Genetic basis of cancer

A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma.

Clinical genetics·2014

Isolation of tumor suppressor genes in melanoma by cDNA microarray.

Methods in molecular medicine·2012

Chromosome Microdissection for Detection of Subchromosomal Alterations by FISH.

Methods in molecular medicine·2011

Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.

Oncogene·2007

The value of molecular haplotypes in a family-based linkage study.

American journal of human genetics·2006

A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.

Journal of medical genetics·2005

Antibody-drug conjugates in breast cancer: the first-line and curative setting.

Current opinion in oncology·2026

Peripheral neuropathies associated with immunoglobulin M monoclonal gammopathies and low-grade B-cell lymphomas: diagnostic and therapeutic approach.

Current opinion in oncology·2026

The many facets of Kaposi sarcoma-associated herpesvirus/human herpes virus-8 multicentric Castleman disease: clinical spectrum, diagnostic innovations, and therapeutic management.

Current opinion in oncology·2026

Haemophagocytic lymphohistiocytosis: a life threatening complication of lymphoma.

Current opinion in oncology·2026

Artificial intelligence for systemic therapy selection and prediction of outcomes in advanced gynecological cancers.

Current opinion in oncology·2026

Artificial intelligence-augmented robotic surgery in gynecologic oncology: intraoperative assistance and analytics.

Current opinion in oncology·2026

Systems genetics analysis reveals immune mediators of coronavirus disease severity in mice.

Genetics·2026

Molecular clusters and precision medicine in pheochromocytomas and paragangliomas.

Endocrine-related cancer·2026

Short-term outcomes of a randomized, mixed-methods trial to improve hereditary cancer test results disclosure and follow-up communication with family.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

Genetic associations and candidate functional genes linking depression and obesity: a multi-omics integrative study.

Frontiers in genetics·2026

Multi-Site Aggregation of p53: Insights from Self- and Co-Aggregation of Multiple Aggregation-Prone Regions.

ACS omega·2026

Sex differences in the pathogenesis of degenerative knee osteoarthritis: a comparative transcriptomics analysis.

Frontiers in aging·2026

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Genetic basis of cancer

Related Concept Videos

A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma.

Isolation of tumor suppressor genes in melanoma by cDNA microarray.

Chromosome Microdissection for Detection of Subchromosomal Alterations by FISH.

Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.

The value of molecular haplotypes in a family-based linkage study.

A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.

Antibody-drug conjugates in breast cancer: the first-line and curative setting.

Peripheral neuropathies associated with immunoglobulin M monoclonal gammopathies and low-grade B-cell lymphomas: diagnostic and therapeutic approach.

The many facets of Kaposi sarcoma-associated herpesvirus/human herpes virus-8 multicentric Castleman disease: clinical spectrum, diagnostic innovations, and therapeutic management.

Haemophagocytic lymphohistiocytosis: a life threatening complication of lymphoma.

Artificial intelligence for systemic therapy selection and prediction of outcomes in advanced gynecological cancers.

Artificial intelligence-augmented robotic surgery in gynecologic oncology: intraoperative assistance and analytics.

Systems genetics analysis reveals immune mediators of coronavirus disease severity in mice.

Molecular clusters and precision medicine in pheochromocytomas and paragangliomas.

Short-term outcomes of a randomized, mixed-methods trial to improve hereditary cancer test results disclosure and follow-up communication with family.

Genetic associations and candidate functional genes linking depression and obesity: a multi-omics integrative study.

Multi-Site Aggregation of p53: Insights from Self- and Co-Aggregation of Multiple Aggregation-Prone Regions.

Sex differences in the pathogenesis of degenerative knee osteoarthritis: a comparative transcriptomics analysis.

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Genetic basis of cancer

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