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| 37533140 | Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait. | Clin J Am Soc Nephrol | 2023 |
| 36226494 | Variation and impact of polygenic hematologic traits in monogenic sickle cell disease. | Haematologica | 2023 |
| 36096903 | Evaluating Associations between Average Pain Intensity and Genetic Variation in People with Sickle Cell Disease: An Exploratory Study. | Pain Manag Nurs | 2023 |
| 36399516 | Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy. | Blood Adv | 2023 |
| 37662265 | WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. | medRxiv | 2023 |
| 37886496 | Genomic Structural Equation Modeling Reveals Latent Phenotypes in the Human Cortex with Distinct Genetic Architecture. | Res Sq | 2023 |
| 37789374 | Integrative single-nucleus multi-omics analysis prioritizes candidate cis and trans regulatory networks and their target genes in Alzheimer's disease brains. | Cell Biosci | 2023 |
| 37967379 | Characterizing epigenetic aging in an adult sickle cell disease cohort. | | 2023 |
| 36778386 | Structural variation across 138,134 samples in the TOPMed consortium. | Res Sq | 2023 |
| 37398366 | Polarized Desmosome and Hemidesmosome Shedding via Exosomes is an Early Indicator of Outer Blood-Retina Barrier Dysfunction. | | 2023 |
| 36702996 | Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing. | Nat Genet | 2023 |
| 36940203 | Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veteran Program. | PLoS Genet | 2023 |
| 36747810 | Structural variation across 138,134 samples in the TOPMed consortium. | bioRxiv | 2023 |
| 37377737 | Gene-nutrient interactions that impact magnesium homeostasis increase risk for neural tube defects in mice exposed to dolutegravir. | | 2023 |
| 36546431 | Sex differences in progression of kidney disease in sickle cell disease. | Haematologica | 2023 |
| 36542982 | Impact of traumatic life events and polygenic risk scores for major depression and posttraumatic stress disorder on Iraq/Afghanistan Veterans. | | 2023 |
| 36993312 | Genetic regulation of fetal hemoglobin across global populations. | medRxiv | 2023 |
| 36993181 | Gene-metabolite annotation with shortest reactional distance enhances metabolite genome-wide association studies results. | | 2023 |
| 37540217 | Lysyl oxidase-like 1-antisense 1 (LOXL1-AS1) lncRNA differentially regulates gene and protein expression, signaling and morphology of human ocular cells. | | 2023 |
| 35347246 | A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. | Mol Psychiatry | 2022 |
| 36183486 | Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. | EBioMedicine | 2022 |
| 35696734 | Longitudinal study of glomerular hyperfiltration in adults with sickle cell anemia: a multicenter pooled analysis. | Blood Adv | 2022 |
| 35367939 | Alcohol use and alcohol use disorder differ in their genetic relationships with PTSD: A genomic structural equation modelling approach. | Drug Alcohol Depend | 2022 |
| 35927319 | Rare genetic variants explain missing heritability in smoking. | Nat Hum Behav | 2022 |
| 36400533 | Genetic Modifiers of Sickle Cell Disease. | Hematology/Oncology Clinics of North America | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 34990411 | Clonal hematopoiesis in sickle cell disease. | J Clin Invest | 2022 |
| 34429139 | Sex dependent glial-specific changes in the chromatin accessibility landscape in late-onset Alzheimer's disease brains. | Mol Neurodegener | 2021 |
| 33860118 | Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD. | Hepatology Communications | 2021 |
| 33545031 | Rare and de novo coding variants in chromodomain genes in Chiari I malformation. | American Journal of Human Genetics | 2021 |
| 34017130 | Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation. | Nat Neurosci | 2021 |
| 33574475 | Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration. | Scientific Reports | 2021 |
| 33667397 | Rare and de novo coding variants in chromodomain genes in Chiari I malformation. | American Journal of Human Genetics | 2021 |
| 34248484 | Examining Individual and Synergistic Contributions of PTSD and Genetics to Blood Pressure: A Trans-Ethnic Meta-Analysis. | Front Neurosci | 2021 |
| 33974636 | Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1. | PLoS One | 2021 |
| 33352116 | Rare and de novo coding variants in chromodomain genes in Chiari I malformation. | American Journal of Human Genetics | 2021 |
| 33346869 | Correction to: Effects of Environmental Stress and Gender on Associations among Symptoms of Depression and the Serotonin Transporter Gene Linked Polymorphic Region (5-HTTLPR). | Behav Genet | 2021 |
| 33179474 | Rapid decline in estimated glomerular filtration rate in sickle cell anemia: results of a multicenter pooled analysis. | Haematologica | 2021 |
| 33231305 | Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program. | Transfusion | 2021 |
| 32949984 | Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis. | Blood Cells Mol Dis | 2021 |
| 33326061 | Correction to: 5-HTTLPR and Gender Moderate Changes in Negative Affect Responses to Tryptophan Infusion. | Behavior Genetics | 2021 |
| 34916497 | Trauma and posttraumatic stress disorder modulate polygenic predictors of hippocampal and amygdala volume. | Transl Psychiatry | 2021 |
| 33214552 | PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia. | Nat Commun | 2020 |
| 31691959 | Genetic variation in dopamine neurotransmission and motor development of infants born extremely-low-birthweight. | Dev Med Child Neurol | 2020 |
| 32641180 | Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression. | International Psychogeriatrics | 2020 |
| 33029326 | Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. | Eur J Psychotraumatol | 2020 |
| 32970752 | Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients. | PLoS ONE | 2020 |
| 33235198 | Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR. | Nat Commun | 2020 |
| 32960507 | Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks. | Molecular genetics & genomic medicine | 2020 |
| 33339817 | Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. | Nat Commun | 2020 |