Louise R. Simard

3.1k citations

55 papers · 2.3k indexed · h-index 26

Molecular Biology top 5%
Genetics top 0.5%
Surgery top 5%
Genetics top 10%
Neurology

Co-authors: Camille Rochette Arthur H.M. Burghes Thomas W. Prior Peter N. Ray Jerry R. Mendell Nicolas Gilbert Patricia McAndrew D. Williams Parsons
Topics: Neurogenetic and Muscular Disorders Research (28 papers)RNA modifications and cancer (22 papers)Congenital Anomalies and Fetal Surgery (11 papers)
Cited by: Genetics Molecular Biology Surgery
Journals: Proceedings of the National Academy of Sciences Nucleic Acids Research Journal of Biological Chemistry
Partner nations: Canada United States France

In The Last Decade

Louise R. Simard

54 papers receiving 2.3k citations

Peers

Countries citing papers authored by Louise R. Simard

Since Specialization

Citations

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

Fields of papers citing papers by Louise R. Simard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louise R. Simard. 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 Louise R. Simard. The network helps show where Louise R. Simard may publish in the future.

Co-authorship network of co-authors of Louise R. Simard

This figure shows the co-authorship network connecting the top 25 collaborators of Louise R. Simard. A scholar is included among the top collaborators of Louise R. Simard 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 Louise R. Simard. Louise R. Simard 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

#	Work	Indexed citations
1	Generation of Conditional Knockout Alleles for PRUNE-1 2023 ·Cells ·Xiaoli Wu,Louise R. Simard,Hao Ding	2
2	Constraining the Side Chain of C-Terminal Amino Acids in Apelin-13 Greatly Increases Affinity, Modulates Signaling, and Improves the Pharmacokinetic Profile 2021 ·Journal of Medicinal Chemistry ·Kien Trân,(unknown),Xavier Sainsily,(unknown),Jérôme Côté,Louise R. Simard,(unknown),Alexandre Murza,(unknown),(unknown),(unknown),Lounès Haroune,Jean‐Michel Longpré,Olivier Lesur,Mannix Auger‐Messier,Claude Spino,Michel Bouvier,Philippe Sarret,Steven Ballet,Éric Marsault	11
3	A homozygous canonical splice acceptor site mutation in PRUNE1 is responsible for a rare childhood neurodegenerative disease in Manitoba Cree families 2018 ·American Journal of Medical Genetics Part A ·(unknown),Louise R. Simard,(unknown),Marc R. Del Bigio,Patrick Frosk	9
4	A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis 2017 ·Journal of Medical Genetics ·Patrick Frosk,Heleen H. Arts,Julien Philippe,(unknown),(unknown),(unknown),Louise R. Simard,Jacek Majewski,Somayyeh Fahiminiya,(unknown),Yangfan P. Liu,(unknown),Robert A. Hegele,Nicholas Katsanis,(unknown),Marc R. Del Bigio,Erica E. Davis	35
5	Protective effects of butyrate-based compounds on a mouse model for spinal muscular atrophy 2016 ·Experimental Neurology ·Matthew E.R. Butchbach,(unknown),(unknown),Luciano Saieva,Jonathan Edwards,Eileen Workman,Louise R. Simard,Livio Pellizzoni,Arthur H.M. Burghes	25
6	Spinal Muscular Atrophy Biomarker Measurements from Blood Samples in a Clinical Trial of Valproic Acid in Ambulatory Adults 2015 ·Journal of Neuromuscular Diseases ·Samantha Renusch,Sean W. Harshman,(unknown),Eileen Workman,Allison Wehr,Xiaobai Li,Thomas W. Prior,Bakri Elsheikh,Kathryn J. Swoboda,Louise R. Simard,John T. Kissel,Daniel J. Battle,Mark R. Parthun,Michael A. Freitas,Stephen J. Kolb	14
7	SMA CARNI-VAL Trial Part I: Double-Blind, Randomized, Placebo-Controlled Trial of L-Carnitine and Valproic Acid in Spinal Muscular Atrophy 2010 ·PLoS ONE ·Kathryn J. Swoboda,Charles Scott,Thomas O. Crawford,Louise R. Simard,Sandra P. Reyna,Kristin J. Krosschell,Gyula Acsádi,(unknown),Mary Schroth,Guy D’Anjou,Bernard LaSalle,Thomas W. Prior,(unknown),Jo Anne Maczulski,Mark B. Bromberg,Gary M. Chan,John T. Kissel,(unknown)	124
8	Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy 2009 ·Human Molecular Genetics ·Matthew E.R. Butchbach,J. J. Singh,Margrét Þorsteinsdóttir,Luciano Saieva,(unknown),John B. Thurmond,Þorkell Andrésson,Jun Zhang,Jonathan Edwards,Louise R. Simard,Livio Pellizzoni,Jill Jarecki,Arthur H.M. Burghes,Mark E. Gurney	94
9	Association of the dopamine transporter gene and ADHD symptoms in a Canadian population‐based sample of same‐age twins 2007 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Isabelle Ouellet‐Morin,Karen Wigg,Yu Feng,Ginette Dionne,Philippe Robaey,Mara Brendgen,Frank Vitaro,Louise R. Simard,Russell Schachar,Richard E. Tremblay,Daniel Pérusse,Michel Boivin,Cathy L. Barr	18
10	The SMN genes are subject to transcriptional regulation during cellular differentiation 2001 ·Gene ·(unknown),Thierry Brun,Camille Rochette,Alexandre Semionov,Raphaël Rouget,Louise R. Simard	29
11	Novel 3678delA mutation in exon 26 of the dystrophin gene causing duchenne muscular dystrophy 1998 ·Human Mutation ·Alka Agarwal-Mawal,Michel Vanasse,Louise R. Simard	1
12	Intragenic complementation at the argininosuccinate lyase locus: Reconstruction of the active site 1998 ·Journal of Inherited Metabolic Disease ·P. Lynne Howell,Mary Ann Turner,John Christodoulou,Daniel Walker,(unknown),Louise R. Simard,Lynda Ploder,Roderick R. McInnes	16
13	Cloning, Characterization, and Copy Number of the Murine Survival Motor Neuron Gene: Homolog of the Spinal Muscular Atrophy-Determining Gene 1997 ·Genome Research ·Christine J. DiDonato,Xiao–Ning Chen,David Noya,Julie R. Korenberg,Joseph H. Nadeau,Louise R. Simard	104
14	SMNT and NAIP mutations in Canadian families with spinal muscular atrophy (SMA): Genotype/phenotype correlations with disease severity 1997 ·American Journal of Medical Genetics ·Louise R. Simard,Camille Rochette,Alexandre Semionov,Kenneth Morgan,Michel Vanasse	37
15	Genetic and physical mapping of the mouse host resistance locus Lgn1 1997 ·Mammalian Genome ·(unknown),Marie‐Claire Beckers,(unknown),Christine J. DiDonato,Louise R. Simard,Céline Morissette,Francine Gervais,Shin-ichi Yoshida,Philippe Gros	19
16	Intragenic Complementation at the Human Argininosuccinate Lyase Locus 1997 ·Journal of Biological Chemistry ·David C. Walker,John Christodoulou,(unknown),Louise R. Simard,Lynda Ploder,P. Lynne Howell,Roderick R. McInnes	24
17	Clinical and genetic study of chronic (types II and III) childhood onset spinal muscular atrophy 1996 ·Neuromuscular Disorders ·(unknown),Louise R. Simard,(unknown),Camille Rochette,Jean Lambert,Michel Vanasse	19
18	A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients 1995 ·Nature Genetics ·Terri G. Thompson,Christine J. DiDonato,Louise R. Simard,Susan E. Ingraham,Arthur H.M. Burghes,Thomas O. Crawford,Camille Rochette,Jerry R. Mendell,John J. Wasmuth	69
19	Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French — Canadian population 1994 ·Human Molecular Genetics ·Louise R. Simard,(unknown),Camille Rochette,Kenneth Morgan,(unknown),(unknown),Serge B. Melançon,Michel Vanasse	24
20	Alumorphs—Human DNA polymorphisms detected by polymerase chain reaction using Alu-specific primers 1990 ·Genomics ·Daniel Sinnett,Jean‐Marc Deragon,Louise R. Simard,Damian Labuda	53

About Louise R. Simard

Louise R. Simard is a scholar working on Genetics, Biochemistry and Molecular Biology, having authored 55 papers that have together received 2.3k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (28 papers), RNA modifications and cancer (22 papers) and Congenital Anomalies and Fetal Surgery (11 papers). The work is most often cited by research in Genetics (1.7k citations), Molecular Biology (1.7k citations) and Surgery (687 citations). Louise R. Simard has collaborated with scholars based in Canada, United States and France. Frequent co-authors include Camille Rochette, Arthur H.M. Burghes, Thomas W. Prior, Peter N. Ray, Jerry R. Mendell, Nicolas Gilbert, Patricia McAndrew, D. Williams Parsons, Christine J. DiDonato and Thomas O. Crawford. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

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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