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  1. Article ; Online: Editorial for the special issue on the molecular genetics of male infertility.

    Krausz, Csilla

    Human genetics

    2020  Volume 140, Issue 1, Page(s) 1–5

    MeSH term(s) Genetics ; Humans ; Infertility, Male/genetics ; Male ; Molecular Biology/methods ; Spermatogenesis
    Language English
    Publishing date 2020-12-18
    Publishing country Germany
    Document type Editorial
    ZDB-ID 223009-4
    ISSN 1432-1203 ; 0340-6717
    ISSN (online) 1432-1203
    ISSN 0340-6717
    DOI 10.1007/s00439-020-02245-0
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  2. Article ; Online: Educational activities of the European Academy of Andrology.

    Jannini, Emmanuele A / Krausz, Csilla

    Andrology

    2022  Volume 10 Suppl 2, Page(s) 97–99

    MeSH term(s) Academies and Institutes ; Andrology ; Urology
    Language English
    Publishing date 2022-09-19
    Publishing country England
    Document type Journal Article
    ZDB-ID 2696108-8
    ISSN 2047-2927 ; 2047-2919
    ISSN (online) 2047-2927
    ISSN 2047-2919
    DOI 10.1111/andr.13246
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  3. Article ; Online: European Academy of Andrology (EAA): Annual report 2022.

    Rajpert-De Meyts, Ewa / Krausz, Csilla

    Andrology

    2023  Volume 11, Issue 7, Page(s) 1528–1536

    Language English
    Publishing date 2023-09-21
    Publishing country England
    Document type News
    ZDB-ID 2696108-8
    ISSN 2047-2927 ; 2047-2919
    ISSN (online) 2047-2927
    ISSN 2047-2919
    DOI 10.1111/andr.13527
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  4. Article: Genetic Factors of Non-Obstructive Azoospermia: Consequences on Patients' and Offspring Health.

    Krausz, Csilla / Cioppi, Francesca

    Journal of clinical medicine

    2021  Volume 10, Issue 17

    Abstract: Non-Obstructive Azoospermia (NOA) affects about 1% of men in the general population and is characterized by clinical heterogeneity implying the involvement of several different acquired and genetic factors. NOA men are at higher risk to be carriers of ... ...

    Abstract Non-Obstructive Azoospermia (NOA) affects about 1% of men in the general population and is characterized by clinical heterogeneity implying the involvement of several different acquired and genetic factors. NOA men are at higher risk to be carriers of known genetic anomalies such as karyotype abnormalities and Y-chromosome microdeletions in respect to oligo-normozoospermic men. In recent years, a growing number of novel monogenic causes have been identified through Whole Exome Sequencing (WES). Genetic testing is useful for diagnostic and pre-TESE prognostic purposes as well as for its potential relevance for general health. Several epidemiological observations show a link between azoospermia and higher morbidity and mortality rate, suggesting a common etiology for NOA and some chronic diseases, including cancer. Since on average 50% of NOA patients has a positive TESE outcome, the identification of genetic factors in NOA patients has relevance also to the offspring's health. Although still debated, the observed increased risk of certain neurodevelopmental disorders, as well as impaired cardiometabolic and reproductive health profile in children conceived with ICSI from NOA fathers may indicate the involvement of transmissible genetic factors. This review provides an update on the reproductive and general health consequences of known genetic factors causing NOA, including offspring's health.
    Language English
    Publishing date 2021-09-05
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm10174009
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  5. Article ; Online: EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: State of the art 2023.

    Krausz, Csilla / Navarro-Costa, Paulo / Wilke, Martina / Tüttelmann, Frank

    Andrology

    2023  Volume 12, Issue 3, Page(s) 487–504

    Abstract: Testing for AZoospermia Factor (AZF) deletions of the Y chromosome is a key component of the diagnostic workup of azoospermic and severely oligozoospermic men. This revision of the 2013 European Academy of Andrology (EAA) and EMQN CIC (previously known ... ...

    Abstract Testing for AZoospermia Factor (AZF) deletions of the Y chromosome is a key component of the diagnostic workup of azoospermic and severely oligozoospermic men. This revision of the 2013 European Academy of Andrology (EAA) and EMQN CIC (previously known as the European Molecular Genetics Quality Network) laboratory guidelines summarizes recent clinically relevant advances and provides an update on the results of the external quality assessment program jointly offered by both organizations. A basic multiplex PCR reaction followed by a deletion extension analysis remains the gold-standard methodology to detect and correctly interpret AZF deletions. Recent data have led to an update of the sY84 reverse primer sequence, as well as to a refinement of what were previously considered as interchangeable border markers for AZFa and AZFb deletion breakpoints. More specifically, sY83 and sY143 are no longer recommended for the deletion extension analysis, leaving sY1064 and sY1192, respectively, as first-choice markers. Despite the transition, currently underway in several countries, toward a diagnosis based on certified kits, it should be noted that many of these commercial products are not recommended due to an unnecessarily high number of tested markers, and none of those currently available are, to the best of our knowledge, in accordance with the new first-choice markers for the deletion extension analysis. The gr/gr partial AZFc deletion remains a population-specific risk factor for impaired sperm production and a predisposing factor for testicular germ cell tumors. Testing for this deletion type is, as before, left at the discretion of the diagnostic labs and referring clinicians. Annual participation in an external quality control program is strongly encouraged, as the 22-year experience of the EMQN/EAA scheme clearly demonstrates a steep decline in diagnostic errors and an improvement in reporting practice.
    MeSH term(s) Humans ; Male ; Andrology ; Semen ; Infertility, Male/diagnosis ; Infertility, Male/genetics ; Infertility, Male/pathology ; Azoospermia/diagnosis ; Azoospermia/genetics ; Azoospermia/pathology ; Chromosome Deletion ; Oligospermia/diagnosis ; Oligospermia/genetics ; Chromosomes, Human, Y/genetics ; Multiplex Polymerase Chain Reaction ; Sertoli Cell-Only Syndrome/genetics ; Sex Chromosome Aberrations ; Sex Chromosome Disorders of Sex Development
    Language English
    Publishing date 2023-09-06
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2696108-8
    ISSN 2047-2927 ; 2047-2919
    ISSN (online) 2047-2927
    ISSN 2047-2919
    DOI 10.1111/andr.13514
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  6. Article ; Online: European academy of andrology newsletter 1-2015.

    Krausz, Csilla

    Andrology

    2015  Volume 3, Issue 2, Page(s) 417–419

    Language English
    Publishing date 2015-03
    Publishing country England
    Document type Journal Article
    ZDB-ID 2696108-8
    ISSN 2047-2927 ; 2047-2919
    ISSN (online) 2047-2927
    ISSN 2047-2919
    DOI 10.1111/andr.12029
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  7. Article ; Online: European Academy of Andrology (EAA): Annual Report 2021.

    Rajpert-De Meyts, Ewa / Krausz, Csilla

    Andrology

    2022  Volume 10, Issue 4, Page(s) 619–624

    MeSH term(s) Academies and Institutes ; Andrology
    Language English
    Publishing date 2022-04-20
    Publishing country England
    Document type News
    ZDB-ID 2696108-8
    ISSN 2047-2927 ; 2047-2919
    ISSN (online) 2047-2927
    ISSN 2047-2919
    DOI 10.1111/andr.13165
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  8. Article ; Online: ANDRONET: A new European network to boost research coordination, education and public awareness in andrology.

    Oliva, Rafael / Krausz, Csilla / Rajpert-De Meyts, Ewa

    Andrology

    2022  Volume 10, Issue 3, Page(s) 423–425

    MeSH term(s) Andrology/education ; Urology
    Language English
    Publishing date 2022-02-10
    Publishing country England
    Document type Editorial
    ZDB-ID 2696108-8
    ISSN 2047-2927 ; 2047-2919
    ISSN (online) 2047-2927
    ISSN 2047-2919
    DOI 10.1111/andr.13144
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  9. Article ; Online: ANDRONET: A new European network to boost research coordination, education and public awareness in andrology.

    Oliva, Rafael / Krausz, Csilla / Rajpert-De Meyts, Ewa

    Andrology

    2022  Volume 10 Suppl 2, Page(s) 144–146

    MeSH term(s) Andrology/education ; Urology
    Language English
    Publishing date 2022-10-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 2696108-8
    ISSN 2047-2927 ; 2047-2919
    ISSN (online) 2047-2927
    ISSN 2047-2919
    DOI 10.1111/andr.13253
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  10. Article ; Online: In memoriam: Paolo Sassone-Corsi.

    Krausz, Csilla / Carrell, Douglas T

    Andrology

    2020  Volume 8, Issue 6, Page(s) 1502–1503

    Language English
    Publishing date 2020-08-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 2696108-8
    ISSN 2047-2927 ; 2047-2919
    ISSN (online) 2047-2927
    ISSN 2047-2919
    DOI 10.1111/andr.12905
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