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Tytuł:
Significance of LHCGR polymorphisms in polycystic ovary syndrome: an association study.
Autorzy:
Singh S; Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Kaur M; Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
Beri A; Beri Maternity Hospital, Southend Beri Fertility and IVF, Amritsar, Punjab, 143001, India.
Kaur A; Department of Human Genetics, Guru Nanak Dev University, Amritsar, Punjab, 143005, India. .
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Źródło:
Scientific reports [Sci Rep] 2023 Dec 21; Vol. 13 (1), pp. 22841. Date of Electronic Publication: 2023 Dec 21.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Polycystic Ovary Syndrome*/genetics
Polycystic Ovary Syndrome*/complications
Female ; Humans ; Case-Control Studies ; Gene Frequency ; Genotype ; Luteinizing Hormone/genetics ; Polymorphism, Single Nucleotide ; Receptors, G-Protein-Coupled/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
NTHL1 is a recessive cancer susceptibility gene.
Autorzy:
Nurmi AK; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Biomedicum Helsinki, P.O. Box 700, 00290, Helsinki, Finland.
Pelttari LM; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Biomedicum Helsinki, P.O. Box 700, 00290, Helsinki, Finland.
Kiiski JI; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Biomedicum Helsinki, P.O. Box 700, 00290, Helsinki, Finland.
Khan S; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Biomedicum Helsinki, P.O. Box 700, 00290, Helsinki, Finland.
Nurmikolu M; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Biomedicum Helsinki, P.O. Box 700, 00290, Helsinki, Finland.
Suvanto M; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Biomedicum Helsinki, P.O. Box 700, 00290, Helsinki, Finland.
Aho N; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Biomedicum Helsinki, P.O. Box 700, 00290, Helsinki, Finland.
Tasmuth T; Department of Anaesthesiology, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Kalso E; Department of Anaesthesiology, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Schleutker J; Institute of Biomedicine, University of Turku, and FICAN West Cancer Centre, and Department of Genomics, Laboratory Division, Turku University Hospital, Turku, Finland.
Kallioniemi A; Tays Cancer Center, Tampere University Hospital, and BioMediTech Institute and Faculty of Medicine and Health Technology, Tampere University, and Fimlab Laboratories, Tampere, Finland.
Heikkilä P; Department of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Aittomäki K; Department of Clinical Genetics, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Blomqvist C; Department of Oncology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Nevanlinna H; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Biomedicum Helsinki, P.O. Box 700, 00290, Helsinki, Finland. .
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Corporate Authors:
FinnGen
Źródło:
Scientific reports [Sci Rep] 2023 Nov 30; Vol. 13 (1), pp. 21127. Date of Electronic Publication: 2023 Nov 30.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Predisposition to Disease*
Breast Neoplasms*/genetics
Humans ; Female ; Heterozygote ; Breast ; Finland ; Deoxyribonuclease (Pyrimidine Dimer)/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genetic determinants of severe COVID-19 in young Asian and Middle Eastern patients: a case series.
Autorzy:
Badla BA; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, UAE.
Hanifa MS; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, UAE.
Jain R; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Naofal ME; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Halabi N; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Yaslam S; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Ramaswamy S; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Taylor A; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Alfalasi R; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Shenbagam S; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Khansaheb H; Medical Education and Research Department, Dubai Health, Dubai, UAE.
Al Suwaidi H; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, UAE.
Nowotny N; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, UAE.; Institute of Virology, University of Veterinary Medicine Vienna, Vienna, Austria.
Popatia R; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, UAE.
Al Khayat A; Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE.
Alsheikh-Ali A; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, UAE.; Dubai Health, Dubai, UAE.
Loney T; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, UAE.
AlDabal LM; Medical Affairs Department, Rashid Hospital, Dubai Health, Dubai, UAE.
Abou Tayoun A; Al Jalila Genomics Center of Excellence, Al Jalila Children's Specialty Hospital, Dubai Health, Dubai, UAE. .; Center for Genomic Discovery, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai Health, Dubai, UAE. .
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Źródło:
Scientific reports [Sci Rep] 2023 Nov 20; Vol. 13 (1), pp. 20294. Date of Electronic Publication: 2023 Nov 20.
Typ publikacji:
Journal Article
MeSH Terms:
COVID-19*/genetics
Genetic Predisposition to Disease*
Adult ; Humans ; Young Adult ; Asian ; Interferons/genetics ; Middle Eastern and North Africans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Comprehensive analysis of genes associated with migraine in the Indian population: a meta-analysis of genetic association studies with trial sequential analysis.
Autorzy:
Sudershan A; Institute of Human Genetics, University of Jammu, Jammu, Jammu and Kashmir, 180006, India.; Department of Human Genetics, Sri Pratap College, Cluster University of Srinagar, Kashmir, Jammu and Kashmir, India.
Pushap AC; Department of Education, Dakshina Bharat Hindi Prachar Sabha, Madras, 600017, India.
Bhagat M; Department of Zoology and Institute of Human Genetics, University of Jammu, Jammu, Jammu and Kashmir, 180006, India.
Sharma I; Department of Zoology and Institute of Human Genetics, University of Jammu, Jammu, Jammu and Kashmir, 180006, India.
Kumar H; Department of Neurology, Super Specialty Hospital, Jammu, Jammu and Kashmir, 180006, India.
Digra SK; Department of Paediatrics, Sri Maharaja Gulab Singh Hospital, Government Medical College, Jammu, Jammu and Kashmir, 180006, India. .
Kumar P; Institute of Human Genetics, University of Jammu, Jammu, Jammu and Kashmir, 180006, India. .; Department of Zoology and Institute of Human Genetics, University of Jammu, Jammu, Jammu and Kashmir, 180006, India. .
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Źródło:
Scientific reports [Sci Rep] 2023 Nov 04; Vol. 13 (1), pp. 19070. Date of Electronic Publication: 2023 Nov 04.
Typ publikacji:
Systematic Review; Meta-Analysis; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Migraine Disorders*/genetics
Migraine Disorders*/epidemiology
Humans ; Genetic Association Studies ; Alleles ; Asian People
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Interaction between genetic susceptibility to obesity and food intake on BMI in Finnish school-aged children.
Autorzy:
Viljakainen H; Folkhälsan Research Center, Topeliuksenkatu 20, 00250, Helsinki, Finland. .; Faculty of Medicine, University of Helsinki, Helsinki, Finland. .
Sorlí JV; Department of Preventive Medicine and Public Health, University of Valencia, Valencia, Spain.; CIBER Fisiopatología de la Obesidad y Nutrición, Madrid, Spain.
Dahlström E; Folkhälsan Research Center, Topeliuksenkatu 20, 00250, Helsinki, Finland.; Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, 00290, Helsinki, Finland.; Department of Nephrology, University of Helsinki and Helsinki University Hospital, 00290, Helsinki, Finland.
Agrawal N; Folkhälsan Research Center, Topeliuksenkatu 20, 00250, Helsinki, Finland.; Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Portolés O; Department of Preventive Medicine and Public Health, University of Valencia, Valencia, Spain.; CIBER Fisiopatología de la Obesidad y Nutrición, Madrid, Spain.
Corella D; Department of Preventive Medicine and Public Health, University of Valencia, Valencia, Spain.; CIBER Fisiopatología de la Obesidad y Nutrición, Madrid, Spain.
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Źródło:
Scientific reports [Sci Rep] 2023 Sep 14; Vol. 13 (1), pp. 15265. Date of Electronic Publication: 2023 Sep 14.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Obesity*/epidemiology
Obesity*/genetics
Female ; Male ; Adolescent ; Humans ; Child ; Body Mass Index ; Finland/epidemiology ; Eating ; Alpha-Ketoglutarate-Dependent Dioxygenase FTO/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Race-specific association of an IRGM risk allele with cytokine expression in human subjects.
Autorzy:
Ajayi T; Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Sciences, 111 T.W. Alexander Drive, MD D2-01, P.O. Box 12233, Research Triangle Park, NC, 27709, USA.
Rai P; Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Sciences, 111 T.W. Alexander Drive, MD D2-01, P.O. Box 12233, Research Triangle Park, NC, 27709, USA.
Shi M; Biostatistics & Computational Biology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.
Gabor KA; Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Sciences, 111 T.W. Alexander Drive, MD D2-01, P.O. Box 12233, Research Triangle Park, NC, 27709, USA.
Karmaus PWF; Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Sciences, 111 T.W. Alexander Drive, MD D2-01, P.O. Box 12233, Research Triangle Park, NC, 27709, USA.
Meacham JM; Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Sciences, 111 T.W. Alexander Drive, MD D2-01, P.O. Box 12233, Research Triangle Park, NC, 27709, USA.
Katen K; Signal Transduction Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.
Madenspacher JH; Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Sciences, 111 T.W. Alexander Drive, MD D2-01, P.O. Box 12233, Research Triangle Park, NC, 27709, USA.
Schurman SH; Clinical Research Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.; Clinical Research Unit, National Institute on Aging, Baltimore, MD, 21225, USA.
Fessler MB; Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Sciences, 111 T.W. Alexander Drive, MD D2-01, P.O. Box 12233, Research Triangle Park, NC, 27709, USA. .
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Źródło:
Scientific reports [Sci Rep] 2023 Aug 09; Vol. 13 (1), pp. 12911. Date of Electronic Publication: 2023 Aug 09.
Typ publikacji:
Journal Article; Research Support, N.I.H., Intramural
MeSH Terms:
Genetic Predisposition to Disease*
Cytokines*/genetics
Humans ; Alleles ; CD8-Positive T-Lymphocytes ; Case-Control Studies ; GTP-Binding Proteins/genetics ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Hypertrophic cardiomyopathy in purpose-bred cats with the A31P mutation in cardiac myosin binding protein-C.
Autorzy:
Stern JA; Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California-Davis, One Shields Avenue, Davis, CA, 95616, USA.; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, 1038 William Moore Dr, Raleigh, NC, 27606, USA.
Rivas VN; Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California-Davis, One Shields Avenue, Davis, CA, 95616, USA.; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, 1038 William Moore Dr, Raleigh, NC, 27606, USA.
Kaplan JL; Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California-Davis, One Shields Avenue, Davis, CA, 95616, USA.
Ueda Y; Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, 1038 William Moore Dr, Raleigh, NC, 27606, USA.
Oldach MS; VCA Sacramento Veterinary Referral Center, 9801 Old Winery Place, Sacramento, CA, 95827, USA.
Ontiveros ES; Rady Children's Institute for Genomic Medicine, 7910 Frost Street, San Diego, CA, 92123, USA.
Kooiker KB; Division of Cardiology, Department of Medicine, University of Washington, Seattle, 98109, USA.
van Dijk SJ; Department of Neurobiology, Physiology, and Behavior, University of California-Davis, One Shields Avenue, Davis, CA, 95616, USA.
Harris SP; Department of Neurobiology, Physiology, and Behavior, University of California-Davis, One Shields Avenue, Davis, CA, 95616, USA. .; Department of Physiology, College of Medicine-Tucson, University of Arizona, 313 Medical Research Building, 1656 E Mabel St., Tucson, AZ, 85724, USA. .
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Źródło:
Scientific reports [Sci Rep] 2023 Jun 26; Vol. 13 (1), pp. 10319. Date of Electronic Publication: 2023 Jun 26.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Cardiomyopathy, Hypertrophic*/genetics
Cardiomyopathy, Hypertrophic*/veterinary
Animals ; Male ; Semen ; Mutation ; Phenotype ; Cytoskeletal Proteins/genetics ; Cardiac Myosins/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Association of MTR gene polymorphisms with the occurrence of non-syndromic congenital heart disease: a case-control study.
Autorzy:
Liu Y; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Zhong T; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Song X; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Zhang S; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Sun M; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Wei J; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Shu J; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.
Yang T; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.; Hunan Provincial Key Laboratory of Clinical Epidemiology, Changsha, Hunan, China.
Wang T; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China.; NHC Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, 53 Xiangchun Road, Changsha, 410028, Hunan, China.
Qin J; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, 110 Xiangya Road, Changsha, 410078, Hunan, China. .; Hunan Provincial Key Laboratory of Clinical Epidemiology, Changsha, Hunan, China. .; NHC Key Laboratory of Birth Defect for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, 53 Xiangchun Road, Changsha, 410028, Hunan, China. .
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Źródło:
Scientific reports [Sci Rep] 2023 Jun 09; Vol. 13 (1), pp. 9424. Date of Electronic Publication: 2023 Jun 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Predisposition to Disease*
Heart Defects, Congenital*/genetics
Infant ; Humans ; 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase/genetics ; Case-Control Studies ; Polymorphism, Single Nucleotide ; Risk Factors ; Genotype
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Novel genetic variants of HLA gene associated with Thai Behcet's disease (BD) patients using next generation sequencing technology.
Autorzy:
Sornsamdang G; Division of Pharmacogenomics and Personalized Medicine, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.; Laboratory for Pharmacogenomics, Somdech Phra Debaratana Medical Center (SDMC), Ramathibodi Hospital, Bangkok, Thailand.
Shobana J; Division of Pharmacogenomics and Personalized Medicine, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.; Laboratory for Pharmacogenomics, Somdech Phra Debaratana Medical Center (SDMC), Ramathibodi Hospital, Bangkok, Thailand.
Chanprapaph K; Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Chantratita W; Center for Medical Genomics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Chotewutmontri S; Faculty of Medicine and Public Health, HRH Princess Chulabhorn College of Medical Science, Chulabhorn Royal Academy, Bangkok, Thailand.
Limtong P; Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
O-Charoen P; Division of Allergy, Immunology, and Rheumatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Sukasem C; Division of Pharmacogenomics and Personalized Medicine, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand. .; Laboratory for Pharmacogenomics, Somdech Phra Debaratana Medical Center (SDMC), Ramathibodi Hospital, Bangkok, Thailand. .; Pharmacogenomics and Precision Medicine, The Preventive Genomics & Family Check-Up Services Center, Bumrungrad International Hospital, Bangkok, Thailand. .; Department of Pharmacology and Therapeutics, MRC Centre for Drug Safety Science, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK. .
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Źródło:
Scientific reports [Sci Rep] 2024 Apr 04; Vol. 14 (1), pp. 7967. Date of Electronic Publication: 2024 Apr 04.
Typ publikacji:
Journal Article
MeSH Terms:
Behcet Syndrome*/epidemiology
Female ; Humans ; HLA-DRB1 Chains/genetics ; High-Throughput Nucleotide Sequencing ; HLA-C Antigens/genetics ; Thailand ; HLA-B Antigens/genetics ; Alleles ; Technology ; Genetic Predisposition to Disease ; Aminopeptidases/genetics ; Minor Histocompatibility Antigens
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genetic predisposition to childhood obesity does not influence the risk of developing skin cancer in adulthood.
Autorzy:
Keatley J; Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.
Law MH; Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.; Departments of Population Health and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.; School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia.
Seviiri M; Departments of Population Health and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Olsen CM; Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.; Departments of Population Health and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Pandeya N; Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.; Departments of Population Health and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Ong JS; Departments of Population Health and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
MacGregor S; Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.; Departments of Population Health and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Whiteman DC; Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.; Departments of Population Health and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Dusingize JC; Departments of Population Health and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. .
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Źródło:
Scientific reports [Sci Rep] 2024 Apr 03; Vol. 14 (1), pp. 7854. Date of Electronic Publication: 2024 Apr 03.
Typ publikacji:
Journal Article
MeSH Terms:
Skin Neoplasms*/epidemiology
Skin Neoplasms*/genetics
Skin Neoplasms*/complications
Melanoma*/etiology
Melanoma*/genetics
Carcinoma, Squamous Cell*/pathology
Pediatric Obesity*/complications
Pediatric Obesity*/genetics
Carcinoma, Basal Cell*/epidemiology
Carcinoma, Basal Cell*/genetics
Humans ; Child ; Genome-Wide Association Study ; Body Mass Index ; Mendelian Randomization Analysis ; Genetic Predisposition to Disease ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
17 variants interaction of Wnt/β-catenin pathway associated with development of osteonecrosis of femoral head in Chinese Han population.
Autorzy:
Shi C; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.
Li X; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.
Sun Y; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.
Du Z; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.
Zhang G; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.; Gene Testing Centre of Changchun Tumor Hospital, Changchun City, 130012, Jilin Province, China.
Che Z; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.
Li Q; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.
Song S; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.
Guo J; Gene Testing Centre of Changchun Tumor Hospital, Changchun City, 130012, Jilin Province, China.
Sun H; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China.
Song Y; Medical Centre of Orthopedics, The Second Hospital of Jilin University, Ziqiang Street No.218, Nanguan District, Changchun City, 130041, Jilin Province, China. .
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Źródło:
Scientific reports [Sci Rep] 2024 Mar 27; Vol. 14 (1), pp. 7301. Date of Electronic Publication: 2024 Mar 27.
Typ publikacji:
Journal Article
MeSH Terms:
Femur Head Necrosis*/genetics
Osteonecrosis*/genetics
Humans ; Femur Head ; beta Catenin/genetics ; Glycogen Synthase Kinase 3 beta/genetics ; Polymorphism, Single Nucleotide ; Lipids ; China ; Case-Control Studies ; Genetic Predisposition to Disease
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
New role of fat-free mass in cancer risk linked with genetic predisposition.
Autorzy:
Harris BHL; Department of Oncology, University of Oxford, Oxford, UK. .; Cutrale Perioperative and Ageing Group, Imperial College London, London, UK. .
Di Giovannantonio M; Department of Oncology, University of Oxford, Oxford, UK.
Zhang P; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Harris DA; St Anne's College, University of Oxford, 56 Woodstock Rd, Oxford, UK.
Lord SR; Department of Oncology, University of Oxford, Oxford, UK.; Early Phase Clinical Trials Unit, Churchill Hospital, Oxford, UK.
Allen NE; Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Maughan TS; Department of Oncology, University of Oxford, Oxford, UK.
Bryant RJ; Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
Harris AL; Department of Oncology, University of Oxford, Oxford, UK.
Bond GL; Institute of Cancer & Genomics Sciences, University of Birmingham, Bimingham, UK.
Buffa FM; Department of Oncology, University of Oxford, Oxford, UK. .; Department of Computing Sciences, Bocconi University, Milan, Italy. .; IFOM - Istituto Fondazione di Oncologia Molecolare ETS, Milan, Italy. .
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Źródło:
Scientific reports [Sci Rep] 2024 Mar 27; Vol. 14 (1), pp. 7270. Date of Electronic Publication: 2024 Mar 27.
Typ publikacji:
Journal Article
MeSH Terms:
Body Composition*/genetics
Neoplasms*/etiology
Neoplasms*/genetics
Male ; Humans ; Body Mass Index ; Genetic Predisposition to Disease ; Electric Impedance
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Interaction between Fokl polymorphism and vitamin D deficiency in the symptoms of mental disorders in adults: a population-based study.
Autorzy:
da Silva Sabião T; School of Nutrition, Postgraduate Program in Health and Nutrition, Research and Study Group on Nutrition and Public Health (GPENSC), Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil. .
Alves de Menezes-Júnior LA; School of Nutrition, Postgraduate Program in Health and Nutrition, Research and Study Group on Nutrition and Public Health (GPENSC), Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil.
Batista AP; Postgraduate Program in Biological Sciences, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil.
Silva de Moura S; School of Nutrition, Postgraduate Program in Health and Nutrition, Research and Study Group on Nutrition and Public Health (GPENSC), Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil.
Meireles AL; Department of Clinical and Social Nutrition, Research and Study Group on Nutrition and Public Health (GPENSC), School of Nutrition, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil.
Carvalho de Menezes M; Department of Clinical and Social Nutrition, Research and Study Group on Nutrition and Public Health (GPENSC), School of Nutrition, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil.
Lins Machado-Coelho GL; Epidemiology Laboratory, Medical School, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil.
Cardoso Carraro JC; Department of Clinical and Social Nutrition, Research and Study Group on Nutrition and Public Health (GPENSC), School of Nutrition, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG, 35400-000, Brazil.
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Źródło:
Scientific reports [Sci Rep] 2024 Mar 22; Vol. 14 (1), pp. 6925. Date of Electronic Publication: 2024 Mar 22.
Typ publikacji:
Journal Article
MeSH Terms:
Vitamin D Deficiency*/complications
Vitamin D Deficiency*/epidemiology
Vitamin D Deficiency*/genetics
Avitaminosis*
Adult ; Humans ; Cross-Sectional Studies ; Receptors, Calcitriol/genetics ; Polymorphism, Genetic ; Anxiety Disorders ; Vitamin D/genetics ; Genotype ; Polymorphism, Single Nucleotide ; Genetic Predisposition to Disease ; Case-Control Studies
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Risk prediction and interaction analysis using polygenic risk score of type 2 diabetes in a Korean population.
Autorzy:
Song M; Department of Statistics & Research Institute of Natural Sciences, Sookmyung Women's University, Seoul, 04310, Korea.
Kwak SH; Department of Internal Medicine, Seoul National University Hospital, Seoul, 03080, Korea. .
Kim J; Department of Statistics, Sookmyung Women's University, Seoul, 04310, Korea.
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Źródło:
Scientific reports [Sci Rep] 2024 Mar 21; Vol. 14 (1), pp. 6790. Date of Electronic Publication: 2024 Mar 21.
Typ publikacji:
Journal Article
MeSH Terms:
Diabetes Mellitus, Type 2*/epidemiology
Diabetes Mellitus, Type 2*/genetics
Male ; Female ; Humans ; Genetic Risk Score ; Genome-Wide Association Study ; Risk Factors ; Republic of Korea/epidemiology ; Genetic Predisposition to Disease
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Association of HLA-DRB1 locus with treatment response to abatacept or TNF inhibitors in patients with seropositive rheumatoid arthritis.
Autorzy:
Cha S; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Hanyang Institute of Bioscience and Biotechnology, Seoul, Republic of Korea.
Bang SY; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Hanyang Institute of Bioscience and Biotechnology, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Joo YB; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Cho SK; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Choi CB; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Sung YK; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Kim TH; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Jun JB; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Yoo DH; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Lee HS; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea.; Hanyang Institute of Bioscience and Biotechnology, Seoul, Republic of Korea.; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea.
Bae SC; Hanyang University Institute for Rheumatology Research, Seoul, Republic of Korea. .; Hanyang Institute of Bioscience and Biotechnology, Seoul, Republic of Korea. .; Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea. .
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Źródło:
Scientific reports [Sci Rep] 2024 Mar 21; Vol. 14 (1), pp. 6763. Date of Electronic Publication: 2024 Mar 21.
Typ publikacji:
Journal Article
MeSH Terms:
Tumor Necrosis Factor Inhibitors*/therapeutic use
Arthritis, Rheumatoid*/drug therapy
Arthritis, Rheumatoid*/genetics
Humans ; Abatacept/pharmacology ; Abatacept/therapeutic use ; Abatacept/genetics ; HLA-DRB1 Chains/genetics ; Epitopes/genetics ; Amino Acids/genetics ; Alleles ; Genetic Predisposition to Disease
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Polygenic risk score-based prediction of breast cancer risk in Taiwanese women with dense breast using a retrospective cohort study.
Autorzy:
Hung CC; Division of Breast Surgery, Department of Surgery, Taichung Veterans General Hospital, Taichung, 407, Taiwan.; Department of Applied Cosmetology, College of Human Science and Social Innovation, Hung Kuang University, Taichung, 433, Taiwan.; College of Life Sciences, National Chung Hsing University, Taichung, 402, Taiwan.
Moi SH; Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, 807, Taiwan.; Research Center for Precision Environmental Medicine, Kaohsiung Medical University, Kaohsiung, 807, Taiwan.; Department of Medical Research, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, 807, Taiwan.
Huang HI; Department of Information Management, National Sun Yat-Sen University, Kaohsiung, 804, Taiwan.; International Integrated Systems, INC, Kaohsiung, 806, Taiwan.
Hsiao TH; Department of Medical Research, Taichung Veterans General Hospital, 1650 Taiwan Boulevard Sect. 4, Taichung, 407219, Taiwan. .; Department of Public Health, Fu Jen Catholic University, New Taipei City, 242, Taiwan. .; Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung, 402, Taiwan. .
Huang CC; Division of Breast Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, 112, Taiwan. .; Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, No.17, Xuzhou Rd., Taipei City, 100, Taiwan. .
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Źródło:
Scientific reports [Sci Rep] 2024 Mar 15; Vol. 14 (1), pp. 6324. Date of Electronic Publication: 2024 Mar 15.
Typ publikacji:
Journal Article
MeSH Terms:
Breast Neoplasms*/diagnosis
Humans ; Female ; Breast Density ; Mammography ; Genetic Risk Score ; Retrospective Studies ; Genetic Predisposition to Disease ; Risk Factors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genetic variants associated with osteosarcoma risk: a systematic review and meta-analysis.
Autorzy:
Hassanain O; Epidemiology and Biostatistics Unit, Clinical Research, Children's Cancer Hospital Egypt-57357 (CCHE-57357), 1 Seket el Emam, el Sayeda Zeinab, Cairo, 11441, Egypt. .
Alaa M; Basic Research, Children's Cancer Hospital Egypt-57357 (CCHE-57357), Cairo, Egypt.
Khalifa MK; Molecular Pathology Laboratory, Children's Cancer Hospital Egypt-57357 (CCHE-57357), Cairo, Egypt.
Kamal N; Basic Research, Children's Cancer Hospital Egypt-57357 (CCHE-57357), Cairo, Egypt.
Albagoury A; Basic Research, Children's Cancer Hospital Egypt-57357 (CCHE-57357), Cairo, Egypt.
El Ghoneimy AM; Department of Orthopedic Oncology, Children's Cancer Hospital-57357 (CCHE-57357), Cairo, Egypt.; Department of Orthopedics, Faculty of Medicine, Cairo University, Cairo, Egypt.
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Źródło:
Scientific reports [Sci Rep] 2024 Feb 15; Vol. 14 (1), pp. 3828. Date of Electronic Publication: 2024 Feb 15.
Typ publikacji:
Meta-Analysis; Systematic Review; Journal Article
MeSH Terms:
Bone Neoplasms*/genetics
Bone Neoplasms*/pathology
Osteosarcoma*/genetics
Osteosarcoma*/pathology
Humans ; Genetic Predisposition to Disease ; Polymorphism, Single Nucleotide ; Asian People ; White People
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Correlations of SDF-1ɑ and XRCC1 gene polymorphisms with the risk of renal cancer development and bioinformatics studies of SDF-1α and XRCC1 and the prognosis of renal cancer.
Autorzy:
Zhang W; School of Public Health, Inner Mongolia Medical University, Hohhot, China.
Su Y; School of Public Health, Inner Mongolia Medical University, Hohhot, China.
Yue G; Department of Urology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China.
Zhao L; School of Public Health, Inner Mongolia Medical University, Hohhot, China.; Key Laboratory of Molecular Epidemiology of Chronic Diseases, Inner Mongolia Medical University, Hohhot, China.
Li H; School of Public Health, Inner Mongolia Medical University, Hohhot, China.; Key Laboratory of Molecular Epidemiology of Chronic Diseases, Inner Mongolia Medical University, Hohhot, China.
Jia M; School of Public Health, Inner Mongolia Medical University, Hohhot, China.
Wang Y; School of Public Health, Inner Mongolia Medical University, Hohhot, China.
Liu D; School of Public Health, Inner Mongolia Medical University, Hohhot, China.
Wang H; School of Public Health, Inner Mongolia Medical University, Hohhot, China. .; Department of Biochemistry and Molecular Biology, School of Basic Medicine, Inner Mongolia Medical University, Hohhot, China. .
Gao Y; School of Public Health, Inner Mongolia Medical University, Hohhot, China. .; Key Laboratory of Molecular Epidemiology of Chronic Diseases, Inner Mongolia Medical University, Hohhot, China. .
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Źródło:
Scientific reports [Sci Rep] 2024 Feb 09; Vol. 14 (1), pp. 3367. Date of Electronic Publication: 2024 Feb 09.
Typ publikacji:
Journal Article
MeSH Terms:
Carcinoma, Renal Cell*/genetics
Kidney Neoplasms*/genetics
Humans ; DNA-Binding Proteins/genetics ; Chemokine CXCL12/genetics ; Genetic Predisposition to Disease ; X-ray Repair Cross Complementing Protein 1/genetics ; Polymorphism, Single Nucleotide ; Genotype ; Prognosis ; Computational Biology ; Case-Control Studies
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Epigenetic role of LINE-1 methylation and key genes in pregnancy maintenance.
Autorzy:
Tisato V; Department of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy. .; University Strategic Centre for Studies On Gender Medicine, University of Ferrara, 44121, Ferrara, Italy. .; Centre Haemostasis & Thrombosis, University of Ferrara, 44121, Ferrara, Italy. .; LTTA Centre, University of Ferrara, 44121, Ferrara, Italy. .
Silva JA; Department of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Scarpellini F; Centre for Reproductive Medicine, CERM Hungaria, 00193, Rome, Italy.
Capucci R; Department of Medical Sciences, University of Ferrara, 44121, Ferrara, Italy.
Marci R; Department of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Gallo I; Department of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Salvatori F; Department of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
D'Aversa E; Department of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Secchiero P; Department of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Serino ML; Centre Haemostasis & Thrombosis, University of Ferrara, 44121, Ferrara, Italy.
Zauli G; Department of Environmental Sciences and Prevention, University of Ferrara, 44121, Ferrara, Italy.
Singh AV; Department of Chemical and Product Safety, German Federal Institute for Risk Assessment (BfR), 10589, Berlin, Germany.
Gemmati D; Department of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy. .; University Strategic Centre for Studies On Gender Medicine, University of Ferrara, 44121, Ferrara, Italy. .; Centre Haemostasis & Thrombosis, University of Ferrara, 44121, Ferrara, Italy. .
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Źródło:
Scientific reports [Sci Rep] 2024 Feb 08; Vol. 14 (1), pp. 3275. Date of Electronic Publication: 2024 Feb 08.
Typ publikacji:
Journal Article
MeSH Terms:
Epigenesis, Genetic*
Abortion, Spontaneous*/genetics
Pregnancy ; Humans ; Female ; Interleukin-10/genetics ; Interleukin-6/genetics ; Genetic Predisposition to Disease ; DNA Methylation ; Pregnancy Maintenance ; Inflammation/genetics ; Apolipoproteins E/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death.
Autorzy:
Minnai F; Institute of Biomedical Technologies, National Research Council, Via F.lli Cervi, 93, 20054, Segrate, MI, Italy.; Department of Medical Biotechnology and Translational Medicine (BioMeTra), Università degli Studi di Milano, Milan, Italy.
Biscarini F; Institute of Agricultural Biology and Biotechnology, National Research Council, Milan, Italy.
Esposito M; Institute of Biomedical Technologies, National Research Council, Via F.lli Cervi, 93, 20054, Segrate, MI, Italy.
Dragani TA; Aspidia S.R.L., Milan, Italy.
Bujanda L; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Biodonostia Health Research Institute, Universidad del País Vasco (UPV/EHU), San Sebastián, Spain.
Rahmouni S; GIGA-Medical Genomics Unit, Uliege, Liege, Belgium.
Alarcón-Riquelme ME; GENYO, University of Granada, Andalusian Regional Government, Granada, Spain.; Institute for Environmental Medicine, Karolinska Institute, Solna, Sweden.
Bernardo D; Centro de Investigación Biomédica en Red en Enfermedades Hepáticas y Digestivas (CIBEREHD), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Mucosal Immunology Lab, Unit of Excellence, Institute of Biomedicine and Molecular Genetics (IBGM), University of Valladolid-CSIC, Valladolid, Spain.
Carnero-Montoro E; GENYO, University of Granada, Andalusian Regional Government, Granada, Spain.; University of Granada, Granada, Spain.
Buti M; Vall D'Hebron Institut de Recerca, Barcelona, Spain.
Zeberg H; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Asselta R; Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.; IRCCS Humanitas Research Hospital, Rozzano, MI, Italy.
Romero-Gómez M; Digestive Diseases Unit and CiberehdVirgen del Rocío University HospitalInstitute of Biomedicine of Seville (HUVR/CSIC/US), University of Seville, Seville, Spain.
Fernandez-Cadenas I; Stroke Pharmacogenomics and Genetics Group, Sant Pau Hospital Research Institute, Barcelona, Spain.
Fallerini C; Medical Genetics, University of Siena, 53100, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Center, University of Siena, 53100, Siena, Italy.
Zguro K; Medical Genetics, University of Siena, 53100, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Center, University of Siena, 53100, Siena, Italy.
Croci S; Medical Genetics, University of Siena, 53100, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Center, University of Siena, 53100, Siena, Italy.
Baldassarri M; Medical Genetics, University of Siena, 53100, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Center, University of Siena, 53100, Siena, Italy.
Bruttini M; Medical Genetics, University of Siena, 53100, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Center, University of Siena, 53100, Siena, Italy.; Genetica Medica, Azienda Ospedaliero-Universitaria Senese, 53100, Siena, Italy.
Furini S; Dipartimento di Ingegneria dell'Energia Elettrica e dell'Informazione 'Guglielmo Marconi', Alma Mater Studiorum - Università di Bologna, Bologna, Italy.
Renieri A; Medical Genetics, University of Siena, 53100, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Center, University of Siena, 53100, Siena, Italy.; Genetica Medica, Azienda Ospedaliero-Universitaria Senese, 53100, Siena, Italy.
Colombo F; Institute of Biomedical Technologies, National Research Council, Via F.lli Cervi, 93, 20054, Segrate, MI, Italy. .
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Corporate Authors:
GEN-COVID Multicenter Study
Źródło:
Scientific reports [Sci Rep] 2024 Feb 06; Vol. 14 (1), pp. 3000. Date of Electronic Publication: 2024 Feb 06.
Typ publikacji:
Multicenter Study; Journal Article
MeSH Terms:
COVID-19*
Humans ; Genome-Wide Association Study/methods ; Genetic Predisposition to Disease ; SARS-CoV-2 ; Genotype
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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