Charu Deshpande

8.0k total citations · 1 hit paper
24 papers, 1.1k citations indexed

About

Charu Deshpande is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Charu Deshpande has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Surgery. Recurrent topics in Charu Deshpande's work include Mitochondrial Function and Pathology (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA modifications and cancer (3 papers). Charu Deshpande is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA modifications and cancer (3 papers). Charu Deshpande collaborates with scholars based in United Kingdom, United States and Germany. Charu Deshpande's co-authors include P.M. Shah, Praful Dalal, Michael A. Simpson, Richard C. Trembath, Dimitra Dafou, Wesley J. Woollard, Wendy D. Jones, Frances Elmslie, Muriel Holder‐Espinasse and Sarah Smithson and has published in prestigious journals such as The Lancet, JAMA and PLoS ONE.

In The Last Decade

Charu Deshpande

23 papers receiving 1.0k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

CEREBRAL EMBOLISM

1965 458 citations Praful Dalal, P.M. Shah et al. The Lancet profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Charu Deshpande United Kingdom	13	436	344	127	122	105	24	1.1k
Maria Piccione Italy	21	408 0.9×	384 1.1×	90 0.7×	192 1.6×	40 0.4×	78	1.0k
Salvatore Savasta Italy	23	542 1.2×	366 1.1×	110 0.9×	182 1.5×	286 2.7×	120	1.6k
Raphael David United States	21	282 0.6×	170 0.5×	82 0.6×	149 1.2×	74 0.7×	52	1.2k
Neil Stoodley United Kingdom	17	328 0.8×	185 0.5×	78 0.6×	451 3.7×	158 1.5×	39	1.2k
Alison Gardner Australia	17	799 1.8×	569 1.7×	143 1.1×	194 1.6×	54 0.5×	30	1.6k
Anke Lux Germany	21	446 1.0×	121 0.4×	105 0.8×	70 0.6×	58 0.6×	62	1.1k
Che‐Sheng Ho Taiwan	17	170 0.4×	116 0.3×	172 1.4×	215 1.8×	47 0.4×	56	789
Michael Harbord Australia	19	354 0.8×	424 1.2×	89 0.7×	227 1.9×	57 0.5×	49	1.1k
Aravindhan Veerapandiyan United States	16	389 0.9×	163 0.5×	62 0.5×	73 0.6×	111 1.1×	72	775
Padraic J. Grattan‐Smith Australia	22	324 0.7×	189 0.5×	134 1.1×	115 0.9×	452 4.3×	60	1.5k

Countries citing papers authored by Charu Deshpande

Since Specialization

Citations

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

Fields of papers citing papers by Charu Deshpande

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charu Deshpande

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

Marmarelis, Melina E., Cindy McGrath, Jacquelyn J. Roth, et al.. (2024). Brief Report: Impact of Reflex Testing on Tissue-Based Molecular Genotyping in Patients With Advanced Non-Squamous Non-Small Cell Lung Cancer. Clinical Lung Cancer. 25(3). 262–265.e2. 1 indexed citations

Marquez, Jonathan, Nina Mann, Engin Deniz, et al.. (2020). DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes. Journal of Medical Genetics. 58(7). 453–464. 10 indexed citations

Henderson, Robert, Sahar Mansour, Charu Deshpande, et al.. (2020). Expanding the phenotypic spectrum consequent upon de novo WDR37 missense variants. Clinical Genetics. 98(2). 191–197. 8 indexed citations

Giri, Dinesh, Detlef Böckenhauer, Charu Deshpande, et al.. (2020). Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB Mutations. Hormone Research in Paediatrics. 93(2). 137–142. 2 indexed citations

Ardıçlı, Didem, Anna Sárközy, Irina Zaharieva, et al.. (2019). A novel case of MSTO1 gene related congenital muscular dystrophy with progressive neurological involvement. Neuromuscular Disorders. 29(6). 448–455. 8 indexed citations

Taylor, Rachel L., Mark T. Handley, Sarah Waller, et al.. (2017). Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature. Investigative Ophthalmology & Visual Science. 58(1). 594–594. 24 indexed citations

Balasubramanian, Meena, Josh Willoughby, Andrew E. Fry, et al.. (2017). Delineating the phenotypic spectrum of Bainbridge-Ropers syndrome: 12 new patients with de novo, heterozygous, loss-of-function mutations in ASXL3 and review of published literature. Journal of Medical Genetics. 54(8). 537–543. 44 indexed citations

Fratter, Carl, Eszter Dombi, Janet Carver, et al.. (2017). Mitochondrial disease and lipid storage myopathy due to mutation in CHCHD10 or DNM1L and disordered mitochondrial dynamics. Neuromuscular Disorders. 27. S21–S21. 1 indexed citations

Thompson, Kyle, Inês A. Barbosa, Langping He, et al.. (2017). Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits. Neurogenetics. 18(4). 227–235. 12 indexed citations

10.

Blanchet, Patricia, Martina Bebin, Gregory M. Cooper, et al.. (2017). MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus. PLoS Genetics. 13(8). e1006957–e1006957. 49 indexed citations

11.

Oláhová, Monika, Kyle Thompson, Steven Hardy, et al.. (2016). Pathogenic variants in HTRA2 cause an early‐onset mitochondrial syndrome associated with 3‐methylglutaconic aciduria. Journal of Inherited Metabolic Disease. 40(1). 121–130. 23 indexed citations

12.

Schottmann, Gudrun, Heinz Jungbluth, Ulrike Schara, et al.. (2015). Recessive truncating IGHMBP2 mutations presenting as axonal sensorimotor neuropathy. Neurology. 84(5). 523–531. 27 indexed citations

13.

Simpson, Michael A., Charu Deshpande, Dimitra Dafou, et al.. (2012). De Novo Mutations of the Gene Encoding the Histone Acetyltransferase KAT6B Cause Genitopatellar Syndrome. The American Journal of Human Genetics. 90(2). 290–294. 72 indexed citations

14.

Jones, Wendy D., Dimitra Dafou, Meriel McEntagart, et al.. (2012). De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome. The American Journal of Human Genetics. 91(2). 358–364. 187 indexed citations

15.

Chandra, Aman, José Antonio Aragon-Martin, Sabiha Gati, et al.. (2012). A Genotype-Phenotype Comparison ofADAMTSL4andFBN1in Isolated Ectopia Lentis. Investigative Ophthalmology & Visual Science. 53(8). 4889–4889. 46 indexed citations

16.

Vilboux, Thierry, Carla Ciccone, Jan Blancato, et al.. (2011). Molecular Analysis of the Retinoic Acid Induced 1 Gene (RAI1) in Patients with Suspected Smith-Magenis Syndrome without the 17p11.2 Deletion. PLoS ONE. 6(8). e22861–e22861. 31 indexed citations

17.

Shilo, Konstantin, Charu Deshpande, İrem Hicran Özbudak, et al.. (2010). Diffuse Thymic Fibrosis. The American Journal of Surgical Pathology. 34(2). 211–215. 3 indexed citations

18.

Deshpande, Charu & Raoul C. M. Hennekam. (2008). Genetic syndromes and prenatally detected renal anomalies. Seminars in Fetal and Neonatal Medicine. 13(3). 171–180. 21 indexed citations

19.

Dalal, Praful, et al.. (1965). CEREBRAL EMBOLISM. The Lancet. 285(7376). 61–64. 458 indexed citations breakdown →

20.

Chitnis, V, Suman Thakur, & Charu Deshpande. (1963). Endometrial Stromal Sarcoma. JAMA. 183(12). 173–173. 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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