Rekha Athiyarath

9PUBLICATIONS
42CO-AUTHORS
Developmental genetics (incl. sex determination)Access to justiceInfant and child healthGene expression (incl. microarray and other genome-wide approaches)Language documentation and description
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Publications (9)

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

|May 16, 2026
Prevalence and carrier frequency of Canavan disease in a South Indian community with implications for research and public health.

|Sep 22, 2025
Exceptionally High Cystic Fibrosis-Related Morbidity and Mortality in Infants and Young Children in India: The Need for Newborn Screening and CF-Specific Capacity Building.

Priyanka Medhi, Grace R Paul, Madhan Kumar

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

Madeline Komar, Jashanpreet Sidhu, Jiju Joseph

|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

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Frequent Collaborators

7 joint publications

Sumita Danda

4 joint publications

Noel Deep Luke

3 joint publications

Preethi Raja Navaneethan

2 joint publications

Lois Sara James