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Author Details
Full Name
Jo Knight
Affiliation
Data Science Institute and Lancaster University Medical School
ORCID
Career Start Year
2000
Papers
102
H Index
43
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
33300144
Transferability of Ancestry-Specific and Cross-Ancestry CYP2A6 Activity Genetic Risk Scores in African and European Populations.
Clin Pharmacol Ther
2021
33713409
A Genome-Wide Association Study of Nausea Incidence in Varenicline-Treated Cigarette Smokers.
Nicotine Tob Res
2021
33334717
Late-onset epilepsy predicts stroke: Systematic review and meta-analysis.
Epilepsy Behav
2021
33243167
Routinely collected patient data in neurology research: a systematic mapping review.
BMC Neurol
2020
33681802
COVID-19 exposes the urgent need for coding of outpatient neurology episodes.
BMJ Neurol Open
2020
29274736
Can we accurately classify schizophrenia patients from healthy controls using magnetic resonance imaging and machine learning? A multi-method and multi-dataset study.
Schizophr Res
2019
31211845
Cross-disorder analysis of schizophrenia and 19 immune-mediated diseases identifies shared genetic risk.
Hum Mol Genet
2019
31575706
<i>APOE</i> ε4, white matter hyperintensities, and cognition in Alzheimer and Lewy body dementia.
Neurology
2019
30527956
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.
Lancet Respir Med
2019
28921760
Genome-wide association study of a nicotine metabolism biomarker in African American smokers: impact of chromosome 19 genetic influences.
Addiction
2018
30224653
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Nat Genet
2018
30429575
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
Nat Genet
2018
29782824
APOE-ε4 associates with hippocampal volume, learning, and memory across the spectrum of Alzheimer's disease and dementia with Lewy bodies.
Alzheimers Dement
2018
29742386
Heritability estimates of cortical anatomy: The influence and reliability of different estimation strategies.
Neuroimage
2018
29370225
Examining the role of common and rare mitochondrial variants in schizophrenia.
PLoS One
2018
29282334
Comment: Unraveling DNA sequence to identify cerebral indicators of dementia risk.
Neurology
2018
27869829
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Nat Genet
2017
28135244
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.
Nat Genet
2017
28277565
Pharmacogenetic Analysis of Functional Glutamate System Gene Variants and Clinical Response to Clozapine.
Mol Neuropsychiatry
2017
28322202
Genetic epistasis regulates amyloid deposition in resilient aging.
Alzheimers Dement
2017
28951623
Corrigendum: Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.
Nat Genet
2017
28561418
Heritability of hippocampal subfield volumes using a twin and non-twin siblings design.
Hum Brain Mapp
2017
28739976
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.
Hypertension
2017
28658209
Fine-mapping inflammatory bowel disease loci to single-variant resolution.
Nature
2017
26876050
Genetic association analysis of N-methyl-D-aspartate receptor subunit gene GRIN2B and clinical response to clozapine.
Hum Psychopharmacol
2016
28097204
Genomics implicates adaptive and innate immunity in Alzheimer's and Parkinson's diseases.
Ann Clin Transl Neurol
2016
26512135
IBD Genetic Risk Profile in Healthy First-Degree Relatives of Crohn's Disease Patients.
J Crohns Colitis
2016
27242348
Genome-Wide Association Studies Suggest Limited Immune Gene Enrichment in Schizophrenia Compared to 5 Autoimmune Diseases.
Schizophr Bull
2016
27327646
Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study.
PLoS Med
2016
27190009
Dopamine D2 receptor gene variants and response to rasagiline in early Parkinson's disease: a pharmacogenetic study.
Brain
2016
27092072
Gene Prioritization for Imaging Genetics Studies Using Gene Ontology and a Stratified False Discovery Rate Approach.
Front Neuroinform
2016
27087318
Allele-Skewed DNA Modification in the Brain: Relevance to a Schizophrenia GWAS.
Am J Hum Genet
2016
25266122
Addiction-related genes in gambling disorders: new insights from parallel human and pre-clinical models.
Mol Psychiatry
2015
26300220
Smoking Gun or Circumstantial Evidence? Comparison of Statistical Learning Methods using Functional Annotations for Prioritizing Risk Variants.
Sci Rep
2015
26177304
Predictors of Outcome in Ulcerative Colitis.
Inflamm Bowel Dis
2015
25917933
A genome-wide association study of suicide severity scores in bipolar disorder.
J Psychiatr Res
2015
25939698
Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci.
Nat Commun
2015
25997848
Assessing models for genetic prediction of complex traits: a comparison of visualization and quantitative methods.
BMC Genomics
2015
25671699
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
PLoS Genet
2015
25416559
CYP2A6 reduced activity gene variants confer reduction in lung cancer risk in African American smokers--findings from two independent populations.
Carcinogenesis
2015
25560467
Investigation of TSPO variants in schizophrenia and antipsychotic treatment outcomes.
Pharmacogenomics
2015
24387768
Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1.
BMC Med Genet
2014
25587358
Complex host genetics influence the microbiome in inflammatory bowel disease.
Genome Med
2014
24831852
The role of leptin, melanocortin, and neurotrophin system genes on body weight in anorexia nervosa and bulimia nervosa.
J Psychiatr Res
2014
24737441
Protein kinase cAMP-dependent regulatory type II beta (PRKAR2B) gene variants in antipsychotic-induced weight gain.
Hum Psychopharmacol
2014
24844982
A Bayesian method to incorporate hundreds of functional characteristics with association evidence to improve variant prioritization.
PLoS One
2014
24927181
Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
Nat Commun
2014
22383645
Introduction to genetic association studies.
Cold Spring Harb Protoc
2012
23143594
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
Nat Genet
2012
22914738
Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis.
Hum Mol Genet
2012
1 - 50 of 102
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William Harvey Research Institute, Queen Mary University of London
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William Harvey Research Institute, Queen Mary University of London
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University of Ioannina
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Harvard Medical School, Harvard University
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