ArticleBrain : a journal of neurology2015
A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
Article in Brain : a journal of neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.
What it found
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The trial behind it
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Who cites it
25 citing papers in PubMed.
- Clinical, neuropathological, and biochemical characterization of ALS in a large CHCHD10 R15L family.medRxiv : the preprint server for health sciences · 2025Article
- CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signature.Human molecular genetics · 2023Article
- Review
- Neurodegeneration-associated mitochondrial proteins, CHCHD2 and CHCHD10-what distinguishes the two?Frontiers in cell and developmental biology · 2022Review
- Multi-OMICS study of a CHCHD10 variant causing ALS demonstrates metabolic rewiring and activation of endoplasmic reticulum and mitochondrial unfolded protein responses.Human molecular genetics · 2021Article
- Early death of ALS-linked CHCHD10-R15L transgenic mice with central nervous system, skeletal muscle, and cardiac pathology.iScience · 2021Article
- Mitochondrial inner membrane protein, Mic60/mitofilin in mammalian organ protection.Journal of cellular physiology · 2019Review
- PD-linked CHCHD2 mutations impair CHCHD10 and MICOS complex leading to mitochondria dysfunction.Human molecular genetics · 2019Article
- Twin CHCH Proteins, CHCHD2, and CHCHD10: Key Molecules of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Frontotemporal Dementia.International journal of molecular sciences · 2019Review
- CHCHD10 variants in amyotrophic lateral sclerosis: Where is the evidence?Annals of neurology · 2018Article
- A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALS.EMBO molecular medicine · 2018Article
- The cellular stress proteins CHCHD10 and MNRR1 (CHCHD2): Partners in mitochondrial and nuclear function and dysfunction.The Journal of biological chemistry · 2018Article
- Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications.The Lancet. Neurology · 2018Review
- Identification of CHCHD10 Mutation in Chinese Patients with Alzheimer Disease.Molecular neurobiology · 2017Article
- Mutation Screening of the CHCHD10 Gene in Chinese Patients with Amyotrophic Lateral Sclerosis.Molecular neurobiology · 2017Article
- Loss of function CHCHD10 mutations in cytoplasmic TDP-43 accumulation and synaptic integrity.Nature communications · 2017Article
- MNRR1, a Biorganellar Regulator of Mitochondria.Oxidative medicine and cellular longevity · 2017Review
- ALS: Recent Developments from Genetics Studies.Current neurology and neuroscience reports · 2016Review
- Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.Brain : a journal of neurology · 2016Article
- New ALS-Related Genes Expand the Spectrum Paradigm of Amyotrophic Lateral Sclerosis.Brain pathology (Zurich, Switzerland) · 2016Review
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4 authors.
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Abstract
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.