Found: 42
Select item for more details and to access through your institution.
Maximum-Likelihood Estimation of Site-Specific Mutation Rates in Human Mitochondrial DNA From Partial Phylogenetic Classification.
- Published in:
- Genetics, 2008, v. 180, n. 3, p. 1511, doi. 10.1534/genetics.108.091116
- By:
- Publication type:
- Article
Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 11, p. 3390, doi. 10.1002/ajmg.a.62456
- By:
- Publication type:
- Article
Exome Sequencing Reveals SYCE1 Mutation Associated With Autosomal Recessive Primary Ovarian Insufficiency.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Performance comparison: exome sequencing as a single test replacing Sanger sequencing.
- Published in:
- Molecular Genetics & Genomics, 2021, v. 296, n. 3, p. 653, doi. 10.1007/s00438-021-01772-3
- By:
- Publication type:
- Article
Uniparental Genetic Heritage of Belarusians: Encounter of Rare Middle Eastern Matrilineages with a Central European Mitochondrial DNA Pool.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066499
- By:
- Publication type:
- Article
Genetic Continuity in the Franco-Cantabrian Region: New Clues from Autochthonous Mitogenomes.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032851
- By:
- Publication type:
- Article
The Druze: A Population Genetic Refugium of the Near East.
- Published in:
- PLoS ONE, 2008, v. 3, n. 5, p. 1, doi. 10.1371/journal.pone.0002105
- By:
- Publication type:
- Article
Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora.
- Published in:
- PLoS ONE, 2008, v. 3, n. 4, p. 1, doi. 10.1371/journal.pone.0002062
- By:
- Publication type:
- Article
Reconstructing the demographic history of the Himalayan and adjoining populations.
- Published in:
- Human Genetics, 2018, v. 137, n. 2, p. 129, doi. 10.1007/s00439-018-1867-2
- By:
- Publication type:
- Article
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.
- Published in:
- 2010
- By:
- Publication type:
- Report
Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthood.
- Published in:
- Human Genetics, 2009, v. 126, n. 5, p. 707, doi. 10.1007/s00439-009-0727-5
- By:
- Publication type:
- Article
Response.
- Published in:
- 2009
- By:
- Publication type:
- Letter
Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations.
- Published in:
- Human Genetics, 2004, v. 114, n. 4, p. 354, doi. 10.1007/s00439-003-1073-7
- By:
- Publication type:
- Article
The phylogenetic and geographic structure of Y-chromosome haplogroup R1a.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 1, p. 124, doi. 10.1038/ejhg.2014.50
- By:
- Publication type:
- Article
Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 12, p. 1275, doi. 10.1038/ejhg.2012.86
- By:
- Publication type:
- Article
MtDNA evidence for a genetic bottleneck in the early history of the Ashkenazi Jewish population.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 5, p. 355, doi. 10.1038/sj.ejhg.5201156
- By:
- Publication type:
- Article
The Caucasus as an Asymmetric Semipermeable Barrier to Ancient Human Migrations.
- Published in:
- Molecular Biology & Evolution, 2012, v. 29, n. 7, p. 1891, doi. 10.1093/molbev/mss141
- By:
- Publication type:
- Article
The Caucasus as an Asymmetric Semipermeable Barrier to Ancient Human Migrations.
- Published in:
- Molecular Biology & Evolution, 2012, v. 29, n. 1, p. 359, doi. 10.1093/molbev/msr221
- By:
- Publication type:
- Article
The genome-wide structure of the Jewish people.
- Published in:
- Nature, 2010, v. 466, n. 7303, p. 238, doi. 10.1038/nature09103
- By:
- Publication type:
- Article
West Asian sources of the Eurasian component in Ethiopians: a reassessment.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-55344-y
- By:
- Publication type:
- Article
Most of the extant mtDNA boundaries in South and Southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humans.
- Published in:
- 2005
- By:
- Publication type:
- Correction Notice
Most of the extant mtDNA boundaries in South and Southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humans.
- Published in:
- BMC Genetics, 2004, v. 5, p. 26, doi. 10.1186/1471-2156-5-26
- By:
- Publication type:
- Article
Phylogenetic applications of whole Y-chromosome sequences and the Near Eastern origin of Ashkenazi Levites.
- Published in:
- Nature Communications, 2013, v. 4, n. 12, p. 2928, doi. 10.1038/ncomms3928
- By:
- Publication type:
- Article
Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans.
- Published in:
- Nature Communications, 2013, v. 4, n. 4, p. 1764, doi. 10.1038/ncomms2656
- By:
- Publication type:
- Article
Insights into the Demographic History of African Pygmies from Complete Mitochondrial Genomes.
- Published in:
- Molecular Biology & Evolution, 2011, v. 28, n. 2, p. 1099, doi. 10.1093/molbev/msq294
- By:
- Publication type:
- Article
Population Genetic Structure in Indian Austroasiatic Speakers: The Role of Landscape Barriers and Sex-Specific Admixture.
- Published in:
- Molecular Biology & Evolution, 2011, v. 28, n. 2, p. 1013, doi. 10.1093/molbev/msq288
- By:
- Publication type:
- Article
Nationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screening.
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 3, p. 223, doi. 10.1002/mgg3.278
- By:
- Publication type:
- Article
Origin and diffusion of human Y chromosome haplogroup J1-M267.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-85883-2
- By:
- Publication type:
- Article
The novel founder homozygous V225M mutation in the HSD17B3 gene causes aberrant splicing and XY-DSD.
- Published in:
- Endocrine (1355008X), 2020, v. 69, n. 3, p. 650, doi. 10.1007/s12020-020-02327-z
- By:
- Publication type:
- Article
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel.
- Published in:
- Familial Cancer, 2018, v. 17, n. 1, p. 79, doi. 10.1007/s10689-017-0009-7
- By:
- Publication type:
- Article
No Evidence from Genome-Wide Data of a Khazar Origin for the Ashkenazi Jews.
- Published in:
- Human Biology, 2013, v. 85, n. 6, p. 859, doi. 10.3378/027.085.0604
- By:
- Publication type:
- Article
Absence of APOL1 Risk Variants Protects against HIV-Associated Nephropathy in the Ethiopian Population.
- Published in:
- American Journal of Nephrology, 2011, v. 34, n. 5, p. 452, doi. 10.1159/000332378
- By:
- Publication type:
- Article
The Genographic Project Public Participation Mitochondrial DNA Database.
- Published in:
- PLoS Genetics, 2007, v. 3, n. 6, p. e104, doi. 10.1371/journal.pgen.0030104
- By:
- Publication type:
- Article
Mutations in TAX1BP3 Cause Dilated Cardiomyopathy with Septo-Optic Dysplasia.
- Published in:
- Human Mutation, 2015, v. 36, n. 4, p. 439, doi. 10.1002/humu.22759
- By:
- Publication type:
- Article
A novel 154-bp deletion in the human mitochondrial DNA control region in healthy individuals.
- Published in:
- Human Mutation, 2008, v. 29, n. 12, p. 1387, doi. 10.1002/humu.20835
- By:
- Publication type:
- Article
African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 9, p. 1816, doi. 10.1093/hmg/ddq040
- By:
- Publication type:
- Article
Evolutionary insights into the high worldwide prevalence of MBL2 deficiency alleles.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 17, p. 2650, doi. 10.1093/hmg/ddl193
- By:
- Publication type:
- Article
Severe Hypertriglyceridemia in an Infant of Arab Descent.
- Published in:
- Israel Medical Association Journal, 2013, v. 15, n. 1, p. 53
- By:
- Publication type:
- Article
Divorcing the Late Upper Palaeolithic demographic histories of mtDNA haplogroups M1 and U6 in Africa.
- Published in:
- BMC Evolutionary Biology, 2012, v. 12, n. 1, p. 1, doi. 10.1186/1471-2148-12-234
- By:
- Publication type:
- Article
Population expansion in the North African Late Pleistocene signalled by mitochondrial DNA haplogroup U6.
- Published in:
- BMC Evolutionary Biology, 2010, v. 10, p. 390, doi. 10.1186/1471-2148-10-390
- By:
- Publication type:
- Article
Long-term prognosis of acute pulmonary oedema--an ominous outcome.
- Published in:
- 2000
- By:
- Publication type:
- journal article
Consanguinity Rates Predict Long Runs of Homozygosity in Jewish Populations.
- Published in:
- Human Heredity, 2017, v. 82, n. 3/4, p. 87, doi. 10.1159/000478897
- By:
- Publication type:
- Article