Frank X. Donovan
National Human Genome Research Institute(US)
Publications by Year
Research Areas
DNA Repair Mechanisms, Acute Myeloid Leukemia Research, CRISPR and Genetic Engineering, Epigenetics and DNA Methylation, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Low Incidence of DNA Sequence Variation in Human Induced Pluripotent Stem Cells Generated by Nonintegrating Plasmid Expression(2012)242 cited
- → Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia(2015)131 cited
- → Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia(2013)89 cited
- → iPSCs and fibroblast subclones from the same fibroblast population contain comparable levels of sequence variations(2017)86 cited
- → Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer(2022)84 cited
- → Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation(2017)83 cited
- → Neuroanatomic, epigenetic and genetic differences in monozygotic twins discordant for attention deficit hyperactivity disorder(2017)68 cited
- → A comprehensive approach to identification of pathogenic FANCA variants in Fanconi anemia patients and their families(2017)64 cited
- → Somatic mutational landscape of AML with inv(16) or t(8;21) identifies patterns of clonal evolution in relapse leukemia(2015)59 cited
- → Deficiency of Interleukin-1 Receptor Antagonist (DIRA): Report of the First Indian Patient and a Novel Deletion Affecting IL1RN(2017)54 cited