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Author Details

Carl D Langefeld
Wake Forest University School of Medicine
1990
568
89
Jake Y. Chen (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37787451Deep Resequencing of the 1q22 Locus in Non-Lobar Intracerebral Hemorrhage.Ann Neurol2024
37787451Deep Resequencing of the 1q22 Locus in Non-Lobar Intracerebral Hemorrhage.Ann Neurol2024
36630956Multi-omic integration reveals cell-type-specific regulatory networks of insulin resistance in distinct ancestry populations.Cell Syst2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37720000Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease.Obstet Med2023
37770635Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.Nat Genet2023
37345795Social Determinants of Health and Cerebral Small Vessel Disease: Is Epigenetics a Key Mediator?J Am Heart Assoc2023
37158120Geographic Disparities in Case Fatality and Discharge Disposition Among Patients With Primary Intracerebral Hemorrhage.J Am Heart Assoc2023
37326643Predicting chronic postsurgical pain: current evidence and a novel program to develop predictive biomarker signatures.Pain2023
37005925Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS).Metabolomics2023
37005464Molecular pathways identified from single nucleotide polymorphisms demonstrate mechanistic differences in systemic lupus erythematosus patients of Asian and European ancestry.Sci Rep2023
36630956Multi-omic integration reveals cell-type-specific regulatory networks of insulin resistance in distinct ancestry populations.Cell Syst2023
36803404Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis.Clin Epigenetics2023
37439560Validation of Epigenetic Markers for the Prediction of Response to Topical Corticosteroid Treatment in Eosinophilic Esophagitis.Clin Transl Gastroenterol2023
36799223A Genomic Risk Score Identifies Individuals at High Risk for Intracerebral Hemorrhage.Stroke2023
36462311DNA methylation of the TPMT gene and azathioprine pharmacokinetics in children with very early onset inflammatory bowel disease.Biomed Pharmacother2023
37221924Identification of influential rare variants in aggregate testing using random forest importance measures.Ann Hum Genet2023
37162822Deep resequencing of the 1q22 locus in non-lobar intracerebral hemorrhage.medRxiv2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37720000Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease.Obstet Med2023
37770635Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.Nat Genet2023
37326643Predicting chronic postsurgical pain: current evidence and a novel program to develop predictive biomarker signatures.Pain2023
37221924Identification of influential rare variants in aggregate testing using random forest importance measures.Ann Hum Genet2023
37158120Geographic Disparities in Case Fatality and Discharge Disposition Among Patients With Primary Intracerebral Hemorrhage.J Am Heart Assoc2023
37345795Social Determinants of Health and Cerebral Small Vessel Disease: Is Epigenetics a Key Mediator?J Am Heart Assoc2023
37439560Validation of Epigenetic Markers for the Prediction of Response to Topical Corticosteroid Treatment in Eosinophilic Esophagitis.Clin Transl Gastroenterol2023
37005925Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS).Metabolomics2023
37005464Molecular pathways identified from single nucleotide polymorphisms demonstrate mechanistic differences in systemic lupus erythematosus patients of Asian and European ancestry.Sci Rep2023
37162822Deep resequencing of the 1q22 locus in non-lobar intracerebral hemorrhage.medRxiv2023
36803404Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis.Clin Epigenetics2023
36462311DNA methylation of the TPMT gene and azathioprine pharmacokinetics in children with very early onset inflammatory bowel disease.Biomed Pharmacother2023
36799223A Genomic Risk Score Identifies Individuals at High Risk for Intracerebral Hemorrhage.Stroke2023
34750102Antifibrotic factor KLF4 is repressed by the miR-10/TFAP2A/TBX5 axis in dermal fibroblasts: insights from twins discordant for systemic sclerosis.Ann Rheum Dis2022
36181103Alzheimer's disease related single nucleotide polymorphisms and correlation with intracerebral hemorrhage incidence.Medicine (Baltimore)2022
35768168Social Factors, Epigenomics and Lupus in African American Women (SELA) Study: protocol for an observational mechanistic study examining the interplay of multiple individual and social factors on lupus outcomes in a health disparity population.Lupus Sci Med2022
35704681Gut dysbiosis and the clinical spectrum in anti-Ro positive mothers of children with neonatal lupus.Gut Microbes2022
35443984Initial antihypertensive agent effects on acute blood pressure after intracerebral haemorrhage.Stroke Vasc Neurol2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
36334592Mendelian randomization and pathway analysis demonstrate shared genetic associations between lupus and coronary artery disease.Cell Rep Med2022
36268164Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.HGG Adv2022
36327221COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection.PLoS Genet2022
35547202Multi-Site Observational Study to Assess Biomarkers for Susceptibility or Resilience to Chronic Pain: The Acute to Chronic Pain Signatures (A2CPS) Study Protocol.Front Med (Lausanne)2022
35853889TGFBR1*6A as a modifier of breast cancer risk and progression: advances and future prospects.NPJ Breast Cancer2022
35720397Relationship Between a Vitamin D Genetic Risk Score and Autoantibodies Among First-Degree Relatives of Probands With Rheumatoid Arthritis and Systemic Lupus Erythematosus.Front Immunol2022
35403514Shared genetic background between SARS-CoV-2 infection and large artery stroke.Int J Stroke2022
35467982Transcriptome-wide analyses of adipose tissue in outbred rats reveal genetic regulatory mechanisms relevant for human obesity.Physiol Genomics2022
36591257Comparison of different gene addition strategies to modify placental derived-mesenchymal stromal cells to produce FVIII.Front Immunol2022
37397545The modifying influence of HLA class II DQB1â¿¿06:02 on the <i>Streptococcus</i> and clinical phenotype correlation among anti-Ro+ mothers of children with neonatal lupus.Genes Dis2022
36550147Reply to: A balanced measure shows superior performance of pseudobulk methods in single-cell RNA-sequencing analysis.Nat Commun2022
35289861Risk Factors Associated With Mortality and Neurologic Disability After Intracerebral Hemorrhage in a Racially and Ethnically Diverse Cohort.JAMA Netw Open2022
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