M. Leach

718 total citations
21 papers, 187 citations indexed

About

M. Leach is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, M. Leach has authored 21 papers receiving a total of 187 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in M. Leach's work include Muscle Physiology and Disorders (12 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Cardiomyopathy and Myosin Studies (4 papers). M. Leach is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Neurogenetic and Muscular Disorders Research (9 papers) and Cardiomyopathy and Myosin Studies (4 papers). M. Leach collaborates with scholars based in United States, France and United Kingdom. M. Leach's co-authors include Carsten G. Bönnemann, Sandra Donkervoort, Payam Mohassel, Diana Bharucha‐Goebel, Ying Hu, David Nguyen, Yaqun Zou, Jahannaz Dastgir, Katherine G. Meilleur and Juliana Gurgel‐Giannetti and has published in prestigious journals such as Blood, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

M. Leach

19 papers receiving 187 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Leach United States	8	92	54	34	29	28	21	187
Caterina Marconi Italy	8	86 0.9×	38 0.7×	39 1.1×	19 0.7×	47 1.7×	18	243
C. Bönnemann United States	8	123 1.3×	51 0.9×	39 1.1×	26 0.9×	34 1.2×	24	178
Nicole P. Safina United States	6	111 1.2×	20 0.4×	36 1.1×	12 0.4×	66 2.4×	7	174
Luca Pradotto Italy	11	157 1.7×	42 0.8×	18 0.5×	32 1.1×	33 1.2×	21	283
Alasdair J. Wood Australia	9	200 2.2×	29 0.5×	14 0.4×	63 2.2×	18 0.6×	18	305
Kristina Martens Canada	11	83 0.9×	35 0.6×	29 0.9×	23 0.8×	10 0.4×	16	264
Batoul Baz Saudi Arabia	10	124 1.3×	15 0.3×	30 0.9×	28 1.0×	68 2.4×	19	273
Marius Kuhn Germany	10	107 1.2×	37 0.7×	50 1.5×	7 0.2×	34 1.2×	16	207
Debora Pehl Germany	10	106 1.2×	22 0.4×	47 1.4×	16 0.6×	6 0.2×	15	321

Countries citing papers authored by M. Leach

Since Specialization

Citations

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

Fields of papers citing papers by M. Leach

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Leach

This figure shows the co-authorship network connecting the top 25 collaborators of M. Leach. A scholar is included among the top collaborators of M. Leach 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 M. Leach. M. Leach 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

Hayes, Leslie H., Sarah Neuhaus, Sandra Donkervoort, et al.. (2024). Taking on the Titin: Muscle imaging as a diagnostic marker of biallelic TTN- related myopathy. Journal of Neuromuscular Diseases. 11(6). 1211–1220. 1 indexed citations

Hayes, Leslie H., Payam Mohassel, Gina Norato, et al.. (2020). Hypoglycemia in patients with congenital muscle disease. BMC Pediatrics. 20(1). 57–57. 8 indexed citations

Ball, Laura J., et al.. (2019). Communication skills among children with spinal muscular atrophy type 1: A parent survey. Assistive Technology. 33(1). 38–48. 16 indexed citations

Zou, Yaqun, Sandra Donkervoort, Antti M. Salo, et al.. (2017). P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye. Human Molecular Genetics. 26(12). 2207–2217. 33 indexed citations

Donkervoort, Sandra, H.S. Chan, Leslie H. Hayes, et al.. (2017). Cytoplasmic body pathology in severe ACTA1-related myopathy in the absence of typical nemaline rods. Neuromuscular Disorders. 27(6). 531–536. 11 indexed citations

Leach, M., A. Reghan Foley, Yuzheng Hu, et al.. (2017). Congenital muscular dystrophy ascending multiple dose cohort study analyzing pharmacokinetics at three dose levels in children and adolescents with assessment of safety and tolerability of omigapil (CALLISTO) trial update. Neuromuscular Disorders. 27. S107–S107. 2 indexed citations

Jain, Minal, Katherine G. Meilleur, Tianxia Wu, et al.. (2017). Electrical impedance myography in individuals with collagen 6 and laminin α‐2 congenital muscular dystrophy: a cross‐sectional and 2‐year analysis. Muscle & Nerve. 57(1). 54–60. 11 indexed citations

Meilleur, Katherine G., Joseph R. Fontana, Anne Rutkowski, et al.. (2017). Comparison of sitting and supine forced vital capacity in collagen VI‐related dystrophy and laminin α2‐related dystrophy. Pediatric Pulmonology. 52(4). 524–532. 17 indexed citations

Donkervoort, Sandra, M. Leach, Payam Mohassel, et al.. (2016). Novel De Novo Mutations in KIF1A as a Cause of Hereditary Spastic Paraplegia With Progressive Central Nervous System Involvement. Journal of Child Neurology. 31(9). 1114–1119. 32 indexed citations

10.

Donkervoort, Sandra, Antti M. Salo, Aileen M. Barnes, et al.. (2016). P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye. Neuromuscular Disorders. 26. S211–S212.

11.

Bharucha‐Goebel, Diana, James J. Collins, Ying Hu, et al.. (2016). Serum biomarker discovery for congenital muscular dystrophies. Neuromuscular Disorders. 26. S189–S189.

12.

Donkervoort, Sandra, Michele Yang, M. Leach, et al.. (2015). Cardiomyopathy in patients with ACTA1-myopathy. Neuromuscular Disorders. 25. S287–S287. 1 indexed citations

13.

Vuillerot, Carole, Katherine G. Meilleur, Minal Jain, et al.. (2014). English cross-cultural translation and validation of the NM-Score: A system for motor function classification in patients with neuromuscular diseases. Annals of Physical and Rehabilitation Medicine. 57. e105–e105. 1 indexed citations

14.

Vuillerot, Carole, Katherine G. Meilleur, Minal Jain, et al.. (2014). English Cross-Cultural Translation and Validation of the Neuromuscular Score: A System for Motor Function Classification in Patients With Neuromuscular Diseases. Archives of Physical Medicine and Rehabilitation. 95(11). 2064–2070.e1. 7 indexed citations

15.

Dastgir, Jahannaz, Carole Vuillerot, David Nguyen, et al.. (2014). T.P.48. Neuromuscular Disorders. 24(9-10). 908–908. 2 indexed citations

16.

Dastgir, Jahannaz, Carole Vuillerot, Kathleen A. Harrison, et al.. (2013). P.13.9 Acoustic radiation force impulse imaging for the differentiation of muscle tissue stiffness in neuromuscular disorders. Neuromuscular Disorders. 23(9-10). 811–811. 3 indexed citations

17.

Donkervoort, Sandra, Alice B. Schindler, Carolina Tesi Rocha, et al.. (2013). ‘Double trouble’: Diagnostic challenges in Duchenne muscular dystrophy in patients with an additional hereditary skeletal dysplasia. Neuromuscular Disorders. 23(12). 955–961. 4 indexed citations

18.

Jain, Minal, M. Waite, Jahannaz Dastgir, et al.. (2013). P.10.11 Validity of the 2 min walk test as an outcome measure in individuals with CMD and other neuromuscular diseases. Neuromuscular Disorders. 23(9-10). 792–792. 1 indexed citations

19.

Foley, A. Reghan, Ying Hu, Yaqun Zou, et al.. (2010). Large genomic deletions: A novel cause of Ullrich congenital muscular dystrophy. Annals of Neurology. 69(1). 206–211. 33 indexed citations

20.

Alhaq, Anwar, et al.. (2000). Novel mutations in heterozygous factor XI deficiency and hemorrhagic tendency. Blood. 96(11). 3 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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