Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patientsLaura Bryant, Heiko Reutter, Alexandrea Wadley et al.|Science Advances|2020Cited by 99
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphologyAndrew K. Sobering, Elizabeth Bhoj, Laura Bryant et al.|Human Genetics and Genomics Advances|2022Cited by 26
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and miceSarah E. Sheppard, Jessica Maffeo, Laura Bryant et al.|Science Advances|2023Cited by 18
Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphologyAndrew K. Sobering, Elizabeth Bhoj, Laura Bryant et al.|Human Genetics and Genomics Advances|2022Cited by 8
Identification of a novel pathogenic missense mutation in<i>PRPF31</i>using whole exome sequencing: a case reportLaura Bryant, Jean Bennett|British Journal of Ophthalmology|2018Cited by 8