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1. Use of the linear regression method to evaluate population accuracy of predictions from non-linear models.

2. Orthogonal Decomposition of the Genetic Variance for Epistatic Traits Under Linkage Disequilibrium—Applications to the Analysis of Bateson-Dobzhansky-Müller Incompatibilities and Sign Epistasis.

3. Genotype-phenotype pattern analysis of pathogenic PAX9 variants in Chinese Han families with non-syndromic oligodontia.

4. Genetics of Inherited Retinal Diseases in Understudied Ethnic Groups in Italian Hospitals.

5. A Comparison of Methods for Gene-Based Testing That Account for Linkage Disequilibrium.

6. Identification of a Rare Case With Nagashima-Type Palmoplantar Keratoderma and 18q Deletion Syndrome via Exome Sequencing and Low-Coverage Whole-Genome Sequencing.

7. Comparative Analyses of Gene Co-expression Networks: Implementations and Applications in the Study of Evolution.

8. Comparing Statistical Tests for Differential Network Analysis of Gene Modules.

9. An Effective Method to Measure Disease Similarity Using Gene and Phenotype Associations.

10. Social parasitism and the molecular basis of phenotypic evolution.

11. Bivariate Causal Discovery and Its Applications to Gene Expression and Imaging Data Analysis.

12. AsmMix: an efficient haplotype-resolved hybrid de novo genome assembling pipeline.

13. Deciphering complexity: TULP1 variants linked to an atypical retinal dystrophy phenotype.

14. Review of the phenotypes and genotypes of Bardet-Biedl syndrome from China.

15. Uniparental disomy: expanding the clinical and molecular phenotypes of whole chromosomes.

16. Gamma irradiation-induced genetic variability and its effects on the phenotypic and agronomic traits of groundnut (Arachis hypogaeaL.).

17. Gamma irradiation-induced genetic variability and its effects on the phenotypic and agronomic traits of groundnut (Arachis hypogaeaL.).

18. Novel variants and phenotypic heterogeneity in a cohort of 11 Chinese children with Wiedemann-Steiner syndrome.

19. Editorial: Gene Regulation as a Driver of Adaptation and Speciation.

20. Phenotypic and genetic parameters of circadian rhythms from core body temperature profiles and their relationships with beef steers' production efficiency profiles during successive winter feeding periods.

21. Phenotypic and genetic characteristics of 130 patients with mucopolysaccharidosis type II: A single-center retrospective study in China.

22. Kalpra: A kernel approach for longitudinal pathway regression analysis integrating network information with an application to the longitudinal PsyCourse Study.

23. Evaluation of GENESIS, SAIGE, REGENIE and fastGWA-GLMM for genome-wide association studies of binary traits in correlated data.

24. Genotype-phenotype correlations of marfan syndrome and related fibrillinopathies: Phenomenon and molecular relevance.

25. Prenatal phenotype analysis and mutation identification of a fetus with meckel gruber syndrome.

26. New observations in the fragile X-associated tremor/ataxia syndrome (FXTAS) phenotype.

27. Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy.

28. Case Report: Identification of a Novel Heterozygous Missense Mutation in COL4A3 Gene Causing Variable Phenotypes in an Autosomal-Dominant Alport Syndrome Family.

29. Improving the Accuracy of Multi-Breed Prediction in Admixed Populations by Accounting for the Breed Origin of Haplotype Segments.

30. Extracellular Vesicle-Derived miR-105-5p Promotes Malignant Phenotypes of Esophageal Squamous Cell Carcinoma by Targeting SPARCL1 via FAK/AKT Signaling Pathway.

31. A Systematic Evaluation of Supervised Machine Learning Algorithms for Cell Phenotype Classification Using Single-Cell RNA Sequencing Data.

32. Skeletal Muscle Expression of Actinin-3 (ACTN3) in Relation to Feed Efficiency Phenotype of F2 Bos indicus - Bos taurus Steers.

33. Identification of Heterotic Groups and Patterns Based on Genotypic and Phenotypic Characteristics Among Rice Accessions of Diverse Origins.

34. Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees.

35. Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype.

36. Genetic Variation and the Distribution of Variant Types in the Horse.

37. RAD52: Paradigm of Synthetic Lethality and New Developments.

38. A Novel Loss-of-Function Mutation in the NPRL3 Gene Identified in Chinese Familial Focal Epilepsy with Variable Foci.

39. Improving the Classification of Alzheimer's Disease Using Hybrid Gene Selection Pipeline and Deep Learning.

40. Accuracy of Genomic Prediction for Milk Production Traits in Philippine Dairy Buffaloes.

41. Apolipoprotein E Genetic Variation and Its Association With Cognitive Function in Rural-Dwelling Older South Africans.

42. Using Summary Statistics to Model Multiplicative Combinations of Initially Analyzed Phenotypes With a Flexible Choice of Covariates.

43. hGATA1 Under the Control of a μLCR/β-Globin Promoter Rescues the Erythroid but Not the Megakaryocytic Phenotype Induced by the Gata1 low Mutation in Mice.

44. Targeted Sequencing of 242 Clinically Important Genes in the Russian Population From the Ivanovo Region.

45. Newborn Screening for G6PD Deficiency in Xiamen, China: Prevalence, Variant Spectrum, and Genotype-Phenotype Correlations.

46. Cis -Regulatory Logic Produces Gene-Expression Noise Describing Phenotypic Heterogeneity in Bacteria.

47. High Genetic Diversity but Absence of Population Structure in Local Chickens of Sri Lanka Inferred by Microsatellite Markers.

48. Dystrophic Epidermolysis Bullosa: Secondary Disease Mechanisms and Disease Modifiers.

49. Species and Phenotypic Distribution Models Reveal Population Differentiation in Ethiopian Indigenous Chickens.

50. Case Report: Two New Cases of Chromosome 12q14 Deletions and Review of the Literature.