32 results on '"Fallin, M Daniele"'
Search Results
2. Multicohort Epigenome-Wide Association Study of All-Cause Cardiovascular Disease and Cancer Incidence: A Cardio-Oncology Approach
3. Smoking, blood DNA methylation sites and lung cancer risk
4. Examining Prenatal Dietary Factors in Association with Child Autism-Related Traits Using a Bayesian Mixture Approach: Results from 2 United States Cohorts
5. Associations of prenatal exposure to a mixture of persistent organic pollutants with social traits and cognitive and adaptive function in early childhood: Findings from the EARLI study
6. Tooth biomarkers to characterize the temporal dynamics of the fetal and early-life exposome
7. Maternal Psychiatric Conditions, Treatment With Selective Serotonin Reuptake Inhibitors, and Neurodevelopmental Disorders
8. The association between maternal lipid profile after birth and offspring risk of autism spectrum disorder
9. Associations Between Media Exposure and Mental Distress Among U.S. Adults at the Beginning of the COVID-19 Pandemic
10. A prospective birth cohort study on cord blood folate subtypes and risk of autism spectrum disorder
11. Mental distress during the COVID-19 pandemic among US adults without a pre-existing mental health condition: Findings from American trend panel survey
12. Epigenetic marks of prenatal air pollution exposure found in multiple tissues relevant for child health
13. Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans
14. DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis
15. Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk
16. New insights and updated guidelines for epigenome-wide association studies
17. Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans
18. GeMes, Clusters of DNA Methylation under Genetic Control, Can Inform Genetic and Epigenetic Analysis of Disease
19. Methods: Genetic Epidemiology
20. Methods: Genetic Epidemiology
21. Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia
22. Stage II follow-up on a linkage scan for bipolar disorder in the Ashkenazim provides suggestive evidence for chromosome 12p and the GRIN2B gene
23. Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations
24. Relative Contribution of Genetic and Nongenetic Modifiers to Intestinal Obstruction in Cystic Fibrosis
25. Phenotypic and genetic characterization of patients with features of “nonclassic” forms of cystic fibrosis
26. Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios
27. Genomewide Linkage Scan for Bipolar-Disorder Susceptibility Loci among Ashkenazi Jewish Families
28. Genomewide Linkage Scan for Schizophrenia Susceptibility Loci among Ashkenazi Jewish Families Shows Evidence of Linkage on Chromosome 10q22
29. TARGETED SEQUENCING OF AFRICAN AMERICAN ALZHEIMER’S DISEASE RISK GENES IMPLICATES SEVERAL POTENTIAL AD RISK VARIANTS
30. TAU PHOSPHORYLATION IS IMPACTED BY RARE AD-ASSOCIATED AKAP9 MUTATIONS SPECIFIC TO AFRICAN AMERICANS
31. Genetic dissection methods: designs used for tests of gene–environment interaction
32. Variation in a Repeat Sequence Determines Whether a Common Variant of the Cystic Fibrosis Transmembrane Conductance Regulator Gene Is Pathogenic or Benign
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