Gabrielle Lemire

1.6k total citations
16 papers, 165 citations indexed

About

Gabrielle Lemire is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Gabrielle Lemire has authored 16 papers receiving a total of 165 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Gabrielle Lemire's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (3 papers) and RNA regulation and disease (2 papers). Gabrielle Lemire is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (3 papers) and RNA regulation and disease (2 papers). Gabrielle Lemire collaborates with scholars based in Canada, United States and Saudi Arabia. Gabrielle Lemire's co-authors include Kym M. Boycott, Kristin D. Kernohan, Heather Howley, Taila Hartley, David R. Adams, Marie‐Ange Delrue, Julie Gauthier, Philippe M. Campeau, Yoko Itō and Wai‐Man Chan and has published in prestigious journals such as Nature Communications, The American Journal of Human Genetics and Annual Review of Genomics and Human Genetics.

In The Last Decade

Gabrielle Lemire

15 papers receiving 164 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gabrielle Lemire Canada 7 91 72 17 16 15 16 165
Berardo Rinaldi Italy 7 99 1.1× 90 1.3× 32 1.9× 10 0.6× 10 0.7× 26 170
Juliane Eckhold Germany 8 116 1.3× 66 0.9× 10 0.6× 18 1.1× 18 1.2× 10 202
Neïla Belguith Tunisia 9 150 1.6× 123 1.7× 13 0.8× 15 0.9× 21 1.4× 34 226
Michael Kennemer United States 4 92 1.0× 92 1.3× 16 0.9× 25 1.6× 13 0.9× 4 181
Agostino Seresini Italy 6 96 1.1× 35 0.5× 13 0.8× 16 1.0× 12 0.8× 8 160
Salima El Chehadeh-Djebbar France 4 72 0.8× 154 2.1× 10 0.6× 12 0.8× 14 0.9× 4 222
Samantha Penney United States 5 68 0.7× 76 1.1× 9 0.5× 27 1.7× 8 0.5× 5 157
Bianca Russell United States 7 77 0.8× 71 1.0× 8 0.5× 8 0.5× 9 0.6× 18 142
Monika Weisz Hubshman Israel 6 79 0.9× 108 1.5× 8 0.5× 18 1.1× 6 0.4× 7 165

Countries citing papers authored by Gabrielle Lemire

Since Specialization
Citations

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

Fields of papers citing papers by Gabrielle Lemire

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabrielle Lemire

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

All Works

16 of 16 papers shown
1.
Lemire, Gabrielle, Thierry Laliberté, Katia Turcot, Véronique H. Flamand, & Alexandre Campeau‐Lecours. (2025). Preliminary development and evaluation of a mechanical handwriting assistive device to support individuals with movement disorders. Frontiers in Rehabilitation Sciences. 5. 1418534–1418534.
2.
Shimada, Ayako, Ashley Buchanan, Natallia Katenka, et al.. (2024). Evaluating attitudes on health-seeking behavior among a network of people who inject drugs. Applied Network Science. 9(1). 1 indexed citations
3.
Lemire, Gabrielle, et al.. (2023). Pathogenic variant in the X‐linked ARR3 gene associated with variable early‐onset myopia. American Journal of Medical Genetics Part A. 194(2). 397–399. 1 indexed citations
4.
Marshall, Aren E., Gabrielle Lemire, Jorge Dávila, et al.. (2023). RNA sequencing reveals deep intronic CEP120 variant: A report of the diagnostic odyssey for two siblings with Joubert syndrome type 31. American Journal of Medical Genetics Part A. 194(4). e63485–e63485. 1 indexed citations
5.
Lemire, Gabrielle, Alison Eaton, Angela L. Duker, et al.. (2023). Specific heterozygous variants in MGP lead to endoplasmic reticulum stress and cause spondyloepiphyseal dysplasia. Nature Communications. 14(1). 7054–7054. 5 indexed citations
6.
Lemire, Gabrielle, et al.. (2023). DNM1L Variant Presenting as Adolescent-Onset Sensory Neuronopathy, Spasticity, Dystonia, and Ataxia. Journal of Pediatric Neurology. 21(6). 475–478. 2 indexed citations
7.
Huang, Yan, Gabrielle Lemire, Lauren C. Briere, et al.. (2022). The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. The American Journal of Human Genetics. 109(10). 1923–1931. 10 indexed citations
8.
Lemire, Gabrielle, Taila Hartley, Alison Eaton, et al.. (2022). The implementation of an enhanced clinical model to improve the diagnostic yield of exome sequencing for patients with a rare genetic disease: A Canadian experience. American Journal of Medical Genetics Part A. 191(2). 338–347. 2 indexed citations
9.
Jurgens, Julie A., Brenda J. Barry, Gabrielle Lemire, et al.. (2021). Novel variants in TUBA1A cause congenital fibrosis of the extraocular muscles with or without malformations of cortical brain development. European Journal of Human Genetics. 29(5). 816–826. 12 indexed citations
10.
Lemire, Gabrielle, Bixia Zheng, Ruobing Zou, et al.. (2021). Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia. American Journal of Medical Genetics Part A. 185(10). 3005–3011. 4 indexed citations
11.
Lemire, Gabrielle, et al.. (2021). A disease‐causing variant in HNRNPH2 inherited from an unaffected mother with skewed X‐inactivation. American Journal of Medical Genetics Part A. 188(2). 668–671. 3 indexed citations
12.
Makrythanasis, Periklis, Gabrielle Lemire, Justine Rousseau, et al.. (2020). De Novo KAT5 Variants Cause a Syndrome with Recognizable Facial Dysmorphisms, Cerebellar Atrophy, Sleep Disturbance, and Epilepsy. The American Journal of Human Genetics. 107(3). 564–574. 19 indexed citations
13.
Alzahrani, Fatema, Hiroyuki Kuwahara, Mohammed Al‐Owain, et al.. (2020). Recessive, Deleterious Variants in SMG8 Expand the Role of Nonsense-Mediated Decay in Developmental Disorders in Humans. The American Journal of Human Genetics. 107(6). 1178–1185. 19 indexed citations
14.
Hartley, Taila, Gabrielle Lemire, Kristin D. Kernohan, et al.. (2020). New Diagnostic Approaches for Undiagnosed Rare Genetic Diseases. Annual Review of Genomics and Human Genetics. 21(1). 351–372. 60 indexed citations
15.
Lemire, Gabrielle, Philippe M. Campeau, Stefan Parent, et al.. (2019). Retrospective analysis of fetal vertebral defects: Associated anomalies, etiologies, and outcome. American Journal of Medical Genetics Part A. 182(4). 664–672. 11 indexed citations
16.
Lemire, Gabrielle, et al.. (2017). A case of familial transmission of the newly described DNMT3A‐Overgrowth Syndrome. American Journal of Medical Genetics Part A. 173(7). 1887–1890. 15 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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