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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 18, 2024
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Autoimmune[original query]>>Original Studies[Product Type]
Exemplar MobileNetV2-Based Artificial Intelligence for Robust and Accurate Diagnosis of Multiple Sclerosis.
Tuba Ekmekyapar et al. Diagnostics (Basel) 2023 13(19)
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Genetic relationships between high blood eosinophil count, asthma susceptibility and asthma severity.
Huashi Li et al. J Asthma 2023 1-15
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A machine learning model identifies patients in need of autoimmune disease testing using electronic health records.
Iain S Forrest et al. Nat Commun 2023 14(1) 2385
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A Review of Laboratory Practices Using the HLA-B27 Survey by the College of American Pathologists: How Important Is Allele-Level Typing?
Jeremy Ryan Andrew Peña et al. Arch Pathol Lab Med 2023
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Characterization of Chronic Urticaria and Associated Conditions - A Web-Based Survey.
Weronika Zysk et al. Dermatology practical & conceptual 2023 13(1)
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Cohort profile: Celiac disease genomic, environmental, microbiome and metabolome study; a prospective longitudinal birth cohort study of children at-risk for celiac disease.
Maureen M Leonard et al. PloS one 2023 18(3) e0282739
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Co-occurring conditions in children with Down syndrome and autism: a retrospective study.
Noemi A Spinazzi et al. Journal of neurodevelopmental disorders 2023 15(1) 9
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Genetic determinants of type 1 diabetes in individuals with weak evidence of islet autoimmunity at disease onset.
Paola Carrera et al. Diabetologia 2023
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DNAH7 mutations benefit colorectal cancer patients receiving immune checkpoint inhibitors.
Yang Wenjuan et al. Annals of translational medicine 2023 10(24) 1335
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The effects of heparin, aspirin, and maternal clinical factors on the rate of non-reportable cell-free DNA results: A retrospective cohort study.
Nitsche Joshua F et al. American journal of obstetrics & gynecology MFM 2022 100846
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Longitudinal Trend Monitoring of Multiple Sclerosis Ambulation Using Smartphones.
Creagh Andrew P et al. IEEE open journal of engineering in medicine and biology 2022 3202-210
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Prevalence of familial autoimmune diseases in juvenile idiopathic arthritis: results from the international Pharmachild registry.
van Straalen Joeri W et al. Pediatric rheumatology online journal 2022 20(1) 103
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The relationship between islet autoantibody status and the genetic risk of type 1 diabetes in adult-onset type 1 diabetes.
Thomas Nicholas J et al. Diabetologia 2022
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The effect of a 18 bp deletion/insertion variant of VEGF gene on the FMF development.
Sezer Ozlem et al. Nucleosides, nucleotides & nucleic acids 2022 1-12
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The impact of family history of type 2 diabetes on the clinical heterogeneity in idiopathic type 1 diabetes.
Chen Yan et al. Diabetes, obesity & metabolism 2022
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Monogenic diabetes clinic (MDC): 3-year experience.
Rapini Novella et al. Acta diabetologica 2022
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Familial autoimmunity in patients with idiopathic inflammatory myopathies.
Che Weng Ian et al. Journal of internal medicine 2022
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Characterization of Autoimmune Thyroid Disease in a Cohort of 73 Paediatric Patients Affected by 22q11.2 Deletion Syndrome: Longitudinal Single-Centre Study.
Ricci Silvia et al. Genes 2022 13(9)
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Relationship Between a Vitamin D Genetic Risk Score and Autoantibodies Among First-Degree Relatives of Probands With Rheumatoid Arthritis and Systemic Lupus Erythematosus.
Vanderlinden Lauren A et al. Frontiers in immunology 2022 13881332
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HLA Genotyping in Romanian Adult Patients with Celiac Disease, their First-degree Relatives and Healthy Persons.
Maruntelu Ion et al. Journal of gastrointestinal and liver diseases : JGLD 2022 31(2) 191-197
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A distinctive profile of family genetic risk scores in a Swedish national sample of cases of fibromyalgia, irritable bowel syndrome, and chronic fatigue syndrome compared to rheumatoid arthritis and major depression.
Kendler Kenneth S et al. Psychological medicine 2022 1-8
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Common Variable Immunodeficiency in Elderly Patients: A Long-Term Clinical Experience.
Danieli Maria Giovanna et al. Biomedicines 2022 10(3)
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Familial autoimmunity in pediatric patients with type 1 diabetes (T1D) and its associations with the severity of clinical presentation at diabetes diagnosis and with coexisting autoimmunity.
Kossiva Lydia et al. Hormones (Athens, Greece) 2022
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An appraisal of the frequency and severity of non-infectious manifestations in primary immunodeficiencies. A study of a national retrospective cohort of 1375 patients over 10 years.
Alligon Mickaël et al. The Journal of allergy and clinical immunology 2022
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Detection of Neoplasms by Metagenomic Next-Generation Sequencing of Cerebrospinal Fluid.
Gu Wei et al. JAMA neurology 2021
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The predictive value of PNH clones, 6p CN-LOH, and clonal TCR gene rearrangement for aplastic anemia diagnosis.
Shah Yash B et al. Blood advances 2021 5(16) 3216-3226
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Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients.
Qu Jingchun et al. Scientific reports 2021 11(1) 16013
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Familial History of Autoimmune Disorders Among Patients With Pediatric Multiple Sclerosis.
Greenberg Benjamin M et al. Neurology(R) neuroimmunology & neuroinflammation 2021 8(5)
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Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK.
Buonocore Federica et al. Journal of the Endocrine Society 2021 5(8) bvab086
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Genetic characterization of short stature patients with overlapping features of growth hormone insensitivity syndromes.
Andrews Afiya et al. The Journal of clinical endocrinology and metabolism 2021
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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