Found: 49
Select item for more details and to access through your institution.
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 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
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
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
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
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
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
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
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
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.
- Published in:
- Nature Genetics, 2004, v. 36, n. 6, p. 579, doi. 10.1038/ng1358
- 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
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
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
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
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
Ashkenazi Jewish Centenarians Do Not Demonstrate Enrichment in Mitochondrial Haplogroup.
- Published in:
- PLoS ONE, 2008, v. 3, n. 10, p. 1, doi. 10.1371/journal.pone.0003425
- 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
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
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
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.
- Published in:
- Human Genetics, 2015, v. 134, n. 3, p. 305, doi. 10.1007/s00439-014-1522-5
- By:
- Publication type:
- Article
Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.
- Published in:
- 2015
- By:
- Publication type:
- Erratum
Exome Sequencing Reveals SYCE1 Mutation Associated With Autosomal Recessive Primary Ovarian Insufficiency.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Adolescent BMI and early-onset type 2 diabetes among Ethiopian immigrants and their descendants: a nationwide study.
- Published in:
- Cardiovascular Diabetology, 2020, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12933-020-01143-z
- 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
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
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
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
Identification of a recurrent mutation inGALNT3demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders.
- Published in:
- 2005
- By:
- Publication type:
- Correction notice
Identification of a recurrent mutation inGALNT3demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disorders.
- Published in:
- Journal of Molecular Medicine, 2005, v. 83, n. 1, p. 33, doi. 10.1007/s00109-004-0610-8
- 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
Long-term prognosis of acute pulmonary oedema--an ominous outcome.
- Published in:
- 2000
- 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
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
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
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
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
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