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Bleomycin-induced chromosomal damage and shortening of telomeres in peripheral blood lymphocytes of incident cancer patients.
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- Genes, Chromosomes & Cancer, 2018, v. 57, n. 2, p. 61, doi. 10.1002/gcc.22508
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Metabolic gene variants associated with chromosomal aberrations in healthy humans.
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- Genes, Chromosomes & Cancer, 2015, v. 54, n. 4, p. 260, doi. 10.1002/gcc.22239
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Telomere length in circulating lymphocytes: Association with chromosomal aberrations.
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- Genes, Chromosomes & Cancer, 2015, v. 54, n. 3, p. 194, doi. 10.1002/gcc.22225
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Somatic alterations in the melanoma genome: A high-resolution array-based comparative genomic hybridization study.
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- Genes, Chromosomes & Cancer, 2010, v. 49, n. 8, p. 733, doi. 10.1002/gcc.20785
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Polymorphisms in the transforming growth factor beta 1 pathway in relation to colorectal cancer progression.
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- Genes, Chromosomes & Cancer, 2010, v. 49, n. 3, p. 270, doi. 10.1002/gcc.20738
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Differential gene expression in melanocytic nevi with the V600E BRAF mutation.
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- Genes, Chromosomes & Cancer, 2007, v. 46, n. 11, p. 1019, doi. 10.1002/gcc.20488
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Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.
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- Molecular Medicine, 2018, v. 24, n. 1, p. N.PAG, doi. 10.1186/s10020-018-0031-8
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Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis?
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- Cancer Immunology, Immunotherapy, 2010, v. 59, n. 2, p. 303, doi. 10.1007/s00262-009-0751-2
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- Article
Familial associations for rheumatoid autoimmune diseases.
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- Rheumatology Advances in Practice, 2020, v. 4, n. 2, p. 1, doi. 10.1093/rap/rkaa048
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SNP microarray analysis for genome-wide detection of crossover regions.
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- Human Genetics, 2005, v. 117, n. 4, p. 389, doi. 10.1007/s00439-005-1323-y
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A genetic study of Hodgkin's lymphoma: an estimate of heritability and anticipation based on the familial cancer database in Sweden.
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- Human Genetics, 2000, v. 106, n. 5, p. 553, doi. 10.1007/s004390050024
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Inbreeding and homozygosity in breast cancer survival.
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- Scientific Reports, 2015, p. 16467, doi. 10.1038/srep16467
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Subsequent Type 2 Diabetes in Patients with Autoimmune Disease.
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- Scientific Reports, 2015, p. 13871, doi. 10.1038/srep13871
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Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches.
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- Scientific Reports, 2015, p. 13889, doi. 10.1038/srep13889
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Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.
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- Scientific Reports, 2015, p. 8922, doi. 10.1038/srep08922
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Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.
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- Cells (2073-4409), 2023, v. 12, n. 1, p. 96, doi. 10.3390/cells12010096
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Familial risks in urolithiasis in the population of Sweden.
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- BJU International, 2018, v. 121, n. 3, p. 479, doi. 10.1111/bju.14096
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Breast Cancer Histology in Immigrants to Sweden: Do Ethnic Differences Exist?
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- Breast Journal, 2012, v. 18, n. 4, p. 392, doi. 10.1111/j.1524-4741.2012.01268.x
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VHL gene alterations in renal cell carcinoma patients: novel hotspot or founder mutations and linkage disequilibrium.
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- Oncogene, 2001, v. 20, n. 38, p. 5393, doi. 10.1038/sj.onc.1204692
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Cancer risk in patients hospitalized with polymyalgia rheumatica and giant cell arteritis: a follow-up study in Sweden.
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- Rheumatology, 2010, v. 49, n. 6, p. 1158, doi. 10.1093/rheumatology/keq040
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Influence of education level on breast cancer risk and survival in Sweden between 1990 and 2004.
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- International Journal of Cancer, 2008, v. 122, n. 1, p. 165, doi. 10.1002/ijc.23007
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Second primary malignancies in females with primary fallopian tube cancer.
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- International Journal of Cancer, 2007, v. 120, n. 9, p. 2047, doi. 10.1002/ijc.22562
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Risk of second malignant neoplasms among lymphoma patients with a family history of cancer.
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- International Journal of Cancer, 2007, v. 120, n. 5, p. 1099, doi. 10.1002/ijc.22414
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Second malignancies among survivors of germ-cell testicular cancer: A pooled analysis between 13 cancer registries.
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- International Journal of Cancer, 2007, v. 120, n. 3, p. 623, doi. 10.1002/ijc.22345
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Single nucleotide polymorphisms in the DMBT1 promoter and the progression of breast cancer.
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- International Journal of Cancer, 2007, v. 120, n. 2, p. 447, doi. 10.1002/ijc.22182
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Associations between ocular melanoma and other primary cancers: An international population-based study.
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- International Journal of Cancer, 2007, v. 120, n. 1, p. 152, doi. 10.1002/ijc.22159
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Reply to 'No major impact of mammography screening on the age specific incidence rates of breast cancer in the Netherlands'.
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- International Journal of Cancer, 2006, v. 119, n. 12, p. 2989, doi. 10.1002/ijc.22254
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Heritable and environmental components in cervical tumors.
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- International Journal of Cancer, 2006, v. 119, n. 11, p. 2699, doi. 10.1002/ijc.22226
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ARLTS1 variants and melanoma risk.
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- International Journal of Cancer, 2006, v. 119, n. 7, p. 1736, doi. 10.1002/ijc.22008
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Second primary malignancies among patients with soft tissue tumors in Sweden.
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- International Journal of Cancer, 2006, v. 119, n. 4, p. 909, doi. 10.1002/ijc.21910
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Familial characteristics of autoimmune and hematologic disorders in 8,406 multiple myeloma patients: A population-based case-control study.
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- International Journal of Cancer, 2006, v. 118, n. 12, p. 3095, doi. 10.1002/ijc.21745
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Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer.
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- International Journal of Cancer, 2006, v. 118, n. 11, p. 2917, doi. 10.1002/ijc.21696
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Polymorphisms in the growth hormone receptor: A case-control study in breast cancer.
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- International Journal of Cancer, 2006, v. 118, n. 11, p. 2903, doi. 10.1002/ijc.21703
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Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk.
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- International Journal of Cancer, 2006, v. 118, n. 10, p. 2505, doi. 10.1002/ijc.21687
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Risk of second cancer among women with breast cancer.
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- International Journal of Cancer, 2006, v. 118, n. 9, p. 2285, doi. 10.1002/ijc.21651
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Ala228 variant of trail receptor 1 affecting the ligand binding site is associated with chronic lymphocytic leukemia, mantle cell lymphoma, prostate cancer, head and neck squamous cell carcinoma and bladder cancer.
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- International Journal of Cancer, 2006, v. 118, n. 7, p. 1831, doi. 10.1002/ijc.21502
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Parental lung cancer as predictor of cancer risks in offspring: Clues about multiple routes of harmful influence?
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- International Journal of Cancer, 2006, v. 118, n. 3, p. 744, doi. 10.1002/ijc.21387
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Associations between small intestine cancer and other primary cancers: An international population-based study.
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- International Journal of Cancer, 2006, v. 118, n. 1, p. 189, doi. 10.1002/ijc.21284
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c-MYC Asn11Ser is associated with increased risk for familial breast cancer.
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- International Journal of Cancer, 2005, v. 117, n. 4, p. 638, doi. 10.1002/ijc.21225
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Effects of screening for breast cancer on its age-incidence relationships and familial risk.
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- International Journal of Cancer, 2005, v. 117, n. 1, p. 145, doi. 10.1002/ijc.21149
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Incidence differences for gallbladder cancer between occupational groups suggest an etiological role for alcohol.
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- International Journal of Cancer, 2005, v. 116, n. 3, p. 492, doi. 10.1002/ijc.21055
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Low frequency of BRAF and CDKN2A mutations in endometrial cancer.
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- International Journal of Cancer, 2005, v. 115, n. 6, p. 930, doi. 10.1002/ijc.20702
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Familial risks for colorectal cancer show evidence on recessive inheritance.
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- International Journal of Cancer, 2005, v. 115, n. 5, p. 835, doi. 10.1002/ijc.20938
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p53 autoantibodies predict subsequent development of cancer.
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- International Journal of Cancer, 2005, v. 114, n. 1, p. 157, doi. 10.1002/ijc.20715
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Influence of GSTM1, GSTT1, GSTP1 and NAT2 genotypes on the p53 mutational spectrum in bladder tumours.
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- International Journal of Cancer, 2005, v. 113, n. 5, p. 761, doi. 10.1002/ijc.20650
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Prostate cancer screening, changing age-specific incidence trends and implications on familial risk.
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- International Journal of Cancer, 2005, v. 113, n. 2, p. 312, doi. 10.1002/ijc.20568
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B- RAF mutations in tumors from melanoma-breast cancer families.
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- International Journal of Cancer, 2005, v. 113, n. 2, p. 336, doi. 10.1002/ijc.20560
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Inherited predisposition to early onset lung cancer according to histological type.
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- International Journal of Cancer, 2004, v. 112, n. 3, p. 451, doi. 10.1002/ijc.20436
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Polymorphisms and haplotype structures in genes for transforming growth factor β1 and its receptors in familial and unselected breast cancers.
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- International Journal of Cancer, 2004, v. 112, n. 1, p. 94, doi. 10.1002/ijc.20370
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Genetic epidemiology of cancer: From families to heritable genes.
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- International Journal of Cancer, 2004, v. 111, n. 6, p. 944, doi. 10.1002/ijc.20355
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