Author

Hiba Ali

Indian Institute of Science Bangalore

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· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1 Research Focus:polygenic risk· 1

Frequent Co-Authors

Khader Valli RupanagudiiD· 2 shared Shweta RamdasiD· 2 shared Albert SteziniD· 1 shared Andie Pinto· 1 shared B. K. Panda· 1 shared Banashree MondaliD· 1 shared Camellia SarkariD· 1 shared Divya Tej SowpatiiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenomics

Khader Valli RupanagudiORCID

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2 papers

Recent·Most cited

Population-Scale Landscape of Mobile Element Insertions Across 82 Diverse Indian Populations

Sagar S, Shreya Ganjigatte Srinivas, Ruchitha Gangaiah Byrohalli, Vidushi Dwivedi, Hiba Ali, Khader Valli Rupanagudi, Ramesh Yelagandula, Divya Tej Sowpati, Ishaan Gupta, Pankaj Yadav, Shweta Ramdas

The paper catalogs mobile element insertions in 82 Indian populations, revealing population-specific variants not present in European databases and highlighting their potential impact on disease associations.

bioRxiv · Aug 2, 2026 · PreprintGenomics

Whole-genome sequencing of 197 cases with Parkinson's Disease reveals novel pathogenic variants in the Indian population

Hiba Ali, Banashree Mondal, Andie Pinto, Camellia Sarkar, B. K. Panda, Khader Valli Rupanagudi, Vikram Venkappayya Holla, Tarunya Nagaraj, Shubha GS Bhat, Shweta Prasad, Mahima Bhardwaj, Pooja Mailankody, Rohan Ramachandra Mahale, Nitish L. Kamble, Ravi Yadav, , Shweta Ramdas

The paper performs whole-genome sequencing on Parkinson's Disease cases in India to identify novel pathogenic variants and quantify polygenic risk.

npj Parkinson s Disease · Jul 6, 2026Peer-reviewedGenetic & Genomic Medicine