Search Results - "EMANUELSSON, Monica"
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Genetic Analysis of the RNASEL Gene in Hereditary, Familial, and Sporadic Prostate Cancer
Published in Clinical cancer research (01-11-2004)“…Purpose: The RNASEL gene has been proposed as a candidate gene for the HPC1 locus through a positional cloning and candidate gene approach. Cosegregation…”
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Bilateral Prophylactic Mastectomy in Swedish Women at High Risk of Breast Cancer: A National Survey
Published in Annals of surgery (2011)“…This study attempted a national inventory of all bilateral prophylactic mastectomies performed in Sweden between 1995 and 2005 in high-risk women without a…”
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Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease
Published in Human genetics (01-03-2014)“…Previous GWAS studies have reported significant associations between various common SNPs and prostate cancer risk using cases unselected for family history…”
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A Combined Genomewide Linkage Scan of 1,233 Families for Prostate Cancer–Susceptibility Genes Conducted by the International Consortium for Prostate Cancer Genetics
Published in American journal of human genetics (01-08-2005)“…Evidence of the existence of major prostate cancer (PC)–susceptibility genes has been provided by multiple segregation analyses. Although genomewide screens…”
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High risk of contralateral breast carcinoma in women with hereditary/familial non‐BRCA1/BRCA2 breast carcinoma
Published in Cancer (15-03-2006)“…BACKGROUND The objectives of the current study were to estimate the risk of developing contralateral breast carcinoma (CBC) among women with…”
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Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)
Published in Human genetics (01-07-2012)“…Multiple prostate cancer (PCa) risk-related loci have been discovered by genome-wide association studies (GWAS) based on case–control designs. However, GWAS…”
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Women with Saethre-Chotzen syndrome are at increased risk of breast cancer
Published in Genes chromosomes & cancer (01-07-2007)“…The Saethre‐Chotzen syndrome is an autosomal, dominantly inherited craniosynostosis caused by mutations in the basic helix‐loop‐helix transcription factor gene…”
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Pooled genome linkage scan of aggressive prostate cancer : results from the International Consortium for Prostate Cancer Genetics
Published in Human genetics (01-11-2006)“…While it is widely appreciated that prostate cancers vary substantially in their propensity to progress to a life-threatening stage, the molecular events…”
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Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG
Published in The Prostate (01-03-2012)“…BACKGROUND In spite of intensive efforts, understanding of the genetic aspects of familial prostate cancer (PC) remains largely incomplete. In a previous…”
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Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for prostate cancer Genetics using novel sumLINK and sumLOD analyses
Published in The Prostate (15-05-2010)“…BACKGROUND Prostate cancer (PC) is generally believed to have a strong inherited component, but the search for susceptibility genes has been hindered by the…”
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Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome
Published in Clinical genetics (01-12-2005)“…Lynch syndrome, or hereditary non‐polyposis colorectal cancer (HNPCC), is a cancer susceptibility syndrome caused by germline mutations in mismatch‐repair…”
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Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics
Published in Human molecular genetics (01-06-2007)“…Previously, an analysis of 14 extended, high-risk Utah pedigrees localized in the chromosome 22q linkage region to 3.2 Mb at 22q12.3-13.1 (flanked on each side…”
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Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population‐based study in northern Sweden
Published in International journal of cancer (10-04-2004)“…Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder that predisposes to predominantly colorectal and endometrial cancers due to…”
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Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families
Published in BMC genetics (19-06-2012)“…Genetic variants are likely to contribute to a portion of prostate cancer risk. Full elucidation of the genetic etiology of prostate cancer is difficult…”
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Genome-wide scan of Swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3
Published in The Prostate (01-12-2003)“…BACKGROUND Prostate cancer (CaP) is a common disorder with multiple genetic and environmental factors contributing to the disease. CaP susceptibility loci can…”
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Cancer risk in families with hereditary prostate carcinoma : A possible link between prostate, breast, and gastric carcinoma
Published in Cancer (15-09-2000)Get full text
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A population based cohort study of patients with multiple colon and endometrial cancer: correlation of microsatellite instability (MSI) staus, age at diagnosis and cancer risk
Published in International journal of cancer (2001)“…Hereditary non-polyposis colorectal cancer, HNPCC, is an autosomal dominant condition predisposing to cancers of primarily the colorectum and the endometrium…”
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