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210 results on '"Kirk C. Wilhelmsen"'

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1. Metabolism as a biomarker for treatment success in anti-amyloid therapy: A case report

2. A greedy regression algorithm with coarse weights offers novel advantages

3. Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing

4. Blood‐based protein predictors of dementia severity as measured by δ: Replication across biofluids and cohorts

5. Genetic loci associated with heart rate variability and their effects on cardiac disease risk

6. Serum Granulocyte Colony-Stimulating Factor and Alzheimer’s Disease

7. Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk

8. Focused ultrasound–mediated blood-brain barrier opening in Alzheimer’s disease: long-term safety, imaging, and cognitive outcomes

9. New insights into the genetic etiology of Alzheimer's disease and related dementias

10. Association of Predicted Expression and Multimodel Association Analysis of Substance Abuse Traits

12. Pleiotropic Loci for Cannabis Use Disorder Severity in Multi-Ancestry High-Risk Populations

13. Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction

14. scRNA-seq in medulloblastoma shows cellular heterogeneity and lineage expansion support resistance to SHH inhibitor therapy

15. Effects of genetic risk for alcohol dependence and onset of regular drinking on the progression to alcohol dependence: A polygenic risk score approach

16. Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing

17. Effects of Common and Rare Chromosome 4 GABAergic Gene Variation on Alcohol Use and Antisocial Behavior

18. Cryptic developmental events determine medulloblastoma radiosensitivity and cellular heterogeneity without altering transcriptomic profile

19. TWO-SIGMA-G: A New Competitive Gene Set Testing Framework for scRNA-seq Data Accounting for Inter-Gene and Cell-Cell Correlation

20. Noninvasive prenatal exome sequencing inefficient for detecting single-gene disorders – problems and possible solutions

21. Frisky CALF sometimes outruns LASSO

22. Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations

23. SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection

24. An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

25. Blood-based protein predictors of dementia severity as measured by δ: Replication across biofluids and cohorts

26. Projected t-SNE for batch correction

27. Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy

28. Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology

29. Genetic Influences on Evening Preference Overlap with Those for Bipolar Disorder in a Sample of Mexican Americans and American Indians

31. Associations Between Genomic Variants in Alcohol Dehydrogenase Genes and Alcohol Symptomatology in American Indians and European Americans: Distinctions and Convergence

32. Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations

33. Whole genome sequence study of cannabis dependence in two independent cohorts

34. Genetic loci for alcohol-related life events and substance-induced affective symptoms: indexing the 'dark side' of addiction

35. Germline Analysis from Tumor–Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings

36. Single nucleotide polymorphisms in theREG-CTNNA2region of chromosome 2 andNEIL3associated with impulsivity in a Native American sample

37. A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

38. Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

40. Indexing the 'dark side of addiction': Substance-induced affective symptoms and alcohol use disorders

41. Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group

42. MaPSeq, A Service-Oriented Architecture for Genomics Research within an Academic Biomedical Research Institution

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

44. Erratum

45. Erratum: 'Genome-wide Association Study of Susceptibility to Particulate Matter-Associated QT Prolongation'

46. Genetic loci associated with heart rate variability and their effects on cardiac disease risk

47. Odorant Item Specific Olfactory Identification Deficit May Differentiate Alzheimer Disease From Aging

48. Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease

49. A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium

50. Genetic variation in the exome: Associations with alcohol and tobacco co-use

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