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Your search keyword '"Pankratz N"' showing total 247 results

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1. Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

2. Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations.

3. Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores

4. Cross-ancestry investigation of venousc genomic predictors

5. Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus (vol 13, 1222, 2022)

6. Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

7. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts

8. Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

9. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

10. A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology

13. Evaluation of mitochondrial DNA copy number estimation techniques

16. A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

17. Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18))

18. Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

19. Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

21. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

22. Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals

23. Erratum: Meta-analysis of dense genecentric association studies reveals common and uncommon variants associated with height ((The American Journal of Human Genetics (2010) 88 (6-18))

24. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

25. A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

30. Variation in GIGYF2 is not associated with Parkinson disease

32. LRRK2 MUTATION ANALYSIS IN PARKINSON DISEASE FAMILIES WITH EVIDENCE OF LINKAGE TO PARK8

34. A mutation in myotilin causes spheroid body myopathy

38. Parkindosage mutations have greater pathogenicity in familial PD than simple sequence mutations

39. Variation in GIGYF2is not associated with Parkinson diseaseSYMBOL

40. Mutations in GBAare associated with familial Parkinson disease susceptibility and age at onsetSYMBOL

41. LRRK2mutation analysis in Parkinson disease families with evidence of linkage to PARK8

42. Heterozygosity for a mutation in the parkingene leads to later onset Parkinson disease

43. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.

44. Linkage stratification and mutation analysis at the parkin locus identifies mutation positive Parkinson's disease families [1]

45. Les mutations germinales du gène CDKN1Bsont une cause de maladie de Cushing chez l’enfant

46. Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

47. Genomewide association study for onset age in Parkinson disease

48. The Familial Intracranial Aneurysm (FIA) study protocol

49. Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment

50. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

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