Leigh B. Waddell

2.8k total citations
20 papers, 648 citations indexed

About

Leigh B. Waddell is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Leigh B. Waddell has authored 20 papers receiving a total of 648 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 10 papers in Genetics and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Leigh B. Waddell's work include Muscle Physiology and Disorders (11 papers), Cardiomyopathy and Myosin Studies (10 papers) and Neurogenetic and Muscular Disorders Research (9 papers). Leigh B. Waddell is often cited by papers focused on Muscle Physiology and Disorders (11 papers), Cardiomyopathy and Myosin Studies (10 papers) and Neurogenetic and Muscular Disorders Research (9 papers). Leigh B. Waddell collaborates with scholars based in Australia, United States and France. Leigh B. Waddell's co-authors include Nigel F. Clarke, Kathryn N. North, Sandra T. Cooper, Daniel G. MacArthur, Monkol Lek, Mark R. Davis, Nigel G. Laing, Roula Ghaoui, Andrew J. Kornberg and Nicole Monnier and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Leigh B. Waddell

20 papers receiving 641 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leigh B. Waddell Australia 14 536 317 217 122 90 20 648
Anni Evilä Finland 12 525 1.0× 322 1.0× 186 0.9× 141 1.2× 57 0.6× 20 644
Hernán Gonorazky Canada 12 532 1.0× 122 0.4× 208 1.0× 76 0.6× 182 2.0× 43 710
Nasim Vasli France 10 353 0.7× 203 0.6× 109 0.5× 78 0.6× 125 1.4× 16 466
Lidia González‐Quereda Spain 13 476 0.9× 156 0.5× 109 0.5× 119 1.0× 59 0.7× 35 540
Lindsay M. Wallace United States 12 573 1.1× 126 0.4× 147 0.7× 100 0.8× 74 0.8× 21 665
Svetlana Gorokhova France 9 409 0.8× 200 0.6× 59 0.3× 101 0.8× 53 0.6× 25 553
M.P. Freda Italy 10 559 1.0× 280 0.9× 87 0.4× 157 1.3× 62 0.7× 11 616
Sini Penttilä Finland 13 427 0.8× 248 0.8× 153 0.7× 147 1.2× 28 0.3× 31 550
Tiina Suominen Finland 15 595 1.1× 361 1.1× 125 0.6× 278 2.3× 29 0.3× 25 702
C. Bönnemann United States 8 256 0.5× 123 0.4× 115 0.5× 50 0.4× 95 1.1× 17 346

Countries citing papers authored by Leigh B. Waddell

Since Specialization
Citations

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

Fields of papers citing papers by Leigh B. Waddell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leigh B. Waddell. 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 Leigh B. Waddell. The network helps show where Leigh B. Waddell may publish in the future.

Co-authorship network of co-authors of Leigh B. Waddell

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

All Works

20 of 20 papers shown
1.
Sandaradura, Sarah A., Adam Bournazos, Amali Mallawaarachchi, et al.. (2017). Nemaline myopathy and distal arthrogryposis associated with an autosomal recessive TNNT3 splice variant. Human Mutation. 39(3). 383–388. 46 indexed citations
2.
Ghaoui, Roula, Tatiana Benavides Damm, Monkol Lek, et al.. (2016). TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophy. Neuromuscular Disorders. 26(8). 500–503. 29 indexed citations
3.
O’Grady, Gina, Alan Ma, Deborah A. Sival, et al.. (2016). Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related disease. European Journal of Human Genetics. 24(8). 1216–1219. 2 indexed citations
4.
O’Grady, Gina, Monkol Lek, Shireen R. Lamandé, et al.. (2016). Diagnosis and etiology of congenital muscular dystrophy: We are halfway there. Annals of Neurology. 80(1). 101–111. 49 indexed citations
5.
Cabrera‐Serrano, Macarena, Roula Ghaoui, Gianina Ravenscroft, et al.. (2015). Expanding the phenotype of GMPPB mutations. Brain. 138(4). 836–844. 43 indexed citations
6.
Ghaoui, Roula, Sandra T. Cooper, Monkol Lek, et al.. (2015). Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy. JAMA Neurology. 72(12). 1424–1424. 142 indexed citations
7.
Menezes, Manoj P., Leigh B. Waddell, Guy M. Lenk, et al.. (2014). Whole exome sequencing identifies three recessive FIG4 mutations in an apparently dominant pedigree with Charcot–Marie–Tooth disease. Neuromuscular Disorders. 24(8). 666–670. 11 indexed citations
8.
Clarke, Nigel F., Kimberly Amburgey, James W. Teener, et al.. (2013). A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathies. Neuromuscular Disorders. 23(5). 432–436. 29 indexed citations
9.
Tajsharghi, Homa, Simon Hammans, Christopher Lindberg, et al.. (2013). Recessive myosin myopathy with external ophthalmoplegia associated with MYH2 mutations. European Journal of Human Genetics. 22(6). 801–808. 28 indexed citations
10.
Tasca, Giorgio, Zagaa Odgerel, Mauro Monforte, et al.. (2012). Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late‐onset cerebellar ataxia. Muscle & Nerve. 46(2). 275–282. 22 indexed citations
11.
Clarke, Nigel F., Leigh B. Waddell, L.T.L. Sie, et al.. (2012). Mutations in TPM2 and congenital fibre type disproportion. Neuromuscular Disorders. 22(11). 955–958. 15 indexed citations
12.
Waddell, Leigh B., Monkol Lek, Melanie Bahlo, et al.. (2012). G.P.41 The identification of LGMD2G (TCAP) in Australia. Neuromuscular Disorders. 22(9-10). 831–832. 13 indexed citations
13.
Menezes, Manoj P., Leigh B. Waddell, Frances J. Evesson, et al.. (2012). Importance and challenge of making an early diagnosis in LMNA -related muscular dystrophy. Neurology. 78(16). 1258–1263. 29 indexed citations
14.
Yiu, Eppie M., Alfred Klausegger, Leigh B. Waddell, et al.. (2011). Epidermolysis bullosa with late‐onset muscular dystrophy and plectin deficiency. Muscle & Nerve. 44(1). 135–141. 10 indexed citations
15.
Waddell, Leigh B., Nicole Monnier, Sandra T. Cooper, Kathryn N. North, & Nigel F. Clarke. (2011). Using complementary DNA from MyoD‐transduced fibroblasts to sequence large muscle genes. Muscle & Nerve. 44(2). 280–282. 4 indexed citations
16.
Yiu, Eppie M., Alfred Klausegger, Leigh B. Waddell, et al.. (2010). 59. Epidermolysis bullosa with late-onset muscular dystrophy and plectin deficiency. Journal of Clinical Neuroscience. 17(12). 1628–1628. 1 indexed citations
17.
Waddell, Leigh B., Andrew J. Kornberg, Paul Kennedy, et al.. (2010). Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3. Neuromuscular Disorders. 20(7). 464–466. 17 indexed citations
18.
Clarke, Nigel F., Leigh B. Waddell, Sandra T. Cooper, et al.. (2010). Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion. Human Mutation. 31(7). E1544–E1550. 126 indexed citations
19.
Clarke, Nigel F., Ana Domazetovska, Leigh B. Waddell, et al.. (2009). Cap disease due to mutation of the beta-tropomyosin gene (TPM2). Neuromuscular Disorders. 19(5). 348–351. 31 indexed citations
20.
Clarke, Nigel F., Nicole Monnier, R. L. Smith, et al.. (2009). G.P.1.05 RYR1 is a common cause of congenital fibre type disproportion with ptosis, ophthalmoplegia, scoliosis and pronounced axial muscle weakness. Neuromuscular Disorders. 19(8-9). 557–557. 1 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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