Patroula Smpokou

512 total citations
12 papers, 279 citations indexed

About

Patroula Smpokou is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Clinical Biochemistry. According to data from OpenAlex, Patroula Smpokou has authored 12 papers receiving a total of 279 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 3 papers in Clinical Biochemistry. Recurrent topics in Patroula Smpokou's work include Protein Tyrosine Phosphatases (4 papers), Metabolism and Genetic Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Patroula Smpokou is often cited by papers focused on Protein Tyrosine Phosphatases (4 papers), Metabolism and Genetic Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Patroula Smpokou collaborates with scholars based in United States, Germany and Canada. Patroula Smpokou's co-authors include Raju Kucherlapati, Amy E. Roberts, Erica Tworog‐Dube, Wen‐Hann Tan, Victor L. Fox, Dina J. Zand, Kenneth N. Rosenbaum, Marshall Summar, Leah Hecht and Uta Lichter‐Konecki and has published in prestigious journals such as Clinical Pharmacology & Therapeutics, Archives of Disease in Childhood and Human Mutation.

In The Last Decade

Patroula Smpokou

12 papers receiving 276 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patroula Smpokou United States	9	195	67	42	32	31	12	279
Hassan Dastsooz Iran	10	191 1.0×	28 0.4×	34 0.8×	13 0.4×	24 0.8×	32	295
Rana Chakrabarti Canada	5	146 0.7×	19 0.3×	15 0.4×	15 0.5×	28 0.9×	7	227
Enrico La Spina Italy	9	156 0.8×	39 0.6×	58 1.4×	8 0.3×	15 0.5×	25	286
Laura J. Zitur United States	7	298 1.5×	45 0.7×	33 0.8×	6 0.2×	26 0.8×	10	478
Seo‐Yun Tong South Korea	7	190 1.0×	25 0.4×	45 1.1×	17 0.5×	19 0.6×	7	275
Ling Jin China	9	166 0.9×	49 0.7×	62 1.5×	20 0.6×	8 0.3×	26	292
Jiantuan Xiong China	10	191 1.0×	50 0.7×	16 0.4×	7 0.2×	17 0.5×	17	318
Xuan Tao China	9	178 0.9×	25 0.4×	29 0.7×	7 0.2×	27 0.9×	24	339
Jia Hu China	7	225 1.2×	100 1.5×	81 1.9×	14 0.4×	45 1.5×	21	417

Countries citing papers authored by Patroula Smpokou

Since Specialization

Citations

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

Fields of papers citing papers by Patroula Smpokou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patroula Smpokou

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

Hon, Yuen Yi, Jie Wang, Henrietta Abodakpi, et al.. (2023). Dose selection for biological enzyme replacement therapy indicated for inborn errors of metabolism. Clinical and Translational Science. 16(12). 2438–2457. 6 indexed citations

Suzuki, Mari, Linda Jo Bone Jeng, Yan Wang, et al.. (2022). FDA approval summary for lonafarnib (Zokinvy) for the treatment of Hutchinson-Gilford progeria syndrome and processing-deficient progeroid laminopathies. Genetics in Medicine. 25(2). 100335–100335. 20 indexed citations

Weaver, James L., Wendy Wu, Paula L. Hyland, et al.. (2021). Expanding Approved Patient Populations for Rare Disease Treatment Using In Vitro Data. Clinical Pharmacology & Therapeutics. 112(1). 58–61. 4 indexed citations

Alaimo, Joseph T., Arnaud Besse, Charlotte L. Alston, et al.. (2018). Loss-of-function mutations inISCA2disrupt 4Fe-4S cluster machinery and cause a fatal leukodystrophy with hyperglycinemia and mtDNA depletion. Human Mutation. 39(4). 537–549. 21 indexed citations

Hofherr, Sean, et al.. (2016). Childhood Rhabdomyosarcoma in Association With a RASopathy Clinical Phenotype and Mosaic Germline SOS1 Duplication. Journal of Pediatric Hematology/Oncology. 38(8). e278–e282. 12 indexed citations

Smpokou, Patroula, Brendan C. Lanpher, & Kenneth N. Rosenbaum. (2015). Important Considerations in the Initial Clinical Evaluation of the Dysmorphic Neonate. Advances in Neonatal Care. 15(4). 248–252. 1 indexed citations

Smpokou, Patroula, Dina J. Zand, Kenneth N. Rosenbaum, & Marshall Summar. (2015). Malignancy in Noonan syndrome and related disorders. Clinical Genetics. 88(6). 516–522. 34 indexed citations

Gripp, Karen W., Katia Sol‐Church, Patroula Smpokou, et al.. (2015). An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences. American Journal of Medical Genetics Part A. 167(9). 2085–2097. 18 indexed citations

Smpokou, Patroula, et al.. (2014). Menkes disease in affected females: The clinical disease spectrum. American Journal of Medical Genetics Part A. 167(2). 417–420. 22 indexed citations

10.

Smpokou, Patroula, Victor L. Fox, & Wen‐Hann Tan. (2014). PTEN hamartoma tumour syndrome: early tumour development in children. Archives of Disease in Childhood. 100(1). 34–37. 44 indexed citations

11.

Fraser, Jamie L., Adeline Vanderver, Sandra Yang, et al.. (2014). Thiamine pyrophosphokinase deficiency causes a Leigh Disease like phenotype in a sibling pair: identification through whole exome sequencing and management strategies. Molecular Genetics and Metabolism Reports. 1. 66–70. 29 indexed citations

12.

Smpokou, Patroula, Erica Tworog‐Dube, Raju Kucherlapati, & Amy E. Roberts. (2012). Medical complications, clinical findings, and educational outcomes in adults with Noonan syndrome. American Journal of Medical Genetics Part A. 158A(12). 3106–3111. 68 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.

Explore authors with similar magnitude of impact