Sumita Danda

18PUBLICATIONS
65CO-AUTHORS
Developmental genetics (incl. sex determination)Infant and child healthCancer geneticsGene expression (incl. microarray and other genome-wide approaches)Language documentation and description
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Publications (18)

|Sep 26, 2026
Considering Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in Prenatal Genetic Assessment of Cystic Renal Anomalies.

|May 22, 2025
PRRT 2-Related Epilepsy: From Self-Limited Infantile Epilepsy to Atypical Epilepsy Phenotypes.

Madeline Komar, Jashanpreet Sidhu, Jiju Joseph

|May 20, 2025
Ovarian/Tubal Pathology in Premenopausal Women with Breast Cancer: A Prospective Study.

Sahana Punneshetty, Sherin Daniel, Shawn Thomas

|May 19, 2025
Investigating Trends and Challenges in Prenatal Diagnosis of Monogenic Conditions in India-An LMIC Setting-Over Half a Decade.

Lois Sara James, Noel Deep Luke, Eunice Sindhuvi

|May 03, 2025
A Novel Presentation and Variable Phenotypic Spectrum of Homozygous Start-Loss Variant in LYRM7-Associated Mitochondrial Complex III Deficiency.

Noel Deep Luke, Aditya Vijayakrishnan Nair, Ajith Sivadasan

|Mar 06, 2025
COL1A1 and COL1A2 Gene Variants Causing Osteogenesis Imperfecta in a Major Referral Center of India.

Agnes Selina, Madhavi Kandagaddala, Nihal Thomas

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Frequent Collaborators

7 joint publications

Rekha Athiyarath

5 joint publications

Noel Deep Luke

3 joint publications

Preethi Raja Navaneethan

2 joint publications

Hemalatha Illangovan