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Jabasteen Johnson

Observed names: J Jabasteen, Jabasteen J
ORCID: 0000-0002-5220-9215
Observed ORCID: 0000-0002-5220-9215
OpenAlex ID: A5087834767
The BRCA mutation spectrum among breast and ovarian cancers in India: highlighting the need to screen BRCA1 185delAG among South Indians
2024 · Ajoy Oommen John, Ashish Singh, et al. · European Journal of Human Genetics · 12
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Genetic Heterogeneity and Challenges in the Management of Permanent Neonatal Diabetes Mellitus: A Single-Centre Study from South India
2022 · Sophy Korula, Lavanya Ravichandran, et al. · Indian Journal of Endocrinology and Metabolism · 11
A series of genetically confirmed congenital lipodystrophy and diabetes in adult southern Indian patients
2024 · Remya Rajan, Aaron Chapla, et al. · Scientific Reports · 10
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WFS1 Gene–associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India
2022 · Aaron Chapla, Jabasteen Johnson, et al. · The Journal of Clinical Endocrinology & Metabolism · 10
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Allele-specific PCR and Next-generation sequencing based genetic screening for Congenital Adrenal Hyperplasia in India
2021 · Lavanya Ravichandran, Sophy Korula, et al. · European Journal of Medical Genetics · 9
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BRCA1 and BRCA2 gene mutation spectrum and high frequency of BRCA1 185delAG among breast and ovarian cancer patients from Southern India.
2023 · Aaron Chapla, Ajoy John, et al. · Research Square · 4
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Glucokinase-Related Maturity-Onset Diabetes of the Young in India and the Clinical Utility of the MODY Probability Calculator for Identifying Underdiagnosed and Rare Forms
2025 · Aaron Chapla, Jabasteen Johnson, et al. · Research Square
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Etiological profile of young diabetes mellitus in south indian population
2024 · Sadishkumar Kamalanathan, Kg Rashmi, et al. · Endocrine Abstracts
BRCA1 and BRCA2 gene mutation spectrum and a high frequency of BRCA1 185delAG among breast and ovarian cancer patients from Southern India.
2022 · Ajoy Oommen John, Ashish Singh, et al. · Research Square
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Abstract 114: WFS1 gene associated diabetes phenotypes and identification of a novel founder mutation in Southern India
2022 · Aaron Chapla, Jabasteen Johnson, et al. · Indian Journal of Endocrinology and Metabolism
Abstract 109: Long-range PCRs and MLPA for molecular analysis of large rearrangements in 21 hydroxylase deficiency
2022 · Lavanya Ravichandran, Sophy Korula, et al. · Indian Journal of Endocrinology and Metabolism
Comprehensive and Cost-Effective Strategy for Genetic Screening of Congenital Adrenal Hyperplasia (CAH) in India
2021 · Lavanya Ravichandran, Sophy Korula, et al. · Journal of the Endocrine Society
Works count: 12
Citation count: 56
H-index: 5
I10-index: 4
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