Featured
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Genetic structure of the Newfoundland and Labrador population: founder effects modulate variability
- Guangju Zhai
- , Jiayi Zhou
- & Roger C Green
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The Italian genome reflects the history of Europe and the Mediterranean basin
- Giovanni Fiorito
- , Cornelia Di Gaetano
- & Giuseppe Matullo
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| Open AccessGenetic evidence for an origin of the Armenians from Bronze Age mixing of multiple populations
- Marc Haber
- , Massimo Mezzavilla
- & Chris Tyler-Smith
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Effect of six type II diabetes susceptibility loci and an FTO variant on obesity in Pakistani subjects
- Shabana
- , Saleem Ullah Shahid
- & Stephen E Humphries
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Origins, admixture and founder lineages in European Roma
- Begoña Martínez-Cruz
- , Isabel Mendizabal
- & David Comas
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Letter |
On the use of Chinese population as a proxy of Amerindian ancestors in genetic admixture studies with Latin American populations
- Ronald R de Moura
- , Valdir de Queiroz Balbino
- & Lucas A C Brandão
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The Greeks in the West: genetic signatures of the Hellenic colonisation in southern Italy and Sicily
- Sergio Tofanelli
- , Francesca Brisighelli
- & Cristian Capelli
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| Open AccessShared language, diverging genetic histories: high-resolution analysis of Y-chromosome variability in Calabrian and Sicilian Arbereshe
- Stefania Sarno
- , Sergio Tofanelli
- & Davide Pettener
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New clues to the evolutionary history of the main European paternal lineage M269: dissection of the Y-SNP S116 in Atlantic Europe and Iberia
- Laura Valverde
- , Maria José Illescas
- & Marian M de Pancorbo
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Transfer of genetic therapy across human populations: molecular targets for increasing patient coverage in repeat expansion diseases
- Miguel A Varela
- , Helen J Curtis
- & Matthew JA Wood
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Association analysis of copy numbers of FC-gamma receptor genes for rheumatoid arthritis and other immune-mediated phenotypes
- Lude Franke
- , Hanane el Bannoudi
- & Alexandra Zhernakova
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Are all the previously reported genetic variants in limb girdle muscular dystrophy genes pathogenic?
- Giuseppina Di Fruscio
- , Arcomaria Garofalo
- & Vincenzo Nigro
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Y-chromosome diversity in Catalan surname samples: insights into surname origin and frequency
- Neus Solé-Morata
- , Jaume Bertranpetit
- & Francesc Calafell
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Extensive genome-wide autozygosity in the population isolates of Daghestan
- Tatiana M Karafet
- , Kazima B Bulayeva
- & Michael F Hammer
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Genome-wide inbreeding estimation within Lebanese communities using SNP arrays
- Nadine Jalkh
- , Mourad Sahbatou
- & Jean-Louis Serre
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Heritability of liver enzyme levels estimated from genome-wide SNP data
- Jenny H D A van Beek
- , Gitta H Lubke
- & Dorret I Boomsma
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Isolation and prominent aboriginal maternal legacy in the present-day population of La Gomera (Canary Islands)
- Rosa Fregel
- , Vicente M Cabrera
- & Ana M González
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Letter |
Reply to letter from Felice L. Bedford and Doron Yacobi
- Inês Nogueiro
- , João Teixeira
- & Luis Alvarez
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Letter |
Reply to ‘The ‘extremely ancient’ chromosome that isn’t’ by Elhaik et al
- Fernando L Mendez
- , Krishna R Veeramah
- & Michael F Hammer
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The correlation between ancestry and color in two cities of Northeast Brazil with contrasting ethnic compositions
- Thiago Magalhães da Silva
- , M R Sandhya Rani
- & Ronald E Blanton
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Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs
- Giorgio Pistis
- , Eleonora Porcu
- & Serena Sanna
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Fine-scale human genetic structure in Western France
- Matilde Karakachoff
- , Nicolas Duforet-Frebourg
- & Christian Dina
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| Open AccessIdentity-by-descent mapping in a Scandinavian multiple sclerosis cohort
- Helga Westerlind
- , Kerstin Imrell
- & Jan Hillert
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Short Report |
Common variants modify the age of onset for basal cell carcinomas in Gorlin syndrome
- Binnaz Yasar
- , Helen J Byers
- & D Gareth Evans
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A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine
- Se-Kyung Oh
- , Jeong-In Baek
- & Kyu-Yup Lee
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Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility
- Jia-Chi Wang
- , Leslie Ross
- & Trilochan Sahoo
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Echoes from Sepharad: signatures on the maternal gene pool of crypto-Jewish descendants
- Inês Nogueiro
- , João Teixeira
- & Luis Alvarez
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| Open AccessEvaluation of European coeliac disease risk variants in a north Indian population
- Sabyasachi Senapati
- , Javier Gutierrez-Achury
- & Gosia Trynka
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| Open AccessImproved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’
- Patrick Deelen
- , Androniki Menelaou
- & Morris A Swertz
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The peopling of Greenland: further insights from the analysis of genetic diversity using autosomal and X-chromosomal markers
- Vania Pereira
- , Carmen Tomas
- & Niels Morling
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Improving power for robust trans-ethnic meta-analysis of rare and low-frequency variants with a partitioning approach
- Sergii Zakharov
- , Xu Wang
- & Yik-Ying Teo
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Short Report |
Machado–Joseph disease in a Nigerian family: mutational origin and review of the literature
- Shamsideen Abayomi Ogun
- , Sandra Martins
- & Michael F Finkel
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Unravelling the distinct strains of Tharu ancestry
- Gyaneshwer Chaubey
- , Manvendra Singh
- & Kumarasamy Thangaraj
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The phylogenetic and geographic structure of Y-chromosome haplogroup R1a
- Peter A Underhill
- , G David Poznik
- & Richard Villems
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Haplotype differences for copy number variants in the 22q11.23 region among human populations: a pigmentation-based model for selective pressure
- Renato Polimanti
- , Sara Piacentini
- & Maria Fuciarelli
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Letter |
Common variant rs10033900 near the complement factor I gene is associated with age-related macular degeneration risk in Han Chinese population
- Dingguo Qian
- , Mengyuan Kan
- & Yun Liu
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Human genetics of the Kula Ring: Y-chromosome and mitochondrial DNA variation in the Massim of Papua New Guinea
- Mannis van Oven
- , Silke Brauer
- & Manfred Kayser
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| Open AccessUsing ancestry-informative markers to identify fine structure across 15 populations of European origin
- Laura M Huckins
- , Vesna Boraska
- & Ioanna Tachmazidou
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Genetic ancestry is associated with colorectal adenomas and adenocarcinomas in Latino populations
- Gustavo Hernandez-Suarez
- , Maria Carolina Sanabria
- & Albert Tenesa
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Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia
- Carla Aimé
- , Paul Verdu
- & Frédéric Austerlitz
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| Open AccessVariation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population
- Shengting Li
- , Soren Besenbacher
- & Mikkel H Schierup
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The ‘extremely ancient’ chromosome that isn’t: a forensic bioinformatic investigation of Albert Perry’s X-degenerate portion of the Y chromosome
- Eran Elhaik
- , Tatiana V Tatarinova
- & Dan Graur
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Face shape differs in phylogenetically related populations
- Saskia M J Hopman
- , Johannes H M Merks
- & Peter Hammond
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Population-level expression variability of mitochondrial DNA-encoded genes in humans
- Gang Wang
- , Ence Yang
- & James J Cai
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Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests
- Matthew Zawistowski
- , Mark Reppell
- & Sebastian Zöllner
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Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American Indians
- V Saroja Voruganti
- , Nora Franceschini
- & Shelley A Cole
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Short Report |
BRCA1/2 mutations and FMR1 alleles are randomly distributed: a case control study
- Efrat Dagan
- , Yoram Cohen
- & Ruth Gershoni-Baruch
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Genealogical analysis as a new approach for the investigation of drug intolerance heritability
- Marc Tremblay
- , Tarek Bouhali
- & Diane Brisson