Published in JAMA on May 26, 2015
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No association between general cognitive ability and rare copy number variation. Behav Genet (2013) 0.84
No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort. PLoS One (2013) 0.82
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Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder. JAMA Psychiatry (2015) 1.27
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat Genet (2016) 1.24
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. Hum Mol Genet (2014) 1.08
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index. PLoS Genet (2014) 0.93
Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nat Neurosci (2016) 0.87
Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes. PLoS Genet (2016) 0.86
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. Biol Psychiatry (2016) 0.85
Mitochondrial DNA variants in obesity. PLoS One (2014) 0.83
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behav Genet (2015) 0.83
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies. Gastroenterology (2016) 0.80
De novo PIK3R2 variant causes polymicrogyria, corpus callosum hyperplasia and focal cortical dysplasia. Eur J Hum Genet (2016) 0.78
Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq). Nat Commun (2016) 0.78
West syndrome caused by homozygous variant in the evolutionary conserved gene encoding the mitochondrial elongation factor GUF1. Eur J Hum Genet (2015) 0.77
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium. Aging Cell (2016) 0.76
The inverse link between genetic risk for schizophrenia and migraine through NMDA (N-methyl-D-aspartate) receptor activation via D-serine. Eur Neuropsychopharmacol (2016) 0.76
Inflammatory myopathy in a patient with Aicardi-Goutières syndrome. Eur J Med Genet (2017) 0.76
A New Split Hand/Foot Malformation with Long Bone Deficiency Familial Case. J Pediatr Genet (2016) 0.75
Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. PLoS One (2017) 0.75
Inactivation of AMMECR1 is associated with growth, bone and heart alterations. Hum Mutat (2017) 0.75
Investigation of Naturally Occurring Single-Nucleotide Variants in Human TAAR1. Front Pharmacol (2017) 0.75
Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations. JAMA Psychiatry (2017) 0.75
Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD. Am J Med Genet B Neuropsychiatr Genet (2017) 0.75
Low number of fixed somatic mutations in a long-lived oak tree. Nat Plants (2017) 0.75
Full exploitation of high dimensionality in brain imaging: The JPND working group statement and findings. Alzheimers Dement (Amst) (2019) 0.75
A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2. Gene (2020) 0.75
PIGN encephalopathy: Characterizing the epileptology. Epilepsia (2022) 0.75