Co-Authors
This is a "connection" page, showing publications co-authored by HUDA ZOGHBI and DAVUT PEHLIVAN.
Connection Strength
0.861
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Comprehensive assessment reveals numerous clinical and neurophysiological differences between MECP2-allelic disorders. Ann Clin Transl Neurol. 2025 02; 12(2):433-447.
Score: 0.222
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Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression. Genome Med. 2024 12 18; 16(1):146.
Score: 0.221
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Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levels. Hum Mol Genet. 2024 11 08; 33(22):1986-2001.
Score: 0.219
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Using the linear references from the pangenome to discover missing autism variants. Nat Commun. 2026 Jan 23; 17(1):1681.
Score: 0.060
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MECP2 Duplication Uncouples Mitochondrial and Purine Metabolism During neuronal maturation. bioRxiv. 2025 Dec 26.
Score: 0.059
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Pangenome discovery of missing autism variants. medRxiv. 2025 Jul 22.
Score: 0.058
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Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome. Nat Genet. 2011 Oct 02; 43(11):1074-81.
Score: 0.022