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Genome Sequencing Reveals Loci under Artificial Selection that Underlie Disease Phenotypes in the Laboratory Rat

Cell, 2013-08, Vol.154 (3), p.691-703

2013

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Identification of somatic mutations in non-small cell lung carcinomas using whole-exome sequencing

Carcinogenesis (New York), 2012-07, Vol.33 (7), p.1270-1276

2012

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Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

Genetics in medicine, 2011-03, Vol.13 (3), p.255-262

2011

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De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1

European journal of human genetics : EJHG, 2018-11, Vol.26 (11), p.1635-1647

2018

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Plasma exosomal miRNAs-based prognosis in metastatic kidney cancer

Oncotarget, 2017-09, Vol.8 (38), p.63703-63714

2017

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Genomics in clinical practice: lessons from the front lines

Science translational medicine, 2013-07, Vol.5 (194), p.194cm5

2013

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Plasma genetic and genomic abnormalities predict treatment response and clinical outcome in advanced prostate cancer

Oncotarget, 2015-06, Vol.6 (18), p.16411-16421

2015

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Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant

American journal of medical genetics. Part A, 2018-03, Vol.176 (3), p.692-698

2018

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Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays

BMC genomics, 2004-02, Vol.5 (1), p.12-12, Article 12

2004

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Mapping the Genetic Determinants of Hypertension, Metabolic Diseases, and Related Phenotypes in the Lyon Hypertensive Rat

Hypertension (Dallas, Tex. 1979), 2004-11, Vol.44 (5), p.695-701

2004

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Genetically hypertensive Brown Norway congenic rat strains suggest intermediate traits underlying genetic hypertension

Croatian medical journal, 2008-10, Vol.49 (5), p.586-599

2008

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Genetically Hypertensive Brown Norway Congenic Rat Strains Suggest Intermediate Traits Underlying Genetic Hypertension

Croatian medical journal, 2008-10, Vol.49 (5), p.586

2008

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Effect of permanent right internal mammary artery occlusion on right coronary artery supply: A randomized placebo-controlled clinical trial

The American heart journal, 2020-12, Vol.230, p.1-12

2020

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Genetic Fine‐Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats

Obesity (Silver Spring, Md.), 2018-01, Vol.26 (1), p.213-222

2018

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Genetic Mapping of Multiple Traits Identifies Novel Genes for Adiposity, Lipids, and Insulin Secretory Capacity in Outbred Rats

Diabetes (New York, N.Y.), 2023-01, Vol.72 (1), p.135-148

2023

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Mild riboflavin deficiency is highly prevalent in school-age children but does not increase risk for anaemia in Côte d'Ivoire

British journal of nutrition, 2007-05, Vol.97 (5), p.970-976

2007

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Differential gene expression and genomic patient stratification following left ventricular assist device support. Commentary

Journal of the American College of Cardiology, 2003, Vol.41 (7), p.1096-1108

2003

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Bridging or buffering?

Journal of educational administration, 2005-02, Vol.43 (1), p.60-71

2005

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Genome Sequencing Reveals Loci under Artificial Selection that Underlie Disease Phenotypes in the Laboratory Rat

Identification of somatic mutations in non-small cell lung carcinomas using whole-exome sequencing

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1

Plasma exosomal miRNAs-based prognosis in metastatic kidney cancer

Genomics in clinical practice: lessons from the front lines

Plasma genetic and genomic abnormalities predict treatment response and clinical outcome in advanced prostate cancer

Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant

Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays

Mapping the Genetic Determinants of Hypertension, Metabolic Diseases, and Related Phenotypes in the Lyon Hypertensive Rat

Genetically hypertensive Brown Norway congenic rat strains suggest intermediate traits underlying genetic hypertension

Genetically Hypertensive Brown Norway Congenic Rat Strains Suggest Intermediate Traits Underlying Genetic Hypertension

Effect of permanent right internal mammary artery occlusion on right coronary artery supply: A randomized placebo-controlled clinical trial

Genetic Fine‐Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats

Genetic Mapping of Multiple Traits Identifies Novel Genes for Adiposity, Lipids, and Insulin Secretory Capacity in Outbred Rats

Mild riboflavin deficiency is highly prevalent in school-age children but does not increase risk for anaemia in Côte d'Ivoire

Differential gene expression and genomic patient stratification following left ventricular assist device support. Commentary

Bridging or buffering?

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