Population history and its impact on medical genetics in Quebec.
about
Twin Town in South Brazil: a Nazi's experiment or a genetic founder effect?GENLIB: an R package for the analysis of genealogical dataThe Quebec Pregnancy Cohort--prevalence of medication use during gestation and pregnancy outcomesEpigenome data release: a participant-centered approach to privacy protectionExome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaReport on the 3rd Ottawa International Conference on Neuromuscular Biology, Disease and Therapy - September 24-26, 2015, Ottawa, Canada.Haplotype analysis of TP53 polymorphisms, Arg72Pro and Ins16, in BRCA1 and BRCA2 mutation carriers of French Canadian descent.Identification of a novel CHEK2 variant and assessment of its contribution to the risk of breast cancer in French Canadian women.Impact of inbreeding on fertility in a pre-industrial population.Of founder populations, long QT syndrome, and destiny.High mammographic density in women of Ashkenazi Jewish descent.Genealogical analysis as a new approach for the investigation of drug intolerance heritability.Geographical variation of Crohn's disease residual incidence in the Province of Quebec, Canada.Saturation of the human phenomeHomozygosity mapping on homozygosity haplotype analysis to detect recessive disease-causing genes from a small number of unrelated, outbred patientsTremor-ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3-10q23.31.Admixed ancestry and stratification of Quebec regional populations.Cohort profile of the CARTaGENE study: Quebec's population-based biobank for public health and personalized genomics.Demographic inference using spectral methods on SNP data, with an analysis of the human out-of-Africa expansion.A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian populationRare copy number variants contribute to congenital left-sided heart disease.Oculopharyngeal muscular dystrophy as a paradigm for muscle aging.Multiple intestinal atresia with combined immune deficiency related to TTC7A defect is a multiorgan pathology: study of a French-Canadian-based cohort.Contribution of the PALB2 c.2323C>T [p.Q775X] founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent.Native American admixture in the Quebec founder population.Deciphering the fine-structure of tribal admixture in the Bedouin population using genomic dataWhole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans.HMGCR is a genetic modifier for risk, age of onset and MCI conversion to Alzheimer's disease in a three cohorts study.A targeted analysis identifies a high frequency of BRCA1 and BRCA2 mutation carriers in women with ovarian cancer from a founder population.Rheumatoid arthritis prevalence in Quebec.FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide.Germline TP53 mutational spectrum in French Canadians with breast cancer.Double PALB2 and BRCA1/BRCA2 mutation carriers are rare in breast cancer and breast-ovarian cancer syndrome families from the French Canadian founder populationConstructing populations in biobanking.How evolutionary principles improve the understanding of human health and diseaseFounder mutations in Tunisia: implications for diagnosis in North Africa and Middle East.Community genetics and dignity in diversity in the Quebec Network of Genetic Medicine.Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancerGenetic isolates in ophthalmic diseases.Phenotypic and genotypic characteristics of inflammatory bowel disease in French Canadians: comparison with a large North American repository.
P2860
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P2860
Population history and its impact on medical genetics in Quebec.
description
2005 nî lūn-bûn
@nan
2005 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Population history and its impact on medical genetics in Quebec.
@ast
Population history and its impact on medical genetics in Quebec.
@en
Population history and its impact on medical genetics in Quebec.
@nl
type
label
Population history and its impact on medical genetics in Quebec.
@ast
Population history and its impact on medical genetics in Quebec.
@en
Population history and its impact on medical genetics in Quebec.
@nl
prefLabel
Population history and its impact on medical genetics in Quebec.
@ast
Population history and its impact on medical genetics in Quebec.
@en
Population history and its impact on medical genetics in Quebec.
@nl
P2093
P1433
P1476
Population history and its impact on medical genetics in Quebec.
@en
P2093
Laberge AM
Mitchell GA
P304
P356
10.1111/J.1399-0004.2005.00497.X
P577
2005-10-01T00:00:00Z