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Alec Reginald Errol Correa

Observed names: Alec Correa, Alec R. E. Correa
ORCID: 0000-0002-9441-9536
Observed ORCID: 0000-0002-9441-9536
OpenAlex ID: A5089627107
Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalis
2021 · Alec Reginald Errol Correa, Kamal Naini, et al. · Prenatal Diagnosis · 26
The spectrum of neurological manifestations and genotype–phenotype correlation in Indian children with Gaucher disease
2023 · Mahesh Venkatachari, Soumalya Chakraborty, et al. · American Journal of Medical Genetics Part A · 8
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First case report of Penttinen syndrome from India
2021 · Bhawana Aggarwal, Alec R. E. Correa, et al. · American Journal of Medical Genetics Part A · 8
Hydrops fetalis in PKD1L1 ‐related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum
2021 · Alec Reginald Errol Correa, Mounika Endrakanti, et al. · Annals of Human Genetics · 8
Methylene Tetrahydrofolate Reductase Deficiency
2020 · Ravneet Kaur, Alec Reginald Errol Correa, et al. · The Indian Journal of Pediatrics · 6
Mevalonate Kinase Deficiency as Cause of Periodic Fever in Two Siblings
2020 · Alec Reginald Errol Correa, Neerja Gupta, et al. · Indian Pediatrics · 4
Report of a Novel Homozygous Nonsense DDR2 Mutation in an Indian Adult Male with Spondylo-meta-epiphyseal Dysplasia, Short Limb-Abnormal Calcification Type
2019 · Neerja Gupta, Alec Reginald Errol Correa, et al. · Journal of Pediatric Genetics · 3
Ethylmalonic encephalopathy masquerading as malabsorption syndrome - A case report
2017 · Amit Kumar Satapathy, Alec Correa, et al. · Meta Gene · 3
Early-onset nephrolithiasis and persistent microscopic hematuria in a child with a novel pathogenic COL4A5 variant in Alport syndrome: A case report and literature review
2025 · Firoz Ahmad, Niladri Bose, et al. · Human Gene · 1
Epigenetic Abnormalities of 11p15.5 Region in Beckwith-Wiedemann Syndrome - A Report of Eight Indian Cases
2020 · Alec Reginald Errol Correa, Puneeta Mishra, et al. · The Indian Journal of Pediatrics · 1
WITHDRAWN: A Decade of Hereditary Cancer Genetic Testing Results in Asian Indian population: Retrospective Study
2026 · Ramesh Menon, Lakshmi Mahadevan, et al. · medRxiv
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ID #866 Liquid biopsy using multiple functional genomic tools reveals clinical and biological insights into replication repair deficient gliomas
2026 · Yoshiko Nakano, Robert Siddaway, et al. · Neuro-Oncology Pediatrics
A novel NMD-escaping STAG2 variant associated with syndromic neurodevelopmental delay, growth failure, and distinctive dysmorphism: expanding the phenotype in male patients and literature review
2026 · Firoz Ahmad, Sapna Sandal, et al. · Gene
Works count: 13
Citation count: 68
H-index: 5
I10-index: 1
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