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Elevated Cardiac Troponin T Levels in Critically Ill Patients with Sepsis

The American journal of medicine, 2013-12, Vol.126 (12), p.1114-1121

2013

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A novel bioinformatics pipeline for identification and characterization of fusion transcripts in breast cancer and normal cell lines

Nucleic acids research, 2011-08, Vol.39 (15), p.e100-e100

2011

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Significance of Elevated Cardiac Troponin T Levels in Critically Ill Patients with Acute Respiratory Disease

The American journal of medicine, 2010-11, Vol.123 (11), p.1049-1058

2010

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Mayo Genome Consortia: A Genotype-Phenotype Resource for Genome-Wide Association Studies With an Application to the Analysis of Circulating Bilirubin Levels

Mayo Clinic proceedings, 2011-07, Vol.86 (7), p.606-614

2011

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GLOSSI: a method to assess the association of genetic loci-sets with complex diseases

BMC bioinformatics, 2009-04, Vol.10 (102), p.102-102, Article 102

2009

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Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases

Scientific data, 2016-10, Vol.3 (1), p.160089-160089, Article 160089

2016

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Genomic Association Analysis Identifies Multiple Loci Influencing Antihypertensive Response to an Angiotensin II Receptor Blocker

Hypertension (Dallas, Tex. 1979), 2012-06, Vol.59 (6), p.1204-1211

2012

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Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes

Diabetes (New York, N.Y.), 2012-05, Vol.61 (5), p.1004-1016

2012

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TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data

Bioinformatics, 2012-01, Vol.28 (2), p.277-278

2012

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Genomic Association Analysis Suggests Chromosome 12 Locus Influencing Antihypertensive Response to Thiazide Diuretic

Hypertension (Dallas, Tex. 1979), 2008-08, Vol.52 (2), p.359-365

2008

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Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy

Circulation. Cardiovascular genetics, 2011-12, Vol.4 (6), p.585-594

2011

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Measures of arterial stiffness and wave reflection are associated with walking distance in patients with peripheral arterial disease

Atherosclerosis, 2007-04, Vol.191 (2), p.384-390

2007

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Long-term prognostic significance of elevated cardiac troponin levels in critically ill patients with acute gastrointestinal bleeding

Critical care medicine, 2009, Vol.37 (1), p.140-147

2009

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An integrated model of the transcriptome of HER2-positive breast cancer

PloS one, 2013-11, Vol.8 (11), p.e79298

2013

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Spatial normalization improves the quality of genotype calling for Affymetrix SNP 6.0 arrays

BMC bioinformatics, 2010-06, Vol.11 (1), p.356-356, Article 356

2010

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Use of log-skew-normal distribution in analysis of continuous data with a discrete component at zero

Statistics in medicine, 2008-08, Vol.27 (18), p.3643-3655

2008

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Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies

American journal of human genetics, 2011-10, Vol.89 (4), p.529-542

2011

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Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitus

Journal of the American Medical Informatics Association : JAMIA, 2012-03, Vol.19 (2), p.219-224

2012

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Batch effect correction for genome-wide methylation data with Illumina Infinium platform

BMC medical genomics, 2011-12, Vol.4 (1), p.84-84, Article 84

2011

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Novel late-onset Alzheimer disease loci variants associate with brain gene expression

Neurology, 2012-07, Vol.79 (3), p.221-228

2012

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Late-onset Alzheimer disease risk variants mark brain regulatory loci

Neurology. Genetics, 2015-08, Vol.1 (2), p.e15-e15

2015

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Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach

BMC genomics, 2010-06, Vol.11 (1), p.357-357, Article 357

2010

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Elevated Cardiac Troponin T Levels in Critically Ill Patients with Sepsis

A novel bioinformatics pipeline for identification and characterization of fusion transcripts in breast cancer and normal cell lines

Significance of Elevated Cardiac Troponin T Levels in Critically Ill Patients with Acute Respiratory Disease

Mayo Genome Consortia: A Genotype-Phenotype Resource for Genome-Wide Association Studies With an Application to the Analysis of Circulating Bilirubin Levels

GLOSSI: a method to assess the association of genetic loci-sets with complex diseases

Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases

Genomic Association Analysis Identifies Multiple Loci Influencing Antihypertensive Response to an Angiotensin II Receptor Blocker

Concordance of Changes in Metabolic Pathways Based on Plasma Metabolomics and Skeletal Muscle Transcriptomics in Type 1 Diabetes

TREAT: a bioinformatics tool for variant annotations and visualizations in targeted and exome sequencing data

Genomic Association Analysis Suggests Chromosome 12 Locus Influencing Antihypertensive Response to Thiazide Diuretic

Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy

Measures of arterial stiffness and wave reflection are associated with walking distance in patients with peripheral arterial disease

Long-term prognostic significance of elevated cardiac troponin levels in critically ill patients with acute gastrointestinal bleeding

An integrated model of the transcriptome of HER2-positive breast cancer

Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with and without Oncogenic KRAS Mutations

Spatial normalization improves the quality of genotype calling for Affymetrix SNP 6.0 arrays

Use of log-skew-normal distribution in analysis of continuous data with a discrete component at zero

Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies

Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitus

Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels

Batch effect correction for genome-wide methylation data with Illumina Infinium platform

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

Late-onset Alzheimer disease risk variants mark brain regulatory loci

Assessing the effect of the brain-derived neurotrophic factor (BDNF) Val66Met polymorphism on mRNA transcript levels, Alzheimer’s disease (AD) risk and cognitive performance (P2.163)

Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach

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