Author

Melissa A. Roberts

Denali Therapeutics (United States)

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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Cell Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Approach:statistical model· 1

Frequent Co-Authors

Adreesh MukherjeeiD· 1 shared Akshi BassiiD· 1 shared Alyssa J. Mathiowetz· 1 shared Ana Paula ArrudaiD· 1 shared Anastasia G. HenryiD· 1 shared Anbu Kayalvizhi· 1 shared Andrew S. PetersoniD· 1 shared Atanu BiswasiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adreesh MukherjeeORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

CLCC1 promotes hepatic neutral lipid flux and nuclear pore complex assembly

Alyssa J. Mathiowetz, Emily S. Meymand, Güneş Parlakgül, Niek van Hilten, Emily F. Torres, Leonardo Luís Artico, Kirandeep K. Deol, Mike Lange, Stephany P. Pang, Cody E. Doubravsky, Melissa A. Roberts, Danielle M. Jorgens, Reena Zalpuri, Misun Kang, Casadora C. A. Boone, , James A. Olzmann

This study identifies CLCC1 as a regulator of hepatic neutral lipid flux and nuclear pore complex assembly through CRISPR screens and functional analyses.

Nature · Feb 25, 2026Peer-reviewedCell Biology

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