Author

Miika M. Mehine

Memorial Sloan Kettering Cancer CenterORCID 0000-0003-0443-0625Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genomics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Assay:whole-exome sequencing· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Chaitanya BandlamudiiD· 2 shared Diana L. MandelkeriD· 2 shared Fergus J. CouchiD· 2 shared Mark E. RobsoniD· 2 shared Susan M. DomchekiD· 2 shared Álvaro N.A. MonteiroiD· 1 shared Anton Mikhailovich SafonoviD· 1 shared Antonio MarraiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenomics

Chaitanya BandlamudiORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

GenomicsbioRxivPreprintFeb 5, 2024

Tumor suppressor heterozygosity and homologous recombination deficiency mediate resistance to front-line therapy in breast cancer

Anton Mikhailovich Safonov, Antonio Marra, Chaitanya Bandlamudi…·Pedram Razavi

The paper identifies how germline and somatic mutations interact to cause resistance to CDK4/6 inhibitors in breast cancer and proposes a sequential treatment strategy using PARP inhibitors.

18 citations

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsbioRxivPreprintDec 14, 2023

Saturation genome editing-based functional evaluation and clinical classification of BRCA2 single nucleotide variants

Huaizhi Huang, Chunling Hu, Jie Na…·Fergus J. Couch

The paper functionally characterizes BRCA2 variants using saturation genome editing and classifies them clinically, finding functionally abnormal variants are associated with increased cancer risk.

5 citations

humanwhole-exome sequencing

𝕏 PostBluesky