Author

Sogol Mostoufi‐Moab

Children's Hospital of PhiladelphiaORCID 0000-0002-8623-1138Unclaimed 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 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:GWAS / association mapping· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Achal NeupaneiD· 1 shared Aime T. FrancoiD· 1 shared Amber R. IsazaiD· 1 shared Andrew J. BaueriD· 1 shared Angela DelaneyiD· 1 shared Carmen Louise WilsoniD· 1 shared Cindy ImiD· 1 shared Deanne TayloriD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Achal NeupaneORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 2, 2023

Trans-ancestral genetic study of diabetes mellitus risk in survivors of childhood cancer: a report from the St. Jude Lifetime Cohort and the Childhood Cancer Survivor Study

Cindy Im, Achal Neupane, Jessica L. Baedke…·Yadav Sapkota

This study identifies novel diabetes risk loci in childhood cancer survivors using whole-genome sequencing and shows higher risk for African ancestry survivors with risk alleles.

DOI 10.1101/2023.06.02.23290868

humanwhole-genome sequencing

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GeneticsJournal of Clinical OncologyPeer-reviewedJan 11, 2022

Fusion-oncogenes are associated with increased metastatic capacity and persistent disease in pediatric thyroid cancers

Aime T. Franco, Julio C. Ricarte-Filho, Amber R. Isaza…·Andrew J. Bauer

This study shows that genetic subtypes of pediatric thyroid cancer, particularly RET/NTRK fusions, are linked to worse clinical outcomes compared to RAS- or BRAF-mutant subtypes.

103 citationstop 1%

humanwhole-exome sequencing

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