Anita M. Quintana

Agammaglobulinemia and absent B lineage cells in a patient lacking the p85α subunit of PI3K

Mary Ellen Conley, Kerry Dobbs, Anita M. Quintana et al. · The Journal of Experimental Medicine · 2012 · 210 citations · Full text

Kabuki syndrome genes<i>KMT2D</i>and<i>KDM6A</i>: functional analyses demonstrate critical roles in craniofacial, heart and brain development

Peter M. Van Laarhoven, Leif R. Neitzel, Anita M. Quintana et al. · Human Molecular Genetics · 2015 · 177 citations · Full text

Brain Development, Genetics, Kmt2d Morphants +20

An X-Linked Cobalamin Disorder Caused by Mutations in Transcriptional Coregulator HCFC1

Hung‐Chun Yu, Jennifer L. Sloan, Gunter Scharer et al. · The American Journal of Human Genetics · 2013 · 130 citations · Full text

Systems Biology, Genetic Disorder, Medicine +6

Identification and Regulation of c-Myb Target Genes in MCF-7 Cells

Anita M. Quintana, Fan Liu, John P. O’Rourke et al. · BMC Cancer · 2011 · 88 citations · Full text

Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities

Anita M. Quintana, Hung‐Chun Yu, Alison Brebner et al. · Human Molecular Genetics · 2017 · 62 citations · Full text