48 results on '"Ashley-Koch, A"'
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2. An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels
3. Transcriptome analysis of adult and fetal trabecular meshwork, cornea, and ciliary body tissues by RNA sequencing
4. Epigenome‐wide association of PTSD from heterogeneous cohorts with a common multi‐site analysis pipeline
5. Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample
6. Single nucleotide polymorphisms in the oxytocin receptor and GRK6 are associated with oxytocin dosing requirements and labor outcomes: 27
7. Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus
8. Evidence for fumonisin inhibition of ceramide synthase in humans consuming maize-based foods and living in high exposure communities in Guatemala
9. Pregnancy continuation and organizational religious activity following prenatal diagnosis of a lethal fetal defect are associated with improved psychological outcome†
10. A common variant near TGFBR3 is associated with primary open angle glaucoma
11. Alloimmunization in sickle cell disease: changing antibody specificities and association with chronic pain and decreased survival
12. EFFECT OF THE APOE ε4 ALLELE AND COMBAT EXPOSURE ON PTSD AMONG IRAQ/AFGHANISTAN-ERA VETERANS
13. Angiogenic, neurotrophic, and inflammatory system SNPs moderate the association between birth weight and ADHD symptom severity
14. No association between RORA polymorphisms and PTSD in two independent samples
15. Urinary fumonisin B1 and estimated fumonisin intake in women from high- and low-exposure communities in Guatemala
16. Hepatic Gene Expression Profiles Differentiate Presymptomatic Patients With Mild Versus Severe Nonalcoholic Fatty Liver Disease
17. Genetic Evaluation and Application of Posterior Cranial Fossa Traits as Endophenotypes for Chiari Type I Malformation
18. Fiber tract-specific white matter lesion severity Findings in late-life depression and by AGTR1 A1166C genotype
19. The kinetics of urinary fumonisin B1 excretion in humans consuming maize-based diets
20. Design, methodological issues and participation in a multiple sclerosis case–control study
21. Impact of BDNF Val66Met and 5-HTTLPR polymorphism variants on neural substrates related to sadness and executive function
22. A Preliminary Analysis of Interactions Between Genotype, Retrospective ADHD Symptoms, and Initial Reactions to Smoking in a Sample of Young Adults
23. MYH9 and APOL1 are both associated with sickle cell disease nephropathy
24. Maternal vitamin D receptor genetic variation contributes to infant birthweight among black mothers
25. BDNF Val66Met genotype and 6-month remission rates in late-life depression
26. The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects
27. Angiotensin receptor gene polymorphisms and 2-year change in hyperintense lesion volume in men
28. Epidemiologic and Genetic Aspects of Spina Bifida and Other Neural Tube Defects
29. Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study
30. Influence of the MTHFR C677T Polymorphism on Magnetic Resonance Imaging Hyperintensity Volume and Cognition in Geriatric Depression
31. Interactions Between Genotype and Depressive Symptoms on Obesity
32. Duffy (Fy), DARC, and neutropenia among women from the United States, Europe and the Caribbean
33. Multiple rare SAPAP3 missense variants in trichotillomania and OCD
34. 5–HTTLPR and Gender Moderate Changes in Negative Affect Responses to Tryptophan Infusion
35. Lack of Duffy antigen expression is associated with organ damage in patients with sickle cell disease
36. β2-Adrenergic receptor and adenylate cyclase gene polymorphisms affect sickle red cell adhesion
37. Pulmonary hypertension associated with sickle cell disease: Clinical and laboratory endpoints and disease outcomes
38. Effects of Environmental Stress and Gender on Associations among Symptoms of Depression and the Serotonin Transporter Gene Linked Polymorphic Region (5-HTTLPR)
39. Linkage to a Known Gene But No Mutation Identified: Comprehensive Reanalysis of SPG4 HSP Pedigrees Reveals Large Deletions as the Sole Cause
40. HLA-DR15 Haplotype and Multiple Sclerosis: A HuGE Review
41. Genetic polymorphisms associated with priapism in sickle cell disease
42. SLITRK1 mutations in Trichotillomania
43. SLITRK1 mutations in trichotillomania
44. Lack of Association Between Autism and SLC25A12
45. An Analysis Paradigm for Investigating Multi-locus Effects in Complex Disease: Examination of Three GABAA Receptor Subunit Genes on 15q11-q13 as Risk Factors for Autistic Disorder.
46. Analysis of the RELN gene as a genetic risk factor for autism
47. Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class
48. Sickle Hemoglobin (Hb S) Allele and Sickle Cell Disease: A HuGE Review
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