Author

Manjari Deshmukh

University of California, San Francisco

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:database / resource· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Akshi BassiiD· 2 shared Andrew S. PetersoniD· 2 shared Ramesh MenoniD· 2 shared Ravi Kr GuptaiD· 2 shared Abhijit Chowdhury· 1 shared Adam S. ButterworthiD· 1 shared Adreesh MukherjeeiD· 1 shared Aliya NaheediD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Akshi BassiORCID

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2 papers

Recent·Most cited

The genetic drivers of juvenile, young, and early-onset Parkinson's Disease in India

Shan V. Andrews, Prashanth Lingappa Kukkle, Ramesh Menon, Thenral S. Geetha, Vinay Goyal, Rukmini Mridula Kandadai, Hrishikesh Kumar, Rupam Borgohain, Adreesh Mukherjee, Pettarusp Murzban Wadia, Ravi Yadav, Soaham Desai, Niraj Kumar, Deepika Joshi, Sakthivel Murugan, , Vedam Lakshmi Ramprasad

This study identifies genetic risk factors for early-onset Parkinson's Disease in a South Asian population, finding a genome-wide significant signal in the SNCA region and associations with BSN gene variants.

Movement Disorders · Nov 28, 2023Peer-reviewedGenetic & Genomic Medicine

South Asian patient population genetics reveal strong founder effects and high rates of homozygosity - new resources for precision medicine

Jeffrey D. Wall, J. Fah Sathirapongsasuti, Ravi Kr Gupta, Anamitra Barik, Rajesh Kumar, Asif Rasheed, Venkatesan Radha, Saurabh Belsare, Ramesh Menon, Sameer Phalke, Anuradha Mittal, John Z. Fang, Deepak Tanneeru, Manjari Deshmukh, Akshi Bassi, , Andrew S. Peterson

The paper characterizes the genetic structure of South Asian populations, identifies founder effects and high homozygosity, and develops a custom SNP array for genetic studies in the region.

bioRxiv · Oct 2, 2020 · PreprintGenomics