about
The DNA sequence of the human X chromosomeSpeeding disease gene discovery by sequence based candidate prioritizationMarkers close to the dopamine D5 receptor gene (DRD5) show significant association with schizophrenia but not bipolar disorderA neuregulin 1 variant associated with abnormal cortical function and psychotic symptomsExpression of DISC1-interactome members correlates with cognitive phenotypes related to schizophrenia.SuRFing the genomics wave: an R package for prioritising SNPs by functionalityComputational comparison of human genomic sequence assemblies for a region of chromosome 4.Preliminary investigation of miRNA expression in individuals at high familial risk of bipolar disorder.Genetics of schizophrenia and bipolar affective disorder: strategies to identify candidate genes.Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression.Impact of a microRNA MIR137 susceptibility variant on brain function in people at high genetic risk of schizophrenia or bipolar disorderDNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorderDirect microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia.Preliminary assessment of pre-morbid DNA methylation in individuals at high genetic risk of mood disordersA case-control association study and family-based expression analysis of the bipolar disorder candidate gene PI4K2BThe DISC1 promoter: characterization and regulation by FOXP2.Identification of polymorphic and off-target probe binding sites on the Illumina Infinium MethylationEPIC BeadChipRare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank.DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan.Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.SUSPECTS: enabling fast and effective prioritization of positional candidatesAssociation of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish populationCohort Profile: Stratifying Resilience and Depression Longitudinally (STRADL): a questionnaire follow-up of Generation Scotland: Scottish Family Health Study (GS:SFHS).Juvenile stress produces long-lasting changes in hippocampal DISC1, GSK3ß and NRG1 expression.Dinucleotide repeat polymorphism at the human olfactory marker protein (OMP) locus on chromosome 11q13.5 near tyrosinase (TYR).A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.Alzheimer's disease risk factor complement receptor 1 is associated with depression.Altered DNA methylation associated with a translocation linked to major mental illness.GWAS on family history of Alzheimer's disease.DNA Methylation Signatures of Depressive Symptoms in Middle-aged and Elderly Persons: Meta-analysis of Multiethnic Epigenome-wide StudiesDNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disordersInvestigating the relationship between DNA methylation age acceleration and risk factors for Alzheimer's diseaseThe effects of a neuregulin 1 variant on white matter density and integrityConvergence of linkage, association and GWAS findings for a candidate region for bipolar disorder and schizophrenia on chromosome 4pAssociation analysis of the chromosome 4p15–p16 candidate region for bipolar disorder and schizophreniaHaplotype Analysis and a Novel Allele-Sharing Method Refines a Chromosome 4p Locus Linked to Bipolar Affective DisorderIn silico identification of transcripts and SNPs from a region of 4p linked with bipolar affective disorderAssociation analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorderEpigenetic signatures of starting and stopping smoking
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description
researcher ORCID ID = 0000-0002-7884-5877
@en
wetenschapper
@nl
name
Kathryn L Evans
@ast
Kathryn L Evans
@en
Kathryn L Evans
@es
Kathryn L Evans
@nl
type
label
Kathryn L Evans
@ast
Kathryn L Evans
@en
Kathryn L Evans
@es
Kathryn L Evans
@nl
prefLabel
Kathryn L Evans
@ast
Kathryn L Evans
@en
Kathryn L Evans
@es
Kathryn L Evans
@nl
P106
P1153
7402215340
P21
P31
P496
0000-0002-7884-5877