Judy Chernos

Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome

Twila M. Yobb, Martin J. Somerville, Lionel Willatt et al. · The American Journal of Human Genetics · 2005 · 259 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags et al. · Human Molecular Genetics · 2013 · 175 citations · Full text

Life Sciences, Genetics, Neuroscience +17

A Comparison of the Frequency of Sperm Chromosome Abnormalities in Men with Mild, Moderate, and Severe Oligozoospermia1

Renée H. Martin, Alfred Rademaker, Calvin Greene et al. · Biology of Reproduction · 2003 · 111 citations · Full text

Veterinary Medicine, Genetics, Molecular Genetics +17

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

Rosanna Weksberg, Ikuko Teshima, Bryan Williams et al. · Human Molecular Genetics · 1993 · 100 citations

Life Sciences, Genetics, Molecular Genetics +17

Analysis of chromosome segregation in sperm from a chromosome 2 inversion heterozygote and assessment of an interchromosomal effect

M. Mikhaail-Philips, Evelyn Ko, Judy Chernos et al. · American Journal of Medical Genetics Part A · 2004 · 93 citations

Life Sciences, Genetics, Molecular Genetics +10