Zih-hua Fang

Otfried Müller Str. 23
Tuebingen, BW 72076, Germany

Last Updated: 09/26/2026

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Found 47 publications

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort.

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort.

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

Multi-ancestry analysis of POLG variants in Parkinson's disease.

Multi-ancestry analysis of POLG variants in Parkinson's disease.

Journal: medRxiv : the preprint server for health sciences

Published: June 22, 2026

Pathology and Genetics in a Global Cohort of Parkinsonian Disorders.

Pathology and Genetics in a Global Cohort of Parkinsonian Disorders.

Journal: JAMA neurology

Published: June 08, 2026

Bridging Genetics and Precision Medicine in Parkinson's Disease through GP2.

Bridging Genetics and Precision Medicine in Parkinson's Disease through GP2.

Journal: medRxiv : the preprint server for health sciences

Published: April 29, 2026

Pathology and genetics in a global cohort of Parkinsonian Disorders.

Pathology and genetics in a global cohort of Parkinsonian Disorders.

Journal: medRxiv : the preprint server for health sciences

Published: April 03, 2026

Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's disease.

Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's disease.

Journal: bioRxiv : the preprint server for biology

Published: March 23, 2026

Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.

Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.

Journal: European journal of human genetics : EJHG

Published: March 16, 2026

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Journal: medRxiv : the preprint server for health sciences

Published: February 12, 2026

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders.

Journal: medRxiv : the preprint server for health sciences

Published: February 12, 2026

Showing 1-12 of 47

Last Updated: 09/26/2026