المؤلفون: David E. Goldgar, Sophie Belman, Bing Jian Feng, Amanda B. Spurdle, Michael T. Parsons

المصدر: Genetics in Medicine. 22:2052-2059

مصطلحات موضوعية: 0301 basic medicine, education.field_of_study, medicine.medical_specialty, medicine.diagnostic_test, Cosegregation, Computer science, Population, Genomics, Bayes factor, Computational biology, 030105 genetics & heredity, Penetrance, 03 medical and health sciences, symbols.namesake, 030104 developmental biology, medicine, Mendelian inheritance, symbols, Medical genetics, education, Genetics (clinical), Genetic testing

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::2a129a0602a7b38340a9e49f5b0eb484Test
https://doi.org/10.1038/s41436-020-0920-4Test

المؤلفون: Bing Jian Feng, Gerald G. Krueger, Kristina Callis Duffin, Michael Milliken, Jessica A. Walsh, Courtney Carroll, Sophie Belman, Benjamin Haaland

المصدر: J Rheumatol

مصطلحات موضوعية: medicine.medical_specialty, Immunology, Population, Article, Psoriatic arthritis, Rheumatology, Quality of life, Internal medicine, Psoriasis, Immunology and Allergy, Medicine, Humans, education, Survival analysis, education.field_of_study, business.industry, Incidence (epidemiology), Incidence, Hazard ratio, Arthritis, Psoriatic, medicine.disease, Early Diagnosis, Quality of Life, business, Cohort study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c70f9fa58f513dbf606f18d850c3653eTest
https://pubmed.ncbi.nlm.nih.gov/33858978Test

المؤلفون: Chad D. Huff, N. Scott Reading, Binay Kumar Thakur, Hao Hu, Sarah Abdelaziz, Anna Shestakova, Chin Bahadur Pun, Lucie Lanikova, Bhola Siwakoti, Bing Jian Feng, Josef T. Prchal, Amir Sapkota, Mia Hashibe, Tatiana Burjanivova, Tsewang Tashi

المصدر: Oncotarget

مصطلحات موضوعية: 0301 basic medicine, Gerontology, Male, medicine.medical_specialty, Lung Neoplasms, Huntsman Cancer Institute, Acclimatization, Population, EPAS1/HIF-2α, Mongoloid, Tibet, Salt lake, 03 medical and health sciences, medicine, Humans, Lung cancer, education, ENGL1/PHD2, Preventive healthcare, Aged, Aged, 80 and over, education.field_of_study, business.industry, hypoxia, Public health, high-altitude adaptation, Middle Aged, medicine.disease, Hypoxia-Inducible Factor 1, alpha Subunit, 3. Good health, lung cancer, 030104 developmental biology, Increased risk, Oncology, Female, business, Demography, Research Paper

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59a1861976a97d672e62074d19d08a0eTest
https://pubmed.ncbi.nlm.nih.gov/28036300Test

المؤلفون: Jeffrey N. Weitzel, Eswary Thirthagiri, Paul Duncan, Soo Hwang Teo, David E. Goldgar, D. Gareth Evans, Ayse Latif, Ruth Gershoni-Baruch, Eitan Friedman, Itay Zamir, Yael Laitman, Bing Jian Feng, Shani Shimon-Paluch, William G. Newman, Jamal Zidan, Danielle Port

المصدر: European Journal of Human Genetics. 21:212-216

مصطلحات موضوعية: Genetics, education.field_of_study, medicine.medical_specialty, BRCA1 Protein, Population, Haplotype, Locus (genetics), Single-nucleotide polymorphism, Biology, Article, Founder Effect, Ashkenazi jews, Genetics, Population, Haplotypes, Jews, Ethnicity, medicine, Humans, Microsatellite, Medical genetics, education, Genetics (clinical), Sequence Deletion, Founder effect

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d08e5896b023cab42db0353f8c4bc64aTest
https://doi.org/10.1038/ejhg.2012.124Test

المؤلفون: Peter Heutink, Christine Van Broeckhoven, Cornelia M. van Duijn, Tatiana I. Axenovich, Bing Jian Feng, Manfred Kayser, Pascual Sánchez-Juan, Aida M. Bertoli-Avella, John C. van Swieten, Fan Liu, Ben A. Oostra, Yurii S. Aulchenko, Alejandro Arias-Vásquez, Kristel Sleegers

المساهمون: Epidemiology, Genetic Identification, Clinical Genetics, Neurology

المصدر: The American journal of human genetics
American Journal of Human Genetics, 81, 17-31
American Journal of Human Genetics, 81, 1, pp. 17-31
American Journal of Human Genetics, 81(1), 17-31. Cell Press

مصطلحات موضوعية: Male, Genetic Linkage, Population, SORL1, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Article, White People, Cognitive neurosciences [UMCN 3.2], Alzheimer Disease, Genetic linkage, Perception and Action [DCN 1], Genetics, Humans, Genetics(clinical), Age of Onset, education, Genetics (clinical), Aged, Netherlands, Aged, 80 and over, education.field_of_study, Genome, Human, Haplotype, Genomics, Middle Aged, Pedigree, Genetic defects of metabolism [UMCN 5.1], Haplotypes, Endophenotype, Microsatellite, Female, Human genome, Lod Score, Functional Neurogenomics [DCN 2]

وصف الملف: pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25b440bf9e186ee387a95cfe7688177aTest
https://doi.org/10.1086/518720Test

المؤلفون: Luba M. Pardo, Aaron Isaacs, Alejandro Arias-Vásquez, Albert Hofman, Lonneke M. L. de Lau, Ben A. Oostra, Cornelia M. van Duijn, Yurii S. Aulchenko, Bing Jian Feng, Aida M. Bertoli-Avella, Fan Liu, Monique M.B. Breteler

المساهمون: Epidemiology, Neurology, Clinical Genetics

المصدر: Neuroscience Letters, 424, 1-5. Elsevier Ireland Ltd
Neuroscience Letters, 424, 1-5
Neuroscience Letters, 424, 1, pp. 1-5

مصطلحات موضوعية: Male, Oncology, Heterozygote, medicine.medical_specialty, Parkinson's disease, Genotype, Genetic Linkage, DNA Mutational Analysis, Population, Autophagy-Related Proteins, Cell Cycle Proteins, Polymorphism, Single Nucleotide, UBQLN1, Cohort Studies, Rotterdam Study, Degenerative disease, Cognitive neurosciences [UMCN 3.2], Alzheimer Disease, Polymorphism (computer science), Internal medicine, Perception and Action [DCN 1], medicine, Humans, SNP, Genetic Predisposition to Disease, Genetic Testing, Age of Onset, education, Adaptor Proteins, Signal Transducing, Aged, Netherlands, Brain Chemistry, education.field_of_study, General Neuroscience, Parkinson Disease, Middle Aged, medicine.disease, Logistic Models, Genetic defects of metabolism [UMCN 5.1], Female, Alzheimer's disease, Carrier Proteins, Cognition Disorders, Psychology, Functional Neurogenomics [DCN 2], Neuroscience

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b39e8da12b9b79dc10f84ef96fc31489Test
https://doi.org/10.1016/j.neulet.2007.07.015Test

المؤلفون: Wided Bedadra, Wided Ben Ayoub, S. Mesli, Noureddine Bouaouina, Marilys Corbex, Meriem Abdoun, Fatima Maachi, M. Hamdi-Cherif, Majida Jalbout, M. Ayad, David E. Goldgar, Sami Dahmoul, Bing Jian Feng, Lotfi Chouchane, Abdellatif Benider, K. Boualga, Meriem Khyatti, Farhat Ben Ayed

المصدر: International Journal of Cancer. 121:1550-1555

مصطلحات موضوعية: Adult, Male, Rural Population, Cancer Research, medicine.medical_specialty, Pathology, Tunisia, Multivariate analysis, Adolescent, Urban Population, Population, Risk Factors, Food Preservation, Environmental health, Fish Products, Epidemiology, medicine, Animals, Humans, Risk factor, Child, education, Aged, education.field_of_study, Sheep, business.industry, Dietary risk, Public health, Case-control study, food and beverages, Nasopharyngeal Neoplasms, Middle Aged, medicine.disease, Dietary Fats, Diet, Meat Products, Morocco, Logistic Models, Oncology, Nasopharyngeal carcinoma, Algeria, Case-Control Studies, Multivariate Analysis, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c90c4a1d833570db135bc48d08ff52fTest
https://doi.org/10.1002/ijc.22813Test

المؤلفون: Bing Jian Feng, Xiao Shi Zhang, Ming Hong Yao, Li Xi Huang, Wei Hua Jia, Qi Sheng Feng, Yin Yao Shugart, Yi Xin Zeng, Zongli Xu, Ping Huang, Xing Juan Yu

المصدر: Cancer. 101:363-369

مصطلحات موضوعية: Adult, Male, Oncology, China, Cancer Research, medicine.medical_specialty, Pathology, Population, Risk Factors, Neoplasms, Internal medicine, Epidemiology, Humans, Medicine, Genetic Predisposition to Disease, Age of Onset, Risk factor, education, Family Health, education.field_of_study, business.industry, Incidence, Incidence (epidemiology), Family aggregation, Nasopharyngeal Neoplasms, medicine.disease, Standardized mortality ratio, Nasopharyngeal carcinoma, Female, Age of onset, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3189a4900261e35ff5d3b301a4f63cb5Test
https://doi.org/10.1002/cncr.20372Test

المؤلفون: Mary B. Daly, Fabrice Odefrey, John L. Hopper, Andrew Lonie, Sean V. Tavtigian, Erin L. Young, Jun Li, Igor V. Makunin, Kayoko Tao, Hao Hu, Fleur Hammet, Graham G. Giles, Terrell C Roane, Jonathan Ellis, Russell Bell, Irene L. Andrulis, Nivonirina Robinot, Melissa C. Southey, Catherine Voegele, Carrie Snyder, Louise B. Thingholm, David E. Goldgar, Mary Beth Terry, Esther M. John, Daniel J. Park, Tu Nguyen-Dumont, Zhi Ling Teo, Shankaracharya, Henry T. Lynch, Bing Jian Feng, Saundra S. Buys, Fabienne Lesueur, Peter Devilee, Florence Le Calvez-Kelm, Helen Tsimiklis, Bernard J. Pope, Chad D. Huff

المصدر: Cancer Discovery, 4(7), 804-815

مصطلحات موضوعية: Oncology, Male, medicine.medical_specialty, Population, Breast Neoplasms, Cell Cycle Proteins, Biology, Bioinformatics, Breast cancer, Internal medicine, medicine, Humans, Exome, Genetic Predisposition to Disease, education, Exome sequencing, Genetic testing, education.field_of_study, medicine.diagnostic_test, Cancer, Family aggregation, Genetic Variation, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Lynch syndrome, Pedigree, Case-Control Studies, Mutation, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::234443dd802321aefd30efdffd0956d7Test
https://pubmed.ncbi.nlm.nih.gov/25002613Test

المؤلفون: Bing Jian Feng, Thomas Hansen, Fergus J. Couch, Dominique Stoppa-Lyonnet, Finn Cilius Nielsen, Sona Ciernikova, David E. Goldgar, Celia M. T. Greenwood, Jacek Gronwald, Nancy Hamel, Bohdan Górski, Olga M. Sinilnikova, Mads Thomassen, Laima Tihomirova, Steven A. Narod, Irene Konstantopoulou, Evgeny N. Imyanitov, Jan Lubinski, Drakoulis Yannoukakos, William D. Foulkes, Lenka Foretova, Vladimir Zajac

المساهمون: Masaryk Memorial Cancer Institute, Service de Génétique Oncologique, INSTITUT CURIE, Unité de génétique et biologie des cancers ( U830 ), Université Paris Descartes - Paris 5 ( UPD5 ) -Institut Curie-Institut National de la Santé et de la Recherche Médicale ( INSERM ), Laboratory of Molecular Oncology, N.N. Petrov Institute of Oncology, Equipe 6, Centre de Recherche en Cancérologie de Lyon ( CRCL ), Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 ( UCBL ), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ) -Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 ( UCBL ), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale ( INSERM ) -Centre National de la Recherche Scientifique ( CNRS ) -Unité Mixte de Génétique Constitutionnelle des Cancers Fréquents, Centre Léon Bérard [Lyon]-Hospices Civils de Lyon ( HCL ) -Hospices Civils de Lyon ( HCL ), Latvian Biomedical Research and Study Centre [Rīga], Department of Genetics and Pathology, Pomeranian Medical University-International Hereditary Cancer Centre, Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Department of Clinical Genetics, Rigshospitalet [Copenhagen]-University of Copenhagen ( KU ), Odense University Hospital, Molecular Diagnostics Laboratory, IRRP, National Centre for Scientific Research 'Demokritos', National Center for Scientific Research 'Demokritos' ( NCSR ), McGill University, Masaryk Memorial Cancer Institute (RECAMO), Institut Curie, Unité de génétique et biologie des cancers (U830), Université Paris Descartes - Paris 5 (UPD5)-Institut Curie-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de Recherche en Cancérologie de Lyon (CRCL), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre Léon Bérard [Lyon]-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre Léon Bérard [Lyon]-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Unité Mixte de Génétique Constitutionnelle des Cancers Fréquents, Centre Léon Bérard [Lyon]-Hospices Civils de Lyon (HCL)-Hospices Civils de Lyon (HCL), Department of Clinical Genetics [Copenhagen], Rigshospitalet [Copenhagen], National Center for Scientific Research 'Demokritos' (NCSR), Institut Curie [Paris], Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Descartes - Paris 5 (UPD5), Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL), Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Unité Mixte de Génétique Constitutionnelle des Cancers Fréquents, Copenhagen University Hospital-Copenhagen University Hospital, McGill University = Université McGill [Montréal, Canada]

المصدر: European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2011, 19 (3), pp.300-6. 〈10.1038/ejhg.2010.203〉
European Journal of Human Genetics, Nature Publishing Group, 2011, 19 (3), pp.300-6. ⟨10.1038/ejhg.2010.203⟩
Hamel, N, Feng, B-J, Foretova, L, Stoppa-Lyonnet, D, Narod, S A, Imyanitov, E, Sinilnikova, O, Tihomirova, L, Lubinski, J, Gronwald, J, Gorski, B, Hansen, T V O, Nielsen, F C, Thomassen, M, Yannoukakos, D, Konstantopoulou, I, Zajac, V, Ciernikova, S, Couch, F J, Greenwood, C M T, Goldgar, D E & Foulkes, W D 2011, ' On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations ', European Journal of Human Genetics, vol. 19, no. March, pp. 300-306 . https://doi.org/10.1038/ejhg.2010.203Test

مصطلحات موضوعية: MESH : Genes, BRCA1, Genes, BRCA1, MESH : Genotype, MESH: Founder Effect, MESH : Breast Neoplasms, MESH : Microsatellite Repeats, [ SDV.CAN ] Life Sciences [q-bio]/Cancer, MESH: Genotype, 0302 clinical medicine, Gene Frequency, Ethnicity, MESH : Female, MESH : Gene Frequency, Genetics (clinical), Genetics, Ovarian Neoplasms, 0303 health sciences, education.field_of_study, MESH: Genetic Testing, MESH: Genetic Predisposition to Disease, MESH: European Continental Ancestry Group, Founder Effect, 3. Good health, Europe, MESH: Ovarian Neoplasms, MESH : Jews, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), MESH: Jews, Microsatellite, MESH: Ethnic Groups, Female, Gene pool, MESH : Mutation, Brazil, MESH : Ethnic Groups, MESH: Mutation, Genotype, Population, MESH : Europe, MESH : Founder Effect, [SDV.CAN]Life Sciences [q-bio]/Cancer, Breast Neoplasms, Biology, White People, Article, MESH : European Continental Ancestry Group, 03 medical and health sciences, Molecular evolution, MESH : Genetic Testing, MESH: Gene Frequency, MESH : Brazil, Humans, Genetic Predisposition to Disease, Genetic Testing, education, Allele frequency, MESH : Haplotypes, 030304 developmental biology, MESH: Humans, MESH : Ovarian Neoplasms, Haplotype, MESH : Humans, MESH: Haplotypes, Haplotypes, Jews, Mutation, MESH : Genetic Predisposition to Disease, MESH: Microsatellite Repeats, MESH: Europe, MESH: Brazil, MESH: Female, MESH: Genes, BRCA1, MESH: Breast Neoplasms, Founder effect, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ae2911b38e54ed4a780b019403dd822Test
https://pubmed.ncbi.nlm.nih.gov/21119707Test