Skip to main content

ResearchHubLoading navigation…

Loading ResearchHub…

Neurogenetics - ResearchHub

Explore the network

Research, people, journals and institutions — all in one place.

Explore

01Research 02Smart search 03Researchers 04Journals 05Institutions 06RHR Rankings 07ResearchHub platform 08Events

Work together

Turn ideas into projects, questions and reusable datasets.

Connect

01Projects 02Questions 03Datasets

Stay informed

Follow trends, opportunities and your research library.

Insights

01Research trends 02Opportunities 03Library 04Research services 05ResearchHub Pro 06Pricing

ResearchHub

Explore ResearchHub.

Personal

01Recommended research 02Research intelligence

Home Search Network Library Log in

ResearchHub

Research, connected

Explore the graph

X

Download ResearchHub

GET IT ONGoogle PlayComing soonDownload on theApp StoreComing soonEXPLORE IT ONAppGalleryComing soon

Research

Research Researchers Journals Institutions RHR Rankings

Contribute

Projects Questions Datasets Opportunities

Platform

ResearchHub platform About Blog Community Help API Licensing

Shopping

Contact and support

Need help, have a question, or want to contact the ResearchHub team?

Contact and support support@aresearch.uk

© 2026 ResearchHub. Built for responsible scholarly connection.

Help Article feed Privacy Terms Cookies This work is licensed under Creative Commons Attribution 4.0 InternationalCC BY 4.0

Privacy-aware community infrastructure

Journal

Neurogenetics

1364-6753 · Springer Science and Business Media LLC

6 verified public works

Browse all journals →

Genetic findings in a Turkish clinical cohort with hereditary Parkinson’s disease

2026 · 0 citations

Founder mutations in movement disorders: global distribution, molecular mechanisms, and clinical consequences—a scoping review

2026 · 0 citations

Short-chain enoyl-CoA hydratase deficiency: a systematic review of clinical spectrum, genotype-phenotype correlations and survival predictors

2026 · 0 citations

Expanding the adult spectrum of TUBB4A disease: a spasticity–tremor phenotype with network imaging correlates

2026 · 0 citations

Further delineation of 2p13.2–p11.2 deletion syndrome by optical genome mapping

2026 · 0 citations

Clinical and genetic findings in Parkinson’s disease in a Turkish cohort: a retrospective exome sequencing study

2026 · 0 citations

Page 1 of 1