Steven H. Laval

3.2k total citations
51 papers, 2.0k citations indexed

About

Steven H. Laval is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Steven H. Laval has authored 51 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 14 papers in Genetics and 9 papers in Rheumatology. Recurrent topics in Steven H. Laval's work include Muscle Physiology and Disorders (15 papers), Rheumatoid Arthritis Research and Therapies (7 papers) and Spondyloarthritis Studies and Treatments (5 papers). Steven H. Laval is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Rheumatoid Arthritis Research and Therapies (7 papers) and Spondyloarthritis Studies and Treatments (5 papers). Steven H. Laval collaborates with scholars based in United Kingdom, United States and Germany. Steven H. Laval's co-authors include Kate Bushby, K. Bushby, Matthew A. Brown, Hanns Lochmüller, Volker Straub, Yvonne Boyd, B P Wordsworth, Lon R. Cardon, Andrew E. Timms and Andrei Călin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Brain.

In The Last Decade

Steven H. Laval

49 papers receiving 2.0k citations

Peers

Steven H. Laval

GENET

RHEUM

IMMUN

Mohnish Suri United Kingdom

Bradley L. Hodges United States

Hans G. Dauwerse Netherlands

Diana Baralle United Kingdom

Arnold Munnich France

M A Patton United Kingdom

Gergana Dobreva Germany

Isabelle Schrauwen United States

Kaya Bilgüvar United States

Beyhan Tüysüz Türkiye

Mohnish Suri United Kingdom

Steven H. Laval

1.2k ×1.0

736 ×1.4

GENET

171 ×0.4

RHEUM

131 ×0.5

IMMUN

260 ×1.0

Citations per year, relative to Steven H. Laval Steven H. Laval (= 1×) peers Mohnish Suri

Countries citing papers authored by Steven H. Laval

Since Specialization

Citations

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

Fields of papers citing papers by Steven H. Laval

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven H. Laval. 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 Steven H. Laval. The network helps show where Steven H. Laval may publish in the future.

Co-authorship network of co-authors of Steven H. Laval

This figure shows the co-authorship network connecting the top 25 collaborators of Steven H. Laval. A scholar is included among the top collaborators of Steven H. Laval 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 Steven H. Laval. Steven H. Laval 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

Richardson, Gavin D., Steven H. Laval, & W. Andrew Owens. (2015). Cardiomyocyte Regeneration in the mdx Mouse Model of Nonischemic Cardiomyopathy. Stem Cells and Development. 24(14). 1672–1679. 20 indexed citations

Blain, A., Elizabeth Greally, Steven H. Laval, et al.. (2015). Absence of Cardiac Benefit with Early Combination ACE Inhibitor and Beta Blocker Treatment in mdx Mice. Journal of Cardiovascular Translational Research. 8(3). 198–207. 8 indexed citations

Blain, A., Elizabeth Greally, Steven H. Laval, et al.. (2014). Assessment of ventricular function in mouse models of muscular dystrophy: A comparison of MRI with conductance catheter. Neuromuscular Disorders. 25(1). 24–31. 2 indexed citations

Dick, Emily, Spandan Kalra, D. N. Anderson, et al.. (2013). Exon Skipping and Gene Transfer Restore Dystrophin Expression in Human Induced Pluripotent Stem Cells-Cardiomyocytes Harboring DMD Mutations. Stem Cells and Development. 22(20). 2714–2724. 51 indexed citations

Laval, Steven H., et al.. (2013). Muscular dystrophy in dysferlin-deficient mouse models. Neuromuscular Disorders. 23(5). 377–387. 34 indexed citations

Cossins, Judith, Katsiaryna Belaya, Debbie Hicks, et al.. (2013). Congenital myasthenic syndromes due to mutations inALG2andALG14. Brain. 136(3). 944–956. 89 indexed citations

Müller, Juliane, Catherine D. Jepson, Steven H. Laval, et al.. (2010). Dok-7 promotes slow muscle integrity as well as neuromuscular junction formation in a zebrafish model of congenital myasthenic syndromes. Human Molecular Genetics. 19(9). 1726–1740. 18 indexed citations

Chiu, Yen‐Hui, Lars Klinge, Louise Helskov Jørgensen, et al.. (2009). Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophy. Human Molecular Genetics. 18(11). 1976–1989. 85 indexed citations

Hernández-Deviez, Delia J., Mark T. Howes, Steven H. Laval, et al.. (2007). Caveolin Regulates Endocytosis of the Muscle Repair Protein, Dysferlin. Journal of Biological Chemistry. 283(10). 6476–6488. 74 indexed citations

10.

Hagen, Maja von der, Steven H. Laval, Lynsey Cree, et al.. (2005). The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice. Neuromuscular Disorders. 15(12). 863–877. 41 indexed citations

11.

Laval, Steven H., et al.. (2003). Characterisation of the dysferlin skeletal muscle promoter. European Journal of Human Genetics. 12(2). 127–131. 7 indexed citations

12.

Eyre, Stephen, Anne Myerscough, Anne Barton, et al.. (2002). Whole-genome linkage analysis of rheumatoid arthritis susceptibility loci in 252 affected sibling pairs in the United Kingdom (vol 46,pg 632, 2002). Queensland's institutional digital repository (The University of Queensland). 46(5). 1406–1406. 15 indexed citations

13.

Brophy, Sinéad, L Bradbury, Andrew E. Timms, et al.. (2001). Towards defining the genetic determinants of disease severity in ankylosing spondylitis.. Queensland's institutional digital repository (The University of Queensland). 44(9). 5 indexed citations

14.

Laval, Steven H., Andrew E. Timms, Steve Edwards, et al.. (2001). Whole-Genome Screening in Ankylosing Spondylitis: Evidence of Non-MHC Genetic-Susceptibility Loci. The American Journal of Human Genetics. 68(4). 918–926. 179 indexed citations

15.

Laval, Steven H., et al.. (2000). The X‐chromosome and susceptibility to ankylosing spondylitis. Arthritis & Rheumatism. 43(6). 1353–1355. 34 indexed citations

16.

Laval, Steven H., et al.. (1999). The role of IL-10 in rheumatoid arthritis (RA) in two ethnically diverse populations.. Oxford University Research Archive (ORA) (University of Oxford). 42.

17.

Laval, Steven H., Robert J. Butler, J. Loftus, et al.. (1998). Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosome. American Journal of Medical Genetics. 81(5). 420–427. 80 indexed citations

18.

Rider, Sue, G. Maslen, Eli Hatchwell, et al.. (1994). A 2-Mb YAC Contig Encompassing Three Loci (DXF34, DXS14, and DXS390) That Lie between Xp11.2 Translocation Breakpoints Associated with Incontinentia Pigmenti Type 1. Genomics. 20(3). 341–346. 7 indexed citations

19.

Reed, Victoria, Steven H. Laval, G. Maslen, & Yvonne Boyd. (1993). Partial sequence data from three evolutionarily conserved loci from the proximal short arm of the human X chromosome; assignment of DXF34S1 to Xp11.21-cen. Cytogenetic and Genome Research. 62(2-3). 153–155. 1 indexed citations

20.

Laval, Steven H., Helen J. Blair, Mark C. Hirst, Kay E. Davies, & Yvonne Boyd. (1992). Mapping of FMR1, the gene implicated in fragile X-linked mental retardation, on the mouse X chromosome. Genomics. 12(4). 818–821. 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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