392 results on '"Behar, Doron M."'
Search Results
2. Human Y chromosome haplogroup L1-M22 traces Neolithic expansion in West Asia and supports the Elamite and Dravidian connection
3. Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomes
4. Performance comparison: exome sequencing as a single test replacing Sanger sequencing
5. Dissecting the paternal founders of Mundari (Austroasiatic) speakers associated with the language dispersal in South Asia
6. Teaching clinicians practical genomic medicine: 7 years’ experience in a tertiary care center
7. Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third
8. Genomic analyses inform on migration events during the peopling of Eurasia
9. The Simons Genome Diversity Project: 300 genomes from 142 diverse populations
10. Origin and diffusion of human Y chromosome haplogroup J1-M267
11. The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD
12. Preconception carrier screening yield: effect of variants of unknown significance in partners of carriers with clinically significant variants
13. A recent bottleneck of Y chromosome diversity coincides with a global change in culture
14. Preliminary Report: Missense mutations in the APOL gene family are associated with end stage kidney disease risk previously attributed to the MYH9 gene
15. Correction: Determination of the phylogenetic origins of the Árpád Dynasty based on Y chromosome sequencing of Béla the Third
16. Reconstructing the demographic history of the Himalayan and adjoining populations
17. Genomic analyses of hair from Ludwig van Beethoven
18. Consanguinity Rates Predict Long Runs of Homozygosity in Jewish Populations
19. Author Correction: The genetic legacy of continental scale admixture in Indian Austroasiatic speakers
20. The genetic legacy of continental scale admixture in Indian Austroasiatic speakers
21. Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel
22. North Africans traveling north
23. Homozygous MED25 mutation implicated in eye–intellectual disability syndrome
24. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5
25. Origin and spread of human mitochondrial DNA haplogroup U7
26. Maternal Traces of Deep Common Ancestry and Asymmetric Gene Flow between Pygmy Hunter-Gatherers and Bantu-Speaking Farmers
27. Timing of a Back-Migration into Africa [with Response]
28. The mtDNA Legacy of the Levantine Early Upper Palaeolithic in Africa
29. Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry
30. Mutations in TAX1BP3 Cause Dilated Cardiomyopathy with Septo-Optic Dysplasia
31. Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene
32. The genome-wide structure of the Jewish people
33. Strong maternal khoisan contribution to the South African coloured population: a case of gender-biased admixture
34. Exome Sequencing Reveals SYCE1 Mutation Associated With Autosomal Recessive Primary Ovarian Insufficiency
35. Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthood
36. Mitochondrial haplogroup U5b3: a distant echo of the epipaleolithic in Italy and the legacy of the early Sardinians
37. The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula
38. Maximum-likelihood estimation of site-specific mutation rates in human mitochondrial DNA from partial phylogenetic classification
39. The dawn of human matrilineal diversity
40. The matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder event
41. Deciphering the ancient and complex evolutionary history of human arylamine N-acetyltransferase genes
42. Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations
43. Performance comparison: exome-sequencing as a single test replacing Sanger-sequencing
44. Where west meets east: the complex mtDNA landscape of the Southwest and Central Asian corridor
45. Multiple origins of Ashkenazi Levites: Y chromosome evidence for both Near Eastern and European ancestries
46. Evaluating the forensic informativeness of mtDNA haplogroup H sub-typing on a Eurasian scale
47. The Caucasus as an Asymmetric Semipermeable Barrier to Ancient Human Migrations
48. The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus
49. Insights into the Demographic History of African Pygmies from Complete Mitochondrial Genomes
50. Population Genetic Structure in Indian Austroasiatic Speakers: The Role of Landscape Barriers and Sex-Specific Admixture
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