Published in Mol Genet Metab on September 07, 2006
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Expression and functional analysis of Tgif during mouse midline development. Dev Dyn (2006) 0.95
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A functional screen for sonic hedgehog regulatory elements across a 1 Mb interval identifies long-range ventral forebrain enhancers. Development (2006) 2.90
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Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features. Proc Natl Acad Sci U S A (2003) 1.98
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The molecular genetics of holoprosencephaly. Am J Med Genet C Semin Med Genet (2010) 1.57
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Analysis of genotype-phenotype correlations in human holoprosencephaly. Am J Med Genet C Semin Med Genet (2010) 1.51
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A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum. Am J Med Genet A (2011) 1.44
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly. Am J Hum Genet (2008) 1.43
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TGIF inhibits retinoid signaling. Mol Cell Biol (2006) 1.40
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Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation. Development (2010) 1.12
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. J Med Genet (2009) 1.10
Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway. PLoS Genet (2012) 1.10
A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects. Hum Genet (2002) 1.09
Sumoylation at chromatin governs coordinated repression of a transcriptional program essential for cell growth and proliferation. Genome Res (2013) 1.08
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature. Am J Med Genet A (2007) 1.07
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis. Am J Hum Genet (2010) 1.06
A novel SIX3 mutation segregates with holoprosencephaly in a large family. Am J Med Genet A (2009) 1.05
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Fetal alcohol spectrum disorders. Am Fam Physician (2005) 1.04
How a Hedgehog might see holoprosencephaly. Hum Mol Genet (2003) 1.03
The Tgif2 gene contains a retained intron within the coding sequence. BMC Mol Biol (2006) 1.03
Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effects. J Pediatr Psychol (2006) 1.03
Silencing of FLRG, an antagonist of activin, inhibits human breast tumor cell growth. Cancer Res (2007) 1.02
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Holoprosencephaly: recommendations for diagnosis and management. Curr Opin Pediatr (2010) 1.02
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Missense substitutions in the GAS1 protein present in holoprosencephaly patients reduce the affinity for its ligand, SHH. Hum Genet (2011) 0.98
Maternal Tgif is required for vascularization of the embryonic placenta. Dev Biol (2008) 0.98
Holoprosencephaly due to numeric chromosome abnormalities. Am J Med Genet C Semin Med Genet (2010) 0.98
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility. Am J Med Genet B Neuropsychiatr Genet (2010) 0.96
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