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| 35671390 | The genetic landscape of germline DDX41 variants predisposing to myeloid neoplasms. | Blood | 2022 |
| 33855780 | Indolent T-cell prolymphocytic leukemia with no expression of surface T-cell receptors or surface CD3. | Int J Lab Hematol | 2021 |
| 32217764 | Comparison of commonly used solid tumor targeted gene sequencing panels for estimating tumor mutation burden shows analytical and prognostic concordance within the cancer genome atlas cohort. | J Immunother Cancer | 2020 |
| 31933193 | Genetic variation in alcohol dehydrogenase is associated with neurocognition in men with HIV and history of alcohol use disorder: preliminary findings. | J Neurovirol | 2020 |
| 31837433 | Multi-Institutional Evaluation of Interrater Agreement of Variant Classification Based on the 2017 Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer. | J Mol Diagn | 2020 |
| 30503783 | Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. | Eur Neuropsychopharmacol | 2019 |
| 30132795 | JAK2 double minutes with resultant simultaneous amplification of JAK2 and CD274 in a therapy-related myelodysplastic syndrome evolving into an acute myeloid leukaemia. | Br J Haematol | 2019 |
| 31301644 | Adverse effect of catechol-O-methyltransferase (COMT) Val158Met met/met genotype in methamphetamine-related executive dysfunction. | Addict Behav | 2019 |
| 31551593 | A perturbed gene network containing PI3K-AKT, RAS-ERK and WNT-β-catenin pathways in leukocytes is linked to ASD genetics and symptom severity. | Nat Neurosci | 2019 |
| 30649720 | Annotation of Variant Data from High-Throughput DNA Sequencing from Tumor Specimens: Filtering Strategies to Identify Driver Mutations. | Methods Mol Biol | 2019 |
| 30649719 | Bioinformatics Basics for High-Throughput Hybridization-Based Targeted DNA Sequencing from FFPE-Derived Tumor Specimens: From Reads to Variants. | Methods Mol Biol | 2019 |
| 30649718 | Library Preparation Using FFPE-Derived Tumor DNA for High-Throughput Hybridization-Based Targeted or Exome Sequencing. | Methods Mol Biol | 2019 |
| 30388399 | Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. | Am J Hum Genet | 2018 |
| 29088295 | Expression of LDL receptor-related proteins (LRPs) in common solid malignancies correlates with patient survival. | PLoS One | 2017 |
| 25953057 | Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children. | Brain Imaging Behav | 2016 |
| 27412137 | Gray matter maturation and cognition in children with different APOE ε genotypes. | Neurology | 2016 |
| 27577874 | Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans. | Hum Mol Genet | 2016 |
| 26183468 | Anxiety is related to indices of cortical maturation in typically developing children and adolescents. | Brain Struct Funct | 2016 |
| 25937488 | The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. | Neuroimage | 2016 |
| 25821911 | Family income, parental education and brain structure in children and adolescents. | Nat Neurosci | 2015 |
| 26668231 | Cell cycle networks link gene expression dysregulation, mutation, and brain maldevelopment in autistic toddlers. | Mol Syst Biol | 2015 |
| 25660813 | Genetic variants associated with sleep disorders. | Sleep Med | 2015 |
| 25739104 | Prediction of autism by translation and immune/inflammation coexpressed genes in toddlers from pediatric community practices. | JAMA Psychiatry | 2015 |
| 24219608 | The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING). | Neuropsychology | 2014 |
| 25439791 | Precision phenotyping, panomics, and system-level bioinformatics to delineate complex biologies of atherosclerosis: rationale and design of the "Genetic Loci and the Burden of Atherosclerotic Lesions" study. | J Cardiovasc Comput Tomogr | 2014 |
| 25395965 | Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles. | Psychiatry Investig | 2014 |
| 24560520 | Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. | Am J Hum Genet | 2014 |
| 24345515 | Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations. | Hum Mol Genet | 2014 |
| 23183192 | Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants. | Heart Rhythm | 2013 |
| 24024963 | Genome-wide association study of shared components of reading disability and language impairment. | Genes Brain Behav | 2013 |
| 23972371 | Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. | Am J Hum Genet | 2013 |
| 23599027 | Genome-wide association study of age at menarche in African-American women. | Hum Mol Genet | 2013 |
| 23521777 | FMR1, circadian genes and depression: suggestive associations or false discovery? | J Circadian Rhythms | 2013 |
| 22355368 | Longitudinal replication studies of GWAS risk SNPs influencing body mass index over the course of childhood and adulthood. | PLoS One | 2012 |
| 23169628 | Long-term influence of normal variation in neonatal characteristics on human brain development. | Proc Natl Acad Sci U S A | 2012 |
| 23166209 | Impact of ancestry and common genetic variants on QT interval in African Americans. | Circ Cardiovasc Genet | 2012 |
| 23063622 | Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. | Am J Hum Genet | 2012 |
| 23139255 | Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. | Circ Cardiovasc Genet | 2012 |
| 23150548 | Multimodal imaging of the self-regulating developing brain. | Proc Natl Acad Sci U S A | 2012 |
| 22902750 | Neuroanatomical assessment of biological maturity. | Curr Biol | 2012 |
| 22842737 | Influences of FTO gene on onset age of adult overweight. | Hum Genet | 2012 |
| 22457638 | Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. | PLoS Genet | 2012 |
| 22624833 | Influence of genetic polymorphisms on the effect of high- and standard-dose clopidogrel after percutaneous coronary intervention: the GIFT (Genotype Information and Functional Testing) study. | J Am Coll Cardiol | 2012 |
| 22247754 | Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias. | PLoS One | 2012 |
| 22295058 | Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--a meta-analysis of three independent studies. | PLoS One | 2012 |
| 22343285 | Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. | Proc Natl Acad Sci U S A | 2012 |
| 21498463 | Analysis of 94 candidate genes and 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia. | Am J Psychiatry | 2011 |
| 22025373 | Genetic variants and blood pressure in a population-based cohort: the Cardiovascular Risk in Young Finns study. | Hypertension | 2011 |
| 21827647 | Polymorphisms in melatonin synthesis pathways: possible influences on depression. | J Circadian Rhythms | 2011 |
| 21843359 | Gene expression profiling of human whole blood samples with the Illumina WG-DASL assay. | BMC Genomics | 2011 |