Author

Swapnil Mittal

University of California San Diego

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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Genetics· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Assay:whole-exome sequencing· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1

Frequent Co-Authors

Joseph G. GleesoniD· 3 shared Changuk ChungiD· 2 shared Chelsea BarrowsiD· 2 shared Keng Ioi VongiD· 2 shared Martin W. BreussiD· 2 shared Valentina StanleyiD· 2 shared Xiaoxu YangiD· 2 shared Alexej S. AbyzoviD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Joseph G. GleesonORCID

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Author profile →

3 papers

Recent·Most cited

Cell-type-resolved somatic mosaicism reveals clonal dynamics of the human forebrain

Changuk Chung, Xiaoxu Yang, Robert F. Hevner, Katie L. Kennedy, Keng Ioi Vong, Yang Liu, Arzoo M. Patel, Rahul Nedunuri, Scott T. Barton, Geoffroy P. J. C. Noël, Chelsea Barrows, Valentina Stanley, Swapnil Mittal, Martin W. Breuss, Johannes C. M. Schlachetzki, , Joseph G. Gleeson

The paper uses mosaic variant barcodes to analyze clonal dynamics in human forebrain cell types, revealing lineage relationships and clonal spread patterns.

Nature · Apr 10, 2024Peer-reviewedNeuroscience

Comprehensive multiomic profiling of somatic mutations in malformations of cortical development

Changuk Chung, Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels, H. Westley Phillips, Zhen Li, Ashley P.L. Marsh, Martin W. Breuss, Laurel Ball, Camila Araújo Bernardino Garcia, Renee D. George, Jing Gu, Mingchu Xu, , Eduardo Maury

This study identifies 69 mutated genes in malformations of cortical development using multiomic profiling of 317 brain resections and single-cell sequencing.

Nature Genetics · Jan 12, 2023Peer-reviewedGenetics

Evaluating Human Mutation Databases for 'Treatability' Using Personalized Antisense Oligonucleotides

Swapnil Mittal, Isaac Tang, Joseph G. Gleeson

The paper evaluates human mutation databases to identify treatable variants using antisense oligonucleotides, finding most pathogenic variants could be targeted therapeutically.

bioRxiv · Jan 4, 2022 · PreprintGenetics