Neha Dagaonkar

Diagnostic Utility of Exome Sequencing for Kidney Disease

Emily Groopman, Maddalena Marasà, Sophia Cameron‐Christie et al. · New England Journal of Medicine · 2018 · 722 citations · Full text

Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis

Omar Niss, Satheesh Chonat, Neha Dagaonkar et al. · Blood Cells Molecules and Diseases · 2016 · 82 citations · Full text

Genotype-phenotype Correlations, Genetic Disorder, Genetics +4

The Spectrum of SPTA1-Associated Hereditary Spherocytosis

Satheesh Chonat, Mary Risinger, Haripriya Sakthivel et al. · Frontiers in Physiology · 2019 · 56 citations · Full text

A comprehensive next‐generation sequencing assay for the diagnosis of epidermolysis bullosa

Anne W. Lucky, Neha Dagaonkar, Karen M. Lammers et al. · Pediatric Dermatology · 2018 · 36 citations

Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia

Anna Alkelai, Shahar Shohat, Lior Greenbaum et al. · Journal of Human Genetics · 2020 · 26 citations

Function Mutation, Psychiatry, Genetic Disorder +9