Zdeněk Sedláček

6.2k total citations
70 papers, 1.5k citations indexed

About

Zdeněk Sedláček is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Zdeněk Sedláček has authored 70 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 33 papers in Genetics and 14 papers in Oncology. Recurrent topics in Zdeněk Sedláček's work include Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (13 papers) and Cancer-related Molecular Pathways (11 papers). Zdeněk Sedláček is often cited by papers focused on Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (13 papers) and Cancer-related Molecular Pathways (11 papers). Zdeněk Sedláček collaborates with scholars based in Czechia, Germany and United Kingdom. Zdeněk Sedláček's co-authors include Markéta Havlovičová, Annemarie Poustka, Marie Trková, Miroslava Hančárová, Michal Hrdlička, Tomáš Urbánek, Bernhard Korn, Anna Křepelová, David Konecki and Roman Kodet and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Zdeněk Sedláček

67 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Zdeněk Sedláček Czechia	24	879	612	232	223	207	70	1.5k
Maria Antonietta Mencarelli Italy	26	982 1.1×	1.2k 1.9×	161 0.7×	81 0.4×	354 1.7×	65	1.9k
Bertrand Isidor France	26	1.3k 1.5×	908 1.5×	165 0.7×	144 0.6×	77 0.4×	112	2.1k
Maria Grazia Pomponi Italy	21	748 0.9×	662 1.1×	79 0.3×	270 1.2×	196 0.9×	56	1.2k
Willy M. Nillesen Netherlands	23	1.3k 1.4×	1.3k 2.0×	119 0.5×	142 0.6×	156 0.8×	42	2.2k
Francisco Martı́nez Spain	24	1.1k 1.2×	837 1.4×	76 0.3×	301 1.3×	98 0.5×	118	1.8k
Katherina Walz United States	26	1.1k 1.2×	965 1.6×	90 0.4×	79 0.4×	193 0.9×	59	1.7k
Livia Tomasini United States	12	1.5k 1.8×	585 1.0×	87 0.4×	332 1.5×	216 1.0×	16	2.1k
Francesca Ariani Italy	29	1.3k 1.5×	1.6k 2.6×	165 0.7×	106 0.5×	581 2.8×	70	2.4k
Fiorella Gurrieri Italy	27	1.4k 1.6×	1.3k 2.1×	86 0.4×	131 0.6×	290 1.4×	88	2.4k
Anath C. Lionel Canada	21	940 1.1×	866 1.4×	174 0.8×	85 0.4×	274 1.3×	36	1.7k

Countries citing papers authored by Zdeněk Sedláček

Since Specialization

Citations

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

Fields of papers citing papers by Zdeněk Sedláček

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zdeněk Sedláček

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

All Works

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20 of 20 papers shown

Vlčková, Markéta, Darina Prchalová, Jana Haberlová, et al.. (2023). A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype–phenotype correlation. Molecular Genetics & Genomic Medicine. 11(6). e2154–e2154. 1 indexed citations

Prchalová, Darina, Markéta Havlovičová, Katalin Štěrbová, et al.. (2017). Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report. BMC Medical Genetics. 18(1). 62–62. 23 indexed citations

Mušová, Zuzana, Miroslava Hančárová, Markéta Havlovičová, et al.. (2016). Expanded <em>DMPK </em>repeats in dizygotic twins referred for diagnosis of autism versus absence of expanded <em>DMPK </em>repeats at screening of 330 children with autism. Neuropsychiatric Disease and Treatment. Volume 12. 2367–2372. 1 indexed citations

Vlčková, Markéta, Viktor Stránecký, Hana Hartmannová, et al.. (2015). A patient showing features of both SBBYSS and GPS supports the concept of a KAT6B-related disease spectrum, with mutations in mid-exon 18 possibly leading to combined phenotypes. European Journal of Medical Genetics. 58(10). 550–555. 24 indexed citations

Vlčková, Markéta, Miroslava Hančárová, Monika Koudová, et al.. (2014). Monozygotic Twins with 17q21.31 Microdeletion Syndrome. Twin Research and Human Genetics. 17(5). 405–410. 3 indexed citations

Brisset, Sophie, Petra Dušátková, Audrey Briand‐Suleau, et al.. (2014). Anophthalmia, hearing loss, abnormal pituitary development and response to growth hormone therapy in three children with microdeletions of 14q22q23. Molecular Cytogenetics. 7(1). 17–17. 11 indexed citations

Hančárová, Miroslava, et al.. (2012). Identification of a patient with intellectual disability and de novo 3.7Mb deletion supports the existence of a novel microdeletion syndrome in 2p14–p15. Gene. 516(1). 158–161. 9 indexed citations

Mejstříková, Ester, Aleš Janda, Ondřej Hrušák, et al.. (2012). Skin Lesions in a Boy With X-linked Lymphoproliferative Disorder: Comparison of 5 SH2D1A Deletion Cases. PEDIATRICS. 129(2). e523–e528. 6 indexed citations

Minárik, Marek, et al.. (2008). Somatic TP53 mutation mosaicism in a patient with Li–Fraumeni syndrome. American Journal of Medical Genetics Part A. 149A(2). 206–211. 30 indexed citations

10.

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

11.

Hrdlička, Michal, Iva Dudová, Jiří Lisý, et al.. (2005). Subtypes of autism by cluster analysis based on structural MRI data. European Child & Adolescent Psychiatry. 14(3). 138–144. 51 indexed citations

12.

Trková, Marie, Julie Fleitz, Anna Křepelová, et al.. (2005). Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations. European Journal of Cancer. 41(11). 1597–1603. 54 indexed citations

13.

Trková, Marie, et al.. (2003). A Li-Fraumeni syndrome family with retained heterozygosity for a germline TP53 mutation in two tumors. Cancer Genetics and Cytogenetics. 145(1). 60–64. 16 indexed citations

14.

Havlovičová, Markéta, et al.. (2002). [Genetic study of 20 patients with autism disorders].. PubMed. 141(12). 381–7. 1 indexed citations

15.

Babjuk, M., Viktor Soukup, J. Mareš, et al.. (2002). The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue. Correlation with pathological findings and clinical outcome. International Urology and Nephrology. 34(4). 495–501. 17 indexed citations

16.

Sedláček, Zdeněk, Ewald Münstermann, Sophie Dhorne‐Pollet, et al.. (1999). Human and Mouse XAP-5 and XAP-5-like (X5L) Genes: Identification of an Ancient Functional Retroposon Differentially Expressed in Testis. Genomics. 61(2). 125–132. 28 indexed citations

17.

Sedláček, Zdeněk, Roman Kodet, E Seemanová, et al.. (1998). Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours. British Journal of Cancer. 77(7). 1034–1039. 35 indexed citations

18.

Coy, Johannes F., Zdeněk Sedláček, Dietmar Bächner, et al.. (1995). Highly conserved 3′ UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1. Human Molecular Genetics. 4(12). 2209–2218. 58 indexed citations

19.

Youngman, S, Gillian P. Bates, Andrea I. McClatchey, et al.. (1992). The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p. Genomics. 14(2). 350–356. 28 indexed citations

20.

Bates, Gillian P., Marcy E. MacDonald, Sarah Baxendale, et al.. (1990). A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.. PubMed. 46(4). 762–75. 56 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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