Vazken M. Der Kaloustian

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda Peters, Saima Riazuddin et al. · The American Journal of Human Genetics · 2001 · 557 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems

Stephen R. Williams, Micheala A. Aldred, Vazken M. Der Kaloustian et al. · The American Journal of Human Genetics · 2010 · 305 citations · Full text

Medicine, Genetics, Molecular Genetics +8

X-Linked Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency: Heterozygote Has Two Clonal Populations

Barbara R. Migeon, Vazken M. Der Kaloustian, William L. Nyhan et al. · Science · 1968 · 194 citations

Life Sciences, Genetics, Molecular Genetics +13

Molecular Analysis of Collagen XVIII Reveals Novel Mutations, Presence of a Third Isoform, and Possible Genetic Heterogeneity in Knobloch Syndrome

Oscar Suzuki, Andréa L. Sertié, Vazken M. Der Kaloustian et al. · The American Journal of Human Genetics · 2002 · 157 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome

C. S. Kogan, Armando Bertone, Kim Cornish et al. · Neurology · 2004 · 113 citations

Medicine, Neurology, Neuroscience +17