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Megan F. Hoenig
Observed names:
Hoenig, Megan,
Megan F.H. Bishop,
Megan Hoenig
Institution:
Mayo Clinic
Observed institution:
Mayo Clinic
ORCID:
0000-0001-7770-9841
Observed ORCID:
0000-0001-7770-9841
OpenAlex ID:
A5050809666
Renal Neoplasia in Birt-Hogg-Dubé Syndrome: Integrated Histopathologic, Bulk, and Single-cell Transcriptomic Analysis
2025
·
Sounak Gupta
, Surendra Dasari
, et al.
·
European Urology
·
26
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline PALB2 sequence variants
2025
·
Marcy E. Richardson
, Megan F.H. Bishop
, et al.
·
The American Journal of Human Genetics
·
6
PDF
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
PDF
P086: Mosaic Li-Fraumeni syndrome identified in patient with a previously presumed germline variant following preimplantation genetic testing: A case report
2023
·
Rhianna Urban
, Megan Holdren
, et al.
·
Genetics in Medicine Open
·
1
PDF
Genetic testing outcomes in utilization management genetic counseling clinic compared to genetic testing ordered by non-genetics providers
2019
·
Hoenig, Megan
·
D-Scholarship@Pitt (University of Pittsburgh)
·
1
Mosaic Li Fraumeni Syndrome Not Identified in Germinal Tissue
2026
·
Rhianna M. Urban
, Nisha Kanwar
, et al.
·
Molecular Genetics & Genomic Medicine
PDF
P060: Spectrum of genetic alterations for hereditary paraganglioma-pheochromocytoma syndrome testing: Eight-year experience from a single diagnostic laboratory
2023
·
Megan Holdren
, Rhianna Urban
, et al.
·
Genetics in Medicine Open
Somatic genetic testing in cancer: how the medical genetics provider can help
2021
·
Megan Hoenig
, Nicholas Mitsiades
, et al.
·
Molecular Genetics and Metabolism
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Works count:
8
Citation count:
36
H-index:
2
I10-index:
1
Year
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