Mridul Johari

1.2k total citations
28 papers, 194 citations indexed

About

Mridul Johari is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Mridul Johari has authored 28 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 12 papers in Cardiology and Cardiovascular Medicine and 7 papers in Genetics. Recurrent topics in Mridul Johari's work include Cardiomyopathy and Myosin Studies (12 papers), Muscle Physiology and Disorders (11 papers) and Genomics and Rare Diseases (5 papers). Mridul Johari is often cited by papers focused on Cardiomyopathy and Myosin Studies (12 papers), Muscle Physiology and Disorders (11 papers) and Genomics and Rare Diseases (5 papers). Mridul Johari collaborates with scholars based in Finland, Australia and Italy. Mridul Johari's co-authors include Marco Savarese, Peter Hackman, Bjarne Udd, Per Harald Jonson, Anna Vihola, J. Sarparanta, Bjarne Udd, Svetlana Konovalova, Henna Tyynismaa and L. Pajunen and has published in prestigious journals such as Neurology, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Mridul Johari

24 papers receiving 194 citations

Peers

Mridul Johari

CCM

CMN

GENET

EPIDE

Irene Colombo Italy

О. П. Рыжкова Russia

C. Bönnemann United States

Mark Screen Finland

Giuseppina Di Fruscio Italy

Marius Kuhn Germany

Ara Kaprelyan Bulgaria

M. Leach United States

Giovanni Marrosu Italy

Irene Colombo Italy

Mridul Johari

155 ×1.2

63 ×1.0

CCM

30 ×0.6

CMN

53 ×1.4

GENET

8 ×0.3

EPIDE

Citations per year, relative to Mridul Johari Mridul Johari (= 1×) peers Irene Colombo

Countries citing papers authored by Mridul Johari

Since Specialization

Citations

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

Fields of papers citing papers by Mridul Johari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mridul Johari

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

Jokela, Manu, Sanna Huovinen, Cornelia Kornblum, et al.. (2025). Characterization of novel CASQ1 variants in two families with unusual phenotypic features. Journal of Neurology. 272(12). 789–789.

Božović, Ivana Babič, Annalaura Torella, Mridul Johari, et al.. (2025). Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohort. Journal of Medical Genetics. 62(5). 350–357. 1 indexed citations

Johari, Mridul, Ozan Özışık, Peter A.C. ’t Hoen, et al.. (2025). Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression. Orphanet Journal of Rare Diseases. 20(1). 27–27. 1 indexed citations

Patil, Asawari, et al.. (2025). 535 Clinicopathological Spectrum of High-Grade Follicular Cell-Derived Non-Anaplastic Thyroid Carcinoma: A Series of 106 Cases. Laboratory Investigation. 105(3). 102765–102765. 1 indexed citations

Oghabian, Ali, Per Harald Jonson, Mridul Johari, et al.. (2025). OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development. Skeletal Muscle. 15(1). 5–5. 2 indexed citations

Clayton, Joshua S., Mridul Johari, Rhonda L. Taylor, et al.. (2024). An Update on Reported Variants in the Skeletal Muscle α‐Actin (ACTA1) Gene. Human Mutation. 2024(1). 6496088–6496088. 4 indexed citations

Zhong, Huahua, Mridul Johari, Shintaro Katayama, et al.. (2024). Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions. Communications Biology. 7(1). 438–438. 2 indexed citations

Johari, Mridul, et al.. (2024). Termination of pregnancy for fetal malformations and severe genetic disorders: what are the laws in Europe?. European Journal of Human Genetics. 33(2). 151–153.

Johari, Mridul, Ana Töpf, Jennifer Duff, et al.. (2024). Loss-of-function variants in JPH1 cause congenital myopathy with prominent facial and ocular involvement. Journal of Medical Genetics. 61(10). 992–998.

10.

Sulonen, Anna-Maija, Henrikki Almusa, Vilma‐Lotta Lehtokari, et al.. (2024). Haplotype information of large neuromuscular disease genes provided by linked-read sequencing has a potential to increase diagnostic yield. Scientific Reports. 14(1). 4306–4306.

11.

Sarparanta, J., Per Harald Jonson, Jens Reimann, et al.. (2023). Extension of the DNAJB2a isoform in a dominant neuromyopathy family. Human Molecular Genetics. 32(21). 3029–3039. 4 indexed citations

12.

Pelin, Katarina, K. Kiiski, Olli Tynninen, et al.. (2023). Novel Compound Heterozygous Splice-Site Variants in TPM3 Revealed by RNA Sequencing in a Patient with an Unusual Form of Nemaline Myopathy: A Case Report. Journal of Neuromuscular Diseases. 10(5). 977–984. 2 indexed citations

13.

Johari, Mridul, Anna Vihola, Johanna Palmio, et al.. (2022). Comprehensive transcriptomic analysis shows disturbed calcium homeostasis and deregulation of T lymphocyte apoptosis in inclusion body myositis. Journal of Neurology. 269(8). 4161–4173. 14 indexed citations

14.

Olivé, Montse, Cristina Domínguez‐González, Mridul Johari, et al.. (2022). Mutation update for the ACTN2 gene. Human Mutation. 43(12). 1745–1756. 15 indexed citations

15.

Johari, Mridul, George K. Papadimas, Constantinos Papadopoulos, et al.. (2022). Adult‐onset dominant muscular dystrophy in Greek families caused by Annexin A11. Annals of Clinical and Translational Neurology. 9(10). 1660–1667. 12 indexed citations

16.

Savarese, Marco, Anna Vihola, Manu Jokela, et al.. (2021). Out-of-Frame Mutations in ACTN2 Last Exon Cause a Dominant Distal Myopathy With Facial Weakness. Neurology Genetics. 7(5). e619–e619. 7 indexed citations

17.

Savarese, Marco, et al.. (2020). Is Gene-Size an Issue for the Diagnosis of Skeletal Muscle Disorders?. Journal of Neuromuscular Diseases. 7(3). 203–216. 7 indexed citations

18.

Jokela, Manu, Giorgio Tasca, Anna Vihola, et al.. (2019). An unusual ryanodine receptor 1 (RYR1) phenotype. Neurology. 92(14). e1600–e1609. 12 indexed citations

19.

Berardo, Andrés, Xavière Lornage, Mridul Johari, et al.. (2019). HNRNPDL-related muscular dystrophy: expanding the clinical, morphological and MRI phenotypes. Journal of Neurology. 266(10). 2524–2534. 19 indexed citations

20.

Johari, Mridul, Meharji Arumilli, Johanna Palmio, et al.. (2017). Association study reveals novel risk loci for sporadic inclusion body myositis. European Journal of Neurology. 24(4). 572–577. 9 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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