Vincent P. Stanton

Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

J. David Brook, Mila E. McCurrach, H G Harley et al. · Cell · 1992 · 2.8K citations

Signal Transduction, Mendelian Disorder, Genetic Disorder +7

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein

Julian Borrow, Vincent P. Stanton, J. Michael Andresen et al. · Nature Genetics · 1996 · 776 citations

Hematological Malignancy, Signal Transduction, Creb–binding Protein +10

The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9

Julian Borrow, Amanda M. Shearman, Vincent P. Stanton et al. · Nature Genetics · 1996 · 445 citations

Hematological Malignancy, Chromatin, Genetics +9

The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A

Linda J. Valentijn, Pieter A. Bolhuis, Ina Zorn et al. · Nature Genetics · 1992 · 317 citations

Genetics, Experimental Neuropathology, Pathology +5

Single-nucleotide polymorphisms can cause different structural folds of mRNA

Ling X. Shen, James P. Basilion, Vincent P. Stanton · Proceedings of the National Academy of Sciences · 1999 · 316 citations · Full text

Single-nucleotide Polymorphisms, Enzymatic Probing, Human Mrnas +12