162 results on '"Bailey-Wilson, J."'
Search Results
2. A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
3. Recruitment strategies and comparison of prostate cancer-specific clinical data on African-American and Caucasian males with and without family history
4. Clinical characteristics of African-American men with hereditary prostate cancer: the AAHPC study
5. Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate
6. A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD
7. Population Isolates in South Tyrol and Their Value for Genetic Dissection of Complex Diseases
8. A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history
9. A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability
10. Evaluation of widely used models for predicting BRCA1 and BRCA 2 mutations
11. ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies
12. Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
13. Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies
14. Attention-Deficit/Hyperactivity Disorder (ADHD): Power simulations to detect linkage in extended pedigrees in the Paisa community of Colombia
15. Linkage simulation enhances decision making strategies for study of lung cancer (LC) pedigrees
16. Genome-wide scanning for linkage in Finnish breast cancer families
17. Toward a gene at Xq27.3 responsible for hereditary prostate cancer (HPC-X)
18. International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16
19. NIA Aging and Genetic Epidemiology Working Group:Genetic Epidemiologic Studies on Age-Specified Traits
20. A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD
21. Identification of BRCA1 and BRCA2 genetic modifiers.
22. Familial aggregation of myopia in the Tehran eye study: estimation of the sibling and parent offspring recurrence risk ratios
23. Combined Genome-Wide Scan for Prostate Cancer Susceptibility Genes
24. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome
25. Germline mutations in the ribonuclease L gene in families showing linkage with HPC1
26. DETERMINATION OF GENETIC SUSCEPTIBILITY TO LUNG CANCER IN FAMILIES FROM SOUTHERN LOUISIANA, AN UPDATE
27. Evidence for a Prostate Cancer Susceptibility Locus on the X Chromosome
28. Segregation analysis of autosomal dominant polycystic kidney disease
29. Response
30. A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.
31. Evidence for Mendelian Inheritance in the Pathogenesis of Lung Cancer
32. Stepwise oligogenic segregation and linkage analysis illustrated with dopamine‐β‐hydroxylase activity
33. Evaluation of widely used models for predicting BRCA1 and BRCA2 mutations.
34. A more powerful robust sib-pair test of linkage for quantitative traits.
35. Autosomal dominant inheritance of prostate cancer: a confirmatory study
36. Increased familial risk for non-lung cancer among relatives of lung cancer patients.
37. Lung cancer detection and prevention: Evidence for an interaction between smoking and genetic predisposition
38. Regional replication of association with refractive error on 15q14 and 15q25 in the age-related eye disease study cohort
39. Myopia in chinese families shows linkage to 10q26.13
40. Replication of linkage results using MALDI-TOF detection of single nucleotide polymorphisms (SNPS)
41. The Value of Molecular Haplotypes in a Family-Based Linkage Study.
42. Rare deleterious germline variants and risk of lung cancer.
43. Rare Variants in Known Susceptibility Loci and Their Contribution to Risk of Lung Cancer.
44. Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge.
45. Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.
46. Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer.
47. Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease.
48. Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22.
49. Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics.
50. A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics.
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