Articles with public access mandates - Sarah MathaiLearn more
Not available anywhere: 1
Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinent
SSC Abraham, S Yoganathan, B Koshy, SP Oommen, A Simon, S Mathai, ...
European Journal of Medical Genetics 64 (9), 104291, 2021
Mandates: Department of Science & Technology, India
Available somewhere: 5
Maturity onset diabetes of the young in India–a distinctive mutation pattern identified through targeted next‐generation sequencing
A Chapla, MD Mruthyunjaya, HS Asha, D Varghese, M Varshney, ...
Clinical Endocrinology 82 (4), 533-542, 2015
Mandates: Council of Scientific and Industrial Research, India
WFS1 Gene–associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India
A Chapla, J Johnson, S Korula, N Mohan, A Ahmed, D Varghese, ...
The Journal of Clinical Endocrinology & Metabolism 107 (5), 1328-1336, 2022
Mandates: Department of Biotechnology, India
First report on the draft genome sequences of Corynebacterium diphtheriae isolates from India
B Veeraraghavan, S Anandan, SK Rajamani Sekar, R Gopi, ...
Genome Announcements 4 (6), 10.1128/genomea. 01316-16, 2016
Mandates: World Health Organization
Congenital Adrenal Hyperplasia–A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from India
L Ravichandran, HS Asha, S Mathai, N Thomas, A Chapla
Indian Journal of Endocrinology and Metabolism 28 (2), 117-128, 2024
Mandates: Department of Science & Technology, India
High carrier frequency of CYP21A2 gene mutations in Southern India – underscoring the need for genetic testing in Congenital Adrenal Hyperplasia
L Ravichandran, S Paul, A HS, S Mathai, A Simon, S Danda, N Thomas, ...
Endocrine, 1-7, 2024
Mandates: Department of Science & Technology, India
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