Author

Monia Benhamed Hammer

National Institutes of HealthORCID 0000-0001-9693-2459Unclaimed 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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Approach:statistical model· 2 Assay:DNA methylation· 1 Research Focus:GWAS / association mapping· 1 Organism:mouse· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alexandra Foubert‐SamieriD· 1 shared Alexey A. ShadriniD· 1 shared Amanda Thomas‐WilsoniD· 1 shared Ana S.A. CoheniD· 1 shared André FrankeiD· 1 shared Andreas Arnold· 1 shared Andrew SingletoniD· 1 shared Anna SzutoiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Alexandra Foubert‐SamierORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedJul 30, 2023

The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change

Heidi L. Rehm, Joseph T. Alaimo, Swaroop Aradhya…·Stephen Francis Kingsmore

The paper analyzes VUS rates in genetic testing and finds lower rates in exome/genome sequencing compared to multi-gene panels, suggesting improvements in variant reporting practices.

138 citationstop 1%

whole-exome sequencingwhole-genome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintAug 31, 2019

A genome-wide genetic pleiotropy approach identified shared loci between multiple system atrophy and inflammatory bowel disease

Alexey A. Shadrin, Sören Mucha, David Ellinghaus…·Manu Sharma

This study identifies shared genetic loci between multiple system atrophy and inflammatory bowel disease using conjFDR, highlighting immune and gut-related molecular mechanisms.

DOI 10.1101/751354

mouseDNA methylation

𝕏 PostBluesky