DISCLAIMER
These data are provided "as is", and
without warranty, for scientific and educational use only. If you
download these data, you acknowledge that these data will be used
only for non-commercial research purposes; that the investigator is
in compliance with all applicable state, local, and federal laws or
regulations and institutional policies regarding human subjects and
genetics research; that secondary distribution of the data without
registration by secondary parties is prohibited; and that the
investigator will cite the appropriate publication in any
communications or publications arising directly or indirectly from
these data. You also acknowledge that yourself or any member of your
research team will never attempt to identify any participant
in these studies.
"Genome-wide common and rare
variant analysis provides novel insights into clozapine-associated
neutropenia" (2017)
Publication.
Description:
Summary
statistics files in various formats (maximum N=5649), please see
header lines (commented with hashes #) for data and column
descriptions.
Citation:
Legge SE, Hamshere ML, Ripke S, Pardiñas AF, Goldstein JI, Rees E,
et al. Genome-wide common and rare variant analysis provides novel
insights into clozapine-associated neutropenia. Mol Psychiatry.
2017. doi: 10.1038/mp.2016.97.
"Common schizophrenia
alleles are enriched in mutation-intolerant genes and in regions
under strong background selection" (2018)
Publication.
Description:
Meta-analysis
of schizophrenia GWAS data from samples of European ancestry
(N=105318; 40675 cases and 64643 controls)
Freq.A1: Frequency of effect allele in 1000
Genomes EUR
super-population.
CHR: Chromosome code.
BP: Base-pair position.
A1: Effect allele.
A2: Non-effect allele.
OR: Odds ratio.
SE: Standard error of the regression beta
(log OR).
P: P-value.
Companion
file supplies SNP names of high-quality imputed (INFO > 0.9)
markers, in LD-Score --merge-alleles
format.
Citation:
Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S,
Carrera N, et al. Common schizophrenia alleles are enriched in
mutation-intolerant genes and in regions under strong background
selection. Nat Genet. 2018. doi: 10.1038/s41588-018-0059-2.
Update
31/05/2018: Corrected OR of X-chromosome SNP rs5937157, which was
shown as a regression beta. Thanks to Lucy Riglin for
reporting this error.
"A genome-wide association
study in individuals of African ancestry reveals the importance of
the Duffy-null genotype in the assessment of clozapine-related
neutropenia" (2019)
Publication.
Description:
GWAS
of lowest absolute neutrophil count during clozapine treatment in
individuals of African ancestry (N=552)
Chr:
Chromosome code.
SNP:
SNP name in HRC
format.
bp:
Base-pair position.
A1:
Effect allele.
A2: Non-effect allele.
Freq: Frequency of effect allele.
b:
Linear mixed model regression statistic.
se: Standard error of the regression beta.
p: P-value.
Citation:
Legge SE, Pardiñas
AF, Helthuis M, Jansen JA, Jollie K, Knapper S, et al. A
genome-wide association study in individuals of African ancestry
reveals the importance of the Duffy-null genotype in the assessment of
clozapine-related neutropenia. Mol Psych. 2019. doi:
10.1038/s41380-018-0335-7.
"Pharmacogenomic variants
and drug interactions identified through the genetic analysis of
clozapine metabolism" (2019)
Publication.
Description:
GWAS
of plasma concentrations of clozapine metabolites in individuals of
European ancestry (N=2989)
Chr:
Chromosome code.
SNP:
SNP name in HRC
format.
bp:
Base-pair position.
A1:
Effect allele.
A2: Non-effect allele.
Freq: Frequency of effect allele.
b:
Linear mixed model regression statistic.
se: Standard error of the regression beta.
p: P-value.
Citation:
Pardiñas AF, Nalmpanti M, Pocklington AJ, Legge SE, Medway C, King A,
et al. Pharmacogenomic Variants and Drug Interactions Identified
Through the Genetic Analysis of Clozapine Metabolism. Am J
Psychiatry. 2019. doi: 10.1176/appi.ajp.2019.18050589.
"Genetic association study
of psychotic experiences in UK Biobank" (2019)
Publication.
Description:
GWAS
of psychotic experiences reported by adults in a population-based
study of European ancestry (N=127966; 6123 cases and 121843
controls; see manuscript for details)
CHR: Chromosome code.
BP: Base-pair position.
A1: Effect allele.
A2: Non-effect allele.
FRQ_A: Frequency of A1 in cases.
FRQ_U: Frequency of A1 in comparator group
("controls").
INFO: Imputation quality score.
OR: Odds ratio.
SE: Standard error of the regression beta
(log OR).
P: P-value.
Citation:
Legge SE, Jones HJ, Kendall KK, Pardiñas AF, Menzies G, Bracher-Smith M, et al. Genetic
association study of psychotic experiences in UK Biobank. JAMA
Psychiatry. 2019. doi: 10.1001/jamapsychiatry.2019.2508.
"Web-Based Cognitive
Testing in Psychiatric Research: Validation and Usability Study"
(2022)
Publication.
Description:
Cognitive
and limited clinical data on the participants recruited online
as part of the Cognition in Mood, Psychosis and Schizophrenia
Study (CoMPaSS Web, N=1227).
Please
note, some information has been stripped or grouped to prevent
identification of participants.
Companion
file provides full variable descriptions and codings.
Citation: Lynham AJ,
Jones IR, Walters, JT. Web-Based Cognitive Testing in Psychiatric
Research: Validation and Usability Study. Journal of Medical
Internet Research. 2022. doi: 10.2196/28233.
"Interaction testing and
polygenic risk scoring to estimate the contribution of common
genetic variants to treatment resistance in schizophrenia"
(2022)
Publication.
Description:
Interaction
analysis of a TRS GWAS (N=35043; 10501 cases and 24542 controls)
against a non-TRS GWAS (N=50447; 20325 cases and 30122
controls). See manuscript for details.
CHR:
Chromosome code (the notation "23" is used for the
X-chromosome).
BP:
Base-pair position.
A1:
Effect allele.
A2: Non-effect allele.
N:
Total sample size (cases+controls) across both GWAS.
MAF: Weighted average minor allele
frequency across both GWAS.
Z:
Interaction Z-score.
P: Interaction P-value.
Citation: Pardiñas AF,
Smart SE, Willcocks IR, Holmans PA, Dennison CA, Lynham AJ, et al.
Interaction testing and polygenic risk scoring to estimate the
contribution of common genetic variants to treatment resistance in
schizophrenia. JAMA
Psychiatry. 2022. doi: 10.1001/jamapsychiatry.2021.3799.
"Genetic Liabilities
Differentiating Bipolar Disorder, Schizophrenia, and Major
Depressive Disorder, and Phenotypic Heterogeneity in Bipolar
Disorder" (2022)
Publication.
Description:
Genomic
SEM (gSEM) summary statistics from a common factor analysis
model of schizophrenia (SZ; N=130644), bipolar disorder (BD;
N=398495) and major depressive disorder (MDD; N=173005). See
manuscript for details.
SNP:
SNP name.
CHR:
Chromosome code.
BP:
Base-pair position.
MAF:
Minor allele frequency.
A1:
Effect allele.
A2: Non-effect allele.
est:
gSEM effect size.
SE: Standard error.
Z_estimate:
Z-score.
P: P-value.
Citation: Richards
AL, Cardno A, Harold G, Craddock NJ, DiFlorio A, Jones L, et al.
Genetic Liabilities Differentiating Bipolar Disorder,
Schizophrenia, and Major Depressive Disorder, and Phenotypic
Heterogeneity in Bipolar Disorder. JAMA
Psychiatry. 2022. doi: 10.1001/jamapsychiatry.2022.2594.
"Pharmacokinetics and
pharmacogenomics of clozapine in an ancestrally diverse
sample: a longitudinal analysis and genome-wide association
study using UK clinical monitoring data" (2023)
Publication.
Description:
GWAS
of plasma concentrations of clozapine metabolites (N=4495;
longitudinal cross-ancestry analysis; see manuscript for
details)
chr: Chromosome code.
pos: Base-pair position.
snpid:
SNP
name in HRC
format.
A1: Effect allele.
A2: Non-effect allele.
Freq:
Frequency of effect allele.
se: Standard error of the regression
beta.
p: P-value.
.
Citation:
Pardiñas
AF, Kappel DB, Roberts M, Tipple F, Shitomi-Jones LM, King A, et al. Pharmacokinetics and
pharmacogenomics of clozapine in an ancestrally diverse sample:
a longitudinal analysis and genome-wide association study using
UK clinical monitoring data. Lancet Psychiatry. 2023.
doi: 10.1016/S2215-0366(23)00002-0.