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1q42

A chromosome band present on 1q
National Institutes of Health

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5 relations
ChromosomesPARP1 wt AlleleTOMM20 wt AlleleWNT9A wt Allele

Papers overview

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Highly Cited
2009
Highly Cited
2009
Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.
Highly Cited
2008
Highly Cited
2008
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
Blood concentrations of lipoproteins and lipids are heritable risk factors for cardiovascular disease. Using genome-wide… 
Review
2006
Review
2006
The Genetics and Biology of Disc1—An Emerging Role in Psychosis and Cognition
Review
2005
Review
2005
The genetics of schizophrenia and bipolar disorder: dissecting psychosis
Much work has been done to identify susceptibility genes in schizophrenia and bipolar disorder. Several well established linkages… 
Highly Cited
2005
Highly Cited
2005
Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory.
CONTEXT Chromosome 1q42 is among several genomic regions showing replicated evidence of linkage with schizophrenia, but the… 
Highly Cited
2004
Highly Cited
2004
Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder.
Schizophrenia, schizoaffective disorder, and bipolar disorder are common psychiatric disorders with high heritabilities and… 
Highly Cited
2003
Highly Cited
2003
Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects.
We have previously reported a linkage peak on 1q42 in a Finnish schizophrenia sample. In this study we genotyped 28 single… 
Highly Cited
2001
Highly Cited
2001
Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.
A family with a (1;11)(q42;q14.3) translocation significantly linked to a clinical phenotype that includes schizophrenia and… 
Highly Cited
2001
Highly Cited
2001
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2).
Arrhythmogenic right ventricular dysplasia type 2 (ARVD2, OMIM 600996) is an autosomal dominant cardiomyopathy, characterized by… 
Highly Cited
2001
Highly Cited
2001
Paternal contribution to the risk for pre-eclampsia
Coeliac disease (CD) is a malabsorption disorder characterised by a small intestinal enteropathy that reverts to normal on… 
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