Sateesh Maddirevula

3.0k total citations
37 papers, 647 citations indexed

About

Sateesh Maddirevula is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sateesh Maddirevula has authored 37 papers receiving a total of 647 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sateesh Maddirevula's work include Renal and related cancers (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Sateesh Maddirevula is often cited by papers focused on Renal and related cancers (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Sateesh Maddirevula collaborates with scholars based in Saudi Arabia, South Korea and United States. Sateesh Maddirevula's co-authors include Fowzan S. Alkuraya, Niema Ibrahim, Firdous Abdulwahab, Serdar Coşkun, Saad S. M. Hassan, Mais Hashem, Hessa S. Alsaif, Ranad Shaheen, Eissa Faqeih and Myungchull Rhee and has published in prestigious journals such as Biochemical and Biophysical Research Communications, The American Journal of Human Genetics and Gene.

In The Last Decade

Sateesh Maddirevula

35 papers receiving 642 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sateesh Maddirevula Saudi Arabia 13 351 206 114 82 70 37 647
Cynthia A. Ballenger United States 6 160 0.5× 104 0.5× 50 0.4× 89 1.1× 53 0.8× 6 528
Kazumasa Ogawa Japan 14 276 0.8× 86 0.4× 39 0.3× 44 0.5× 15 0.2× 43 536
Lakshmi Rambhatla United States 8 572 1.6× 151 0.7× 97 0.9× 174 2.1× 56 0.8× 9 704
Toru Arase Japan 13 204 0.6× 82 0.4× 111 1.0× 79 1.0× 51 0.7× 18 829
Christine M. Smyth Australia 12 273 0.8× 287 1.4× 28 0.2× 149 1.8× 15 0.2× 24 666
K Matsushita Japan 13 175 0.5× 60 0.3× 133 1.2× 63 0.8× 19 0.3× 28 544
Lap Chee Tsui Canada 10 323 0.9× 124 0.6× 24 0.2× 60 0.7× 54 0.8× 13 918
Heleen Roose Belgium 9 201 0.6× 35 0.2× 82 0.7× 41 0.5× 15 0.2× 13 583
Maï Thu Vu Hai France 8 180 0.5× 201 1.0× 66 0.6× 26 0.3× 8 0.1× 9 552
Joanna Budna Poland 15 304 0.9× 99 0.5× 321 2.8× 56 0.7× 12 0.2× 60 737

Countries citing papers authored by Sateesh Maddirevula

Since Specialization
Citations

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

Fields of papers citing papers by Sateesh Maddirevula

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sateesh Maddirevula

This figure shows the co-authorship network connecting the top 25 collaborators of Sateesh Maddirevula. A scholar is included among the top collaborators of Sateesh Maddirevula 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 Sateesh Maddirevula. Sateesh Maddirevula 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.
Al‐Hamed, Mohamed H., Sateesh Maddirevula, Nabil Moghrabi, et al.. (2025). Detection of Chromosomal Aneuploidy Using Exome Sequencing. Genes. 16(9). 992–992.
2.
Echahidi, Najmeddine, et al.. (2024). Genetic Analysis of Heterotaxy in a Consanguineous Cohort. Clinical Genetics. 107(2). 224–230. 1 indexed citations
3.
AlAbdi, Lama, Zuhair Rahbeeni, Sateesh Maddirevula, et al.. (2024). A founder variant expands the phenotype of WNT7B ‐related PDAC syndrome. Clinical Genetics. 106(1). 66–71.
4.
Blakemore, Karin J., Jena L. Miller, Hanan E. Shamseldin, et al.. (2023). The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction. Prenatal Diagnosis. 44(2). 196–204. 5 indexed citations
5.
Almannai, Mohammed, Lama AlAbdi, Sateesh Maddirevula, et al.. (2022). KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon. Human Genetics. 142(3). 399–405. 3 indexed citations
6.
Maddirevula, Sateesh, Khalid Awartani, Serdar Coşkun, et al.. (2020). A genomics approach to females with infertility and recurrent pregnancy loss. Human Genetics. 139(5). 605–613. 58 indexed citations
7.
Maddirevula, Sateesh, et al.. (2020). Confirming the involvement of PIEZO2 in the etiology of Marden–Walker syndrome. American Journal of Medical Genetics Part A. 185(3). 945–948. 7 indexed citations
8.
Peer‐Zada, Abdul Ali, Abdulrahman Al‐Hussaini, Sateesh Maddirevula, et al.. (2020). New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin. Journal of Human Genetics. 66(2). 151–159. 25 indexed citations
9.
Alhathal, Naif, Sateesh Maddirevula, Serdar Coşkun, et al.. (2020). A genomics approach to male infertility. Genetics in Medicine. 22(12). 1967–1975. 51 indexed citations
10.
Maddirevula, Sateesh, Tawfeg Ben‐Omran, Mariam Al‐Mureikhi, et al.. (2020). Further delineation of HIDEA syndrome. American Journal of Medical Genetics Part A. 182(12). 2999–3006. 5 indexed citations
11.
Shaheen, Ranad, Sateesh Maddirevula, Ghada M. H. Abdel‐Salam, et al.. (2019). PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly. Human Genetics. 138(3). 231–239. 68 indexed citations
12.
Al‐Qattan, Mohammad M., Sateesh Maddirevula, & Fowzan S. Alkuraya. (2019). A de novo TBX3 mutation presenting as dorsalization of the little fingers: A forme fruste phenotype of ulnar-mammary syndrome. European Journal of Medical Genetics. 63(1). 103615–103615. 7 indexed citations
13.
Nashabat, Marwan, Waleed Altwaijri, Khalid Hundallah, et al.. (2019). The landscape of early infantile epileptic encephalopathy in a consanguineous population. Seizure. 69. 154–172. 38 indexed citations
14.
Maddirevula, Sateesh, et al.. (2017). Expression patterns of prune2 is regulated by Notch and retinoic acid signaling pathways in the zebrafish embryogenesis. Gene Expression Patterns. 23-24. 45–51. 5 indexed citations
15.
Jeong, Yun-Mi, Mi‐Sun Lee, Sateesh Maddirevula, et al.. (2017). Mind Bomb-Binding Partner RanBP9 Plays a Contributory Role in Retinal Development. Molecules and Cells. 40(4). 271–279. 4 indexed citations
16.
Yoo, Kyeong‐Won, et al.. (2017). Sinup is essential for the integrity of centrosomes and mitotic spindles in zebrafish embryos. Animal Cells and Systems. 21(2). 93–99. 2 indexed citations
17.
Maddirevula, Sateesh, Fatema Alzahrani, Shams Anazi, et al.. (2017). GWAS signals revisited using human knockouts. Genetics in Medicine. 20(1). 64–68. 3 indexed citations
18.
Shamseldin, Hanan E., Sateesh Maddirevula, Eissa Faqeih, et al.. (2016). Increasing the sensitivity of clinical exome sequencing through improved filtration strategy. Genetics in Medicine. 19(5). 593–598. 43 indexed citations
19.
Patel, Nisha, Deepti Anand, Dorota Monies, et al.. (2016). Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract. Human Genetics. 136(2). 205–225. 64 indexed citations
20.
Maddirevula, Sateesh, et al.. (2015). Antibacterial activity of novel Cu₂ZnSnS₄ nanoparticles against pathogenic strains. RSC Advances. 1 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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