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| 35101336 | Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC). | Genet Med | 2022 |
| 35771717 | Characterization of unusual iAMP21 B-lymphoblastic leukemia (iAMP21-ALL) from the Mayo Clinic and Children's Oncology Group. | Genes Chromosomes Cancer | 2022 |
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| 34020826 | Re: Stanley Weng, Renzo G. DiNatale, Andrew Silagy, et al. The Clinicopathologic and Molecular Landscape of Clear Cell Papillary Renal Cell Carcinoma: Implications in Diagnosis and Management. Eur Urol 2021;79:468-77. | Eur Urol | 2021 |
| 33563889 | Myeloid malignancies with 5q and 7q deletions are associated with extreme genomic complexity, biallelic TP53 variants, and very poor prognosis. | Blood Cancer J | 2021 |
| 34767027 | Assessment of Risk of Hereditary Predisposition in Patients With Melanoma and/or Mesothelioma and Renal Neoplasia. | JAMA Netw Open | 2021 |
| 34505882 | Lymphoid blast transformation in an MPN with BCR-JAK2 treated with ruxolitinib: putative mechanisms of resistance. | Blood Adv | 2021 |
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| 31919873 | Clinical utility of fluorescence in situ hybridization-based diagnosis of BCR-ABL1 like (Philadelphia chromosome like) B-acute lymphoblastic leukemia. | Am J Hematol | 2020 |
| 31913406 | Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish Community. | JAMA Cardiol | 2020 |
| 32827877 | Integrated genomic analysis using chromosomal microarray, fluorescence in situ hybridization and mate pair analyses: Characterization of a cryptic t(9;22)(p24.1;q11.2)/BCR-JAK2 in myeloid/lymphoid neoplasm with eosinophilia. | Cancer Genet | 2020 |
| 32820244 | Limited diagnostic impact of duplications <1â¿¿Mb of uncertain clinical significance: a 10-year retrospective analysis of reporting practices at the Mayo Clinic. | Genet Med | 2020 |
| 32644817 | Collaborative, Multidisciplinary Evaluation of Cancer Variants Through Virtual Molecular Tumor Boards Informs Local Clinical Practices. | JCO Clin Cancer Inform | 2020 |
| 32246132 | A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer. | Nat Genet | 2020 |
| 32302940 | Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia. | Cancer Genet | 2020 |
| 32272434 | Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisis. | Cancer Genet | 2020 |
| 32165485 | <i>IGH</i> rearrangement in myeloid neoplasms. | Haematologica | 2020 |
| 30267776 | Use of mate-pair sequencing to characterize a complex cryptic BCR/ABL1 rearrangement observed in a newly diagnosed case of chronic myeloid leukemia. | Hum Pathol | 2019 |
| 31844041 | Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma. | Blood Cancer J | 2019 |
| 31695749 | Stable transmission of complex chromosomal rearrangements involving chromosome 1q derived from constitutional chromoanagenesis. | Mol Cytogenet | 2019 |
| 29992858 | Cryptic ETV6-PDGFRB fusion in a highly complex rearrangement of chromosomes 1, 5, and 12 due to a chromothripsis-like event in a myelodysplastic syndrome/myeloproliferative neoplasm. | Leuk Lymphoma | 2019 |
| 31015206 | Characterization of a cryptic <i>IGH/CCND1</i> rearrangement in a case of mantle cell lymphoma with negative <i>CCND1</i> FISH studies. | Blood Adv | 2019 |
| 30707474 | Acute leukemias harboring KMT2A/MLLT10 fusion: a 10-year experience from a single genomics laboratory. | Genes Chromosomes Cancer | 2019 |
| 30767316 | RNA sequencing identifies a novel USP9X-USP6 promoter swap gene fusion in a primary aneurysmal bone cyst. | Genes Chromosomes Cancer | 2019 |
| 30936193 | Detection of a cryptic <i>NUP214/ABL1</i> gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemia. | Cold Spring Harb Mol Case Stud | 2019 |
| 31160360 | Elucidating a false-negative <i>MYC</i> break-apart fluorescence in situ hybridization probe study by next-generation sequencing in a patient with high-grade B-cell lymphoma with <i>IGH/MYC</i> and <i>IGH/BCL2</i> rearrangements. | Cold Spring Harb Mol Case Stud | 2019 |
| 30497985 | Constitutional chromosome rearrangements that mimic the 2017 world health organization "acute myeloid leukemia with recurrent genetic abnormalities": A study of three cases and review of the literature. | Cancer Genet | 2019 |
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