Darren G. Monckton

NeuroscienceBiochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 15 papers. Top paper: “Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects”.

Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.012

N/A

0.652DataRank · unranked

76 citations

Eun Pyo Hong, Jun Wan Shin, Michael J. Chao, Jacob M. Loupe, Tammy Gillis +12 more

Huntington’s Disease Pathogenesis: Two Sequential Components

Journal of Huntington s Disease(2021)10.3233/jhd-200427

N/A

0DataRank · unranked

114 citations

Marcy E. MacDonald, Vanessa C. Wheeler, Lesley Jones, Peter Holmans, Michael Orth +6 more

Cognitive Deficits, Apathy, and Hypersomnolence Represent the Core Brain Symptoms of Adult-Onset Myotonic Dystrophy Type 1

Frontiers in Neurology(2021)10.3389/fneur.2021.700796

N/A

0DataRank · unranked

27 citations

Alison Kruger, David J. Moser, Laurie Gutmann, Ellen van der Plas, Timothy R. Koscik +4 more

Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent

Human Molecular Genetics(2021)10.1093/hmg/ddab243

N/A

0DataRank · unranked

22 citations

Eyleen Corrales, Baili Zhang, Melissa Vásquez, Carolina Santamaría‐Ulloa, Hazel Quesada +5 more

Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington’s Disease

Journal of Huntington s Disease(2021)10.3233/jhd-210485

N/A

0DataRank · unranked

8 citations

Michael J. Chao, Thomas H. Massey, Branduff McAllister, S. V. Lobanov, Lesley Jones +12 more

Neurocognitive Features of Motor Premanifest Individuals With Myotonic Dystrophy Type 1

Neurology Genetics(2021)10.1212/nxg.0000000000000577

N/A

0DataRank · unranked

6 citations

Timothy R. Koscik, Vincent A. Magnotta, Sarah A. Cumming, Darren G. Monckton, Laurie Gutmann +2 more

FAN1 nuclease activity affects CAG expansion and age at onset of Huntington’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.13.439716

N/A

0DataRank · unranked

3 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Genetic modifiers of Huntington disease differentially influence motor and cognitive domains

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.004

N/A

0DataRank · unranked

121 citations

Yuan Huang, Michael Orth, Tammy Gillis, Jacqueline Siciliano, Eunpyo Hong +23 more

Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

Nature Neuroscience(2022)10.1038/s41593-022-01033-5

N/A

0DataRank · unranked

92 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Blood-Based Markers of Neuronal Injury in Adult-Onset Myotonic Dystrophy Type 1

Frontiers in Neurology(2022)10.3389/fneur.2021.791065

N/A

0DataRank · unranked

12 citations

Jeffrey D. Long, Timothy R. Koscik, Vincent A. Magnotta, Darren G. Monckton, Sarah A. Cumming +5 more

Genetic modifiers of Huntington’s disease differentially influence motor and cognitive domains

medRxiv(2022)10.1101/2022.01.03.22268687

N/A

0DataRank · unranked

1 citations

Yuan Huang, Michael Orth, Tammy Gillis, Jacqueline Siciliano, Eunpyo Hong +23 more

Longitudinal changes in white matter as measured with diffusion tensor imaging in adult-onset myotonic dystrophy type 1

Neuromuscular Disorders(2023)10.1016/j.nmd.2023.05.010

N/A

0DataRank · unranked

9 citations

Ellen van der Plas, Jeffrey D. Long, Stephen Cross, Laurie Gutmann, Sarah A. Cumming +5 more

Modification of Huntington’s disease by short tandem repeats

Brain Communications(2024)10.1093/braincomms/fcae016

N/A

0DataRank · unranked

12 citations

Eliana Marisa Ramos, N. Ahmad Aziz, Thomas H. Massey, Branduff McAllister, S. V. Lobanov +16 more

Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington’s disease

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322924121

N/A

0DataRank · unranked

10 citations

Eun Pyo Hong, Yukyeong Lee, Zachariah L. McLean, Emanuela Elezi, Ramee Lee +15 more

Genetic modifiers of somatic expansion and clinical phenotypes in Huntington’s disease highlight shared and tissue-specific effects

Nature Genetics(2025)10.1038/s41588-025-02191-5

N/A

0DataRank · unranked

45 citations

Jong-Min Lee, Zachariah L. McLean, Kevin Correia, Jun Wan Shin, Sujin Lee +38 more