Co-Authors
This is a "connection" page, showing publications co-authored by Shabab Hannan and HUGO BELLEN.
Connection Strength
0.574
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Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder. Genet Med. 2026 Apr; 28(4):101685.
Score: 0.242
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De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features. Am J Hum Genet. 2024 04 04; 111(4):742-760.
Score: 0.213
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Revealing the nervous system requirements of Alzheimer disease risk genes in Drosophila. Am J Hum Genet. 2025 12 04; 112(12):2870-2887.
Score: 0.060
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Revealing the nervous system requirements of Alzheimer's disease risk genes in Drosophila. bioRxiv. 2025 Jul 30.
Score: 0.059