Pawaree Saisawat

1.8k total citations
18 papers, 603 citations indexed

About

Pawaree Saisawat is a scholar working on Molecular Biology, Nephrology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Pawaree Saisawat has authored 18 papers receiving a total of 603 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Nephrology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Pawaree Saisawat's work include Renal and related cancers (5 papers), Pediatric Urology and Nephrology Studies (5 papers) and Renal Diseases and Glomerulopathies (3 papers). Pawaree Saisawat is often cited by papers focused on Renal and related cancers (5 papers), Pediatric Urology and Nephrology Studies (5 papers) and Renal Diseases and Glomerulopathies (3 papers). Pawaree Saisawat collaborates with scholars based in Thailand, United States and Germany. Pawaree Saisawat's co-authors include Friedhelm Hildebrandt, Virginia Vega-Warner, Velibor Tasić, Elijah O. Kehinde, Gabriel C. Dworschak, Asaf Vivante, Radovan Bogdanović, Buğsu Övünç, Gil Chernin and Alina C. Hilger and has published in prestigious journals such as Kidney International, Journal of the American Society of Nephrology and World Journal of Gastroenterology.

In The Last Decade

Pawaree Saisawat

18 papers receiving 597 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pawaree Saisawat Thailand 9 424 239 167 162 119 18 603
Audrey Pawtowski France 5 268 0.6× 192 0.8× 90 0.5× 192 1.2× 71 0.6× 6 442
Mireille Lacoste France 9 175 0.4× 105 0.4× 252 1.5× 68 0.4× 72 0.6× 10 511
Gianfranco Rizzoni Italy 7 213 0.5× 243 1.0× 77 0.5× 145 0.9× 69 0.6× 8 538
Isabella Zalewski United States 8 254 0.6× 418 1.7× 62 0.4× 117 0.7× 103 0.9× 8 520
Jonathan D. Porath United States 8 292 0.7× 147 0.6× 130 0.8× 228 1.4× 164 1.4× 13 503
Achra Sumboonnanonda Thailand 12 215 0.5× 155 0.6× 118 0.7× 30 0.2× 85 0.7× 35 536
Stephanie M. Karle Germany 11 421 1.0× 660 2.8× 68 0.4× 168 1.0× 106 0.9× 13 836
Sandrine Beaufils France 7 478 1.1× 66 0.3× 183 1.1× 560 3.5× 60 0.5× 8 865
Agnes Trautmann Germany 8 168 0.4× 428 1.8× 35 0.2× 41 0.3× 130 1.1× 10 581
Matthew L. Lemer United States 4 155 0.4× 150 0.6× 40 0.2× 21 0.1× 74 0.6× 4 521

Countries citing papers authored by Pawaree Saisawat

Since Specialization
Citations

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

Fields of papers citing papers by Pawaree Saisawat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pawaree Saisawat

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

All Works

18 of 18 papers shown
1.
Tangnararatchakit, Kanchana, et al.. (2024). Control of blood pressure in hypertensive children and adolescents assessed by ambulatory blood pressure monitoring. BMC Pediatrics. 24(1). 269–269. 1 indexed citations
2.
Chuansumrit, Ampaiwan, Duantida Songdej, Nongnuch Sirachainan, et al.. (2024). Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload. Hemoglobin. 48(1). 47–55. 1 indexed citations
3.
Saisawat, Pawaree, et al.. (2023). Waist-to-height-ratio is associated with sustained hypertension in children and adolescents with high office blood pressure. Frontiers in Cardiovascular Medicine. 9. 1026606–1026606. 2 indexed citations
4.
Saisawat, Pawaree, et al.. (2022). Clinical Outcomes of Renal Replacement Therapy in Pediatric Acute Kidney Injury: A 10-Year Retrospective Observational Study. Global Pediatric Health. 9. 2333794X221142415–2333794X221142415. 8 indexed citations
5.
Santanirand, Pitak, et al.. (2019). Outcomes of Empirical Antimicrobial Therapy for Pediatric Community-onset Febrile Urinary Tract Infection in the Era of Increasing Antimicrobial Resistance. The Pediatric Infectious Disease Journal. 39(2). 121–126. 7 indexed citations
6.
Tangnararatchakit, Kanchana, et al.. (2019). Inadequate blood pressure control demonstrated by ambulatory blood pressure monitoring in pediatric renal transplant recipients. Pediatric Transplantation. 23(6). e13499–e13499. 5 indexed citations
7.
Tangnararatchakit, Kanchana, et al.. (2017). Clinical Outcomes in Pediatric Renal Transplant Recipients Who Received Steroid-Based Immunosuppressive Regimen. Transplantation Proceedings. 49(5). 971–976. 5 indexed citations
8.
Saisawat, Pawaree, et al.. (2017). Unusual cause of anemia in a child with end-stage renal disease: Questions. Pediatric Nephrology. 32(12). 2259–2260. 1 indexed citations
9.
Saisawat, Pawaree, et al.. (2017). Unusual cause of anemia in a child with end-stage renal disease: Answers. Pediatric Nephrology. 32(12). 2261–2262. 1 indexed citations
10.
Lerkvaleekul, Butsabong, et al.. (2016). Henoch-Schönlein purpura from vasculitis to intestinal perforation: A case report and literature review. World Journal of Gastroenterology. 22(26). 6089–6089. 12 indexed citations
11.
Kohl, Stefan, Daw‐Yang Hwang, Gabriel C. Dworschak, et al.. (2014). Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract. Journal of the American Society of Nephrology. 25(9). 1917–1922. 67 indexed citations
12.
Hwang, Daw‐Yang, Gabriel C. Dworschak, Stefan Kohl, et al.. (2014). Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract. Kidney International. 85(6). 1429–1433. 154 indexed citations
13.
Lovric, Svjetlana, Humphrey Fang, Virginia Vega-Warner, et al.. (2014). Rapid Detection of Monogenic Causes of Childhood-Onset Steroid-Resistant Nephrotic Syndrome. Clinical Journal of the American Society of Nephrology. 9(6). 1109–1116. 55 indexed citations
14.
Övünç, Buğsu, Edgar A. Otto, Virginia Vega-Warner, et al.. (2011). Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of Proteinuria. Journal of the American Society of Nephrology. 22(10). 1815–1820. 80 indexed citations
15.
Saisawat, Pawaree, Velibor Tasić, Virginia Vega-Warner, et al.. (2011). Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis. Kidney International. 81(2). 196–200. 65 indexed citations
16.
Chernin, Gil, Virginia Vega-Warner, Dominik S. Schoeb, et al.. (2010). Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations. Clinical Journal of the American Society of Nephrology. 5(9). 1655–1662. 70 indexed citations
17.
Schoeb, Dominik S., Gil Chernin, Saskia F. Heeringa, et al.. (2010). Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS). Nephrology Dialysis Transplantation. 25(9). 2970–2976. 57 indexed citations
18.
Ashraf, Shazia, Bethan E. Hoskins, H. Chaib, et al.. (2009). Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24. Nephrology Dialysis Transplantation. 25(5). 1496–1501. 12 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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