Vicki L. McGovern

3.4k citations

32 papers · 1.7k indexed · h-index 18

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

Co-authors: Arthur H.M. Burghes Kevin D. Foust Tatiana Gavrilina Adam K. Bevan Brian K. Kaspar Leah Schmelzer Christine E. Beattie Lyndsey Braun
Topics: Neurogenetic and Muscular Disorders Research (26 papers)RNA modifications and cancer (16 papers)Congenital Anomalies and Fetal Surgery (12 papers)
Cited by: Genetics Molecular Biology Surgery
Journals: Nature Medicine PLoS ONE Molecular and Cellular Biology
Partner nations: United States United Kingdom Australia

In The Last Decade

Vicki L. McGovern

32 papers receiving 1.6k citations

Peers

Countries citing papers authored by Vicki L. McGovern

Since Specialization

Citations

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

Fields of papers citing papers by Vicki L. McGovern

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vicki L. McGovern. 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 Vicki L. McGovern. The network helps show where Vicki L. McGovern may publish in the future.

Co-authorship network of co-authors of Vicki L. McGovern

This figure shows the co-authorship network connecting the top 25 collaborators of Vicki L. McGovern. A scholar is included among the top collaborators of Vicki L. McGovern 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 Vicki L. McGovern. Vicki L. McGovern 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	In-depth comparison of Anc80L65 and AAV9 retinal targeting and characterization of cross-reactivity to multiple AAV serotypes in humans 2023 ·Molecular Therapy — Methods & Clinical Development ·(unknown),Shibi Likhite,(unknown),(unknown),Vicki L. McGovern,(unknown),(unknown),Arthur H.M. Burghes,Kathrin Meyer	5
2	Dual SMN inducing therapies can rescue survival and motor unit function in symptomatic ∆7SMA mice 2021 ·Neurobiology of Disease ·(unknown),Vicki L. McGovern,Deepti Chugh,W. David Arnold,Arthur H.M. Burghes	14
3	Biodistribution of onasemnogene abeparvovec DNA, mRNA and SMN protein in human tissue 2021 ·Nature Medicine ·Gretchen M. Thomsen,Arthur H.M. Burghes,(unknown),(unknown),(unknown),Stephanie T. Perry,Basam Z. Barkho,Petra Kaufmann,Douglas M. Sproule,Douglas E. Feltner,Wendy K. Chung,Vicki L. McGovern,Robert F. Hevner,Miriam Conces,Christopher R. Pierson,Mariacristina Scoto,Francesco Muntoni,Jerry R. Mendell,Kevin D. Foust	67
4	Complete sequencing of the SMN2 gene in SMA patients detects SMN gene deletion junctions and variants in SMN2 that modify the SMA phenotype 2019 ·Human Genetics ·(unknown),Vicki L. McGovern,Matthew R. Avenarius,Pamela J. Snyder,Thomas W. Prior,Flávia C. Nery,(unknown),Jennifer Roggenbuck,John T. Kissel,Valeria Sansone,(unknown),(unknown),(unknown),(unknown),Kathryn J. Swoboda,Arthur H.M. Burghes	63
5	Normalization of Patient-Identified Plasma Biomarkers in SMNΔ7 Mice following Postnatal SMN Restoration 2016 ·PLoS ONE ·W. David Arnold,Sandra Duqué,Chitra C. Iyer,Phillip G. Zaworski,Vicki L. McGovern,(unknown),Katharine M. von Herrmann,Dione Kobayashi,Karen Chen,Stephen J. Kolb,Sergey Paushkin,Arthur H.M. Burghes	10
6	Variable phenotypic expression and onset in MYH14 distal hereditary motor neuropathy phenotype in a large, multigenerational North American family 2016 ·Muscle & Nerve ·Stanley Iyadurai,W. David Arnold,John T. Kissel,(unknown),Vicki L. McGovern,Pamela J. Snyder,Thomas W. Prior,Jennifer Roggenbuck,Arthur H.M. Burghes,Stephen J. Kolb	10
7	Electrical Impedance Myography as a Pharmacodynamic Biomarker in Spinal Muscular Atrophy (P2.004) 2015 ·Neurology ·W. David Arnold,Vicki L. McGovern,Jia Li,Xiaohui Li,Stephen J. Kolb,Seward B. Rutkove,Arthur H.M. Burghes	1
8	SMN expression is required in motor neurons to rescue electrophysiological deficits in the SMNΔ7 mouse model of SMA 2015 ·Human Molecular Genetics ·Vicki L. McGovern,Chitra C. Iyer,W. David Arnold,Sara E. Gombash,Phillip G. Zaworski,(unknown),Kevin D. Foust,Arthur H.M. Burghes	47
9	The neuromuscular impact of symptomatic SMN restoration in a mouse model of spinal muscular atrophy 2015 ·Neurobiology of Disease ·W. David Arnold,Vicki L. McGovern,Benjamin Sanchez,Jia Li,(unknown),Stephen J. Kolb,Seward B. Rutkove,Arthur H.M. Burghes	38
10	Low levels of Survival Motor Neuron protein are sufficient for normal muscle function in the SMNΔ7 mouse model of SMA 2015 ·Human Molecular Genetics ·Chitra C. Iyer,Vicki L. McGovern,Jason D. Murray,Sara E. Gombash,Phillip G. Zaworski,Kevin D. Foust,Paul M.L. Janssen,Arthur H.M. Burghes	32
11	SMN deficiency disrupts gastrointestinal and enteric nervous system function in mice 2015 ·Human Molecular Genetics ·Sara E. Gombash,Christopher Cowley,Julie C. Fitzgerald,Chitra C. Iyer,David Fried,Vicki L. McGovern,Kent C. Williams,Arthur H.M. Burghes,Fedias L. Christofi,Brian D. Gulbransen,Kevin D. Foust	42
12	Plastin 3 Expression Does Not Modify Spinal Muscular Atrophy Severity in the ∆7 SMA Mouse 2015 ·PLoS ONE ·Vicki L. McGovern,Aurélie Massoni‐Laporte,Xueyong Wang,Thanh T. Le,(unknown),Christine E. Beattie,Mark M. Rich,Arthur H.M. Burghes	39
13	Deletion of atrophy enhancing genes fails to ameliorate the phenotype in a mouse model of spinal muscular atrophy 2014 ·Neuromuscular Disorders ·Chitra C. Iyer,Vicki L. McGovern,(unknown),David J. Glass,Arthur H.M. Burghes	9
14	Improving Single Injection CSF Delivery of AAV9-mediated Gene Therapy for SMA: A Dose–response Study in Mice and Nonhuman Primates 2014 ·Molecular Therapy ·Kathrin Meyer,Laura Ferraiuolo,Leah Schmelzer,Lyndsey Braun,Vicki L. McGovern,Shibi Likhite,(unknown),Alessandra Govoni,Julie C. Fitzgerald,Pablo Morales,Kevin D. Foust,Jerry R. Mendell,Arthur H.M. Burghes,Brian K. Kaspar	216
15	A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mouse 2011 ·Human Molecular Genetics ·Paul Porensky,Chalermchai Mitrpant,Vicki L. McGovern,Adam K. Bevan,Kevin D. Foust,(unknown),Steve D. Wilton,Arthur H.M. Burghes	209
16	Early heart failure in the SMNΔ7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery 2010 ·Human Molecular Genetics ·Adam K. Bevan,Kirk R. Hutchinson,Kevin D. Foust,Lyndsey Braun,Vicki L. McGovern,Leah Schmelzer,Jennifer Ward,Jeffrey C. Petruska,Pamela A. Lucchesi,Arthur H.M. Burghes,Brian K. Kaspar	170
17	Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect 2008 ·Human Molecular Genetics ·Tatiana Gavrilina,Vicki L. McGovern,Eileen Workman,Thomas O. Crawford,Rocky G. Gogliotti,Christine J. DiDonato,U. R. Monani,Glenn E. Morris,Arthur H.M. Burghes	169
18	Embryonic motor axon development in the severe SMA mouse 2008 ·Human Molecular Genetics ·Vicki L. McGovern,Tatiana Gavrilina,Christine E. Beattie,Arthur H.M. Burghes	121
19	A targeted gain of function screen in the embryonic CNS of Drosophila 2003 ·Mechanisms of Development ·Vicki L. McGovern,Christina A. Pacak,(unknown),Michelle L. Turski,Mark A. Seeger	20
20	Mosaic analysis reveals a cell-autonomous, neuronal requirement for Commissureless in the Drosophila CNS 2003 ·Development Genes and Evolution ·Vicki L. McGovern,Mark A. Seeger	6

About Vicki L. McGovern

Vicki L. McGovern is a scholar working on Genetics, Surgery and Molecular Biology, having authored 32 papers that have together received 1.7k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (26 papers), RNA modifications and cancer (16 papers) and Congenital Anomalies and Fetal Surgery (12 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (1.4k citations) and Surgery (478 citations). Vicki L. McGovern has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Arthur H.M. Burghes, Kevin D. Foust, Tatiana Gavrilina, Adam K. Bevan, Brian K. Kaspar, Leah Schmelzer, Christine E. Beattie, Lyndsey Braun, Paul Porensky and Chalermchai Mitrpant. Their work appears in journals such as Nature Medicine, PLoS ONE and Molecular and Cellular Biology.

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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