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Author

Nayla Y. León

Observed name: Nayla Y León
Institution: Centogene (Germany)
ORCID: 0000-0002-8009-0872
Observed ORCID: 0000-0002-8009-0872
OpenAlex ID: A5029017355
A clinical algorithm to diagnose differences of sex development
2019 · Nayla Y León, Alejandra P Reyes, et al. · The Lancet Diabetes & Endocrinology · 68
Genetic control of typical and atypical sex development
2023 · Alejandra P. Reyes, Nayla Y. León, et al. · Nature Reviews Urology · 59
ATR-X syndrome: genetics, clinical spectrum, and management
2021 · Nayla Y. León, Vincent R. Harley · Human Genetics · 28
Biallelic Variants in TMEM17 Cause Meckel‐Gruber Syndrome Within the Ciliopathy Spectrum
2025 · Luba M. Pardo, Javier Martini, et al. · Clinical Genetics · 2
Clinical challenges of an Xp21 contiguous gene deletion syndrome in a newborn and 15 months of follow-up - case report
2026 · Ignacy Frulenko, Iwona Ostrowska, et al. · Frontiers in Endocrinology
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Author response for "Biallelic Variants in TMEM17 Cause Meckel‐Gruber Syndrome Within the Ciliopathy Spectrum"
2025 · Luba M. Pardo, Javier Martini, et al. · Publons reviews and discussion
Y chromosome damage underlies testicular abnormalities in ATR-X syndrome
2024 · Nayla Y. León, Thanh Nha Uyen Le, et al. · iScience
Works count: 7
Citation count: 157
H-index: 3
I10-index: 3
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