Detection of mutations in SF3B1, EIF1AX and GNAQ in primary orbital melanoma by candidate gene analysis

Genomic determinants of chronic myelomonocytic leukemia

(2017) B J Patel et al.   LEUKEMIA

KRAS, NRAS and BRAF mutations in colorectal cancer and melanoma

(2017) Jonas Cicenas et al.   MEDICAL ONCOLOGY

Whole-exome sequencing identifies recurrent SF3B1 R625 mutation and comutation of NF1 and KIT in mucosal melanoma

(2017) Jennifer D. Hintzsche et al.   MELANOMA RESEARCH

SF3B1 and BAP1 mutations in blue nevus-like melanoma

(2017) Klaus G Griewank et al.   MODERN PATHOLOGY

Primary Orbital Melanoma: Presentation, Treatment, and Long-term Outcomes for 13 Patients

(2017) Anna M. Rose et al.   Frontiers in Oncology

Presentation, Treatment, and Prognosis of Secondary Melanoma within the Orbit

(2017) Anna M. Rose et al.   Frontiers in Oncology

Comparing the Prognostic Value of BAP1 Mutation Pattern, Chromosome 3 Status, and BAP1 Immunohistochemistry in Uveal Melanoma

(2016) Johannes A.P. van de Nes et al.   AMERICAN JOURNAL OF SURGICAL PATHOLOGY

Recurrent activating mutations of G-protein-coupled receptor CYSLTR2 in uveal melanoma

(2016) Amanda R Moore et al.   NATURE GENETICS

Uveal Melanomas with SF3B1 Mutations

(2016) Serdar Yavuzyigitoglu et al.   OPHTHALMOLOGY

Driver Mutations in Uveal Melanoma

(2016) Christina L. Decatur et al.   JAMA Ophthalmology

SF3B1 and EIF1AX mutations occur in primary leptomeningeal melanocytic neoplasms; yet another similarity to uveal melanomas

(2016) Heidi V. N. Küsters-Vandevelde et al.   Acta Neuropathologica Communications

Deep sequencing of uveal melanoma identifies a recurrent mutation in PLCB4

(2015) Peter Johansson et al.   Oncotarget

Rare SF3B1 R625 mutations in cutaneous melanoma

(2014) Yong Kong et al.   MELANOMA RESEARCH

Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma

(2014) Anna E Koopmans et al.   MODERN PATHOLOGY

The genetic basis of myelodysplasia and its clinical relevance

(2013) M. Cazzola et al.   BLOOD

Lack of SF3B1 R625 mutations in cutaneous melanoma

(2013) Bastian Schilling et al.   Diagnostic Pathology

Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3

(2013) Marcel Martin et al.   NATURE GENETICS

Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma

(2013) J William Harbour et al.   NATURE GENETICS

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

(2011) L. Malcovati et al.   BLOOD

Frequent pathway mutations of splicing machinery in myelodysplasia

(2011) Kenichi Yoshida et al.   NATURE

Mutations inGNA11in Uveal Melanoma

(2010) Catherine D. Van Raamsdonk et al.   NEW ENGLAND JOURNAL OF MEDICINE

Translating Uveal Melanoma Cytogenetics Into Clinical Care

(2009) Bertil Damato   ARCHIVES OF OPHTHALMOLOGY

Frequent somatic mutations of GNAQ in uveal melanoma and blue naevi

(2008) Catherine D. Van Raamsdonk et al.   NATURE