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1. Author Correction: Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

2. Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes

5. Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome

6. Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

12. Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

13. Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

14. A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.

15. Genome-wide associations for birth weight and correlations with adult disease

16. Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network

17. Facilitating phenotype transfer using a common data model

19. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

22. AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate

23. GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network

25. Rare variants at 16p11.2 are associated with common variable immunodeficiency

26. Multiancestral polygenic risk score for pediatric asthma

27. Probing the Virtual Proteome to Identify Novel Disease Biomarkers

31. Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis

33. Additional file 1 of An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities

34. Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

35. The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth

37. Desiderata for computable representations of electronic health records-driven phenotype algorithms

38. Directional dominance on stature and cognition in diverse human populations

39. A novel common variant in DCST2 is associated with length in early life and height in adulthood

40. Erratum to: AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate

42. A genome-wide study reveals copy number variants exclusive to childhood obesity cases

43. Neuroimaging of the Philadelphia Neurodevelopmental Cohort

47. Integrative Genetics Analysis of Juvenile Idiopathic Arthritis Identifies Novel Loci

48. The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

49. Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (Scientific Reports (2017) 7 (3847) DOI: 10.1038/s41598-017-01674-8)

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