Lauren Brady

2.2k total citations
40 papers, 558 citations indexed

About

Lauren Brady is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Lauren Brady has authored 40 papers receiving a total of 558 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 15 papers in Cellular and Molecular Neuroscience and 9 papers in Clinical Biochemistry. Recurrent topics in Lauren Brady's work include Mitochondrial Function and Pathology (16 papers), Genetic Neurodegenerative Diseases (11 papers) and Metabolism and Genetic Disorders (9 papers). Lauren Brady is often cited by papers focused on Mitochondrial Function and Pathology (16 papers), Genetic Neurodegenerative Diseases (11 papers) and Metabolism and Genetic Disorders (9 papers). Lauren Brady collaborates with scholars based in Canada, United States and Denmark. Lauren Brady's co-authors include Mark A. Tarnopolsky, Lauren MacNeil, John M. Shoffner, Jeremy Schwartzentruber, Lily Wu, Bekim Sadiković, Dennis E. Bulman, Mamta Giri, Eric P. Hoffman and Mandeep S. Sidhu and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Lauren Brady

39 papers receiving 544 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lauren Brady Canada 17 360 122 120 102 72 40 558
Carola Hedberg‐Oldfors Sweden 15 335 0.9× 106 0.9× 152 1.3× 47 0.5× 74 1.0× 42 570
Imen Dorboz France 14 492 1.4× 50 0.4× 94 0.8× 59 0.6× 40 0.6× 30 650
Morad Khayat Israel 16 422 1.2× 115 0.9× 162 1.4× 46 0.5× 18 0.3× 50 664
Cristina Domínguez‐González Spain 13 277 0.8× 82 0.7× 88 0.7× 111 1.1× 101 1.4× 80 503
Chiara Aiello Italy 16 397 1.1× 100 0.8× 41 0.3× 110 1.1× 24 0.3× 34 583
Luc Régal Belgium 15 336 0.9× 84 0.7× 117 1.0× 51 0.5× 119 1.7× 33 689
Alessandro Malandrini Italy 16 448 1.2× 112 0.9× 67 0.6× 246 2.4× 134 1.9× 48 734
Hamad Alzaidan Saudi Arabia 14 283 0.8× 132 1.1× 173 1.4× 46 0.5× 15 0.2× 39 578
Sietske H. Kevelam Netherlands 10 283 0.8× 86 0.7× 83 0.7× 32 0.3× 100 1.4× 11 473
Sander Pajusalu Estonia 14 349 1.0× 68 0.6× 211 1.8× 76 0.7× 26 0.4× 37 555

Countries citing papers authored by Lauren Brady

Since Specialization
Citations

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

Fields of papers citing papers by Lauren Brady

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lauren Brady

This figure shows the co-authorship network connecting the top 25 collaborators of Lauren Brady. A scholar is included among the top collaborators of Lauren Brady 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 Lauren Brady. Lauren Brady is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Krag, Thomas, Lauren Brady, France Leturcq, et al.. (2025). Variants in CAPN3 Causing Autosomal Dominant Limb–Girdle Muscular Dystrophy Combined With Calpain‐3 Deficiency. Human Mutation. 2025(1). 9301465–9301465. 1 indexed citations
2.
Nath, Siddharth, Nicholas S. Caron, Jill E. Kolesar, et al.. (2022). Functional characterization of variants of unknown significance in a spinocerebellar ataxia patient using an unsupervised machine learning pipeline. Human Genome Variation. 9(1). 10–10. 3 indexed citations
3.
Brady, Lauren, et al.. (2022). Pre- and Postnatal Characterization of Autosomal Recessive <b><i>KIDINS220</i></b>-Associated Ventriculomegaly. Molecular Syndromology. 13(5). 419–424. 3 indexed citations
4.
Ngo, Kathie J., John Provias, Steven K. Baker, et al.. (2021). De novo pathogenic variant in SETX causes a rapidly progressive neurodegenerative disorder of early childhood-onset with severe axonal polyneuropathy. Acta Neuropathologica Communications. 9(1). 194–194. 5 indexed citations
5.
Brady, Lauren, et al.. (2020). A mitochondrial disorder with ptosis and exercise intolerance without ophthalmoparesis secondary to m.5865 T > C variant. Mitochondrion. 53. 150–153. 1 indexed citations
6.
Brady, Lauren, et al.. (2020). Phenotypic convergence in Charcot-Marie-Tooth 2Y with novel VCP mutation. Neuromuscular Disorders. 30(3). 232–235. 7 indexed citations
7.
Fagerberg, Christina, Adrian Taylor, Felix Distelmaier, et al.. (2019). Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. Brain. 143(1). 94–111. 18 indexed citations
8.
Tarnopolsky, Mark A., Lauren Brady, & Lauren MacNeil. (2019). Myasthenia graves-like symptoms associated with rare mitochondrial mutation (m.5728T>C). Mitochondrion. 47. 139–140. 5 indexed citations
9.
Hannah‐Shmouni, Fady, Lauren MacNeil, Lauren Brady, Mats I. Nilsson, & Mark A. Tarnopolsky. (2019). Expanding the Clinical Spectrum of LONP1-Related Mitochondrial Cytopathy. Frontiers in Neurology. 10. 981–981. 10 indexed citations
10.
Brady, Lauren, et al.. (2019). Genotypes of chronic progressive external ophthalmoplegia in a large adult-onset cohort. Mitochondrion. 49. 227–231. 17 indexed citations
11.
Choi, May Y., Mark A. Tarnopolsky, Lauren Brady, et al.. (2019). Anti-NT5c1A Autoantibodies as Biomarkers in Inclusion Body Myositis. Frontiers in Immunology. 10. 745–745. 34 indexed citations
12.
Wu, Lily, Lauren Brady, John M. Shoffner, & Mark A. Tarnopolsky. (2018). Next-Generation Sequencing to Diagnose Muscular Dystrophy, Rhabdomyolysis, and HyperCKemia. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45(3). 262–268. 25 indexed citations
13.
Brady, Lauren, Bekim Sadiković, C. Anthony Rupar, & Mark A. Tarnopolsky. (2018). Complete elimination of a pathogenic homoplasmic mtDNA mutation in one generation. Mitochondrion. 45. 18–21. 1 indexed citations
14.
Sidhu, Mandeep S., Lauren Brady, Mark A. Tarnopolsky, & Gabriel M. Ronen. (2017). Clinical Manifestations Associated With the N-Terminal-Acetyltransferase NAA10 Gene Mutation in a Girl: Ogden Syndrome. Pediatric Neurology. 76. 82–85. 19 indexed citations
15.
16.
Okur, Volkan, Megan T. Cho, Lindsay B. Henderson, et al.. (2016). De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. Human Genetics. 135(7). 699–705. 53 indexed citations
17.
Brady, Lauren, Mamta Giri, John Provias, Eric P. Hoffman, & Mark A. Tarnopolsky. (2015). Proximal myopathy with focal depletion of mitochondria and megaconial congenital muscular dystrophy are allelic conditions caused by mutations in CHKB. Neuromuscular Disorders. 26(2). 160–164. 10 indexed citations
18.
Lines, Matthew A., Rebekah Jobling, Lauren Brady, et al.. (2014). Peroxisomal D-bifunctional protein deficiency. Neurology. 82(11). 963–968. 47 indexed citations
19.
Forbes, Nauzer, Kevin Woodward, David Morgan, et al.. (2014). Evidence for synergistic effects of PRNP and ATP7Bmutations in severe neuropsychiatric deterioration. BMC Medical Genetics. 15(1). 22–22. 8 indexed citations
20.
Brady, Lauren, Lauren MacNeil, & Mark A. Tarnopolsky. (2014). Impact of Habitual Exercise on the Strength of Individuals with Myotonic Dystrophy Type 1. American Journal of Physical Medicine & Rehabilitation. 93(9). 739–750. 19 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Carola Hedberg‐Oldfors Breakdown of academic impact, for papers by Imen Dorboz Breakdown of academic impact, for papers by Morad Khayat Breakdown of academic impact, for papers by Cristina Domínguez‐González Breakdown of academic impact, for papers by Chiara Aiello Breakdown of academic impact, for papers by Luc Régal Breakdown of academic impact, for papers by Alessandro Malandrini Breakdown of academic impact, for papers by Hamad Alzaidan Breakdown of academic impact, for papers by Sietske H. Kevelam Breakdown of academic impact, for papers by Sander Pajusalu
Rankless by CCL
2026