133 results on '"Wilhelmsen Kirk C"'
Search Results
2. More Similar than Different: Memory, Executive Functions, Cortical Thickness, and Glucose Metabolism in Biomarker-Positive Alzheimer’s Disease and Behavioral Variant Frontotemporal Dementia
3. LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry
4. Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifiesLRRC4C, LHX5-AS1and nominates ancestry-specific lociPTPRK,GRB14, andKIAA0825as novel risk loci for Alzheimer’s disease: the Alzheimer’s Disease Genetics Consortium
5. Pleiotropic loci for cannabis use disorder severity in multi-ancestry high-risk populations
6. Pleiotropic Loci for Cannabis Use Disorder Severity in Multi-Ancestry High-Risk Populations
7. Focused ultrasound–mediated blood-brain barrier opening in Alzheimer’s disease: long-term safety, imaging, and cognitive outcomes
8. A greedy regression algorithm with coarse weights offers novel advantages
9. Association of Predicted Expression and Multimodel Association Analysis of Substance Abuse Traits
10. Effects of genetic risk for alcohol dependence and onset of regular drinking on the progression to alcohol dependence: A polygenic risk score approach
11. Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction
12. Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing
13. Noninvasive prenatal exome sequencing inefficient for detecting single-gene disorders – problems and possible solutions
14. SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection
15. Frisky CALF sometimes outruns LASSO
16. Projected t-SNE for batch correction
17. Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations
18. 784: Novel sequencing-based framework for non-invasive fetal genotyping
19. Effects of Common and Rare Chromosome 4 GABAergic Gene Variation on Alcohol Use and Antisocial Behavior
20. SMNN: Batch Effect Correction for Single-cell RNA-seq data via Supervised Mutual Nearest Neighbor Detection
21. Genetic loci for alcohol-related life events and substance-induced affective symptoms: indexing the “dark side” of addiction
22. Increasing the diagnostic yield of exome sequencing by copy number variant analysis
23. Indexing the ‘dark side of addiction’: substance-induced affective symptoms and alcohol use disorders
24. Odorant Item Specific Olfactory Identification Deficit May Differentiate Alzheimer Disease From Aging
25. Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy
26. Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders
27. Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly
28. Genetic Influences on Evening Preference Overlap with Those for Bipolar Disorder in a Sample of Mexican Americans and American Indians
29. Identification of Alcoholism Susceptibility Genes
30. Identification of Alcoholism Susceptibility Genes
31. Associations Between Genomic Variants in Alcohol Dehydrogenase Genes and Alcohol Symptomatology in American Indians and European Americans: Distinctions and Convergence
32. Erratum: “Genome-wide Association Study of Susceptibility to Particulate Matter-Associated QT Prolongation”
33. Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk
34. Fifteen Genetic Loci Associated With the Electrocardiographic P Wave
35. Genome-wide Association Study of Susceptibility to Particulate Matter–Associated QT Prolongation
36. Genetic loci associated with heart rate variability and their effects on cardiac disease risk
37. Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease
38. Genetic variation in the exome: Associations with alcohol and tobacco co-use.
39. Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence
40. Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population
41. Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations
42. Whole genome sequence study of cannabis dependence in two independent cohorts
43. Integration of expression quantitative trait loci and pleiotropy identifies a novel psoriasis susceptibility gene,PTPN1
44. 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
45. Common susceptibility variants are shared between schizophrenia and psoriasis in the Han Chinese population
46. Polygenic risk scores for cigarettes smoked per day do not generalize to a Native American population
47. A Novel Tobacco Use Phenotype Suggests the 15q25 and 19q13 Loci May be Differentially Associated With Cigarettes per Day and Tobacco-Related Problems
48. Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans
49. Germline Analysis from Tumor–Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings
50. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine
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