Sateesh Maddirevula

13PUBLICATIONS
103CO-AUTHORS
Genetic immunologyInfant and child healthMedical biochemistry - inorganic elements and compoundsNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (13)

|Jun 01, 2026
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.

|Feb 20, 2026
WDR59 Is Mutated in Individuals With Autosomal Recessive Syndromic Dilated Cardiomyopathy.

Lama Alabdi, Benjamin Cogne, Ali S Almasood

|Jan 20, 2026
Biallelic STEAP3 Variant in Neonatal Hemophagocytic Lymphohistiocytosis.

Abdullah H Alfalah, Mohamed Y Elsaid, Ahmed Alrajjal

|Nov 24, 2025
Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy.

Pritha Bisarad, Yung-Chun Wang, Peter T Skidmore

|Sep 27, 2025
Detection of Chromosomal Aneuploidy Using Exome Sequencing.

Mohamed H Al-Hamed, Sateesh Maddirevula, Nabil Moghrabi

|Nov 28, 2024
Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome.

Efil Bayam, Peggy Tilly, Stephan C Collins

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Frequent Collaborators

5 joint publications

Ahmed Alfares

3 joint publications

Fowzan S Alkuraya

3 joint publications

Abdullah H Alfalah

2 joint publications

Norah Altuwaijri