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Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

PLoS genetics, 2011-02, Vol.7 (2), p.e1001308

2011

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Discovering genetic interactions bridging pathways in genome-wide association studies

Nature communications, 2019-09, Vol.10 (1), p.4274-18, Article 4274

2019

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Genetic and Nongenetic Risk Factors for Childhood Cancer

The Pediatric clinics of North America, 2015-02, Vol.62 (1), p.11-25

2015

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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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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

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Copy number variations and cognitive phenotypes in unselected populations

JAMA : the journal of the American Medical Association, 2015-05, Vol.313 (20), p.2044

2015

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Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

NeuroImage (Orlando, Fla.), 2010-11, Vol.53 (3), p.1051-1063

2010

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Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores

PloS one, 2023-01, Vol.18 (1), p.e0280657-e0280657

2023

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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.84-17, Article 84

2020

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Human genetics, 2009-01, Vol.124 (6), p.593-605

2009

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Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing’s disease

Endocrine-related cancer, 2017-08, Vol.24 (8), p.379-392

2017

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

Nature communications, 2023-09, Vol.14 (1), p.6113-16, Article 6113

2023

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Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: A Mendelian randomization study

PloS one, 2018-04, Vol.13 (4), p.e0195719-e0195719

2018

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Association between MICA polymorphisms, s-MICA levels, and pancreatic cancer risk in a population-based case-control study

PloS one, 2019-06, Vol.14 (6), p.e0217868-e0217868

2019

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Mitochondrial DNA copy number and incident atrial fibrillation

BMC medicine, 2020-09, Vol.18 (1), p.246-246, Article 246

2020

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Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number

HGG advances, 2023-01, Vol.4 (1), p.100147, Article 100147

2023

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Exome sequencing findings in children with annular pancreas

Molecular genetics & genomic medicine, 2023-10, Vol.11 (10), p.e2233-n/a

2023

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Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study

Journal of human genetics, 2018-03, Vol.63 (3), p.327-337

2018

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Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

PLoS genetics, 2012-06, Vol.8 (6), p.e1002794

2012

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Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study

PloS one, 2019-10, Vol.14 (10), p.e0223574

2019

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Heritability of Vascular Structure and Function: A Parent–Child Study

Journal of the American Heart Association, 2017-02, Vol.6 (2), p.n/a

2017

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Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls

Frontiers in molecular neuroscience, 2023-02, Vol.16, p.1069375-1069375

2023

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Copy number variation in familial Parkinson disease

PloS one, 2011-08, Vol.6 (8), p.e20988

2011

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Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?

Frontiers in endocrinology (Lausanne), 2020-07, Vol.11, p.433-433

2020

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Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Nature communications, 2022-12, Vol.13 (1), p.7592-18, Article 7592

2022

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Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

Discovering genetic interactions bridging pathways in genome-wide association studies

Genetic and Nongenetic Risk Factors for Childhood Cancer

Evaluation of mitochondrial DNA copy number estimation techniques

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

Copy number variations and cognitive phenotypes in unselected populations

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores

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

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing’s disease

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

Evaluation of the relationship between plasma lipids and abdominal aortic aneurysm: A Mendelian randomization study

Association between MICA polymorphisms, s-MICA levels, and pancreatic cancer risk in a population-based case-control study

Mitochondrial DNA copy number and incident atrial fibrillation

Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number

Exome sequencing findings in children with annular pancreas

Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study

Heritability of Vascular Structure and Function: A Parent–Child Study

Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls

Copy number variation in familial Parkinson disease

Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

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