Monika Koudova

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 19 publications

First-Trimester Bilateral Choanal Atresia as a Marker of a De Novo Pathogenic KMT2D Variant Associated With BCAHH Syndrome.

First-Trimester Bilateral Choanal Atresia as a Marker of a De Novo Pathogenic KMT2D Variant Associated With BCAHH Syndrome.

Journal: Prenatal diagnosis

Published: May 30, 2026

Reporting framework in the testing of predisposition to common adult solid tumors using next-generation sequencing.

Reporting framework in the testing of predisposition to common adult solid tumors using next-generation sequencing.

Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti

Published: May 25, 2026

Serum and urinary D-lactate in pediatric intestinal failure: clinical associations and reference values.

Serum and urinary D-lactate in pediatric intestinal failure: clinical associations and reference values.

Journal: Pediatric research

Published: April 30, 2026

The guidelines for clinical practice for carriers of germline mutations in the Lynch syndrome predisposition genes MLH1, MSH2, MSH6, PMS2 and large deletions of EPCAM (4.2024).

The guidelines for clinical practice for carriers of germline mutations in the Lynch syndrome predisposition genes MLH1, MSH2, MSH6, PMS2 and large deletions of EPCAM (4.2024).

Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti

Published: November 08, 2024

Hereditary α-tryptasemia is Associated With Anaphylaxis to Antibiotics and Monoclonal Antibodies.

Hereditary α-tryptasemia is Associated With Anaphylaxis to Antibiotics and Monoclonal Antibodies.

Journal: The journal of allergy and clinical immunology. In practice

Published: October 02, 2024

The guidelines for clinical practice for carriers of germline mutations in hereditary breast, ovarian, prostate, and pancreatic cancer predisposition genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 (4.2024).

The guidelines for clinical practice for carriers of germline mutations in hereditary breast, ovarian, prostate, and pancreatic cancer predisposition genes BRCA1, BRCA2, PALB2, ATM, and CHEK2 (4.2024).

Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti

Published: August 22, 2024

A comprehensive analysis of germline predisposition to early-onset ovarian cancer.

A comprehensive analysis of germline predisposition to early-onset ovarian cancer.

Journal: Scientific reports

Published: February 26, 2024

A deep intronic recurrent CHEK2 variant c.1009-118_1009-87delinsC affects pre-mRNA splicing and contributes to hereditary breast cancer predisposition.

A deep intronic recurrent CHEK2 variant c.1009-118_1009-87delinsC affects pre-mRNA splicing and contributes to hereditary breast cancer predisposition.

Journal: Breast (Edinburgh, Scotland)

Published: February 21, 2024

A comprehensive study evaluating germline FANCG variants in predisposition to breast and ovarian cancer.

A comprehensive study evaluating germline FANCG variants in predisposition to breast and ovarian cancer.

Journal: Cancer medicine

Published: February 15, 2024

Genetic Predisposition to Male Breast Cancer.

Genetic Predisposition to Male Breast Cancer.

Journal: Folia biologica

Published: January 01, 2024

Germline multigene panel testing of patients with endometrial cancer.

Germline multigene panel testing of patients with endometrial cancer.

Journal: Oncology letters

Published: November 22, 2022

Stepwise molecular-genetic examination in aborted fetuses.

Stepwise molecular-genetic examination in aborted fetuses.

Journal: Ceska gynekologie

Published: June 06, 2022

Showing 1-12 of 19

Last Updated: 09/26/2026