László Sztriha

4.7k total citations
66 papers, 1.8k citations indexed

About

László Sztriha is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, László Sztriha has authored 66 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 26 papers in Pediatrics, Perinatology and Child Health and 22 papers in Genetics. Recurrent topics in László Sztriha's work include Fetal and Pediatric Neurological Disorders (20 papers), Neonatal and fetal brain pathology (11 papers) and Hedgehog Signaling Pathway Studies (11 papers). László Sztriha is often cited by papers focused on Fetal and Pediatric Neurological Disorders (20 papers), Neonatal and fetal brain pathology (11 papers) and Hedgehog Signaling Pathway Studies (11 papers). László Sztriha collaborates with scholars based in United Arab Emirates, Hungary and United States. László Sztriha's co-authors include Aithala Gururaj, Lihadh Al‐Gazali, Michael Nork, L.I. Al-Gazali, Renzo Guerrini, Abdülbari Bener, Abdulbari Bener, Sarah Marsh, A. James Barkovich and William B. Dobyns and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Annals of Neurology.

In The Last Decade

László Sztriha

64 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
László Sztriha United Arab Emirates 23 817 751 672 355 301 66 1.8k
Laura Flores‐Sarnat Canada 25 732 0.9× 693 0.9× 557 0.8× 264 0.7× 308 1.0× 66 1.8k
Simone Mandelstam Australia 23 726 0.9× 478 0.6× 771 1.1× 685 1.9× 384 1.3× 60 2.1k
Davide Mei Italy 30 888 1.1× 577 0.8× 1.2k 1.7× 1.0k 2.9× 482 1.6× 81 2.4k
Byung Chan Lim South Korea 23 750 0.9× 375 0.5× 436 0.6× 481 1.4× 244 0.8× 165 1.8k
Antonietta Coppola Italy 28 474 0.6× 438 0.6× 607 0.9× 763 2.1× 384 1.3× 87 2.0k
E Peeters Netherlands 23 447 0.5× 560 0.7× 220 0.3× 650 1.8× 197 0.7× 46 1.7k
Carlo Fusco Italy 21 565 0.7× 296 0.4× 258 0.4× 353 1.0× 276 0.9× 118 1.8k
Kenji Yokochi Japan 20 587 0.7× 460 0.6× 197 0.3× 285 0.8× 131 0.4× 72 1.4k
Michael C. Kruer United States 25 746 0.9× 218 0.3× 412 0.6× 342 1.0× 449 1.5× 74 2.2k
Jillian S. Parboosingh Canada 29 936 1.1× 306 0.4× 617 0.9× 87 0.2× 215 0.7× 85 2.0k

Countries citing papers authored by László Sztriha

Since Specialization
Citations

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

Fields of papers citing papers by László Sztriha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of László Sztriha

This figure shows the co-authorship network connecting the top 25 collaborators of László Sztriha. A scholar is included among the top collaborators of László Sztriha 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 László Sztriha. László Sztriha 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.
Kalmár, Tibor, Zoltán Maróti, Alíz Zimmermann, & László Sztriha. (2020). Tremor as an early sign of hereditary spastic paraplegia due to mutations in ALDH18A1. Brain and Development. 43(1). 144–151. 5 indexed citations
2.
Nagy, Nikoletta, et al.. (2013). Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases. Molecular Cytogenetics. 6(1). 35–35. 6 indexed citations
3.
Varga, Edina, et al.. (2010). European Association of Young Neurologists and Trainees. Ideggyógyászati Szemle. 63. 429.
4.
Sztriha, László & J. G. Johansen. (2005). Spectrum of malformations of the hindbrain (cerebellum, pons, and medulla) in a cohort of children with high rate of parental consanguinity. American Journal of Medical Genetics Part A. 135A(2). 134–141. 11 indexed citations
5.
Dixon‐Salazar, Tracy, Jennifer L. Silhavy, Sarah Marsh, et al.. (2004). Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria. The American Journal of Human Genetics. 75(6). 979–987. 208 indexed citations
6.
Sztriha, László. (2004). Spectrum of corpus callosum agenesis. Pediatric Neurology. 32(2). 94–101. 34 indexed citations
7.
Marsh, Sarah, Esther P. Leeflang, C. Geoffrey Woods, et al.. (2003). Linkage Analysis in Families with Joubert Syndrome Plus Oculo-Renal Involvement Identifies the CORS2 Locus on Chromosome 11p12-q13.3. The American Journal of Human Genetics. 73(3). 656–662. 59 indexed citations
8.
Gururaj, Aithala, László Sztriha, Abdülbari Bener, Adekunle Dawodu, & Valsamma Eapen. (2003). Epilepsy in children with cerebral palsy. Seizure. 12(2). 110–114. 69 indexed citations
9.
Rudnik‐Schöneborn, Sabine, László Sztriha, Gunnar Houge, et al.. (2002). Extended phenotype of pontocerebellar hypoplasia with infantile spinal muscular atrophy. American Journal of Medical Genetics Part A. 117A(1). 10–17. 43 indexed citations
10.
Sztriha, László & Michael Nork. (2002). Bilateral symmetrical frontoparietal polymicrogyria. European Journal of Paediatric Neurology. 6(4). 229–232. 8 indexed citations
11.
Gururaj, Aithala, et al.. (2002). Are the strokes in moyamoya syndrome associated with Down syndrome due to protein C deficiency?. Brain and Development. 24(7). 719–722. 19 indexed citations
12.
Al-Gazali, L.I., et al.. (2001). Gerodermia osteodysplastica and wrinkly skin syndrome: Are they the same?. American Journal of Medical Genetics. 101(3). 213–220. 30 indexed citations
13.
Sztriha, László, L.I. Al-Gazali, Ronald J. A. Wanders, et al.. (2000). Abnormal myelin formation in rhizomelic chondrodysplasia punctata type 2 (DHAPAT-deficiency). Developmental Medicine & Child Neurology. 42(7). 492–495. 23 indexed citations
14.
Endo, Fumio, Ichiro Matsuda, László Sztriha, et al.. (1999). Congenital Insensitivity to Pain with Anhidrosis: Novel Mutations in the TRKA (NTRK1) Gene Encoding A High-Affinity Receptor for Nerve Growth Factor. The American Journal of Human Genetics. 64(6). 1570–1579. 121 indexed citations
15.
Sztriha, László, et al.. (1999). Joubert’s syndrome: new cases and review of clinicopathologic correlation. Pediatric Neurology. 20(4). 274–281. 34 indexed citations
16.
Sztriha, László, et al.. (1999). Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages. Clinical Genetics. 55(2). 95–102. 30 indexed citations
17.
Bener, Abdulbari, et al.. (1998). Public awareness and attitudes towards epilepsy in the United Arab Emirates. Seizure. 7(3). 219–222. 85 indexed citations
18.
Sztriha, László, et al.. (1998). Mediobasal and Mantle Defect of the Prosencephalon: Lobar Holoprosencephaly, Schizencephaly and Diabetes Insipidus. Neuropediatrics. 29(5). 272–275. 4 indexed citations
19.
Mpofu, Christopher, et al.. (1996). Neuroblastoma-Associated Paraneoplastic Syndrome with anti-Hu Antineuronal Antibodies Presenting at the Time of Recurrence. Pediatric Hematology and Oncology. 13(4). 369–373. 3 indexed citations
20.
Sztriha, László, et al.. (1994). Epilepsia Partialis Continua: Follow-Up with99mTc-HMPAO-SPECT. Neuropediatrics. 25(5). 250–254. 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.

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