Associated Papers
A case report of neonatal incontinentia pigmenti complicated by severe cerebrovascular lesions in one of the male monozygotic twins.
Lin X et al.
Frontiers in Pediatrics, 2024
38832002 (PubMed )
Supplement: Table1.xlsx › filter_variants
Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease.
Shi M et al.
Stroke and Vascular Neurology, 2022
34880113 (PubMed )
Supplement: svn-2021-001157supp001.pdf
Mastermind: A Comprehensive Genomic Association Search Engine for Empirical Evidence Curation and Genetic Variant Interpretation.
Chunn LM et al.
Frontiers in Genetics, 2020
Comprehensive assessment of the association of WNK4 polymorphisms with hypertension: evidence from a meta-analysis.
Guo XG et al.
Scientific Reports, 2014
The WNKs: atypical protein kinases with pleiotropic actions.
McCormick JA et al.
Physiological Reviews, 2011
WNK kinases and the control of blood pressure.
Cope G et al.
Pharmacology & Therapeutics, 2005
Three novel missense mutations of WNK4, a kinase mutated in inherited hypertension, in Japanese hypertensives: implication of clinical phenotypes.
Kamide K et al.
American Journal of Hypertension, 2004
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