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성함이나 학술지명, PMID로 찾아보십시오.
Ahluwalia TS에 대해
38건, 그중 18건 표시.
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
외 180명 — 모두 보기
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,
Marques-Vidal P,
Montgomery GW,
Mosing MA,
Paternoster L,
Pattie A,
Petrovic KE,
Pulkki-Råback L,
Quaye L,
Räikkönen K,
Rudan I,
Scott RJ,
Smith JA,
Sutin AR,
Trzaskowski M,
Vinkhuyzen AE,
Yu L,
Zabaneh D,
Attia JR,
Bennett DA,
Berger K,
Bertram L,
Boomsma DI,
Snieder H,
Chang SC,
Cucca F,
Deary IJ,
van Duijn CM,
Eriksson JG,
Bültmann U,
de Geus EJ,
Groenen PJ,
Gudnason V,
Hansen T,
Hartman CA,
Haworth CM,
Haworth CM,
Hayward C,
Heath AC,
Hinds DA,
Hyppönen E,
Iacono WG,
Järvelin MR,
Jöckel KH,
Kaprio J,
Kardia SL,
Keltikangas-Järvinen L,
Kraft P,
Kubzansky LD,
Lehtimäki T,
Magnusson PK,
Martin NG,
McGue M,
Metspalu A,
Mills M,
de Mutsert R,
Oldehinkel AJ,
Pasterkamp G,
Pedersen NL,
Plomin R,
Polasek O,
Power C,
Rich SS,
Rosendaal FR,
den Ruijter HM,
Schlessinger D,
Schmidt H,
Svento R,
Schmidt R,
Alizadeh BZ,
Sørensen TI,
Spector TD,
Starr JM,
Stefansson K,
Steptoe A,
Terracciano A,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tiemeier H,
Uitterlinden AG,
Vollenweider P,
Vollenweider P,
Wagner GG,
Weir DR,
Yang J,
Conley DC,
Smith GD,
Hofman A,
Johannesson M,
Laibson DI,
Medland SE,
Meyer MN,
Pickrell JK,
Esko T,
Krueger RF,
Beauchamp JP,
Koellinger PD,
Benjamin DJ,
Bartels M,
Cesarini D
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
페이지 10개
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
van der Laan CM,
Ip HF,
Schipper M,
Hottenga JJ,
St Pourcain B,
Zayats T,
Pool R,
Krapohl EML,
Brikell I,
Soler Artigas M,
Cabana-Domínguez J,
Llonga N
외 117명 — 모두 보기
Nolte IM,
Bolhuis K,
Palviainen T,
Zafarmand H,
Gordon S,
Aliev F,
Burt SA,
Wang CA,
Saunders G,
Karhunen V,
Adkins DE,
Border R,
Peterson RE,
Prinz JA,
Thiering E,
Vilor-Tejedor N,
Ahluwalia TS,
Allegrini A,
Rimfeld K,
Chen Q,
Lu Y,
Martin J,
Bosch R,
Ramos-Quiroga JA,
Neumann A,
Ensink J,
Grasby KL,
Morosoli JJ,
Tong X,
Marrington S,
Scott JG,
Shabalin AA,
Corley R,
Evans LM,
Sugden K,
Alemany S,
Sass L,
Vinding R,
Ehli EA,
Hagenbeek FA,
Derks EM,
Larsson H,
Snieder H,
Cecil C,
Whipp AM,
Korhonen T,
Vuoksimaa E,
Rose RJ,
Uitterlinden AG,
Haavik J,
Harris JR,
Helgeland Ø,
Johansson S,
Knudsen GPS,
Njolstad PR,
Lu Q,
Rodriguez A,
Henders AK,
Mamun A,
Najman JM,
Brown S,
Hopfer C,
Krauter K,
Reynolds CA,
Smolen A,
Stallings M,
Wadsworth S,
Wall TL,
Eaves L,
Silberg JL,
Miller A,
Havdahl A,
Llop S,
Lopez-Espinosa MJ,
Bønnelykke K,
Sunyer J,
Arseneault L,
Standl M,
Heinrich J,
Boden J,
Pearson J,
Horwood J,
Kennedy M,
Poulton R,
Maes HH,
Hewitt J,
Copeland WE,
Middeldorp CM,
Williams GM,
Wray N,
Järvelin MR,
McGue M,
Iacono W,
Caspi A,
Moffitt TE,
Whitehouse AJO,
Pennell CE,
Klump KL,
Jiang C,
Dick DM,
Reichborn-Kjennerud T,
Martin NG,
Medland SE,
Vrijkotte T,
Kaprio J,
Tiemeier H,
Davey Smith G,
Hartman CA,
Oldehinkel AJ,
Casas M,
Ribasés M,
Lichtenstein P,
Lundström S,
Plomin R,
Bartels M,
Nivard MG,
Boomsma DI
Nature genetics · 2025 · PMID 40962958
페이지 9개
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
외 99명 — 모두 보기
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 외 컨소시엄 2곳
Human molecular genetics · 2016 · PMID 26604143
페이지 8개
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets
Grarup N,
Sulem P,
Sandholt CH,
Thorleifsson G,
Ahluwalia TS,
Steinthorsdottir V,
Bjarnason H,
Gudbjartsson DF,
Magnusson OT,
Sparsø T,
Albrechtsen A,
Kong A
외 19명 — 모두 보기
Masson G,
Tian G,
Cao H,
Nie C,
Kristiansen K,
Husemoen LL,
Thuesen B,
Li Y,
Nielsen R,
Linneberg A,
Olafsson I,
Eyjolfsson GI,
Jørgensen T,
Wang J,
Wang J,
Hansen T,
Thorsteinsdottir U,
Stefánsson K,
Pedersen O
PLoS genetics · 2013 · PMID 23754956 · open access
페이지 6개
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
Grosche S,
Marenholz I,
Esparza-Gordillo J,
Arnau-Soler A,
Pairo-Castineira E,
Rüschendorf F,
Ahluwalia TS,
Almqvist C,
Arnold A,
Baurecht H,
Bisgaard H,
Bønnelykke K
외 50명 — 모두 보기
Brown SJ,
Bustamante M,
Curtin JA,
Custovic A,
Dharmage SC,
Esplugues A,
Falchi M,
Fernandez-Orth D,
Ferreira MAR,
Franke A,
Gerdes S,
Gieger C,
Hakonarson H,
Holt PG,
Homuth G,
Hubner N,
Hysi PG,
Jarvelin MR,
Karlsson R,
Koppelman GH,
Lau S,
Lutz M,
Magnusson PKE,
Marks GB,
Müller-Nurasyid M,
Nöthen MM,
Paternoster L,
Pennell CE,
Peters A,
Rawlik K,
Robertson CF,
Rodriguez E,
Sebert S,
Simpson A,
Sleiman PMA,
Standl M,
Stölzl D,
Strauch K,
Szwajda A,
Tenesa A,
Thompson PJ,
Ullemar V,
Visconti A,
Vonk JM,
Wang CA,
Weidinger S,
Wielscher M,
Worth CL,
Xu CJ,
Lee YA
Australian Asthma Genetics Consortium (AAGC)
Nature communications · 2021 · PMID 34785669 · open access
페이지 6개
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
외 87명 — 모두 보기
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
페이지 5개
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
Salem RM,
Todd JN,
Sandholm N,
Cole JB,
Chen WM,
Andrews D,
Pezzolesi MG,
McKeigue PM,
Hiraki LT,
Qiu C,
Nair V,
Di Liao C
외 76명 — 모두 보기
Cao JJ,
Valo E,
Onengut-Gumuscu S,
Smiles AM,
McGurnaghan SJ,
Haukka JK,
Harjutsalo V,
Brennan EP,
van Zuydam N,
Ahlqvist E,
Doyle R,
Ahluwalia TS,
Lajer M,
Hughes MF,
Park J,
Skupien J,
Spiliopoulou A,
Liu A,
Menon R,
Boustany-Kari CM,
Kang HM,
Nelson RG,
Klein R,
Klein BE,
Lee KE,
Gao X,
Mauer M,
Maestroni S,
Caramori ML,
de Boer IH,
Miller RG,
Guo J,
Boright AP,
Tregouet D,
Gyorgy B,
Snell-Bergeon JK,
Maahs DM,
Bull SB,
Canty AJ,
Palmer CNA,
Stechemesser L,
Paulweber B,
Weitgasser R,
Sokolovska J,
Rovīte V,
Pīrāgs V,
Prakapiene E,
Radzeviciene L,
Verkauskiene R,
Panduru NM,
Groop LC,
McCarthy MI,
Gu HF,
Möllsten A,
Falhammar H,
Brismar K,
Martin F,
Rossing P,
Costacou T,
Zerbini G,
Marre M,
Hadjadj S,
McKnight AJ,
Forsblom C,
McKay G,
Godson C,
Maxwell AP,
Kretzler M,
Susztak K,
Colhoun HM,
Krolewski A,
Paterson AD,
Groop PH,
Rich SS,
Hirschhorn JN,
Florez JC
SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium
Journal of the American Society of Nephrology : JASN · 2019 · PMID 31537649
페이지 5개
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
외 228명 — 모두 보기
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
페이지 5개
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Barban N,
Jansen R,
de Vlaming R,
Vaez A,
Mandemakers JJ,
Tropf FC,
Shen X,
Wilson JF,
Chasman DI,
Nolte IM,
Tragante V,
van der Laan SW
외 241명 — 모두 보기
Perry JR,
Kong A,
Ahluwalia TS,
Albrecht E,
Yerges-Armstrong L,
Atzmon G,
Auro K,
Ayers K,
Bakshi A,
Ben-Avraham D,
Berger K,
Bergman A,
Bertram L,
Bielak LF,
Bjornsdottir G,
Bonder MJ,
Broer L,
Bui M,
Barbieri C,
Cavadino A,
Chavarro JE,
Turman C,
Concas MP,
Cordell HJ,
Davies G,
Eibich P,
Eriksson N,
Esko T,
Eriksson J,
Falahi F,
Felix JF,
Fontana MA,
Franke L,
Gandin I,
Gaskins AJ,
Gieger C,
Gunderson EP,
Guo X,
Hayward C,
He C,
Hofer E,
Huang H,
Joshi PK,
Kanoni S,
Karlsson R,
Kiechl S,
Kifley A,
Kluttig A,
Kraft P,
Lagou V,
Lecoeur C,
Lahti J,
Li-Gao R,
Lind PA,
Liu T,
Makalic E,
Mamasoula C,
Matteson L,
Mbarek H,
McArdle PF,
McMahon G,
Meddens SF,
Mihailov E,
Miller M,
Missmer SA,
Monnereau C,
van der Most PJ,
Myhre R,
Nalls MA,
Nutile T,
Kalafati IP,
Porcu E,
Prokopenko I,
Rajan KB,
Rich-Edwards J,
Rietveld CA,
Robino A,
Rose LM,
Rueedi R,
Ryan KA,
Saba Y,
Schmidt D,
Smith JA,
Stolk L,
Streeten E,
Tönjes A,
Thorleifsson G,
Ulivi S,
Wedenoja J,
Wellmann J,
Willeit P,
Yao J,
Yengo L,
Zhao JH,
Zhao W,
Zhernakova DV,
Amin N,
Andrews H,
Balkau B,
Barzilai N,
Bergmann S,
Biino G,
Bisgaard H,
Bønnelykke K,
Boomsma DI,
Buring JE,
Campbell H,
Cappellani S,
Ciullo M,
Cox SR,
Cucca F,
Toniolo D,
Davey-Smith G,
Deary IJ,
Dedoussis G,
Deloukas P,
van Duijn CM,
de Geus EJ,
Eriksson JG,
Evans DA,
Faul JD,
Sala CF,
Froguel P,
Gasparini P,
Girotto G,
Grabe HJ,
Greiser KH,
Groenen PJ,
de Haan HG,
Haerting J,
Harris TB,
Heath AC,
Heikkilä K,
Hofman A,
Homuth G,
Holliday EG,
Hopper J,
Hyppönen E,
Jacobsson B,
Jaddoe VW,
Johannesson M,
Jugessur A,
Kähönen M,
Kajantie E,
Kardia SL,
Keavney B,
Kolcic I,
Koponen P,
Kovacs P,
Kronenberg F,
Kutalik Z,
La Bianca M,
Lachance G,
Iacono WG,
Lai S,
Lehtimäki T,
Liewald DC,
Lindgren CM,
Liu Y,
Luben R,
Lucht M,
Luoto R,
Magnus P,
Magnusson PK,
Martin NG,
McGue M,
McQuillan R,
Medland SE,
Meisinger C,
Mellström D,
Metspalu A,
Traglia M,
Milani L,
Mitchell P,
Montgomery GW,
Mook-Kanamori D,
de Mutsert R,
Nohr EA,
Ohlsson C,
Olsen J,
Ong KK,
Paternoster L,
Pattie A,
Penninx BW,
Perola M,
Peyser PA,
Pirastu M,
Polasek O,
Power C,
Kaprio J,
Raffel LJ,
Räikkönen K,
Raitakari O,
Ridker PM,
Ring SM,
Roll K,
Rudan I,
Ruggiero D,
Rujescu D,
Salomaa V,
Schlessinger D,
Schmidt H,
Schmidt R,
Schupf N,
Smit J,
Sorice R,
Spector TD,
Starr JM,
Stöckl D,
Strauch K,
Stumvoll M,
Swertz MA,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tung JY,
Uitterlinden AG,
Vaccargiu S,
Viikari J,
Vitart V,
Völzke H,
Vollenweider P,
Vuckovic D,
Waage J,
Wagner GG,
Wang JJ,
Wareham NJ,
Weir DR,
Willemsen G,
Willeit J,
Wright AF,
Zondervan KT,
Stefansson K,
Krueger RF,
Lee JJ,
Benjamin DJ,
Cesarini D,
Koellinger PD,
den Hoed M,
Snieder H,
Mills MC
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
페이지 4개
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
외 247명 — 모두 보기
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
페이지 3개
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways
Bustamante M,
Standl M,
Bassat Q,
Vilor-Tejedor N,
Medina-Gomez C,
Bonilla C,
Ahluwalia TS,
Bacelis J,
Bradfield JP,
Tiesler CM,
Rivadeneira F,
Ring S
외 27명 — 모두 보기
Vissing NH,
Fink NR,
Jugessur A,
Mentch FD,
Ballester F,
Kriebel J,
Kiefte-de Jong JC,
Wolsk HM,
Llop S,
Thiering E,
Beth SA,
Timpson NJ,
Andersen J,
Schulz H,
Jaddoe VW,
Evans DM,
Waage J,
Hakonarson H,
Grant SF,
Jacobsson B,
Bønnelykke K,
Bisgaard H,
Davey Smith G,
Moll HA,
Heinrich J,
Estivill X,
Sunyer J
Human molecular genetics · 2016 · PMID 27559109
페이지 3개
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
외 21명 — 모두 보기
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
페이지 3개
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
외 233명 — 모두 보기
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 외 컨소시엄 2곳
Nature genetics · 2015 · PMID 26390057
페이지 2개
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Gorski M,
Jung B,
Li Y,
Matias-Garcia PR,
Wuttke M,
Coassin S,
Thio CHL,
Kleber ME,
Winkler TW,
Wanner V,
Chai JF,
Chu AY
외 119명 — 모두 보기
Cocca M,
Feitosa MF,
Ghasemi S,
Hoppmann A,
Horn K,
Li M,
Nutile T,
Scholz M,
Sieber KB,
Teumer A,
Tin A,
Wang J,
Tayo BO,
Ahluwalia TS,
Almgren P,
Bakker SJL,
Banas B,
Bansal N,
Biggs ML,
Boerwinkle E,
Bottinger EP,
Brenner H,
Carroll RJ,
Chalmers J,
Chee ML,
Chee ML,
Cheng CY,
Coresh J,
de Borst MH,
Degenhardt F,
Eckardt KU,
Endlich K,
Franke A,
Freitag-Wolf S,
Gampawar P,
Gansevoort RT,
Ghanbari M,
Gieger C,
Hamet P,
Ho K,
Hofer E,
Holleczek B,
Xian Foo VH,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Josyula NS,
Kähönen M,
Khor CC,
Koenig W,
Kramer H,
Krämer BK,
Kühnel B,
Lange LA,
Lehtimäki T,
Lieb W,
Loos RJF,
Lukas MA,
Lyytikäinen LP,
Meisinger C,
Meitinger T,
Melander O,
Milaneschi Y,
Mishra PP,
Mononen N,
Mychaleckyj JC,
Nadkarni GN,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
O'Donoghue ML,
Orho-Melander M,
Pendergrass SA,
Penninx BWJH,
Preuss MH,
Psaty BM,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rosenkranz AR,
Rossing P,
Rotter JI,
Sabanayagam C,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Sedaghat S,
Shaffer CM,
Strauch K,
Szymczak S,
Taylor KD,
Tremblay J,
Chaker L,
van der Harst P,
van der Most PJ,
Verweij N,
Völker U,
Waldenberger M,
Wallentin L,
Waterworth DM,
White HD,
Wilson JG,
Wong TY,
Woodward M,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang Y,
Snieder H,
Wanner C,
Böger CA,
Köttgen A,
Kronenberg F,
Pattaro C,
Heid IM
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
페이지 2개
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
van Zuydam NR,
Ahlqvist E,
Sandholm N,
Deshmukh H,
Rayner NW,
Abdalla M,
Ladenvall C,
Ziemek D,
Fauman E,
Robertson NR,
McKeigue PM,
Valo E
외 69명 — 모두 보기
Forsblom C,
Harjutsalo V,
Perna A,
Rurali E,
Marcovecchio ML,
Igo RP Jr,
Salem RM,
Perico N,
Lajer M,
Käräjämäki A,
Imamura M,
Kubo M,
Takahashi A,
Sim X,
Liu J,
van Dam RM,
Jiang G,
Tam CHT,
Luk AOY,
Lee HM,
Lim CKP,
Szeto CC,
So WY,
Chan JCN,
Ang SF,
Dorajoo R,
Wang L,
Clara TSH,
McKnight AJ,
Duffy S,
Pezzolesi MG,
Marre M,
Gyorgy B,
Hadjadj S,
Hiraki LT,
Ahluwalia TS,
Almgren P,
Schulz CA,
Orho-Melander M,
Linneberg A,
Christensen C,
Witte DR,
Grarup N,
Brandslund I,
Melander O,
Paterson AD,
Tregouet D,
Maxwell AP,
Lim SC,
Ma RCW,
Tai ES,
Maeda S,
Lyssenko V,
Tuomi T,
Krolewski AS,
Rich SS,
Hirschhorn JN,
Florez JC,
Dunger D,
Pedersen O,
Hansen T,
Rossing P,
Remuzzi G,
Brosnan MJ,
Palmer CNA,
Groop PH,
Colhoun HM,
Groop LC,
McCarthy MI
Finnish Diabetic Nephropathy Study (FinnDiane) · Hong Kong Diabetes Registry Theme-based Research Scheme Project Group 외 컨소시엄 4곳
Diabetes · 2018 · PMID 29703844
페이지 1개
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Jackson VE,
Latourelle JC,
Wain LV,
Smith AV,
Grove ML,
Bartz TM,
Obeidat M,
Province MA,
Gao W,
Qaiser B,
Porteous DJ,
Cassano PA
외 95명 — 모두 보기
Ahluwalia TS,
Grarup N,
Li J,
Altmaier E,
Marten J,
Harris SE,
Manichaikul A,
Pottinger TD,
Li-Gao R,
Lind-Thomsen A,
Mahajan A,
Lahousse L,
Imboden M,
Teumer A,
Prins B,
Lyytikäinen LP,
Eiriksdottir G,
Franceschini N,
Sitlani CM,
Brody JA,
Bossé Y,
Timens W,
Kraja A,
Loukola A,
Tang W,
Liu Y,
Bork-Jensen J,
Justesen JM,
Linneberg A,
Lange LA,
Rawal R,
Karrasch S,
Huffman JE,
Smith BH,
Davies G,
Burkart KM,
Mychaleckyj JC,
Bonten TN,
Enroth S,
Lind L,
Brusselle GG,
Kumar A,
Stubbe B,
Kähönen M,
Wyss AB,
Psaty BM,
Heckbert SR,
Hao K,
Rantanen T,
Kritchevsky SB,
Lohman K,
Skaaby T,
Pisinger C,
Hansen T,
Schulz H,
Polasek O,
Campbell A,
Starr JM,
Rich SS,
Mook-Kanamori DO,
Johansson Å,
Ingelsson E,
Uitterlinden AG,
Weiss S,
Raitakari OT,
Gudnason V,
North KE,
Gharib SA,
Sin DD,
Taylor KD,
O'Connor GT,
Kaprio J,
Harris TB,
Pederson O,
Vestergaard H,
Wilson JG,
Strauch K,
Hayward C,
Kerr S,
Deary IJ,
Barr RG,
de Mutsert R,
Gyllensten U,
Morris AP,
Ikram MA,
Probst-Hensch N,
Gläser S,
Zeggini E,
Lehtimäki T,
Strachan DP,
Dupuis J,
Morrison AC,
Hall IP,
Tobin MD,
London SJ
Understanding Society Scientific Group
Wellcome open research · 2018 · PMID 30175238 · open access
페이지 1개
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group
Irvin MR,
Sitlani CM,
Floyd JS,
Psaty BM,
Bis JC,
Wiggins KL,
Whitsel EA,
Sturmer T,
Stewart J,
Raffield L,
Sun F,
Liu CT
외 32명 — 모두 보기
Xu H,
Cupples AL,
Tanner RM,
Rossing P,
Smith A,
Zilhão NR,
Launer LJ,
Noordam R,
Rotter JI,
Yao J,
Li X,
Guo X,
Limdi N,
Sundaresan A,
Lange L,
Correa A,
Stott DJ,
Ford I,
Jukema JW,
Gudnason V,
Mook-Kanamori DO,
Trompet S,
Palmas W,
Warren HR,
Hellwege JN,
Giri A,
O'donnell C,
Hung AM,
Edwards TL,
Ahluwalia TS,
Arnett DK,
Avery CL
American journal of hypertension · 2019 · PMID 31545351
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Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Ahluwalia TS,
Prins BP,
Abdollahi M,
Armstrong NJ,
Aslibekyan S,
Bain L,
Jefferis B,
Baumert J,
Beekman M,
Ben-Shlomo Y,
Bis JC,
Mitchell BD
외 114명 — 모두 보기
de Geus E,
Delgado GE,
Marek D,
Eriksson J,
Kajantie E,
Kanoni S,
Kemp JP,
Lu C,
Marioni RE,
McLachlan S,
Milaneschi Y,
Nolte IM,
Petrelis AM,
Porcu E,
Sabater-Lleal M,
Naderi E,
Seppälä I,
Shah T,
Singhal G,
Standl M,
Teumer A,
Thalamuthu A,
Thiering E,
Trompet S,
Ballantyne CM,
Benjamin EJ,
Casas JP,
Toben C,
Dedoussis G,
Deelen J,
Durda P,
Engmann J,
Feitosa MF,
Grallert H,
Hammarstedt A,
Harris SE,
Homuth G,
Hottenga JJ,
Jalkanen S,
Jamshidi Y,
Jawahar MC,
Jess T,
Kivimaki M,
Kleber ME,
Lahti J,
Liu Y,
Marques-Vidal P,
Mellström D,
Mooijaart SP,
Müller-Nurasyid M,
Penninx B,
Revez JA,
Rossing P,
Räikkönen K,
Sattar N,
Scharnagl H,
Sennblad B,
Silveira A,
Pourcain BS,
Timpson NJ,
Trollor J,
van Dongen J,
Van Heemst D,
Visvikis-Siest S,
Vollenweider P,
Völker U,
Waldenberger M,
Willemsen G,
Zabaneh D,
Morris RW,
Arnett DK,
Baune BT,
Boomsma DI,
Chang YC,
Deary IJ,
Deloukas P,
Eriksson JG,
Evans DM,
Ferreira MA,
Gaunt T,
Gudnason V,
Hamsten A,
Heinrich J,
Hingorani A,
Humphries SE,
Jukema JW,
Koenig W,
Kumari M,
Kutalik Z,
Lawlor DA,
Lehtimäki T,
März W,
Mather KA,
Naitza S,
Nauck M,
Ohlsson C,
Price JF,
Raitakari O,
Rice K,
Sachdev PS,
Slagboom E,
Sørensen TIA,
Spector T,
Stacey D,
Stathopoulou MG,
Tanaka T,
Wannamethee SG,
Whincup P,
Rotter JI,
Dehghan A,
Boerwinkle E,
Psaty BM,
Snieder H,
Alizadeh BZ
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · open access
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