Shruti Pande

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 5

Top Topics

Escherichia Coli

Duchenne Muscular Dystrophy

Intellectual Disability

Endoplasmic Reticulum

Top Venues

European journal of human genetics : EJHG

American journal of medical genetics. Part A

FASEB journal : official publication of the Federation of American Societies for Experimental Biology

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

Publications

Shruti Pande, Debasish Kumar Ghosh
Nuclear proteostasis imbalance in laminopathy-associated premature aging diseases. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 37 (8) (2023)
Shruti Pande, Selinda Mascarenhas, Aishwarya Venkatraman, Vivekananda Bhat, Dhanya Lakshmi Narayanan, Shahyan Siddiqui, Stephanie L Bielas, Katta Mohan Girisha, Anju Shukla
Further validation of craniosynostosis as a part of phenotypic spectrum of BCL11B-related BAFopathy. American journal of medical genetics. Part A (2023)
Shruti Pande, Purvi Majethia, Karthik Nair, Lakshmi Priya Rao, Selinda Mascarenhas, Namanpreet Kaur, Michelle C do Rosario, Kausthubham Neethukrishna, Ankur Chaurasia, Bhagesh Hunakunti, Nalesh Jadhav, Sruthy Xavier, Jeevan Kumar, Vivekananda Bhat, Gandham SriLakshmi Bhavani, Dhanya Lakshmi Narayanan, B L Yatheesha, Siddaramappa J Patil, Sheela Nampoothiri, Nutan Kamath, Shrikiran Aroor, Ramesh Bhat Y, Leslie E Lewis, Suvasini Sharma, Shruti Bajaj, Naveen Sankhyan, Shahyan Siddiqui, Shalini S Nayak, Stephanie Bielas, Katta Mohan Girisha, Anju Shukla
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India. European journal of human genetics : EJHG (2023)
Shruti Pande, Purvi Majethia, Karthik Nair, Lakshmi Priya Rao, Selinda Mascarenhas, Namanpreet Kaur, Michelle C do Rosario, Kausthubham Neethukrishna, Ankur Chaurasia, Bhagesh Hunakunti, Nalesh Jadhav, Sruthy Xavier, Jeevan Kumar, Vivekananda Bhat, Gandham SriLakshmi Bhavani, Dhanya Lakshmi Narayanan, B L Yatheesha, Siddaramappa J Patil, Sheela Nampoothiri, Nutan Kamath, Shrikiran Aroor, Ramesh Bhat Y, Leslie E Lewis, Suvasini Sharma, Shruti Bajaj, Naveen Sankhyan, Shahyan Siddiqui, Shalini S Nayak, Stephanie Bielas, Katta Mohan Girisha, Anju Shukla
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India. European journal of human genetics : EJHG (2023)
Debasish Kumar Ghosh, Shruti Pande, Jeevan Kumar, Dhanya Yesodharan, Sheela Nampoothiri, Periyasamy Radhakrishnan, Chilakala Gangi Reddy, Akash Ranjan, Katta Mohan Girisha
The E262K mutation in Lamin A links nuclear proteostasis imbalance to laminopathy-associated premature aging. Aging cell 21 (11) (2022)