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#TitleJournalYearCitations
1Mapping genomic loci implicates genes and synaptic biology in schizophreniaNature2022929
2Temporal disease trajectories condensed from population-wide registry data covering 6.2 million patientsNature Communications2014289
3Using Electronic Patient Records to Discover Disease Correlations and Stratify Patient CohortsPLoS Computational Biology2011236
4Common variants on 8p12 and 1q24.2 confer risk of schizophreniaNature Genetics2011224
5Acute COVID-19 severity and mental health morbidity trajectories in patient populations of six nations: an observational studyLancet Public Health, The202299
6A Mouse Model that Recapitulates Cardinal Features of the 15q13.3 Microdeletion Syndrome Including Schizophrenia- and Epilepsy-Related AlterationsBiological Psychiatry201495
7In Vitro Drug Metabolism by Human Carboxylesterase 1: Focus on Angiotensin-Converting Enzyme InhibitorsDrug Metabolism and Disposition201484
8Synthetic cannabimimetic agents metabolized by carboxylesterasesDrug Testing and Analysis201581
9Association Study of Nonsynonymous Single Nucleotide Polymorphisms in SchizophreniaBiological Psychiatry201278
10Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disordersAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics201263
11Digital questionnaire platform in the Danish Blood Donor StudyComputer Methods and Programs in Biomedicine201638
12The impact of CES1 genotypes on the pharmacokinetics of methylphenidate in healthy Danish subjectsBritish Journal of Clinical Pharmacology201735
1322q11.2 Deletion Syndrome Is Associated With Impaired Auditory Steady-State Gamma ResponseSchizophrenia Bulletin201833
14Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndromeJournal of Neurodevelopmental Disorders201627
15Altered auditory processing and effective connectivity in 22q11.2 deletion syndromeSchizophrenia Research201824
16Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorderTranslational Psychiatry201824
17Comorbidity of migraine with ADHD in adultsBMC Neurology201824
18Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric DisordersJAMA Psychiatry202224
19Association Study of CHRNA7 Promoter Variants with Sensory and Sensorimotor Gating in Schizophrenia Patients and Healthy Controls: A Danish Case–Control StudyNeuroMolecular Medicine201523
20Individualization of treatments with drugs metabolized by CES1: combining genetics and metabolomicsPharmacogenomics201519
21Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nationsInternational Journal of Epidemiology202216
22The impact of human CES1 genetic variation on enzyme activity assessed by ritalinic acid/methylphenidate ratiosBasic and Clinical Pharmacology and Toxicology201915
23Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHDAmerican Journal of Psychiatry202115
24The Danish 22q11 research initiativeBMC Psychiatry201514
25The Pharmacokinetics of Enalapril in Relation to CES1 Genotype in Healthy Danish VolunteersBasic and Clinical Pharmacology and Toxicology201714
26Pharmacometabolomics Informs About Pharmacokinetic Profile of MethylphenidateCPT: Pharmacometrics and Systems Pharmacology201814
27Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a familyEuropean Journal of Medical Genetics201512
28Linkage and whole genome sequencing identify a locus on 6q25–26 for formal thought disorder and implicate MEF2A regulationSchizophrenia Research201512
29Quality of life and self-esteem in 7-year-old children with familial high risk of schizophrenia or bipolar disorder: the Danish High Risk and Resilience Study-VIA 7—a population-based cohort studyEuropean Child and Adolescent Psychiatry202010
30Genome-Wide Association Study of Genetic Variants in LPS-Stimulated IL-6, IL-8, IL-10, IL-1ra and TNF-α Cytokine Response in a Danish CohortPLoS ONE201310
31Pharmacogenetic Risk Stratification in Angiotensin-Converting Enzyme Inhibitor-Treated Patients with Congestive Heart Failure: A Retrospective Cohort StudyPLoS ONE20159
32Switch in Therapy from Methylphenidate to Atomoxetine in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: An Analysis of Patient RecordsJournal of Child and Adolescent Psychopharmacology20168
33Predicting treatment response using pharmacy register in migraineJournal of Headache and Pain20198
34Prognostic role of genetic polymorphisms of the interleukin-6 signaling pathway in patients with severe heart failurePharmacogenomics Journal20197
35Combined Ensemble Docking and Machine Learning in Identification of Therapeutic Agents with Potential Inhibitory Effect on Human CES1Molecules20196
36Pharmacodynamic Impact of Carboxylesterase 1 Gene Variants in Patients with Congestive Heart Failure Treated with Angiotensin-Converting Enzyme InhibitorsPLoS ONE20166
37Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome CohortFrontiers in Neuroscience20165
38Novel approach for CES1 genotyping: integrating single nucleotide variants and structural variationPharmacogenomics20185
39Reappraisal of the genetic diversity and pharmacogenetic assessment of CES1Pharmacogenomics20174
40A manual-based vocational rehabilitation program for patients with an acquired brain injury: study protocol of a pragmatic randomized controlled trial (RCT)Trials20174
41Carboxylesterase 1 genes: systematic review and evaluation of existing genotyping proceduresDrug Metabolism and Personalized Therapy20184
42Outcomes of a 12-week ecologically valid observational study of first treatment with methylphenidate in a representative clinical sample of drug naïve children with ADHDPLoS ONE20213
43Life-time Actionable Pharmacogenetic Drug Use: A Population-based Cohort Study in 86 040 Young People With and Without Mental Disorders in DenmarkPharmacopsychiatry20223
44Carboxylesterase 1A2 encoding gene with increased transcription and potential rapid drug metabolism in Asian populationsDrug Metabolism and Personalized Therapy20172
45Carboxylesterase 1 gene duplication and mRNA expression in adipose tissue are linked to obesity and metabolic functionFASEB Journal20130