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21 matches for
Tyrrell J,
showing the first 20.
Genome-wide associations for birth weight and correlations with adult disease
Horikoshi M,
Beaumont RN,
Day FR,
Warrington NM,
Kooijman MN,
Fernandez-Tajes J,
Feenstra B,
van Zuydam NR,
Gaulton KJ,
Grarup N,
Bradfield JP,
Strachan DP
and 157 more — show all
Li-Gao R,
Ahluwalia TS,
Kreiner E,
Rueedi R,
Lyytikäinen LP,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Hottenga JJ,
Vilor-Tejedor N,
Joshi PK,
Boh ETH,
Ntalla I,
Pitkänen N,
Mahajan A,
van Leeuwen EM,
Joro R,
Lagou V,
Nodzenski M,
Diver LA,
Zondervan KT,
Bustamante M,
Marques-Vidal P,
Mercader JM,
Bennett AJ,
Rahmioglu N,
Nyholt DR,
Ma RCW,
Tam CHT,
Tam WH,
Ganesh SK,
van Rooij FJ,
Jones SE,
Loh PR,
Ruth KS,
Tuke MA,
Tyrrell J,
Wood AR,
Yaghootkar H,
Scholtens DM,
Paternoster L,
Prokopenko I,
Kovacs P,
Atalay M,
Willems SM,
Panoutsopoulou K,
Wang X,
Carstensen L,
Geller F,
Schraut KE,
Murcia M,
van Beijsterveldt CE,
Willemsen G,
Appel EVR,
Fonvig CE,
Trier C,
Tiesler CM,
Standl M,
Kutalik Z,
Bonas-Guarch S,
Hougaard DM,
Sánchez F,
Torrents D,
Waage J,
Hollegaard MV,
de Haan HG,
Rosendaal FR,
Medina-Gomez C,
Ring SM,
Hemani G,
McMahon G,
Robertson NR,
Groves CJ,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Mentch FD,
MacKenzie SM,
Reynolds RM,
Lowe WL Jr,
Tönjes A,
Stumvoll M,
Lindi V,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Sørensen TI,
Niinikoski H,
Pahkala K,
Raitakari OT,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Melbye M,
Campbell H,
Wilson JF,
Vrijheid M,
de Geus EJ,
Boomsma DI,
Kadarmideen HN,
Holm JC,
Holm JC,
Hansen T,
Sebert S,
Hattersley AT,
Beilin LJ,
Newnham JP,
Newnham JP,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Kähönen M,
Viikari JS,
Lehtimäki T,
Vollenweider P,
Vollenweider P,
Bønnelykke K,
Bisgaard H,
Mook-Kanamori DO,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pisinger C,
Pisinger C,
Pedersen O,
Power C,
Hyppönen E,
Wareham NJ,
Hakonarson H,
Davies E,
Walker BR,
Jaddoe VW,
Jarvelin MR,
Grant SF,
Vaag AA,
Lawlor DA,
Frayling TM,
Frayling TM,
Davey Smith G,
Morris AP,
Ong KK,
Felix JF,
Timpson NJ,
Perry JR,
Evans DM,
McCarthy MI,
McCarthy MI,
Freathy RM
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
Justice AE,
Winkler TW,
Feitosa MF,
Graff M,
Fisher VA,
Young K,
Barata L,
Deng X,
Czajkowski J,
Hadley D,
Ngwa JS,
Ahluwalia TS
and 305 more — show all
Chu AY,
Heard-Costa NL,
Lim E,
Perez J,
Eicher JD,
Kutalik Z,
Xue L,
Mahajan A,
Renström F,
Wu J,
Qi Q,
Ahmad S,
Alfred T,
Amin N,
Bielak LF,
Bonnefond A,
Bragg J,
Cadby G,
Chittani M,
Coggeshall S,
Corre T,
Direk N,
Eriksson J,
Fischer K,
Gorski M,
Neergaard Harder M,
Horikoshi M,
Huang T,
Huffman JE,
Jackson AU,
Justesen JM,
Kanoni S,
Kinnunen L,
Kleber ME,
Komulainen P,
Kumari M,
Lim U,
Luan J,
Lyytikäinen LP,
Mangino M,
Manichaikul A,
Marten J,
Middelberg RPS,
Müller-Nurasyid M,
Navarro P,
Pérusse L,
Pervjakova N,
Sarti C,
Smith AV,
Smith JA,
Stančáková A,
Strawbridge RJ,
Stringham HM,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van der Most PJ,
Van Vliet-Ostaptchouk JV,
Vedantam SL,
Verweij N,
Vink JM,
Vitart V,
Wu Y,
Yengo L,
Zhang W,
Hua Zhao J,
Zimmermann ME,
Zubair N,
Abecasis GR,
Adair LS,
Afaq S,
Afzal U,
Bakker SJL,
Bartz TM,
Beilby J,
Bergman RN,
Bergmann S,
Biffar R,
Blangero J,
Boerwinkle E,
Bonnycastle LL,
Bottinger E,
Braga D,
Buckley BM,
Buyske S,
Campbell H,
Chambers JC,
Collins FS,
Curran JE,
de Borst GJ,
de Craen AJM,
de Geus EJC,
Dedoussis G,
Delgado GE,
den Ruijter HM,
Eiriksdottir G,
Eriksson AL,
Esko T,
Faul JD,
Ford I,
Forrester T,
Gertow K,
Gigante B,
Glorioso N,
Gong J,
Grallert H,
Grammer TB,
Grarup N,
Haitjema S,
Hallmans G,
Hamsten A,
Hansen T,
Harris TB,
Hartman CA,
Hassinen M,
Hastie ND,
Heath AC,
Hernandez D,
Hindorff L,
Hocking LJ,
Hollensted M,
Holmen OL,
Homuth G,
Jan Hottenga J,
Huang J,
Hung J,
Hutri-Kähönen N,
Ingelsson E,
James AL,
Jansson JO,
Jarvelin MR,
Jhun MA,
Jørgensen ME,
Juonala M,
Kähönen M,
Karlsson M,
Koistinen HA,
Kolcic I,
Kolovou G,
Kooperberg C,
Krämer BK,
Kuusisto J,
Kvaløy K,
Lakka TA,
Langenberg C,
Launer LJ,
Leander K,
Lee NR,
Lind L,
Lindgren CM,
Linneberg A,
Lobbens S,
Loh M,
Lorentzon M,
Luben R,
Lubke G,
Ludolph-Donislawski A,
Lupoli S,
Madden PAF,
Männikkö R,
Marques-Vidal P,
Martin NG,
McKenzie CA,
McKnight B,
Mellström D,
Menni C,
Montgomery GW,
Musk AB,
Narisu N,
Nauck M,
Nolte IM,
Oldehinkel AJ,
Olden M,
Ong KK,
Padmanabhan S,
Peyser PA,
Pisinger C,
Porteous DJ,
Raitakari OT,
Rankinen T,
Rao DC,
Rasmussen-Torvik LJ,
Rawal R,
Rice T,
Ridker PM,
Rose LM,
Bien SA,
Rudan I,
Sanna S,
Sarzynski MA,
Sattar N,
Savonen K,
Schlessinger D,
Scholtens S,
Schurmann C,
Scott RA,
Sennblad B,
Siemelink MA,
Silbernagel G,
Slagboom PE,
Snieder H,
Staessen JA,
Stott DJ,
Swertz MA,
Swift AJ,
Taylor KD,
Tayo BO,
Thorand B,
Thuillier D,
Tuomilehto J,
Uitterlinden AG,
Vandenput L,
Vohl MC,
Völzke H,
Vonk JM,
Waeber G,
Waldenberger M,
Westendorp RGJ,
Wild S,
Willemsen G,
Wolffenbuttel BHR,
Wong A,
Wright AF,
Zhao W,
Zillikens MC,
Baldassarre D,
Balkau B,
Bandinelli S,
Böger CA,
Boomsma DI,
Bouchard C,
Bruinenberg M,
Chasman DI,
Chen YD,
Chines PS,
Cooper RS,
Cucca F,
Cusi D,
Faire U,
Ferrucci L,
Franks PW,
Froguel P,
Gordon-Larsen P,
Grabe HJ,
Gudnason V,
Haiman CA,
Hayward C,
Hveem K,
Johnson AD,
Wouter Jukema J,
Kardia SLR,
Kivimaki M,
Kooner JS,
Kuh D,
Laakso M,
Lehtimäki T,
Marchand LL,
März W,
McCarthy MI,
Metspalu A,
Morris AP,
Ohlsson C,
Palmer LJ,
Pasterkamp G,
Pedersen O,
Peters A,
Peters U,
Polasek O,
Psaty BM,
Qi L,
Rauramaa R,
Smith BH,
Sørensen TIA,
Strauch K,
Tiemeier H,
Tremoli E,
van der Harst P,
Vestergaard H,
Vollenweider P,
Wareham NJ,
Weir DR,
Whitfield JB,
Wilson JF,
Tyrrell J,
Frayling TM,
Barroso I,
Boehnke M,
Deloukas P,
Fox CS,
Hirschhorn JN,
Hunter DJ,
Spector TD,
Strachan DP,
van Duijn CM,
Heid IM,
Mohlke KL,
Marchini J,
Loos RJF,
Kilpeläinen TO,
Liu CT,
Borecki IB,
North KE,
Cupples LA
Nature communications · 2017 · PMID 28443625 · open access
12 pages+
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers
Pilling LC,
Atkins JL,
Duff MO,
Beaumont RN,
Jones SE,
Tyrrell J,
Kuo CL,
Ruth KS,
Tuke MA,
Yaghootkar H,
Wood AR,
Murray A
and 6 more — show all
PloS one · 2017 · PMID 28957414 · open access
12 pages+
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry
Pulit SL,
Stoneman C,
Morris AP,
Wood AR,
Glastonbury CA,
Tyrrell J,
Yengo L,
Ferreira T,
Marouli E,
Ji Y,
Yang J,
Jones S
and 10 more — show all
GIANT Consortium
Human molecular genetics · 2019 · PMID 30239722 · open access
12 pages+
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms
Jones SE,
Lane JM,
Wood AR,
van Hees VT,
Tyrrell J,
Beaumont RN,
Jeffries AR,
Dashti HS,
Hillsdon M,
Ruth KS,
Tuke MA,
Yaghootkar H
and 20 more — show all
Sharp SA,
Jie Y,
Thompson WD,
Harrison JW,
Dawes A,
Byrne EM,
Tiemeier H,
Allebrandt KV,
Bowden J,
Ray DW,
Freathy RM,
Murray A,
Mazzotti DR,
Gehrman PR,
Lawlor DA,
Frayling TM,
Rutter MK,
Hinds DA,
Saxena R,
Weedon MN
Nature communications · 2019 · PMID 30696823 · open access
12 pages+
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates
Dashti HS,
Jones SE,
Wood AR,
Lane JM,
van Hees VT,
Wang H,
Rhodes JA,
Song Y,
Patel K,
Anderson SG,
Beaumont RN,
Bechtold DA
and 20 more — show all
Bowden J,
Cade BE,
Garaulet M,
Kyle SD,
Little MA,
Loudon AS,
Luik AI,
Scheer FAJL,
Spiegelhalder K,
Tyrrell J,
Gottlieb DJ,
Tiemeier H,
Ray DW,
Purcell SM,
Frayling TM,
Redline S,
Lawlor DA,
Rutter MK,
Weedon MN,
Saxena R
Nature communications · 2019 · PMID 30846698 · open access
12 pages+
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Warrington NM,
Beaumont RN,
Horikoshi M,
Day FR,
Helgeland Ø,
Laurin C,
Bacelis J,
Peng S,
Hao K,
Feenstra B,
Wood AR,
Mahajan A
and 196 more — show all
Tyrrell J,
Robertson NR,
Rayner NW,
Qiao Z,
Moen GH,
Vaudel M,
Marsit CJ,
Chen J,
Nodzenski M,
Schnurr TM,
Zafarmand MH,
Bradfield JP,
Grarup N,
Kooijman MN,
Li-Gao R,
Geller F,
Ahluwalia TS,
Paternoster L,
Rueedi R,
Huikari V,
Hottenga JJ,
Lyytikäinen LP,
Cavadino A,
Metrustry S,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Vilor-Tejedor N,
Joshi PK,
Painter JN,
Ntalla I,
Myhre R,
Pitkänen N,
van Leeuwen EM,
Joro R,
Lagou V,
Richmond RC,
Espinosa A,
Barton SJ,
Inskip HM,
Holloway JW,
Santa-Marina L,
Estivill X,
Ang W,
Marsh JA,
Reichetzeder C,
Marullo L,
Hocher B,
Lunetta KL,
Murabito JM,
Relton CL,
Kogevinas M,
Chatzi L,
Allard C,
Bouchard L,
Hivert MF,
Zhang G,
Muglia LJ,
Heikkinen J,
Morgen CS,
van Kampen AHC,
van Schaik BDC,
Mentch FD,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Hemani G,
Ring SM,
Bennett AJ,
Gaulton KJ,
Fernandez-Tajes J,
van Zuydam NR,
Medina-Gomez C,
de Haan HG,
Rosendaal FR,
Kutalik Z,
Marques-Vidal P,
Das S,
Willemsen G,
Mbarek H,
Müller-Nurasyid M,
Standl M,
Appel EVR,
Fonvig CE,
Trier C,
van Beijsterveldt CEM,
Murcia M,
Bustamante M,
Bonas-Guarch S,
Hougaard DM,
Mercader JM,
Linneberg A,
Schraut KE,
Lind PA,
Medland SE,
Shields BM,
Knight BA,
Chai JF,
Panoutsopoulou K,
Bartels M,
Sánchez F,
Stokholm J,
Torrents D,
Vinding RK,
Willems SM,
Atalay M,
Chawes BL,
Kovacs P,
Prokopenko I,
Tuke MA,
Yaghootkar H,
Ruth KS,
Jones SE,
Loh PR,
Murray A,
Weedon MN,
Tönjes A,
Stumvoll M,
Michaelsen KF,
Eloranta AM,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Niinikoski H,
Pahkala K,
Raitakari OT,
Jacobsson B,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Montgomery GW,
Campbell H,
Wilson JF,
Vrijkotte TGM,
Vrijheid M,
de Geus EJCN,
Hayes MG,
Kadarmideen HN,
Holm JC,
Beilin LJ,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Hattersley AT,
Spector TD,
Kähönen M,
Viikari JS,
Lehtimäki T,
Boomsma DI,
Sebert S,
Vollenweider P,
Sørensen TIA,
Bisgaard H,
Bønnelykke K,
Murray JC,
Melbye M,
Nohr EA,
Mook-Kanamori DO,
Rivadeneira F,
Hofman A,
Felix JF,
Jaddoe VWV,
Hansen T,
Pisinger C,
Vaag AA,
Pedersen O,
Uitterlinden AG,
Järvelin MR,
Power C,
Hyppönen E,
Scholtens DM,
Lowe WL Jr,
Davey Smith G,
Timpson NJ,
Morris AP,
Wareham NJ,
Hakonarson H,
Grant SFA,
Frayling TM,
Lawlor DA,
Njølstad PR,
Johansson S,
Ong KK,
McCarthy MI,
Perry JRB,
Evans DM,
Freathy RM
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
Using human genetics to understand the disease impacts of testosterone in men and women
Ruth KS,
Day FR,
Tyrrell J,
Thompson DJ,
Wood AR,
Mahajan A,
Beaumont RN,
Wittemans L,
Martin S,
Busch AS,
Erzurumluoglu AM,
Hollis B
and 10 more — show all
Endometrial Cancer Association Consortium
Nature medicine · 2020 · PMID 32042192 · open access
12 pages+
Genetic Evidence for Different Adiposity Phenotypes and Their Opposing Influences on Ectopic Fat and Risk of Cardiometabolic Disease
Martin S,
Cule M,
Basty N,
Tyrrell J,
Beaumont RN,
Wood AR,
Frayling TM,
Sorokin E,
Whitcher B,
Liu Y,
Bell JD,
Thomas EL
and 1 more — show all
Diabetes · 2021 · PMID 33980691
12 pages+
Genetic insights into biological mechanisms governing human ovarian ageing
Ruth KS,
Day FR,
Hussain J,
Martínez-Marchal A,
Aiken CE,
Azad A,
Thompson DJ,
Knoblochova L,
Abe H,
Tarry-Adkins JL,
Gonzalez JM,
Fontanillas P
and 256 more — show all
Claringbould A,
Bakker OB,
Sulem P,
Walters RG,
Terao C,
Turon S,
Horikoshi M,
Lin K,
Onland-Moret NC,
Sankar A,
Hertz EPT,
Timshel PN,
Shukla V,
Borup R,
Olsen KW,
Aguilera P,
Ferrer-Roda M,
Huang Y,
Stankovic S,
Timmers PRHJ,
Ahearn TU,
Alizadeh BZ,
Naderi E,
Andrulis IL,
Arnold AM,
Aronson KJ,
Augustinsson A,
Bandinelli S,
Barbieri CM,
Beaumont RN,
Becher H,
Beckmann MW,
Benonisdottir S,
Bergmann S,
Bochud M,
Boerwinkle E,
Bojesen SE,
Bolla MK,
Boomsma DI,
Bowker N,
Brody JA,
Broer L,
Buring JE,
Campbell A,
Campbell H,
Castelao JE,
Catamo E,
Chanock SJ,
Chenevix-Trench G,
Ciullo M,
Corre T,
Couch FJ,
Cox A,
Crisponi L,
Cross SS,
Cucca F,
Czene K,
Smith GD,
de Geus EJCN,
de Mutsert R,
De Vivo I,
Demerath EW,
Dennis J,
Dunning AM,
Dwek M,
Eriksson M,
Esko T,
Fasching PA,
Faul JD,
Ferrucci L,
Franceschini N,
Frayling TM,
Gago-Dominguez M,
Mezzavilla M,
García-Closas M,
Gieger C,
Giles GG,
Grallert H,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Haiman CA,
Håkansson N,
Hall P,
Hayward C,
He C,
He W,
Heiss G,
Høffding MK,
Hopper JL,
Hottenga JJ,
Hu F,
Hunter D,
Ikram MA,
Jackson RD,
Joaquim MDR,
John EM,
Joshi PK,
Karasik D,
Kardia SLR,
Kartsonaki C,
Karlsson R,
Kitahara CM,
Kolcic I,
Kooperberg C,
Kraft P,
Kurian AW,
Kutalik Z,
La Bianca M,
LaChance G,
Langenberg C,
Launer LJ,
Laven JSE,
Lawlor DA,
Le Marchand L,
Li J,
Lindblom A,
Lindstrom S,
Lindstrom T,
Linet M,
Liu Y,
Liu S,
Luan J,
Mägi R,
Magnusson PKE,
Mangino M,
Mannermaa A,
Marco B,
Marten J,
Martin NG,
Mbarek H,
McKnight B,
Medland SE,
Meisinger C,
Meitinger T,
Menni C,
Metspalu A,
Milani L,
Milne RL,
Montgomery GW,
Mook-Kanamori DO,
Mulas A,
Mulligan AM,
Murray A,
Nalls MA,
Newman A,
Noordam R,
Nutile T,
Nyholt DR,
Olshan AF,
Olsson H,
Painter JN,
Patel AV,
Pedersen NL,
Perjakova N,
Peters A,
Peters U,
Pharoah PDP,
Polasek O,
Porcu E,
Psaty BM,
Rahman I,
Rennert G,
Rennert HS,
Ridker PM,
Ring SM,
Robino A,
Rose LM,
Rosendaal FR,
Rossouw J,
Rudan I,
Rueedi R,
Ruggiero D,
Sala CF,
Saloustros E,
Sandler DP,
Sanna S,
Sawyer EJ,
Sarnowski C,
Schlessinger D,
Schmidt MK,
Schoemaker MJ,
Schraut KE,
Scott C,
Shekari S,
Shrikhande A,
Smith AV,
Smith BH,
Smith JA,
Sorice R,
Southey MC,
Spector TD,
Spinelli JJ,
Stampfer M,
Stöckl D,
van Meurs JBJ,
Strauch K,
Styrkarsdottir U,
Swerdlow AJ,
Tanaka T,
Teras LR,
Teumer A,
Þorsteinsdottir U,
Timpson NJ,
Toniolo D,
Traglia M,
Troester MA,
Truong T,
Tyrrell J,
Uitterlinden AG,
Ulivi S,
Vachon CM,
Vitart V,
Völker U,
Vollenweider P,
Völzke H,
Wang Q,
Wareham NJ,
Weinberg CR,
Weir DR,
Wilcox AN,
van Dijk KW,
Willemsen G,
Wilson JF,
Wolffenbuttel BHR,
Wolk A,
Wood AR,
Zhao W,
Zygmunt M,
Chen Z,
Li L,
Franke L,
Burgess S,
Deelen P,
Pers TH,
Grøndahl ML,
Andersen CY,
Pujol A,
Lopez-Contreras AJ,
Daniel JA,
Stefansson K,
Chang-Claude J,
van der Schouw YT,
Lunetta KL,
Chasman DI,
Easton DF,
Visser JA,
Ozanne SE,
Namekawa SH,
Solc P,
Murabito JM,
Ong KK,
Hoffmann ER,
Murray A,
Roig I,
Perry JRB
Biobank-based Integrative Omics Study (BIOS) Consortium · eQTLGen Consortium and 6 more consortia
Nature · 2021 · PMID 34349265
12 pages+
Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood
Hawkes G,
Beaumont RN,
Tyrrell J,
Power GM,
Wood A,
Laakso M,
Fernandes Silva L,
Boehnke M,
Yin X,
Richardson TG,
Smith GD,
Frayling TM
Diabetologia · 2023 · PMID 37280435 · open access
12 pages+
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Erzurumluoglu AM,
Liu M,
Jackson VE,
Barnes DR,
Datta G,
Melbourne CA,
Young R,
Batini C,
Surendran P,
Jiang T,
Adnan SD,
Afaq S
and 164 more — show all
Agrawal A,
Altmaier E,
Antoniou AC,
Asselbergs FW,
Baumbach C,
Bierut L,
Bertelsen S,
Boehnke M,
Bots ML,
Brazel DM,
Chambers JC,
Chang-Claude J,
Chen C,
Corley J,
Chou YL,
David SP,
de Boer RA,
de Leeuw CA,
Dennis JG,
Dominiczak AF,
Dunning AM,
Easton DF,
Eaton C,
Elliott P,
Evangelou E,
Faul JD,
Foroud T,
Goate A,
Gong J,
Grabe HJ,
Haessler J,
Haiman C,
Hallmans G,
Hammerschlag AR,
Harris SE,
Hattersley A,
Heath A,
Hsu C,
Iacono WG,
Kanoni S,
Kapoor M,
Kaprio J,
Kardia SL,
Karpe F,
Kontto J,
Kooner JS,
Kooperberg C,
Kuulasmaa K,
Laakso M,
Lai D,
Langenberg C,
Le N,
Lettre G,
Loukola A,
Luan J,
Madden PAF,
Mangino M,
Marioni RE,
Marouli E,
Marten J,
Martin NG,
McGue M,
Michailidou K,
Mihailov E,
Moayyeri A,
Moitry M,
Müller-Nurasyid M,
Naheed A,
Nauck M,
Neville MJ,
Nielsen SF,
North K,
Perola M,
Pharoah PDP,
Pistis G,
Polderman TJ,
Posthuma D,
Poulter N,
Qaiser B,
Rasheed A,
Reiner A,
Renström F,
Rice J,
Rohde R,
Rolandsson O,
Samani NJ,
Samuel M,
Schlessinger D,
Scholte SH,
Scott RA,
Sever P,
Shao Y,
Shrine N,
Smith JA,
Starr JM,
Stirrups K,
Stram D,
Stringham HM,
Tachmazidou I,
Tardif JC,
Thompson DJ,
Tindle HA,
Tragante V,
Trompet S,
Turcot V,
Tyrrell J,
Vaartjes I,
van der Leij AR,
van der Meer P,
Varga TV,
Verweij N,
Völzke H,
Wareham NJ,
Warren HR,
Weir DR,
Weiss S,
Wetherill L,
Yaghootkar H,
Yavas E,
Jiang Y,
Chen F,
Zhan X,
Zhang W,
Zhao W,
Zhao W,
Zhou K,
Amouyel P,
Blankenberg S,
Caulfield MJ,
Chowdhury R,
Cucca F,
Deary IJ,
Deloukas P,
Di Angelantonio E,
Ferrario M,
Ferrières J,
Franks PW,
Frayling TM,
Frossard P,
Hall IP,
Hayward C,
Jansson JH,
Jukema JW,
Kee F,
Männistö S,
Metspalu A,
Munroe PB,
Nordestgaard BG,
Palmer CNA,
Salomaa V,
Sattar N,
Spector T,
Strachan DP,
van der Harst P,
Zeggini E,
Saleheen D,
Butterworth AS,
Wain LV,
Abecasis GR,
Danesh J,
Tobin MD,
Vrieze S,
Liu DJ,
Howson JMM
Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
Molecular psychiatry · 2020 · PMID 30617275 · open access
7 pages
Biological and clinical insights from genetics of insomnia symptoms
Lane JM,
Jones SE,
Dashti HS,
Wood AR,
Aragam KG,
van Hees VT,
Strand LB,
Winsvold BS,
Wang H,
Bowden J,
Song Y,
Patel K
and 31 more — show all
Anderson SG,
Beaumont RN,
Bechtold DA,
Cade BE,
Haas M,
Kathiresan S,
Little MA,
Luik AI,
Loudon AS,
Purcell S,
Richmond RC,
Scheer FAJL,
Schormair B,
Tyrrell J,
Winkelman JW,
Winkelmann J,
Hveem K,
Zhao C,
Nielsen JB,
Willer CJ,
Redline S,
Spiegelhalder K,
Kyle SD,
Ray DW,
Zwart JA,
Brumpton B,
Frayling TM,
Lawlor DA,
Rutter MK,
Weedon MN,
Saxena R
HUNT All In Sleep
Nature genetics · 2019 · PMID 30804566 · open access
6 pages
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci
Jones SE,
Tyrrell J,
Wood AR,
Beaumont RN,
Ruth KS,
Tuke MA,
Yaghootkar H,
Hu Y,
Teder-Laving M,
Hayward C,
Roenneberg T,
Wilson JF
and 15 more — show all
Del Greco F,
Hicks AA,
Shin C,
Yun CH,
Lee SK,
Metspalu A,
Byrne EM,
Gehrman PR,
Tiemeier H,
Allebrandt KV,
Freathy RM,
Murray A,
Hinds DA,
Frayling TM,
Weedon MN
PLoS genetics · 2016 · PMID 27494321 · open access
5 pages
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
Giannakopoulou O,
Lin K,
Meng X,
Su MH,
Kuo PH,
Peterson RE,
Awasthi S,
Moscati A,
Coleman JRI,
Bass N,
Millwood IY,
Chen Y
and 25 more — show all
Chen Z,
Chen HC,
Lu ML,
Huang MC,
Chen CH,
Stahl EA,
Loos RJF,
Mullins N,
Ursano RJ,
Kessler RC,
Stein MB,
Sen S,
Scott LJ,
Burmeister M,
Fang Y,
Tyrrell J,
Jiang Y,
Tian C,
McIntosh AM,
Ripke S,
Dunn EC,
Kendler KS,
Walters RG,
Lewis CM,
Kuchenbaecker K
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
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
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms
Schafmayer C,
Harrison JW,
Buch S,
Lange C,
Reichert MC,
Hofer P,
Cossais F,
Kupcinskas J,
von Schönfels W,
Schniewind B,
Kruis W,
Tepel J
and 51 more — show all
Zobel M,
Rosendahl J,
Jacobi T,
Walther-Berends A,
Schroeder M,
Vogel I,
Sergeev P,
Boedeker H,
Hinrichsen H,
Volk A,
Erk JU,
Burmeister G,
Hendricks A,
Hinz S,
Wolff S,
Böttner M,
Wood AR,
Tyrrell J,
Beaumont RN,
Langheinrich M,
Kucharzik T,
Brezina S,
Huber-Schönauer U,
Pietsch L,
Noack LS,
Brosch M,
Herrmann A,
Thangapandi RV,
Schimming HW,
Zeissig S,
Palm S,
Focke G,
Andreasson A,
Schmidt PT,
Weitz J,
Krawczak M,
Völzke H,
Leeb G,
Michl P,
Lieb W,
Grützmann R,
Franke A,
Lammert F,
Becker T,
Kupcinskas L,
D'Amato M,
Wedel T,
Datz C,
Gsur A,
Weedon MN,
Hampe J
Gut · 2019 · PMID 30661054
1 page
Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour
Jones SE,
van Hees VT,
Mazzotti DR,
Marques-Vidal P,
Sabia S,
van der Spek A,
Dashti HS,
Engmann J,
Kocevska D,
Tyrrell J,
Beaumont RN,
Hillsdon M
and 20 more — show all
Ruth KS,
Tuke MA,
Yaghootkar H,
Sharp SA,
Ji Y,
Harrison JW,
Freathy RM,
Murray A,
Luik AI,
Amin N,
Lane JM,
Saxena R,
Rutter MK,
Tiemeier H,
Kutalik Z,
Kumari M,
Frayling TM,
Weedon MN,
Gehrman PR,
Wood AR
Nature communications · 2019 · PMID 30952852 · open access
1 page
A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio
Casanova F,
Tyrrell J,
Beaumont RN,
Ji Y,
Jones SE,
Hattersley AT,
Weedon MN,
Murray A,
Shore AC,
Frayling TM,
Wood AR
Human molecular genetics · 2019 · PMID 31630189 · open access
1 page
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