Chiara Chianese

Florence, 50139, Italy

Last Updated: 09/26/2026

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Found 17 publications

Correction: gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study.

Correction: gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study.

Journal: European journal of human genetics : EJHG

Published: August 14, 2020

Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.

Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.

Journal: Human reproduction (Oxford, England)

Published: July 12, 2019

Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.

Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.

Journal: Human reproduction (Oxford, England)

Published: January 07, 2019

gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study.

gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study.

Journal: European journal of human genetics : EJHG

Published: December 27, 2018

Impact of circulating tumor DNA mutant allele fraction on prognosis in RAS-mutant metastatic colorectal cancer.

Impact of circulating tumor DNA mutant allele fraction on prognosis in RAS-mutant metastatic colorectal cancer.

Journal: Molecular oncology

Published: October 21, 2018

From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia.

From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: November 23, 2017

Genetics of male infertility: from research to clinic.

Genetics of male infertility: from research to clinic.

Journal: Reproduction (Cambridge, England)

Published: October 09, 2015

Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia.

Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia.

Journal: Andrology

Published: November 05, 2014

Genetic testing and counselling for male infertility.

Genetic testing and counselling for male infertility.

Journal: Current opinion in endocrinology, diabetes, and obesity

Published: April 18, 2014

Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency.

Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency.

Journal: Human reproduction (Oxford, England)

Published: March 18, 2014

Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility.

Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility.

Journal: Journal of medical genetics

Published: January 15, 2014

X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance.

X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance.

Journal: PloS one

Published: December 06, 2013

Showing 1-12 of 17

Last Updated: 09/26/2026