Andrew E. Timms
Publications by Year
Research Areas
Spondyloarthritis Studies and Treatments, Rheumatoid Arthritis Research and Therapies, Genomics and Rare Diseases, Acute Myeloid Leukemia Research, Retinal Development and Disorders
Most-Cited Works
- → Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia(2011)596 cited
- → A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia(2013)324 cited
- → A search for type 1 diabetes susceptibility genes in families from the United Kingdom(1998)323 cited
- → Association of MTOR Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism(2016)275 cited
- → Whole-Genome Screening in Ankylosing Spondylitis: Evidence of Non-MHC Genetic-Susceptibility Loci(2001)228 cited
- → Spatial and cell type transcriptional landscape of human cerebellar development(2021)217 cited
- → Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum(2019)191 cited
- → PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution(2016)185 cited
- → A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair(2016)150 cited
- → Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina(2021)150 cited