Found: 9
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Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 8, p. 1319, doi. 10.1093/hmg/ddl052
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- Article
Large, rare chromosomal deletions associated with severe early-onset obesity.
- Published in:
- Nature, 2010, v. 463, n. 7281, p. 666, doi. 10.1038/nature08689
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- Article
Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.
- Published in:
- Nature Genetics, 2013, v. 45, n. 9, p. 1055, doi. 10.1038/ng.2716
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- Article
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
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- Nature Genetics, 2013, v. 45, n. 5, p. 513, doi. 10.1038/ng.2607
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- Publication type:
- Article
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-08737-6
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- Article
CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in <i>COL8A1</i> and <i>NRXN1</i>.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059061
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- Article
Rare variants in single-minded 1 (SIM1) are associated with severe obesity.
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- Journal of Clinical Investigation, 2013, v. 123, n. 7, p. 3042, doi. 10.1172/JCI68016
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- Article
Human SH2B1 mutations are associated with maladaptive behaviors and obesity.
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- Journal of Clinical Investigation, 2012, v. 122, n. 12, p. 4732, doi. 10.1172/JCI62696
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- Article
Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily.
- Published in:
- Human Mutation, 2009, v. 30, n. 2, p. 204, doi. 10.1002/humu.20825
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- Article