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Author Details
Full Name
Carl D Langefeld
Affiliation
Wake Forest University School of Medicine
ORCID
Career Start Year
1990
Papers
568
H Index
89
Expertise
CM4AI Collaborator
Jake Y. Chen (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37787451
Deep Resequencing of the 1q22 Locus in Non-Lobar Intracerebral Hemorrhage.
Ann Neurol
2024
37787451
Deep Resequencing of the 1q22 Locus in Non-Lobar Intracerebral Hemorrhage.
Ann Neurol
2024
36630956
Multi-omic integration reveals cell-type-specific regulatory networks of insulin resistance in distinct ancestry populations.
Cell Syst
2023
38028628
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
Front Genet
2023
37720000
Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease.
Obstet Med
2023
37770635
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.
Nat Genet
2023
37345795
Social Determinants of Health and Cerebral Small Vessel Disease: Is Epigenetics a Key Mediator?
J Am Heart Assoc
2023
37158120
Geographic Disparities in Case Fatality and Discharge Disposition Among Patients With Primary Intracerebral Hemorrhage.
J Am Heart Assoc
2023
37326643
Predicting chronic postsurgical pain: current evidence and a novel program to develop predictive biomarker signatures.
Pain
2023
37005925
Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS).
Metabolomics
2023
37005464
Molecular pathways identified from single nucleotide polymorphisms demonstrate mechanistic differences in systemic lupus erythematosus patients of Asian and European ancestry.
Sci Rep
2023
36630956
Multi-omic integration reveals cell-type-specific regulatory networks of insulin resistance in distinct ancestry populations.
Cell Syst
2023
36803404
Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis.
Clin Epigenetics
2023
37439560
Validation of Epigenetic Markers for the Prediction of Response to Topical Corticosteroid Treatment in Eosinophilic Esophagitis.
Clin Transl Gastroenterol
2023
36799223
A Genomic Risk Score Identifies Individuals at High Risk for Intracerebral Hemorrhage.
Stroke
2023
36462311
DNA methylation of the TPMT gene and azathioprine pharmacokinetics in children with very early onset inflammatory bowel disease.
Biomed Pharmacother
2023
37221924
Identification of influential rare variants in aggregate testing using random forest importance measures.
Ann Hum Genet
2023
37162822
Deep resequencing of the 1q22 locus in non-lobar intracerebral hemorrhage.
medRxiv
2023
38028628
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
Front Genet
2023
37720000
Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease.
Obstet Med
2023
37770635
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.
Nat Genet
2023
37326643
Predicting chronic postsurgical pain: current evidence and a novel program to develop predictive biomarker signatures.
Pain
2023
37221924
Identification of influential rare variants in aggregate testing using random forest importance measures.
Ann Hum Genet
2023
37158120
Geographic Disparities in Case Fatality and Discharge Disposition Among Patients With Primary Intracerebral Hemorrhage.
J Am Heart Assoc
2023
37345795
Social Determinants of Health and Cerebral Small Vessel Disease: Is Epigenetics a Key Mediator?
J Am Heart Assoc
2023
37439560
Validation of Epigenetic Markers for the Prediction of Response to Topical Corticosteroid Treatment in Eosinophilic Esophagitis.
Clin Transl Gastroenterol
2023
37005925
Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS).
Metabolomics
2023
37005464
Molecular pathways identified from single nucleotide polymorphisms demonstrate mechanistic differences in systemic lupus erythematosus patients of Asian and European ancestry.
Sci Rep
2023
37162822
Deep resequencing of the 1q22 locus in non-lobar intracerebral hemorrhage.
medRxiv
2023
36803404
Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis.
Clin Epigenetics
2023
36462311
DNA methylation of the TPMT gene and azathioprine pharmacokinetics in children with very early onset inflammatory bowel disease.
Biomed Pharmacother
2023
36799223
A Genomic Risk Score Identifies Individuals at High Risk for Intracerebral Hemorrhage.
Stroke
2023
34750102
Antifibrotic factor KLF4 is repressed by the miR-10/TFAP2A/TBX5 axis in dermal fibroblasts: insights from twins discordant for systemic sclerosis.
Ann Rheum Dis
2022
36181103
Alzheimer's disease related single nucleotide polymorphisms and correlation with intracerebral hemorrhage incidence.
Medicine (Baltimore)
2022
35768168
Social 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 Med
2022
35704681
Gut dysbiosis and the clinical spectrum in anti-Ro positive mothers of children with neonatal lupus.
Gut Microbes
2022
35443984
Initial antihypertensive agent effects on acute blood pressure after intracerebral haemorrhage.
Stroke Vasc Neurol
2022
35697829
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Commun Biol
2022
36334592
Mendelian randomization and pathway analysis demonstrate shared genetic associations between lupus and coronary artery disease.
Cell Rep Med
2022
36268164
Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.
HGG Adv
2022
36327221
COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection.
PLoS Genet
2022
35547202
Multi-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
35853889
TGFBR1*6A as a modifier of breast cancer risk and progression: advances and future prospects.
NPJ Breast Cancer
2022
35720397
Relationship Between a Vitamin D Genetic Risk Score and Autoantibodies Among First-Degree Relatives of Probands With Rheumatoid Arthritis and Systemic Lupus Erythematosus.
Front Immunol
2022
35403514
Shared genetic background between SARS-CoV-2 infection and large artery stroke.
Int J Stroke
2022
35467982
Transcriptome-wide analyses of adipose tissue in outbred rats reveal genetic regulatory mechanisms relevant for human obesity.
Physiol Genomics
2022
36591257
Comparison of different gene addition strategies to modify placental derived-mesenchymal stromal cells to produce FVIII.
Front Immunol
2022
37397545
The 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 Dis
2022
36550147
Reply to: A balanced measure shows superior performance of pseudobulk methods in single-cell RNA-sequencing analysis.
Nat Commun
2022
35289861
Risk Factors Associated With Mortality and Neurologic Disability After Intracerebral Hemorrhage in a Racially and Ethnically Diverse Cohort.
JAMA Netw Open
2022
1 - 50 of 1,136
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Co-authored papers
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Co-authored papers
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Wake Forest School of Medicine.
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83
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US Department of Veterans Affairs Medical Center
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74
Patrick M Gaffney
Co-authored papers
70
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University of Cincinnati
Co-authored papers
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Julie T Ziegler
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Jill M Norris
Co-authored papers
56
Timothy J Vyse
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55
Jerome I Rotter
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Michelle Petri
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51
Lindsey A Criswell
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49
Adrienne H Williams
Co-authored papers
47
John D Reveille
University of Texas
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45
Yii-Der Ida Chen
Co-authored papers
44
Kent D Taylor
Co-authored papers
40
Maggie C Y Ng
Co-authored papers
39
Jonathan Rosand
Center for Genomic Medicine, Massachusetts General Hospital
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37
Xiuqing Guo
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33
Joel M Guthridge
Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation
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33
Michèle M Sale
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31
Bradford B Worrall
University of Virginia
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30
Timothy D Howard
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29
Charles J Moomaw
University of Cincinnati College of Medicine
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28
Lingyi Lu
Co-authored papers
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