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ISSUE INFORMATION
EDITORIAL
Free Access
free
The rising role of genetics in andrology research and clinical practice
- Pages: 983-985
- First Published: 22 June 2025
REVIEW ARTICLE
Free Access
free
Introduction to androgenetics: terminology, approaches, and impactful studies across 60 years
- Pages: 986-998
- First Published: 08 January 2025
Free Access
free
Utility of exome sequencing in primary spermatogenic disorders: From research to diagnostics
- Pages: 999-1010
- First Published: 19 September 2024
Open Access
oa
How exome sequencing improves the diagnostics and management of men with non-syndromic infertility
- Pages: 1011-1024
- First Published: 09 August 2024
Open Access
oa
Genomic technologies and the diagnosis of 46, XY differences of sex development
- Pages: 1025-1043
- First Published: 31 July 2024
Open Access
oa
Human asthenozoospermia: Update on genetic causes, patient management, and clinical strategies
- Pages: 1044-1064
- First Published: 02 January 2025
Free Access
free
Preconception carrier screening and preimplantation genetic testing in the infertility management
- Pages: 1065-1077
- First Published: 21 August 2024
ORIGINAL ARTICLE
Open Access
oa
Innovative all-in-one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10-month experience
- Pages: 1078-1092
- First Published: 24 August 2024
no
Genome sequencing of Pakistani families with male infertility identifies deleterious genotypes in SPAG6, CCDC9, TKTL1, TUBA3C, and M1AP
- Pages: 1093-1104
- First Published: 10 December 2023
no
Whole-exome sequencing identifies ADGB as a novel causative gene for male infertility in humans: from motility to fertilization
- Pages: 1105-1116
- First Published: 22 February 2024
Open Access
oa
Novel ACTL7A variants in males lead to fertilization failure and male infertility
- Pages: 1117-1126
- First Published: 22 November 2023
no
Genetic anomalies in infertile Egyptian men and their impact on sperm retrieval rates and intracytoplasmic sperm injection outcome: A retrospective cohort study
- Pages: 1127-1136
- First Published: 27 March 2025
Open Access
oa
Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants
- Pages: 1137-1148
- First Published: 09 August 2024
REVIEW ARTICLE
Free Access
free
Prostate cancer and genetic contributions
- Pages: 1149-1157
- First Published: 29 November 2024
Free Access
free
Relevance, strategies, and added value of mouse models in androgenetics
- Pages: 1158-1169
- First Published: 19 September 2024
Free Access
free
Telomeric function and regulation during male meiosis in mice and humans
- Pages: 1170-1180
- First Published: 21 March 2024
Open Access
oa
Applications of spatial transcriptomics in studying spermatogenesis
- Pages: 1181-1189
- First Published: 09 April 2025
ORIGINAL ARTICLE
no
The human infertility single-cell testis atlas (HISTA): an interactive molecular scRNA-Seq reference of the human testis
- Pages: 1190-1200
- First Published: 05 April 2024
no
Role of Kctd13 in modulating AR and SOX9 expression in different penile cell populations
- Pages: 1201-1212
- First Published: 29 January 2025
Open Access
oa
Phenotype and gene signature of testicular tumors in 129.MOLF-Chr19 mice resemble human teratomas
- Pages: 1213-1222
- First Published: 29 July 2024
no
Loss of lncRNAs 1700101O22Rik and 1700027A15Rik causes sperm malformation and subfertility
- Pages: 1223-1235
- First Published: 14 February 2025
no
PWWP3A deficiency accelerates testicular senescence in aged mice
- Pages: 1236-1250
- First Published: 03 October 2024
Open Access
oa
CRISPR/Cas9-mediated genome editing reveals seven testis-enriched transmembrane glycoproteins dispensable for male fertility in mice
- Pages: 1251-1260
- First Published: 12 December 2023
no
Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription
- Pages: 1261-1269
- First Published: 27 August 2024
no
Homozygous deleterious variants in the C-terminal of TDRD5 impair spermiogenesis, causing severe oligoasthenoteratozoospermia in humans
- Pages: 1270-1284
- First Published: 07 June 2024
SHORT COMMUNICATION
no
A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans
- Pages: 1285-1291
- First Published: 26 December 2024