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eating disorders
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Ophoff, R.A.
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(1 - 24 of 27)
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Childhood abuse v. neglect and risk for major psychiatric disorders
Common genetic variation and age of onset of anorexia nervosa
Genetic variants associated with longitudinal changes in brain structure across the lifespan
Virtual histology of cortical thickness and shared neurobiology in 6 psychiatric disorders
Shared genetic risk between eating disorder- and substance-use-related phenotypes
Genetic architecture of subcortical brain structures in 38,851 individuals
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
Identification of an Amino Acid Motif in HLA-DR1 That Distinguishes Uveitis in Patients With Juvenile Idiopathic Arthritis
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Rare and low-frequency coding variants alter human adult height
Novel genetic loci associated with hippocampal volume
Novel genetic loci underlying human intracranial volume identified through genome-wide association
High educational performance is a distinctive feature of bipolar disorder: a study on cognition in bipolar disorder, schizophrenia patients, relatives and controls
High educational performance is a distinctive feature of bipolar disorder: A study on cognition in bipolar disorder, schizophrenia patients, relatives and controls
Common genetic variants influence human subcortical brain structures
A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
A genome-wide association study of anorexia nervosa
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data
A Genome Wide Association Study Of Rheumatoid Arthritis Without Antibodies Against Citrullinated Peptides
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Identification of common variants associated with human hippocampal and intracranial volumes
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Identification of Novel Genetic Markers Associated with Clinical Phenotypes of Systemic Sclerosis through a Genome-Wide Association Strategy
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