Found: 131
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Lack of germline CDK6 mutations in familial melanoma.
- Published in:
- Oncogene, 2000, v. 19, n. 14, p. 1849, doi. 10.1038/sj.onc.1203507
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- Publication type:
- Article
Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries.
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- International Journal of Cancer, 2007, v. 121, n. 4, p. 825, doi. 10.1002/ijc.22712
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- Publication type:
- Article
Family history of gallstones and the risk of biliary tract cancer and gallstones: A population-based study in Shanghai, China.
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- International Journal of Cancer, 2007, v. 121, n. 4, p. 832, doi. 10.1002/ijc.22756
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- Publication type:
- Article
Distribution of Epstein-Barr viral load in serum of individuals from nasopharyngeal carcinoma high-risk families in Taiwan.
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- International Journal of Cancer, 2006, v. 118, n. 3, p. 780, doi. 10.1002/ijc.21396
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- Publication type:
- Article
Family history as a co-factor for adenocarcinoma and squamous cell carcinoma of the uterine cervix: Results from two studies conducted in Costa Rica and the United States.
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- International Journal of Cancer, 2005, v. 116, n. 4, p. 599, doi. 10.1002/ijc.21048
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- Publication type:
- Article
Corroboration of a familial chordoma locus on chromosome 7q and evidence of genetic heterogeneity using single nucleotide polymorphisms (SNPs).
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- International Journal of Cancer, 2005, v. 116, n. 3, p. 487, doi. 10.1002/ijc.21006
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- Publication type:
- Article
Epstein-Barr virus seroreactivity among unaffected individuals within high-risk nasopharyngeal carcinoma families in Taiwan.
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- International Journal of Cancer, 2004, v. 111, n. 1, p. 117, doi. 10.1002/ijc.20222
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- Publication type:
- Article
Analysis of mutations and identification of several polymorphisms in the putative promoter region of the P34.
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- International Journal of Cancer, 2002, v. 99, n. 6, p. 834, doi. 10.1002/ijc.10422
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- Publication type:
- Article
A PROBLEM IN IDENTIFYiNG RISK FACTORS FOR DISEASE USING SURROGATE EXPOSURE VARIABLES THAT ARE UNDER GENETIC CONTROL.
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- American Journal of Epidemiology, 1990, v. 132, n. 6, p. 1171, doi. 10.1093/oxfordjournals.aje.a115760
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- Publication type:
- Article
Integrative genomics analysis of genes with biallelic loss and its relation to the expression of mRNA and micro-RNA in esophageal squamous cell carcinoma.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1919-0
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- Publication type:
- Article
Robustness of inference on measured covariates to misspecification of genetic random effects in family studies.
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- Genetic Epidemiology, 2003, v. 24, n. 1, p. 14, doi. 10.1002/gepi.10191
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- Publication type:
- Article
Comparison of Likelihood Approaches for Combined Segregation and Linkage Analysis of a Complex Disease and a Candidate Gene Marker Under Different Ascertainment Schemes.
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- Genetic Epidemiology, 2001, v. 21, p. S760, doi. 10.1002/gepi.2001.21.s1.s760
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- Publication type:
- Article
Gene×Environment Interaction from Case-Control and Case-Case Approaches.
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- Genetic Epidemiology, 2001, v. 21, p. S825, doi. 10.1002/gepi.2001.21.s1.s825
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- Publication type:
- Article
Use of Weighted p-Values in Regional Inference Procedures.
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- Genetic Epidemiology, 2001, v. 21, p. S484, doi. 10.1002/gepi.2001.21.s1.s484
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- Publication type:
- Article
A genome-wide search for loci contributing to smoking and alcoholism.
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- Genetic Epidemiology, 1999, v. 17, p. S55, doi. 10.1002/gepi.1370170710
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- Publication type:
- Article
Preface.
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- Genetic Epidemiology, 1999, v. 17, p. Sxxxi, doi. 10.1002/gepi.1370170702
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- Publication type:
- Article
Sib-pair linkage analyses of alcoholism: Dichotomous and quantitative measures.
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- Genetic Epidemiology, 1999, v. 17, p. S205, doi. 10.1002/gepi.1370170735
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- Publication type:
- Article
Sib-pair linkage analyses of nuclear family data: Quantitative versus dichotomous disease classification.
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- Genetic Epidemiology, 1997, v. 14, n. 6, p. 827, doi. 10.1002/(SICI)1098-2272(1997)14:6<827::AID-GEPI44>3.0.CO;2-P
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- Publication type:
- Article
Detecting gene-environment interactions using a case-control design.
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- Genetic Epidemiology, 1997, v. 14, n. 6, p. 1085, doi. 10.1002/(SICI)1098-2272(1997)14:6<1085::AID-GEPI87>3.0.CO;2-D
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- Publication type:
- Article
Clustering of high density lipoprotein cholesterol levels in premenopausal and postmenopausal female twins.
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- Genetic Epidemiology, 1993, v. 10, n. 6, p. 563, doi. 10.1002/gepi.1370100639
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- Publication type:
- Article
Genetic epidemiology of bilateral breast cancer: A linkage analysis using the affected-pedigree-member method.
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- Genetic Epidemiology, 1990, v. 7, n. 1, p. 47, doi. 10.1002/gepi.1370070112
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- Publication type:
- Article
Cleft lip with or without cleft palate: Reanalysis of a three-generation family study from England.
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- Genetic Epidemiology, 1986, v. 3, n. 5, p. 335, doi. 10.1002/gepi.1370030506
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- Publication type:
- Article
Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk.
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- Carcinogenesis, 2010, v. 31, n. 4, p. 634, doi. 10.1093/carcin/bgp334
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- Publication type:
- Article
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma.
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- Human Molecular Genetics, 2006, v. 15, n. 18, p. 2682, doi. 10.1093/hmg/ddl199
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- Publication type:
- Article
Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls.
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- Genome Medicine, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13073-018-0607-5
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- Publication type:
- Article
Genome wide analysis of DNA copy number neutral loss of heterozygosity (CNNLOH) and its relation to gene expression in esophageal squamous cell carcinoma.
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- BMC Genomics, 2010, v. 11, n. 1, p. 1, doi. 10.1186/1471-2164-11-576
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- Publication type:
- Article
Genome wide analysis of DNA copy number neutral loss of heterozygosity (CNNLOH) and its relation to gene expression in esophageal squamous cell carcinoma.
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- BMC Genomics, 2010, v. 11, p. 576, doi. 10.1186/1471-2164-11-576
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- Publication type:
- Article
Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array.
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- BMC Genomics, 2006, v. 7, p. 299, doi. 10.1186/1471-2164-7-299
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- Publication type:
- Article
Allelotyping of esophageal squamous‐cell carcinoma on chromosome 13 defines deletions related to family historyThis article is a US Government work and, as such, is in the public domain in the United States of America.
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- Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 271, doi. 10.1002/gcc.20242
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- Article
High frequency of CDKN2A alterations in esophageal squamous cell carcinoma from a high-risk Chinese population.
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- Genes, Chromosomes & Cancer, 2004, v. 39, n. 3, p. 205, doi. 10.1002/gcc.10315
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- Publication type:
- Article
Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effect.
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- Genes, Chromosomes & Cancer, 2001, v. 32, n. 3, p. 195, doi. 10.1002/gcc.1183
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- Publication type:
- Article
Allelic loss on chromosome bands 13q11-q13 in esophageal squamous cell carcinoma.
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- Genes, Chromosomes & Cancer, 2001, v. 31, n. 4, p. 390, doi. 10.1002/gcc.1158
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- Publication type:
- Article
Mutation screening of the CDKN2A promoter in melanoma families.
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- Genes, Chromosomes & Cancer, 2000, v. 28, n. 1, p. 45, doi. 10.1002/(SICI)1098-2264(200005)28:1<45::AID-GCC6>3.0.CO;2-F
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- Publication type:
- Article
Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 217, doi. 10.1002/(SICI)1098-2264(200003)27:3<217::AID-GCC1>3.0.CO;2-A
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- Publication type:
- Article
Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germline PTEN mutation.
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- Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 61, doi. 10.1002/(SICI)1098-2264(199801)21:1<61::AID-GCC8>3.0.CO;2-6
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- Publication type:
- Article
Affected members of melanoma-prone families with linkage to 9p21 but lacking mutations in CDKN2A do not harbor mutations in the coding regions of either CDKN2B or p19<sup>ARF</sup>.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 1, p. 52, doi. 10.1002/(SICI)1098-2264(199705)19:1<52::AID-GCC8>3.0.CO;2-#
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- Publication type:
- Article
High-risk pregnancy and neonatal complications in the DNA repair and transcription disorder trichothiodystrophy: report of 27 affected pregnancies.
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- Prenatal Diagnosis, 2011, v. 31, n. 11, p. 1046, doi. 10.1002/pd.2829
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- Publication type:
- Article
Assessment of Human Papillomavirus in Lung Tumor Tissue.
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- JNCI: Journal of the National Cancer Institute, 2011, v. 103, n. 6, p. 501, doi. 10.1093/jnci/djr003
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- Publication type:
- Article
A Piece of the Melanoma Puzzle.
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- 2005
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- Publication type:
- Editorial
MC1R, ASIP, and DNA Repair in Sporadic and Familial Melanoma in a Mediterranean Population.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2005, v. 97, n. 13, p. 998, doi. 10.1093/jnci/dji176
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- Publication type:
- Article
Geographical variation in the penetrance of CDKN2A mutations for melanoma.
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- 2002
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- Publication type:
- journal article
A mutation hotspot at the p14ARF splice site.
- Published in:
- Oncogene, 2005, v. 24, n. 28, p. 4604, doi. 10.1038/sj.onc.1208678
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- Publication type:
- Article
Evaluation of BRCA2 in the genetic susceptibility of familial esophageal cancer.
- Published in:
- Oncogene, 2004, v. 23, n. 3, p. 852, doi. 10.1038/sj.onc.1207150
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- Publication type:
- Article
Germline splicing mutations of CDKN2A predispose to melanoma.
- Published in:
- Oncogene, 2003, v. 22, n. 41, p. 6387, doi. 10.1038/sj.onc.1206736
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- Publication type:
- Article
CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16<sup>INK4a</sup> and p14<sup>ARF</sup>.
- Published in:
- Oncogene, 2003, v. 22, n. 28, p. 4444, doi. 10.1038/sj.onc.1206564
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- Publication type:
- Article
Melanoma etiology: where are we?
- Published in:
- Oncogene, 2003, v. 22, n. 20, p. 3042, doi. 10.1038/sj.onc.1206444
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- Publication type:
- Article
Allelic loss on chromosome 13q14 and mutation in deleted in cancer 1 gene in esophageal squamous cell carcinoma.
- Published in:
- Oncogene, 2003, v. 22, n. 2, p. 314, doi. 10.1038/sj.onc.1206098
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- Publication type:
- Article
Effect of mutations in XPD(ERCC2) on pregnancy and prenatal development in mothers of patients with trichothiodystrophy or xeroderma pigmentosum.
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- European Journal of Human Genetics, 2012, v. 20, n. 12, p. 1308, doi. 10.1038/ejhg.2012.90
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- Publication type:
- Article
Familial Melanoma Aggregation in North-Eastern Italy.
- Published in:
- Journal of Investigative Dermatology, 2000, v. 115, n. 4, p. 764, doi. 10.1046/j.1523-1747.2000.00124-4.x
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- Publication type:
- Article
Fine Mapping of the Locus for Nevoid Basal Cell Carcinoma Syndrome on Chromosome 9q.
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- Journal of Investigative Dermatology, 1994, v. 103, n. 2, p. 178, doi. 10.1111/1523-1747.ep12392682
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- Publication type:
- Article