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| 37852782 | Characterization of human transcription factor function and patterns of gene regulation in HepG2 cells. | Genome Res | 2023 |
| 37873117 | Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLs. | bioRxiv | 2023 |
| 36778651 | Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3' Breakpoints. | Complex Psychiatry | 2023 |
| 37090552 | <i>MAPT</i> expression is mediated by long-range interactions with <i>cis</i>-regulatory elements. | bioRxiv | 2023 |
| 37031222 | Neurotransmission-related gene expression in the frontal pole is altered in subjects with bipolar disorder and schizophrenia. | Transl Psychiatry | 2023 |
| 36586412 | Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype. | Am J Hum Genet | 2023 |
| 36951251 | Genetic associations with age at dementia onset in the PSEN1 E280A Colombian kindred. | Alzheimers Dement | 2023 |
| 36950385 | Single nucleus multiomics identifies ZEB1 and MAFB as candidate regulators of Alzheimer's disease-specific <i>cis</i>-regulatory elements. | Cell Genom | 2023 |
| 37308299 | Contributions of rare and common variation to early-onset and atypical dementia risk. | Cold Spring Harb Mol Case Stud | 2023 |
| 36798301 | Contributions of rare and common variation to early-onset and atypical dementia risk. | medRxiv | 2023 |
| 37506491 | Genome-wide DNA methylation analysis implicates enrichment of interferon pathway in African American patients with Systemic Lupus Erythematosus and European Americans with lupus nephritis. | J Autoimmun | 2023 |
| 37852782 | Characterization of human transcription factor function and patterns of gene regulation in HepG2 cells. | Genome Res | 2023 |
| 37506491 | Genome-wide DNA methylation analysis implicates enrichment of interferon pathway in African American patients with Systemic Lupus Erythematosus and European Americans with lupus nephritis. | J Autoimmun | 2023 |
| 37873117 | Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLs. | bioRxiv | 2023 |
| 37090552 | <i>MAPT</i> expression is mediated by long-range interactions with <i>cis</i>-regulatory elements. | bioRxiv | 2023 |
| 36951251 | Genetic associations with age at dementia onset in the PSEN1 E280A Colombian kindred. | Alzheimers Dement | 2023 |
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| 37308299 | Contributions of rare and common variation to early-onset and atypical dementia risk. | Cold Spring Harb Mol Case Stud | 2023 |
| 37031222 | Neurotransmission-related gene expression in the frontal pole is altered in subjects with bipolar disorder and schizophrenia. | Transl Psychiatry | 2023 |
| 36586412 | Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype. | Am J Hum Genet | 2023 |
| 36778651 | Large Common Mitochondrial DNA Deletions Are Associated with a Mitochondrial SNP T14798C Near the 3' Breakpoints. | Complex Psychiatry | 2023 |
| 35260199 | A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects. | Genome Med | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 36042222 | Mitochondria DNA copy number, mitochondria DNA total somatic deletions, Complex I activity, synapse number, and synaptic mitochondria number are altered in schizophrenia and bipolar disorder. | Transl Psychiatry | 2022 |
| 35576644 | Longitudinal analysis of blood DNA methylation identifies mechanisms of response to tumor necrosis factor inhibitor therapy in rheumatoid arthritis. | EBioMedicine | 2022 |
| 35422091 | Identification of potential blood biomarkers associated with suicide in major depressive disorder. | Transl Psychiatry | 2022 |
| 35474001 | Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes. | Nature | 2022 |
| 36411364 | Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. | Nat Genet | 2022 |
| 35260199 | A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects. | Genome Med | 2022 |
| 35474001 | Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes. | Nature | 2022 |
| 35576644 | Longitudinal analysis of blood DNA methylation identifies mechanisms of response to tumor necrosis factor inhibitor therapy in rheumatoid arthritis. | EBioMedicine | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 35422091 | Identification of potential blood biomarkers associated with suicide in major depressive disorder. | Transl Psychiatry | 2022 |
| 36411364 | Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. | Nat Genet | 2022 |
| 36042222 | Mitochondria DNA copy number, mitochondria DNA total somatic deletions, Complex I activity, synapse number, and synaptic mitochondria number are altered in schizophrenia and bipolar disorder. | Transl Psychiatry | 2022 |
| 33411788 | Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy. | PLoS Genet | 2021 |
| 34075090 | Targeting of the CD80/86 proinflammatory axis as a therapeutic strategy to prevent severe COVID-19. | Sci Rep | 2021 |
| 34234242 | Three dimensional modeling of biologically relevant fluid shear stress in human renal tubule cells mimics in vivo transcriptional profiles. | Sci Rep | 2021 |
| 34002096 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. | Nat Genet | 2021 |
| 33843487 | The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible Life. | AJOB Empir Bioeth | 2021 |
| 33674754 | Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. | Mol Psychiatry | 2021 |
| 34049503 | Pooled CRISPR screening in pancreatic cancer cells implicates co-repressor complexes as a cause of multiple drug resistance via regulation of epithelial-to-mesenchymal transition. | BMC Cancer | 2021 |
| 33776890 | The Multi-Partner Consortium to Expand Dementia Research in Latin America (ReDLat): Driving Multicentric Research and Implementation Science. | Front Neurol | 2021 |
| 34144992 | Predicting future from past: The genomic basis of recurrent and rapid stickleback evolution. | Sci Adv | 2021 |
| 34313030 | A study of elective genome sequencing and pharmacogenetic testing in an unselected population. | Mol Genet Genomic Med | 2021 |
| 33411788 | Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy. | PLoS Genet | 2021 |
| 33674754 | Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. | Mol Psychiatry | 2021 |
| 33843487 | The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible Life. | AJOB Empir Bioeth | 2021 |
| 33776890 | The Multi-Partner Consortium to Expand Dementia Research in Latin America (ReDLat): Driving Multicentric Research and Implementation Science. | Front Neurol | 2021 |