Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Single-Nucleotide Polymorphism Array for Histologically Ambiguous Melanocytic Tumors.

The Journal of molecular diagnostics : JMD - 1 Nov 2022

Geiersbach Katherine B, Gliem Troy J, Jenkins Sarah M, Gaitatzes Athanasios G, Brodersen Pamela R, Negro Megan E, Clees Megan J, Swanson Kirsten E, Boeckman Riley M, Natrop Travis J, Sukov William R, Shah Kabeer K, Greipp Patricia T, Rowsey Ross A, Flotte Thomas J, Erickson Lori A, Guo Ruifeng

Abstract excerpt

Genome-wide copy number profiling by single-nucleotide polymorphism (SNP) array is increasingly employed in the clinical diagnostic workup of melanocytic tumors. We present our SNP array results on 675 melanocytic tumors, including 615 histologically ambiguous tumors evaluated by our institution's dermatopathology consultation service and a separate validation cohort of 26 known benign nevi and 34 known malignant...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cancer Genomics and Diagnostics
Share to Chromosome Aberrations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cutaneous Melanoma Detection and Management

Share to Melanoma

Share to Melanoma and MAPK Pathways

Share to Polymorphism, Single Nucleotide

Share to Skin Neoplasms

Source

Identifiers

PMID: 36115511
DOI: 10.1016/j.jmoldx.2022.08.004

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Single-Nucleotide Polymorphism Array for Histologically Ambiguous Melanocytic Tumors.PMID 36115511Read ↗

Evaluating melanocytic lesions with single nucleotide polymorphism (SNP) chromosomal microarray.Semantic proximity Read ↗

DNA copy number changes correlate with clinical behavior in melanocytic neoplasms: proposal of an algorithmic approach.Semantic proximity Read ↗

Copy number variation in archival melanoma biopsies versus benign melanocytic lesions.Semantic proximity Read ↗

Molecular pathology as a diagnostic aid in difficult-to-classify melanocytic tumours with spitzoid morphology.Semantic proximity Read ↗

Differentiation of Malignant Melanoma From Benign Nevus Using a Novel Genomic Microarray With Low Specimen RequirementsSemantic proximity Read ↗

The impact of next generation sequencing studies on the diagnosis of BAP1 inactivated melanocytic tumors.Semantic proximity Read ↗

MAP2K1 ‐mutated melanocytic tumors have reproducible histopathologic features and share similarities with melanocytic tumors with BRAF V600E mutationsSemantic proximity Read ↗

Role of single‐nucleotide polymorphism microarray in the classification of BAP1 ‐inactivated melanocytic tumoursSemantic proximity Read ↗

Melanotic tumors of the nervous system are characterized by distinct mutational, chromosomal and epigenomic profiles.Semantic proximity Read ↗

Comparison of melanoma gene expression score with histopathology, fluorescence in situ hybridization, and SNP array for the classification of melanocytic neoplasms.Semantic proximity Read ↗

Towards diagnostic criteria for malignant deep penetrating melanocytic tumors using single nucleotide polymorphism array and next-generation sequencing.Semantic proximity Read ↗

Copy Number Analysis in Congenital Nevi: Concordance and Diagnostic Limitations of aCGH, sWGS, and Methylation ProfilingSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.