I completed my Ph.D. in Human Genetics at the Radboud University Medical Center, the Netherlands in December 2015. I joined the Chakravarti lab as a postdoctoral research fellow in November 2016. My projects primarily involve sequencing and genotyping methods to further understand the roles of RET, SEMA3, and NRG1 gene loci in Hirschsprung disease biology.
Duvvari MR, van de Ven JPH, Geerlings MJ, Saksens NT, Bakker B, Henkes A, Neveling K, Rosario M, Westra D, van den Heuvel LP, Schick T, Fauser S, Boon CJ, Hoyng CB, de Jong EK, den Hollander AI. Whole exome sequencing in patients with the cuticular drusen subtype of age-related macular degeneration. PLoS One 2016, 11(3), e0152047.
Helgason H, Sulem P, Duvvari MR, Luo H, Thorleifsson G, Stefansson H, Jonsdottir I, Masson G, Gudbjartsson DF, Walters GB, Magnusson OT, Kong A, Rafnar T, Kiemeney LA, Schoenmaker-Koller FE, Zhao L, Boon CJ, Song Y, Fauser S, Pei M, Ristau T, Patel S, Liakopoulos S, van de Ven JPH, Hoyng CB, Ferreyra H, Duan Y, Bernstein PS, Geirsdottir A, Helgadottir G, Stefansson E, den Hollander AI, Zhang K, Jonasson F, Sigurdsson H, Thorsteinsdottir U, Stefansson K. A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration. Nature Genetics 2013, 45(11), 1371-1374.