Zhilian Xia

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

Paweł Stankiewicz, Partha Sen, Samarth Bhatt et al. · The American Journal of Human Genetics · 2009 · 513 citations · Full text

Detection of clinically relevant exonic copy-number changes by array CGH

Philip M. Boone, Carlos A. Bacino, Chad A. Shaw et al. · Human Mutation · 2010 · 237 citations

Array Cgh, Genetics, Diagnosis +18

Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture

Lisenka E.L.M. Vissers, Samarth Bhatt, Irene M. Janssen et al. · Human Molecular Genetics · 2009 · 193 citations · Full text

Dna Breakage, Genetics, Tandem Duplications +22

Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment

Nicola Brunetti‐Pierri, Alex R. Paciorkowski, Roberto Ciccone et al. · European Journal of Human Genetics · 2010 · 187 citations · Full text

Developmental Biology, Mendelian Disorder, Severe Speech Impairment +10

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

Marwan Shinawi, Christian P. Schaaf, Samarth Bhatt et al. · Nature Genetics · 2009 · 180 citations

Neurodevelopmental Disorders, Developmental Biology, Brain Development +10