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Thanh Nha Uyen Le

MFSD7c functions as a transporter of choline at the blood–brain barrier
2024 · Xuan Thi Anh Nguyen, Thanh Nha Uyen Le, et al. · Cell Research · 30
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Mfsd2b and Spns2 are essential for maintenance of blood vessels during development and in anaphylactic shock
2022 · Thanh Nha Uyen Le, Toan Q. Nguyen, et al. · Cell Reports · 19
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An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32-11.22.
2020 · Thanh Nha Uyen Le, Viet Nhan Nguyen, et al. · PubMed Central · 6
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Association of TP53 gene codon 72 polymorphism with Helicobacter pylori-positive non-cardia gastric cancer in Vietnam
2019 · Thi Minh Thi Ha, Thanh Nha Uyen Le, et al. · The Journal of Infection in Developing Countries · 6
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MBD5‐ related intellectual disability in a Vietnamese child
2021 · Thanh Nha Uyen Le, Thi Minh Thi Ha · American Journal of Medical Genetics Part A · 3
A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications
2025 · Marcello Scala, Nancy C. P. Leong, et al. · European Journal of Human Genetics · 2
Y chromosome damage underlies testicular abnormalities in ATR-X syndrome
2024 · Nayla Y. León, Thanh Nha Uyen Le, et al. · iScience · 1
An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome.
2023 · Thi Minh Thi Ha, Phan Tuong Quynh Le, et al. · PubMed Central · 1
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Association of C677t Polymorphisms of Mthfr Gene With Recurrent Pregnancy Loss in Vietnamese Woman
2019 · Thanh Nha Uyen Le, Thi Minh Thi Ha, et al. · Journal of Medicine and Pharmacy · 1
Supplementary material for Biallelic CYB5A disruptions in 46,XY DSD: Novel missense and deep intronic variants manuscript
2026 · Shirin Moradifard, Thanh Nha Uyen Le, et al. · Figshare
Biallelic CYB5A disruptions in 46, XY DSD: Novel missense and deep intronic variants
2026 · Shirin Moradifard, Thanh Nha Uyen Le, et al. · The Journal of Clinical Endocrinology & Metabolism
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MAP3K7 novel variants in syndromic 46,XY DSD
2026 · Thanh Nha Uyen Le, Shirin Moradi Fard, et al. · medRxiv
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An Extremely Rare SRD5A2 Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam
2022 · Phan Tuong Quynh Le, Thanh Nha Uyen Le, et al. · Case Reports in Endocrinology
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Works count: 13
Citation count: 69
H-index: 4
I10-index: 2
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