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المؤلفون: Jan Loeffen, Saskia M. J. Hopman, Natasha K. A. van Eijkelenburg, Cora M. Aalfs, Fonnet E. Bleeker, Lieke P.V. Berger, Peter Hammond, Floor A. M. Postema, Charlotte J. Dommering, Jakob K. Anninga, Janna A. Hol, Raoul C.M. Hennekam, Anja Wagner, Maran J. W. Olderode-Berends, Marry M. van den Heuvel-Eibrink, Tom G.W. Letteboer, Lisethe Meijer, Johannes H. M. Merks, Corianne A. J. M. de Borgie, Wijnanda A. Kors
المساهمون: Clinical Genetics, Human genetics, CCA - Cancer biology and immunology
المصدر: Familial Cancer, 20, 263-271. SPRINGER
Familial Cancer
Familial Cancer, 20(4), 263-271. Springer Netherlands
Postema, F A M, Hopman, S M J, de Borgie, C A J M, Aalfs, C M, Anninga, J K, Berger, L P V, Bleeker, F E, Dommering, C J, van Eijkelenburg, N K A, Hammond, P, van den Heuvel-Eibrink, M M, Hol, J A, Kors, W A, Letteboer, T G W, Loeffen, J L C M, Meijer, L, Olderode-Berends, M J W, Wagner, A, Hennekam, R C & Merks, J H M 2021, ' Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS) : a prospective, observational, multi-center study ', Familial Cancer, vol. 20, no. 4, pp. 263-271 . https://doi.org/10.1007/s10689-021-00237-1مصطلحات موضوعية: 0301 basic medicine, Cancer Research, medicine.medical_specialty, media_common.quotation_subject, Genetic predisposition to disease, Pediatrics, Imaging, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Neoplasms, Internal medicine, Genetic screening, Epidemiology, Genetics, medicine, Humans, Mass Screening, Clinical significance, Prospective Studies, Child, Early Detection of Cancer, Genetics (clinical), media_common, Selection bias, business.industry, Cancer, Syndrome, medicine.disease, Checklist, 030104 developmental biology, Oncology, 030220 oncology & carcinogenesis, Cohort, Clinical value, Original Article, Observational study, Three-dimensional, business
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المؤلفون: Rachel H. Giles, Thera P. Links, Wim J. Sluiter, Roeliene C. Kruizinga, Maran J. W. Olderode-Berends, Anouk N A van der Horst-Schrivers, Rachel S van Leeuwaarde
المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Damage and Repair in Cancer Development and Cancer Treatment (DARE), Internal medicine
المصدر: Familial Cancer, 18(3), 369. Springer Netherlands
Familial Cancer, 18(3), 369-376. SPRINGER
Familial Cancer
van der Horst-Schrivers, A N A, Sluiter, W J, Kruizinga, R C, van Leeuwaarde, R S, Giles, R, Olderode-Berends, M J W & Links, T P 2019, ' The incidence of consecutive manifestations in Von Hippel-Lindau disease ', Familial Cancer, vol. 18, no. 3, pp. 369-376 . https://doi.org/10.1007/s10689-019-00131-x
Familial Cancer, 18(3), 369-376. Springer Netherlandsمصطلحات موضوعية: 0301 basic medicine, Male, Pathology, Cancer Research, Time Factors, endocrine system diseases, PROGRESSION, Disease, Kaplan-Meier Estimate, 030105 genetics & heredity, urologic and male genital diseases, Central Nervous System Neoplasms, 0302 clinical medicine, Epidemiology, Genetics(clinical), MUTATION, Genetics (clinical), Surveillance, Incidence (epidemiology), Age Factors, Middle Aged, Kidney Neoplasms, female genital diseases and pregnancy complications, Hemangioblastoma, Natural history, medicine.anatomical_structure, PREGNANCY, Oncology, 030220 oncology & carcinogenesis, symbols, Original Article, Female, Pancreas, Adult, Von Hippel-Lindau disease, medicine.medical_specialty, Heterozygote, Adolescent, Retinal Neoplasms, HEMANGIOBLASTOMAS, 03 medical and health sciences, symbols.namesake, Young Adult, medicine, Genetics, Journal Article, Humans, Poisson regression, Von Hippel–Lindau disease, Allele, neoplasms, Aged, Retrospective Studies, Disease progression, business.industry, CENTRAL-NERVOUS-SYSTEM, VHL-related manifestations, NATURAL-HISTORY, medicine.disease, Pancreatic Neoplasms, MODEL, business
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المؤلفون: Stefan Aretz, Jenny von Salomé, Liesbeth Spruijt, Inge Bernstein, Tom G.W. Letteboer, Theo A. M. van Os, Kristina Lagerstedt-Robinson, Magnus von Knebel Doeberitz, Encarna B. Gomez-Garcia, Verena Steinke-Lange, Sanne W. ten Broeke, Maran J. W. Olderode-Berends, Hans K. Schackert, Marta Pineda, Manon Suerink, Gabriel Capellá, Nils Rahner, Carli M. J. Tops, Mar Rodríguez-Girondo, Christoph Engel, Anja Wagner, Pål Møller, Liselotte P. van Hest, Maartje Nielsen
المساهمون: Human genetics, CCA - Cancer biology and immunology, Klinische Genetica, MUMC+: DA KG Polikliniek (9), RS: GROW - R4 - Reproductive and Perinatal Medicine, Clinical Genetics, Human Genetics
المصدر: Ten Broeke, S W, Rodríguez-Girondo, M, Suerink, M, Aretz, S, Bernstein, I, Capella, G, Engel, C, Gomez-Garcia, E B, van Hest, L P, von Knebel Doeberitz, M, Lagerstedt-Robinson, K, Letteboer, T G W, Møller, P, van Os, T A M, Pineda, M, Rahner, N, Olderode-Berends, M J W, von Salomé, J, Schackert, H K, Spruijt, L, Steinke-Lange, V, Wagner, A, Tops, C M J & Nielsen, M 2019, ' The apparent genetic anticipation in PMS2-associated Lynch syndrome families is explained by birth cohort effect ', Cancer Epidemiology, Biomarkers & Prevention, vol. 28, no. 6, pp. 1010-1014 . https://doi.org/10.1158/1055-9965.EPI-18-0576
Cancer Epidemiology, Biomarkers & Prevention, 28, 6, pp. 1010-1014
Cancer Epidemiology, Biomarkers and Prevention, 28(6), 1010-1014
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 28(6), 1010-1014. AMER ASSOC CANCER RESEARCH
Cancer Epidemiology Biomarkers and Prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer Epidemiology Biomarkers & Prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer epidemiology, biomarkers & prevention, 28(6), 1010-1014. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers and Prevention, 28(6), 1010-1014. AMER ASSOC CANCER RESEARCH
Cancer Epidemiology, Biomarkers & Prevention, 28, 1010-1014
ten Broeke, S W, Rodríguez-Girondo, M, Suerink, M, Aretz, S, Bernstein, I, Capella, G, Engel, C, Gomez-Garcia, E B, van Hest, L P, von Knebel Doeberitz, M, Lagerstedt-Robinson, K, Letteboer, T G W, Moller, P, van Os, T A, Pineda, M, Rahner, N, Olderode-Berends, M J W, von Salome, J, Schackert, H K, Spruijt, L, Steinke-Lange, V, Wagner, A, Tops, C M J & Nielsen, M 2019, ' The apparent genetic anticipation in PMS2-associated lynch syndrome families is explained by birth-cohort effect ', Cancer Epidemiology Biomarkers and Prevention, vol. 28, no. 6, pp. 1010-1014 . https://doi.org/10.1158/1055-9965.EPI-18-0576مصطلحات موضوعية: 0301 basic medicine, Proband, Male, medicine.medical_specialty, Epidemiology, Colorectal cancer, Penetrance, DNA Mismatch Repair, COLORECTAL-CANCER, 03 medical and health sciences, 0302 clinical medicine, Cohort Effect, medicine, Humans, HETEROGENEITY, Age of Onset, Aged, Mismatch Repair Endonuclease PMS2, Netherlands, Proportional Hazards Models, RISK, Models, Statistical, business.industry, Anticipation, Genetic, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Confidence interval, Lynch syndrome, Pedigree, 030104 developmental biology, Oncology, 030220 oncology & carcinogenesis, Anticipation (genetics), Mutation, Medical genetics, Female, Age of onset, NO EVIDENCE, business, Demography, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9]
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المؤلفون: Maartje Nielsen, Marjolijn J. L. Ligtenberg, Yvonne Tiersma, Juul T. Wijnen, Maran J. W. Olderode-Berends, Encarna Gomez Garcia, B. Redeker, José B. M. Zonneveld, Sanne W. ten Broeke, Frederik J. Hes, Carli M. J. Tops, Peter Devilee, Theo A. M. van Os, Christi J. van Asperen, Hans J. J. P. Gille, Niels de Wind, Heleen M. van der Klift, Arjen R. Mensenkamp, Tom G.W. Letteboer, Yvonne J. Vos, Elsa C. Bik, Mark Drost, S. Verhoef, Liselotte P. van Hest, Anja Wagner
المساهمون: Human Genetics, Human genetics, CCA - Cancer biology, RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Polikliniek (9), Klinische Genetica, Medical Genetics, Clinical Genetics
المصدر: Human mutation, 37(11), 1162-1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162-1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162–1179. Wiley-Liss Inc.
Human Mutation, 37(11), 1162-1179. Wiley
Human Mutation, 37(11), 1162-1179
Human Mutation, 37, 11, pp. 1162-1179
Human Mutation, 37, 1162-1179
van der Klift, H M, Mensenkamp, A R, Drost, M, Bik, E C, Vos, Y J, Gille, H J J P, Redeker, B E J W, Tiersma, Y, Zonneveld, J B M, Garcia, E G, Letteboer, T G W, Olderode-Berends, M J W, van Hest, L P, van Os, T A, Verhoef, S, Wagner, A, van Asperen, C J, Ten Broeke, S W, Hes, F J, de Wind, N, Nielsen, M, Devilee, P, Ligtenberg, M J L, Wijnen, J T & Tops, C M J 2016, ' Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome ', Human Mutation, vol. 37, no. 11, pp. 1162-1179 . https://doi.org/10.1002/humu.23052مصطلحات موضوعية: 0301 basic medicine, DNA Mutational Analysis, pseudogenes, COLORECTAL-CANCER, Cohort Studies, 0302 clinical medicine, Mutation Carrier, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], PMS2, Missense mutation, Genetics (clinical), Mismatch Repair Endonuclease PMS2, Netherlands, Medicine(all), Genetics, Brain Neoplasms, MLH1, Neoplastic Syndromes, Hereditary/genetics, Lynch syndrome, CMMRD, missense variants, immunohistochemistry, mismatch repair, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), DNA mismatch repair, Microsatellite Instability, Colorectal Neoplasms, EUROPEAN CONSORTIUM CARE, PSEUDOGENE INTERFERENCE, congenital, hereditary, and neonatal diseases and abnormalities, DNA Mutational Analysis/methods, Biology, 03 medical and health sciences, Germline mutation, Neoplastic Syndromes, Hereditary, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, SYNDROME FAMILIES, CFR PARTICIPANTS, medicine, Journal Article, Humans, Genetic Predisposition to Disease, Germ-Line Mutation, Brain Neoplasms/genetics, Microsatellite instability, Genetic Variation, Mismatch Repair Endonuclease PMS2/genetics, medicine.disease, Colorectal Neoplasms/genetics, Colorectal Neoplasms, Hereditary Nonpolyposis, GENE, digestive system diseases, 030104 developmental biology, PROMOTER HYPERMETHYLATION, 3' DELETIONS, Cancer research, NONPOLYPOSIS COLON-CANCER
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المؤلفون: Liesbeth Spruijt, Encarna Gomez Garcia, Maartje Nielsen, Tom van Wezel, Maran J. W. Olderode-Berends, Ewout W. Steyerberg, Hans J. J. P. Gille, Liselot P. van Hest, Juul T. Wijnen, Lisa Pagan, Manon Suerink, Sanne W. ten Broeke, Carli M. J. Tops, Theo A. M. van Os, Arjen R. Mensenkamp, B. Redeker, Tom G.W. Letteboer, Yvonne J. Vos, Fadwa A. Elsayed, Lizet E. van der Kolk, Anja Wagner
المساهمون: CCA - Cancer biology and immunology, Human genetics, Human Genetics, RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Polikliniek (9), Klinische Genetica, Clinical Genetics
المصدر: Familial Cancer, 17(4), 507-515. Springer Netherlands
Familial Cancer, 17, 507-515
Ten Broeke, S W, Elsayed, F A, Pagan, L, Olderode-Berends, M J W, Garcia, E G, Gille, H J P, van Hest, L P, Letteboer, T G W, van der Kolk, L E, Mensenkamp, A R, van Os, T A, Spruijt, L, Redeker, B J W, Suerink, M, Vos, Y J, Wagner, A, Wijnen, J T, Steyerberg, E W, Tops, C M J, van Wezel, T & Nielsen, M 2018, ' SNP association study in PMS2-associated Lynch syndrome ', Familial Cancer, vol. 17, no. 4, pp. 507-515 . https://doi.org/10.1007/s10689-017-0061-3
Familial Cancer, 17(4), 507-515. SPRINGER
Familial Cancer
Familial cancer, 17(4), 507-515. Springer Netherlands
Familial Cancer, 17(4), 507. Springer Netherlands
Familial Cancer, 17(4), 507-515. Springer, Cham
Familial Cancer, 17(4), 507-515
Familial Cancer, 17, 4, pp. 507-515مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Cancer Research, Genome-wide association study, Kaplan-Meier Estimate, VARIANTS, Cancer risk, 0302 clinical medicine, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Genetics(clinical), 8Q23.3, Genetics (clinical), Mismatch Repair Endonuclease PMS2, Aged, 80 and over, Hazard ratio, MLH1, Middle Aged, Lynch syndrome, 3. Good health, 030220 oncology & carcinogenesis, Female, Original Article, Colorectal Neoplasms, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], Chromosomes, Human, Pair 8, Adult, Heterozygote, 11Q23.1, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, GENES, Concordance, SNP, Single-nucleotide polymorphism, MUTATION CARRIERS, Polymorphism, Single Nucleotide, 03 medical and health sciences, All institutes and research themes of the Radboud University Medical Center, Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, COHORT, Allele, Aged, COLORECTAL-CANCER RISK, PMS2 MUTATIONS, Proportional hazards model, business.industry, Chromosomes, Human, Pair 11, Modifiers, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Colorectal cancer, digestive system diseases, BODY-MASS INDEX, PMS2, 030104 developmental biology, Case-Control Studies, business, Genome-Wide Association Study
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المؤلفون: Maran J. W. Olderode-Berends, Mercedes Robledo, J. de Vries, M. F. van Dooren, Karin Eijkelenkamp, R. B. van der Luijt, Thera P. Links, Richard A Feelders, A. N. A. van der Horst-Schrivers, Michiel N. Kerstens
المساهمون: Damage and Repair in Cancer Development and Cancer Treatment (DARE), Guided Treatment in Optimal Selected Cancer Patients (GUTS), Clinical Genetics, Internal Medicine
المصدر: Clinical Genetics, 93(5), 1049-1056
Clinical Genetics, 93(5), 1049-1056. Wiley
Clinical Genetics, 93(5), 1049-1056. Wiley-Blackwell Publishing Ltdمصطلحات موضوعية: Adult, Male, 0301 basic medicine, CARCINOMA, SDHB, Adrenal Gland Neoplasms, SUSCEPTIBILITY, Neuroendocrine tumors, COMPLEX II DEFICIENCY, medicine.disease_cause, homozygous, DISEASE, Pheochromocytoma, 03 medical and health sciences, chemistry.chemical_compound, paraganglioma, 0302 clinical medicine, Germline mutation, Paraganglioma, TMEM127 mutation carriers, MANAGEMENT, Genetics, Humans, Medicine, Genetic Predisposition to Disease, Genetic Testing, Gene, Metanephrine, Germ-Line Mutation, Genetics (clinical), Mutation, business.industry, Homozygote, Membrane Proteins, GERMLINE MUTATIONS, Middle Aged, medicine.disease, GENE, pheochromocytoma, FAMILY, 030104 developmental biology, chemistry, 030220 oncology & carcinogenesis, Female, business
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المؤلفون: Eveline J. Kamping, Wojciech Młynarski, Diede A G van Bladel, Nicoline Hoogerbrugge, Anja Wagner, Roland P. Kuiper, Marjolijn J. L. Ligtenberg, Marjolijn C.J. Jongmans, Jan Loeffen, Denisa Ilencikova, Dylan A. Mordaunt, Lesley M McGregor, Eveline S. J. M. de Bont, Antonis Kattamis, Gijs W. E. Santen, Thatjana Gardeitchik, Arjen R. Mensenkamp, Elizabeth Thompson, Agata Pastorczak, Martine J. van Belzen, Saskia M. J. Hopman, Maran J. W. Olderode-Berends, Anneke Vulto van Silfhout, Carlo Marcelis, David A. Koolen, Esmé Waanders, Illja J. Diets, Peter M. Hoogerbrugge, Erica H. Gerkes
المساهمون: Damage and Repair in Cancer Development and Cancer Treatment (DARE), Stem Cell Aging Leukemia and Lymphoma (SALL), Pediatrics, Clinical Genetics
المصدر: Clinical Cancer Research, 24(7), 1594-1603. AMER ASSOC CANCER RESEARCH
Clinical Cancer Research, 24, 1594-1603
Clinical Cancer Research, 24, 7, pp. 1594-1603
Clinical Cancer Research, 24(7), 1594-1603. American Association for Cancer Research Inc.
Clinical Cancer Research, 24(7), 1594. American Association for Cancer Research Inc.مصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, INTELLECTUAL DISABILITY, WEAVER SYNDROME, Craniofacial Abnormalities, 0302 clinical medicine, Neoplasms, Genotype, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], Medicine, Exome, Child, Exome sequencing, Genetics, Rubinstein-Taybi Syndrome, GENETIC-VARIATION, Metabolic Disorders Radboud Institute for Molecular Life Sciences [Radboudumc 6], Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Phenotype, Oncology, 030220 oncology & carcinogenesis, Child, Preschool, Female, LI-FRAUMENI SYNDROME, Hand Deformities, Congenital, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], Adolescent, Micrognathism, ACUTE MYELOID-LEUKEMIA, 03 medical and health sciences, Germline mutation, SDG 3 - Good Health and Well-being, WINTER CEREBROFRONTOFACIAL SYNDROME, Exome Sequencing, Genetic predisposition, Congenital Hypothyroidism, Humans, Abnormalities, Multiple, Genetic Predisposition to Disease, Coffin–Siris syndrome, Germ-Line Mutation, ACUTE LYMPHOBLASTIC-LEUKEMIA, PEDIATRIC CANCER, CHILDHOOD-CANCER, business.industry, COFFIN-SIRIS SYNDROME, Cancer, Infant, medicine.disease, Pediatric cancer, 030104 developmental biology, Li–Fraumeni syndrome, Face, business, Neck
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المؤلفون: Karl Heinimann, Susanne Timshel, Shirley Hodgson, Noralane M. Lindor, E. B. Gomez Garcia, Pål Møller, Stefan Aretz, Fiona Douglas, Maran J. W. Olderode-Berends, C. M. Kets, Chrystelle Colas, Hans F. A. Vasen, Maureen Murphy-Ryan, Allan D. Spigelman, Frederik J. Hes, Marry H. Nieuwenhuis
المصدر: Colorectal Disease. 14:e562-e566
مصطلحات موضوعية: Oncology, medicine.medical_specialty, education.field_of_study, biology, Colorectal cancer, business.industry, Population, Gastroenterology, Cancer, Multiple hamartoma syndrome, Cowden syndrome, medicine.disease, Internal medicine, medicine, biology.protein, Tensin, PTEN, Gastrointestinal Polyp, education, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::fbac7c71e0b57253bda934f640e07c17
https://doi.org/10.1111/j .1463-1318.2012.03121.x -
9
المؤلفون: Sónia Sousa, Renee C. Niessen, Robert M.W. Hofstra, Ana Ferreira, Maran J. W. Olderode-Berends, Helga Westers, Jan H. Kleibeuker, Tineke van der Sluis, Raquel Seruca, Rolf H. Sijmons, Harry Hollema, Peter Reuvekamp, Ying Wu
المصدر: The Journal of Pathology. 219:96-102
مصطلحات موضوعية: Genome instability, congenital, hereditary, and neonatal diseases and abnormalities, Pathology, medicine.medical_specialty, Cancer, Microsatellite instability, Colorectal adenoma, Biology, Gene mutation, medicine.disease, digestive system diseases, Lynch syndrome, Pathology and Forensic Medicine, Germline mutation, medicine, Cancer research, DNA mismatch repair
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المؤلفون: Anneke T. van Silfhout, Trijnie Dijkhuizen, Birgit Sikkema-Raddatz, Conny M. A. van Ravenswaaij-Arts, Peter C. van den Akker, Maran J. W. Olderode-Berends, Joke B. G. M. Verheij, Klaas Kok
المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Translational Immunology Groningen (TRIGR)
المصدر: European Journal of Human Genetics, 17(11), 1432-1438. Nature Publishing Group
مصطلحات موضوعية: Male, CANDIDATE GENE, EXPRESSION, Candidate gene, LIMB DEVELOPMENT, Foot Deformities, Congenital, Locus (genetics), Biology, Article, split hand/foot malformation (SHFM), Gene mapping, LOCUS, Genetics, medicine, Humans, Abnormalities, Multiple, P63 GENE, chromosome 7q21q22, DLX5, DLX6, Genetics (clinical), Chromosome Aberrations, medicine.diagnostic_test, DSS1, MUTATIONS, Infant, Newborn, Infant, REARRANGEMENT, HAND FOOT MALFORMATION, FAMILY, Female, Haploinsufficiency, Hand Deformities, Congenital, Chromosomes, Human, Pair 7, Fluorescence in situ hybridization, Comparative genomic hybridization
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المؤلفون: Marco J. Bruno, Jan-Werner Poley, Irma Kluijt, Anja Wagner, Rolf H. Sijmons, Cora M. Aalfs, Maran J. W. Olderode-Berends, Theo A. M. van Os, Femme Harinck, Quinten Waisfisz, Paul Fockens, Saskia E. van Mil, Ernst J. Kuipers
المساهمون: Gastroenterology & Hepatology, Clinical Genetics, Human Genetics, Amsterdam Gastroenterology Endocrinology Metabolism, Cancer Center Amsterdam, Gastroenterology and Hepatology, Other departments, Human genetics, CCA - Quality of life, Science in Healthy Ageing & healthcaRE (SHARE), Ethical, Legal, Social Issues in Genetics (ELSI), Guided Treatment in Optimal Selected Cancer Patients (GUTS)
المصدر: European Journal of Human Genetics, 20(5), 577-579. Nature Publishing Group
European journal of human genetics, 20(5), 577-579. Nature Publishing Group
Harinck, F, Kluijt, I, van Mil, S E, Waisfisz, Q, van Os, T A M, Aalfs, C M, Wagner, A, Olderode-Berends, M, Sijmons, R H, Kuipers, E J, Poley, J W, Fockens, P & Bruno, M J 2012, ' Routine testing for PALB2 mutations in familial pancreatic cancer families and breast cancer families with pancreatic cancer is not indicated ', European Journal of Human Genetics, vol. 20, no. 5, pp. 577-579 . https://doi.org/10.1038/ejhg.2011.226مصطلحات موضوعية: Oncology, Adult, Male, medicine.medical_specialty, PALB2, pancreatic cancer susceptibility, Short Report, Breast Neoplasms, familial pancreatic cancer, Gene mutation, BRCA2-INTERACTING PROTEIN, Cohort Studies, Breast cancer, SDG 3 - Good Health and Well-being, Pancreatic cancer, Internal medicine, Genetics, Prevalence, Medicine, Humans, Genetic Predisposition to Disease, Multiplex ligation-dependent probe amplification, Family history, Genetics (clinical), mutation analysis, business.industry, Tumor Suppressor Proteins, breast cancer susceptibility, Nuclear Proteins, Middle Aged, medicine.disease, Pancreatic Neoplasms, SUSCEPTIBILITY GENE, hereditary cancer, Cohort, Mutation, Female, business, Fanconi Anemia Complementation Group N Protein, Cohort study
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المؤلفون: Harry Hollema, Helga Westers, Renee C. Niessen, Maran J. W. Olderode-Berends, Rolf H. Sijmons, Marjolijn J. L. Ligtenberg, Trijnie Dijkhuizen, Paul O. J. Jager, Marloes L. de Groote, Krista Kooi, Jan H. Kleibeuker, Robert M.W. Hofstra
المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Targeted Gynaecologic Oncology (TARGON)
المصدر: GENES CHROMOSOMES & CANCER, 48(8), 737-744. Wiley
Genes, Chromosomes & Cancer, 48, 8, pp. 737-44
Genes, Chromosomes & Cancer, 48, 737-44مصطلحات موضوعية: Male, Cancer Research, MICROSATELLITE INSTABILITY, medicine.disease_cause, Germline, FAMILIES, Cohort Studies, Promoter Regions, Genetic, Mutation, METHYLATION, Nuclear Proteins, NONPOLYPOSIS COLORECTAL-CANCER, Epithelial Cell Adhesion Molecule, TUMORS, Immunohistochemistry, Lynch syndrome, HMLH1, DNA-Binding Proteins, EPIMUTATION, MutS Homolog 2 Protein, DNA methylation, Female, MutL Protein Homolog 1, EXPRESSION, congenital, hereditary, and neonatal diseases and abnormalities, Biology, MLH1, Translational research [ONCOL 3], Antigens, Neoplasm, Genetics, medicine, Humans, neoplasms, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Hereditary cancer and cancer-related syndromes [ONCOL 1], Microsatellite instability, nutritional and metabolic diseases, DNA Methylation, medicine.disease, Molecular biology, GENE, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, MSH2, MSH6, Cancer research, Cell Adhesion Molecules, Gene Deletion
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المؤلفون: Ana Ferreira, Renee C. Niessen, Harry Hollema, Helga Westers, Jan H. Kleibeuker, Maran J. W. Olderode-Berends, Ying Wu, Tineke van der Sluis, Ate G. van der Zee, Robert M.W. Hofstra, Rolf H. Sijmons
المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Targeted Gynaecologic Oncology (TARGON)
المصدر: GENES CHROMOSOMES & CANCER, 48(7), 552-557. Wiley
مصطلحات موضوعية: Adult, Cancer Research, Base Pair Mismatch, DNA Mutational Analysis, INSERTION, Endometrial Carcinomas, Biology, HEREDITARY, medicine.disease_cause, SEQUENCE, SACCHAROMYCES-CEREVISIAE, Genetics, medicine, Humans, DELETION MUTATIONS, MISMATCH REPAIR PROFICIENT, neoplasms, Aged, Mutation, RELATIVE RATES, Analysis of Variance, Endometrial epithelium, Age Factors, Microsatellite instability, Cancer, DNA, Gene deletion, Middle Aged, medicine.disease, Molecular biology, CANCER, Lynch syndrome, digestive system diseases, Endometrial Neoplasms, Mutagenesis, Insertional, Deletion mutation, CELLS, Female, Microsatellite Instability, Colorectal Neoplasms, Gene Deletion, Microsatellite Repeats
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المؤلفون: Charlotte J. Dommering, Lieke P.V. Berger, Fonnet E. Bleeker, Saskia M. J. Hopman, Raoul C.M. Hennekam, Tom G.W. Letteboer, Maran J. W. Olderode-Berends, Floor A. M. Postema, Johannes H. M. Merks, Anja Wagner, Marjolijn C.J. Jongmans, Cora M. Aalfs
المساهمون: Clinical Genetics
المصدر: Pediatric blood & cancer, 64, S404-S405. Wiley
European Journal of Cancer, 80, pp. 48-54
European Journal of Cancer, 80, 48-54. Elsevier Ltd.
European Journal of Cancer, 80, 48. Elsevier Limited
Postema, F A M, Hopman, S M J, Aalfs, C M, Berger, L P V, Bleeker, F E, Dommering, C J, Jongmans, M C J, Letteboer, T G W, Olderode-Berends, M J W, Wagner, A, Hennekam, R C & Merks, J H M 2017, ' Childhood tumours with a high probability of being part of a tumour predisposition syndrome; reason for referral for genetic consultation ', European Journal of Cancer, vol. 80, pp. 48-54 . https://doi.org/10.1016/j.ejca.2017.04.021
European Journal of Cancer, 80, 48-54مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Pediatrics, medicine.medical_specialty, Consensus, Referral, CARCINOMA, Genetic predisposition to disease, CHILDREN, Genetic Counseling, Review, FREQUENCY, RECOMMENDATIONS, 03 medical and health sciences, 0302 clinical medicine, Neoplastic Syndromes, Hereditary, SURVEILLANCE, Carcinoma, Journal Article, Medicine, Humans, Clinical significance, Genetic Predisposition to Disease, Child, Referral and Consultation, Cancer, GORLIN SYNDROME, PEDIATRIC CANCER, business.industry, Paediatric oncology, MUTATIONS, Incidence (epidemiology), Incidence, MALFORMATION SYNDROMES, Paediatrics, Geneticist, medicine.disease, Pediatric cancer, 030104 developmental biology, Oncology, MEDULLOBLASTOMA, 030220 oncology & carcinogenesis, business, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9]
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