المؤلفون: Molly Went, Ben Kinnersley, Amit Sud, David C. Johnson, Niels Weinhold, Asta Försti, Mark van Duin, Giulia Orlando, Jonathan S. Mitchell, Rowan Kuiper, Brian A. Walker, Walter M. Gregory, Per Hoffmann, Graham H. Jackson, Markus M. Nöthen, Miguel Inacio da Silva Filho, Hauke Thomsen, Annemiek Broyl, Faith E. Davies, Unnur Thorsteinsdottir, Markus Hansson, Martin Kaiser, Pieter Sonneveld, Hartmut Goldschmidt, Kari Stefansson, Kari Hemminki, Björn Nilsson, Gareth J. Morgan, Richard S. Houlston

المصدر: Human Genomics, Vol 13, Iss 1, Pp 1-8 (2019)

مصطلحات موضوعية: Genome-wide association study, Gene expression, Multiple myeloma, Transcriptome-wide association study, Medicine, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s40246-019-0231-5; https://doaj.org/toc/1479-7364

URL الوصول: https://doaj.org/article/921d6df1bf474729aae772a11dae5420

المؤلفون: Tobias Möllers, Laura Perna, Bernd Holleczek, Hannah Stocker, Hauke Thomsen, Hermann Brenner, Dan Rujescu, Korbinian Weigl, Ben Schöttker

المصدر: Molecular Psychiatry

مصطلحات موضوعية: 0301 basic medicine, Apolipoprotein E, medicine.medical_specialty, Genotype, Apolipoprotein E4, Diseases, Disease, Logistic regression, Article, 03 medical and health sciences, Cellular and Molecular Neuroscience, Apolipoproteins E, 0302 clinical medicine, Alzheimer Disease, Risk Factors, Internal medicine, Genetics, medicine, Humans, Dementia, Prospective Studies, Allele, Molecular Biology, Receiver operating characteristic, business.industry, Correction, medicine.disease, Psychiatry and Mental health, 030104 developmental biology, Clinical diagnosis, Cohort, business, 030217 neurology & neurosurgery, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0de8a8e98d4edfbe8bfbae27e218e687
https://doi.org/10.1038/s41380-020-0764-y

المؤلفون: Subhayan Chattopadhyay, Miguel Inacio da Silva Filho, Stefanie Huhn, Niels Weinhold, Hauke Thomsen, Markus M. Nöthen, Gareth J. Morgan, Pankaj Yadav, Uta Bertsch, Kari Hemminki, Hartmut Goldschmidt, Asta Försti, Richard S. Houlston, Per Hoffman

المصدر: Communications Biology, Vol 2, Iss 1, Pp 1-10 (2019)
Communications Biology

مصطلحات موضوعية: Cellular differentiation, Gene regulatory network, Medicine (miscellaneous), Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Genome, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, immune system diseases, hemic and lymphatic diseases, medicine, Genetic predisposition, Humans, Gene Regulatory Networks, Genetic Predisposition to Disease, Gene, lcsh:QH301-705.5, Multiple myeloma, 030304 developmental biology, Bone morphogenesis, Genetics, 0303 health sciences, Chromosome Mapping, medicine.disease, 3. Good health, lcsh:Biology (General), Genetic Loci, 030220 oncology & carcinogenesis, Disease Susceptibility, Multiple Myeloma, General Agricultural and Biological Sciences, Genome-Wide Association Study, Signal Transduction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76dba05d998a4ef0bff602630d52d9b7
http://link.springer.com/article/10.1038/s42003-019-0329-2

المؤلفون: Marcel Romanos, Johannes Hebebrand, Anke Hinney, Zsofia Nemoda, Susanne Walitza, Edna Grünblatt, Anna Maria Werling, Alexander Roth, Hauke Thomsen, Klaus-Peter Lesch, Zsanett Tarnok, Triinu Peters, Nora Angyal

المساهمون: University of Zurich, Grünblatt, Edna, Psychiatrie & Neuropsychologie, RS: MHeNs - R3 - Neuroscience

المصدر: American Journal of Medical Genetics
American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 180 (6)
American Journal of Medical Genetics Part B-neuropsychiatric Genetics, 180(6), 365-376. Wiley

مصطلحات موضوعية: 0301 basic medicine, Oncology, Male, 2804 Cellular and Molecular Neuroscience, Medizin, Genome-wide association study, polymorphism, 2738 Psychiatry and Mental Health, 0302 clinical medicine, gender, genetics, 10064 Neuroscience Center Zurich, Child, Wnt Signaling Pathway, Genetics (clinical), Research Articles, RISK, Sex Characteristics, LRP6, LRP5, BIPOLAR DISORDER, 10058 Department of Child and Adolescent Psychiatry, OVERLAP, Psychiatry and Mental health, DIFFERENTIATION, Low Density Lipoprotein Receptor-Related Protein-5, Meta-analysis, 10076 Center for Integrative Human Physiology, Low Density Lipoprotein Receptor-Related Protein-6, Medical genetics, NEURAL-TUBE DEFECTS, Female, BONE-MINERAL DENSITY, FUNCTIONAL ANNOTATION, Research Article, Adult, medicine.medical_specialty, 2716 Genetics (clinical), Adolescent, DEFICIT HYPERACTIVITY DISORDER, attention‐deficit hyperactivity disorder, SNP, 610 Medicine & health, 03 medical and health sciences, Cellular and Molecular Neuroscience, Sex Factors, Internal medicine, attention-deficit hyperactivity disorder, medicine, Attention deficit hyperactivity disorder, Humans, Bipolar disorder, GENOME-WIDE ASSOCIATION, business.industry, Genetic Variation, medicine.disease, 030104 developmental biology, Attention Deficit Disorder with Hyperactivity, LOW-DENSITY-LIPOPROTEIN-RECEPTOR-RELATED-PROTEIN-6, business, 030217 neurology & neurosurgery

وصف الملف: Grunblatt_et_al-2018_The_involvement_of_the_canonical_Wnt-signaling_receptor_LRP5.pdf - application/pdf; application/application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7163c75c42bc7b7c5c3bf40c510f3bd7
http://europepmc.org/articles/PMC6767385

المؤلفون: Alena Kazimirova, Magdalena Barancokova, Sona Vodenkova, Marta Staruchova, Markus M. Nöthen, Maria Dusinska, Asta Försti, Ludovit Musak, Ludmila Vodickova, Per Hoffmann, Yasmeen Niazi, Kari Hemminki, Katarina Volkovova, Pavel Vodicka, Hauke Thomsen, Michal Kroupa, Bozena Smolkova, Veronika Vymetalkova

المصدر: Environmental and Molecular Mutagenesis. 60:17-28

مصطلحات موضوعية: Adult, Male, Slovakia, medicine.medical_specialty, DNA Repair, Epidemiology, Health, Toxicology and Mutagenesis, Single-nucleotide polymorphism, Genome-wide association study, 010501 environmental sciences, Biology, Polymorphism, Single Nucleotide, 01 natural sciences, 03 medical and health sciences, Neoplasms, Genetic variation, medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, Autistic Disorder, Promoter Regions, Genetic, Gene, Genetics (clinical), Czech Republic, 030304 developmental biology, 0105 earth and related environmental sciences, Chromosome Aberrations, Genetics, 0303 health sciences, Chromosome, Cancer, Middle Aged, medicine.disease, Cytogenetic Analysis, Medical genetics, Female, Down Syndrome, DNA Damage, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2441aac88c214a6919d336ab2794f30b
https://doi.org/10.1002/em.22236

المؤلفون: Pierre Laurent-Puig, Yan Ren, Frédérique Rachédi, Pascal Guénel, Sandya Liyanarachchi, Asta Försti, Albert de la Chapelle, Om Kulkarni, Claire Mulot, Huiling He, Federica Gemignani, Julie Guibon, Anne-Valérie Guizard, Fabienne Lesueur, Rossella Elisei, Ausrele Kesminiene, Anthony F. Herzig, Mojgan Karimi, Pierre-Emmanuel Sugier, Thérèse Truong, Delphine Bacq-Daian, Anne-Louise Leutenegger, Constance Xhaard, Daniel F. Comiskey, Celia M Pereda, Evgenia Ostroumova, Florent de Vathaire, Elisabeth Adjadj, Françoise Borson-Chazot, Jean-François Deleuze, Carole Rubino, Anne Boland-Auge, Hauke Thomsen, Elise A. Lucotte, Marie-Christine Boutron-Ruault, Juan J Lence-Anta, Rosa Ortiz, Claire Schvartz

المساهمون: Institut Gustave Roussy (IGR), Centre de recherche en épidémiologie et santé des populations (CESP), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris-Saclay, Université Paris-Saclay, Cancer et génome: Bioinformatique, biostatistiques et épidémiologie d'un système complexe, Institut Curie [Paris]-MINES ParisTech - École nationale supérieure des mines de Paris, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM), Défaillance Cardiovasculaire Aiguë et Chronique (DCAC), Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL), Épidémiologie des radiations, épidémiologie clinique des cancers et survie (U1018 (Équipe 3) ), Institut Gustave Roussy (IGR)-Centre de recherche en épidémiologie et santé des populations (CESP), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris-Saclay-Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Paul Brousse-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris-Saclay, Centre d'investigation clinique plurithématique Pierre Drouin [Nancy] (CIC-P), Centre d'investigation clinique [Nancy] (CIC), Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL)-Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL), Cardiovascular and Renal Clinical Trialists [Vandoeuvre-les-Nancy] (INI-CRCT), Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu [Nancy], French-Clinical Research Infrastructure Network - F-CRIN [Paris] (Cardiovascular & Renal Clinical Trialists - CRCT ), Service de biostatistique et d'épidémiologie (SBE), Direction de la recherche clinique [Gustave Roussy], Institut Gustave Roussy (IGR)-Institut Gustave Roussy (IGR), Centre National de Recherche en Génomique Humaine (CNRGH), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Centre de Recherche des Cordeliers (CRC (UMR_S_1138 / U1138)), École pratique des hautes études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Université de Paris (UP), Université Paris Diderot, Sorbonne Paris Cité, Paris, France, Université Paris Diderot - Paris 7 (UPD7), Institut Jean Godinot [Reims], UNICANCER, Registre Général des Tumeurs du Calvados, CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Centre Régional de Lutte contre le Cancer François Baclesse [Caen] (UNICANCER/CRLC), Normandie Université (NU)-UNICANCER-Tumorothèque de Caen Basse-Normandie (TCBN)-UNICANCER, Unité de recherche interdisciplinaire pour la prévention et le traitement des cancers (ANTICIPE), Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN)-Centre Régional de Lutte contre le Cancer François Baclesse [Caen] (UNICANCER/CRLC), Normandie Université (NU)-UNICANCER-Tumorothèque de Caen Basse-Normandie (TCBN)-UNICANCER-Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital de Taaone, Hôpital Louis Pradel [CHU - HCL], Hospices Civils de Lyon (HCL), Health Service and Performance Research (HESPER), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon, Institute of Oncology and Radiobiology, Ohio State University [Columbus] (OSU), University of Pisa - Università di Pisa, Molecular Genetics of Breast Cancer, German Cancer Research Center (DKFZ), German Cancer Research Center - Deutsches Krebsforschungszentrum [Heidelberg] (DKFZ), Hopp Children's Cancer Center Heidelberg [Heidelber, Germany] (KITZ), German Cancer Research Center - Deutsches Krebsforschungszentrum [Heidelberg] (DKFZ)-Heidelberg University Hospital [Heidelberg], German Cancer Consortium [Heidelberg] (DKTK), Génétique, génomique fonctionnelle et biotechnologies (UMR 1078) (GGB), Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO)-Université de Brest (UBO)-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM), Maladies neurodéveloppementales et neurovasculaires (NeuroDiderot (UMR_S_1141 / U1141)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP), Centre International de Recherche contre le Cancer - International Agency for Research on Cancer (CIRC - IARC), Organisation Mondiale de la Santé / World Health Organization Office (OMS / WHO), Ministère de l'Enseignement supérieur, de la Recherche et de l'Innovation, MESRI: 2102 918823 National Institute of Ecology, NIE Agence Nationale de la Recherche, ANR: ANR‐10‐COHO‐0006 Fondation ARC pour la Recherche sur le Cancer, ARC: PGA120150202302 Ligue Contre le Cancer Fondation de France Institut National Du Cancer, INCa: 9533 Agence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du Travail, ANSES Mutuelle Générale de l'Education Nationale, MGEN Electricité de France, EDF: EP 2019‐01, We thank Dr Yannick Rougier and Dr Dominique Baron-Dubourdieu for providing pathological reports for the NC study, as well as Dr Sylvie Laumond, Dr Jean-Paul Grangeon (Direction des affaires sanitaires et sociales de Nouvelle-Cal?donie) and the country's provincial health authorities (DPASS Sud, DPASS Nord, DPASS Iles Loyaut?) for support during data collection in the NC study. We thank Milagros Velasco, Mae Chappe and Idalmis Infante (Institute of Oncology and Radiobiology, La Havana, Cuba) and Silvia Turcios (National Institute of Endocrinology, La Havana, Cuba) for helping in the collection of the data in the Cuban Study. We thank John Paoaafaite and Joseph Teuri who contacted and interviewed cases and controls for the study. Finally, we also thank P. Morales, J. Iltis, P. Giraud, P. Didiergeorge, M. Brisard, G. Soubiran, B. Caillou, P. Dupire, J. Ienfa, G. de Clermont, N. Cerf, B. Oddo, M. Bambridge, C. Baron, A. Mouchard-Rachet, O. Simonet, D. Lamarque, J. Vabret, J. Delacre, M.P. Darquier and J. Leninger, for their help in the collection of the cases or in the organization of study in French Polynesia. We would like to thank the Association Centre de Regroupement Informatique et Statistique en Anatomie Pathologique en Provence-Alpes-C?te d'Azur (CRISAP PACA), as well as Dr Arlette Danzon, Dr Genevi?ve Sasolas, Dr Marc Christophe Sattonnet, Dr Marc Colonna, Dr Brigitte Lacour, Dr Michel Velten, Dr Enora Clero, Dr St?phane Maillard, Dr Laurent Bailly, Dr Eug?nia Marin? Barjoan, Dr Jean-Luc Lassalle, Dr Z Hafdi-Nejjari, Dr P Delafosse, Dr Elisabeth Adjadj, Kami-Marie Moreau, Cyrielle Orenes, Laurianne Sarrazin, St?phanie Bonnay, Fr?d?rique Chatelain, Maryse Barouh, Evelyne Rapp, Julie Festra?ts, Julie Valbousquet, Yusuf Atilgan, Jean Chappellet, Lallia Bedhouche, Florent Dayet and Ziyan Fami, for their help in the collection of cases, the organization and the management of the Young-Thyr study. We acknowledge Stefano Landi for the Italian GWAS data and Subhayan Chattopadhyay and Yasmeen Niazi (Division of Molecular Genetic Epidemiology, German Cancer Research Center?DKFZ) for technical assistance in these data analysis. We are grateful to Dr Herv? Perdry for his help in using the GASTON package. The EPITHYR GWAS was supported by Institut National du Cancer (grant number 9533) and Fondation ARC (grant number PGA120150202302). The E3N cohort received support from the MGEN, Gustave Roussy and Ligue contre le cancer for its setup and maintenance. The E3N cohort was also supported by a state grant from the Agence Nationale pour la Recherche (ANR) (grant number ANR-10-COHO-0006) within the Investissement d'Avenir program and from the French Ministry of Higher Education, Research and Innovation (MESRI, grant number 2102 918823). The other participating studies were funded by Ligue Nationale Contre le Cancer, ANR, the Direction G?n?rale de la Sante, the Agence Fran?aise de S?curit? Sanitaire de l'alimentation, de l'environnement et du travail (ANSES), CHILDTHYR EEC program, and the Fondation de France. JG was the recipient of a PhD fellowship from R?gion Ile-de-France, part of OK was the recipient of a post-doc fellowship from Electricit? de France (conseil scientifique de Radioprotection d'EDF, grant EP 2019-01)., The EPITHYR GWAS was supported by Institut National du Cancer (grant number 9533) and Fondation ARC (grant number PGA120150202302). The E3N cohort received support from the MGEN, Gustave Roussy and Ligue contre le cancer for its setup and maintenance. The E3N cohort was also supported by a state grant from the Agence Nationale pour la Recherche (ANR) (grant number ANR‐10‐COHO‐0006) within the Investissement d'Avenir program and from the French Ministry of Higher Education, Research and Innovation (MESRI, grant number 2102 918823). The other participating studies were funded by Ligue Nationale Contre le Cancer, the Direction Générale de la Sante, the Agence Française de Sécurité Sanitaire de l'alimentation, and the Fondation de France. JG was the recipient of a PhD fellowship from Région Ile‐de‐France, part of OK was the recipient of a post‐doc fellowship from Electricité de France (conseil scientifique de Radioprotection d'EDF, grant EP 2019‐01)., Mines Paris - PSL (École nationale supérieure des mines de Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM), École Pratique des Hautes Études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Université Paris Cité (UPCité), EFS-Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Brestois Santé Agro Matière (IBSAM), Université de Brest (UBO), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)

المصدر: International Journal of Cancer
International Journal of Cancer, Wiley, 2021, 148 (12), pp.2935-2946. ⟨10.1002/ijc.33488⟩
International Journal of Cancer, 2021, 148 (12), pp.2935-2946. ⟨10.1002/ijc.33488⟩

مصطلحات موضوعية: Male, Cancer Research, Native Hawaiian or Other Pacific Islander, [SDV]Life Sciences [q-bio], Ethnic group, Genome-wide association study, 0302 clinical medicine, Gene Frequency, Informed consent, Epidemiology, thyroid cancer, Chromosomes, Human, Medicine, Prospective cohort study, Thyroid cancer, Genetics, 0303 health sciences, education.field_of_study, Incidence (epidemiology), Middle Aged, Checklist, 3. Good health, Oncology, 030220 oncology & carcinogenesis, Pacific islanders, Female, Adult, medicine.medical_specialty, case-control study, education, Population, Biology, Pacific Islands, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, Humans, Genetic Predisposition to Disease, Thyroid Neoplasms, Aged, 030304 developmental biology, genome-wide association study, business.industry, Case-control study, medicine.disease, Clinical trial, Case-Control Studies, Family medicine, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fce6416820f02c763882048815b64fc0
https://hdl.handle.net/11568/1105339

المؤلفون: Asta Försti, Alena Kazimirova, Yasmeen Niazi, Per Hoffmann, Hauke Thomsen, Katarina Volkovova, Magdalena Barancokova, Veronika Vymetalkova, Kari Hemminki, Maria Dusinska, Pavel Vodicka, Markus M. Nöthen, Marta Staruchova, Soňa Vodenkova, Ludmila Vodickova, Ludovit Musak, Michal Kroupa, Bozena Smolkova

المصدر: DNA repair. 101

مصطلحات موضوعية: Male, DNA Repair, Biochemistry, DNA Mismatch Repair, 0302 clinical medicine, Fanconi anemia, Replication Protein A, Czech Republic, Genetics, Aged, 80 and over, 0303 health sciences, education.field_of_study, RecQ Helicases, Middle Aged, Healthy Volunteers, Association study, DNA-Binding Proteins, 030220 oncology & carcinogenesis, Chromatid, DNA mismatch repair, Female, Poly(ADP-ribose) Polymerases, Adult, Slovakia, Werner Syndrome Helicase, Adolescent, DNA repair, Double-strand breaks, Population, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, Young Adult, medicine, Humans, Computer Simulation, education, Molecular Biology, Gene, 030304 developmental biology, Aged, Chromosome Aberrations, Chromosomal aberrations, Cell Biology, Non-Smokers, medicine.disease, Telomere, DNA Repair Enzymes, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02dd4cb27782b57c9d648b1c244d8433
https://pubmed.ncbi.nlm.nih.gov/33676360

المؤلفون: Markus M. Nöthen, Jost B. Jonas, Sarah E. Coupland, Hauke Thomsen, Subhayan Chattopadhyay, Helen Kalirai, Per Hoffmann, Kari Hemminki, Asta Försti

المصدر: Melanoma research. 30(2)

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Uveal Neoplasms, Cancer Research, Skin Neoplasms, DNA Repair, DNA repair, Locus (genetics), Dermatology, Biology, 03 medical and health sciences, Young Adult, 0302 clinical medicine, medicine, Eye color, Humans, Allele, Melanoma, Aged, Aged, 80 and over, BAP1, Phosphoric Diester Hydrolases, Middle Aged, medicine.disease, eye diseases, 030104 developmental biology, Oncology, 030220 oncology & carcinogenesis, Eye melanoma, Cutaneous melanoma, Cancer research, Female, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2bd4bf9731c2f236ccce5a750594c12
https://pubmed.ncbi.nlm.nih.gov/31626034

المؤلفون: Miguel Inacio da Silva Filho, Markus M. Nöthen, Stefanie Huhn, Pavel Vodicka, Stefan Schönland, Göran Hallmans, Roman Hájek, Ludmila Vodickova, Giovanni Palladini, Kari Hemminki, Börge Schmidt, Paolo Milani, Ulrika Pettersson-Kymmer, Philip N. Hawkins, Per Hoffmann, Ashutosh D. Wechalekar, Hartmut Goldschmidt, Karl-Heinz Jöckel, Iman Meziane, Niels Weinhold, Stefano Landi, Hauke Thomsen, Ute Hegenbart, Claes Ohlsson, Richard S. Houlston, Dorota Rowcieno, Asta Försti, Subhayan Chattopadhyay, Giampaolo Merlini

المصدر: Leukemia. 34(4)

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Monoclonal Gammopathy of Undetermined Significance, Polymorphism, Single Nucleotide, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Unknown Significance, Polymorphism (computer science), Genetic etiology, hemic and lymphatic diseases, medicine, AL amyloidosis, Biomarkers, Tumor, Humans, Immunoglobulin Light-chain Amyloidosis, Polymorphism, Multiple myeloma, Tumor, business.industry, Hematology, Single Nucleotide, medicine.disease, Prognosis, Monoclonal gammopathy, 030104 developmental biology, Oncology, Genetic Loci, 030220 oncology & carcinogenesis, Immunology, medicine.symptom, business, Multiple Myeloma, Genome-Wide Association Study, Biomarkers

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4babe0014983572c1664537311dfaf11
https://pubmed.ncbi.nlm.nih.gov/31695157

المؤلفون: Asta Försti, Ludmila Vodickova, Alena Kazimirova, Markus M. Nöthen, Marta Staruchova, Per Hoffmann, Yasmeen Niazi, Katarina Volkovova, Kari Hemminki, Maria Dusinska, Veronika Vymetalkova, Soňa Vodenkova, Ludovit Musak, Hauke Thomsen, Pavel Vodicka, Michal Kroupa, Bozena Smolkova, Magdalena Barancokova

المصدر: Mutagenesis. 34(4)

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Health, Toxicology and Mutagenesis, Population, Genome-wide association study, Biology, Toxicology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Gene Frequency, Meta-Analysis as Topic, Chromosome instability, Genetics, medicine, Odds Ratio, Humans, Genetic Predisposition to Disease, education, Gene, Genetics (clinical), Alleles, 030304 developmental biology, Genetic association, Aged, Aged, 80 and over, Chromosome Aberrations, 0303 health sciences, education.field_of_study, Middle Aged, medicine.disease, Genetics, Population, 030220 oncology & carcinogenesis, Cytogenetic Analysis, Chromosome abnormality, Medical genetics, Chromatid, Female, DNA Damage, Genome-Wide Association Study, Mutagens

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ff13cd138fb15fabeb23db8ecec8787
https://pubmed.ncbi.nlm.nih.gov/31586183