Ashwin Dalal

4.5k total citations
151 papers, 1.4k citations indexed

About

Ashwin Dalal is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ashwin Dalal has authored 151 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 74 papers in Genetics and 21 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ashwin Dalal's work include Genomic variations and chromosomal abnormalities (23 papers), Genomics and Rare Diseases (21 papers) and Connective tissue disorders research (17 papers). Ashwin Dalal is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Genomics and Rare Diseases (21 papers) and Connective tissue disorders research (17 papers). Ashwin Dalal collaborates with scholars based in India, United States and Germany. Ashwin Dalal's co-authors include Shubha R. Phadke, Aneek Das Bhowmik, Shagun Aggarwal, Vijaya Kumar Pidugu, Prajnya Ranganath, Mandakini Pradhan, Katta M. Girisha, Neerja Gupta, Anju Shukla and Hitesh Shah and has published in prestigious journals such as Nature, PLoS ONE and Gene.

In The Last Decade

Ashwin Dalal

138 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ashwin Dalal India 20 651 543 202 192 150 151 1.4k
Giovanni Sorge Italy 22 486 0.7× 553 1.0× 153 0.8× 207 1.1× 135 0.9× 75 1.3k
Ulrike Hüffmeier Germany 24 534 0.8× 586 1.1× 132 0.7× 221 1.2× 252 1.7× 45 1.8k
Shubha R. Phadke India 23 908 1.4× 826 1.5× 437 2.2× 209 1.1× 194 1.3× 268 2.4k
Dusica Babovic‐Vuksanovic United States 27 863 1.3× 540 1.0× 144 0.7× 138 0.7× 176 1.2× 99 2.2k
Shalini N. Jhangiani United States 25 1.1k 1.7× 801 1.5× 115 0.6× 76 0.4× 75 0.5× 80 2.0k
Éric Bieth France 24 1.1k 1.7× 690 1.3× 348 1.7× 75 0.4× 182 1.2× 72 2.1k
Lucia Bartoloni Italy 19 724 1.1× 834 1.5× 191 0.9× 78 0.4× 65 0.4× 38 1.9k
Peter Gustavsson Sweden 20 1.3k 1.9× 476 0.9× 189 0.9× 86 0.4× 87 0.6× 38 1.8k
Francesca Faravelli Italy 22 869 1.3× 1.2k 2.1× 294 1.5× 79 0.4× 128 0.9× 61 2.9k
Wadih M. Zein United States 21 762 1.2× 369 0.7× 122 0.6× 112 0.6× 65 0.4× 86 1.4k

Countries citing papers authored by Ashwin Dalal

Since Specialization
Citations

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

Fields of papers citing papers by Ashwin Dalal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ashwin Dalal

This figure shows the co-authorship network connecting the top 25 collaborators of Ashwin Dalal. A scholar is included among the top collaborators of Ashwin Dalal 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 Ashwin Dalal. Ashwin Dalal 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.
Tyagi, Shweta, Aditi Arora, Prajnya Ranganath, & Ashwin Dalal. (2025). CEP72 Emerges as a Key Centriolar Satellite Protein in Health and Disease. Cytoskeleton. 82(11). 737–746.
2.
Dalal, Ashwin, Ajay Kumar Mahato, Kapaettu Satyamoorthy, et al.. (2024). Mitochondria in biology and medicine – 2023. Mitochondrion. 76. 101853–101853. 9 indexed citations
3.
Jacob, Prince, Neethukrishna Kausthubham, Gandham SriLakshmi Bhavani, et al.. (2024). PRKACA‐related, atrial defects‐polydactyly‐multiple congenital malformation syndrome in an Indian patient. American Journal of Medical Genetics Part A. 194(7). e63566–e63566.
4.
Mohan, Chandra, et al.. (2024). Diagnostic outcome of pro bono neurogenetic diagnostic service in Sri Lanka: A wealth creation. European Journal of Human Genetics. 32(10). 1299–1306. 2 indexed citations
5.
Dalal, Ashwin, et al.. (2024). Rare genetic diseases in India: Steps toward a nationwide mission program. Journal of Biosciences. 49(1). 4 indexed citations
6.
Hathout, Yetrib, Harry W.M. Steinbusch, Chandra Mohan, et al.. (2023). Gene therapy for selected neuromuscular and trinucleotide repeat disorders – An insight to subsume South Asia for multicenter clinical trials. IBRO Neuroscience Reports. 14. 146–153. 7 indexed citations
7.
Dalal, Ashwin, et al.. (2023). Familial monoallelic CYP26B1 truncating variant causes a syndromic craniosynostosis due to haploinsufficiency ?. European Journal of Medical Genetics. 66(7). 104772–104772. 1 indexed citations
8.
Amaratunga, Dhammika, Yetrib Hathout, Chandra Mohan, et al.. (2023). Duchenne Muscular Dystrophy from Brain to Muscle: The Role of Brain Dystrophin Isoforms in Motor Functions. Journal of Clinical Medicine. 12(17). 5637–5637. 8 indexed citations
9.
Jacob, Prince, Gandham SriLakshmi Bhavani, Zheng Wang, et al.. (2023). Exome Sequencing in Monogenic Forms of Rickets. The Indian Journal of Pediatrics. 90(12). 1182–1190. 3 indexed citations
10.
11.
Aggarwal, Shagun, et al.. (2022). Fetal presentation of chondrodysplasia with joint dislocations, GPAPP type, caused by novel biallelic IMPAD1 variants. American Journal of Medical Genetics Part A. 188(4). 1287–1292.
12.
Saxena, Deepti, Madhulika Kabra, Neerja Gupta, et al.. (2022). Genotype-phenotype spectrum of 130 unrelated Indian families with Mucopolysaccharidosis type II. European Journal of Medical Genetics. 65(3). 104447–104447. 3 indexed citations
13.
Dalal, Ashwin, et al.. (2022). Next Generation Sequencing in a Case of Early Onset Hydrops: Closing the Loop on the Diagnostic Odyssey!. Fetal and Pediatric Pathology. 42(1). 103–109. 2 indexed citations
14.
Chaudhary, Ajay Kumar, Hampapathalu Adimurthy Nagarajaram, Ashwin Dalal, et al.. (2021). Ectodysplasin pathogenic variants affecting the furin‐cleavage site and unusual clinical features define X‐linked hypohidrotic ectodermal dysplasia in India. American Journal of Medical Genetics Part A. 188(3). 788–805. 2 indexed citations
15.
Srivastava, Priyanka, Neerja Gupta, Madhulika Kabra, et al.. (2021). Phenotypic and genotypic spectrum of CTSK variants in a cohort of twenty-five Indian patients with pycnodysostosis. European Journal of Medical Genetics. 64(7). 104235–104235. 7 indexed citations
16.
Girisha, Katta M., et al.. (2020). Untapped opportunities for rare disease gene discovery in India. American Journal of Medical Genetics Part A. 182(12). 3056–3059. 1 indexed citations
17.
Tallapaka, Karthik Bharadwaj, et al.. (2018). Novel RSPO1 mutation causing 46,XX testicular disorder of sex development with palmoplantar keratoderma: A review of literature and expansion of clinical phenotype. American Journal of Medical Genetics Part A. 176(4). 1006–1010. 17 indexed citations
18.
Patil, Siddaramappa J., et al.. (2018). Autosomal recessive otofaciocervical syndrome type 2 with novel homozygous small insertion in PAX1 gene. American Journal of Medical Genetics Part A. 176(5). 1200–1206. 21 indexed citations
19.
Narayanan, Dhanya Lakshmi, et al.. (2017). Familial choreoathetosis due to novel heterozygous mutation in PDE10A. American Journal of Medical Genetics Part A. 176(1). 146–150. 11 indexed citations
20.
Bhavani, Gandham SriLakshmi, Hitesh Shah, Anju Shukla, Ashwin Dalal, & Katta M. Girisha. (2015). Progressive Pseudorheumatoid Dysplasia. 7 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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