Anushree Acharya

1.2k total citations
50 papers, 551 citations indexed

About

Anushree Acharya is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Anushree Acharya has authored 50 papers receiving a total of 551 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 17 papers in Sensory Systems and 11 papers in Genetics. Recurrent topics in Anushree Acharya's work include Hearing, Cochlea, Tinnitus, Genetics (17 papers), Congenital heart defects research (7 papers) and Genomics and Rare Diseases (5 papers). Anushree Acharya is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (17 papers), Congenital heart defects research (7 papers) and Genomics and Rare Diseases (5 papers). Anushree Acharya collaborates with scholars based in United States, Pakistan and India. Anushree Acharya's co-authors include Suzanne M. Leal, Isabelle Schrauwen, Wasim Ahmad, Shiva Raj Mishra, Devendra Bansal, Binaya Kumar Baral, Abdul Nasır, Saruna Ghimire, Ali A. Sultan and Michael J. Bamshad and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Anushree Acharya

46 papers receiving 545 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anushree Acharya United States 13 211 100 81 80 67 50 551
Chang‐Huei Tsao Taiwan 18 225 1.1× 25 0.3× 34 0.4× 132 1.6× 199 3.0× 54 884
Iram Haq United Kingdom 12 209 1.0× 53 0.5× 9 0.1× 139 1.7× 17 0.3× 30 931
Sabine Blouquit‐Laye France 11 262 1.2× 25 0.3× 24 0.3× 125 1.6× 27 0.4× 19 732
Takako Ito Japan 13 71 0.3× 18 0.2× 27 0.3× 83 1.0× 51 0.8× 52 580
Mansour Salehi Iran 14 147 0.7× 29 0.3× 9 0.1× 60 0.8× 45 0.7× 72 611
Christine Boone United States 12 78 0.4× 42 0.4× 291 3.6× 28 0.3× 30 0.4× 27 932
Rodrigo San-Cristóbal Spain 11 204 1.0× 81 0.8× 13 0.2× 47 0.6× 105 1.6× 28 516
Trina C. Uwiera Canada 8 172 0.8× 68 0.7× 49 0.6× 39 0.5× 21 0.3× 17 447
Helen Maureen Massa Australia 12 120 0.6× 41 0.4× 7 0.1× 167 2.1× 81 1.2× 29 695
Sohyun Bae South Korea 14 163 0.8× 19 0.2× 11 0.1× 49 0.6× 17 0.3× 49 813

Countries citing papers authored by Anushree Acharya

Since Specialization
Citations

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

Fields of papers citing papers by Anushree Acharya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anushree Acharya

This figure shows the co-authorship network connecting the top 25 collaborators of Anushree Acharya. A scholar is included among the top collaborators of Anushree Acharya 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 Anushree Acharya. Anushree Acharya 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.
Acharya, Anushree, et al.. (2025). The Diverse Genetic Landscape of Hearing Impairment in South African Families. Clinical Genetics. 108(5). 511–520.
2.
Kalsoom, Umme, et al.. (2025). A pathogenic COL7A1 variant highlights semi-dominant inheritance in dystrophic epidermolysis bullosa. BMC Medical Genomics. 18(1). 26–26.
3.
Schrauwen, Isabelle, Anushree Acharya, Susanna Öhman, et al.. (2024). Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders. Scientific Reports. 14(1). 11239–11239. 7 indexed citations
4.
Acharya, Anushree, Saadullah Khan, Irfan Ullah, et al.. (2024). THBS1 is a new autosomal recessive non-syndromic hearing impairment gene. BMC Medical Genomics. 17(1). 291–291. 1 indexed citations
5.
Hussain, A., et al.. (2023). A Novel Variant in VPS13B Underlying Cohen Syndrome. BioMed Research International. 2023(1). 9993801–9993801.
6.
Saqib, Muhammad Arif Nadeem, Edwin Mientjes, Anushree Acharya, et al.. (2023). A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndrome. European Journal of Human Genetics. 31(12). 1447–1454. 3 indexed citations
7.
Parkkola, Riitta, Anushree Acharya, Suzanne M. Leal, et al.. (2023). A novel variant in CYFIP2 in a girl with severe disabilities and bilateral perisylvian polymicrogyria. American Journal of Medical Genetics Part A. 194(4). e63478–e63478. 1 indexed citations
8.
Bilal, Muhammad, Tobias B. Haack, Rebecca Buchert, et al.. (2023). Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly. European Journal of Human Genetics. 31(11). 1270–1274. 3 indexed citations
9.
Li, Guangyou, Anushree Acharya, Yin Huang, et al.. (2023). Rare-variant association analysis reveals known and new age-related hearing loss genes. European Journal of Human Genetics. 31(6). 638–647. 9 indexed citations
10.
Schrauwen, Isabelle, Anushree Acharya, Marja‐Leena Väisänen, et al.. (2022). Autosomal recessive nonsyndromic hearing impairment in two Finnish families due to the population enriched CABP2 c.637+1G>T variant. Molecular Genetics & Genomic Medicine. 10(3). e1866–e1866. 1 indexed citations
11.
Adadey, Samuel Mawuli, Kevin Esoh, Anushree Acharya, et al.. (2022). A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana. BMC Medical Genomics. 15(1). 237–237. 4 indexed citations
12.
Adadey, Samuel Mawuli, Isabelle Schrauwen, Kevin Esoh, et al.. (2021). Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment. Journal of Human Genetics. 66(12). 1169–1175. 10 indexed citations
13.
Melegh, Béla, Györgyi Csábí, Anushree Acharya, et al.. (2020). Maternal mosaicism underlies the inheritance of a rare germline AKT3 variant which is responsible for megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome in two Roma half-siblings. Experimental and Molecular Pathology. 115. 104471–104471. 4 indexed citations
14.
Schrauwen, Isabelle, Béla Melegh, Imen Chakchouk, et al.. (2019). Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma. European Journal of Human Genetics. 27(6). 869–878. 10 indexed citations
15.
Schrauwen, Isabelle, Syed Irfan Raza, Kwanghyuk Lee, et al.. (2018). Identification of CACNA1D variants associated with sinoatrial node dysfunction and deafness in additional Pakistani families reveals a clinical significance. Journal of Human Genetics. 64(2). 153–160. 28 indexed citations
16.
Acharya, Anushree, Devendra Bansal, Praveen K. Bharti, et al.. (2017). Molecular surveillance of chloroquine drug resistance markers (Pfcrt and Pfmdr1) among imported Plasmodium falciparum malaria in Qatar. Pathogens and Global Health. 112(2). 57–62. 4 indexed citations
17.
Ansar, Muhammad, Regie Lyn P. Santos‐Cortez, Xin Wang, et al.. (2015). Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability. European Journal of Human Genetics. 24(8). 1223–1227. 20 indexed citations
18.
Ranjit‬, Manoranjan, et al.. (2009). Chloroquine-resistant P. falciparum parasites and severe malaria in Orissa.. Current Science. 96(12). 1608–1611. 9 indexed citations
19.
Ranjit‬, Manoranjan, et al.. (2004). The PfCRT (K76T) point mutation favours clone multiplicity and disease severity in Plasmodium falciparum infection. Tropical Medicine & International Health. 9(8). 857–861. 22 indexed citations
20.
Acharya, Anushree, et al.. (1991). Software for estimating LD50 and LD90 by logit analysis. Computer Methods and Programs in Biomedicine. 34(4). 255–256. 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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