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2,076 results on '"Department of Genomics"'

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

2. Associations of autozygosity with a broad range of human phenotypes

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

4. Associations of the Intellectual Disability Gene MYT1L with Helix–Loop–Helix Gene Expression, Hippocampus Volume and Hippocampus Activation During Memory Retrieval

5. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

6. Novel genetic loci associated with hippocampal volume

7. Novel genetic loci underlying human intracranial volume identified through genome-wide association

8. Common genetic variants influence human subcortical brain structures

9. Multi-PGS enhances polygenic prediction: weighting 937 polygenic scores

10. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

11. Adiposity, hormone replacement therapy use and breast cancer risk by age and hormone receptor status: a large prospective cohort study

12. Gut microbiota steroid sexual dimorphism and its impact on gonadal steroids: influences of obesity and menopausal status

14. Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells

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

16. Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

17. Exploring Cuba’s population structure and demographic history using genome-wide data

18. Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant

19. Quantifying the effects of 16p11.2 copy number variants on brain structure: A multisite genetic-first study

20. Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder

21. Iron affinity gel and gallium immobilized metal affinity chromatographic technique for phosphopeptide enrichment: a comparative study

22. Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach

23. High-quality de novo assembly of the apple genome and methylome dynamics of early fruit development

24. Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis

25. DNA damage and the activation of the p53 pathway mediate alterations in metabolic and secretory functions of adipocytes Running title: DNA damage and p53 in obese adipocytes

26. Genetic variability of the forkhead box O3 and prostate cancer risk in the European Prospective Investigation on Cancer

27. Immunochip analysis identifies association of the RAD50/IL13 region with human longevity

28. The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

29. Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer

30. Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder

31. High-resolution genetic and physical map of the Rvi1 (Vg) apple scab resistance locus

32. Genome-wide association study identifies multiple susceptibility loci for glioma

33. New genetic loci link adipose and insulin biology to body fat distribution

34. Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

35. Two Antarctic penguin genomes reveal insights into their evolutionary history and molecular changes related to the Antarctic environment

36. RFX6 Regulates Insulin Secretion by Modulating Ca2+ Homeostasis in Human β Cells

37. Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability

38. Low copy number of the salivary amylase gene predisposes to obesity

39. Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report

40. Development of the Paris definition of early Crohn's disease for disease-modification trials: results of an international expert opinion process

41. On the Futility of Screening for Genes That Make You Fat

42. Large-scale fine mapping of the HNF1B locus and prostate cancer risk

43. Systems medicine and integrated care to combat chronic noncommunicable diseases

44. Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature

45. Genetic variability of the mTOR pathway and prostate cancer risk in the European Prospective Investigation on Cancer (EPIC)

46. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

47. Hereditary angioedema with normal C1 inhibitor gene in a family with affected women and men is associated with the p.Thr328Lys mutation in the F12 gene

48. A case of hereditary angio-oedema type III presenting with C1-inhibitor cleavage and a missense mutation in the F12 gene

49. The PPARG Pro12Ala polymorphism is associated with a decreased risk of developing hyperglycemia over 6 years and combines with the effect of the APM1 G-11391A single nucleotide polymorphism: the Data From an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) study

50. What Is the Contribution of Two Genetic Variants Regulating VEGF Levels to Type 2 Diabetes Risk and to Microvascular Complications?

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