A. Boday

Most-cited papers

1. Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes

   J. Čopíková, J. Paděrová, Věra Románková, M. Havlovicová +15 more

   2020Annals of Human Genetics19 citations

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2. Absence of spinocerebellar ataxia type 3/Machado–Joseph disease within ataxic patients in the Czech population

   P. Bauer, A. Zumrova, V. Mat'oška, T. Maříková +4 more

   2005European Journal of Neurology19 citations

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3. Fluorescent Multiplex PCR: Fast Method for Autosomal Dominant Spinocerebellar Ataxias Screening

   P. Bauer, S. Kotliarova, V. Maťoška, Z. Mušová +5 more

   2005Russian Journal of Genetics17 citations

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4. Newly designed 11-gene panel reveals first case of hereditary amyloidosis captured by massive parallel sequencing

   Zuzana Chyra Kufova, T. Ševčíková, J. Januška, Petr Vojta +7 more

   2018Journal of Clinical Pathology14 citations Open access

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5. [Malignant Melanoma - from Classical Histology towards Molecular Genetic Testing].

   A. Ryška, O. Horký, J. Berkovcová, I. Ticha +8 more

   2017Klinicka onkologie8 citations Open access

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6. Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion.

   P. Bauer, V. Maťoška, A. Zumrová, A. Boday +3 more

   2005Journal of Applied Genetics7 citations

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7. [Screening of celiac disease in patients with osteoporosis and osteopenia].

   P. Fojtík, Pavel Novosad, Martin Kliment, Petr Hrdý +3 more

   2011Vnitrni lekarstvi5 citations

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8. Prognostic and predictive molecular biological markers in prostate cancer - significance of expression of genes PCA3 and TMPRSS2.

   R. Soumarová, A. Boday, V. Krhutova, A. Janotová +4 more

   2015Neoplasma (Bratislava)4 citations Open access

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9. P02.235 Biological markers of the hyperkinetic syndrome in children of age 6 to 10 years

   Ivo Paclt, P. Uhlíková, J. Koudelová, Peter Bauer +4 more

   2000European psychiatry4 citations Open access

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10. [KRAS mutation testing in therapeutic algorithm for treatment of metastatic colorectal carcinoma].

    L. Dubská, M. Vyskočilová, R. Nenutil, D. Valík +18 more

    2011Casopis lekaru ceskych2 citations

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11. [DNA diagnosis of the fragile X chromosome syndrome--FRAXA using PCR].

    A. Boday, V. Mat'oška, V. Konrádová, M. Havlovicová +3 more

    1998Casopis lekaru ceskych2 citations

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12. [Use of CA repeat polymorphism in direct and indirect diagnosis of Duchenne and Becker muscular dystrophy].

    Z. Mušová, V. Mat'oška, Š. Krejčová, A. Boday

    1997Casopis lekaru ceskych2 citations

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13. Leber congenital amaurosis and early onset severe retinal dystrophy in the Czech Republic: Mutational spectrum and clinical findings

    M. Vajter, B. Kousal, J. Moravíková, Monika Chylova +5 more

    2022Acta ophthalmologica1 citations

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14. CHARACTERIZATION OF MUTATIONS THROUGH WHOLE GENE SEQUENCING OF THE GLUCOSE-6-PHOSPHATE DEHYDROGENASE GENE AMONG FILIPINO CHILDREN

    P. Cibulková, R. Krenkova, P., Vanickova +7 more

    20150 citations

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15. Cytology, CEA and K-RAS analysis of cyst fluid aspirate obtained by EUS-FNA in diagnosing pancreatic cystic neoplasia – A prospective study

    M. Kliment, O. Urban, L. Ceganova, A. Boday +4 more

    20120 citations

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16. 242 Neurophysiological findings in patients with spinocerebellar ataxias

    J. Kraus, V. Mat'oška, A. Zumrová, A. Boday +1 more

    19990 citations

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17. 243 Genotype/phenotype correlations in Duchenne/Becker muscular dystrophy

    J. Kraus, Š. Krejčová, A. Boday, V. Mat'oška +1 more

    19990 citations

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18. 205 Hereditary ataxias in the Czech republic

    V. Mat'oška, A. Zumrová, T. Maříková, A. Boday +3 more

    19990 citations

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