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KCTD13 gene

Known as: KCTD13, PDIP1, TNFAIP1-LIKE 
 
National Institutes of Health

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KCTD1 gene

Papers overview

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2019
2019
CRISPR/Cas9-mediated Knockout of the Neuropsychiatric Risk Gene KCTD13 Causes Developmental Deficits in Human Cortical Neurons Derived from Induced Pluripotent Stem Cells
The human KCTD13 gene is located within the 16p11.2 locus and copy number variants of this locus are associated with a high risk… Expand
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Review
2019
Review
2019
KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders
Abstract The underlying molecular basis for neurodevelopmental or neuropsychiatric disorders is not known. In contrast… Expand
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2016
2016
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2
Duplications in 16p11.2 are a risk factor for schizophrenia (SCZ). Using genetically modified zebrafish, Golzio and colleagues… Expand
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Highly Cited
2012
Highly Cited
2012
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
Copy number variants (CNVs) are major contributors to genetic disorders. We have dissected a region of the 16p11.2 chromosome… Expand
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2012
2012
Earth science: Geomagnetism under scrutiny
New calculations show that the electrical resistance of Earth's liquid-iron core is lower than had been thought. The results… Expand
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