Dr Paul Kalitsis
Dr Paul Kalitsis
Details
Role
Medical Scientist
Group
Cytogenetics Laboratory
Top Publications
- Kim, JH, Kalitsis, P, Pertile, MD, Magliano, D, Wong, L, Choo, A, Hudson, DF. Nucleic Acids: Hybridisation. 2026 view publication
- Gear, R, Kalitsis, P, Glass, M, Isidor, B, Vincent-Delorme, C, Petit, F, Verhagen, JMA, Jorge, A, Krepischi, ACV, Osei-Owusu, I, et al. AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions.. Am J Med Genet A 197(11) : e64153 2025 view publication
- Francis, D, Lall, P, Ayres, S, Van Bergen, NJ, Christodoulou, J, Brown, NJ, Kalitsis, P. De novo enhancer deletion of LMX1B produces a mild nail-patella clinical phenotype.. Clin Genet 105(2) : 214 -219 2024 view publication
- Francis, DI, Stark, Z, Scheffer, IE, Tan, TY, Murali, K, Gallacher, L, Amor, DJ, Goel, H, Downie, L, Stutterd, CA, et al. Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability.. Eur J Hum Genet 31(5) : 521 -525 2023 view publication
- Udugama, M, Vinod, B, Chan, FL, Hii, L, Garvie, A, Collas, P, Kalitsis, P, Steer, D, Das, PP, Tripathi, P, et al. Histone H3.3 phosphorylation promotes heterochromatin formation by inhibiting H3K9/K36 histone demethylase.. Nucleic Acids Res 50(8) : 4500 -4514 2022 view publication
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