Common polymorphism in <it>H19 </it>associated with birthweight and cord blood IGF-II levels in humans by Petry Clive J, Ong Ken K, Barratt Bryan J, Wingate Diane, Cordell Heather J, Ring Susan M, Pembrey Marcus E, Reik Wolf, Todd John A, Dunger David B

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Investigating the utility of combining Φ29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray™ genotyping by Smink Luc J, Lam Alex C, Smith Anne, Twells Rebecca CJ, Sebastian Meera, Smyth Deborah J, Nutland Sarah, Barratt Bryan J, Rance Helen E, Pask Rebecca, Walker Neil M, Todd John A

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Development of an integrated genome informatics, data management and workflow infrastructure: A toolbox for the study of complex disease genetics by Burren Oliver S, Healy Barry C, Lam Alex C, Schuilenburg Helen, Dolman Geoffrey E, Everett Vincent H, Laneri Davide, Nutland Sarah, Rance Helen E, Payne Felicity, Smyth Deborah, Lowe Chris, Barratt Bryan J, Twells Rebecca CJ, Rainbow Daniel B, Wicker Linda S, Todd John A, Walker Neil M, Smink Luc J

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Sequencing and association analysis of the type 1 diabetes – linked region on chromosome 10p12-q11 by Barratt Bryan J, Twells Rebecca, Smith Anne, Walker Neil M, Nutland Sarah, Stevens Helen, Burren Oliver, Lam Alex, Godfrey Lisa, Masters Jennifer, Payne Felicity, Lowe Christopher E, Bailey Rebecca, Smyth Deborah, Smink Luc J, Nejentsev Sergey, Wright Charmain, French Lisa, Chen Yuan, Deloukas Panagiotis, Rogers Jane, Dunham Ian, Todd John A

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