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Query Trace: Hypertension[original query]>>Evidence Synthesis [Product Type]
Methylenetetrahydrofolate Reductase Polymorphism (rs1801133) and the Risk of Hypertension among African Populations: A Narrative Synthesis of Literature. Mabhida Sihle E et al. Genes 2022 13(4) Similar articles in PubMed
Use of technology to prevent, detect, manage and control hypertension in sub-Saharan Africa: a systematic review. Stokes Katy et al. BMJ open 2022 12(4) e058840 Similar articles in PubMed
Prediction of hypertension using traditional regression and machine learning models: A systematic review and meta-analysis. Chowdhury Mohammad Ziaul Islam et al. PloS one 2022 17(4) e0266334 Similar articles in PubMed
Number of Affected Relatives, Age, Smoking, and Hypertension Prediction Score for Intracranial Aneurysms in Persons With a Family History for Subarachnoid Hemorrhage. Zuurbier Charlotte C M et al. Stroke 2022 STROKEAHA121034612 Similar articles in PubMed
Artificial intelligence in disease diagnosis: a systematic literature review, synthesizing framework and future research agenda. Kumar Yogesh et al. Journal of ambient intelligence and humanized computing 2022 1-28 Similar articles in PubMed
Association between circulating microRNAs and the metabolic syndrome in adult populations: A systematic review. Solís-Toro Daniel et al. Diabetes & metabolic syndrome 2021 16(1) 102376 Similar articles in PubMed
Pharmacogenomics of ketamine: A systematic review. Meshkat Shakila et al. Journal of psychiatric research 2021 14527-34 Similar articles in PubMed
Prediction of incident atrial fibrillation in community-based electronic health records: a systematic review with meta-analysis. Nadarajah Ramesh et al. Heart (British Cardiac Society) 2021 Similar articles in PubMed
Diagnostic test accuracy of artificial intelligence analysis of cross-sectional imaging in pulmonary hypertension: a systematic literature review. Hardacre Conor Joseph et al. The British journal of radiology 2021 20210332 Similar articles in PubMed
CLINGEN Actionability Report for Marfan Syndrome - FBN1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Hereditary Hemorrhagic Telangiectasia - ENG, ACVRL1, SMAD4, GDF2 ClinGen Actionability Working Group
CLINGEN Actionability Report for Dilated cardiomyopathy - DMD, LMNA, TNNT2 ClinGen Actionability Working Group
CLINGEN Actionability Report for Von Hippel-Lindau Syndrome - VHL ClinGen Actionability Working Group
CLINGEN Actionability Report for Acute Intermittent Porphyria - HMBS ClinGen Actionability Working Group
CLINGEN Actionability Report for Glutaric Acidemia I - GCDH ClinGen Actionability Working Group
CLINGEN Actionability Report for Fabry Disease - GLA ClinGen Actionability Working Group
CLINGEN Actionability Report for Thrombophilia due to protein S deficiency - PROS1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Wilms tumor-WT1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Multiple Endocrine Neoplasia IIA, Familial Medullary Thyroid Cancer - RET ClinGen Actionability Working Group
CLINGEN Actionability Report for Li-Fraumeni Syndrome - TP53 ClinGen Actionability Working Group
CLINGEN Actionability Report for Familial Hypertrophic Cardiomyopathy - ACTC1, CSRP3, MYBPC3, MYH7, MYL2, MYL3, PRKAG2, TNNI3, TNNT2, TPM1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Hemochromatosis, Type 1-HFE ClinGen Actionability Working Group
CLINGEN Actionability Report for Neurofibromatosis type 1 - NF1 ClinGen Actionability Working Group
CLINGEN Actionability Report for Autosomal Dominant Polycystic Kidney Disease - DNAJB11, GANAB, PKD1, PKD2 ClinGen Actionability Working Group
CLINGEN Actionability Report for Wilson Disease - ATP7B ClinGen Actionability Working Group
CLINGEN Actionability Report for Familial thoracic aortic aneurysms and dissections (FTAAD)- FBN1, TGFBR1, TGFBR2, SMAD3, ACTA2, MYLK, MYH11 ClinGen Actionability Working Group
CLINGEN Actionability Report for Thrombophilia due to protein C deficiency - PROC ClinGen Actionability Working Group
CLINGEN Actionability Report for Primary pulmonary hypertension 1- BMPR2 ClinGen Actionability Working Group
CLINGEN Actionability Report for Arterial tortuosity syndrome - SLC2A10 ClinGen Actionability Working Group
CLINGEN Actionability Report for Paragangliomas 1, 2, 3, 4, 5; Pheochromocytoma- MAX, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127 ClinGen Actionability Working Group

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