Found: 236
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Breast and prostate cancer: familial associations.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Functional germline variants in driver genes of breast cancer.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
- Published in:
- Genes, Chromosomes & Cancer, 2015, v. 54, n. 4, p. 260, doi. 10.1002/gcc.22239
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- Publication type:
- Article
Telomere length in circulating lymphocytes: Association with chromosomal aberrations.
- Published in:
- Genes, Chromosomes & Cancer, 2015, v. 54, n. 3, p. 194, doi. 10.1002/gcc.22225
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- Publication type:
- Article
Polymorphisms in the transforming growth factor beta 1 pathway in relation to colorectal cancer progression.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 3, p. 270, doi. 10.1002/gcc.20738
- By:
- Publication type:
- Article
Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.
- Published in:
- Molecular Medicine, 2018, v. 24, n. 1, p. N.PAG, doi. 10.1186/s10020-018-0031-8
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- Publication type:
- Article
Familial associations for rheumatoid autoimmune diseases.
- Published in:
- Rheumatology Advances in Practice, 2020, v. 4, n. 2, p. 1, doi. 10.1093/rap/rkaa048
- By:
- Publication type:
- Article
Inbreeding and homozygosity in breast cancer survival.
- Published in:
- Scientific Reports, 2015, p. 16467, doi. 10.1038/srep16467
- By:
- Publication type:
- Article
Subsequent Type 2 Diabetes in Patients with Autoimmune Disease.
- Published in:
- Scientific Reports, 2015, p. 13871, doi. 10.1038/srep13871
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- Publication type:
- Article
Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 1, p. 96, doi. 10.3390/cells12010096
- By:
- Publication type:
- Article
Familial risks in urolithiasis in the population of Sweden.
- Published in:
- BJU International, 2018, v. 121, n. 3, p. 479, doi. 10.1111/bju.14096
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- Publication type:
- Article
Single nucleotide polymorphisms in the DMBT1 promoter and the progression of breast cancer.
- Published in:
- International Journal of Cancer, 2007, v. 120, n. 2, p. 447, doi. 10.1002/ijc.22182
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- Publication type:
- Article
Polymorphisms in the growth hormone receptor: A case-control study in breast cancer.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 11, p. 2903, doi. 10.1002/ijc.21703
- By:
- Publication type:
- Article
c-MYC Asn11Ser is associated with increased risk for familial breast cancer.
- Published in:
- International Journal of Cancer, 2005, v. 117, n. 4, p. 638, doi. 10.1002/ijc.21225
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- Publication type:
- Article
B- RAF mutations in tumors from melanoma-breast cancer families.
- Published in:
- International Journal of Cancer, 2005, v. 113, n. 2, p. 336, doi. 10.1002/ijc.20560
- By:
- Publication type:
- Article
Polymorphisms and haplotype structures in genes for transforming growth factor β1 and its receptors in familial and unselected breast cancers.
- Published in:
- International Journal of Cancer, 2004, v. 112, n. 1, p. 94, doi. 10.1002/ijc.20370
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- Publication type:
- Article
Single nucleotide polymorphisms in the XPG gene: Determination of role in DNA repair and breast cancer risk.
- Published in:
- International Journal of Cancer, 2003, v. 103, n. 5, p. 671, doi. 10.1002/ijc.10870
- By:
- Publication type:
- Article
Single nucleotide polymorphism analyses of the human proliferating cell nuclear antigen (pCNA) and flap endonuclease (FEN1) genes.
- Published in:
- International Journal of Cancer, 2000, v. 88, n. 6, p. 938, doi. 10.1002/1097-0215(20001215)88:6<938::AID-IJC16>3.0.CO;2-G
- By:
- Publication type:
- Article
Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Familial Risks between Pernicious Anemia and Other Autoimmune Diseases in the Population of Sweden.
- Published in:
- Autoimmune Diseases (2090-0422), 2021, v. 2021, p. 1, doi. 10.1155/2021/8815297
- By:
- Publication type:
- Article
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS).
- Published in:
- European Journal of Haematology, 2017, v. 99, n. 1, p. 70, doi. 10.1111/ejh.12892
- By:
- Publication type:
- Article
Correction: Familial risks of ovarian cancer by age at diagnosis, proband type and histology.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Familial risks of ovarian cancer by age at diagnosis, proband type and histology.
- Published in:
- PLoS ONE, 2018, v. 13, n. 10, p. 1, doi. 10.1371/journal.pone.0205000
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- Publication type:
- Article
Correction: Inherited variants in genes somatically mutated in thyroid cancer.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer.
- Published in:
- PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0192385
- By:
- Publication type:
- Article
Single nucleotide polymorphisms (SNPs) are inherited from parents and they measure heritable events.
- Published in:
- Journal of Carcinogenesis, 2005, v. 4, n. 1, p. 2, doi. 10.1186/1477-3163-4-2
- By:
- Publication type:
- Article
Gene–Environment Interactions in Cancer.
- Published in:
- Annals of the New York Academy of Sciences, 2006, v. 1076, n. 1, p. 137, doi. 10.1196/annals.1371.029
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- Publication type:
- Article
The balance between heritable and environmental aetiology of human disease.
- Published in:
- Nature Reviews Genetics, 2006, v. 7, n. 12, p. 958, doi. 10.1038/nrg2009
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- Publication type:
- Article
Neurological and psychiatric associations in bullous pemphigoid-more than skin deep?
- Published in:
- Experimental Dermatology, 2017, v. 26, n. 12, p. 1228, doi. 10.1111/exd.13401
- By:
- Publication type:
- Article
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29952-z
- By:
- Publication type:
- Article
Familial Ovarian Cancer Clusters with Other Cancers.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29888-4
- By:
- Publication type:
- Article
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.
- Published in:
- Carcinogenesis, 2010, v. 31, n. 9, p. 1612, doi. 10.1093/carcin/bgq146
- By:
- Publication type:
- Article
Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer: ITGB4 as prognostic marker.
- Published in:
- Carcinogenesis, 2008, v. 29, n. 7, p. 1394, doi. 10.1093/carcin/bgn126
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- Publication type:
- Article
Interleukin promoter polymorphisms and prognosis in colorectal cancer.
- Published in:
- Carcinogenesis, 2008, v. 29, n. 6, p. 1202, doi. 10.1093/carcin/bgn101
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- Publication type:
- Article
Controls need to be selected for the type of SNP study.
- Published in:
- Carcinogenesis, 2002, v. 23, n. 12, p. 2137, doi. 10.1093/carcin/23.12.2137
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- Publication type:
- Article
Proper controls for SNP studies?
- Published in:
- Carcinogenesis, 2002, v. 23, n. 8, p. 1405, doi. 10.1093/carcin/23.8.1405
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- Publication type:
- Article
Sex hormone-binding globulin polymorphisms in familial and sporadic breast cancer.
- Published in:
- Carcinogenesis, 2002, v. 23, n. 8, p. 1315, doi. 10.1093/carcin/23.8.1315
- By:
- Publication type:
- Article
Allelic imbalance on chromosomes 13 and 17 and mutation analysis of BRCA1 and BRCA2 genes in monozygotic twins concordant for breast cancer.
- Published in:
- Carcinogenesis, 2001, v. 22, n. 1, p. 27, doi. 10.1093/carcin/22.1.27
- By:
- Publication type:
- Article
Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility.
- Published in:
- Nature Communications, 2017, v. 8, n. 12, p. 1, doi. 10.1038/s41467-017-00320-1
- By:
- Publication type:
- Article
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma.
- Published in:
- Nature Communications, 2016, v. 7, n. 7, p. 12050, doi. 10.1038/ncomms12050
- By:
- Publication type:
- Article
Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma.
- Published in:
- Nature Communications, 2016, v. 7, n. 1, p. 10290, doi. 10.1038/ncomms10290
- By:
- Publication type:
- Article
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
- Published in:
- Nature Communications, 2013, v. 4, n. 10, p. 2549, doi. 10.1038/ncomms3549
- By:
- Publication type:
- Article
Survival in Lung Cancer in the Nordic Countries Through A Half Century.
- Published in:
- Clinical Epidemiology, 2023, v. 15, p. 503, doi. 10.2147/CLEP.S406606
- By:
- Publication type:
- Article
Second Primary Cancers After Liver, Gallbladder and Bile Duct Cancers, and These Cancers as Second Primary Cancers.
- Published in:
- Clinical Epidemiology, 2021, v. 13, p. 683, doi. 10.2147/CLEP.S318737
- By:
- Publication type:
- Article
Second Primary Cancers After Gastric Cancer, and Gastric Cancer as Second Primary Cancer.
- Published in:
- Clinical Epidemiology, 2021, v. 13, p. 515, doi. 10.2147/clep.s318737
- By:
- Publication type:
- Article
Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 824, doi. 10.1038/ejhg.2014.184
- By:
- Publication type:
- Article
Incidence and survival in laryngeal and lung cancers in Finland and Sweden through a half century.
- Published in:
- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0268922
- By:
- Publication type:
- Article
Survival in bladder and upper urinary tract cancers in Finland and Sweden through 50 years.
- Published in:
- PLoS ONE, 2022, v. 17, n. 1, p. 1, doi. 10.1371/journal.pone.0261124
- By:
- Publication type:
- Article
GWAS-Identified Variants for Obesity Do Not Influence the Risk of Developing Multiple Myeloma: A Population-Based Study and Meta-Analysis.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 7, p. 6029, doi. 10.3390/ijms24076029
- By:
- Publication type:
- Article
Recurrent Germline Variant in RAD21 Predisposes Children to Lymphoblastic Leukemia or Lymphoma.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 9, p. 5174, doi. 10.3390/ijms23095174
- By:
- Publication type:
- Article