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Author Details
Full Name
Nathan Pankratz
Affiliation
University of Minnesota
ORCID
Career Start Year
2001
Papers
164
H Index
50
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36194249
Proteomic analysis of diabetes genetic risk scores identifies complement C2 and neuropilin-2 as predictors of type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) Study.
Diabetologia
2023
36194249
Proteomic analysis of diabetes genetic risk scores identifies complement C2 and neuropilin-2 as predictors of type 2 diabetes: the Atherosclerosis Risk in Communities (ARIC) Study.
Diabetologia
2023
37745480
Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.
bioRxiv
2023
37635636
Exome sequencing findings in children with annular pancreas.
Mol Genet Genomic Med
2023
36716319
Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores.
PLoS One
2023
37153111
Exploratory Study of the Association of Genetic Factors With Recovery of Adrenal Function in Cushing Disease.
J Endocr Soc
2023
36778386
Structural variation across 138,134 samples in the TOPMed consortium.
Res Sq
2023
36960714
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.
Circ Genom Precis Med
2023
36765944
Lower Expression of <i>CFTR</i> Is Associated with Higher Mortality in a Meta-Analysis of Individuals with Colorectal Cancer.
Cancers (Basel)
2023
36579647
Proteomics Analysis of Genetic Liability of Abdominal Aortic Aneurysm Identifies Plasma Neogenin and Kit Ligand: The ARIC Study.
Arterioscler Thromb Vasc Biol
2023
36958849
Associations between MICA and MICB Genetic Variants, Protein Levels, and Colorectal Cancer: Atherosclerosis Risk in Communities (ARIC).
Cancer Epidemiol Biomarkers Prev
2023
37398003
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
medRxiv
2023
37192320
Long-Term Air Pollution Exposure and Mitochondrial DNA Copy Number: An Analysis of UK Biobank Data.
Environ Health Perspect
2023
36747810
Structural variation across 138,134 samples in the TOPMed consortium.
bioRxiv
2023
37531260
Predicted leukocyte telomere length and risk of myeloid neoplasms.
Hum Mol Genet
2023
36846569
Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls.
Front Mol Neurosci
2023
37635636
Exome sequencing findings in children with annular pancreas.
Mol Genet Genomic Med
2023
37745480
Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.
bioRxiv
2023
37531260
Predicted leukocyte telomere length and risk of myeloid neoplasms.
Hum Mol Genet
2023
37192320
Long-Term Air Pollution Exposure and Mitochondrial DNA Copy Number: An Analysis of UK Biobank Data.
Environ Health Perspect
2023
36958849
Associations between MICA and MICB Genetic Variants, Protein Levels, and Colorectal Cancer: Atherosclerosis Risk in Communities (ARIC).
Cancer Epidemiol Biomarkers Prev
2023
37153111
Exploratory Study of the Association of Genetic Factors With Recovery of Adrenal Function in Cushing Disease.
J Endocr Soc
2023
37398003
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
medRxiv
2023
36960714
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.
Circ Genom Precis Med
2023
36747810
Structural variation across 138,134 samples in the TOPMed consortium.
bioRxiv
2023
36716319
Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores.
PLoS One
2023
36846569
Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls.
Front Mol Neurosci
2023
36579647
Proteomics Analysis of Genetic Liability of Abdominal Aortic Aneurysm Identifies Plasma Neogenin and Kit Ligand: The ARIC Study.
Arterioscler Thromb Vasc Biol
2023
36778386
Structural variation across 138,134 samples in the TOPMed consortium.
Res Sq
2023
36765944
Lower Expression of <i>CFTR</i> Is Associated with Higher Mortality in a Meta-Analysis of Individuals with Colorectal Cancer.
Cancers (Basel)
2023
34553764
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Hum Mol Genet
2022
36311265
Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number.
HGG Adv
2022
36042976
Whole Exome Sequencing in Patients With Ectopic Posterior Pituitary.
J Endocr Soc
2022
35591888
A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data.
NAR Genom Bioinform
2022
35388009
Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.
Nat Commun
2022
35385311
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.
Sci Adv
2022
36154123
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.
Circulation
2022
36149413
Genetic drivers of Cushing's disease: Frequency and associated phenotypes.
Genet Med
2022
35552711
Whole-exome sequencing of 14â¿¿389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Hum Mol Genet
2022
35368045
Predicted leukocyte telomere length and risk of germ cell tumours.
Br J Cancer
2022
36198488
Progressive reduction in circulating levels of carotenoids and other micronutrients in patients with chronic pancreatitis.
Pancreatology
2022
36481753
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.
Nat Commun
2022
35274497
Exome sequencing identifies variants in infants with sacral agenesis.
Birth Defects Res
2022
35264566
Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.
Nat Commun
2022
34553764
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Hum Mol Genet
2022
35368045
Predicted leukocyte telomere length and risk of germ cell tumours.
Br J Cancer
2022
35388009
Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus.
Nat Commun
2022
35591888
A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data.
NAR Genom Bioinform
2022
35552711
Whole-exome sequencing of 14â¿¿389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Hum Mol Genet
2022
35385311
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.
Sci Adv
2022
1 - 50 of 328
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