Ishwar Chandar Verma (Ishwar Verma, Ishwar C Verma, Ishwar Chander Verma)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 10

Top Topics

Botulinum Toxin

Children With Cerebral Palsy

Top Venues

European journal of human genetics : EJHG

American journal of medical genetics. Part A

Indian journal of pediatrics

Congenital anomalies

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

Publications

Sameer Bhatia, Swasti Pal, Samarth Kulshrestha, Dhiren Gupta, Arun Soni, Renu Saxena, Sunita Bijarnia Mahay, Ishwar Chandar Verma, Ratna Dua Puri
Role of next generation sequencing in diagnosis and management of critically ill children with suspected monogenic disorder. European journal of human genetics : EJHG (2024)
Sameer Bhatia, Swasti Pal, Samarth Kulshrestha, Dhiren Gupta, Arun Soni, Renu Saxena, Sunita Bijarnia Mahay, Ishwar Chandar Verma, Ratna Dua Puri
Role of next generation sequencing in diagnosis and management of critically ill children with suspected monogenic disorder. European journal of human genetics : EJHG 32 (9) (2024)
Ishwar Chandar Verma
Practical Approach to Pediatric and Adolescent Endocrinology: IPS Kochar (Ed), Smita Ramachandran (Co-Ed) and Aashish Sethi (Co-Ed) : Published by Thieme Medical Publisher; Stuttgart. 47 Illustrations; 1st Edition; 2021; ISBN: 978-93-90553-06-8; Pages: 212; Price: Rs. 920. Indian journal of pediatrics (2023)
Sudha Kohli, Renu Saxena, Ratna Dua Puri, Sunita Bijarnia Mahay, Swasti Pal, Sudhisha Dubey, Veronica Arora, Ishwar Chandar Verma
The molecular landscape of oculocutaneous albinism in India and its therapeutic implications. European journal of human genetics : EJHG (2023)
Ranjana Mishra, Samarth Kulshreshtha, Kausik Mandal, Ashok Khurana, Dan Diego-Álvarez, Laura Pradas, Renu Saxena, Shubha Rao Phadke, Amita Moirangthem, Suzena Masih, Seema Sud, Ishwar Chandar Verma, Ratna Dua Puri
COASY related pontocerebellar hypoplasia type 12: A common Indian mutation with expansion of the phenotypic spectrum. American journal of medical genetics. Part A 188 (8) (2022)
Ishwar Chandar Verma, Sudha Kohli, Shruti Shenbagam, Sunita Bijarnia Mahay, Ratna DuaPuri, Renu Saxena
Carrier screening of spinal muscular atrophy in North Indian population and its public health implications. Clinical genetics 98 (2) (2021)
Sapna Sandal, Veronica Arora, Ishwar Chandar Verma
ANO5-associated Gnathodiaphyseal dysplasia with calvarial doughnut lesions: First report in an Asian Indian with an expanded phenotype. Congenital anomalies 61 (1) (2020)
Veronica Arora, Ratna Dua Puri, Sunita Bijarnia-Mahay, Ishwar Chandar Verma
Expanding the phenotypic and genotypic spectrum of Wiedemann-Steiner syndrome: First patient from India. American journal of medical genetics. Part A 182 (5) (2020)
Ishwar Chandar Verma, Sameer Bhatia, Veronica Arora
Genetic Testing in Pediatric Epilepsy. Indian journal of pediatrics 88 (10) (2020)
Veronica Arora, Sunita Bijarnia Mahay, Samarth Kulshreshtra, Kanika Singh, Ratna Dua Puri, Ishwar Chandar Verma
Prenatal presentation of a rare genetic disorder: a clinical, autopsy and molecular correlation. Autopsy & case reports 9 (4) (2019)