Search

Your search keyword '"Tsetsos F"' showing total 27 results

Search Constraints

Start Over You searched for: Author "Tsetsos F" Remove constraint Author: "Tsetsos F"
27 results on '"Tsetsos F"'

Search Results

1. Analysis of shared heritability in common disorders of the brain

2. Analysis of shared heritability in common disorders of the brain

4. Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree

5. Analysis of shared heritability in common disorders of the brain

6. Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome.

7. Assembly of 43 human Y chromosomes reveals extensive complexity and variation.

8. Myasthenia gravis genome-wide association study implicates AGRN as a risk locus.

9. Variants in clock genes could be associated with lower risk of type 2 diabetes in an elderly Greek population.

10. Oxidative Stress Genes in Diabetes Mellitus Type 2: Association with Diabetic Kidney Disease.

11. Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum.

12. Association of rs11780592 Polymorphism in the Human Soluble Epoxide Hydrolase Gene (EPHX2) with Oxidized LDL and Mortality in Patients with Diabetic Chronic Kidney Disease.

13. Synaptic processes and immune-related pathways implicated in Tourette syndrome.

14. Genetic variation in CARD8 , a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 diabetes mellitus.

15. Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population.

16. Genetic history of the population of Crete.

17. Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.

18. Analysis of shared heritability in common disorders of the brain.

19. Association of ALOX12 gene polymorphism with all-cause and cardiovascular mortality in diabetic nephropathy.

20. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.

21. Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean Greeks.

22. Rapporteur summaries of plenary, symposia, and oral sessions from the XXIIIrd World Congress of Psychiatric Genetics Meeting in Toronto, Canada, 16-20 October 2015.

23. Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort.

24. Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.

25. Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis.

26. Genetic association signal near NTN4 in Tourette syndrome.

27. Maritime route of colonization of Europe.

Catalog

Books, media, physical & digital resources