Deepa Selvi Rani

A novel BRCA1 mutation in an Indian family with hereditary breast/ovarian cancer

K. Thangaraj, Thanemozhi Natarajan, P. Gajalakshmi, 2006, Breast Cancer Research and Treatment.

A novel missense mutation C11994T in the mitochondrial ND4 gene as a cause of low sperm motility in the Indian subcontinent.

L. Singh, K. Thangaraj, B. Chakravarty, 2006, Fertility and sterility.

Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.

K. Thangaraj, P. Nallari, Perundurai S. Dhandapany, 2015, DNA and cell biology.

Genetic affinities of the Jewish populations of India

R. Tamang, G. Chaubey, N. Rai, 2016, Scientific Reports.

An In Silico Analysis of Troponin I Mutations in Hypertrophic Cardiomyopathy of Indian Origin

M. Kumar, P. Kaur, P. Nallari, 2013, PloS one.

Maternal Footprints of Southeast Asians in North India

C. Tyler-Smith, G. Chaubey, M. Metspalu, 2008, Human Heredity.

Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.

K. Thangaraj, P. Nallari, Perundurai S. Dhandapany, 2015, DNA and cell biology.