A. Manzur

1.8k total citations
28 papers, 856 citations indexed

About

A. Manzur is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, A. Manzur has authored 28 papers receiving a total of 856 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 6 papers in Surgery and 5 papers in Genetics. Recurrent topics in A. Manzur's work include Muscle Physiology and Disorders (17 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Cardiomyopathy and Myosin Studies (5 papers). A. Manzur is often cited by papers focused on Muscle Physiology and Disorders (17 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Cardiomyopathy and Myosin Studies (5 papers). A. Manzur collaborates with scholars based in United Kingdom, Italy and Finland. A. Manzur's co-authors include Maria Kinali, Francesco Muntoni, Eugenio Mercuri, Francesco Muntoni, Caroline A. Sewry, Victor Dubowitz, Heinz Jungbluth, S. Brown, Sonia Messina and G. Edge and has published in prestigious journals such as Neurology, Archives of Disease in Childhood and Developmental Medicine & Child Neurology.

In The Last Decade

A. Manzur

27 papers receiving 846 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Manzur United Kingdom 13 649 292 221 119 118 28 856
Luigia Passamano Italy 11 645 1.0× 336 1.2× 153 0.7× 71 0.6× 56 0.5× 28 794
Justin Robison United States 6 680 1.0× 142 0.5× 229 1.0× 92 0.8× 81 0.7× 8 905
L. Feng United Kingdom 13 674 1.0× 254 0.9× 187 0.8× 52 0.4× 122 1.0× 19 795
Marina Pedemonte Italy 21 1.0k 1.6× 176 0.6× 243 1.1× 169 1.4× 214 1.8× 57 1.3k
Madoka Mori‐Yoshimura Japan 18 522 0.8× 213 0.7× 168 0.8× 45 0.4× 109 0.9× 87 881
Gerardo Nigro Italy 14 517 0.8× 358 1.2× 132 0.6× 67 0.6× 33 0.3× 41 854
L.I. Comi Italy 11 975 1.5× 649 2.2× 125 0.6× 84 0.7× 71 0.6× 16 1.1k
G.W. Padberg Netherlands 16 784 1.2× 247 0.8× 169 0.8× 60 0.5× 54 0.5× 22 1.0k
Tina Duong United States 14 691 1.1× 151 0.5× 316 1.4× 155 1.3× 48 0.4× 60 945
Julia R. Dahlqvist Denmark 17 537 0.8× 209 0.7× 165 0.7× 86 0.7× 49 0.4× 35 797

Countries citing papers authored by A. Manzur

Since Specialization
Citations

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

Fields of papers citing papers by A. Manzur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Manzur

This figure shows the co-authorship network connecting the top 25 collaborators of A. Manzur. A scholar is included among the top collaborators of A. Manzur 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 A. Manzur. A. Manzur 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.
Muntoni, Francesco, et al.. (2018). DUCHENNE MUSCULAR DYSTROPHY - PHYSIOTHERAPY. Neuromuscular Disorders. 28. S121–S121. 2 indexed citations
2.
Ricotti, Valeria, A. Manzur, E. Scott, & Francesco Muntoni. (2011). 2FC2.6 Benefits and adverse effects of glucocorticoids in boys with Duchenne Muscular Dystrophy: A UK perspective. European Journal of Paediatric Neurology. 15. S21–S21. 2 indexed citations
3.
4.
Nadeau, Amélie, Maria Kinali, Marion Main, et al.. (2009). Natural history of Ullrich congenital muscular dystrophy. Neurology. 73(1). 25–31. 107 indexed citations
5.
Manzur, A., Maria Kinali, & Francesco Muntoni. (2008). Update on the management of Duchenne muscular dystrophy. Archives of Disease in Childhood. 93(11). 986–990. 114 indexed citations
6.
Jimenez‐Mallebrera, C., Haiyan Zhou, A. Manzur, et al.. (2007). C.P.4.16 Core myopathy without mutations in RYR1 or SEPN1 genes. Neuromuscular Disorders. 17(9-10). 883–883. 1 indexed citations
7.
Kinali, Maria, R. H. Robinson, A. Manzur, Christine Burren, & S. Robb. (2007). Backache in a Duchenne boy. Neuromuscular Disorders. 17(4). 346–348. 1 indexed citations
8.
Kinali, Maria, Marion Main, Joseph Eliahoo, et al.. (2007). Predictive factors for the development of scoliosis in Duchenne muscular dystrophy. European Journal of Paediatric Neurology. 11(3). 160–166. 56 indexed citations
9.
Kinali, Maria, Sonia Messina, Eugenio Mercuri, et al.. (2006). Management of scoliosis in Duchenne muscular dystrophy: a large 10-year retrospective study. Developmental Medicine & Child Neurology. 48(6). 513–513. 58 indexed citations
10.
Kinali, Maria, A. Manzur, Eugenio Mercuri, et al.. (2006). UK physicians’ attitudes and practices in long-term non-invasive ventilation of Duchenne Muscular Dystrophy. Pediatric Rehabilitation. 9(4). 351–364. 21 indexed citations
11.
Kinali, Maria, Linda M. Banks, Eugenio Mercuri, A. Manzur, & F. Muntoni. (2004). Bone Mineral Density in a Paediatric Spinal Muscular Atrophy Population. Neuropediatrics. 35(6). 325–328. 38 indexed citations
12.
Jungbluth, Heinz, C. R. Müller, B. Halliger–Keller, et al.. (2002). Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores. Neurology. 59(2). 284–287. 114 indexed citations
13.
Jungbluth, Heinz, Caroline A. Sewry, S. Brown, et al.. (2001). Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle α-actin (ACTA1) gene. Neuromuscular Disorders. 11(1). 35–40. 78 indexed citations
14.
Sewry, Caroline A., S. Brown, Katarina Pelin, et al.. (2001). Abnormalities in the expression of nebulin in chromosome-2 linked nemaline myopathy. Neuromuscular Disorders. 11(2). 146–153. 36 indexed citations
15.
Jungbluth, Heinz, Mark I. Rees, A. Manzur, et al.. (2000). An unusual case of hyperekplexia. European Journal of Paediatric Neurology. 4(2). 77–80. 7 indexed citations
16.
Mercuri, Eugenio, Caroline A. Sewry, S. Brown, et al.. (2000). Congenital Muscular Dystrophy with Secondary Merosin Deficiency and Normal Brain MRI: A Novel Entity?. Neuropediatrics. 31(4). 186–189. 12 indexed citations
17.
Mercuri, Eugenio, A. Manzur, Heinz Jungbluth, et al.. (2000). Early and severe presentation of autosomal dominant Emery-Dreifuss muscular dystrophy (EMD2). Neurology. 54(8). 1704–1705. 12 indexed citations
18.
Manzur, A., et al.. (1998). A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance. Neuromuscular Disorders. 8(7). 467–473. 30 indexed citations
19.
Naom, Isam, Mariella D’Alessandro, Caroline A. Sewry, et al.. (1998). Laminin α2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy. Neuromuscular Disorders. 8(7). 495–501. 43 indexed citations
20.
Hodgson, Shirley, Stephen Abbs, A. Manzur, et al.. (1992). Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability. Neuromuscular Disorders. 2(4). 269–276. 45 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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