Dinah Yaeger

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

Ian D. Krantz, Jennifer McCallum, Cheryl DeScipio et al. · Nature Genetics · 2004 · 715 citations · Full text

Genome Instability, Developmental Biology, Genetic Disorder +8

Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation

Matthew A. Deardorff, Maninder Kaur, Dinah Yaeger et al. · The American Journal of Human Genetics · 2007 · 518 citations · Full text

Developmental Anomaly, Smc1a Cause, Mendelian Disorder +11

NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations

Lynette A. Gillis, Jennifer McCallum, Maninder Kaur et al. · The American Journal of Human Genetics · 2004 · 312 citations · Full text

Genotype-phenotype Correlations, Mendelian Disorder, Genetic Disorder +9

Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome

Maninder Kaur, Cheryl DeScipio, Jennifer McCallum et al. · American Journal of Medical Genetics Part A · 2005 · 129 citations · Full text

Developmental Biology, Cell Division, Genetic Disorder +13

Fine‐mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals

Cheryl DeScipio, Nancy B. Spinner, Maninder Kaur et al. · American Journal of Medical Genetics Part A · 2008 · 59 citations · Full text