Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

Laura Crisponi, Manila Deiana, Angela Loi et al. · Nature Genetics · 2001 · 977 citations

Life Sciences, Genetics, Molecular Genetics +5

The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance

Dirk Schmidt, Catherine E. Ovitt, Katrin Anlag et al. · Development · 2004 · 756 citations · Full text

Medicine, Developmental Biology, Genetics +17

The 11q terminal deletion disorder: A prospective study of 110 cases

Paul Grossfeld, Teresa Mattina, Zona Lai et al. · American Journal of Medical Genetics Part A · 2004 · 343 citations

Life Sciences, Genetics, Molecular Genetics +16

Involvement of neurogranin in the modulation of calcium/calmodulin-dependent protein kinase II, synaptic plasticity, and spatial learning: A study with knockout mice

Jhang Ho Pak, Freesia L. Huang, Junfa Li et al. · Proceedings of the National Academy of Sciences · 2000 · 277 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

An (11;21) Translocation in Four Generations with Chromosome 11 Abnormalities in the Offspring

Petrea Jacobsen, M. Hauge, K. Henningsen et al. · Human Heredity · 1973 · 238 citations

Life Sciences, Genetics, Molecular Genetics +14