Samantha J.L. Knight

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

Heather C. Mefford, Andrew J. Sharp, Carl Baker et al. · New England Journal of Medicine · 2008 · 803 citations · Full text

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

Andrew J. Sharp, S.K. Hansen, Rebecca R. Selzer et al. · Nature Genetics · 2006 · 663 citations

Mendelian Disorder, Genetic Disorder, Unidentified Genomic Disorders +11

The autophagy protein Atg7 is essential for hematopoietic stem cell maintenance

Monika Mortensen, Elizabeth J. Soilleux, Gordana Djordjević et al. · The Journal of Experimental Medicine · 2011 · 628 citations · Full text

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

Andrew J. Sharp, Heather C. Mefford, Kelly Li et al. · Nature Genetics · 2008 · 588 citations

Mendelian Disorder, Genetic Disorder, Psychiatric Genetics +9

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation

Samantha J.L. Knight, A Flannery, Mark C. Hirst et al. · Cell · 1993 · 520 citations

Cpg Island, Genetic Disorder, Genetics +6