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Jan Diblík

Observed names: Diblík, Jan, J Diblik, J Diblík, J. Diblik, J. Diblík, Jan Diblik
Institution: Gennet
ORCID: 0000-0002-0627-9124
Observed ORCID: 0000-0002-0627-9124
OpenAlex ID: A5052251126
Accumulation of the Proteolytic Marker Peptide Ubiquitin in the Trophoblast of Mammalian Blastocysts
2001 · Peter Sutovsky, Jan Motlik, et al. · Cloning and Stem Cells · 15
An ADP-ribosyltransferase 3 (ART3) variant is associated with reduced sperm counts in Czech males: case/control association study replicating results from the Japanese population.
2012 · Patricia Alejandra Norambuena, Jan Diblík, et al. · PubMed · 6
Chromosome topology in normal and aneuploid blastomeres from human embryos
2007 · Jan Diblík, Milan Macek, et al. · Prenatal Diagnosis · 6
Increased sperm aneuploidy in two male carriers of germline TP53 mutations
2011 · Petra Paulasova, Jan Diblik, et al. · Cancer Genetics · 4
Topology of Chromosomes 18 and X in Human Blastomeres from 3- to 4-Day-old Embryos
2005 · Jan Diblík, Milan Macek, et al. · Journal of Histochemistry & Cytochemistry · 4
[Medical genetics in reproductive medicine].
2002 · M Macek, S Vilímová, et al. · PubMed · 2
Prevalence of Smith–Lemli–Opitz Syndrome Carriers and the Spectrum of DHCR7 Pathogenic Variants in Representative Czech and Hungarian Population Cohorts
2026 · Eszter Kovács, Zsuzsanna Szűcs, et al. · Genes · 1
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Poster Viewing Session - Reproductive Endocrinology
2011 · M. Colakoglu, H. Toy, et al. · Human Reproduction · 1
L26/P-671 A retrospective genetic cohort study of patients with Azoospermia using whole exome sequencing
2026 · J. Diblik, Š. Lednický, et al. · Human Reproduction
P-581 A prospective multicentric genetic study of a cohort of 50 patients with diminished ovarian reserve using whole exome sequencing
2025 · S Lednicky, M Koudova, et al. · Human Reproduction
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EP06.45: Prenatal diagnosis of Temple syndrome in the second trimester
2024 · M. Hynek, J. Diblík, et al. · Ultrasound in Obstetrics and Gynecology
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O-146 Extended carrier testing of inherited disorders for reproductive risk assessment in preconception care
2022 · J Diblik, R Jarošová, et al. · Human Reproduction
47. Pgt-m in Families Carrying "de Novo" Mutation by Combination of Embryo Sanger Sequencing and Karyomapping
2019 · V. Becvarova, I. Soldatova, et al. · Reproductive BioMedicine Online
Uniparental disomy testing in robertsonian translocation carriers
2018 · Marie Trková, Inna Soldátová, et al. · Reproductive BioMedicine Online
EP10.03: A case of unilateral choanal atresia
2017 · S. Brezinova, J. Diblík, et al. · Ultrasound in Obstetrics and Gynecology
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P61 Risk of the ovarian hyperstimulation syndrome and FSH receptor Asn680Ser and −29A/G polymorphisms
2012 · M. Macek, P. Feldmár, et al. · Reproductive BioMedicine Online
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102 the Relationship of the Fsh-r Polymorphism to Moderate and Severe Types of Ohss in Czech Women
2010 · P. Feldmar, M. Macek, et al. · Reproductive BioMedicine Online
Posters * Reproductive Genetics (PGD/PGS)
2010 · A. Crippa, M. C. Magli, et al. · Human Reproduction
P60 FSH-R polymorphism in severe types of OHSS
2010 · M. Macek, P. Feldmar, et al. · Reproductive BioMedicine Online
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P8 Case report: high polar bodies aneuploidy rate in a patient with severe ovarian hyperstimulation syndrome
2010 · J. Diblík, M. Macek, et al. · Reproductive BioMedicine Online
A study of aneuploidy in gametes and embryos
2006 · Diblík, Jan · Digital Repository (National Repository of Grey Literature)
P-19. Simplified method for molecular cytogenetic examination of human sperm cells
2002 · M Macek, Y Yurov, et al. · Reproductive BioMedicine Online
Quantitative fluorescent PCR in the examination of microquantity of fetal cells
2001 · Milan Maçek, Alice Krebsová, et al. · Fetal Diagnosis and Therapy
Works count: 23
Citation count: 39
H-index: 4
I10-index: 1
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