Author

Anmol Kumar

University of HelsinkiORCID 0000-0002-5626-4190Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Aarno V. PalotieiD· 1 shared Anastasia Kytölä· 1 shared Anna SyreeniiD· 1 shared Anni A. AntikaineniD· 1 shared Anni YlineniD· 1 shared Elina Kilpeläinen· 1 shared Jani K. HaukkaiD· 1 shared Jukka Putaala AiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Aarno V. PalotieORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineScientific ReportsPeer-reviewedJun 11, 2024

Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes

Anni A. Antikainen, Jani K. Haukka, Anmol Kumar…·the FinnDiane Study Group

The paper uses whole-genome sequencing to identify genetic variants associated with stroke in type 1 diabetes and finds replication evidence for several loci in both diabetic and non-diabetic populations.

5 citations

humanwhole-genome sequencing

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