Alexandre D. Laporte

687 total citations
5 papers, 99 citations indexed

About

Alexandre D. Laporte is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Alexandre D. Laporte has authored 5 papers receiving a total of 99 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Neurology and 2 papers in Genetics. Recurrent topics in Alexandre D. Laporte's work include Neurological disorders and treatments (2 papers), RNA regulation and disease (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Alexandre D. Laporte is often cited by papers focused on Neurological disorders and treatments (2 papers), RNA regulation and disease (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Alexandre D. Laporte collaborates with scholars based in Canada, Italy and Austria. Alexandre D. Laporte's co-authors include Guy A. Rouleau, Dan Spiegelman, Patrick A. Dion, Fulya Akçimen, Calwing Liao, Ridha Joober, Judith St‐Onge, Myriam Srour, Andrea Accogli and Jean‐Baptiste Rivière and has published in prestigious journals such as Nature Communications, Movement Disorders and Frontiers in Genetics.

In The Last Decade

Alexandre D. Laporte

5 papers receiving 99 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alexandre D. Laporte Canada	5	52	40	21	16	14	5	99
Ahmed N. Sahly Saudi Arabia	8	29 0.6×	34 0.8×	22 1.0×	18 1.1×	14 1.0×	14	96
Cheuk Wing Fung China	9	67 1.3×	54 1.4×	31 1.5×	21 1.3×	6 0.4×	18	177
Zeyu Zhu China	7	41 0.8×	19 0.5×	12 0.6×	28 1.8×	12 0.9×	25	113
Dana Marafi United States	8	88 1.7×	70 1.8×	13 0.6×	22 1.4×	5 0.4×	24	171
Hormos Salimi Dafsari Germany	8	70 1.3×	55 1.4×	10 0.5×	28 1.8×	40 2.9×	18	173
Naomi Meeks United States	8	86 1.7×	50 1.3×	15 0.7×	9 0.6×	3 0.2×	16	169
Suad Alyamani Saudi Arabia	4	67 1.3×	22 0.6×	23 1.1×	35 2.2×	10 0.7×	8	118
Michela Stagnaro Italy	5	66 1.3×	38 0.9×	18 0.9×	7 0.4×	8 0.6×	9	99
Yuko Shimizu‐Motohashi Japan	6	45 0.9×	27 0.7×	31 1.5×	16 1.0×	11 0.8×	30	121
Sara Nuovo Italy	8	77 1.5×	68 1.7×	5 0.2×	37 2.3×	15 1.1×	12	168

Countries citing papers authored by Alexandre D. Laporte

Since Specialization

Citations

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

Fields of papers citing papers by Alexandre D. Laporte

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexandre D. Laporte. 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 Alexandre D. Laporte. The network helps show where Alexandre D. Laporte may publish in the future.

Co-authorship network of co-authors of Alexandre D. Laporte

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

All Works

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5 of 5 papers shown

1.

Liao, Calwing, Daniel Rochefort, Fulya Akçimen, et al.. (2020). Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor. Frontiers in Genetics. 11. 813–813. 9 indexed citations

2.

Liao, Calwing, Daniel Rochefort, Fulya Akçimen, et al.. (2020). Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor. Movement Disorders. 35(7). 1153–1162. 7 indexed citations

3.

Accogli, Andrea, Laura Russell, Guillaume Sébire, et al.. (2019). Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia. Neurogenetics. 20(2). 103–108. 13 indexed citations

4.

Liao, Calwing, Alexandre D. Laporte, Dan Spiegelman, et al.. (2019). Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes. Nature Communications. 10(1). 4450–4450. 63 indexed citations

5.

Accogli, Andrea, Judith St‐Onge, Joël Lafond‐Lapalme, et al.. (2019). Heterozygous Missense Pathogenic Variants Within the Second Spectrin Repeat of SPTBN2 Lead to Infantile-Onset Cerebellar Ataxia. Journal of Child Neurology. 35(2). 106–110. 7 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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