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181 results on '"Ehm, Margaret G"'

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1. Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

2. High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases

3. FinnGen provides genetic insights from a well-phenotyped isolated population

4. The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

5. Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

6. Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations.

7. Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women

8. Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population

9. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.

10. Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank

11. The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

13. FinnGen provides genetic insights from a well-phenotyped isolated population

15. An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People

19. FinnGen: Unique genetic insights from combining isolated population and national health register data

22. The Population Reference Sample, POPRES: A Resource for Population, Disease, and Pharmacological Genetics Research

23. Contrasting linkage-disequilibrium patterns between cases and controls as a novel association-mapping method

24. Effect of two- and three-locus linkage disequilibrium on the power to detect marker/phenotype associations

26. Deep Sequencing of The LRRK2 Gene in 14,002 Individuals Reveals Evidence of Purifying Selection and Independent Origin of the p.Arg1628pro Mutation in Europe

27. Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation

28. Meta-Analysis of 26 638 Individuals Identifies Two Genetic Loci Associated With Left Ventricular Ejection Fraction

29. Candidate Single-Nucleotide Polymorphisms From a Genomewide Association Study of Alzheimer Disease

31. An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

33. Integration of Real‐World Data and Genetics to Support Target Identification and Validation.

35. Genome-Wide Scan of Obesity in the Old Order Amish*

38. Assessment of rosacea symptom severity by genome-wide association study and expression analysis highlights immuno-inflammatory and skin pigmentation genes

39. High-Resolution Genotyping of Formalin-Fixed Tissue Accurately Estimates Polygenic Risk Scores in Human Diseases

40. Phenome-wide association study using research participants’ self-reported data provides insight into the Th17 and IL-17 pathway

41. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

42. A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

43. A Genome-Wide Scan for Susceptibility Loci to Insulin Levels in the Old Order Amish

44. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

45. A Genome-Wide Scan for Susceptibility Loci to Obesity in the Old Order Amish

46. Genome-Wide Search for Type 2 Diabetes Susceptibility Genes in Caucasians, Mexican Americans, African Americans, and Japanese Americans

47. Type 2 Diabetes Loci in the Old Order Amish

49. A Low‐Frequency Variant in MAPK14 Provides Mechanistic Evidence of a Link With Myeloperoxidase: A Prognostic Cardiovascular Risk Marker

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