel S,
Elliot P,
McCarthy MI,
Daly MJ,
Järvelin MR,
Freimer NB,
Peltonen L
Nature genetics · 2009 · PMID 19060910
2 pages
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation
Coviello AD,
Haring R,
Wellons M,
Vaidya D,
Lehtimäki T,
Keildson S,
Lunetta KL,
He C,
Fornage M,
Lagou V,
Mangino M,
Onland-Moret NC
and 87 more — show all
Chen B,
Eriksson J,
Garcia M,
Liu YM,
Koster A,
Lohman K,
Lyytikäinen LP,
Petersen AK,
Prescott J,
Stolk L,
Vandenput L,
Wood AR,
Zhuang WV,
Ruokonen A,
Hartikainen AL,
Pouta A,
Bandinelli S,
Biffar R,
Brabant G,
Cox DG,
Chen Y,
Cummings S,
Ferrucci L,
Gunter MJ,
Hankinson SE,
Martikainen H,
Hofman A,
Homuth G,
Illig T,
Jansson JO,
Johnson AD,
Karasik D,
Karlsson M,
Kettunen J,
Kiel DP,
Kraft P,
Liu J,
Ljunggren Ö,
Lorentzon M,
Maggio M,
Markus MR,
Mellström D,
Miljkovic I,
Mirel D,
Nelson S,
Morin Papunen L,
Peeters PH,
Prokopenko I,
Raffel L,
Reincke M,
Reiner AP,
Rexrode K,
Rivadeneira F,
Schwartz SM,
Siscovick D,
Soranzo N,
Stöckl D,
Tworoger S,
Uitterlinden AG,
van Gils CH,
Vasan RS,
Wichmann HE,
Zhai G,
Bhasin S,
Bidlingmaier M,
Chanock SJ,
De Vivo I,
Harris TB,
Hunter DJ,
Kähönen M,
Liu S,
Ouyang P,
Spector TD,
van der Schouw YT,
Viikari J,
Wallaschofski H,
McCarthy MI,
Frayling TM,
Murray A,
Franks S,
Järvelin MR,
de Jong FH,
Raitakari O,
Teumer A,
Ohlsson C,
Murabito JM,
Perry JR
PLoS genetics · 2012 · PMID 22829776 · open access
2 pages
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Cornelis MC,
Byrne EM,
Esko T,
Nalls MA,
Ganna A,
Paynter N,
Monda KL,
Amin N,
Fischer K,
Renstrom F,
Ngwa JS,
Huikari V
and 142 more — show all
Cavadino A,
Nolte IM,
Teumer A,
Yu K,
Marques-Vidal P,
Rawal R,
Manichaikul A,
Wojczynski MK,
Vink JM,
Zhao JH,
Burlutsky G,
Lahti J,
Mikkilä V,
Lemaitre RN,
Eriksson J,
Musani SK,
Tanaka T,
Geller F,
Luan J,
Hui J,
Mägi R,
Dimitriou M,
Garcia ME,
Ho WK,
Wright MJ,
Rose LM,
Magnusson PK,
Pedersen NL,
Couper D,
Oostra BA,
Hofman A,
Ikram MA,
Tiemeier HW,
Uitterlinden AG,
van Rooij FJ,
Barroso I,
Johansson I,
Xue L,
Kaakinen M,
Milani L,
Power C,
Snieder H,
Stolk RP,
Baumeister SE,
Biffar R,
Gu F,
Bastardot F,
Kutalik Z,
Jacobs DR Jr,
Forouhi NG,
Mihailov E,
Lind L,
Lindgren C,
Michaëlsson K,
Morris A,
Jensen M,
Khaw KT,
Luben RN,
Wang JJ,
Männistö S,
Perälä MM,
Kähönen M,
Lehtimäki T,
Viikari J,
Mozaffarian D,
Mukamal K,
Psaty BM,
Döring A,
Heath AC,
Montgomery GW,
Dahmen N,
Carithers T,
Tucker KL,
Ferrucci L,
Boyd HA,
Melbye M,
Treur JL,
Mellström D,
Hottenga JJ,
Prokopenko I,
Tönjes A,
Deloukas P,
Kanoni S,
Lorentzon M,
Houston DK,
Liu Y,
Danesh J,
Rasheed A,
Mason MA,
Zonderman AB,
Franke L,
Kristal BS,
Karjalainen J,
Reed DR,
Westra HJ,
Evans MK,
Saleheen D,
Harris TB,
Dedoussis G,
Curhan G,
Stumvoll M,
Beilby J,
Pasquale LR,
Feenstra B,
Bandinelli S,
Ordovas JM,
Chan AT,
Peters U,
Ohlsson C,
Gieger C,
Martin NG,
Waldenberger M,
Siscovick DS,
Raitakari O,
Eriksson JG,
Mitchell P,
Hunter DJ,
Kraft P,
Rimm EB,
Boomsma DI,
Borecki IB,
Loos RJ,
Wareham NJ,
Vollenweider P,
Caporaso N,
Grabe HJ,
Neuhouser ML,
Wolffenbuttel BH,
Hu FB,
Hyppönen E,
Järvelin MR,
Cupples LA,
Franks PW,
Ridker PM,
van Duijn CM,
Heiss G,
Metspalu A,
North KE,
Ingelsson E,
Nettleton JA,
van Dam RM,
Chasman DI
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeirsson TE,
Gudbjartsson DF,
Surakka I,
Vink JM,
Amin N,
Geller F,
Sulem P,
Rafnar T,
Esko T,
Walter S,
Gieger C,
Rawal R
and 82 more — show all
Mangino M,
Prokopenko I,
Mägi R,
Keskitalo K,
Gudjonsdottir IH,
Gretarsdottir S,
Stefansson H,
Thompson JR,
Aulchenko YS,
Nelis M,
Aben KK,
den Heijer M,
Dirksen A,
Ashraf H,
Soranzo N,
Valdes AM,
Steves C,
Uitterlinden AG,
Hofman A,
Tönjes A,
Kovacs P,
Hottenga JJ,
Willemsen G,
Vogelzangs N,
Döring A,
Dahmen N,
Nitz B,
Pergadia ML,
Saez B,
De Diego V,
Lezcano V,
Garcia-Prats MD,
Ripatti S,
Perola M,
Kettunen J,
Hartikainen AL,
Pouta A,
Laitinen J,
Isohanni M,
Huei-Yi S,
Allen M,
Krestyaninova M,
Hall AS,
Jones GT,
van Rij AM,
Mueller T,
Dieplinger B,
Haltmayer M,
Jonsson S,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Kiemeney LA,
Mayordomo JI,
Lindholt JS,
Pedersen JH,
Franklin WA,
Wolf H,
Montgomery GW,
Heath AC,
Martin NG,
Madden PA,
Giegling I,
Rujescu D,
Järvelin MR,
Salomaa V,
Stumvoll M,
Spector TD,
Wichmann HE,
Metspalu A,
Samani NJ,
Penninx BW,
Oostra BA,
Boomsma DI,
Tiemeier H,
van Duijn CM,
Kaprio J,
Gulcher JR,
McCarthy MI,
Peltonen L,
Thorsteinsdottir U,
Stefansson K
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Day FR,
Thompson DJ,
Helgason H,
Chasman DI,
Finucane H,
Sulem P,
Ruth KS,
Whalen S,
Sarkar AK,
Albrecht E,
Altmaier E,
Amini M
and 204 more — show all
Barbieri CM,
Boutin T,
Campbell A,
Demerath E,
Giri A,
He C,
Hottenga JJ,
Karlsson R,
Kolcic I,
Loh PR,
Lunetta KL,
Mangino M,
Marco B,
McMahon G,
Medland SE,
Nolte IM,
Noordam R,
Nutile T,
Paternoster L,
Perjakova N,
Porcu E,
Rose LM,
Schraut KE,
Segrè AV,
Smith AV,
Stolk L,
Teumer A,
Andrulis IL,
Bandinelli S,
Beckmann MW,
Benitez J,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Brand JS,
Brauch H,
Brenner H,
Broer L,
Brüning T,
Buring JE,
Campbell H,
Catamo E,
Chanock S,
Chenevix-Trench G,
Corre T,
Couch FJ,
Cousminer DL,
Cox A,
Crisponi L,
Czene K,
Davey Smith G,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Dennis J,
Devilee P,
Dos-Santos-Silva I,
Dunning AM,
Eriksson JG,
Fasching PA,
Fernández-Rhodes L,
Ferrucci L,
Flesch-Janys D,
Franke L,
Gabrielson M,
Gandin I,
Giles GG,
Grallert H,
Gudbjartsson DF,
Guénel P,
Hall P,
Hallberg E,
Hamann U,
Harris TB,
Hartman CA,
Heiss G,
Hooning MJ,
Hopper JL,
Hu F,
Hunter DJ,
Ikram MA,
Im HK,
Järvelin MR,
Joshi PK,
Karasik D,
Kellis M,
Kutalik Z,
LaChance G,
Lambrechts D,
Langenberg C,
Launer LJ,
Laven JSE,
Lenarduzzi S,
Li J,
Lind PA,
Lindstrom S,
Liu Y,
Luan J,
Mägi R,
Mannermaa A,
Mbarek H,
McCarthy MI,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Michailidou K,
Milani L,
Milne RL,
Montgomery GW,
Mulligan AM,
Nalls MA,
Navarro P,
Nevanlinna H,
Nyholt DR,
Oldehinkel AJ,
O'Mara TA,
Padmanabhan S,
Palotie A,
Pedersen N,
Peters A,
Peto J,
Pharoah PDP,
Pouta A,
Radice P,
Rahman I,
Ring SM,
Robino A,
Rosendaal FR,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Schmidt MK,
Scott RA,
Shah M,
Sorice R,
Southey MC,
Sovio U,
Stampfer M,
Steri M,
Strauch K,
Tanaka T,
Tikkanen E,
Timpson NJ,
Traglia M,
Truong T,
Tyrer JP,
Uitterlinden AG,
Edwards DRV,
Vitart V,
Völker U,
Vollenweider P,
Wang Q,
Widen E,
van Dijk KW,
Willemsen G,
Winqvist R,
Wolffenbuttel BHR,
Zhao JH,
Zoledziewska M,
Zygmunt M,
Alizadeh BZ,
Boomsma DI,
Ciullo M,
Cucca F,
Esko T,
Franceschini N,
Gieger C,
Gudnason V,
Hayward C,
Kraft P,
Lawlor DA,
Magnusson PKE,
Martin NG,
Mook-Kanamori DO,
Nohr EA,
Polasek O,
Porteous D,
Price AL,
Ridker PM,
Snieder H,
Spector TD,
Stöckl D,
Toniolo D,
Ulivi S,
Visser JA,
Völzke H,
Wareham NJ,
Wilson JF,
Spurdle AB,
Thorsteindottir U,
Pollard KS,
Easton DF,
Tung JY,
Chang-Claude J,
Hinds D,
Murray A,
Murabito JM,
Stefansson K,
Ong KK,
Perry JRB
LifeLines Cohort Study · InterAct Consortium and 4 more consortia
Nature genetics · 2017 · PMID 28436984
1 page
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Beaumont RN,
Warrington NM,
Cavadino A,
Tyrrell J,
Nodzenski M,
Horikoshi M,
Geller F,
Myhre R,
Richmond RC,
Paternoster L,
Bradfield JP,
Kreiner-Møller E
and 74 more — show all
Huikari V,
Metrustry S,
Lunetta KL,
Painter JN,
Hottenga JJ,
Allard C,
Barton SJ,
Espinosa A,
Marsh JA,
Potter C,
Zhang G,
Ang W,
Berry DJ,
Bouchard L,
Das S,
Hakonarson H,
Heikkinen J,
Helgeland Ø,
Hocher B,
Hofman A,
Inskip HM,
Jones SE,
Kogevinas M,
Lind PA,
Marullo L,
Medland SE,
Murray A,
Murray JC,
Njølstad PR,
Nohr EA,
Reichetzeder C,
Ring SM,
Ruth KS,
Santa-Marina L,
Scholtens DM,
Sebert S,
Sengpiel V,
Tuke MA,
Vaudel M,
Weedon MN,
Willemsen G,
Wood AR,
Yaghootkar H,
Muglia LJ,
Bartels M,
Relton CL,
Pennell CE,
Chatzi L,
Estivill X,
Holloway JW,
Boomsma DI,
Montgomery GW,
Murabito JM,
Spector TD,
Power C,
Järvelin MR,
Bisgaard H,
Grant SFA,
Sørensen TIA,
Jaddoe VW,
Jacobsson B,
Melbye M,
McCarthy MI,
Hattersley AT,
Hayes MG,
Frayling TM,
Hivert MF,
Felix JF,
Hyppönen E,
Lowe WL Jr,
Evans DM,
Lawlor DA,
Feenstra B,
Freathy RM
Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
1 page
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.