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Scopus Author ID: 7006367734
ResearcherID: K-4922-2014

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Employment (1)

University Hospital: Olomouc, CZ

1997 to present (Department of Clinical Genetics and Foetal Medicine)
Employment
Source: Self-asserted source
Pavlina Capkova

Education and qualifications (1)

Palacky University, Faculty of Sciences: Olomouc, CZ

1984 to 1989 | Ph.D
Education
Source: Self-asserted source
Pavlina Capkova

Funding (1)

MH CZ-DRO(FNOL, 00098892)

2016-04 to 2017-01 | Grant
Ministry of Health Czech Republic (Prague, CZ)
Source: Self-asserted source
Pavlina Capkova

Works (15)

Clinical-genetic analysis of selected genes involved in the development of the human skeleton in 128 Czech patients with suspected congenital skeletal abnormalities

Gene
2024-01 | Journal article
DOI: 10.1016/j.gene.2023.147881
Contributors: Z Spurná; P Čapková; L Punová; J DuchoslavovÁ; D Aleksijevic; P Venháčová; J Srovnal; J Štellmachová; V Curtisová; V Bitnerová et al.
Source: check_circle
Crossref

Prenatal detection of copy number variants in fetuses with detected congenital devolpmental disordes, from 2015 to 2020 by Multiplex Ligation-Dependent Probe Amplification and microarray analysis

Česká gynekologie
2023-06-21 | Journal article
DOI: 10.48095/cccg2023162
Contributors: Andrea Štefeková; Pavlína Čapková; Václava Curtisová; Enghjargalan Mracká; Hana Filipová; Zuzana Spurná; Martin Procházka; Marek Ľubušký; Radovan Pilka; Radek Vrtěl
Source: check_circle
Crossref

MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism

PeerJ
2019-01-09 | Journal article
DOI: 10.7717/peerj.6183
Contributors: Pavlina Capkova; Josef Srovnal; Zuzana Capkova; Katerina Staffova; Vera Becvarova; Marie Trkova; Katerina Adamova; Alena Santava; Vaclava Curtisova; Marian Hajduch et al.
Source: check_circle
Crossref

Haploinsufficiency of BMP4 and OTX2 in the Foetus with an abnormal facial profile detected in the first trimester of pregnancy

Molecular Cytogenetics
2017-12 | Journal article
DOI: 10.1186/s13039-017-0351-3
Contributors: Pavlina Capkova; Alena Santava; Ivana Markova; Andrea Stefekova; Josef Srovnal; Katerina Staffova; Veronika Durdová
Source: check_circle
Crossref

Partial trisomy and tetrasomy of chromosome 21 without dowsyndrome phenotype and short overview of genotype-phenotype correlation. A case report

2014 | Journal article
DOI:

10.5507/bp.2013.077

EID:

2-s2.0-84903595907
Contributors: Capkova, P.; Misovicova, N.; Vrbickaa, D.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier

Substitution of prenatal karyotyping with targeted QFPCR - Cytogenetic residual risk assessment | Stanovení reziduálního cytogenetického rizika v prenatální diagnostice při nahrazení tradičního karyotypování cílenými molekulárními testy určenými k rychlé detekci aneuploidií - Retrospektivní studie

2011 | Journal article
EID:

2-s2.0-79959596421
Contributors: Čapková, P.; Curtisová, V.; Dhaifalah, I.; Hyjánek, J.; Křepská, J.; Streitová, R.; Šantavý, J.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier

Rethore syndrome (trisomy 9p) | Syndrom rethoreové (trizomie 9p)

2007 | Journal article
EID:

2-s2.0-34547807062
Contributors: Čapková, P.; Šantavá, A.; Holzerová, M.; Jarošová, M.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier

Porod plodu s triploidní mozaikou a chorangiózou placenty

Gynekolog
2006 | Journal article
OTHER-ID:

ISSN: 1210-1133.
Source: Self-asserted source
Pavlina Capkova

Molecular genetic study of causes of the Prader-Willi and Angelman syndrome | Molekulárně-genetická studie příč in Prader-Williho a Angelmanova syndromu

2005 | Journal article
EID:

2-s2.0-14644400554
Contributors: Čapková, P.; Vrtěl, R.; Šantavá, A.; Zapletalová, J.; Kršiaková, J.; Hyjánek, J.; Šantavý, J.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier

The Importance of Genetic Investigation in Couples with Reproduction Impairment | Význam Genetického Vyšetření u Párů s Poruchami Reprodukce

2004 | Journal article
EID:

2-s2.0-1242291899
Contributors: Čapková, P.; Adamová, K.; Šantavá, A.; Braunerová, B.; Kolářová, J.; Polák, P.; Sobek, A.; Oborná, I.; Šantavý, J.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier

Uniparental Paternal Disomia as a Cause of Angelman Syndrome in a Five-Year Girl | Uniparentální Paternální Dizomie jako Příčina Angelmanova Syndromu

2004 | Journal article
EID:

2-s2.0-1542573842
Contributors: Šantavá, A.; Čapková, P.; Vrtěl, R.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier

Atypický ultrazvukový obraz u plodu s Downovým syndromem matky s gonozomální mozaikou.

Gynekolog
2003 | Journal article
OTHER-ID:

bmc04002044

OTHER-ID:

http://www.medvik.cz/link/bmc04002044
Source: Self-asserted source
Pavlina Capkova

Microdeletion of azoospermia factor as one of the possible causes of male infertility | Mikrodelece faktoru azoospermie jako jedna z příčin mužské infertility

2003 | Journal article
EID:

2-s2.0-0038674750
Contributors: Kolářová, J.; Vrtěl, R.; Vodička, R.; Čapková, P.; Šantavý, J.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier

Early fetal karyotyping and its role in prenatal diagnosis | Vcasná karyotypizace fetu a její prínos pro prenatální diagnostiku.

2000 | Journal article
EID:

2-s2.0-0034330056
Contributors: Vodicka, R.; Adamová, K.; Capková, P.; Santavý, J.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier

The importance of ultrasonography in the 1st and 2nd trimester of pregnancy in prenatal diagnosis of chromosome aberrations | Význam ultrazvuku v I. a II. trimestru gravidity pro prenatální diagnostiku chromosomálních aberací.

1998 | Journal article
EID:

2-s2.0-18344401374
Contributors: Polák, P.; Santavý, J.; Hyjánek, J.; Santavá, A.; Capková, P.
Source: Self-asserted source
Pavlina Capkova via Scopus - Elsevier
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