Deciphering the host genetic factors conferring susceptibility to severe COVID-19 using exome sequencing
暂无分享,去创建一个
G. Zararsiz | N. Tutar | H. Akalın | Vahap Eldem | Firat Ozcelik | R. Yuksel | Ahu Cephe | H. Sipahioğlu | Aynur Karayol Akin | Zuhal Ozer simsek | Yusuf Ozkul | Munis Dundar | I. O. Sahin | Kubra Uslu | Osman Baspinar | Yasin Simsek | Kursat Gundogan | Orhan Yıldız
[1] J. Olgin,et al. A common allele of HLA is associated with asymptomatic SARS-CoV-2 infection , 2023, Nature.
[2] Matthew A. Wiles,et al. GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19 , 2023, Nature.
[3] M. Kanai,et al. Single-cell analyses and host genetics highlight the role of innate immune cells in COVID-19 severity , 2023, Nature Genetics.
[4] V. Rimoldi,et al. Genetic susceptibility to severe COVID-19 , 2023, Infection, Genetics and Evolution.
[5] L. Puig,et al. Tyk2 Targeting in Immune-Mediated Inflammatory Diseases , 2023, International journal of molecular sciences.
[6] William T. Harvey,et al. SARS-CoV-2 variant biology: immune escape, transmission and fitness , 2023, Nature Reviews Microbiology.
[7] H. Karabulut,et al. Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia , 2023, Journal of medical virology.
[8] Huanming Yang,et al. Towards precision medicine: Omics approach for COVID-19 , 2023, Biosafety and Health.
[9] M. Bhattacharya,et al. A Detailed Overview of SARS-CoV-2 Omicron: Its Sub-Variants, Mutations and Pathophysiology, Clinical Characteristics, Immunological Landscape, Immune Escape, and Therapies , 2023, Viruses.
[10] Benjamin Bowe,et al. Acute and postacute sequelae associated with SARS-CoV-2 reinfection , 2022, Nature Medicine.
[11] S. Jerônimo,et al. Genome-wide association studies of COVID-19: Connecting the dots , 2022, Infection, Genetics and Evolution.
[12] M. Buti,et al. Detailed stratified GWAS analysis for severe COVID-19 in four European populations , 2022, Human Molecular Genetics.
[13] S. Temel,et al. Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in the Turkish population , 2022, Journal of medical virology.
[14] J. Casanova,et al. Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee , 2022, Journal of Clinical Immunology.
[15] J. Casanova,et al. Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia , 2022, The Journal of experimental medicine.
[16] C. Li,et al. A systematic review and meta-analysis of long term physical and mental sequelae of COVID-19 pandemic: call for research priority and action , 2022, Molecular Psychiatry.
[17] M. Jaeger,et al. The Genetic Risk for COVID-19 Severity Is Associated With Defective Immune Responses , 2022, Frontiers in Immunology.
[18] D. Altmann,et al. COVID-19 vaccination: The road ahead , 2022, Science.
[19] Jin-Jin Zhang,et al. Risk and Protective Factors for COVID-19 Morbidity, Severity, and Mortality , 2022, Clinical Reviews in Allergy & Immunology.
[20] M. Netea,et al. A guide to immunotherapy for COVID-19 , 2022, Nature Medicine.
[21] Aidan N. Gomez,et al. Disease variant prediction with deep generative models of evolutionary data , 2021, Nature.
[22] Shobi Veleri. Neurotropism of SARS-CoV-2 and neurological diseases of the central nervous system in COVID-19 patients , 2021, Experimental brain research.
[23] M. Farzan,et al. Mechanisms of SARS-CoV-2 entry into cells , 2021, Nature reviews. Molecular cell biology.
[24] T. Beccari,et al. COVID-19 vaccine candidates and vaccine development platforms available worldwide , 2021, Journal of Pharmaceutical Analysis.
[25] R. Miceli,et al. Severe COVID-19 in Hospitalized Carriers of Single CFTR Pathogenic Variants , 2021, Journal of personalized medicine.
[26] Mattia G. Bergomi,et al. Mapping the human genetic architecture of COVID-19 , 2021, Nature.
[27] A. Maghazachi,et al. Chemokines and chemokine receptors during COVID-19 infection , 2021, Computational and Structural Biotechnology Journal.
[28] A. Nakhaee,et al. Significant association of LXRβ (NR1H2) polymorphisms (rs28514894, rs2303044) with type 2 diabetes mellitus and laboratory characteristics , 2021, Journal of Diabetes & Metabolic Disorders.
[29] Christopher G Chute,et al. The Human Phenotype Ontology in 2021 , 2020, Nucleic Acids Res..
[30] C. Akdis,et al. Risk factors for severe and critically ill COVID‐19 patients: A review , 2020, Allergy.
[31] Barbara B. Shih,et al. Genetic mechanisms of critical illness in COVID-19 , 2020, Nature.
[32] Jacques Fellay,et al. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19 , 2020, Science.
[33] G. Musumeci,et al. Network perturbation analysis in human bronchial epithelial cells following SARS-CoV2 infection , 2020, Experimental Cell Research.
[34] J. Schuurs-Hoeijmakers,et al. Presence of Genetic Variants Among Young Men With Severe COVID-19. , 2020, JAMA.
[35] L. Álvarez-Vallina,et al. Perforin gene variant A91V in young patients with severe COVID-19. , 2020, Haematologica.
[36] T. Mogensen,et al. Deciphering the Role of Host Genetics in Susceptibility to Severe COVID-19 , 2020, Frontiers in Immunology.
[37] J. Casanova,et al. Severe COVID-19 in the young and healthy: monogenic inborn errors of immunity? , 2020, Nature Reviews Immunology.
[38] S. Klein,et al. Considering how biological sex impacts immune responses and COVID-19 outcomes , 2020, Nature Reviews Immunology.
[39] Jacques Fellay,et al. A Global Effort to Define the Human Genetics of Protective Immunity to SARS-CoV-2 Infection , 2020, Cell.
[40] N. Rezaei,et al. Genetic predisposition models to COVID-19 infection , 2020, Medical Hypotheses.
[41] Ryan L. Collins,et al. The mutational constraint spectrum quantified from variation in 141,456 humans , 2020, Nature.
[42] Benjamin J. Polacco,et al. A SARS-CoV-2 Protein Interaction Map Reveals Targets for Drug-Repurposing , 2020, Nature.
[43] Xin Zhou,et al. Risk Factors Associated With Acute Respiratory Distress Syndrome and Death in Patients With Coronavirus Disease 2019 Pneumonia in Wuhan, China , 2020, The Journal of Emergency Medicine.
[44] Runan Yao,et al. ShinyGO: a graphical gene-set enrichment tool for animals and plants , 2019, Bioinform..
[45] Katherine R. Smith,et al. PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels , 2019, Nature Genetics.
[46] F. Corsolini,et al. FAS‐mediated apoptosis impairment in patients with ALPS/ALPS‐like phenotype carrying variants on CASP10 gene , 2019, British journal of haematology.
[47] J. Casanova,et al. Severe influenza pneumonitis in children with inherited TLR3 deficiency , 2019, The Journal of experimental medicine.
[48] Gregory M. Cooper,et al. CADD: predicting the deleteriousness of variants throughout the human genome , 2018, Nucleic Acids Res..
[49] M. Rovaris,et al. HLA alleles modulate EBV viral load in multiple sclerosis , 2018, Journal of Translational Medicine.
[50] F. Cunningham,et al. The Ensembl Variant Effect Predictor , 2016, Genome Biology.
[51] E. Huang,et al. Clinico-pathological correlation in adenylate kinase 5 autoimmune limbic encephalitis , 2015, Journal of Neuroimmunology.
[52] Philippe Bardou,et al. jvenn: an interactive Venn diagram viewer , 2014, BMC Bioinformatics.
[53] Feng Liu,et al. Defective activities, but not secretions, resulting from gene point mutations of human mannan-binding lectin , 2012, Molecular medicine reports.
[54] Tomohiro Watanabe,et al. NOD2, an Intracellular Innate Immune Sensor Involved in Host Defense and Crohn's Disease , 2011, Mucosal Immunology.
[55] M. Carrington,et al. Possession of HLA class II DRB1*1303 associates with reduced viral loads in chronic HIV-1 clade C and B infection. , 2011, The Journal of infectious diseases.
[56] E. Alnemri,et al. Involvement of the AIM2, NLRC4, and NLRP3 Inflammasomes in Caspase-1 Activation by Listeria monocytogenes , 2010, Journal of Clinical Immunology.
[57] S. Henikoff,et al. Amino acid substitution matrices from protein blocks. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[58] Mohammed A. Eid,et al. Peer Review File Manuscript Title: Whole genome sequencing identifies multiple loci for critical illness caused by COVID-19 Reviewer Comments & Author Rebuttals , 2022 .
[59] I. Touitou,et al. Autoinflammatory diseases. , 2008, Best practice & research. Clinical rheumatology.
[60] Y. Benjamini,et al. Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .