Pages that link to "Q29417123"
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The following pages link to Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk (Q29417123):
Displayed 50 items.
- intracranial aneurysm (Q1198391) (← links)
- CDKN2B-AS1 (Q18062371) (← links)
- Heart Disease and Stroke Statistics--2015 Update: A Report From the American Heart Association (Q22241921) (← links)
- Developing epigenetic diagnostics and therapeutics for brain disorders (Q27022987) (← links)
- Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets (Q28392307) (← links)
- Heart disease and stroke statistics--2014 update: a report from the American Heart Association (Q29547691) (← links)
- Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association (Q30238784) (← links)
- Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7. (Q30370233) (← links)
- Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm (Q30405930) (← links)
- Sox17 is indispensable for acquisition and maintenance of arterial identity (Q30557264) (← links)
- Revealing phenotype-associated functional differences by genome-wide scan of ancient haplotype blocks (Q33606025) (← links)
- Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies (Q33675091) (← links)
- Toward Understanding Non-coding RNA Roles in Intracranial Aneurysms and Subarachnoid Hemorrhage (Q33917323) (← links)
- Genome-wide association studies in neurology (Q34658391) (← links)
- Affected twins in the familial intracranial aneurysm study (Q35143018) (← links)
- Molecular basis and genetic predisposition to intracranial aneurysm (Q35626453) (← links)
- Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal. (Q35694393) (← links)
- Sox7, Sox17, and Sox18 Cooperatively Regulate Vascular Development in the Mouse Retina (Q35859036) (← links)
- Molecular mechanisms of the formation and progression of intracranial aneurysms. (Q35943389) (← links)
- Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals (Q37027180) (← links)
- A Review of the Genetics of Intracranial Berry Aneurysms and Implications for Genetic Counseling (Q37601496) (← links)
- Aberrant expression of lncRNAs and mRNAs in patients with intracranial aneurysm (Q37709316) (← links)
- Unruptured intracranial aneurysms: epidemiology, natural history, management options, and familial screening (Q38197433) (← links)
- Functional genomics of the 9p21.3 locus for atherosclerosis: clarity or confusion? (Q38217345) (← links)
- The emerging roles of long noncoding RNAs in common cardiovascular diseases (Q38374530) (← links)
- Global Gene Expression Patterns and Somatic Mutations in Sporadic Intracranial Aneurysms (Q39037402) (← links)
- RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population (Q39286785) (← links)
- New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics (Q40386684) (← links)
- Genetic associations of intracranial aneurysm formation and sub-arachnoid hemorrhage (Q41165028) (← links)
- Advancing stroke genomic research in the age of Trans-Omics big data science: Emerging priorities and opportunities (Q46650405) (← links)
- CDKN2BAS gene polymorphisms and the risk of intracranial aneurysm in the Chinese population. (Q47107879) (← links)
- Long non-coding RNA ANRIL in gene regulation and its duality in atherosclerosis (Q47262034) (← links)
- Exome Sequencing Identifies LOXL2 Mutation as a Cause of Familial Intracranial Aneurysm (Q47436913) (← links)
- Heritability of circle of Willis variations in families with intracranial aneurysms (Q48149577) (← links)
- APOL1, CDKN2A/CDKN2B, and HDAC9 Polymorphisms and Small Vessel Ischemic Stroke (Q48248566) (← links)
- LncRNA CDKN2BAS rs2157719 genetic variant contributes to medulloblastoma predisposition. (Q48286920) (← links)
- Association of SOX17 Gene Polymorphisms and Intracranial Aneurysm: A Case-Control Study and Meta-Analysis. (Q49390071) (← links)
- Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. (Q51417528) (← links)
- Identification of nine genes as novel susceptibility loci for early-onset ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage. (Q55391862) (← links)
- Cerebrovascular disorders associated with genetic lesions (Q57456322) (← links)
- point mutations and familial intracranial aneurysms (Q58568725) (← links)
- Long Noncoding RNAs in Atherosclerosis: JACC Review Topic of the Week (Q58607301) (← links)
- China Intracranial Aneurysm Project (CIAP): protocol for a registry study on a multidimensional prediction model for rupture risk of unruptured intracranial aneurysms (Q58694989) (← links)
- Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease (Q64044228) (← links)
- Genetic polymorphisms in associated with intracranial aneurysm in Chinese Han people: a genotype-phenotype study (Q64086451) (← links)
- Expression and mechanisms of long non-coding RNA genes MEG3 and ANRIL in gallbladder cancer (Q87161553) (← links)
- Rho Guanine Nucleotide Exchange Factor ARHGEF17 Is a Risk Gene for Intracranial Aneurysms (Q89574589) (← links)
- Translational Genomics in Neurocritical Care: a Review (Q89813391) (← links)
- Associations among Genetic Variants and Intracranial Aneurysm in a Chinese Population (Q93096246) (← links)
- Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (Q102075612) (← links)