C
Csilla Krausz
Researcher at University of Florence
Publications - 216
Citations - 12738
Csilla Krausz is an academic researcher from University of Florence. The author has contributed to research in topics: Male infertility & Infertility. The author has an hindex of 60, co-authored 186 publications receiving 10945 citations. Previous affiliations of Csilla Krausz include Pasteur Institute & University of Edinburgh.
Papers
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Journal ArticleDOI
A de novo paradigm for male infertility
Manon S. Oud,Roos M. Smits,H. Smith,F. Mastrorosa,G. Holt,Brendan J Houston,Petra de Vries,B. Alobaidi,L. E. Batty,H.R. Ismail,J. Greenwood,Harsh Sheth,Aneta Mikulasova,G. Astuti,Christian Gilissen,Kevin McEleny,Helen Turner,John Coxhead,Simon Cockell,D.D.M. Braat,Kathrin Fleischer,K. D’Hauwers,Evelyn Schaafsma,Donald F. Conrad,Liina Nagirnaja,Kenneth I. Aston,Douglas T. Carrell,James M. Hotaling,Timothy G. Jenkins,R. McLachlan,Moira K O'Bryan,Peter N. Schlegel,Michael L. Eisenberg,Jay I. Sandlow,Emily S. Jungheim,Kenan Omurtag,Alexandra M. Lopes,Susana Seixas,Filipa Carvalho,Susana Fernandes,Alberto Barros,João Miguel da Silva Gonçalves,Iris Pereira Caetano,Graça Pinto,Sónia Cristina Heleno Correia,Maris Laan,Margus Punab,Ewa Rajpert-De Meyts,Niels Jørgensen,Kristian Almstrup,Keith Jarvi,Corinna Friedrich,Sabine Kliesch,K. Aston,Antoni Riera-Escamilla,Csilla Krausz,Claudia Gonzaga-Jauregui,Mauro Santibanez-Koref,Dylan J. Elliott,L. E. L. M. Vissers,Frank Tüttelmann,M. O’Bryan,Liliana Ramos,M. Xavier,Gwen van der Heijden,J. Veltman +65 more
TL;DR: In this article , de novo mutations play an important role in severe male infertility and explain a portion of the genetic causes of this understudied disorder, using trio-based exome sequencing.
Journal ArticleDOI
X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance.
Chiara Chianese,Adam C. Gunning,Claudia Giachini,Fabrice Daguin,Giancarlo Balercia,Elisabet Ars,Deborah Lo Giacco,Eduard Ruiz-Castañé,Gianni Forti,Csilla Krausz +9 more
TL;DR: This study allowed the identification of novel spermatogenesis candidate genes linked to the 5 CNVs and the discovery of the first recurrent, X-linked gain with potential clinical relevance.
Book ChapterDOI
Genomic changes in spermatozoa of the aging male.
TL;DR: Most of what is known about the relationship between male aging and changes in the spermatozoa is summarized, giving special focus on the events occurring with age at the genomic level.
Journal ArticleDOI
Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways.
Domenico Vladimiro Libri,Gunnar Kleinau,Valeria Vezzoli,Marta Busnelli,Fabiana Guizzardi,Antonio Agostino Sinisi,Angela Ida Pincelli,Antonio Mancini,Gianni Russo,Paolo Beck-Peccoz,Sandro Loche,Claudio Crivellaro,Mohamad Maghnie,Csilla Krausz,Luca Persani,Marco Bonomi +15 more
TL;DR: It is shown that single PRokR2 missense allelic variants can either affect both signaling pathways differently or selectively, and the integrity of both PROKR2-dependent cAMP and IP signals should be evaluated for a complete functional testing of novel identified allelic variant.
Journal ArticleDOI
European Association of Urology guidelines on vasectomy
TL;DR: These guidelines aim to provide information and recommendations for physicians who perform vasectomies and to promote the provision of adequate information to the patient before the operation to prevent unrealistic expectations and legal procedures.