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93 results on '"Behar, Doron M."'

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1. Genomic analyses of hair from Ludwig van Beethoven

2. Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry

3. Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomes

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

6. Correction: Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third

8. Dissecting the paternal founders of Mundari (Austroasiatic) speakers associated with the language dispersal in South Asia

9. Teaching clinicians practical genomic medicine: 7 years’ experience in a tertiary care center

10. Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third

11. The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD

14. Counting the paternal founders of Austroasiatic speakers associated with the language dispersal in South Asia

15. The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries

16. Influence of genetic copy number variants of the human GLUT3 glucose transporter gene SLC2A3 on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication study

17. Author Correction: The genetic legacy of continental scale admixture in Indian Austroasiatic speakers

18. The genetic legacy of continental scale admixture in Indian Austroasiatic speakers

20. The genetic legacy of continental scale admixture in Indian Austroasiatic speakers

21. Reconstructing the demographic history of the Himalayan and adjoining populations

22. The genetic variation in the R1a clade among the Ashkenazi Levites’ Y chromosome

23. Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel

24. Origin and spread of human mitochondrial DNA haplogroup U7

25. Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screening

26. The Simons Genome Diversity Project: 300 genomes from 142 diverse populations

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

28. Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C

29. Human Y Chromosome Haplogroup N: A Non-trivial Time-Resolved Phylogeography that Cuts across Language Families

34. Homozygous MED25 mutation implicated in eye–intellectual disability syndrome

35. Mutations inTAX1BP3Cause Dilated Cardiomyopathy with Septo-Optic Dysplasia

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

38. Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

42. The phylogenetic and geographic structure of Y-chromosome haplogroup R1a

43. Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency

45. Phylogenetic applications of whole Y-chromosome sequences and the Near Eastern origin of Ashkenazi Levites

46. No Evidence from Genome-Wide Data of a Khazar Origin for the Ashkenazi Jews

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

49. Uniparental Genetic Heritage of Belarusians: Encounter of Rare Middle Eastern Matrilineages with a Central European Mitochondrial DNA Pool

50. Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus

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