 Connection
Emily Bates to Haploinsufficiency
This is a "connection" page, showing publications Emily Bates has written about Haploinsufficiency.
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Connection Strength |
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0.662 |
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Aiken J, Buscaglia G, Aiken AS, Moore JK, Bates EA. Tubulin mutations in brain development disorders: Why haploinsufficiency does not explain TUBA1A tubulinopathies. Cytoskeleton (Hoboken). 2020 03; 77(3-4):40-54.
Score: 0.602
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Kim BJ, Hernández-García A, Curtis DL, Thompson O, Champaigne N, Priolo M, Radio FC, Tartaglia M, Gucsavas-Calikoglu M, Shiloh-Malawsky Y, Perilla-Young Y, Josephi-Taylor S, Bournazos AM, Cooper ST, van Gassen K, van den Boogaard MJ, Ozekin YH, Bates EA, Kongchan N, Hsu CW, Scott DA. SPEN deficiency contributes to the development of orofacial clefts in humans and mice. Hum Mol Genet. 2026 Jul 15; 35(15).
Score: 0.060
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Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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