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Your search keyword '"Mannik K"' showing total 24 results

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1. The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals

2. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

3. Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches

4. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

5. Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease

6. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

7. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

8. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

9. Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa

10. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

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

12. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

13. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

14. Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

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

16. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

17. Genetic modifiers and ascertainment drive variable expressivity of complex disorders.

19. Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.

20. Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.

21. Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.

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

23. Monozygotic twins with 17q21.31 microdeletion syndrome.

24. A patient with de novo 0.45 Mb deletion of 2p16.1: the role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome.

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