Manju Ghosh

2.3k total citations
47 papers, 1.1k citations indexed

About

Manju Ghosh is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Manju Ghosh has authored 47 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 9 papers in Sensory Systems and 9 papers in Genetics. Recurrent topics in Manju Ghosh's work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), RNA regulation and disease (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Manju Ghosh is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (9 papers), RNA regulation and disease (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Manju Ghosh collaborates with scholars based in India, United States and Pakistan. Manju Ghosh's co-authors include Madhulika Kabra, Shobha Broor, Thomas B. Friedman, Sheikh Riazuddin, Rakesh Lodha, Saima Riazuddin, Zubair M. Ahmed, P.S.N. Menon, Edward R. Wilcox and Tarun Singhal and has published in prestigious journals such as Annals of Surgery, The American Journal of Human Genetics and The Journal of Organic Chemistry.

In The Last Decade

Manju Ghosh

47 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manju Ghosh India 16 466 411 184 166 133 47 1.1k
Esther Vivas United States 14 179 0.4× 68 0.2× 225 1.2× 123 0.7× 45 0.3× 38 1.1k
Yi Zhong China 18 298 0.6× 154 0.4× 115 0.6× 80 0.5× 31 0.2× 47 924
Shenglan Wang China 17 310 0.7× 351 0.9× 134 0.7× 13 0.1× 83 0.6× 64 1.1k
Anita Bhandari United States 20 186 0.4× 62 0.2× 108 0.6× 99 0.6× 50 0.4× 76 1.5k
Boris Reidel United States 14 355 0.8× 107 0.3× 55 0.3× 19 0.1× 40 0.3× 20 774
Marilyn D. Farber United States 22 491 1.1× 34 0.1× 139 0.8× 28 0.2× 50 0.4× 35 1.6k
Juan Sabater United States 19 408 0.9× 49 0.1× 71 0.4× 9 0.1× 78 0.6× 45 1.4k
Karen Uray United States 19 487 1.0× 18 0.0× 88 0.5× 66 0.4× 42 0.3× 57 1.3k
Li G China 13 198 0.4× 28 0.1× 62 0.3× 31 0.2× 58 0.4× 175 632
Safarina G. Malik Indonesia 15 278 0.6× 60 0.1× 59 0.3× 25 0.2× 110 0.8× 66 742

Countries citing papers authored by Manju Ghosh

Since Specialization
Citations

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

Fields of papers citing papers by Manju Ghosh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manju Ghosh

This figure shows the co-authorship network connecting the top 25 collaborators of Manju Ghosh. A scholar is included among the top collaborators of Manju Ghosh 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 Manju Ghosh. Manju Ghosh 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.
Gupta, Neerja, Kees E. P. van Roozendaal, Savita Sapra, et al.. (2020). Spectrum of MECP2 mutations in Indian females with Rett Syndrome - a large cohort study. Research Publications (Maastricht University). 3 indexed citations
2.
Singh, Pawan Kumar, Manju Ghosh, Shipra Sharma, et al.. (2017). Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India. The Indian Journal of Medical Research. 145(4). 492–497. 5 indexed citations
3.
Sharma, Pankaj, Neerja Gupta, Shubha R. Phadke, et al.. (2015). Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in India. Cytogenetic and Genome Research. 146(3). 187–194. 5 indexed citations
4.
Jain, Kajal, Trilochan Mohapatra, Prasenjit Das, et al.. (2014). Sequential Occurrence of Preneoplastic Lesions and Accumulation of Loss of Heterozygosity in Patients With Gallbladder Stones Suggest Causal Association With Gallbladder Cancer. Annals of Surgery. 260(6). 1073–1080. 35 indexed citations
5.
Ghosh, Manju, Shipra Sharma, Shivaram Shastri, et al.. (2012). Norrie Disease: First Mutation Report and Prenatal Diagnosis in an Indian Family. The Indian Journal of Pediatrics. 79(11). 1529–1531. 3 indexed citations
6.
Gupta, Neerja, et al.. (2012). Brachytelephalangic chondrodysplasia punctata. Clinical Dysmorphology. 21(3). 113–117. 3 indexed citations
7.
Gupta, Neerja, Manju Ghosh, Manoj Kumar, et al.. (2010). Molecular and structural analysis of metachromatic leukodystrophy patients in Indian population. Journal of the Neurological Sciences. 301(1-2). 38–45. 17 indexed citations
8.
Sapra, Savita, Manju Ghosh, Neerja Gupta, et al.. (2009). Rapid Detection of Deletions in Hotspot C-Terminal Segment Region of MECP2 by Routine PCR Method: Report of Two Classical Rett Syndrome Patients of Indian Origin. Genetic Testing and Molecular Biomarkers. 13(2). 277–280. 4 indexed citations
9.
Ahmed, Zubair M., Özgül M. Alper, Güven Lüleci, et al.. (2007). Mutational spectrum ofMYO15A: the large N-terminal extension of myosin XVA is required for hearing. Human Mutation. 28(10). 1014–1019. 68 indexed citations
10.
Riazuddin, Saima, Shaheen N. Khan, Zubair M. Ahmed, et al.. (2005). Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness. The American Journal of Human Genetics. 78(1). 137–143. 76 indexed citations
11.
Ghosh, Manju, et al.. (2005). In vivo assessment of toxicity and pharmacokinetics of methylglyoxal. Toxicology and Applied Pharmacology. 212(1). 45–58. 62 indexed citations
12.
Kabra, Sushil Kumar, et al.. (2004). Can we identify acute severe viral lower respiratory tract infection clinically?. PubMed. 41(3). 245–9. 10 indexed citations
13.
Ghosh, Manju, et al.. (2004). Genetics of deafness in India. The Indian Journal of Pediatrics. 71(6). 531–533. 10 indexed citations
14.
Kabra, S. K., et al.. (2003). Etiology of acute lower respiratory tract infection. The Indian Journal of Pediatrics. 70(1). 33–36. 30 indexed citations
15.
Maheshwari, M., et al.. (2003). Screening of families with autosomal recessive non‐syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario. American Journal of Medical Genetics Part A. 120A(2). 180–184. 55 indexed citations
16.
Ghosh, Manju, Saima Riazuddin, Sadaf Naz, et al.. (2001). Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome. Human Genetics. 109(5). 535–541. 94 indexed citations
17.
Kabra, Madhulika, et al.. (2000). Infantile-onset leukoencephalopathy with discrepant mild clinical course. The Indian Journal of Pediatrics. 67(10). 769–773. 6 indexed citations
18.
Broor, Shobha, et al.. (2000). Rapid detection of respiratory viruses by centrifugation enhanced cultures from children with acute lower respiratory tract infections. Journal of Clinical Virology. 16(1). 41–47. 60 indexed citations
19.
Ghosh, Manju, et al.. (1997). Evaluation of β-tethymustine, a new anticancer compound, in murine tumour models. Cancer Letters. 119(1). 7–12. 9 indexed citations
20.
Ghosh, Manju, et al.. (1994). Evaluation of toxicity of cypenhymustine, a new anticancer compound, in mice. Cancer Letters. 85(1). 65–72. 2 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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