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Sumita Danda

Christian Medical College and Hospital

SCHOLARLY PAPERS

2

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258

TOTAL CITATIONS

1

Scholarly Papers (2)

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1.

Exome Sequencing in 403 Indian Children with Neurodevelopmental Disorders: Diagnostic Yield, Utility and Challenges in a Resource-Limited Setting

Number of pages: 16 Posted: 05 Dec 2022
Pranav Chand Rayabarapu, Wankhede Vinit, Varsha Vaidya, Anand Subramaniam Iyer, Madhavi Shelke, Shagun Aggarwal, Suvarna Magar, Sumita Danda, Amita Moirangthem, Shubha Rajendra Phadke, Manisha Goyal, Prajnya Ranganath, Mehul Mistri, Parth Shah, Nidhi Shah and Udhaya Hardik Kotecha
Neuberg Centre for Genomic Medicine, Kids Neuro Clinic and Child Rehabilitation Center, Kpond Children Super Specialty hospital, Apollo Hospitals, Integrated Centre for Child Neurodevelopment, Nizam's Institute of Medical Sciences, MGM Medical College, Christian Medical College and Hospital, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Sanjay Gandhi Post Graduate Institute of Medical Sciences, SMS Medical College, Nizam's Institute of Medical Sciences, Neuberg Centre for Genomic Medicine, Neuberg Centre for Genomic Medicine, Neuberg Centre for Genomic Medicine and Neuberg Centre for Genomic Medicine
Downloads 149 (508,926)

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Neurodevelopmental disorders, next generation sequencing, Exome Sequencing, Copy Number Variations

2.

Phenotype-Genotype Data from a Cohort of 120 Patients with Cystic Fibrosis Followed at a Tertiary Referral Hospital in South India

Number of pages: 36 Posted: 08 Sep 2023
Sneha D. Varkki, Rekha A, Aaron Chapla, Sumita Danda, Priyanka Medhi, Jansi Rani N and Grace R. Paul
Christian Medical College and Hospital, Christian Medical College and Hospital, The Chinese University of Hong Kong (CUHK) - Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong, Christian Medical College and Hospital, Christian Medical College and Hospital, Christian Medical College and Hospital and Nationwide Children’s Hospital
Downloads 109 (645,052)
Citation 1

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CF, India, CFTR mutations, Genetics