Search Results - "Runz, Heiko"

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Lipids: new biology and therapeutic targets revealed through human genetics.

Authors: Runz, Heiko (AUTHOR) heiko.runz@med.uni–heidelberg.de

Source: Clinical Lipidology. Jun2013, Vol. 8 Issue 3, p295-298. 4p.

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The genome as pharmacopeia: Association of genetic dose with phenotypic response.

Authors: Wadhawan, Samir Runz, Heiko Burchard, Julja

Source: Biochemical Pharmacology. Apr2015, Vol. 94 Issue 4, p229-240. 12p.

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NTHL1 is a recessive cancer susceptibility gene.

Authors: Nurmi, Anna K. Pelttari, Liisa M. Kiiski, Johanna I. et al.

Source: Scientific Reports. 11/30/2023, Vol. 13 Issue 1, p1-14. 14p.

Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials.

Authors: Loomis, Stephanie J. Sadhu, Nilanjana Fisher, Elizabeth et al.

Source: Scientific Reports. 8/31/2023, Vol. 13 Issue 1, p1-12. 12p.

Genetic Loci Associated With Periodontitis: The FinnGen Study Based on National Health Registers.

Authors: Salminen, Aino Hyvärinen, Kati Ritari, Jarmo et al.

Source: Journal of Clinical Periodontology. Sep2025, Vol. 52 Issue 9, p1263-1275. 13p.

A deaf mother and son with diabetes and renal failure.

Authors: Schanz, Jurik Rudofsky, Gottfried Runz, Heiko et al.

Source: Clinical Kidney Journal. Apr2012, Vol. 5 Issue 2, p137-139. 3p. 1 Diagram.

Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes.

Authors: Tamlander, Max Mars, Nina Pirinen, Matti et al.

Source: Communications Biology. 2/23/2022, Vol. 5 Issue 1, p1-13. 13p.

Sequencing of a Patient with Balanced Chromosome Abnormalities and Neurodevelopmental Disease Identifies Disruption of Multiple High Risk Loci by Structural Variation.

Authors: Blake, Jonathon Riddell, Andrew Theiss, Susanne et al.

Source: PLoS ONE. Mar2014, Vol. 9 Issue 3, p1-11. 11p.

Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation.

Authors: Frühmesser, Anne Blake, Jonathon Haberlandt, Edda et al.

Source: European Journal of Human Genetics. Oct2013, Vol. 21 Issue 10, p1177-1180. 4p.

Niemann-Pick disease type C clinical database: cognitive and coordination deficits are early disease indicators.

Authors: Stampfer, Miriam Theiss, Susanne Amraoui, Yasmina et al.

Source: Orphanet Journal of Rare Diseases. 2013, Vol. 8 Issue 1, p1-11. 11p. 2 Charts, 4 Graphs.

A Frequent PNPLA3 Variant Is a Sex Specific Disease Modifier in PSC Patients with Bile Duct Stenosis.

Authors: Friedrich, Kilian Rupp, Christian Hov, Johannes Roksund et al.

Source: PLoS ONE. Mar2013, Vol. 8 Issue 3, p1-7. 7p.

Characterization of drug-induced transcriptional modules: towards drug repositioning and functional understanding.

Authors: Iskar, Murat Zeller, Georg Blattmann, Peter et al.

Source: Molecular Systems Biology. 2013, Vol. 9 Issue 1, p1-13. 13p. 3 Color Photographs, 2 Graphs.

A cross-sectional single-centre study on the spectrum of Pompe disease, German patients: molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations.

Authors: Herzog, Andreas Hartung, Ralf Reuser, Arnold J. J. et al.

Source: Orphanet Journal of Rare Diseases. 2012, Vol. 7 Issue 1, p35-48. 14p. 1 Diagram, 5 Charts, 4 Graphs.