Samuel Strohbehn
University of Washington(US)
Publications by Year
Research Areas
Cutaneous Melanoma Detection and Management, RNA Research and Splicing, Genetic Neurodegenerative Diseases, Metabolism and Genetic Disorders, Melanoma and MAPK Pathways
Most-Cited Works
- → Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition(2025)28 cited
- → Acute Kidney Injury Following Encorafenib and Binimetinib for Metastatic Melanoma(2020)9 cited
- → Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition(2023)7 cited
- → Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A(2023)7 cited
- → Acute kidney injury after ruxolitinib: Common complication, uncommon cause(2020)4 cited
- → Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome(2023)3 cited
- → Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts(2024)2 cited
- → Acute and chronic kidney function decline in patients receiving BRAF/MEK inhibitors for melanoma(2024)2 cited
- → MO344: Effect of Cancer Stage on Adverse Kidney Outcomes in Patients With Advanced Melanoma Treated With Immune Checkpoint Inhibitors(2022)