B. Petrák

455 total citations
19 papers, 212 citations indexed

About

B. Petrák is a scholar working on Neurology, Epidemiology and Surgery. According to data from OpenAlex, B. Petrák has authored 19 papers receiving a total of 212 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 5 papers in Epidemiology and 4 papers in Surgery. Recurrent topics in B. Petrák's work include Neurofibromatosis and Schwannoma Cases (9 papers), Neuroblastoma Research and Treatments (4 papers) and Meningioma and schwannoma management (3 papers). B. Petrák is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (9 papers), Neuroblastoma Research and Treatments (4 papers) and Meningioma and schwannoma management (3 papers). B. Petrák collaborates with scholars based in Czechia, Germany and Brazil. B. Petrák's co-authors include John C. Carey, H. R. Hill, Markéta Havlovičová, Martin Kynčl, Šárka Bendová, Zdeněk Sedláček, Michal Hrdlička, Josef Zámečnı́k, Michal Tichý and Jiří Lisý and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Journal of Inherited Metabolic Disease.

In The Last Decade

B. Petrák

16 papers receiving 193 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B. Petrák Czechia	8	66	56	53	44	35	19	212
Denise L. Lind United States	6	107 1.6×	26 0.5×	92 1.7×	57 1.3×	16 0.5×	7	335
Nathan R. McGee United States	11	55 0.8×	27 0.5×	194 3.7×	51 1.2×	18 0.5×	18	297
Marie‐Louise Bondeson Sweden	10	108 1.6×	60 1.1×	30 0.6×	202 4.6×	11 0.3×	13	305
Heather Allewelt United States	7	18 0.3×	30 0.5×	27 0.5×	66 1.5×	59 1.7×	12	185
Jürgen Groet United Kingdom	12	98 1.5×	59 1.1×	23 0.4×	213 4.8×	29 0.8×	15	502
Juliane Eckhold Germany	8	66 1.0×	23 0.4×	16 0.3×	116 2.6×	19 0.5×	10	202
Amal Al‐Hemidan Saudi Arabia	10	60 0.9×	22 0.4×	23 0.4×	72 1.6×	14 0.4×	13	307
Katherine S. Elliott United Kingdom	8	59 0.9×	37 0.7×	95 1.8×	71 1.6×	10 0.3×	12	238
Victoria Empson Austria	7	47 0.7×	106 1.9×	55 1.0×	58 1.3×	6 0.2×	12	241
Glenda M. Beaman United Kingdom	9	86 1.3×	64 1.1×	8 0.2×	129 2.9×	17 0.5×	20	278

Countries citing papers authored by B. Petrák

Since Specialization

Citations

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

Fields of papers citing papers by B. Petrák

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Petrák

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

All Works

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19 of 19 papers shown

Petrák, B., et al.. (2021). Monozygotic twins with Legius syndrome and differential diagnosis of Legius syndrome and neurof bromatosis type 1. Česká a slovenská neurologie a neurochirurgie. 84/117(2).

Petrák, B., et al.. (2020). Torcular dural sinus malformations: a grading system proposal. Child s Nervous System. 36(11). 2707–2716. 6 indexed citations

Petrák, B., et al.. (2019). Torcular dural sinus malformations: a single-center case series and a review of literature. Child s Nervous System. 36(2). 333–341. 13 indexed citations

Petrák, B., et al.. (2019). Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 1. Brain and Development. 41(8). 678–690. 13 indexed citations

Beňová, Barbora, B. Petrák, Martin Kynčl, et al.. (2018). Early predictors of clinical and mental outcome in tuberous sclerosis complex: A prospective study. European Journal of Paediatric Neurology. 22(4). 632–641. 17 indexed citations

Petrák, B., et al.. (2018). Neurofibromatosis von Recklinghausen type 1 (NF1) - the most common neurocutaneous disorder. Neurologie pro praxi. 19(2). 104–107.

Fogarasi, András, Liesbeth De Waele, G. Bartalini, et al.. (2016). EFFECTS: an expanded access program of everolimus for patients with subependymal giant cell astrocytoma associated with tuberous sclerosis complex. BMC Neurology. 16(1). 126–126. 15 indexed citations

Brožková, Dana Šafka, B. Petrák, Jana Haberlová, et al.. (2013). HomozygousEXOSC3Mutation c.92G→C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma. Journal of Neurogenetics. 27(4). 163–169. 26 indexed citations

Šnajderová, Marta, Vincent M. Riccardi, B. Petrák, et al.. (2012). The importance of advanced parental age in the origin of neurofibromatosis type 1. American Journal of Medical Genetics Part A. 158A(3). 519–523. 15 indexed citations

10.

Petrák, B., Pavlína Plevová, Jiřı́ Novotný, & Lenka Foretová. (2009). [Neurofibromatosis von Recklinghausen].. PubMed. 22 Suppl. S38–44. 3 indexed citations

11.

Petrák, B., et al.. (2008). FOCAL AREAS OF HIGH-SIGNAL INTENSITY ON BRAIN T2-WEIGHTED MAGNETIC RESONANCE IMAGING SCANS ARE SIGNIFICANT FOR THE DIAGNOSIS OF NEUROFIBROMATOSIS VON RECKLINGHAUSEN TYPE 1. PEDIATRICS. 121(Supplement_2). S147–S147. 3 indexed citations

12.

Bendová, Šárka, et al.. (2007). Novel mutations in the NF1 gene in Czech patients with neurofibromatosis type 1. Journal of Molecular Neuroscience. 31(3). 273–279. 3 indexed citations

13.

Kotaška, Karel, B. Petrák, Jiří Kukačka, Josef Kraus, & Richard Průša. (2007). Anti-vimentin antibodies and neuron-specific enolase in children with neurofibromatosis type-1.. PubMed. 28(6). 761–4. 3 indexed citations

14.

Petrák, B., et al.. (2007). Mid-aortic syndrome with renovascular hypertension and multisystem involvement in a girl with familiar neurofibromatosis von Recklinghausen type 1.. PubMed. 28(6). 734–8.

15.

Havlovičová, Markéta, et al.. (2006). A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17. American Journal of Medical Genetics Part A. 143A(1). 76–81. 34 indexed citations

16.

Petrák, B.. (2001). [Neurofibromatosis von Recklinghausen type 1 (NF1) - clinical picture and molecular-genetics diagnostic].. Medical Entomology and Zoology. 51(1). 34–40. 3 indexed citations

17.

Carey, John C., et al.. (1998). The face of Job. The Journal of Pediatrics. 133(2). 303–305. 54 indexed citations

18.

Hřebı́ček, Martin, J Zeman, B. Petrák, et al.. (1992). Unusual clinical presentation in two boys with cytochromec oxidase deficiency. Journal of Inherited Metabolic Disease. 15(3). 320–322. 3 indexed citations

19.

Petrák, B.. (1966). Sport Activity in the Life of the Population of the Czechomoravian Plateau. International Review of Sport Sociology. 1(1). 141–151. 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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