P Balícek

420 total citations
27 papers, 296 citations indexed

About

P Balícek is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, P Balícek has authored 27 papers receiving a total of 296 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in P Balícek's work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (7 papers). P Balícek is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (7 papers). P Balícek collaborates with scholars based in Czechia, Australia and Denmark. P Balícek's co-authors include Ján Žižka, Fosco Bernasconi, Wendy P. Robinson, Güven Lüleci, Giovanni Neri, F Serville, Memnune Yüksel‐Apak, Johannes Nielsen, K Kozłowski and A Baxová and has published in prestigious journals such as Human Genetics, Acta Paediatrica and American Journal of Medical Genetics.

In The Last Decade

P Balícek

24 papers receiving 258 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P Balícek Czechia 10 217 130 113 101 34 27 296
M Ferguson-Smith United Kingdom 10 242 1.1× 95 0.7× 168 1.5× 153 1.5× 24 0.7× 15 374
Constance J. Sandlin United States 8 316 1.5× 239 1.8× 132 1.2× 138 1.4× 63 1.9× 10 397
M. Crocker United Kingdom 9 183 0.8× 68 0.5× 88 0.8× 52 0.5× 15 0.4× 16 245
Milly Andrle Austria 7 239 1.1× 72 0.6× 191 1.7× 195 1.9× 11 0.3× 11 358
Frank S. Grass United States 8 184 0.8× 122 0.9× 88 0.8× 84 0.8× 24 0.7× 12 256
Carolyn Trunca United States 9 199 0.9× 152 1.2× 98 0.9× 96 1.0× 31 0.9× 14 301
M. Barr United States 6 144 0.7× 93 0.7× 199 1.8× 24 0.2× 62 1.8× 6 346
B. Biederman Canada 11 256 1.2× 56 0.4× 132 1.2× 139 1.4× 15 0.4× 18 292
Christine A Joyce United Kingdom 8 195 0.9× 98 0.8× 145 1.3× 68 0.7× 16 0.5× 10 255
Sorrell H. Waxman United States 13 217 1.0× 143 1.1× 132 1.2× 50 0.5× 37 1.1× 19 387

Countries citing papers authored by P Balícek

Since Specialization
Citations

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

Fields of papers citing papers by P Balícek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P Balícek

This figure shows the co-authorship network connecting the top 25 collaborators of P Balícek. A scholar is included among the top collaborators of P Balícek 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 P Balícek. P Balícek 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.
Balícek, P, et al.. (2011). A case of Down syndrome with acute lymphoblastic leukemia and t(8;14)(q11;q32). Atlas of Genetics and Cytogenetics in Oncology and Haematology.
2.
Žižka, Ján, et al.. (2002). Currarino triad: concurrent US and MRI diagnosis in the fetus and the mother. Prenatal Diagnosis. 22(11). 1005–1010. 12 indexed citations
3.
Balícek, P, et al.. (2001). [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].. PubMed. 140(4). 122–4. 4 indexed citations
4.
Žižka, Ján, et al.. (1998). Brachytelephalangic chondrodysplasia punctata with distinctive phenotype and normal karyotype. American Journal of Medical Genetics. 76(3). 213–216. 11 indexed citations
5.
Robinson, Wendy P., Fosco Bernasconi, Memnune Yüksel‐Apak, et al.. (1994). A somatic origin of homologous Robertsonian translocations and isochromosomes. PubMed. 54(2). 290–302. 102 indexed citations
6.
Balícek, P, et al.. (1983). INTESTINAL AGANGLIONOSIS IN THE SMITH‐LEMLI‐OPITZ SYNDROME. Acta Paediatrica. 72(1). 141–143. 15 indexed citations
7.
Balícek, P, et al.. (1982). RHG-band polymorphism of the short arms of human acrocentric chromosomes and relationship of variants to satellite associations. Human Genetics. 62(3). 237–239. 1 indexed citations
8.
Žižka, Ján, et al.. (1981). [Fetal face syndrome (Robinow syndrome].. PubMed. 36(6). 328–30. 4 indexed citations
9.
Žižka, Ján, et al.. (1981). Trisomy 18 syndrome: analysis of 15 cases.. PubMed. 24(3). 385–405.
10.
Balícek, P & Ján Žižka. (1980). Intercalar satellites of human acrocentric chromosomes as a cytological manifestation of polymorphism in GC-rich material?. Human Genetics. 54(3). 343–347. 7 indexed citations
11.
Balícek, P, et al.. (1979). Chromosomal patterns in patients treated in chronic intermittent haemodialysis programme.. PubMed. 22(1). 9–12. 2 indexed citations
12.
Balícek, P, et al.. (1977). Length of human constitutive heterochromatin in relation to chromosomal contraction. Human Genetics. 38(2). 189–193. 40 indexed citations
13.
Žižka, Ján, et al.. (1977). [Trisomy X in a neonate with esophageal atresia].. PubMed. 32(12). 723–4. 2 indexed citations
14.
Balícek, P, et al.. (1976). An isochromosome of the short arms of the no. 18 chromosome in a mentally retarded girl. Clinical Genetics. 9(2). 192–196. 15 indexed citations
15.
Žižka, Ján, et al.. (1976). Exomphalos and trisomy 18 syndrome. Human Genetics. 32(2). 221–223. 3 indexed citations
16.
Lichy, Jack, et al.. (1975). Proceedings: EEG findings in children with Klinefelter's syndrome.. PubMed. 39(4). 439–439. 2 indexed citations
17.
Žižka, Ján, P Balícek, & Johannes Nielsen. (1975). XXYY son of a triple-X mother. Human Genetics. 26(2). 159–160. 9 indexed citations
18.
Balícek, P, et al.. (1975). A case of trisomy 9p in a family with translocation 9/15. PubMed. 27(4). 353–358. 18 indexed citations
19.
Žižka, Ján, et al.. (1975). [Syndrome of metacentric microchromosome].. PubMed. 30(1-2). 50–3. 8 indexed citations
20.
Žižka, Ján, et al.. (1975). A boy with 48, XXYY karyotype.. PubMed. 19(1). 161–6. 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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