Garth A. Nicholson

26.8k total citations · 3 hit papers
237 papers, 11.7k citations indexed

About

Garth A. Nicholson is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Garth A. Nicholson has authored 237 papers receiving a total of 11.7k indexed citations (citations by other indexed papers that have themselves been cited), including 131 papers in Cellular and Molecular Neuroscience, 93 papers in Molecular Biology and 81 papers in Neurology. Recurrent topics in Garth A. Nicholson's work include Hereditary Neurological Disorders (105 papers), Genetic Neurodegenerative Diseases (63 papers) and Neurological diseases and metabolism (58 papers). Garth A. Nicholson is often cited by papers focused on Hereditary Neurological Disorders (105 papers), Genetic Neurodegenerative Diseases (63 papers) and Neurological diseases and metabolism (58 papers). Garth A. Nicholson collaborates with scholars based in Australia, United States and United Kingdom. Garth A. Nicholson's co-authors include Ian P. Blair, Marina Kennerson, Steve Vucic, Matthew C. Kiernan, Kelly L. Williams, Glenda M. Halliday, Julie Cavanagh, David M. Sharpe, Paul J. Spira and Jennifer C. Durnall and has published in prestigious journals such as Science, The Lancet and Nucleic Acids Research.

In The Last Decade

Garth A. Nicholson

236 papers receiving 11.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

2008 2.0k citations Jemeen Sreedharan, Ian P. Blair et al. Science profile →
DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

2004 602 citations Ian P. Blair, Marina Kennerson et al. The American Journal of Human Genetics profile →
Clinical and pathological features of a parkinsonian syndrome in a family with an Ala53Thr α‐synuclein mutation

2001 536 citations Paul J. Spira, David M. Sharpe et al. profile →

Peers

Countries citing papers authored by Garth A. Nicholson

Since Specialization

Citations

This map shows the geographic impact of Garth A. Nicholson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Garth A. Nicholson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Garth A. Nicholson more than expected).

Fields of papers citing papers by Garth A. Nicholson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Garth A. Nicholson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Garth A. Nicholson. The network helps show where Garth A. Nicholson may publish in the future.

Co-authorship network of co-authors of Garth A. Nicholson

This figure shows the co-authorship network connecting the top 25 collaborators of Garth A. Nicholson. A scholar is included among the top collaborators of Garth A. Nicholson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Garth A. Nicholson. Garth A. Nicholson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Treatment with sodium butyrate induces autophagy resulting in therapeutic benefits for spinocerebellar ataxia type 3 2024 ·The FASEB Journal ·Maxinne Watchon, Katherine J. Robinson, Luan Luu, (unknown), Kristy C. Yuan, (unknown), (unknown), Emily K. Don, Garth A. Nicholson, Albert Lee, Angela S. Laird	7
2	C9orf72-Associated Dipeptide Repeat Expansions Perturb ER-Golgi Vesicular Trafficking, Inducing Golgi Fragmentation and ER Stress, in ALS/FTD 2024 ·Molecular Neurobiology ·(unknown), Audrey Ragagnin, Sonam Parakh, (unknown), Kai Y. Soo, Marta Vidal, Cyril J. Jagaraj, (unknown), (unknown), Sina Shadfar, Emily K. Don, Anand K. Deva, Garth A. Nicholson, Dominic B. Rowe, Ian P. Blair, Shu Yang, Julie D. Atkin	4
3	A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing 2024 ·Journal of the Peripheral Nervous System ·(unknown), J. Parmar, Melina Ellis, Samantha J. Bryen, Cas Simons, (unknown), Igor Stevanovski, Ira W. Deveson, Garth A. Nicholson, Nigel G. Laing, Mathew Wallis, Gianina Ravenscroft, Kishore R. Kumar, Steve Vucic, Marina Kennerson	1
4	A humanized yeast model reveals dominant-negative properties of neuropathy-associated alanyl-tRNA synthetase mutations 2023 ·Human Molecular Genetics ·Rebecca Meyer‐Schuman, (unknown), (unknown), Shawna Feely, Marina Kennerson, Garth A. Nicholson, (unknown), Kristin S. Koutmou, Anthony Antonellis	7
5	Identity-by-descent analysis of CMTX3 links three families through a common founder 2022 ·Journal of Human Genetics ·Lyndal Henden, (unknown), Melina Ellis, Garth A. Nicholson, Marina Kennerson, Kelly L. Williams	3
6	Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy 2022 ·Journal of the Peripheral Nervous System ·(unknown), Igor Stevanovski, Sara Negri, Melina Ellis, Stephanie L. Barnes, Stephen Reddel, Steve Vucic, Garth A. Nicholson, Andrea Cortese, Kishore R. Kumar, Ira W. Deveson, Marina Kennerson	9
7	Novel gene–intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathy 2022 ·Brain ·(unknown), Ramesh K. Narayanan, (unknown), (unknown), Kaitao Lai, (unknown), Melina Ellis, Ruby C.Y. Lin, Brent Neumann, (unknown), Motonari Uesugi, Garth A. Nicholson, Steve Vucic, Mario Saporta, Marina Kennerson	9
8	Sodium valproate increases activity of the sirtuin pathway resulting in beneficial effects for spinocerebellar ataxia-3 in vivo 2021 ·Molecular Brain ·Maxinne Watchon, Luan Luu, Katherine J. Robinson, Kristy C. Yuan, (unknown), (unknown), (unknown), Gilles J. Guillemin, Nicholas J. Cole, Garth A. Nicholson, Roger S. Chung, Albert Lee, Angela S. Laird	14
9	Revisiting the pathogenic mechanism of the GJB1 5’ UTR c.-103C > T mutation causing CMTX1 2021 ·Neurogenetics ·(unknown), John Svaren, (unknown), Garth A. Nicholson, Marina Kennerson	2
10	A Tol2 Gateway-Compatible Toolbox for the Study of the Nervous System and Neurodegenerative Disease 2016 ·Zebrafish ·Emily K. Don, (unknown), Andrew P. Badrock, Thomas E. Hall, Marco Morsch, Elinor Hortle, Alison Hogan, Sharron Chow, (unknown), (unknown), Garth A. Nicholson, Roger S. Chung, Nicholas J. Cole	45
11	Mutations in the SPTLC1 Protein Cause Mitochondrial Structural Abnormalities and Endoplasmic Reticulum Stress in Lymphoblasts 2014 ·DNA and Cell Biology ·Simon J. Myers, Chandra S. Malladi, (unknown), Tara G. Bautista, Ross Boadle, Phillip J. Robinson, Garth A. Nicholson	20
12	A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene 2013 ·Human Molecular Genetics ·Marina Kennerson, Eppie M. Yiu, David Chuang, (unknown), Shih-Chia Tso, (unknown), Rama Chaudhry, Alexander P. Drew, Gary Rance, Martin B. Delatycki, Stephan Züchner, Monique M. Ryan, Garth A. Nicholson	56
13	TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis breakdown → 2008 ·Science ·Jemeen Sreedharan, Ian P. Blair, (unknown), Xun Hu, Caroline Vance, Boris Rogelj, Steven Ackerley, Jennifer C. Durnall, Kelly L. Williams, Emanuele Buratti, Francisco E. Baralle, Jacqueline de Belleroche, John D. Mitchell, P. Nigel Leigh, Ammar Al‐Chalabi, Christopher C.J. Miller, Garth A. Nicholson, Christopher E. Shaw	2037
14	Pedigree with frontotemporal lobar degeneration – motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9 2008 ·BMC Neurology ·Agnes A. Luty, John B. Kwok, Elizabeth M. Thompson, Peter Blumbergs, William S. Brooks, Clement T. Loy, Carol Dobson‐Stone, Peter K. Panegyres, Jane Hecker, Garth A. Nicholson, Glenda M. Halliday, Peter R. Schofield	58
15	Stoichiometric alteration of PMP22 protein determines the phenotype of HNPP 2007 ·Journal of the Peripheral Nervous System ·J. Li, (unknown), (unknown), Rosemary Shy, Krzysztof Krajewski, Michael E. Shy, Garth A. Nicholson	3
16	A Rapid and Definitive Test for Charcot-Marie-Tooth 1A and Hereditary Neuropathy with Liability to Pressure Palsies Using Multiplexed Real-Time PCR 2003 ·Genetic Testing ·(unknown), Thomas Kaiser, Marina Kennerson, Garth A. Nicholson	17
17	Peripheral neuropathies of infancy 2003 ·Developmental Medicine & Child Neurology ·Jo M. Wilmshurst, John D. Pollard, Garth A. Nicholson, Jayne Antony	20
18	Carbohydrate content and monosaccharide composition of dioxygen-binding functional units from Rapana Thomasiana hemocyanin isoform RtH2 2001 ·Comptes Rendus De L Academie Bulgare Des Sciences ·Krassimira Idakieva, (unknown), Garth A. Nicholson, Wolfgang Voelter, (unknown)	4
19	Clinical and pathological features of a Parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutation. 2001 ·PubMed ·Paul J. Spira, David M. Sharpe, Glenda M. Halliday, Julie Cavanagh, Garth A. Nicholson	279
20	Mutational studies in X-linked Charcot-Marie-Tooth disease (CMTX) 1994 ·The American Journal of Human Genetics ·(unknown), (unknown), Marina Kennerson, Garth A. Nicholson	10

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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