Matt Baker

24.1k total citations · 1 hit paper
83 papers, 5.1k citations indexed

About

Matt Baker is a scholar working on Neurology, Physiology and Molecular Biology. According to data from OpenAlex, Matt Baker has authored 83 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Neurology, 37 papers in Physiology and 24 papers in Molecular Biology. Recurrent topics in Matt Baker's work include Amyotrophic Lateral Sclerosis Research (41 papers), Alzheimer's disease research and treatments (37 papers) and Parkinson's Disease Mechanisms and Treatments (32 papers). Matt Baker is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (41 papers), Alzheimer's disease research and treatments (37 papers) and Parkinson's Disease Mechanisms and Treatments (32 papers). Matt Baker collaborates with scholars based in United States, Canada and United Kingdom. Matt Baker's co-authors include Rosa Rademakers, Manuela Neumann, Sigrun Roeber, I. R. A. Mackenzie, Mike Hutton, H. A. Kretzschmar, Dennis W. Dickson, Ian R. Mackenzie, Nicola J. Rutherford and Mariely DeJesus‐Hernandez and has published in prestigious journals such as Journal of Biological Chemistry, Nature Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Matt Baker

81 papers receiving 5.0k 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.

A new subtype of frontotemporal lobar degeneration with FUS pathology

2009 544 citations Rosa Rademakers, Matt Baker et al. Brain profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Matt Baker United States	38	3.4k	2.2k	1.8k	1.3k	1.1k	83	5.1k
Stuart Pickering‐Brown United Kingdom	43	4.5k 1.3×	3.2k 1.4×	2.1k 1.2×	1.5k 1.1×	1.2k 1.1×	111	6.6k
Theresa Schuck United States	15	4.3k 1.3×	1.9k 0.9×	2.7k 1.5×	1.1k 0.8×	1.8k 1.6×	19	6.4k
Matthew C. Micsenyi United States	10	4.0k 1.2×	1.9k 0.9×	2.4k 1.3×	989 0.8×	1.7k 1.5×	11	5.9k
Kuniaki Tsuchiya Japan	35	4.9k 1.4×	2.5k 1.1×	2.4k 1.3×	1.7k 1.3×	1.3k 1.2×	157	7.4k
Deepak M. Sampathu United States	10	4.5k 1.3×	1.6k 0.7×	2.4k 1.3×	1.0k 0.8×	1.8k 1.6×	10	5.9k
Felix Geser United States	25	2.8k 0.8×	951 0.4×	895 0.5×	748 0.6×	945 0.9×	40	3.4k
Tatsuro Oda Japan	20	2.7k 0.8×	1.3k 0.6×	1.5k 0.8×	1.0k 0.8×	1.0k 0.9×	39	3.9k
Luc Dupuis France	43	4.0k 1.2×	842 0.4×	2.1k 1.2×	628 0.5×	2.4k 2.2×	103	5.8k
Hidefumi Ito Japan	38	1.7k 0.5×	785 0.4×	1.5k 0.8×	1.0k 0.8×	564 0.5×	145	3.9k
David R. Beers United States	39	4.2k 1.2×	1.5k 0.7×	1.6k 0.9×	3.3k 2.6×	1.8k 1.7×	70	6.8k

Countries citing papers authored by Matt Baker

Since Specialization

Citations

This map shows the geographic impact of Matt Baker'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 Matt Baker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matt Baker more than expected).

Fields of papers citing papers by Matt Baker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matt Baker. 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 Matt Baker. The network helps show where Matt Baker may publish in the future.

Co-authorship network of co-authors of Matt Baker

This figure shows the co-authorship network connecting the top 25 collaborators of Matt Baker. A scholar is included among the top collaborators of Matt Baker 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 Matt Baker. Matt Baker 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

Vicente, Cristina T., Jolien Perneel, Marleen Van den Broeck, et al.. (2023). C-terminal TMEM106B fragments in human brain correlate with disease-associated TMEM106B haplotypes. Brain. 146(10). 4055–4064. 16 indexed citations

Josephs, Keith A., Shunsuke Koga, Nirubol Tosakulwong, et al.. (2023). Molecular fragment characteristics and distribution of tangle associated TDP-43 (TATs) and other TDP-43 lesions in Alzheimer’s disease. SHILAP Revista de lepidopterología. 4. 22–22. 6 indexed citations

Hirsch‐Reinshagen, Veronica, Ging‐Yuek Robin Hsiung, Cyril Pottier, et al.. (2019). Clinicopathologic correlations in a family with aTBK1mutation presenting as primary progressive aphasia and primary lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 20(7-8). 568–575. 23 indexed citations

Markopoulou, Katerina, Bruce A. Chase, Piotr Robowski, et al.. (2016). Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory Dysfunction. PLoS ONE. 11(11). e0165112–e0165112. 11 indexed citations

Baker, Matt. (2015). Future Selves interventions: A critique of the current evidence base. 1(154). 24–30. 1 indexed citations

Suh, EunRan, Sandra Weıntraub, Bradley T. Hyman, et al.. (2014). A NovelGRNMutation (GRNc.708+6_+9delTGAG) in Frontotemporal Lobar Degeneration With TDP-43–Positive Inclusions. Journal of Neuropathology & Experimental Neurology. 73(5). 467–473. 5 indexed citations

Kertesz, Andrew, Lee Cyn Ang, Sarah Jesso, et al.. (2013). Psychosis and Hallucinations in Frontotemporal Dementia with the C9ORF72 Mutation. Cognitive and Behavioral Neurology. 26(3). 146–154. 55 indexed citations

Baker, Matt, Audrey Strongosky, Mónica Sánchez-Contreras, et al.. (2013). SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia. Neurogenetics. 15(1). 23–30. 46 indexed citations

Sitek, Emilia J., Anna Barczak, Barbara Jasińska‐Myga, et al.. (2012). Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301LMAPTmutation: dysexecutive, aphasic, apraxic or spatial phenomenon?. Neurocase. 20(1). 69–86. 12 indexed citations

10.

Whitwell, Jennifer L., Keith A. Josephs, Ramesh Avula, et al.. (2011). Altered functional connectivity in asymptomatic MAPT subjects. Neurology. 77(9). 866–874. 101 indexed citations

11.

Carrasquillo, Minerva M., Alexandra M. Nicholson, NiCole A. Finch, et al.. (2010). Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma. The American Journal of Human Genetics. 87(6). 890–897. 112 indexed citations

12.

Jasińska‐Myga, Barbara, Christian Wider, Grzegorz Opala, et al.. (2009). GRN 3′UTR+78 C>T is not associated with risk for Parkinson’s disease. European Journal of Neurology. 16(8). 909–911. 8 indexed citations

13.

Coppola, Giovanni, Anna Karydas, Rosa Rademakers, et al.. (2008). Gene expression study on peripheral blood identifies progranulin mutations. Annals of Neurology. 64(1). 92–96. 70 indexed citations

14.

Dächsel, Justus C., Owen A. Ross, Ignácio F. Mata, et al.. (2006). Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions. Acta Neuropathologica. 113(5). 601–606. 48 indexed citations

15.

Wszołek, Zbigniew K., Yasuhiko Baba, Ian R. Mackenzie, et al.. (2006). Autosomal dominant dystonia-plus with cerebral calcifications. Neurology. 67(4). 620–625. 28 indexed citations

16.

Pickering‐Brown, Stuart, Matt Baker, Thomas D. Bird, et al.. (2003). Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 125B(1). 79–82. 18 indexed citations

17.

Friedman, Joseph, Katrina Gwinn, Jennifer DeWolfe, et al.. (2002). A family with a tau P301L mutation presenting with parkinsonism. Parkinsonism & Related Disorders. 9(2). 121–123. 10 indexed citations

18.

Amtul, Zareen, Patrick A. Lewis, Siân C. Piper, et al.. (2002). A Presenilin 1 Mutation Associated with Familial Frontotemporal Dementia Inhibits γ-Secretase Cleavage of APP and Notch. Neurobiology of Disease. 9(2). 269–273. 75 indexed citations

19.

Bigio, Eileen H., Jennifer Adamson, Estelle Sontag, et al.. (2001). Cortical Synapse Loss in progressive Supranuclear palsy. Journal of Neuropathology & Experimental Neurology. 60(5). 403–410. 52 indexed citations

20.

Isaacs, Adrian M., Matt Baker, Fabienne Wavrant‐De Vrièze, & Mike Hutton. (1998). Determination of the Gene Structure of Human GFAP and Absence of Coding Region Mutations Associated with Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17. Genomics. 51(1). 152–154. 25 indexed citations

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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