Phylogeography of Y-Chromosome Haplogroup I Reveals Distinct Domains of Prehistoric Gene Flow in Europe

Siiri Rootsi, Toomas Kivisild, Giorgia Benuzzi, +41

The American Journal of Human Genetics

Haplotype DeterminationPhylogeneticsMedicineGeneticsEvolutionary Biology +8

Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages

Toomas Kivisild, Michael J. Bamshad, Katrin Kaldma, +12

Current Biology

Deep Common AncestryPhylogeneticsMedicineGeneticsEvolutionary Biology +7

The Western and Eastern Roots of the Saami—the Story of Genetic “Outliers” Told by Mitochondrial DNA and Y Chromosomes

Kristiina Tambets, Siiri Rootsi, Toomas Kivisild, +40

The American Journal of Human Genetics

Eastern RootsSaami—the StoryGeneticsEvolutionary BiologyMedicine +6

Lactase Haplotype Diversity in the Old World

Edward J. Hollox, Mark Poulter, Marek Zvarík, +5

The American Journal of Human Genetics

Lactase Haplotype DiversityHaplotype DeterminationMolecular EcologyMedicineGenetics +6

A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe

Siiri Rootsi, Lev A. Zhivotovsky, Marián Baldovič, +13

European Journal of Human Genetics

BiologyY-chromosome Haplogroup NHaplotype DeterminationSoutheast AsiaMedicine +11

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Martina Plášilová, Ivaylo Stoilov, Mansoor Sarfarazi, +3

Journal of Medical Genetics

BiologyCytochrome P450 MoleculeAllelic VariantMendelian DisorderOphthalmology +11

Reconstructing the Population History of European Romani from Genome-wide Data

Isabel Mendizabal, Óscar Lao, Urko M. Marigorta, +19

Current Biology

Population HistoryMolecular EcologyHuman VariationMedicineGenetics +10

Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset

A Genĉík, A Gencíková, V. Ferák

Human Genetics

Ocular DiseaseOphthalmologyPopulation Genetical AspectsGeneticsPrimary Congenital Glaucoma +7

High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in HGO Involving Different Mutational Hot Spots

Andrea Zaťková, Daniel Beltrán Valero de Bernabé, H Poláková, +6

The American Journal of Human Genetics

BiologyAllelic VariantMendelian DisorderMultiple MutationsGenetic Disorder +5

High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL).

Gabriel Minárik, V. Ferák, Eva Feráková, +3

PubMed

Carrier FrequencyGjb2 Mutation W24xMendelian DisorderGenetic DisorderGenetics +11