Miriam Kessi

701 total citations
34 papers, 440 citations indexed

About

Miriam Kessi is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Miriam Kessi has authored 34 papers receiving a total of 440 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Genetics and 11 papers in Psychiatry and Mental health. Recurrent topics in Miriam Kessi's work include Genetics and Neurodevelopmental Disorders (13 papers), Epilepsy research and treatment (10 papers) and Neuroscience and Neuropharmacology Research (8 papers). Miriam Kessi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (13 papers), Epilepsy research and treatment (10 papers) and Neuroscience and Neuropharmacology Research (8 papers). Miriam Kessi collaborates with scholars based in China, Tanzania and Canada. Miriam Kessi's co-authors include Fei Yin, Jing Peng, Lifen Yang, Baiyu Chen, Juan Xiong, Fang He, Nan Pang, Liwen Wu, Ciliu Zhang and Yulin Tang and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Frontiers in Pharmacology.

In The Last Decade

Miriam Kessi

30 papers receiving 437 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Miriam Kessi China	11	160	158	143	117	62	34	440
Noriyuki Akasaka Japan	14	175 1.1×	214 1.4×	245 1.7×	122 1.0×	76 1.2×	27	566
Takeshi Okinaga Japan	14	160 1.0×	99 0.6×	74 0.5×	58 0.5×	26 0.4×	27	411
Yoram Nevo Israel	14	241 1.5×	186 1.2×	80 0.6×	90 0.8×	48 0.8×	31	641
Ilaria Contaldo Italy	13	158 1.0×	219 1.4×	192 1.3×	71 0.6×	26 0.4×	44	449
Lata Vadlamudi Australia	14	215 1.3×	396 2.5×	323 2.3×	148 1.3×	50 0.8×	30	721
Katsuyuki Fukushima Japan	8	231 1.4×	352 2.2×	161 1.1×	228 1.9×	69 1.1×	14	567
Jao‐Shwann Liang Taiwan	13	159 1.0×	136 0.9×	177 1.2×	65 0.6×	23 0.4×	44	458
Yuan Wu China	11	133 0.8×	56 0.4×	77 0.5×	87 0.7×	87 1.4×	32	416
Tine Van Dyck Belgium	6	188 1.2×	332 2.1×	156 1.1×	179 1.5×	23 0.4×	6	472
Antonia Clarke United Kingdom	12	186 1.2×	103 0.7×	48 0.3×	70 0.6×	69 1.1×	15	490

Countries citing papers authored by Miriam Kessi

Since Specialization

Citations

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

Fields of papers citing papers by Miriam Kessi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miriam Kessi

This figure shows the co-authorship network connecting the top 25 collaborators of Miriam Kessi. A scholar is included among the top collaborators of Miriam Kessi 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 Miriam Kessi. Miriam Kessi 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:

20 of 20 papers shown

Kessi, Miriam, Fang He, Ciliu Zhang, et al.. (2025). Anti-GAD65 Antibodies Related Refractory Epilepsy Successfully Treated with Tocilizumab: A Case Report and Systematic Literature Review. ImmunoTargets and Therapy. Volume 14. 491–500.

Wang, Guoli, Miriam Kessi, Xi Huang, et al.. (2024). Treatment of juvenile myasthenia gravis with tacrolimus: A cohort study. European Journal of Neurology. 31(12). e16466–e16466.

Kessi, Miriam, et al.. (2024). Anti-GluK2 Encephalitis in an Asian Child: A Case Report and Literature Review. ImmunoTargets and Therapy. Volume 13. 805–811.

Kessi, Miriam, Yulin Tang, Baiyu Chen, et al.. (2024). Pediatric Ocular Myasthenia Gravis: Single-Center Experience. Pediatric Neurology. 153. 137–143. 2 indexed citations

Kessi, Miriam, Baiyu Chen, Nan Pang, et al.. (2023). The genotype–phenotype correlations of the CACNA1A-related neurodevelopmental disorders: a small case series and literature reviews. Frontiers in Molecular Neuroscience. 16. 1222321–1222321. 9 indexed citations

Kessi, Miriam, Baiyu Chen, Ying Wang, et al.. (2023). Genotype-phenotype correlations of STXBP1 pathogenic variants and the treatment choices for STXBP1-related disorders in China. BMC Medical Genomics. 16(1). 46–46. 5 indexed citations

Yang, Lifen, Yulin Tang, Fang He, et al.. (2022). Clinical characteristics and outcome predictors of a Chinese childhood-onset myasthenia gravis cohort. Frontiers in Pediatrics. 10. 996213–996213. 7 indexed citations

Kessi, Miriam, Jing Peng, Hailan He, et al.. (2022). The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review. Frontiers in Molecular Neuroscience. 15. 807202–807202. 23 indexed citations

Chen, Baiyu, Miriam Kessi, Juan Xiong, et al.. (2021). Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children. Frontiers in Molecular Biosciences. 8. 792319–792319. 7 indexed citations

10.

Xiong, Juan, Miriam Kessi, Fang He, et al.. (2021). Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients. BMC Medical Genomics. 14(1). 182–182. 8 indexed citations

11.

Kessi, Miriam, et al.. (2021). Calcium channelopathies and intellectual disability: a systematic review. Orphanet Journal of Rare Diseases. 16(1). 219–219. 45 indexed citations

12.

Guang, Shiqi, Jiannan Ma, Shuizhen Zhou, et al.. (2021). Immunotherapies for Anti-N-M-methyl-D-aspartate Receptor Encephalitis: Multicenter Retrospective Pediatric Cohort Study in China. Frontiers in Pediatrics. 9. 691599–691599. 9 indexed citations

13.

Yin, Fei, Pan Zou, Ting Xiao, et al.. (2020). The Study of Genetic Susceptibility and Mitochondrial Dysfunction in Mesial Temporal Lobe Epilepsy. Molecular Neurobiology. 57(9). 3920–3930. 19 indexed citations

14.

Kessi, Miriam, Baiyu Chen, Jing Peng, et al.. (2020). Intellectual Disability and Potassium Channelopathies: A Systematic Review. Frontiers in Genetics. 11. 614–614. 34 indexed citations

15.

Chen, Baiyu, Miriam Kessi, Juan Xiong, et al.. (2020). The Recommendations for the Management of Chinese Children With Epilepsy During the COVID-19 Outbreak. Frontiers in Pediatrics. 8. 495–495. 4 indexed citations

16.

Kessi, Miriam, Yulin Tang, Liwen Wu, et al.. (2020). Efficacy of different treatment modalities for acute and chronic phases of the febrile infection-related epilepsy syndrome: A systematic review. Seizure. 79. 61–68. 14 indexed citations

17.

Peng, Jing, Hui Xiao, Liwen Wu, et al.. (2019). [Clinical features and COL4A1 genotype of a toddler with hereditary angiopathy with nephropathy, aneurysms and muscle cramps syndrome].. PubMed. 21(8). 754–760. 4 indexed citations

18.

Peng, Jing, Nan Pang, Ying Wang, et al.. (2018). Next‐generation sequencing improves treatment efficacy and reduces hospitalization in children with drug‐resistant epilepsy. CNS Neuroscience & Therapeutics. 25(1). 14–20. 45 indexed citations

19.

Kessi, Miriam, Jing Peng, Lifen Yang, et al.. (2018). Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic review. BMC Genetics. 19(1). 40–40. 35 indexed citations

20.

Kessi, Miriam, et al.. (2018). A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication Syndromes. SHILAP Revista de lepidopterología. 5. 2329048X18798200–2329048X18798200. 2 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