Moumita Barua

1.9k total citations
32 papers, 877 citations indexed

About

Moumita Barua is a scholar working on Nephrology, Molecular Biology and Genetics. According to data from OpenAlex, Moumita Barua has authored 32 papers receiving a total of 877 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Nephrology, 14 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Moumita Barua's work include Renal Diseases and Glomerulopathies (12 papers), Chronic Kidney Disease and Diabetes (7 papers) and Cell Adhesion Molecules Research (7 papers). Moumita Barua is often cited by papers focused on Renal Diseases and Glomerulopathies (12 papers), Chronic Kidney Disease and Diabetes (7 papers) and Cell Adhesion Molecules Research (7 papers). Moumita Barua collaborates with scholars based in Canada, United States and United Kingdom. Moumita Barua's co-authors include Martin R. Pollak, Elizabeth Brown, Giulio Genovese, York Pei, Michelle Hladunewich, Andrew D. Paterson, Xin Yuan, Steven P. Balk, Andreas Pierratos and Christopher T. Chan and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Moumita Barua

31 papers receiving 859 citations

Peers

Moumita Barua

NEPHR

GENET

PRM

PHEOH

Bernhard Bielesz Austria

Amélie Dendooven Belgium

Jin Nakamura Japan

Gianfranco Rizzoni Italy

R. Riess Germany

Xiaoxia Pan China

Maddalena Gigante Italy

Joshua A. Schwimmer United States

Jianxin Wan China

Nataša Stajić Serbia

Bernhard Bielesz Austria

Moumita Barua

422 ×1.1

541 ×1.4

NEPHR

174 ×0.8

GENET

161 ×1.0

PRM

31 ×0.2

PHEOH

Citations per year, relative to Moumita Barua Moumita Barua (= 1×) peers Bernhard Bielesz

Countries citing papers authored by Moumita Barua

Since Specialization

Citations

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

Fields of papers citing papers by Moumita Barua

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moumita Barua

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

All Works

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20 of 20 papers shown

Barua, Moumita, et al.. (2025). Genotype-Based Molecular Mechanisms in Alport Syndrome. Journal of the American Society of Nephrology. 36(6). 1176–1183. 1 indexed citations

Zhang, Dongke, et al.. (2025). Podocytes in health and glomerular disease. Frontiers in Cell and Developmental Biology. 13. 1564847–1564847. 1 indexed citations

Barua, Moumita, et al.. (2024). Genetic Causes of Nephrotic Syndrome and Focal and Segmental Glomerulosclerosis. PubMed. 31(4). 309–316. 4 indexed citations

Barua, Moumita, et al.. (2024). Comparative Analysis of Deep Learning Models for Stock Price Prediction in the Indian Market. SHILAP Revista de lepidopterología. 3(4). 551–568. 5 indexed citations

Omachi, Kohei, Damian Fermin, Felix Eichinger, et al.. (2024). Association of Genetically Predicted Skipping of COL4A4 Exon 27 with Hematuria and Albuminuria. Journal of the American Society of Nephrology. 36(1). 48–59. 2 indexed citations

Taliun, Sarah A. Gagliano, et al.. (2023). GWAS for the composite traits of hematuria and albuminuria. Scientific Reports. 13(1). 18084–18084. 3 indexed citations

Barua, Moumita, et al.. (2023). Alport Syndrome: Clinical Spectrum and Therapeutic Advances. Kidney Medicine. 5(5). 100631–100631. 16 indexed citations

Barua, Moumita, et al.. (2022). Machine learning in renal pathology. PubMed. 2. 1007002–1007002. 5 indexed citations

Barua, Moumita & Andrew D. Paterson. (2021). Population-based studies reveal an additive role of type IV collagen variants in hematuria and albuminuria. Pediatric Nephrology. 37(2). 253–262. 11 indexed citations

10.

Yao, Tony, Andrew D. Paterson, Rohan John, et al.. (2021). LAMA2 and LOXL4 are candidate FSGS genes. BMC Nephrology. 22(1). 320–320. 2 indexed citations

11.

Yao, Tony, Daniel C. Cattran, Heather N. Reich, et al.. (2021). Type IV Collagen Variants in CKD: Performance of Computational Predictions for Identifying Pathogenic Variants. Kidney Medicine. 3(2). 257–266. 7 indexed citations

12.

Yao, Tony, Rohan John, Amirreza Haghighi, et al.. (2019). Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS. Clinical Journal of the American Society of Nephrology. 14(2). 213–223. 90 indexed citations

13.

Barua, Moumita, et al.. (2018). Advances in molecular diagnosis and therapeutics in nephrotic syndrome and focal and segmental glomerulosclerosis. Current Opinion in Nephrology & Hypertension. 27(3). 194–200. 8 indexed citations

14.

Barua, Moumita, Rohan John, Lorenzo Stella, et al.. (2017). X-Linked Glomerulopathy Due to COL4A5 Founder Variant. American Journal of Kidney Diseases. 71(3). 441–445. 3 indexed citations

15.

Barua, Moumita, Emilia Stellacci, Lorenzo Stella, et al.. (2014). Mutations in PAX2 Associate with Adult-Onset FSGS. Journal of the American Society of Nephrology. 25(9). 1942–1953. 87 indexed citations

16.

Barua, Moumita, et al.. (2013). Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis. Kidney International. 85(1). 124–133. 36 indexed citations

17.

Barua, Moumita, et al.. (2012). Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis. Kidney International. 83(2). 316–322. 88 indexed citations

18.

Barua, Moumita & York Pei. (2010). Diagnosis of Autosomal-Dominant Polycystic Kidney Disease: An Integrated Approach. Seminars in Nephrology. 30(4). 356–365. 18 indexed citations

19.

Barua, Moumita, Onur Çil, Andrew D. Paterson, et al.. (2009). Family History of Renal Disease Severity Predicts the Mutated Gene in ADPKD. Journal of the American Society of Nephrology. 20(8). 1833–1838. 97 indexed citations

20.

Amir, Avital L., et al.. (2003). A Direct β-Catenin-independent Interaction between Androgen Receptor and T Cell Factor 4. Journal of Biological Chemistry. 278(33). 30828–30834. 77 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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