Professor Vardhman Rakyan, PhD, BSc (Hons) Biochemistry (University of Sydney)

Professor of Epigenetics; Deputy Director of Research
Centre: Genomics and Child Health
Email: v.rakyan@qmul.ac.uk Telephone: 020 7882 8140Twitter: @Rakyan_Lab
Profile
For my PhD (1999-2002) I investigated epigenetic inheritance under the supervision of Prof. Emma Whitelaw, University of Sydney, Australia. From 2003-2007, I was a CJ Martin Postdoctoral Fellow at the Sanger Institute, Cambridge, UK; where, under the guidance of Dr Stephan Beck, I developed functional genomics tools for genome-wide DNA methylation analyses. I joined QMUL as a Lecturer in 2007.
Website: www.rakyanlab.com
Teaching
PBLs, SSC, MBBS academic advisor, Experimental Pathology Research Project advisor
Research
Research Interests:
- Francisco Rodriguez Algarra
Publications
Key Publications
Genetic variation at mouse and human ribosomal DNA influences associated epigenetic states.
Rodriguez-Algarra F, Seaborne RAE, Danson AF, Yildizoglu S, Yoshikawa H, Law PP, Ahmad Z, Maudsley VA, Brew A, Holmes N, Ochôa M, Hodgkinson A, Marzi SJ, Pradeepa MM, Loose M, Holland ML, Rakyan VK.
Genome Biol. 2022 Feb 14;23(1):54.
Ageing-associated DNA methylation dynamics are a molecular readout of lifespan variation among mammalian species.
Lowe R, Barton C, Jenkins CA, Ernst C, Forman O, Fernandez-Twinn DS, Bock C, Rossiter SJ, Faulkes CG, Ozanne SE, Walter L, Odom DT, Mellersh C, Rakyan VK.
Genome Biol. 2018 Feb 16;19(1):22.
Early-life nutrition modulates the epigenetic state of specific rDNA genetic variants in mice.
Holland ML, Lowe R, Caton PW, Gemma C, Carbajosa G, Danson AF, Carpenter AA, Loche E, Ozanne SE, Rakyan VK.
Science. 2016 Jul 29;353(6298):495-8.
Epigenome-wide association studies for common human diseases.
Rakyan VK, Down TA, Balding DJ, Beck S.
Nat Rev Genet. 2011 Jul 12;12(8):529-41.
Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains.
Rakyan VK, Down TA, Maslau S, Andrew T, Yang TP, Beyan H, Whittaker P, McCann OT, Finer S, Valdes AM, Leslie RD, Deloukas P, Spector TD.
Genome Res. 2010 Apr;20(4):434-9