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Author

Denise G. Lanza

Observed name: Lanza, Denise G.
Observed institution: Baylor College of Medicine
OpenAlex ID: A5136122234
A rare recurring gain-of-function variant in BMPR2 causes neurodevelopmental phenotypes in humans and flies
2026 · Jung-Wan Mok, Carrie L. Welch, et al. · The American Journal of Human Genetics · 2
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Reversible in vivo regulation of drug metabolizing enzyme CYP1A2 activity through a dTAG knock-in strategy
2026 · Shenzhi Zhou, Xingyu Ji, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 1
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Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder
2026 · Ali H. Bereshneh, Kirkland A. Wilson, et al. · Genetics in Medicine · 1
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Biallelic Variants in KMO Cause a Novel Form of Congenital NAD Deficiency
2026 · Nathalie M. Aceves-Ewing, Nanbing Li-Villarreal, et al. · medRxiv
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Uncovering phenotypic expansion in AXIN2-related disorders through precision animal modeling
2026 · Nathalie M. Aceves-Ewing, Denise G. Lanza, et al. · Genetics in Medicine
Uncovering phenotypic expansion in AXIN2-related disorders through precision animal modeling
2026 · Aceves-Ewing, Nathalie M., Lanza, Denise G., et al. · Radar (Oxford Brookes University)
Works count: 6
Citation count: 4
H-index: 1
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