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Nature genetics. Apr 2024
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ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon.
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Genome biology. Dec 2022
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Nature. Oct 2022
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Nature genetics. Jun 2019
(DOI : PMC7610439)
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Nature communications. Nov 2018
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Human Molecular Genetics. Sep 2018
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Molecular psychiatry. May 2018
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Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
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Nature genetics. Apr 2018
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Nature genetics. Mar 2018
(DOI : 10.1038/s41588-018-0050-y)
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Nature genetics. Mar 2018
(DOI : 10.1038/s41588-018-0082-3)
Feitosa MF, Kraja AT, Chasman DI, Sung YJ, Winkler TW, Ntalla I, Franceschini N, Cheng CY, Marten J, Musani SK, Richard MA, Noordam R, Bartz TM, Bielak LF, Dorajoo R, Hartwig FP, Manning AK, Rankinen T, Smith AV, Tajuddin SM, Wojczynski MK, Alver M, Campbell A, Divers J, Goel A, Harris SE, Jackson AU, Kähönen M, Kasturiratne A, Komulainen P, Kühnel B, Luan J, Nolte IM, Padmanabhan S, Riaz M, Rueedi R, Robino A, Said MA, Scott RA, Stančáková A, Takeuchi F, Tayo BO, van der Most PJ, Varga TV, Vitart V, Wang Y, Ware EB, Warren HR, Weiss S, Yanek LR, Zhang W, Zhao JH, Afaq S, Amin N, Amini M, Arking DE, Aung T, Boerwinkle E, Borecki I, Broeckel U, Brown M, Brumat M, Chakravarti A, Connell JM, Correa A, de Mutsert R, Deng X, Ding J, Eaton CB, Ehret G, Eppinga RN, Evangelou E, Faul JD, Felix SB, Forouhi NG, Forrester T, Franco OH, Friedlander Y, Gandin I, Ghanbari M, Gigante B, Hallmans G, Harris TB, Heng CK, Howard BV, Ikram MA, Katsuya T, Khor CC, Kilpeläinen TO, Koh WP, Kubo M, Kuusisto J, Lakka TA, Langefeld CD, Langenberg C, Launer LJ, Lehne B, Lewis CE, Mägi R, McKenzie CA, Meitinger T, Metspalu A, Milaneschi Y, Milani L, Mohlke KL, Nalls MA, Nelson CP, Sotoodehnia N, Norris JM, O'Connell JR, Palmer ND, Pedersen NL, Peters A, Peyser PA, Poulter N, Raffel LJ, Raitakari OT, Roll K, Rose LM, Rosendaal FR, Rotter JI, Schreiner PJ, Schupf N, Scott WR, Sever PS, Sidney S, Sitlani CM, Smith JA, Snieder H, Starr JM, Strauch K, Stringham HM, Tang H, Taylor KD, Teo YY, Tham YC, Turner ST, Uitterlinden AG, Vollenweider P, Waldenberger M, Wang L, Wang YX, Williams C, Yuan JM, Zhao W, Zonderman AB, Becker DM, Boehnke M, Bowden DW, Chambers JC, Deary IJ, Esko T, Farrall M, Franks PW, Freedman BI, Froguel P, Gasparini P, Gieger C, Jonas JB, Kamatani Y, Kato N, Kooner JS, Kutalik Z, Laakso M, Leander K, Lehtimäki T, Magnusson PKE, Oldehinkel AJ, Penninx BWJH, Polasek O, Porteous DJ, Rauramaa R, Samani NJ, Scott J, Shu XO, van der Harst P, Wagenknecht LE, Wareham NJ, Watkins H, Weir DR, Wickremasinghe AR, Zheng W, Bouchard C, Christensen K, Evans MK, Gudnason V, Horta BL, Kardia SLR, Psaty BM, Ridker PM, van Dam RM, Mook-Kanamori DO, Fornage M, Rotimi CN, Cupples LA, Kelly TN, Hayward C, van Duijn CM, Tai ES, Wong TY, Kooperberg C, Palmas W, Rice K, Morrison AC, Elliott P, Caulfield MJ, Munroe PB, Rao DC, Province MA, Levy D
PLoS ONE. Feb 2018
(DOI : 10.1371/journal.pone.0198166)
Justice AE, Karaderi T, Highland HM, Young KL, Graff M, Turcot V, Auer PL, Fine RS, Schurmann C, Lempradl A, Marouli E, Mahajan A, Winkler TW, Locke AE, Medina-Gomez C, Esko T, Vedantam S, Giri A, Alfred T, Mudgal P, Ng MCY, Heard-Costa NL, Feitosa MF, Manning AK, Willems S, Sivapalaratnam S, Abecasis G, Alam DS, Allison M, Amouyel P, Arzumanyan Z, Balkau B, Bastarache L, Bergmann S, Bielak LF, Blüher M, Boehnke M, Boeing H, Boerwinkle E, Böger CA, Bork-Jensen J, Bottinger EP, Bowden DW, Brandslund I, Broer L, Burt AA, Butterworth AS, Caulfield MJ, Cesana G, Chambers JC, Chasman DI, Chen YI, Chowdhury R, Christensen C, Chu AY, Collins FS, Cook JP, Cox AJ, Crosslin DS, Danesh J, de Bakker PIW, Mutsert R, Dedoussis G, Demerath EW, Dennis JG, Denny JC, Dörr M, Drenos F, Dubé MP, Dunning AM, Easton DF, Elliott P, Evangelou E, Farmaki AE, Feng S, Ferrannini E, Ferrières J, Florez JC, Fornage M, Fox CS, Franks PW, Friedrich N, Gandin I, Gasparini P, Giedraitis V, Girotto G, Gorski M, Grallert H, Grarup N, Grove ML, Gustafsson S, Haessler J, Hansen T, Hattersley AT, Hayward C, Heid IM, Holmen OL, Hovingh GK, Howson JMM, Hung YJ, Hveem K, Ikram MA, Ingelsson E, Jackson AU, Jarvik GP, Jørgensen T, Jousilahti P, Justesen JM, Kahali B, Karaleftheri M, Kardia SLR, Karpe F, Kitajima H, Komulainen P, Kooner JS, Kovacs P, Krämer BK, Kuulasmaa K, Kuusisto J, Laakso M, Lakka TA, Lamparter D, Lange LA, Langenberg C, Larson EB, Lee NR, Lee WJ, Lehtimäki T, Lewis CE, Li-Gao R, Lin LA, Lind L, Lindström J, Linneberg A, Liu CT, Liu DJ, Luan J, Lyytikäinen LP, MacGregor S, Mägi R, Männistö S, Marenne G, Marten J, Masca NGD, McCarthy MI, Meidtner K, Mihailov E, Moilanen L, Moitry M, Mook-Kanamori DO, Morgan A, Morris AP, Müller-Nurasyid M, Munroe PB, Narisu N, Nelson CP, Neville M, Ntalla I, O'Connell JR, Owen KR, Pedersen O, Peloso GM, Pennell CE, Perola M, Perry JA, Perry JR, Pers TH, Polasek O, Raitakari OT, Rasheed A, Rauramaa R, Reilly DF, Reiner AP, Ridker PM, Rivas MA, Robertson NR, Robino A, Rudan I, Ruth KS, Saleheen D, Salomaa V, Samani NJ, Schreiner PJ, Schulze MB, Scott RA, Slater AJ, Small KS, Smith BH, Smith JA, Southam L, Spector TD, Speliotes EK, Stefansson K, Steinthorsdottir V, Stirrups KE, Strauch K, Stringham HM, Stumvoll M, Surendran P, Swart KMA, Tardif JC, Taylor KD, Teumer A, Thompson DJ, Thorleifsson G, Thorsteinsdottir U, Thuesen BH, Tönjes A, Torres M, Tsafantakis E, Tuomilehto J, Uitterlinden AG, Uusitupa M, van Duijn CM, Vanhala M, Varma R, Vermeulen SH, Vestergaard H, Vitart V, Vogt TF, Vuckovic D, Wagenknecht LE, Walker M, Wallentin L, Wang F, Wang CA, Wang S, Wareham NJ, Warren HR, Waterworth DM, Wessel J, White HD, Willer CJ, Wilson JG, Wood AR, Yaghootkar H, Yerges-Armstrong LM, Young R, Zeggini E, Zhan X, Zhang W, Zhao JH, Zhao W, Zheng H, Zhou W, Zillikens MC, Rivadeneira F, Borecki IB, Pospisilik JA, Deloukas P, Frayling TM, Lettre G, Mohlke KL, Rotter JI, Kutalik Z, Hirschhorn JN, Cupples LA, Loos RJF, North KE, Lindgren CM
Nature genetics. Nov 2017
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American journal of human genetics. Oct 2017
(DOI : 10.1016/j.ajhg.2018.01.015)
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Nature genetics. Oct 2017
(DOI : 10.1038/s41588-018-0205-x)
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Nature genetics. Aug 2017
(DOI : 10.1038/s41588-017-0011-x)
New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals.
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Circulation. Cardiovascular genetics. Apr 2017
(DOI : 10.1161/CIRCGENETICS.117.001778)
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Hypertension (Dallas, Tex. : 1979). Mar 2017
(DOI : 10.1161/HYPERTENSIONAHA.117.09438)
Exome-wide association study of plasma lipids in >300,000 individuals.
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Nature genetics. Jan 2017
(DOI : 10.1038/ng.3977)
Rare and low-frequency coding variants alter human adult height.
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Nature. Jul 2016
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Analysis with the exome array identifies multiple new independent variants in lipid loci.
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Nature genetics. Jul 2015
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Nature genetics. Jul 2015
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Nature. Nov 2013
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Nature genetics. Feb 2011
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Nature. Aug 2010
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PLoS genetics. May 2010
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Nature genetics. May 2010
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Hundreds of variants clustered in genomic loci and biological pathways affect human height.
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Nature. Apr 2010
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