Maria Kinali

5.2k total citations
57 papers, 2.4k citations indexed

About

Maria Kinali is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Maria Kinali has authored 57 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 10 papers in Genetics and 9 papers in Physiology. Recurrent topics in Maria Kinali's work include Muscle Physiology and Disorders (24 papers), Nuclear Structure and Function (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Maria Kinali is often cited by papers focused on Muscle Physiology and Disorders (24 papers), Nuclear Structure and Function (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Maria Kinali collaborates with scholars based in United Kingdom, Italy and France. Maria Kinali's co-authors include Eugenio Mercuri, Francesco Muntoni, Francesco Muntoni, A. Manzur, Marion Main, Sonia Messina, Caroline A. Sewry, Marika Pane, A. Aloysius and Heinz Jungbluth and has published in prestigious journals such as Brain, Neurology and Archives of Disease in Childhood.

In The Last Decade

Maria Kinali

54 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maria Kinali United Kingdom 31 1.8k 539 392 344 338 57 2.4k
Nicolas Deconinck Belgium 25 2.2k 1.2× 626 1.2× 336 0.9× 422 1.2× 403 1.2× 91 3.0k
Adnan Y. Manzur United Kingdom 26 1.5k 0.9× 535 1.0× 528 1.3× 151 0.4× 351 1.0× 63 2.1k
Michela Guglieri United Kingdom 31 2.8k 1.6× 813 1.5× 623 1.6× 424 1.2× 430 1.3× 104 3.5k
Carolyn M. Constantin United States 7 1.9k 1.1× 529 1.0× 483 1.2× 161 0.5× 223 0.7× 11 2.4k
Diana M. Escolar United States 20 1.5k 0.8× 288 0.5× 326 0.8× 168 0.5× 241 0.7× 49 2.0k
Martin K. Childers United States 32 1.3k 0.7× 278 0.5× 365 0.9× 219 0.6× 366 1.1× 97 2.9k
Wendy King United States 27 2.5k 1.4× 828 1.5× 529 1.3× 324 0.9× 602 1.8× 45 3.8k
Richard Roxburgh New Zealand 25 1.9k 1.1× 412 0.8× 384 1.0× 264 0.8× 1.3k 3.8× 78 3.0k
Lindsay N. Alfano United States 21 1.6k 0.9× 907 1.7× 338 0.9× 541 1.6× 136 0.4× 88 2.3k
L. Signore United States 10 1.4k 0.8× 410 0.8× 225 0.6× 171 0.5× 222 0.7× 10 1.9k

Countries citing papers authored by Maria Kinali

Since Specialization
Citations

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

Fields of papers citing papers by Maria Kinali

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Kinali

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Kinali. A scholar is included among the top collaborators of Maria Kinali 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 Maria Kinali. Maria Kinali 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.
Martello, Elisa, Emma Wilson, Joanne R Morling, et al.. (2025). Systematic Review Suggests Nutraceuticals Containing Vitamin B2 Could Provide an Alternative Treatment for Paediatric Migraines. Acta Paediatrica. 114(10). 2443–2457.
2.
Topriceanu, Constantin‐Cristian, et al.. (2021). Machine learning with neuroimaging data to identify autism spectrum disorder: a systematic review and meta-analysis. Neuroradiology. 63(12). 2057–2072. 15 indexed citations
3.
Benger, Matthew, Maria Kinali, & Nicholas D. Mazarakis. (2018). Autism spectrum disorder: prospects for treatment using gene therapy. Molecular Autism. 9(1). 39–39. 43 indexed citations
4.
Pavlidou, Efterpi, Vincenzo Salpietro, Rahul Phadke, et al.. (2016). Pontocerebellar hypoplasia type 2D and optic nerve atrophy further expand the spectrum associated with selenoprotein biosynthesis deficiency. European Journal of Paediatric Neurology. 20(3). 483–488. 30 indexed citations
5.
Steel, Dora, Vincenzo Salpietro, Rahul Phadke, et al.. (2015). Whole exome sequencing reveals a MLL de novo mutation associated with mild developmental delay and without ‘hairy elbows’: expanding the phenotype of Wiedemann–Steiner syndrome. Journal of Genetics. 94(4). 755–758. 20 indexed citations
6.
Read, Joy, Anita K. Simonds, Maria Kinali, Francesco Muntoni, & M. Elena Garralda. (2010). Sleep and well-being in young men with neuromuscular disorders receiving non-invasive ventilation and their carers. Neuromuscular Disorders. 20(7). 458–463. 21 indexed citations
7.
Arechavala‐Gomeza, Virginia, Maria Kinali, L. Feng, et al.. (2009). Immunohistological intensity measurements as a tool to assess sarcolemma‐associated protein expression. Neuropathology and Applied Neurobiology. 36(4). 265–274. 66 indexed citations
8.
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
9.
Clement, Emma, E. Mercuri, Mary Rutherford, et al.. (2007). C.P.3.06 Spectrum of brain changes and genotype-phenotype correlations in secondary dystroglycanopathies. Neuromuscular Disorders. 17(9-10). 871–871. 1 indexed citations
10.
Kinali, Maria, et al.. (2007). G.P.9.05 The role of ACE inhibitor therapy in presymptomatic cardiomyopathy in Duchenne muscular dystrophy. Neuromuscular Disorders. 17(9-10). 816–816. 1 indexed citations
11.
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
12.
Hartley, Louise, Maria Kinali, Ravi Knight, et al.. (2007). A congenital myopathy with diaphragmatic weakness not linked to the SMARD1 locus. Neuromuscular Disorders. 17(2). 174–179. 20 indexed citations
13.
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
14.
Kinali, Maria, Heinz Jungbluth, L. H. Eunson, et al.. (2004). Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia. Neuromuscular Disorders. 14(10). 689–693. 43 indexed citations
15.
Mercuri, Eugenio, Maja Poppe, Rosaline C. M. Quinlivan, et al.. (2004). Extreme Variability of Phenotype in Patients With an Identical Missense Mutation in the Lamin A/C Gene. Archives of Neurology. 61(5). 690–690. 85 indexed citations
16.
Mercuri, Eugenio, C. Cini, Anna Pichiecchio, et al.. (2003). Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype. Neuromuscular Disorders. 13(7-8). 554–558. 57 indexed citations
17.
McDonald, Denise, Maria Kinali, Andrew Gallagher, et al.. (2002). Fracture prevalence in Duchenne muscular dystrophy. Developmental Medicine & Child Neurology. 44(10). 695–698. 114 indexed citations
18.
Mercuri, Eugenio, Serena J. Counsell, Joanna Allsop, et al.. (2002). Selective Muscle Involvement on Magnetic Resonance Imaging in Autosomal Dominant Emery-Dreifuss Muscular Dystrophy. Neuropediatrics. 33(1). 10–14. 73 indexed citations
19.
Kinali, Maria, Eugenio Mercuri, Marion Main, Francesco Muntoni, & Victor Dubowitz. (2002). An effective, low-dosage, intermittent schedule of prednisolone in the long-term treatment of early cases of Duchenne dystrophy. Neuromuscular Disorders. 12. S169–S174. 49 indexed citations
20.
Dubowitz, Victor, Maria Kinali, Marion Main, Eugenio Mercuri, & Francesco Muntoni. (2002). Remission of clinical signs in early Duchenne muscular dystrophy on intermittent low-dosage prednisolone therapy. European Journal of Paediatric Neurology. 6(3). 153–159. 34 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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