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المؤلفون: A. Roussel-Jobin, Celia M. T. Greenwood, Jean Latreille, Rachel Laframboise, Olga Aleynikova, George Chong, D. Provencher, Lidia Kasprzak, Serge Nolet, Z. El-Haffaf, A. Volenik, Bruno Maranda, Adrian Gologan, K. Oros-Klein, M. Breguet, Marc Tischkowitz, Laura Palma, Victoria Marcus, Anne Marie Mes-Masson, Sylvie Giroux, R. Gagne, K. Australie, William D. Foulkes, François Rousseau, J. Liu, Ester Castellsagué

المصدر: Clinical Genetics. 87:536-542

مصطلحات موضوعية: Proband, Genetics, education.field_of_study, Endometrial cancer, Population, Haplotype, Odds ratio, Biology, medicine.disease, Lynch syndrome, 3. Good health, MSH6, Mutation (genetic algorithm), medicine, education, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::463b62de44070396fc8430bf0ff98398
https://doi.org/10.1111/cge.12526

المؤلفون: E, Castellsagué, J, Liu, A, Volenik, S, Giroux, R, Gagné, B, Maranda, A, Roussel-Jobin, J, Latreille, R, Laframboise, L, Palma, L, Kasprzak, V A, Marcus, M, Breguet, S, Nolet, Z, El-Haffaf, K, Australie, A, Gologan, O, Aleynikova, K, Oros-Klein, C, Greenwood, A M, Mes-Masson, D, Provencher, M, Tischkowitz, G, Chong, F, Rousseau, W D, Foulkes

المصدر: Clinical genetics. 87(6)

مصطلحات موضوعية: Adult, Male, Risk, Canada, Heterozygote, Adolescent, Quebec, Loss of Heterozygosity, Middle Aged, Colorectal Neoplasms, Hereditary Nonpolyposis, Founder Effect, Endometrial Neoplasms, DNA-Binding Proteins, Young Adult, Haplotypes, Child, Preschool, Mutation, Ethnicity, Humans, Family, Female, Genetic Predisposition to Disease, Child, Genetic Association Studies, Aged

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::d32a22d4fa25ed4ea26c8134f8a4aefc
https://pubmed.ncbi.nlm.nih.gov/25318681

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المؤلفون: Zeng Y; PhD Program in Quantitative Life Sciences, Interfaculty Studies, McGill University, Montréal, QC H3A 1E3, Canada.; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC H3T 1E2, Canada., Zhao K; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC H3T 1E2, Canada.; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, QC H3A 1A2, Canada., Oros Klein K; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC H3T 1E2, Canada., Shao X; Digital Technologies Research Centre, National Research Council Canada, Ottawa, ON K1A 0R6, Canada., Fritzler MJ; Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada., Hudson M; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC H3T 1E2, Canada.; Department of Medicine, McGill University, Montréal, QC H4A 3J1, Canada.; Division of Rheumatology, Jewish General Hospital, Montréal, QC H3T 1E2, Canada., Colmegna I; Department of Medicine, McGill University, Montréal, QC H4A 3J1, Canada.; Division of Rheumatology, McGill University, Montréal, QC H3G 1A4, Canada., Pastinen T; Department of Human Genetics, McGill University, Montréal, QC H3A 0C7, Canada.; Center for Pediatric Genomic Medicine, Children's Mercy, Kansas City, MO 64108, USA., Bernatsky S; Department of Medicine, McGill University, Montréal, QC H4A 3J1, Canada.; Division of Rheumatology, McGill University, Montréal, QC H3G 1A4, Canada., Greenwood CMT; PhD Program in Quantitative Life Sciences, Interfaculty Studies, McGill University, Montréal, QC H3A 1E3, Canada.; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, QC H3T 1E2, Canada.; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, QC H3A 1A2, Canada.; Department of Human Genetics, McGill University, Montréal, QC H3A 0C7, Canada.; Gerald Bronfman Department of Oncology, McGill University, Montréal, QC H4A 3T2, Canada.

المصدر: Genes [Genes (Basel)] 2021 Aug 29; Vol. 12 (9). Date of Electronic Publication: 2021 Aug 29.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

مواضيع طبية MeSH: CpG Islands* , DNA Methylation*, Anti-Citrullinated Protein Antibodies/*blood , Arthritis, Rheumatoid/*genetics, Arthritis, Rheumatoid/blood ; Cytosine/metabolism ; Databases, Factual ; Epigenome ; Female ; Gene Ontology ; Genome-Wide Association Study ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide

المؤلفون: Oros Klein K; Lady Davis Research Institute, Jewish General Hospital Montreal, QC, Canada., Oualkacha K; Département de Mathématiques, Université du Québec à Montréal Montreal, QC, Canada., Lafond MH; Département de Mathématiques, Université du Québec à Montréal Montreal, QC, Canada., Bhatnagar S; Lady Davis Research Institute, Jewish General HospitalMontreal, QC, Canada; Department of Epidemiology, Biostatistics and Occupational Health, McGill UniversityMontreal, QC, Canada., Tonin PN; Cancer Research Program, The Research Institute of the McGill University Health CentreMontreal, QC, Canada; Departments of Medicine and Human Genetics, McGill UniversityMontreal, QC, Canada., Greenwood CM; Lady Davis Research Institute, Jewish General HospitalMontreal, QC, Canada; Department of Epidemiology, Biostatistics and Occupational Health, McGill UniversityMontreal, QC, Canada; Departments of Oncology and Human Genetics, McGill UniversityMontreal, QC, Canada.

المصدر: Frontiers in genetics [Front Genet] 2016 Aug 03; Vol. 7, pp. 137. Date of Electronic Publication: 2016 Aug 03 (Print Publication: 2016).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE