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Role of Hormones, Genes, and Environment in Human Cryptorchidism

Endocrine reviews, 2008-08, Vol.29 (5), p.560-580

2008

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Human papillomavirus found in sperm head of young adult males affects the progressive motility

Fertility and sterility, 2010-02, Vol.93 (3), p.802-806

2010

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Polymorphism rs2274911 of GPRC6A as a Novel Risk Factor for Testis Failure

The journal of clinical endocrinology and metabolism, 2016-03, Vol.101 (3), p.953-961

2016

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Androgens stimulate endothelial progenitor cells through an androgen receptor-mediated pathway

Clinical endocrinology (Oxford), 2008-02, Vol.68 (2), p.284-289

2008

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Past, Present, and Future Strategies for Enhanced Assessment of Embryo's Genome and Reproductive Competence in Women of Advanced Reproductive Age

Frontiers in endocrinology (Lausanne), 2019-03, Vol.10, p.154-154

2019

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Identification of a novel mutation in exon 1 of androgen receptor gene in an azoospermic patient with mild androgen insensitivity syndrome: case report and literature review

Fertility and sterility, 2011-11, Vol.96 (5), p.1165-1169

2011

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Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate

Molecular genetics & genomic medicine, 2020-01, Vol.8 (1), p.e1056-n/a

2020

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Role of estrogen receptors in menstrual cycle–related neoangiogenesis and their influence on endothelial progenitor cell physiology

Fertility and sterility, 2010, Vol.93 (1), p.220-228

2010

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Epigenetics of pregnancy: looking beyond the DNA code

Journal of assisted reproduction and genetics, 2022-04, Vol.39 (4), p.801-816

2022

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Preimplantation Genetic Testing for Genetic Diseases: Limits and Review of Current Literature

Genes, 2023-11, Vol.14 (11), p.2095

2023

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Male infertility: role of genetic background

Reproductive biomedicine online, 2007, Vol.14 (6), p.734-745

2007

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Supporting couples with polycystic kidney disease in a medically assisted reproduction process

Giornale di clinica nefrologica e dialisi, 2024-04, Vol.36 (1)

2024

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The impact of a second embryo biopsy for preimplantation genetic testing for monogenic diseases (PGT-M) with inconclusive results on pregnancy potential: results from a matched case–control study

Journal of assisted reproduction and genetics, 2024-05, Vol.41 (5), p.1173-1179

2024

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Androgen receptor is expressed in both X- and Y-carrier human spermatozoa

Fertility and sterility, 2009, Vol.91 (1), p.193-200

2009

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PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the FMR1 Gene

Genes, 2024-01, Vol.15 (1), p.6

2024

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Challenges of Preimplantation Genetic Counselling in the Context of Cystic Fibrosis and Other CFTR-Related Disorders: A Monocentric Experience in a Cohort of 92 Couples

Genes, 2024-07, Vol.15 (7), p.937

2024

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Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature

Genes, 2023-03, Vol.14 (3), p.748

2023

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Genetic alterations associated with cryptorchidism

JAMA : the journal of the American Medical Association, 2008-11, Vol.300 (19), p.2271

2008

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PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the IFMR1/I Gene

Genes, 2023-12, Vol.15 (1)

2023

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Electroclinical Features in Two Novel STRADA Patients and a Functional Yeast Assay for the Validation of Missense STRADA Mutations

Pediatric neurology, 2023-11, Vol.148, p.152-156

2023

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Public Awareness and Acceptability of PGT-M in Cancer Predisposition Syndromes

Genes, 2023-11, Vol.14 (11), p.2069

2023

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Considerations on the use of carrier screening testing in human reproduction: comparison between recommendations from the Italian Society of Human Genetics and other international societies

Journal of assisted reproduction and genetics, 2022-11, Vol.39 (11), p.2581-2593

2022

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Biallelic mutations in the TOGARAM1 gene cause a novel primary ciliopathy

Journal of medical genetics, 2021-08, Vol.58 (8), p.526-533

2021

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Homozygous ITNNI3/I Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature

Genes, 2023-03, Vol.14 (3)

2023

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An Unclassified Deletion Involving the Proximal Short Arm of Chromosome 10: A New Syndrome?

Genes, 2024-05, Vol.15 (6), p.650

2024

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Role of Hormones, Genes, and Environment in Human Cryptorchidism

Human papillomavirus found in sperm head of young adult males affects the progressive motility

Polymorphism rs2274911 of GPRC6A as a Novel Risk Factor for Testis Failure

Androgens stimulate endothelial progenitor cells through an androgen receptor-mediated pathway

Past, Present, and Future Strategies for Enhanced Assessment of Embryo's Genome and Reproductive Competence in Women of Advanced Reproductive Age

Identification of a novel mutation in exon 1 of androgen receptor gene in an azoospermic patient with mild androgen insensitivity syndrome: case report and literature review

Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate

Role of estrogen receptors in menstrual cycle–related neoangiogenesis and their influence on endothelial progenitor cell physiology

Epigenetics of pregnancy: looking beyond the DNA code

Preimplantation Genetic Testing for Genetic Diseases: Limits and Review of Current Literature

Male infertility: role of genetic background

Supporting couples with polycystic kidney disease in a medically assisted reproduction process

The impact of a second embryo biopsy for preimplantation genetic testing for monogenic diseases (PGT-M) with inconclusive results on pregnancy potential: results from a matched case–control study

Androgen receptor is expressed in both X- and Y-carrier human spermatozoa

PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the FMR1 Gene

Challenges of Preimplantation Genetic Counselling in the Context of Cystic Fibrosis and Other CFTR-Related Disorders: A Monocentric Experience in a Cohort of 92 Couples

Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature

Genetic alterations associated with cryptorchidism

PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the IFMR1/I Gene

Electroclinical Features in Two Novel STRADA Patients and a Functional Yeast Assay for the Validation of Missense STRADA Mutations

Public Awareness and Acceptability of PGT-M in Cancer Predisposition Syndromes

Considerations on the use of carrier screening testing in human reproduction: comparison between recommendations from the Italian Society of Human Genetics and other international societies

Biallelic mutations in the TOGARAM1 gene cause a novel primary ciliopathy

Homozygous ITNNI3/I Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature

An Unclassified Deletion Involving the Proximal Short Arm of Chromosome 10: A New Syndrome?

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