V. Bhat

发表

Exome sequencing and functional studies in zebrafish identify WDR8 as the causative gene for isolated Microspherophakia in Indian families.

U. Nongthomba, M. Madhangi, Debanjan Dutta, 2021, Human molecular genetics.

Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome

V. Bhat, Arun Kumar, M. H. Shah, 2014, Molecular vision.

Genetic analysis of ATP7B in 102 south Indian families with Wilson disease

Saketh Kapoor, A. Taly, S. Sinha, 2019, PloS one.

Evidence that TSC2 acts as a transcription factor and binds to and represses the promoter of Epiregulin

V. Bhat, M. I. Rather, Ankana Tiwari, 2014, Nucleic acids research.

Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex

A. Mahadevan, R. Bharath, Saketh Kapoor, 2016, PloS one.

Clinical phenotype and the lack of mutations in the CHRNG, CHRND, and CHRNA1 genes in two Indian families with Escobar syndrome

V. Bhat, Arun Kumar, M. H. Shah, 2013, Clinical dysmorphology.

Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations

V. Bhat, Arun Kumar, P. Singhmar, 2011, Clinical genetics.

Genetic analysis of ATP7B in 102 south Indian families with Wilson disease

Saketh Kapoor, A. Taly, S. Sinha, 2019, PloS one.