Aneek Das Bhowmik

616 total citations
36 papers, 428 citations indexed

About

Aneek Das Bhowmik is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Aneek Das Bhowmik has authored 36 papers receiving a total of 428 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Aneek Das Bhowmik's work include Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Aneek Das Bhowmik is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Aneek Das Bhowmik collaborates with scholars based in India, France and United States. Aneek Das Bhowmik's co-authors include Ashwin Dalal, Kanchan Mukhopadhyay, Swagata Sinha, Shagun Aggarwal, Manali Das, Keya Chaudhuri, Anindita Chattopadhyay, Neerja Gupta, Shubha R. Phadke and Venkatraman Bhat and has published in prestigious journals such as Gene, Genomics and Human Mutation.

In The Last Decade

Aneek Das Bhowmik

32 papers receiving 412 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aneek Das Bhowmik India 13 179 179 87 68 60 36 428
Matthieu Raveau Japan 10 232 1.3× 229 1.3× 70 0.8× 99 1.5× 93 1.6× 13 535
Madeleine Fannemel Norway 11 173 1.0× 196 1.1× 98 1.1× 58 0.9× 35 0.6× 18 386
Angela Peron Italy 18 261 1.5× 365 2.0× 114 1.3× 127 1.9× 55 0.9× 54 827
Mihaela Bustuchina ̆ Vlaicu France 7 114 0.6× 121 0.7× 117 1.3× 86 1.3× 59 1.0× 10 394
Euthymia Vargìami Greece 13 155 0.9× 158 0.9× 139 1.6× 162 2.4× 42 0.7× 35 543
Claude Cancès France 10 293 1.6× 310 1.7× 115 1.3× 89 1.3× 66 1.1× 15 574
Shino Shimada Japan 15 315 1.8× 318 1.8× 43 0.5× 35 0.5× 68 1.1× 36 545
Sofia Douzgou United Kingdom 16 338 1.9× 321 1.8× 57 0.7× 75 1.1× 53 0.9× 49 679
Laëtitia Lambert France 11 235 1.3× 351 2.0× 59 0.7× 77 1.1× 41 0.7× 32 509
Masato Mori Japan 16 404 2.3× 191 1.1× 61 0.7× 87 1.3× 64 1.1× 31 720

Countries citing papers authored by Aneek Das Bhowmik

Since Specialization
Citations

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

Fields of papers citing papers by Aneek Das Bhowmik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aneek Das Bhowmik. 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 Aneek Das Bhowmik. The network helps show where Aneek Das Bhowmik may publish in the future.

Co-authorship network of co-authors of Aneek Das Bhowmik

This figure shows the co-authorship network connecting the top 25 collaborators of Aneek Das Bhowmik. A scholar is included among the top collaborators of Aneek Das Bhowmik 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 Aneek Das Bhowmik. Aneek Das Bhowmik 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.
Pal, Pinaki, et al.. (2025). Case report of a 21-year-old woman with Gabriele-de Vries syndrome and autoimmune hypothyroidism. Clinical Dysmorphology. 34(3). 79–82.
2.
Bhowmik, Aneek Das, et al.. (2023). IODINE AS A POTENTIAL FRONT-LINE DEFENSE AGAINST COVID-19: A LITERATURE REVIEW. Asian Journal of Pharmaceutical and Clinical Research. 13–19.
3.
Bhowmik, Aneek Das, et al.. (2022). Muscle spasms as presenting feature of Nivelon‐Nivelon‐Mabile syndrome. American Journal of Medical Genetics Part A. 191(1). 238–248. 2 indexed citations
4.
Tallapaka, Karthik Bharadwaj, et al.. (2019). Co-Occurrence of Leber Congenital Amaurosis and Meckel Syndrome Type 1 in a Fetus: Is There a Lesson to Be Learned. Molecular Syndromology. 10(3). 177–182. 2 indexed citations
5.
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
6.
7.
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
8.
Phadke, Shubha R., et al.. (2017). Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly. American Journal of Medical Genetics Part A. 176(1). 34–40. 12 indexed citations
9.
Bhowmik, Aneek Das, et al.. (2017). Tarsal‐carpal coalition syndrome: Report of a novel missense mutation in NOG gene and phenotypic delineation. American Journal of Medical Genetics Part A. 176(1). 219–224. 8 indexed citations
10.
Shukla, Anju, Aneek Das Bhowmik, Malavika Hebbar, et al.. (2017). Homozygosity for a nonsense variant in AIMP2 is associated with a progressive neurodevelopmental disorder with microcephaly, seizures, and spastic quadriparesis. Journal of Human Genetics. 63(1). 19–25. 24 indexed citations
11.
Bhowmik, Aneek Das, et al.. (2016). Identification of a novel splice site HSPG2 mutation and prenatal diagnosis in Schwartz Jampel Syndrome type 1 using whole exome sequencing. Neuromuscular Disorders. 26(11). 809–814. 9 indexed citations
12.
Phadke, Shubha R., et al.. (2016). Complex Camptosynpolydactyly and Mesoaxial synostotic syndactyly with phalangeal reduction are allelic disorders. American Journal of Medical Genetics Part A. 170(6). 1622–1625. 10 indexed citations
13.
Aggarwal, Shagun, Aneek Das Bhowmik, Vedam L. Ramprasad, Sakthivel Murugan, & Ashwin Dalal. (2016). A splice site mutation in HERC1 leads to syndromic intellectual disability with macrocephaly and facial dysmorphism: Further delineation of the phenotypic spectrum. American Journal of Medical Genetics Part A. 170(7). 1868–1873. 29 indexed citations
14.
Bhowmik, Aneek Das & Ashwin Dalal. (2015). Whole exome sequencing identifies a novel frameshift mutation in GPC3 gene in a patient with overgrowth syndrome. Gene. 572(2). 303–306. 14 indexed citations
15.
Bhowmik, Aneek Das, et al.. (2014). Molecular genetic analysis of trinucleotide repeat disorders (TRDs) in Indian population and application of repeat primed PCR. European Journal of Medical Genetics. 58(3). 160–167. 5 indexed citations
16.
Bhowmik, Aneek Das & Kanchan Mukhopadhyay. (2012). MOLECULAR GENETICS OF INTELLECTUAL DISABILITY WITH SPECIAL EMPHASIS ON THE IDIOPATHIC TYPE. 4(3). 99–110. 1 indexed citations
17.
Bhowmik, Aneek Das, Jyoti Shaw, Arpita Chatterjee, et al.. (2011). Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 35(7). 1714–1722. 4 indexed citations
18.
Mukherjee, Sanjit, et al.. (2011). Association of XRCC1, XRCC3, and NAT2 polymorphisms with the risk of oral submucous fibrosis among eastern Indian population. Journal of Oral Pathology and Medicine. 41(4). 292–302. 15 indexed citations
19.
Das, Manali, et al.. (2009). Screening of rural children in West Bengal for fragile-X syndrome.. PubMed. 130(6). 714–9. 3 indexed citations
20.
Bhowmik, Aneek Das, et al.. (2007). Risk of Down syndrome conferred by <i>MTHFR</i> C677T polymorphism: Ethnic variations. Indian journal of human genetics. 13(2). 76–76. 6 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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