Evidence for the role of EPHX2 gene variants in anorexia nervosa
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A genome-wide association study of anorexia nervosa.Association claims in the sequencing eraEffect of soluble epoxide hydrolase polymorphism on substrate and inhibitor selectivity and dimer formationDysregulation of soluble epoxide hydrolase and lipidomic profiles in anorexia nervosaA genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations.Cerebral perfusion differences in women currently with and recovered from anorexia nervosaThe tyrosine kinase receptor Tyro3 enhances lifespan and neuropeptide Y (Npy) neuron survival in the mouse anorexia (anx) mutation.A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.The role of leptin, melanocortin, and neurotrophin system genes on body weight in anorexia nervosa and bulimia nervosa.Allele frequencies of variants in ultra conserved elements identify selective pressure on transcription factor bindingMachine learning derived risk prediction of anorexia nervosaA genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT regionWhole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.Contemporary views on the genetics of anorexia nervosa.Novel and ultra-rare damaging variants in neuropeptide signaling are associated with disordered eating behaviorsIntegrating multi-omics biomarkers and postprandial metabolism to develop personalized treatment for anorexia nervosa.Genetic epidemiology of eating disorders.Emerging Treatments in Eating Disorders.Soluble epoxide hydrolase as a therapeutic target for pain, inflammatory and neurodegenerative diseases.A retrospective analysis of biochemical and haematological parameters in patients with eating disorders.Spectrum of mutations in monogenic diabetes genes identified from high-throughput DNA sequencing of 6888 individuals.Personalized polyunsaturated fatty acids as a potential adjunctive treatment for anorexia nervosa.Early childhood adversities and risk of eating disorders in women: A Danish register-based cohort study.Molecular bases of anorexia nervosa, bulimia nervosa and binge eating disorder: shedding light on the darkness.Genetics of Anorexia Nervosa.Fasting and postprandial soluble epoxide hydrolase-associated eicosanoids of remitted patients with eating disorder.
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Evidence for the role of EPHX2 gene variants in anorexia nervosa
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2014 nî lūn-bûn
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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
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2014 թվականի հունիսին հրատարակված գիտական հոդված
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2014年の論文
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Evidence for the role of EPHX2 gene variants in anorexia nervosa
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Evidence for the role of EPHX2 gene variants in anorexia nervosa
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Evidence for the role of EPHX2 gene variants in anorexia nervosa
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label
Evidence for the role of EPHX2 gene variants in anorexia nervosa
@ast
Evidence for the role of EPHX2 gene variants in anorexia nervosa
@en
Evidence for the role of EPHX2 gene variants in anorexia nervosa
@nl
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Evidence for the role of EPHX2 gene variants in anorexia nervosa
@ast
Evidence for the role of EPHX2 gene variants in anorexia nervosa
@en
Evidence for the role of EPHX2 gene variants in anorexia nervosa
@nl
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Evidence for the role of EPHX2 gene variants in anorexia nervosa
@en
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A A Scott-Van Zeeland
A S Kaplan
A Torkamani
A W Bergen
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P304
P356
10.1038/MP.2013.91
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P577
2014-06-01T00:00:00Z