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Evaluation of mitochondrial DNA copy number estimation techniques

PloS one, 2020-01, Vol.15 (1), p.e0228166

2020

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MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension

PloS one, 2017-08, Vol.12 (8), p.e0176734

2017

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Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci

Human molecular genetics, 2015-08, Vol.24 (15), p.4464-4479

2015

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CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis

The Journal of clinical investigation, 2018-03, Vol.128 (3), p.1106-1124

2018

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Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities Study

Journal of the American Society of Nephrology, 2016-08, Vol.27 (8), p.2467-2473

2016

Volltextzugriff (PDF)

Clinical interpretation and implications of whole-genome sequencing

JAMA : the journal of the American Medical Association, 2014-03, Vol.311 (10), p.1035

2014

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A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos

American journal of human genetics, 2020-11, Vol.107 (5), p.849-863

2020

Volltextzugriff (PDF)

Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting

The New England journal of medicine, 2022-02, Vol.386 (7), p.700-702

2022

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Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

Genome medicine, 2020-09, Vol.12 (1), p.84-84, Article 84

2020

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Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections

American journal of human genetics, 2016-09, Vol.99 (3), p.762-769

2016

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Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers

PloS one, 2019-09, Vol.14 (9), p.e0221957

2019

Volltextzugriff (PDF)

Multiple SCN5A variant enhancers modulate its cardiac gene expression and the QT interval

Proceedings of the National Academy of Sciences - PNAS, 2019-05, Vol.116 (22), p.10636-10645

2019

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Association between mitochondrial DNA copy number and sudden cardiac death: findings from the Atherosclerosis Risk in Communities study (ARIC)

European heart journal, 2017-12, Vol.38 (46), p.3443-3448

2017

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Informed Consent in the Genomics Era

Cold Spring Harbor perspectives in medicine, 2020-08, Vol.10 (8), p.a036582

2020

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Serum sphingolipids and incident diabetes in a US population with high diabetes burden: the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

The American journal of clinical nutrition, 2020-07, Vol.112 (1), p.57-65

2020

Volltextzugriff (PDF)

Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality

Nature communications, 2023-09, Vol.14 (1), p.6113-6113, Article 6113

2023

Volltextzugriff (PDF)

Epigenome‐wide study identifies novel methylation loci associated with body mass index and waist circumference

Obesity (Silver Spring, Md.), 2015-07, Vol.23 (7), p.1493-1501

2015

Volltextzugriff (PDF)

Longitudinal change in blood DNA epigenetic signature after smoking cessation

Epigenetics, 2022-10, Vol.17 (10), p.1098-1109

2022

Volltextzugriff (PDF)

Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing

Nature biotechnology, 2022-07, Vol.40 (7), p.1035-1041

2022

Volltextzugriff (PDF)

Factors associated with blood mercury concentrations and their interactions with three glutathione S-transferase genes (GSTT1, GSTM1, and GSTP1): an exposure assessment study of typically developing Jamaican children

BMC pediatrics, 2024-01, Vol.24 (1), p.14-14, Article 14

2024

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Gut Microbiota and Blood Metabolites Related to Fiber Intake and Type 2 Diabetes

Circulation research, 2024-03, Vol.134 (7), p.842

2024

Volltextzugriff (PDF)

Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans

JAMA : the journal of the American Medical Association, 2014-11, Vol.312 (20), p.2115

2014

Volltextzugriff (PDF)

Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience

Genetics in medicine, 2018-03, Vol.20 (3), p.369-373

2018

Volltextzugriff (PDF)

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Evaluation of mitochondrial DNA copy number estimation techniques

MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension

Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci

CD163+ macrophages promote angiogenesis and vascular permeability accompanied by inflammation in atherosclerosis

Association between Mitochondrial DNA Copy Number in Peripheral Blood and Incident CKD in the Atherosclerosis Risk in Communities Study

Clinical interpretation and implications of whole-genome sequencing

A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos

Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting

Host and gut microbial tryptophan metabolism and type 2 diabetes: an integrative analysis of host genetics, diet, gut microbiome and circulating metabolites in cohort studies

Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs

Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections

Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers

Multiple SCN5A variant enhancers modulate its cardiac gene expression and the QT interval

Association between mitochondrial DNA copy number and sudden cardiac death: findings from the Atherosclerosis Risk in Communities study (ARIC)

Informed Consent in the Genomics Era

Serum sphingolipids and incident diabetes in a US population with high diabetes burden: the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality

Epigenome‐wide study identifies novel methylation loci associated with body mass index and waist circumference

Longitudinal change in blood DNA epigenetic signature after smoking cessation

Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing

Factors associated with blood mercury concentrations and their interactions with three glutathione S-transferase genes (GSTT1, GSTM1, and GSTP1): an exposure assessment study of typically developing Jamaican children

Gut Microbiota and Blood Metabolites Related to Fiber Intake and Type 2 Diabetes

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

Association of sickle cell trait with chronic kidney disease and albuminuria in African Americans

Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience

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