Matthew Velinder

Genomic analyses implicate noncoding de novo variants in congenital heart disease

Felix Richter, Sarah U. Morton, Seong Won Kim et al. · Nature Genetics · 2020 · 167 citations · Full text

Variant Interpretation, Genetics, Congenital Heart Defect +7

Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)?

Whitney Wooderchak‐Donahue, Gülsen Akay, Kevin J. Whitehead et al. · Genetics in Medicine · 2019 · 57 citations · Full text

Much Overlap, Hereditary Hemorrhagic Telangiectasia, Genetic Disorder +9

Growth Factor Independence 1B-Mediated Transcriptional Repression and Lineage Allocation Require Lysine-Specific Demethylase 1-Dependent Recruitment of the BHC Complex

David McClellan, Mattie J. Casey, Diana Bareyan et al. · Molecular and Cellular Biology · 2019 · 34 citations · Full text

Genetics, Gene Regulatory Network, Bhc Complex +17

SUMOylation Regulates Growth Factor Independence 1 in Transcriptional Control and Hematopoiesis

Daniel Andrade, Matthew Velinder, Jason Singer et al. · Molecular and Cellular Biology · 2016 · 18 citations · Full text

Transcriptional Regulation, Developmental Biology, Lineage Allocation +13

GFI1 functions in transcriptional control and cell fate determination require SNAG domain methylation to recruit LSD1

Matthew Velinder, Jason Singer, Diana Bareyan et al. · Biochemical Journal · 2017 · 14 citations · Full text

Pharmaceutical Science, Epigenetic Change, Genetics +25