Author

Alise Blake

St. Jude Children's Research HospitalORCID 0000-0002-1336-7106Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Kim E. NicholsiD· 2 shared Richa SharmaiD· 2 shared Annika MartiniD· 1 shared Barbara C. JonesiD· 1 shared Christian Peter KratziD· 1 shared Christopher PrevitiiD· 1 shared David JonesiD· 1 shared Dirk F. HockemeyeriD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetics

Kim E. NicholsORCID

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2 papers

Recent·Most cited

GeneticsNature CommunicationsPeer-reviewedSep 14, 2026

Telomere length of both parents contributes to heritable POT1 cancer-predisposition syndrome

Annika Martin, Robert Lu, Alise Blake…·Dirk F. Hockemeyer

The paper investigates how POT1 mutations affect telomere inheritance and cancer risk by analyzing telomere length in families with POT1 mutations.

1 citationtop 4%

humanDNA methylation

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Genetic & Genomic MedicineJournal of Clinical OncologyPeer-reviewedOct 9, 2025

Germline variation in DNA damage repair genes in children with cancer: Unveiling SMARCAL1 as novel osteosarcoma predisposition gene

Ninad Oak, Wenan Chen, Alise K. Blake…·Richa Sharma

The paper identifies SMARCAL1 as a novel predisposition gene for osteosarcoma by analyzing germline variants in DNA damage repair genes across childhood cancer cases.

10 citationstop 3%

humanwhole-exome sequencing

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