Author

Siddharth Gahlaut

Indian Institute of Science Education and Research Pune

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Assay:DNA methylation· 1

Frequent Co-Authors

Ashraf ul Mannan· 2 shared Ashwini C. BapatiD· 2 shared Chaitanyanand B. KoppikeriD· 2 shared Laleh Busheri· 2 shared Ruhi R. Reddy· 2 shared Rupa MishraiD· 2 shared Santosh DixitiD· 2 shared Smeeta Nare· 2 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Ashraf ul Mannan

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2 papers

Recent·Most cited

Assessing germline mutational profile and its clinicopathological associations in Triple Negative Breast Cancer

Jisha John, Ashwini C. Bapat, Siddharth Gahlaut, Naveen Luke Demonte, Rahul Kumar, Yashaswi Thakur, Christina Mathew, Aishwarya Konnur, Namrata P. Namewar, Ruhi R. Reddy, Sanket Nagarkar, Smeeta Nare, GEORGE V. THOMAS, Laleh Busheri, Asha Reddy, , Chaitanyanand B. Koppiker

The paper analyzes germline mutations in TNBC patients in India and identifies BRCA1/2 as the most common mutated genes, with novel mutations and a higher proportion of variants of uncertain significance in non-BRCA genes.

Cancer Genetics · Jun 18, 2025Peer-reviewedGenetic & Genomic Medicine

Familial Genetic Cancer Risk Assessment with respect to a Silent BRCA2 mutation

Ashwini C. Bapat, Siddharth Gahlaut, Rupa Mishra, Aijaz Ul Noor, Laleh Busheri, Ruhi R. Reddy, Shahin Shaikh, Ashraf ul Mannan, Smeeta Nare, Santosh Dixit, Chaitanyanand B. Koppiker

This study reports a silent BRCA2 mutation associated with hereditary breast cancer in a male patient and his family, highlighting its potential spliceogenic effect and clinical relevance.

medRxiv · Jul 1, 2021 · PreprintGenetic & Genomic Medicine