Sumita Danda

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 14

Top Topics

Duchenne Muscular Dystrophy

Dna Methylation

Gas Chromatography Mass Spectrometry

Top Venues

Journal of perinatal medicine

American journal of medical genetics. Part A

Indian journal of pediatrics

Journal of pediatric genetics

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

Publications

Hemalatha Ilangovan, Janane Elangovan, Sumita Danda, Manisha Madhai Beck, Preethi Navaneethan, Rekha A
Exploring the clinical utility of exome sequencing/Mono, Duo, Trio in prenatal testing: a retrospective study in a tertiary care centre in South India. Journal of perinatal medicine 52 (5) (2024)
Hemalatha Ilangovan, Janane Elangovan, Sumita Danda, Manisha Madhai Beck, Preethi Navaneethan, Rekha A
Exploring the clinical utility of exome sequencing/Mono, Duo, Trio in prenatal testing: a retrospective study in a tertiary care centre in South India. Journal of perinatal medicine 52 (5) (2024)
Hemalatha Ilangovan, Janane Elangovan, Sumita Danda, Manisha Madhai Beck, Preethi Navaneethan, Rekha A
Exploring the clinical utility of exome sequencing/mono, duo, trio in prenatal testing: a retrospective study in a tertiary care centre in south India. Journal of perinatal medicine (2024)
Debashish Danda, Ruchika Goel, Jayakanthan Kabeerdoss, Celi Sun, Sumita Danda, Anisea Lincy Franklin, George Joseph, Swapan K Nath
Angiogenesis related genes in Takayasu Arteritis (TAK): robust association with Tag SNPs of IL-18 and FGF-2 in a South Asian Cohort. Journal of human genetics (2023)
Sumita Danda, Chaitanya Datar, Archana Kher, Tanmay Deshpande, Maya Mary Thomas, Samuel P Oommen
First reported cases with Xia-Gibbs syndrome from India harboring novel variants in AHDC1. American journal of medical genetics. Part A 188 (8) (2022)
Minu Jose Chiramel, Lydia Mathew, Rekha A, Aaron Chapla, Dharshini Sathishkumar, Thenmozhi Mani, Sumita Danda, Renu George
Genotype of autosomal recessive congenital ichthyosis from a tertiary care center in India. Pediatric dermatology 39 (3) (2022)
Ananthapadmanabha Kotambail, Pavalan Selvam, Karthik Muthusamy, Maya Thomas, Sniya Valsa Sudhakar, Chetan Ghati, Sumita Danda, Gautham Arunachal Udupi
Clustering of Juvenile Canavan disease in an Indian community due to population bottleneck and isolation: genomic signatures of a founder event. European journal of human genetics : EJHG (2022)
Rekha A, Shanu Chandran, Arpita Roy Ghatak, Niranjan Thomas, Sumita Danda
Novel Mutations in CRLF1: Case Reports with Crisponi Syndrome. Indian journal of pediatrics 89 (11) (2022)
Anne George Cherian, Vandana Kamath, Vivi Srivastava, Sumita Danda, Tunny S Purayidathil, Manisha Madhai Beck
Spectrum of Chromosomal Abnormalities Detected by Conventional Cytogenetic Analysis Following Invasive Prenatal Testing of Fetuses with Abnormal Ultrasound Scans. Journal of obstetrics and gynaecology of India 72 (Suppl 1) (2022)
Ajay Kumar Chaudhary, Aishwarya Gholse, Hampapathalu Adimurthy Nagarajaram, Ashwin Bhikaji Dalal, Neerja Gupta, Atanu Kumar Dutta, Sumita Danda, Rekha Gupta, Hariharan V Sankar, Gandham SriLakshmi Bhavani, Katta Mohan Girisha, Shubha Rao Phadke, Prajnya Ranganath, Murali Dharan Bashyam
Ectodysplasin pathogenic variants affecting the furin-cleavage site and unusual clinical features define X-linked hypohidrotic ectodermal dysplasia in India. American journal of medical genetics. Part A (2021)
Parag M Tamhankar, Lakshmi Vasudevan, Pratima Kondurkar, Sarfaraj Niazi, Rita Christopher, Dhaval Solanki, Pooja Dholakia, Mamta Muranjan, Mahesh Kamate, Umesh Kalane, Jayesh Sheth, Vasundhara Tamhankar, Reena Gulati, Madhavi Vasikarla, Sumita Danda, Shaik M Naushad, Katta M Girisha, Shekhar Patil
Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1. Journal of pediatric genetics 10 (3) (2020)
Shruthi Sudarshan, Atin Kumar, Arun Gupta, Neetu Bhari, Gomathy Sethuraman, Tanuja Kaushal, Ankita Pradhan, Savita Sapra, Neerja Gupta, Punit Kaur, Sheffali Gulati, Biswaroop Chakrawarty, Sumita Danda, Meenakshi Bhat, Seema Kapoor, Katta M Girisha, Naveen Sankhyan, Madhulika Kabra, Madhumita Roy Chowdhury
Mutation Spectrum of Tuberous Sclerosis Complex Patients in Indian Population. Journal of pediatric genetics 10 (4) (2020)
Ansa P Sunny, Gautham Arunachal, Sumita Danda
Van der Woude Syndrome: IRF6 Mutations. Indian journal of pediatrics 86 (11) (2019)
Ashwin B Dalal, Prajnya Ranganath, Shubha R Phadke, Madhulika Kabra, Sumita Danda, Ratna Dua Puri, V H Sankar, Neerja Gupta, S J Patil, Kausik Mandal, Parag Tamhankar, Shagun Aggarwal, Meenal Agarwal
Prenatal diagnosis in India is not limited to sex selection. Genetics in medicine : official journal of the American College of Medical Genetics 17 (1) (2015)