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Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28167-1
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- Article
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29133-7
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- Publication type:
- Article
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.
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- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02673-2
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- Article
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
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- 2022
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- Correction Notice
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29133-7
- By:
- Publication type:
- Article
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28167-1
- By:
- Publication type:
- Article
Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00752-9
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- Publication type:
- Article
Thirty novel sequence variants impacting human intracranial volume.
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- Brain Communications, 2022, v. 4, n. 6, p. 1, doi. 10.1093/braincomms/fcac271
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- Publication type:
- Article
A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-82736-w
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- Article