Paper · 39780503
Introduction to androgenetics: terminology, approaches, and impactful studies across 60 years.
Akbari A and 2 others. Andrology, 2025. Cited by 2 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. Introduction to androgenetics: terminology, approaches, and impactful studies across 60 years. Papers, record 39780503. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/39780503
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
Topics7
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Andrology | Major topic |
| Genetics, Medical | Major topic |
| Infertility, Male | Major topic |
| Terminology as Topic | Major topic |
| Humans | |
| Male | |
| History, 21st Century |
Source PubMed
Grants5
Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.
| Grant, as the record writes it | Agency | Country | NIH project | Stated by | Source |
|---|---|---|---|---|---|
| R01 HD078641 | NICHD NIH HHS | United States | R01HD078641 | PubMed and NIH | NIH RePORTER |
| PRG1021 | Eesti Teadusagentuur | PubMed | PubMed | ||
| P50HD096723 | NIH HHS | United States | P50HD096723 | PubMed and NIH | NIH RePORTER |
| P50 HD096723 | NICHD NIH HHS | United States | P50HD096723 | PubMed and NIH | NIH RePORTER |
| R01HD078641 | NIH HHS | United States | R01HD078641 | PubMed and NIH | NIH RePORTER |
Trials0
The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.
None in this release.
Comments and corrections0
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References92
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 31,337,883 | Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome. | Genet Med | 2020 | https://conductscience.org/library/papers/31337883 | PubMed |
| 2 | 34,498,060 | A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships. | Hum Reprod Update | 2021 | https://conductscience.org/library/papers/34498060 | PubMed |
| 3 | 32,673,564 | Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility. | Am J Hum Genet | 2020 | https://conductscience.org/library/papers/32673564 | PubMed |
| 4 | 32,620,854 | Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency. | Sci Rep | 2020 | https://conductscience.org/library/papers/32620854 | PubMed |
| 5 | 37,563,329 | Genome-wide prediction of disease variant effects with a deep protein language model. | Nat Genet | 2023 | https://conductscience.org/library/papers/37563329 | PubMed |
| 6 | 13,632,697 | A case of human intersexuality having a possible XXY sex-determining mechanism. | Nature | 1959 | https://conductscience.org/library/papers/13632697 | PubMed |
| 7 | 38,437,850 | Classes and predictors of reversal in male patients with congenital hypogonadotropic hypogonadism: a cross-sectional study of six international referral centres. | Lancet Diabetes Endocrinol | 2024 | https://conductscience.org/library/papers/38437850 | PubMed |
| 8 | 35,690,514 | Genetic Architecture of Azoospermia-Time to Advance the Standard of Care. | Eur Urol | 2023 | https://conductscience.org/library/papers/35690514 | PubMed |
| 9 | 28,536,242 | Mutation in TDRD9 causes non-obstructive azoospermia in infertile men. | J Med Genet | 2017 | https://conductscience.org/library/papers/28536242 | PubMed |
| 10 | 32,719,396 | A genomics approach to male infertility. | Genet Med | 2020 | https://conductscience.org/library/papers/32719396 | PubMed |
1 to 10 of 92
See all 92 referencesCited by2
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 2 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 41,694,248 | Diagnostic odyssey of a male with 45,X/46,XY mosaicism: case report and review of the literature. | F S Rep | 2026 | https://conductscience.org/library/papers/41694248 | PubMed |
| 40,545,437 | The rising role of genetics in andrology research and clinical practice. | Andrology | 2025 | https://conductscience.org/library/papers/40545437 | PubMed |
Genes0
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
None in this release.
Drugs0
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None in this release.
Data0
The data bank entries PubMed's record names. Trial numbers are under Trials.
None in this release.
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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