Caspar E. Gross

TU Kaiserslautern, Erwin Schrödinger Str. 54
Kaiserslautern, RP 67663, Germany

Last Updated: 09/26/2026

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Found 17 publications

Ultra-deep long-read metagenomics captures diverse taxonomic and biosynthetic potential of soil microbes.

Ultra-deep long-read metagenomics captures diverse taxonomic and biosynthetic potential of soil microbes.

Journal: GigaScience

Published: July 03, 2025

Long-Read Sequencing Identifies Mosaic Sequence Variations in Friedreich's Ataxia-GAA Repeats.

Long-Read Sequencing Identifies Mosaic Sequence Variations in Friedreich's Ataxia-GAA Repeats.

Journal: International journal of molecular sciences

Published: April 10, 2025

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Journal: Nature communications

Published: March 31, 2025

Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefits.

Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefits.

Journal: Breast (Edinburgh, Scotland)

Published: February 16, 2025

Author Correction: Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson's study.

Author Correction: Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson's study.

Journal: NPJ Parkinson's disease

Published: December 18, 2023

A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy.

A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy.

Journal: Nature genetics

Published: November 03, 2023

Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjects.

Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjects.

Journal: NPJ genomic medicine

Published: September 13, 2023

Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene.

Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the DMD Gene.

Journal: International journal of molecular sciences

Published: September 01, 2023

Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson's study.

Accurate long-read sequencing identified GBA1 as major risk factor in the Luxembourgish Parkinson's study.

Journal: NPJ Parkinson's disease

Published: March 29, 2023

Whole genome analysis of two sympatric human Mansonella: Mansonella perstans and Mansonella sp "DEUX".

Whole genome analysis of two sympatric human Mansonella: Mansonella perstans and Mansonella sp "DEUX".

Journal: Frontiers in cellular and infection microbiology

Published: February 06, 2023

Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17.

Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17.

Journal: Cellular and molecular life sciences : CMLS

Published: August 09, 2021

Multisystemic neurodegeneration caused by biallelic pentanucleotide expansions in RFC1.

Multisystemic neurodegeneration caused by biallelic pentanucleotide expansions in RFC1.

Journal: Parkinsonism & related disorders

Published: June 09, 2021

Showing 1-12 of 17

Last Updated: 09/26/2026