دورية أكاديمية
أعرض في EDS

Genetic Predisposition to Neurological Complications in Patients with COVID-19.

التفاصيل البيبلوغرافية
العنوان: Genetic Predisposition to Neurological Complications in Patients with COVID-19.
المؤلفون: Sahajpal NS; Department of Pathology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.; Greenwood Genetic Center, Greenwood, SC 29646, USA., Hastie AR; Bionano Genomics, Inc., San Diego, CA 92121, USA., Schieck M; Hannover Unified Biobank, Hannover Medical School, 30625 Hannover, Germany.; RESIST-Cluster of Excellence 2155, Hannover Medical School, 30625 Hannover, Germany., Mondal AK; Department of Pathology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA., Felde M; Department of Human Genetics, Hannover Medical School, 30625 Hannover, Germany., van der Made CI; Department of Human Genetics, Radboud University Medical Center for Infectious Diseases (RCI), 6525 Nijmegen, The Netherlands.; Department of Internal Medicine, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 Nijmegen, The Netherlands.; Radboud Expertise Center for Immunodeficiency and Autoinflammation, Radboud University Medical Center, 6525 Nijmegen, The Netherlands., Chou JS; Division of Immunology, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA., Randolph AG; Department of Anesthesiology, Critical Care, and Pain Medicine, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.; Departments of Anesthesia and Pediatrics, Harvard Medical School, Boston, MA 02115, USA., Illig T; Hannover Unified Biobank, Hannover Medical School, 30625 Hannover, Germany.; RESIST-Cluster of Excellence 2155, Hannover Medical School, 30625 Hannover, Germany., Zody MC; New York Genome Center, New York, NY 10013, USA., Brownstein CA; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA., Beggs AH; Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA., Hoischen A; Department of Human Genetics, Radboud University Medical Center for Infectious Diseases (RCI), 6525 Nijmegen, The Netherlands.; Department of Internal Medicine, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 Nijmegen, The Netherlands.; Radboud Expertise Center for Immunodeficiency and Autoinflammation, Radboud University Medical Center, 6525 Nijmegen, The Netherlands., Chaubey A; Bionano Genomics, Inc., San Diego, CA 92121, USA., Kolhe R; Department of Pathology, Medical College of Georgia, Augusta University, Augusta, GA 30912, USA.
مؤلفون مشاركون: COVID19hostgenomesv Consortium
المصدر: Biomolecules [Biomolecules] 2023 Jan 09; Vol. 13 (1). Date of Electronic Publication: 2023 Jan 09.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101596414 Publication Model: Electronic Cited Medium: Internet ISSN: 2218-273X (Electronic) Linking ISSN: 2218273X NLM ISO Abbreviation: Biomolecules Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : MDPI, 2011-
مواضيع طبية MeSH: COVID-19*/complications , COVID-19*/genetics , Nervous System Diseases*/genetics, Humans ; Genetic Predisposition to Disease ; Genotype
مستخلص: Several studies have identified rare and common genetic variants associated with severe COVID-19, but no study has reported genetic determinants as predisposition factors for neurological complications. In this report, we identified rare/unique structural variants (SVs) implicated in neurological functions in two individuals with neurological manifestations of COVID-19. This report highlights the possible genetic link to the neurological symptoms with COVID-19 and calls for a collective effort to study these cohorts for a possible genetic linkage.
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معلومات مُعتمدة: P50 HD105351 United States HD NICHD NIH HHS
فهرسة مساهمة: Keywords: COVID-19; genetic predisposition; neurological complications; optical genome mapping; rare SVs
تواريخ الأحداث: Date Created: 20230121 Date Completed: 20230124 Latest Revision: 20230315
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC9855758
DOI: 10.3390/biom13010133
PMID: 36671517
قاعدة البيانات: MEDLINE
الوصف
تدمد:2218-273X
DOI:10.3390/biom13010133