Renu Saxena

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 6

Top Topics

Pulmonary Embolism

Intellectual Disability

Botulinum Toxin

Children With Cerebral Palsy

Top Venues

European journal of human genetics : EJHG

Indian journal of pediatrics

American journal of medical genetics. Part A

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)
Sunita Bijarnia Mahay, Sameer Bhatia, Deepti Gupta, Aditi Sud, Sudhisha Dubey, Renu Saxena
CEDNIK Syndrome - A Report of a Clinically Recognizable Disorder with Prenatal Diagnosis. Indian journal of pediatrics 91 (8) (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)
Sunita Bijarnia Mahay, Sameer Bhatia, Deepti Gupta, Aditi Sud, Sudhisha Dubey, Renu Saxena
CEDNIK Syndrome - A Report of a Clinically Recognizable Disorder with Prenatal Diagnosis. Indian journal of pediatrics (2024)
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)