Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Exome sequencing study revealed novel susceptibility loci in subarachnoid hemorrhage (SAH).

Molecular brain - 25 May 2020

Hao Xiwa, Pang Jiangxia, Li Ruiming, Lv Lin, Liu Guorong, Li Yuechun, Cheng Guojuan, Zhang Jingfen

Abstract excerpt

AIM: To expand our current understanding of the genetic basis of subarachnoid hemorrhage (SAH), and reveal the susceptibility genes in SAH risk. METHODS: We conducted whole-exome sequencing (WES) in a cohort of 196 individuals, including 94 SAH patients and 94 controls, as well as 8 samples that belong to two pedigrees. Systematically examination for rare variations (through direct genotyping) and common...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Exome Sequencing
Share to Genetic Loci
Share to Genome-Wide Association Study

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Inheritance Patterns

Share to Pedigree

Share to Polymorphism, Single Nucleotide

Share to Risk Factors

Share to Subarachnoid Hemorrhage

Source

Open in PubMed Open full text

Identifiers

PMID: 32450902
DOI: 10.1186/s13041-020-00620-6
PMCID: PMC7249693

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Exome sequencing study revealed novel susceptibility loci in subarachnoid hemorrhage (SAH).PMID 32450902Read ↗

Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies.Semantic proximity Read ↗

Longitudinal Genome-wide Association Study of Cognitive Impairment After Subarachnoid Hemorrhage: A Long-term Prospective Cohort StudySemantic proximity Read ↗

Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.Semantic proximity Read ↗

Genetics of intracerebral hemorrhage.Semantic proximity Read ↗

Genetic Epidemiology of Spontaneous Subarachnoid HemorrhageSemantic proximity Read ↗

From GWAS to the clinic: risk factors for intracranial aneurysmsSemantic proximity Read ↗

Monogenic Causes in Familial Stroke Across Intracerebral Hemorrhage and Ischemic Stroke Subtypes Identified by Whole-Exome SequencingSemantic proximity Read ↗

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.Semantic proximity Read ↗

Multi-ancestry proteogenomic analysis identifies risk proteins for intracranial aneurysmsSemantic proximity Read ↗

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors.Semantic proximity Read ↗

Genetic Polymorphisms Associated with Spontaneous Intracerebral HemorrhageSemantic proximity Read ↗

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.