Sandra B. Laurent

2.5k total citations
20 papers, 1.1k citations indexed

About

Sandra B. Laurent is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Sandra B. Laurent has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 9 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Sandra B. Laurent's work include Genetics and Neurodevelopmental Disorders (7 papers), Neurological diseases and metabolism (4 papers) and Autism Spectrum Disorder Research (4 papers). Sandra B. Laurent is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Neurological diseases and metabolism (4 papers) and Autism Spectrum Disorder Research (4 papers). Sandra B. Laurent collaborates with scholars based in Canada, United States and France. Sandra B. Laurent's co-authors include Guy A. Rouleau, Jean‐Pierre Bouchard, François Gros‐Louis, Nicolas Dupré, Patrick A. Dion, Julie Gauthier, Ridha Joober, Laurent Mottron, Dan Spiegelman and Judith St‐Onge and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Annals of Neurology.

In The Last Decade

Sandra B. Laurent

20 papers receiving 1.0k citations

Peers

Sandra B. Laurent

GENET

NEURO

CMN

Weirui Guo United States

Michael R. Akins United States

Anne Noreau Canada

Juan Crespo-Barreto United States

Emmanuelle Buhler France

Sylvia Dobrzeniecka Canada

Jessica L. MacDonald United States

Amy Krans United States

Noam D. Rudnick United States

Caleb Davis United States

Weirui Guo United States

Sandra B. Laurent

464 ×0.8

307 ×0.8

GENET

196 ×0.7

NEURO

298 ×1.2

CMN

215 ×0.8

Citations per year, relative to Sandra B. Laurent Sandra B. Laurent (= 1×) peers Weirui Guo

Countries citing papers authored by Sandra B. Laurent

Since Specialization

Citations

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

Fields of papers citing papers by Sandra B. Laurent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra B. Laurent. 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 Sandra B. Laurent. The network helps show where Sandra B. Laurent may publish in the future.

Co-authorship network of co-authors of Sandra B. Laurent

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra B. Laurent. A scholar is included among the top collaborators of Sandra B. Laurent 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 Sandra B. Laurent. Sandra B. Laurent 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

Laurent, Sandra B., et al.. (2022). Effects of financial inclusion to GDP growth: The case of North Macedonia. Ekonomika. 68(1). 57–79. 3 indexed citations

Yu, Eric, Lynne Krohn, Uladzislau Rudakou, et al.. (2021). LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease. Neurobiology of Aging. 103. 142.e1–142.e5. 15 indexed citations

Saini, Prabhjyot, Uladzislau Rudakou, Eric Yu, et al.. (2020). Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease. Neurobiology of Aging. 100. 119.e7–119.e13. 25 indexed citations

Ross, Jay P., Claire S. Leblond, Sandra B. Laurent, et al.. (2020). Oligogenicity, C9orf72 expansion, and variant severity in ALS. Neurogenetics. 21(3). 227–242. 14 indexed citations

Rudakou, Uladzislau, Bouchra Ouled Amar Bencheikh, Jennifer A. Ruskey, et al.. (2018). Common and rare GCH1 variants are associated with Parkinson's disease. Neurobiology of Aging. 73. 231.e1–231.e6. 17 indexed citations

Ambalavanan, Amirthagowri, Claire S. Leblond, Dan Spiegelman, et al.. (2018). Absence of Mutation Enrichment for Genes Phylogenetically Conserved in the Olivocerebellar Motor Circuitry in a Cohort of Canadian Essential Tremor Cases. Molecular Neurobiology. 56(6). 4317–4321. 2 indexed citations

Leblond, Claire S., Amirthagowri Ambalavanan, Dan Spiegelman, et al.. (2017). Teneurin transmembrane protein 4 is not a cause for essential tremor in a Canadian population. Movement Disorders. 32(2). 292–295. 8 indexed citations

Ambalavanan, Amirthagowri, Claire S. Leblond, Dan Spiegelman, et al.. (2017). No rare deleterious variants from STK32B , PPARGC1A , and CTNNA3 are associated with essential tremor. Neurology Genetics. 3(5). e195–e195. 4 indexed citations

Lemay, Philippe, Patrizia De Marco, Dan Spiegelman, et al.. (2017). Rare deleterious variants in GRHL3 are associated with human spina bifida. Human Mutation. 38(6). 716–724. 30 indexed citations

10.

Leblond, Claire S., Ziv Gan‐Or, Dan Spiegelman, et al.. (2015). Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 37. 209.e17–209.e21. 58 indexed citations

11.

Therrien, Martine, Janet Laganière, Daniel Rochefort, et al.. (2012). Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron models. Human Molecular Genetics. 21(10). 2211–2218. 41 indexed citations

12.

Gauthier, Julie, Dan Spiegelman, Amélie Piton, et al.. (2008). Novel de novo SHANK3 mutation in autistic patients. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(3). 421–424. 245 indexed citations

13.

Meijer, Inge A., Sandra B. Laurent, Judith St‐Onge, et al.. (2008). A Novel Duplication Confirms the Involvement of 5q23.2 in Autosomal Dominant Leukodystrophy. Archives of Neurology. 65(11). 1496–1496. 29 indexed citations

14.

Meijer, Inge A., Patrick A. Dion, Sandra B. Laurent, et al.. (2007). Characterization of a novel SPG3A deletion in a French‐Canadian family. Annals of Neurology. 61(6). 599–603. 18 indexed citations

15.

Gros‐Louis, François, Nicolas Dupré, Patrick A. Dion, et al.. (2006). Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia. Nature Genetics. 39(1). 80–85. 245 indexed citations

16.

Gauthier, Julie, Gevork N. Mnatzakanian, Carol Saunders, et al.. (2005). Clinical Stringency Greatly Improves Mutation Detection in Rett Syndrome. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 32(3). 321–326. 6 indexed citations

17.

Gauthier, Julie, Anna Bonnel, Judith St‐Onge, et al.. (2004). NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 132B(1). 74–75. 90 indexed citations

18.

Gros‐Louis, François, Roxanne Larivière, Genevíève Gowing, et al.. (2004). A Frameshift Deletion in Peripherin Gene Associated with Amyotrophic Lateral Sclerosis. Journal of Biological Chemistry. 279(44). 45951–45956. 141 indexed citations

19.

Gauthier, Julie, et al.. (2003). Mutation screening of FOXP2 in individuals diagnosed with autistic disorder. American Journal of Medical Genetics Part A. 118A(2). 172–175. 42 indexed citations

20.

Dupré, Nicolas, Dominique J. Verlaan, Collette K. Hand, et al.. (2003). Linkage to the CCM2 Locus and Genetic Heterogeneity in Familial Cerebral Cavernous Malformation. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 30(2). 122–128. 24 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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