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Zac Chatterton

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Articles 22
Citations 402
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Recent Articles
1.
Liao S, Kano K, Phanse S, Nguyen M, Margolis E, Fu Y, et al.
bioRxiv . 2024 Sep; PMID: 39257750
Mutations in the mitochondrial cristae protein CHCHD2 lead to a late-onset autosomal dominant form of Parkinson's disease (PD) which closely resembles idiopathic PD, providing the opportunity to gain new insights...
2.
Rademacher K, Doric Z, Haddad D, Mamaligas A, Liao S, Creed R, et al.
bioRxiv . 2024 Apr; PMID: 38645054
Parkinson's disease (PD) is characterized by the death of substantia nigra (SNc) dopamine (DA) neurons, but the pathophysiological mechanisms that precede and drive their death remain unknown. The activity of...
3.
Naaldijk Y, Fernandez B, Fasiczka R, Fdez E, Leghay C, Croitoru I, et al.
NPJ Parkinsons Dis . 2024 Jan; 10(1):12. PMID: 38191886
Parkinson´s disease (PD) is a common neurodegenerative movement disorder and leucine-rich repeat kinase 2 (LRRK2) is a promising therapeutic target for disease intervention. However, the ability to stratify patients who...
4.
de Boer S, Riedl L, Fenoglio C, Rue I, Landin-Romero R, Matis S, et al.
J Alzheimers Dis . 2023 Dec; 97(2):963-973. PMID: 38143357
Background: The behavioral variant of frontotemporal dementia (bvFTD) is very heterogeneous in pathology, genetics, and disease course. Unlike Alzheimer's disease, reliable biomarkers are lacking and sporadic bvFTD is often misdiagnosed...
5.
Togel L, Nightingale R, Wu R, Chueh A, Al-Obaidi S, Luk I, et al.
Sci Rep . 2023 Feb; 13(1):2422. PMID: 36765160
No abstract available.
6.
Chatterton Z, Lamichhane P, Ahmadi Rastegar D, Fitzpatrick L, Lebhar H, Marquis C, et al.
Cell Biosci . 2023 Jan; 13(1):2. PMID: 36600255
Background: DNA methylation is a critical molecular mark involved in cellular differentiation and cell-specific processes. Single-cell whole genome DNA methylation profiling methods hold great potential to resolve the DNA methylation...
7.
Southwood D, Singh S, Chatterton Z
Neural Regen Res . 2022 Mar; 17(10):2213-2214. PMID: 35259835
No abstract available.
8.
Chatterton Z, Mendelev N, Chen S, Carr W, Kamimori G, Ge Y, et al.
Front Mol Neurosci . 2021 Jul; 14:672614. PMID: 34276305
Sampling the live brain is difficult and dangerous, and withdrawing cerebrospinal fluid is uncomfortable and frightening to the subject, so new sources of real-time analysis are constantly sought. Cell-free DNA...
9.
Ye Z, Chatterton Z, Pflueger J, Damiano J, McQuillan L, Harvey A, et al.
Brain Commun . 2021 Mar; 3(1):fcaa235. PMID: 33738444
Brain somatic mutations are an increasingly recognized cause of epilepsy, brain malformations and autism spectrum disorders and may be a hidden cause of other neurodevelopmental and neurodegenerative disorders. At present,...
10.
Oyston L, Chatterton Z, Hallupp M, Rajan N, Kwok J, Dobson-Stone C
Brain . 2020 Jul; 143(8):e68. PMID: 32666099
No abstract available.