A systematic review and evidence assessment of monogenic gene–disease relationships in human female infertility and differences in sex development

A systematic review and standardized clinical validity assessment of genes involved in female reproductive failure

(2022) Ludmila Volozonoka et al.   REPRODUCTION

Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development

(2021) Inas Mazen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation

(2021) Cristina E. Trevino et al.   FERTILITY AND STERILITY

The PRISMA 2020 statement: An updated guideline for reporting systematic reviews

(2021) Matthew J. Page et al.   PLOS MEDICINE

A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene–disease relationships

(2021) Brendan J Houston et al.   HUMAN REPRODUCTION UPDATE

Fragile X Premutation Associated Conditions (FXPAC)

(2020) Kirsten Johnson et al.   Frontiers in Pediatrics

The molecular mechanisms that underlie fragile X-associated premature ovarian insufficiency: is it RNA or protein based?

(2020) Roseanne Rosario et al.   MOLECULAR HUMAN REPRODUCTION

Preconception genome medicine: current state and future perspectives to improve infertility diagnosis and reproductive and health outcomes based on individual genomic data

(2020) Antonio Capalbo et al.   HUMAN REPRODUCTION UPDATE

A systematic review and standardized clinical validity assessment of male infertility genes

(2019) Manon S Oud et al.   HUMAN REPRODUCTION

Genetics of human female infertility

(2019) Svetlana A Yatsenko et al.   BIOLOGY OF REPRODUCTION

Association between the FMR1 CGG repeat lengths and the severity of idiopathic primary ovarian insufficiency: a meta analysis

(2019) Jing Huang et al.   Artificial Cells Nanomedicine and Biotechnology

Comprehensive genetic testing for female and male infertility using next-generation sequencing

(2018) Bonny Patel et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Genetic evaluation of patients with non-syndromic male infertility

(2018) Ozlem Okutman et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians

(2017) Fady Hannah-Shmouni et al.   GENETICS IN MEDICINE

Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications

(2017) Erica D. Smith et al.   HUMAN MUTATION

Genetics of primary ovarian insufficiency

(2016) R. Rossetti et al.   CLINICAL GENETICS

Genetic Considerations in Recurrent Pregnancy Loss

(2015) K. J. Hyde et al.   Cold Spring Harbor Perspectives in Medicine

Definition and Epidemiology of Unexplained Infertility

(2014) Tarek A. Gelbaya et al.   OBSTETRICAL & GYNECOLOGICAL SURVEY

Population-based estimates of the prevalence of FMR1 expansion mutations in women with early menopause and primary ovarian insufficiency

(2013) Anna Murray et al.   GENETICS IN MEDICINE

Bio.Phylo: A unified toolkit for processing, analyzing and visualizing phylogenetic trees in Biopython

(2012) Eric Talevich et al.   BMC BIOINFORMATICS

Male infertility: Pathogenesis and clinical diagnosis

(2011) Csilla Krausz   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

FMR1 and the Continuum of Primary Ovarian Insufficiency

(2011) Shannon Sullivan et al.   SEMINARS IN REPRODUCTIVE MEDICINE

Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

(2010) Maud Bidet et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Primary ovarian insufficiency

(2010) Michel De Vos et al.   LANCET

Biopython: freely available Python tools for computational molecular biology and bioinformatics

(2009) P. J. A. Cock et al.   BIOINFORMATICS