Charu Deshpande

8.0k citations

24 papers · 1.1k indexed · 1 hit paper · h-index 13

Molecular Biology
Genetics top 5%
Epidemiology
Pediatrics, Perinatology and Child Health top 10%
Neurology top 10%

Co-authors: P.M. Shah Praful Dalal Michael A. Simpson Wesley J. Woollard Richard C. Trembath Dimitra Dafou Wendy D. Jones Frances Elmslie
Topics: Mitochondrial Function and Pathology (4 papers)Genomic variations and chromosomal abnormalities (4 papers)RNA modifications and cancer (3 papers)
Cited by: Genetics Neurology Molecular Biology
Journals: The Lancet JAMA PLoS ONE
Partner nations: United Kingdom United States Germany

In The Last Decade

Charu Deshpande

23 papers receiving 1.0k citations

Hit Papers

align trajectories

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

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

#	Work	Indexed citations
1	Brief Report: Impact of Reflex Testing on Tissue-Based Molecular Genotyping in Patients With Advanced Non-Squamous Non-Small Cell Lung Cancer 2024 ·Clinical Lung Cancer ·Melina E. Marmarelis,(unknown),Cindy McGrath,(unknown),Jacquelyn J. Roth,Michael D. Feldman,Jennifer J.D. Morrissette,Leslie A. Litzky,Charu Deshpande,Jeffrey C. Thompson,Abigail Doucette,Peter Gabriel,Lova Sun,Aditi P. Singh,Roger B. Cohen,Corey J. Langer,Erica L. Carpenter,Charu Aggarwal	1
2	Expanding the phenotypic spectrum consequent upon de novo WDR37 missense variants 2020 ·Clinical Genetics ·(unknown),Robert Henderson,Sahar Mansour,Charu Deshpande,Rachel L. Jones,(unknown),Kshitij Mankad,Rodrigo Young,Mariya Moosajee,Gavin Arno	8
3	Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of <b><i>HSD3B2</i></b> and <b><i>CLCNKB</i></b> Mutations 2020 ·Hormone Research in Paediatrics ·Dinesh Giri,Detlef Böckenhauer,Charu Deshpande,John C. Achermann,Norman Taylor,Gill Rumsby,(unknown),Senthil Senniappan,(unknown)	2
4	DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes 2020 ·Journal of Medical Genetics ·Jonathan Marquez,Nina Mann,(unknown),Engin Deniz,Weizhen Ji,Monica Konstantino,Emily K. Mis,Charu Deshpande,(unknown),(unknown),Hannah Hugo,Eugen Widmeier,Martin Konrad,Velibor Tasić,Raffaella Morotti,Júlia Baptista,Sian Ellard,Saquib A. Lakhani,Friedhelm Hildebrandt,Mustafa K. Khokha	10
5	Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature 2017 ·Investigative Ophthalmology & Visual Science ·Rachel L. Taylor,Mark T. Handley,Sarah Waller,Christopher Campbell,Jill Urquhart,Alison Meynert,Jamie M. Ellingford,Deirdre Donnelly,Gisela Wilcox,Iva Lloyd,Helen Mundy,David Fitzpatrick,Charu Deshpande,Jill Clayton‐Smith,Graeme C. Black	24
6	Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits 2017 ·Neurogenetics ·(unknown),Kyle Thompson,Inês A. Barbosa,Langping He,Charlotte L. Alston,Charu Deshpande,Michael A. Simpson,Andrew A. M. Morris,Axel Neu,Ulrike Löbel,(unknown),Holger Prokisch,Tobias B. Haack,Maja Hempel,Robert McFarland,Robert W. Taylor	12
7	Mitochondrial disease and lipid storage myopathy due to mutation in CHCHD10 or DNM1L and disordered mitochondrial dynamics 2017 ·Neuromuscular Disorders ·Carl Fratter,Eszter Dombi,Janet Carver,Kjell Sergeant,Inês A. Barbosa,Monika Hofer,M M Esiri,David Hilton‐Jones,Sandeep Jayawant,S. E. Olpin,Charu Deshpande,(unknown),Joanna Poulton	1
8	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 2017 ·Journal of Medical Genetics ·Meena Balasubramanian,Josh Willoughby,Andrew E. Fry,Astrid Weber,Helen V. Firth,Charu Deshpande,Jonathan Berg,Kate Chandler,Kay Metcalfe,Wayne Lam,Daniela T. Pilz,Susan Tomkins	44
9	MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus 2017 ·PLoS Genetics ·Patricia Blanchet,Martina Bebin,(unknown),Gregory M. Cooper,Michelle L. Thompson,Bénédicte Duban‐Bedu,Bénédicte Gérard,Amélie Piton,(unknown),Charu Deshpande,Virginia Clowes,Julie Vogt,Peter D. Turnpenny,Michael P. Williamson,Yves Alembik,Eric Glasgow,Alisdair McNeill	49
10	Pathogenic variants in HTRA2 cause an early‐onset mitochondrial syndrome associated with 3‐methylglutaconic aciduria 2016 ·Journal of Inherited Metabolic Disease ·Monika Oláhová,Kyle Thompson,Steven Hardy,Inês A. Barbosa,Arnaud Besse,(unknown),Kathryn White,Tracey Davey,Michael A. Simpson,Michael Champion,Greg Enns,Susan Schelley,Robert N. Lightowlers,Zofia M. Chrzanowska‐Lightowlers,Robert McFarland,Charu Deshpande,Penelope E. Bonnen,Robert W. Taylor	23
11	Recessive truncating IGHMBP2 mutations presenting as axonal sensorimotor neuropathy 2015 ·Neurology ·Gudrun Schottmann,Heinz Jungbluth,Ulrike Schara,Ellen Knierim,Susanne Morales-Gonzalez,Esther Gill,Franziska Seifert,Fiona Norwood,Charu Deshpande,Katja von Au,Markus Schuelke,Jan Senderek	27
12	De Novo Mutations of the Gene Encoding the Histone Acetyltransferase KAT6B Cause Genitopatellar Syndrome 2012 ·The American Journal of Human Genetics ·Michael A. Simpson,Charu Deshpande,Dimitra Dafou,Lisenka E.L.M. Vissers,Wesley J. Woollard,Susan Holder,Gabriele Gillessen‐Kaesbach,Ronny Derks,Susan M. White,(unknown),Sarina G. Kant,Lies H. Hoefsloot,William Reardon,Han G. Brunner,Ernie M.H.F. Bongers,Richard C. Trembath	72
13	De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome 2012 ·The American Journal of Human Genetics ·Wendy D. Jones,Dimitra Dafou,Meriel McEntagart,Wesley J. Woollard,Frances Elmslie,Muriel Holder‐Espinasse,Melita Irving,Anand Saggar,Sarah Smithson,Richard C. Trembath,Charu Deshpande,Michael A. Simpson	187
14	Molecular Analysis of the Retinoic Acid Induced 1 Gene (RAI1) in Patients with Suspected Smith-Magenis Syndrome without the 17p11.2 Deletion 2011 ·PLoS ONE ·Thierry Vilboux,Carla Ciccone,Jan Blancato,Gerald F. Cox,Charu Deshpande,Wendy J. Introne,William A. Gahl,Ann C. M. Smith,Marjan Huizing	31
15	Diffuse Thymic Fibrosis 2010 ·The American Journal of Surgical Pathology ·Konstantin Shilo,(unknown),Charu Deshpande,İrem Hicran Özbudak,William D. Travis,Jeffrey R. Galvin,Teri J. Franks	3
16	Genetic syndromes and prenatally detected renal anomalies 2008 ·Seminars in Fetal and Neonatal Medicine ·Charu Deshpande,Raoul C. M. Hennekam	21
17	A randomized, double-blind study of two combined oral contraceptives containing the same progestogen, but different estrogens 1980 ·Contraception ·(unknown),Suporn Koetsawang,(unknown),(unknown),(unknown),Charu Deshpande,(unknown),(unknown),S. S. Ratnam,László Kovács,(unknown),(unknown),M. H. Briggs,Mark A. Belsey,Peter E. Hall,Parker Ra	35
18	Aortic arch syndrome. 1971 ·PubMed ·P M Dalal,Charu Deshpande,(unknown)	0
19	CEREBRAL EMBOLISMbreakdown → 1965 ·The Lancet ·Praful Dalal,P.M. Shah,(unknown),Charu Deshpande	458
20	Endometrial Stromal Sarcoma 1963 ·JAMA ·V Chitnis,Suman Thakur,Charu Deshpande	2

About Charu Deshpande

Charu Deshpande is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology, having authored 24 papers that have together received 1.1k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Genetics (344 citations), Neurology (105 citations) and Molecular Biology (436 citations). Charu Deshpande has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include P.M. Shah, Praful Dalal, Michael A. Simpson, Wesley J. Woollard, Richard C. Trembath, Dimitra Dafou, Wendy D. Jones, Frances Elmslie, Meriel McEntagart and Muriel Holder‐Espinasse. Their work appears in journals such as The Lancet, JAMA and PLoS ONE.

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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