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50 results on '"Peralta, Juan M"'

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1. Metabolic syndrome traits exhibit genotype-by-environment interaction in relation to socioeconomic status in the Mexican American family heart study

2. Genotype-by-socioeconomic status interaction influences heart disease risk scores and carotid artery thickness in Mexican Americans: the predominant role of education in comparison to household income and socioeconomic index

3. Cocktail-party listening and cognitive abilities show strong pleiotropy

4. Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population

5. Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

6. The Genetic contribution to solving the cocktail-party problem

7. Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

8. Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

9. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

10. The G505A Nonsynonymous Single-Nucleotide Polymorphism (SNP) in TAFI, the Gene Encoding Thrombin-Activatable Fibrinolysis Inhibitor (TAFI) Is Pleiotropically Associated with TAFI Antigen Levels and Coronary Heart Disease (CHD) in Mexican Americans of South Texas

11. The Factor II (FII) Expression Quantitative Trait Locus (eQTL) Prothrombin G20210A Is Pleiotropically Associated with Plasma Fibrinogen Levels and Has a Profound Effect on Obesity in Mexican Americans of South Texas

12. Genetic Overlap Profiles of Cognitive Ability in Psychotic and Affective Illnesses: A Multisite Study of Multiplex Pedigrees

13. Identifying the Lipidomic Effects of a Rare Loss-of-Function Deletion in ANGPTL3

14. Transcriptomic Profiling of Fibropapillomatosis in Green Sea Turtles (Chelonia mydas) From South Texas

15. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

16. Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

17. N-Linked Glycans on Therapeutic Factor VIII (FVIII) Proteins Attenuate Immunogenicity Potential: Evidence from Independent HLA-Class-II/FVIII (HLAcII/FVIII) Peptidomes

18. Specific Correction of the Intron-22 Inverted Factor VIII Gene in Autologous Blood Outgrowth Endothelial Cells from Patients with Severe Hemophilia A

19. Disentangling the Effects of HLA DRB1*15:01 and DQB1*06:02 to Establish the True HLA Risk Allele for Inhibitor Development in the Treatment of Hemophilia A

20. Transcriptomic profiling of fibropapillomatosis in green sea turtles (Chelonia mydas) from South Texas

21. Genotype phasing in pedigrees using whole-genome sequence data

22. Quantitative HLA‐class‐II/factor VIII (FVIII) peptidomic variation in dendritic cells correlates with the immunogenic potential of therapeutic FVIII proteins in hemophilia A

23. Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

24. Rare DEGS1 variant significantly alters de novo ceramide synthesis pathway

25. Evidence for genetic correlation between human cerebral white matter microstructure and inflammation

26. Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes

27. Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

32. Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

34. Independent test assessment using the extreme value distribution theory

37. Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure

41. Genetic Effects on DNA Methylation and Its Potential Relevance for Obesity in Mexican Americans

43. Systems genetics of the nuclear factor-κB signal transduction network. I. Detection of several quantitative trait loci potentially relevant to aging

50. A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels

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