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You searched for: Author/Creator Nöthen, Markus M

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1. A common microdeletion affecting a hippocampus‐ and amygdala‐specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. (23rd April 2014)

2. Cis-epistasis at the LPA locus and risk of cardiovascular diseases. Issue 4 (20th April 2021)

3. Cortical Surfaces Mediate the Relationship Between Polygenic Scores for Intelligence and General Intelligence. (11th December 2019)

4. Detailed stratified GWAS analysis for severe COVID-19 in four European populations. Issue 23 (15th July 2022)

5. Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. (4th October 2019)

6. Effects of DRD2/ANKK1 and COMT Val158Met polymorphisms on stabilization against and adaptation to unexpected events. (2nd March 2022)

7. Elucidation of the genetic causes of bicuspid aortic valve disease. Issue 3 (21st June 2022)

8. Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes. (25th January 2021)

9. First genotype-phenotype study reveals HLA-DQβ1 insertion heterogeneity in high-resolution manometry achalasia subtypes. Issue 1 (February 2019)

10. First genotype‐phenotype study reveals HLA‐DQβ1 insertion heterogeneity in high‐resolution manometry achalasia subtypes. Issue 1 (1st February 2019)