Avinash V. Dharmadhikari

2.3k total citations
15 papers, 222 citations indexed

About

Avinash V. Dharmadhikari is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Avinash V. Dharmadhikari has authored 15 papers receiving a total of 222 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Avinash V. Dharmadhikari's work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Renal and related cancers (2 papers). Avinash V. Dharmadhikari is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers) and Renal and related cancers (2 papers). Avinash V. Dharmadhikari collaborates with scholars based in United States, Poland and Australia. Avinash V. Dharmadhikari's co-authors include Przemysław Szafrański, Paweł Stankiewicz, Vladimir V. Kalinichenko, Partha Sen, Francis White, Pirooz Eghtesady, F. Sessions Cole, Gail Deutsch, Jennifer Wambach and R. Mark Grady and has published in prestigious journals such as PLoS ONE, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Avinash V. Dharmadhikari

13 papers receiving 198 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Avinash V. Dharmadhikari United States 8 143 80 61 58 20 15 222
Nadiya Sosonkina United States 8 115 0.8× 40 0.5× 70 1.1× 35 0.6× 41 2.0× 14 212
Rocío Mena Spain 7 65 0.5× 48 0.6× 75 1.2× 20 0.3× 32 1.6× 16 182
Edwin Oole Netherlands 6 119 0.8× 60 0.8× 23 0.4× 13 0.2× 8 0.4× 8 222
Aline Receveur France 9 81 0.6× 21 0.3× 109 1.8× 20 0.3× 50 2.5× 22 200
Florian Erger Germany 7 139 1.0× 81 1.0× 81 1.3× 9 0.2× 44 2.2× 24 230
Patrick R. van den Berg Netherlands 8 240 1.7× 62 0.8× 54 0.9× 15 0.3× 20 1.0× 8 303
Lorraine F. May United States 6 47 0.3× 27 0.3× 96 1.6× 81 1.4× 38 1.9× 6 211
John Lazar United States 5 230 1.6× 18 0.2× 38 0.6× 10 0.2× 16 0.8× 7 274
Meenakshi Maitra United States 4 239 1.7× 151 1.9× 62 1.0× 58 1.0× 4 0.2× 5 361
Xingbo Cheng China 7 167 1.2× 19 0.2× 148 2.4× 18 0.3× 58 2.9× 21 295

Countries citing papers authored by Avinash V. Dharmadhikari

Since Specialization
Citations

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

Fields of papers citing papers by Avinash V. Dharmadhikari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Avinash V. Dharmadhikari. 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 Avinash V. Dharmadhikari. The network helps show where Avinash V. Dharmadhikari may publish in the future.

Co-authorship network of co-authors of Avinash V. Dharmadhikari

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

All Works

15 of 15 papers shown
1.
Hahn, Elan, Avinash V. Dharmadhikari, Simran Maggo, et al.. (2025). Copy number variant analysis improves diagnostic yield in a diverse pediatric exome sequencing cohort. npj Genomic Medicine. 10(1). 16–16.
2.
Dharmadhikari, Avinash V., Jennifer Han, Xu Dong, et al.. (2025). Optical genome mapping improves clinical interpretation of constitutional copy-number gains and reduces their VUS burden. Genetics in Medicine. 27(8). 101452–101452. 1 indexed citations
3.
Tanaka, Akemi, et al.. (2022). Molecular Genetic Testing Approaches for Retinitis Pigmentosa. Methods in molecular biology. 2560. 41–66. 1 indexed citations
4.
Thomas‐Wilson, Amanda, Avinash V. Dharmadhikari, Jonas J. Heymann, et al.. (2022). Whole Exome Sequencing detects PYGM variants in two adults with McArdle disease. Molecular Case Studies. 8(2). mcs.a006173–mcs.a006173. 2 indexed citations
5.
Dharmadhikari, Avinash V., Elaine M. Pereira, Michael J. Macera, et al.. (2022). Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl. Frontiers in Genetics. 13. 906077–906077. 1 indexed citations
6.
Ganapathi, Mythily, Amanda Thomas‐Wilson, Christie M. Buchovecky, et al.. (2022). Clinical exome sequencing for inherited retinal degenerations at a tertiary care center. Scientific Reports. 12(1). 9358–9358. 10 indexed citations
7.
Dharmadhikari, Avinash V., Elaine M. Pereira, Vaidehi Jobanputra, et al.. (2021). Follow-up of an abnormal NIPS result (T13) leads to identification of mosaic 13q31.1q34 tetrasomy associated with a neocentromeric sSMC. Molecular Genetics and Metabolism. 132. S318–S319.
8.
Abdelhakim, Aliaa H., Avinash V. Dharmadhikari, Sara D. Ragi, et al.. (2020). Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency. Orphanet Journal of Rare Diseases. 15(1). 320–320. 7 indexed citations
9.
Dharmadhikari, Avinash V., Krzysztof Gogolewski, Vladimir Ustiyan, et al.. (2016). Lethal lung hypoplasia and vascular defects in mice with conditionalFoxf1overexpression. Biology Open. 5(11). 1595–1606. 19 indexed citations
10.
Dharmadhikari, Avinash V., Przemysław Szafrański, Vladimir V. Kalinichenko, & Paweł Stankiewicz. (2015). Genomic and Epigenetic Complexity of the FOXF1 Locus in 16q24.1: Implications for Development and Disease. Current Genomics. 16(2). 107–116. 52 indexed citations
11.
Dharmadhikari, Avinash V., Tomasz Gambin, Przemysław Szafrański, et al.. (2014). Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatellite. BMC Medical Genetics. 15(1). 128–128. 21 indexed citations
12.
Sen, Partha, Avinash V. Dharmadhikari, Tadeusz Majewski, et al.. (2014). Comparative Analyses of Lung Transcriptomes in Patients with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins and in Foxf1 Heterozygous Knockout Mice. PLoS ONE. 9(4). e94390–e94390. 25 indexed citations
13.
Szafrański, Przemysław, Avinash V. Dharmadhikari, Jennifer Wambach, et al.. (2014). Two deletions overlapping a distant FOXF1 enhancer unravel the role of lncRNA LINC01081 in etiology of alveolar capillary dysplasia with misalignment of pulmonary veins. American Journal of Medical Genetics Part A. 164(8). 2013–2019. 50 indexed citations
14.
Dharmadhikari, Avinash V., Przemysław Szafrański, Richard Person, et al.. (2012). Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148. Human Molecular Genetics. 21(15). 3345–3355. 17 indexed citations
15.
Dharmadhikari, Avinash V., Sheila N.J. Sait, George Deeb, et al.. (2012). CD19 expression in acute leukemia is not restricted to the cytogenetically aberrant populations. Leukemia & lymphoma. 54(7). 1517–1520. 16 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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