| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/J.JAAD.2015.08.037 |
| P8608 | Fatcat ID | release_zrskgplvprfxffiwrs5phvl5iq |
| P932 | PMC publication ID | 4761106 |
| P698 | PubMed publication ID | 26892651 |
| P2093 | author name string | Hensin Tsao | |
| Alexander J Stratigos | |||
| Kristen Shannon | |||
| Philip J Eliades | |||
| Efthymia Soura | |||
| P2860 | cites work | The POT1-TPP1 telomere complex is a telomerase processivity factor | Q24293607 |
| POT1 loss-of-function variants predispose to familial melanoma | Q24563091 | ||
| Germline mutations in BAP1 predispose to melanocytic tumors | Q24594891 | ||
| Frequent mutation of BAP1 in metastasizing uveal melanomas | Q24601069 | ||
| The telomere syndromes | Q24632444 | ||
| Germline BAP1 mutations predispose to malignant mesothelioma | Q24635326 | ||
| Melanoma: from mutations to medicine | Q27024061 | ||
| Variation at the TERT locus and predisposition for cancer | Q28282704 | ||
| Highly recurrent TERT promoter mutations in human melanoma | Q29614798 | ||
| TERT promoter mutations in familial and sporadic melanoma | Q29614920 | ||
| Telomere length and the risk of cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations | Q31131061 | ||
| Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases. | Q33697377 | ||
| Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma | Q33751971 | ||
| Genetic variants in telomere-maintaining genes and skin cancer risk | Q33758326 | ||
| Nevus size and number are associated with telomere length and represent potential markers of a decreased senescence in vivo. | Q34005118 | ||
| Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers | Q34218657 | ||
| The genetics of uveal melanoma: an emerging framework for targeted therapy | Q34249080 | ||
| Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families | Q34251101 | ||
| The effect on melanoma risk of genes previously associated with telomere length | Q34333988 | ||
| A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancers | Q34973438 | ||
| PTEN hamartoma tumor syndrome: an overview | Q34996547 | ||
| Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma | Q35102528 | ||
| Inherited genetic variants associated with occurrence of multiple primary melanoma | Q35674870 | ||
| Lifetime cancer risks in individuals with germline PTEN mutations. | Q35681689 | ||
| A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma | Q35699278 | ||
| A distinct subset of atypical Spitz tumors is characterized by BRAF mutation and loss of BAP1 expression | Q35965678 | ||
| Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors | Q36242298 | ||
| Profiling of UV-induced ATM/ATR signaling pathways. | Q36288898 | ||
| BAP1 cancer syndrome: malignant mesothelioma, uveal and cutaneous melanoma, and MBAITs | Q36384018 | ||
| Telomere maintenance and human bone marrow failure | Q36591289 | ||
| Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer | Q36897003 | ||
| BAP1 and cancer | Q37221089 | ||
| The impact of MITF on melanoma development: news from bench and bedside | Q37507876 | ||
| Telomeres and telomerase in cancer | Q37627017 | ||
| MITF, the Janus transcription factor of melanoma. | Q38081986 | ||
| Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria | Q38153670 | ||
| The Importance of Multidisciplinary Approach in Early Detection of BAP1 Tumor Predisposition Syndrome: Clinical Management and Risk Assessment | Q38214084 | ||
| Cancer. The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancer. | Q38874534 | ||
| Frequency of TERT promoter mutations in human cancers | Q39120274 | ||
| A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma | Q39455824 | ||
| Clinical Characteristics of Uveal Melanoma in Patients With Germline BAP1 Mutations | Q40939840 | ||
| BRCA1-associated protein 1 (BAP1) deubiquitinase antagonizes the ubiquitin-mediated activation of FoxK2 target genes | Q41752870 | ||
| TERT promoter mutations in skin cancer: the effects of sun exposure and X-irradiation. | Q42456732 | ||
| BAP1 has a survival role in cutaneous melanoma | Q43194421 | ||
| High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome | Q44636065 | ||
| A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma | Q44640266 | ||
| Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. | Q45374479 | ||
| Phenotypic characterization of nevus and tumor patterns in MITF E318K mutation carrier melanoma patients. | Q50489618 | ||
| Long telomere length and a TERT-CLPTM1 locus polymorphism association with melanoma risk. | Q55069651 | ||
| Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations | Q57266547 | ||
| Toward an Improved Definition of the Tumor Spectrum Associated WithBAP1Germline Mutations | Q57631287 | ||
| Sunlight and risk of uveal melanoma | Q72198428 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 411-20; quiz 421-2 | |
| P577 | publication date | 2016-03-01 | |
| P1433 | published in | Journal of the American Academy of Dermatology | Q15757046 |
| P1476 | title | Hereditary melanoma: Update on syndromes and management: Emerging melanoma cancer complexes and genetic counseling | |
| P478 | volume | 74 |
| Q50068785 | Atypical Melanocytic Proliferations: A Review of the Literature |
| Q87949115 | A melanoma family |
| Q89699834 | Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients |
| Q50087551 | Comprehensive review of genetic factors contributing to head and neck squamous cell carcinoma development in low-risk, nontraditional patients. |
| Q38812696 | Desmoplastic melanoma: a challenge for the oncologist |
| Q39245116 | Epidemiological trends and clinicopathological features of cutaneous melanoma in sporadic and xeroderma pigmentosum Tunisian patients. |
| Q41178179 | Familial Cancers of Head and Neck Region |
| Q33728131 | Genetic profiling of a rare condition: co-occurrence of albinism and multiple primary melanoma in a Caucasian family |
| Q33851085 | Hereditary pancreatic cancer: related syndromes and clinical perspective |
| Q36304955 | Identification, genetic testing, and management of hereditary melanoma. |
| Q52802985 | Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing. |
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