Author

Samantha E. Roellinger

Observed name: Samantha Roellinger

Institution: Mayo Clinic

Observed institution: Mayo Clinic

OpenAlex ID: A5065337819

Natural underlying mtDNA heteroplasmy as a potential source of intra‐person hiPSC variability

2016 · Ester Perales‐Clemente, Alexandra N Cook, et al. · The EMBO Journal · 75

Development and Clinical Implementation of a Combination Deletion PCR and Multiplex Ligation-Dependent Probe Amplification Assay for Detecting Deletions Involving the Human α-Globin Gene Cluster

2011 · Benjamin R. Kipp, Samantha E. Roellinger, et al. · Journal of Molecular Diagnostics · 32

Variant Detection in 3′ Exons of PMS2 Using Exome Sequencing Data

2024 · Nipun A. Mistry, Samantha E. Roellinger, et al. · Journal of Molecular Diagnostics · 2

P586: A retrospective analysis of mitochondrial genome sequencing data reveals opportunities for improved representation in genomic testing

2026 · Michelle Cox, Samantha Roellinger, et al. · Genetics in Medicine Open

30. A cost-effective bioinformatics triage strategy for testing PMS2 using short-read next generation sequencing

2022 · Wei Shen, Tejaswi Koganti, et al. · Cancer Genetics

Cerebellar Ataxia Renal-failure Neuropathy with Encephalopathy (mt-CARNE): A New Mitochondrial Syndrome Identified by Sequencing Frozen Nerve and Kidney Tissue DNA (P1.330)

2018 · Peng Soon Ng, Jadee Neff, et al. · Neurology

Works count: 6

Citation count: 109

H-index: 2

I10-index: 2