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2. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

3. No Evidence from Genome-wide Data of a Khazar Origin for the Ashkenazi Jews

4. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

5. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

6. Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

7. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

8. A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia

10. Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

11. Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction

12. Genomic analyses inform on migration events during the peopling of Eurasia

13. Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39

14. A recent bottleneck of Y chromosome diversity coincides with a global change in culture

15. Origin and diffusion of human Y chromosome haplogroup J1-M267

17. Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

18. Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium

20. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

21. Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

22. FANCM missense variants and breast cancer risk:a case-control association study of 75,156 European women

23. Identification of a new locus at 16q12 associated with time to asthma onset

25. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

26. Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

27. Genes reveal traces of common recent demographic history for most of the Uralic-speaking populations

31. Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

32. Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci

33. Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

34. Origin and spread of human mitochondrial DNA haplogroup U7

37. A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia

38. A Common Founder Effect of the Splice Site Variant c.-23+1G>A in GJB2 Gene Causing Autosomal Recessive Deafness 1A (DFNB1A) in Eurasia

39. The genome-wide structure of the Jewish people

40. FANCMmissense variants and breast cancer risk: a case-control association study of 75,156 European women

50. A new approach to estimating the prevalence of hereditary hearing loss: An analysis of the distribution of sign language users based on census data in Russia

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