Dr Robin Walters
MA, PhD, PgDip
Dr Robin Walters completed degrees in Natural Sciences (Cambridge) and in Genetics (Liverpool) before working for 17 years on the biophysics, biochemistry and genetics of plant photosynthesis, first in Sheffield and then in Oxford. He then held a post as a Research Fellow at Imperial College London, before moving to CTSU in June 2012.
Dr Walters’s recent research has focussed on investigating the contribution of structural variation in the human genome to disease risk and phenotypic variation, with a particular focus on diabetes and obesity. He played a leading role in work identifying the highly penetrant obesity phenotype associated with a deletion on chromosome 16p, and the reciprocal effects of a duplication at the same locus.
He continues to have an interest in the development of novel methodologies for the identification and analysis of genomic structural variants. His current role is to plan and lead the genetic analysis of stroke risk in the China Kadoorie Biobank.
Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Shrine N. et al, (2019), Nat Genet, 51
Conventional and genetic evidence on alcohol and vascular disease aetiology: a prospective study of 500 000 men and women in China.
Millwood IY. et al, (2019), Lancet, 393, 1831 - 1842
Causal associations of blood lipids with risk of ischemic stroke and intracerebral hemorrhage in Chinese adults.
Sun L. et al, (2019), Nat Med, 25, 569 - 574
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
Shrine N. et al, (2019), Nat Genet, 51, 481 - 493
[Study on genetic structure differences and adjustment strategies in different areas of China].
Zhu M. et al, (2019), Zhonghua Liu Xing Bing Xue Za Zhi, 40, 20 - 25