V.K. Maloney
Salisbury District Hospital(GB)Wessex Regional Genetics Laboratory(GB)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Chromosomal and Genetic Variations, Prenatal Screening and Diagnostics, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Genomics and Chromatin Dynamics
Most-Cited Works
- → A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis(2005)133 cited
- → 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q(2009)128 cited
- → Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development(2008)83 cited
- → Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect(2006)60 cited
- → Characterization of SHOX Deletions in Léri-Weill Dyschondrosteosis (LWD) Reveals Genetic Heterogeneity and No Recombination Hotspots(2006)31 cited
- → Investigation of the origins of human autosomal inversions(2008)30 cited
- → Male breast cancer, age and sex chromosome aneuploidy(2013)21 cited
- → Homozygosity for a novel deletion downstream of the SHOX gene provides evidence for an additional long range regulatory region with a mild phenotypic effect(2014)21 cited
- → Purification and characterization of simian immunodeficiency virus (SIVmac) envelope glycoprotein GP130 from virus-infected cells(1994)13 cited
- → A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGH(2009)12 cited