The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12

By Reed Danielle R.   Zhu Gu   Breslin Paul A.S.   Duke Fujiko F.   Henders Anjali K.   Campbell Megan J.   Montgomery Grant W.   Medland Sarah E.   Martin Nicholas G.   Wright Margaret J.  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4278-4285

Oxford University Press

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Common genetic variants associated with open-angle glaucoma

By Ramdas Wishal D.   van Koolwijk Leonieke M.E.   Lemij Hans G.   Pasutto Francesca   Cree Angela J.   Thorleifsson Gudmar   Janssen Sarah F.   Jacoline ten Brink   Amin Najaf   Rivadeneira Fernando   Wolfs Roger C.W.   Walters G. Bragi   Jonasson Fridbert   Weisschuh Nicole   Mardin Christian Y.   Gibson Jane   Zegers Richard H.C.   Hofman Albert   de Jong Paulus T.V.M.   Uitterlinden André G.   Oostra Ben A.   Thorsteinsdottir Unnur   Gramer Eugen   Welgen-Lüßen Ulrich C.   Kirwan James F.   Bergen Arthur A.B.   Reis André   Stefansson Kari   Lotery Andrew J.   Vingerling Johannes R.   Jansonius Nomdo M.   Klaver Caroline C.W.   van Duijn Cornelia M.  

Human Molecular Genetics, Vol. 20, Iss. 12, 2011-06 ,pp. : 2464-2471

Oxford University Press

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Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

By Johansson sa   Marroni Fabio   Hayward Caroline   Franklin Christopher S.   Kirichenko Anatoly V.   Jonasson Inger   Hicks Andrew A.   Vitart Veronique   Isaacs Aaron   Axenovich Tatiana   Campbell Susan   Dunlop Malcolm G.   Floyd Jamie   Hastie Nick   Hofman Albert   Knott Sara   Kolcic Ivana   Pichler Irene   Polasek Ozren   Rivadeneira Fernando   Tenesa Albert   Uitterlinden Andr G.   Wild Sarah H.   Zorkoltseva Irina V.   Meitinger Thomas   Wilson James F.   Rudan Igor   Campbell Harry   Pattaro Cristian   Pramstaller Peter   Oostra Ben A.   Wright Alan F.   van Duijn Cornelia M.   Aulchenko Yurii S.   Gyllensten Ulf  

Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 373-380

Oxford University Press

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Mapping common regulatory variants to human haplotypes

By Pastinen Tomi   Ge Bing   Gurd Scott   Gaudin Tiffany   Dore Carole   Lemire Mathieu   Lepage Pierre   Harmsen Eef   Hudson Thomas J.  

Human Molecular Genetics, Vol. 14, Iss. 24, 2005-12 ,pp. : 3963-3971

Oxford University Press

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Common variants in KCNQ1 are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population

By Qi Qibin   Li Huaixing   Loos Ruth J.F.   Liu Chen   Wu Ying   Hu Frank B.   Wu Hongyu   Lu Ling   Yu Zhijie   Lin Xu  

Human Molecular Genetics, Vol. 18, Iss. 18, 2009-09 ,pp. : 3508-3515

Oxford University Press

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