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2. CDH1 mutation distribution and type suggests genetic differences between the etiology of orofacial clefting and gastric cancer

4. Risk of pre‐eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case–control study

5. Pairwise linkage analysis of 11 loci on human chromosome 4.

6. Regional assignment of the gene for human liver/bone/kidney alkaline phosphatase to chromosome 1p36.1-p34.

7. Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci.

8. Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma.

9. The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects

11. Defining the role of common variation in the genomic and biological architecture of adult human height

13. Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

14. Risk of pre‐eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case–control study.

15. Biological interpretation of genome-wide association studies using predicted gene functions

16. Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

17. Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development

18. New genetic loci link adipose and insulin biology to body fat distribution.

19. Biological interpretation of genome-wide association studies using predicted gene functions

20. Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate

21. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

22. New genetic loci link adipose and insulin biology to body fat distribution

24. Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

25. Genome-wide association study identifies four loci associated with eruption of permanent teeth

26. Evidence of Gene-Environment Interaction for Two Genes on Chromosome 4 and Environmental Tobacco Smoke in Controlling the Risk of Nonsyndromic Cleft Palate

27. Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate

28. A search for the gene(s) predisposing to idiopathic clubfoot

29. Sequence variants in oxytocin pathway genes and preterm birth: A candidate gene association study

30. Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate

31. Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5CHRNA3CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight

32. Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5- CHRNA3-CHRNB4) interacts with maternal selfreported smoking status during pregnancy to influence birth weight

33. CRISPLD2 variants including a C471T silent mutation may contribute to nonsyndromic cleft lip with or without cleft palate

34. Genome-wide association scan for childhood caries implicates novel genes

35. Coagulation and cancer

36. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

37. Mutations in BMP4 Are Associated with Subepithelial, Microform, and Overt Cleft Lip

38. Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results

39. The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P

41. Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts

42. A genome wide linkage scan for cleft lip and palate and dental anomalies

43. Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis

44. Impaired FGF signaling contributes to cleft lip and palate

45. A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23

46. PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations

47. Genetic evidence for the role of loci at 19q13 in cleft lip and palate.

48. Candidate genes for oral-facial clefts in Guatemalan families

50. Medical sequencing of candidate genes for nonsyndromic cleft lip and palate.

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