Precision Health Database

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Query Trace: Hypertension[original query]>>Evidence Synthesis[Product Type]

Publication
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
CLINGEN Actionability Report for Mucopolysaccharidosis type I-IDUA ClinGen Actionability Working Group
CLINGEN Actionability Report for Maturity Onset Diabetes of the Young Type III - HNF1A ClinGen Actionability Working Group
Clinical biomarker innovation: when is it worthwhile? Kluytmans Anouck et al. Clinical chemistry and laboratory medicine 2019 Jul Similar articles in PubMed
Economic evaluation of a pharmacogenomic multi-gene panel test to optimize anti-hypertension therapy: simulation study. Kelley Eli F et al. Journal of medical economics 2018 Oct 1-19 Similar articles in PubMed
Genetic factors contributing to hypertension in African-based populations: A systematic review and meta-analysis. Yako Yandiswa Y et al. Journal of clinical hypertension (Greenwich, Conn.) 2018 Mar Similar articles in PubMed
A systematic review of genetic mutations in pulmonary arterial hypertension. Garcia-Rivas Gerardo et al. BMC medical genetics 2017 18(1) 82 Similar articles in PubMed
The development and implementation of stroke risk prediction model in National Health Insurance Service's personal health record. Lee Jae-Woo et al. Computer methods and programs in biomedicine 2018 Jan 153253-257 Similar articles in PubMed
Recent development of risk-prediction models for incident hypertension: An updated systematic review. Sun Dongdong et al. PloS one 2017 12(10) e0187240 Similar articles in PubMed
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Surendran Praveen et al. Nature genetics 2016 Sep Similar articles in PubMed