Emanuele Pelosi
Biochemistry, Genetics and Molecular Biology · Indiana University
Publications
55
Citations
1,988
Est. group size
—
Recurring co-author estimate
Active years
26
Publishing since 2001
- Wnt5a Regulates Embryonic Müllerian Duct Development Through the Non-Canonical Wnt PCP Pathway
Cells · 2026
- 7. A patient's personal account of navigating a Mullerian Anomaly diagnosis
Journal of Pediatric and Adolescent Gynecology · 2026
- 147. Prevalence of cervical cancer screening and cervical dysplasia in patients with Müllerian anomalies at a tertiary care center
Journal of Pediatric and Adolescent Gynecology · 2026
- Evidence for FOXL2 Association with the Tsc1 Regulatory Region in Mice
Biomolecules · 2026
- The impact of mercury exposure on male reproduction: Mechanistic insights
Journal of Trace Elements in Medicine and Biology · 2025
- Harnessing Microbiome, Bacterial Extracellular Vesicle, and Artificial Intelligence for Polycystic Ovary Syndrome Diagnosis and Management
Biomolecules · 2025
- Spotlight on Proteases: Roles in Ovarian Health and Disease
Cells · 2025
- Müllerian anomalies and endometriosis: associations and phenotypic variations
Reproductive Biology and Endocrinology · 2024
- 12554 Human Sex Determination: SRY Length Regulates Its Cellular Stability And Hence The Robustness Of Testis Differentiation
Journal of the Endocrine Society · 2024
- Extracellular vesicles as a potential delivery platform for CRISPR-Cas based therapy in epithelial ovarian cancer
Seminars in Cancer Biology · 2023
- Ovarian absence: a systematic literature review and case series report
Journal of Ovarian Research · 2023
- 13. Assessing Clinical Care Experiences of Patients with Congenital Uterine Anomalies: a Pilot Study
Journal of Pediatric and Adolescent Gynecology · 2023
- 55. Challenges to Access to Care in the Mountain West Region of the United States for Patients with Congenital Uterine Anomalies: Results from a Pilot Study
Journal of Pediatric and Adolescent Gynecology · 2023
- Functional genomics analysis identifies loss of<i>HNF1B</i>function as a cause of Mayer–Rokitansky–Küster–Hauser syndrome
Human Molecular Genetics · 2022
- Functional Analysis of Mmd2 and Related PAQR Genes During Sex Determination in Mice
Sexual Development · 2022
- Journal of Pediatric and Adolescent Gynecology×4
- bioRxiv (Cold Spring Harbor Laboratory)×3
- Nature Communications×2
- Sexual Development×2
- Biomolecules×2
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 9, 2026.
Claim or correct this profile