Rati Devendra

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 7

Top Topics

Sickle Cell Disease

Top Venues

Molecular genetics and genomics : MGG

Annals of hematology

Annals of human biology

This page only lists publications with an associated author ORCID identifier.

Publications

Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG 298 (2) (2023)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG 298 (2) (2023)
Rashmi Dongerdiye, Meghana Bokde, Tejashree Anil More, Arati Saptarshi, Rati Devendra, Ashish S Chiddarwar, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population. Annals of hematology (2023)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG 298 (2) (2023)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG 298 (2) (2023)
Tejashree Anil More, Rati Devendra, Rashmi Dongerdiye, Prashant Warang, Prabhakar S Kedar
Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. Molecular genetics and genomics : MGG (2023)
Rati Devendra, Vinod Gupta, Somashekhar S Biradar, Pradeep Bhat, Shantharam Hegde, S L Hoti, Malay B Mukherjee, Harsha V Hegde
G6PD A- is the major cause of G6PD deficiency among the Siddis of Karnataka, India. Annals of human biology 47 (1) (2019)