Abhijit Dixit

3.1k total citations
23 papers, 269 citations indexed

About

Abhijit Dixit is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Abhijit Dixit has authored 23 papers receiving a total of 269 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Surgery. Recurrent topics in Abhijit Dixit's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (4 papers) and Genetic Syndromes and Imprinting (3 papers). Abhijit Dixit is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (4 papers) and Genetic Syndromes and Imprinting (3 papers). Abhijit Dixit collaborates with scholars based in United Kingdom, United States and Cyprus. Abhijit Dixit's co-authors include Mohnish Suri, Margaret Lever, Ajoy Sarkar, Rebecca Poole, H. Bullman, Kate Chandler, M.Z. Mughal, George A. Tanteles, Joanna Jarvis and Dominic McMullan and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Abhijit Dixit

22 papers receiving 233 citations

Peers

Abhijit Dixit

GENET

PRM

PPCH

SURGE

Jian-Liang Cai China

Cara Skraban United States

Caroline Bénech France

Cynthia Lim United States

Mónica Rosello Spain

Holly Dubbs United States

Majdi Nagara Tunisia

Yukiko Kuroda Japan

Tiffany Busa France

Anand Saggar United Kingdom

Jian-Liang Cai China

Abhijit Dixit

285 ×1.7

96 ×0.6

GENET

27 ×0.5

PRM

11 ×0.3

PPCH

39 ×1.6

SURGE

Citations per year, relative to Abhijit Dixit Abhijit Dixit (= 1×) peers Jian-Liang Cai

Countries citing papers authored by Abhijit Dixit

Since Specialization

Citations

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

Fields of papers citing papers by Abhijit Dixit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abhijit Dixit

This figure shows the co-authorship network connecting the top 25 collaborators of Abhijit Dixit. A scholar is included among the top collaborators of Abhijit Dixit 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 Abhijit Dixit. Abhijit Dixit is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Albaba, Shadi, Glenda Sobey, Jessica Bowen, et al.. (2025). Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome. European Journal of Human Genetics. 33(10). 1309–1315.

Holmes, Nadine, Anne‐Sophie Denommé‐Pichon, Marie Vincent, et al.. (2025). An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical Recommendations. American Journal of Medical Genetics Part A. 197(11). e64157–e64157. 1 indexed citations

Hoare, Derek J., et al.. (2024). UK and US risk factors for hearing loss in neonatal intensive care unit infants. PLoS ONE. 19(7). e0291847–e0291847. 1 indexed citations

Tanguy, M., Adam Giess, Abhijit Dixit, et al.. (2024). A Comparison of Structural Variant Calling from Short-Read and Nanopore-Based Whole-Genome Sequencing Using Optical Genome Mapping as a Benchmark. Genes. 15(7). 925–925. 3 indexed citations

Kitterick, Pádraig T., et al.. (2023). Multiple congenital anomalies and adverse developmental outcomes are associated with neonatal intensive care admission and unilateral hearing loss. Frontiers in Pediatrics. 10. 1068884–1068884. 4 indexed citations

Stattin, Eva‐Lena, Karin Lindblom, André Struglics, et al.. (2022). Novel missense ACAN gene variants linked to familial osteochondritis dissecans cluster in the C-terminal globular domain of aggrecan. Scientific Reports. 12(1). 5215–5215. 7 indexed citations

Valluru, Manoj K., Mark Gilchrist, Jackie Cook, et al.. (2022). A founder UMOD variant is a common cause of hereditary nephropathy in the British population. Journal of Medical Genetics. 60(4). 397–405. 2 indexed citations

Walsh, R. J., Dushyant Batra, Abhijit Dixit, & Jayesh Bhatt. (2020). Clues beyond the lung: an unusual diagnosis in an infant with chronic lung disease. Breathe. 16(1). 190319–190319. 1 indexed citations

Georgiou, Michalis, et al.. (2020). Joubert syndrome diagnosed renally late. Clinical Kidney Journal. 14(3). 1017–1019. 2 indexed citations

10.

Forde, Claire, Derek Lim, George J. Burghel, et al.. (2019). Hereditary Leiomyomatosis and Renal Cell Cancer: Clinical, Molecular, and Screening Features in a Cohort of 185 Affected Individuals. European Urology Oncology. 3(6). 764–772. 51 indexed citations

11.

Hastings, Richard & Abhijit Dixit. (2019). Genomic medicine for the paediatrician. Paediatrics and Child Health. 29(4). 185–189. 1 indexed citations

12.

Bashir, Rani A., Abhijit Dixit, Jillian S. Parboosingh, et al.. (2017). Lin‐Gettig syndrome: Craniosynostosis expands the spectrum of the KAT6B related disorders. American Journal of Medical Genetics Part A. 173(10). 2596–2604. 11 indexed citations

13.

Dixit, Abhijit, Chitra Thakur, Jyotsna Gokral, et al.. (2013). Association of progesterone receptor gene polymorphism with male infertility and clinical outcome of ICSI. Journal of Assisted Reproduction and Genetics. 30(9). 1133–1139. 7 indexed citations

14.

Tanteles, George A., Abhijit Dixit, Sunil Dhar, & Mohnish Suri. (2013). Two somali half‐siblings with CHST3‐related chondrodysplasia illustrating the phenotypic spectrum and intrafamilial variability. American Journal of Medical Genetics Part A. 161(10). 2588–2593. 9 indexed citations

15.

Dixit, Abhijit, Shane McKee, Sahar Mansour, et al.. (2012). 7q11.23 Microduplication: a recognizable phenotype. Clinical Genetics. 83(2). 155–161. 37 indexed citations

16.

Dixit, Abhijit, et al.. (2012). Monozygotic twins discordant for trisomy 13: counselling and management issues. Journal of Perinatology. 32(8). 639–641. 6 indexed citations

17.

Dixit, Abhijit, Kate Chandler, Margaret Lever, et al.. (2012). Pseudohypoparathyroidism Type 1b due to Paternal Uniparental Disomy of Chromosome 20q. The Journal of Clinical Endocrinology & Metabolism. 98(1). E103–E108. 61 indexed citations

18.

Dixit, Abhijit, Chirag Patel, Rachel Harrison, et al.. (2012). 17q12 microdeletion syndrome: Three patients illustrating the phenotypic spectrum. American Journal of Medical Genetics Part A. 158A(9). 2317–2321. 37 indexed citations

19.

Dixit, Abhijit, Gabriel Chow, & Ajoy Sarkar. (2011). Neurologic Presentation of Triple A Syndrome. Pediatric Neurology. 45(5). 347–349. 11 indexed citations

20.

Tanteles, George A., Abhijit Dixit, Nigel Smith, Kate Martin, & Mohnish Suri. (2011). Mild phenotype in a patient with a de-novo 2.9-Mb interstitial deletion at 13q12.11. Clinical Dysmorphology. 20(2). 61–65. 3 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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