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Dive into the research topics where Cristina Martínez-Labarga is active.

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Featured researches published by Cristina Martínez-Labarga.


PLOS ONE | 2007

Beringian Standstill and Spread of Native American Founders

Erika Tamm; Toomas Kivisild; Maere Reidla; Mait Metspalu; David Glenn Smith; Connie J. Mulligan; Claudio M. Bravi; Olga Rickards; Cristina Martínez-Labarga; E. K. Khusnutdinova; Sardana A. Fedorova; Maria V. Golubenko; V. A. Stepanov; Marina Gubina; Sergey I. Zhadanov; Ludmila P. Ossipova; Larisa Damba; M. I. Voevoda; José Edgardo Dipierri; Richard Villems; Ripan S. Malhi

Native Americans derive from a small number of Asian founders who likely arrived to the Americas via Beringia. However, additional details about the intial colonization of the Americas remain unclear. To investigate the pioneering phase in the Americas we analyzed a total of 623 complete mtDNAs from the Americas and Asia, including 20 new complete mtDNAs from the Americas and seven from Asia. This sequence data was used to direct high-resolution genotyping from 20 American and 26 Asian populations. Here we describe more genetic diversity within the founder population than was previously reported. The newly resolved phylogenetic structure suggests that ancestors of Native Americans paused when they reached Beringia, during which time New World founder lineages differentiated from their Asian sister-clades. This pause in movement was followed by a swift migration southward that distributed the founder types all the way to South America. The data also suggest more recent bi-directional gene flow between Siberia and the North American Arctic.


American Journal of Human Genetics | 1999

mtDNA History of the Cayapa Amerinds of Ecuador: Detection of Additional Founding Lineages for the Native American Populations

Olga Rickards; Cristina Martínez-Labarga; J.K. Lum; G.F. De Stefano; Rebecca L. Cann

mtDNA variation in the Cayapa, an Ecuadorian Amerindian tribe belonging to the Chibcha-Paezan linguistic branch, was analyzed by use of hypervariable control regions I and II along with two linked regions undergoing insertion/deletion mutations. Three major maternal lineage clusters fit into the A, B, and C founding groups first described by Schurr and colleagues in 1990, whereas a fourth lineage, apparently unique to the Cayapa, has ambiguous affinity to known clusters. The time of divergence from a common maternal ancestor of the four lineage groups is of sufficient age that it indicates an origin in Asia and supports the hypothesis that the degree of variability carried by the Asian ancestral populations into the New World was rather high. Spatial autocorrelation analysis points out (a) statistically significant nonrandom distributions of the founding lineages in the Americas, because of north-south population movements that have occurred since the first Asian migrants spread through Beringia into the Americas, and (b) an unusual pattern associated with the D lineage cluster. The values of haplotype and nucleotide diversity that are displayed by the Cayapa appear to differ from those observed in other Chibchan populations but match those calculated for South American groups belonging to various linguistic stocks. These data, together with the results of phylogenetic analysis performed with the Amerinds of Central and South America, highlight the difficulty in the identification of clear coevolutionary patterns between linguistic and genetic relationships in particular human populations.


American Journal of Physical Anthropology | 2009

Stable isotopic evidence for diet at the Imperial Roman coastal site of Velia (1st and 2nd Centuries AD) in Southern Italy

Oliver E. Craig; Marco Biazzo; Tamsin C. O'Connell; Peter Garnsey; Cristina Martínez-Labarga; Roberta Lelli; Loretana Salvadei; Gianna Tartaglia; Alessia Nava; Lorena Renò; Antonella Fiammenghi; Olga Rickards; Luca Bondioli

Here we report on a stable isotope palaeodietary study of a Imperial Roman population interred near the port of Velia in Southern Italy during the 1st and 2nd centuries AD. Carbon and nitrogen stable isotope analyses were performed on collagen extracted from 117 adult humans as well as a range of fauna to reconstruct individual dietary histories. For the majority of individuals, we found that stable isotope data were consistent with a diet high in cereals, with relatively modest contributions of meat and only minor contributions of marine fish. However, substantial isotopic variation was found within the population, indicating that diets were not uniform. We suggest that a number of individuals, mainly but not exclusively males, had greater access to marine resources, especially high trophic level fish. However, the observed dietary variation did not correlate with burial type, number of grave goods, nor age at death. Also, individuals buried at the necropolis at Velia ate much less fish overall compared with the contemporaneous population from the necropolis of Portus at Isola Sacra, located on the coast close to Rome. Marine and riverine transport and commerce dominated the economy of Portus, and its people were in a position to supplement their own stocks of fish with imported goods in transit to Rome, whereas at Velia marine exploitation existed side-by-side with land-based economic activities.


Scandinavian Journal of Gastroenterology | 2004

Increased Frequency of the Immunoglobulin Enhancer HS1,2 Allele 2 in Coeliac Disease

Domenico Frezza; Vincenzo Giambra; Rossella Cianci; A. Fruscalzo; M. Giufrè; Giovanni Cammarota; Cristina Martínez-Labarga; Olga Rickards; G. Scibilia; Concetta Sferlazzas; F. Bartolozzi; S. Starnino; Giuseppe Magazzù; G. Gasbarrini; Franco Pandolfi

Background: Coeliac disease (CD) is characterized by increased immunological responsiveness to ingested gliadin in genetically predisposed individuals. This genetic predisposition is not completely defined. A dysregulation of immunoglobulins (Ig) is present in CD: since antiendomysium antibodies (anti-EMA) are of the IgA class. One polymorphic enhancer within the locus control region (LCR) of the immunoglobulin heavy chain cluster at the 3′ of the C alpha-1 gene was investigated. The correlation of the penetrance of the four different alleles of the HS1,2-A enhancer of the LCR-1 3′ to C alpha-1 in CD patients compared to a control population was analysed. Methods: A total of 115 consecutive CD outpatients, on a gluten-free diet, and 248 healthy donors, age- and sex-matched, from the same geographical area were enrolled in the study. HS1,2-A allele frequencies were investigated by nested polymerase chain reaction (PCR). Results: The frequency of allele 2 of the enhancer HS1,2-A gene was increased by 30.8% as compared to the control frequency. The frequency of homozygosity for allele 2 was significantly increased in CD patients. Crude odds ratio (OR) showed that those with 2/2 and 2/4 (OR 2.63, P < 0.001 and OR 2.01, P = 0.03) have a significantly higher risk of developing the disease. In contrast, allele 1/2 may represent a protective genetic factor against CD (OR 0.52, P = 0.01). Conclusions: These data provide further evidence of a genetic predisposition in CD. Because of the Ig dysregulation in CD, the enhancer HS1,2-A may be involved in the pathogenesis.


PLOS ONE | 2010

Mitochondrial Haplogroup H1 in North Africa: An Early Holocene Arrival from Iberia

Claudio Ottoni; Giuseppina Primativo; Baharak Hooshiar Kashani; Alessandro Achilli; Cristina Martínez-Labarga; Gianfranco Biondi; Antonio Torroni; Olga Rickards

The Tuareg of the Fezzan region (Libya) are characterized by an extremely high frequency (61%) of haplogroup H1, a mitochondrial DNA (mtDNA) haplogroup that is common in all Western European populations. To define how and when H1 spread from Europe to North Africa up to the Central Sahara, in Fezzan, we investigated the complete mitochondrial genomes of eleven Libyan Tuareg belonging to H1. Coalescence time estimates suggest an arrival of the European H1 mtDNAs at about 8,000–9,000 years ago, while phylogenetic analyses reveal three novel H1 branches, termed H1v, H1w and H1x, which appear to be specific for North African populations, but whose frequencies can be extremely different even in relatively close Tuareg villages. Overall, these findings support the scenario of an arrival of haplogroup H1 in North Africa from Iberia at the beginning of the Holocene, as a consequence of the improvement in climate conditions after the Younger Dryas cold snap, followed by in situ formation of local H1 sub-haplogroups. This process of autochthonous differentiation continues in the Libyan Tuareg who, probably due to isolation and recent founder events, are characterized by village-specific maternal mtDNA lineages.


European Journal of Human Genetics | 2005

The population history of the Croatian linguistic minority of Molise (southern Italy): a maternal view.

Carla Babalini; Cristina Martínez-Labarga; Helle-Viivi Tolk; Toomas Kivisild; Rita Giampaolo; Tiziana Tarsi; Irene Contini; Lovorka Barać; Branka Janićijević; Irena Martinović Klarić; Marijana Peričić; Anita Sujoldžić; Richard Villems; Gianfranco Biondi; Pavao Rudan; Olga Rickards

This study examines the mitochondrial DNA (mtDNA) diversity of the Croatian-speaking minority of Molise and evaluates its potential genetic relatedness to the neighbouring Italian groups and the Croatian parental population. Intermatch, genetic distance, and admixture analyses highlighted the genetic similarity between the Croatians of Molise and the neighbouring Italian populations and demonstrated that the Croatian-Italian ethnic minority presents features lying between Croatians and Italians. This finding was confirmed by a phylogeographic approach, which revealed both the prevalence of Croatian and the penetrance of Italian maternal lineages in the Croatian community of Molise. These results suggest that there was no reproductive isolation between the two geographically proximate, yet culturally distinct populations living in Italy. The gene flow between the Croatian-Italians and the surrounding Italian populations indicate, therefore, that ethnic consciousness has not created reproductive barriers and that the Croatian-speaking minority of Molise does not represent a reproductively isolated entity.


Annals of Human Genetics | 2009

First genetic insight into Libyan Tuaregs: a maternal perspective

Claudio Ottoni; Cristina Martínez-Labarga; Eva-Liis Loogväli; Erwan Pennarun; Alessandro Achilli; Flavio De Angelis; Emiliano Trucchi; Irene Contini; Gianfranco Biondi; Olga Rickards

The Tuaregs are a semi‐nomadic pastoralist people of northwest Africa. Their origins are still a matter of debate due to the scarcity of genetic and historical data. Here we report the first data on the mitochondrial DNA (mtDNA) genetic characterization of a Tuareg sample from Fezzan (Libyan Sahara). A total of 129 individuals from two villages in the Acacus region were genetically analysed. Both the hypervariable regions and the coding region of mtDNA were investigated. Phylogeographic investigation was carried out in order to reconstruct human migratory shifts in central Sahara, and to shed light on the origin of the Libyan Tuaregs. Our results clearly show low genetic diversity in the sample, possibly due to genetic drift and founder effect associated with the separation of Libyan Tuaregs from an ancestral population. Furthermore, the maternal genetic pool of the Libyan Tuaregs is characterized by a major „European” component shared with the Berbers that could be traced to the Iberian Peninsula, as well as a minor ‘south Saharan’ contribution possibly linked to both Eastern African and Near Eastern populations.


Annals of Human Biology | 2009

Human mitochondrial DNA variation in Southern Italy

Claudio Ottoni; Cristina Martínez-Labarga; Luciana Vitelli; Giuseppina Scano; Enrico Fabrini; Irene Contini; Gianfranco Biondi; Olga Rickards

Background: Since prehistoric times Southern Italy has been a cultural crossroads of the Mediterranean basin. Genetic data on the peoples of Basilicata and Calabria are scarce and, particularly, no records on mtDNA variability have been published. Aim: In this study mtDNA haplotypes of populations from Basilicata, Calabria and Sicily are compared with those of other Italian and Mediterranean populations, so as to investigate their genetic relationships. Subjects and methods: A total of 341 individuals was analysed for mtDNA in order to provide their classification into haplogroups. Multivariate analysis was used to compare the studied populations with other Mediterranean samples; median-joining network analysis was applied to observe the relationship between the major lineages of the Southern Italians. Results: The haplogroup distribution in the Southern Italian samples falls within the typical pattern of mtDNA variability of Western Eurasia. The comparison with other Mediterranean countries showed a substantial homogeneity of the area, which is probably related to the historic contact through the Mediterranean Sea. Conclusion: The mtDNA analysis demonstrated that Southern Italy displays a typical pattern of Mediterranean basin variability, even though it appears plausible that Southern Italy was less affected by the effects of the Late Glacial Maximum, which reduced genetic diversity in Europe.


Current Genomics | 2008

Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations

Emiliano Giardina; Ilenia Pietrangeli; Cristina Martínez-Labarga; Claudia Martone; Flavio De Angelis; Aldo Spinella; Gianfranco De Stefano; Olga Rickards; Giuseppe Novelli

Ancestry informative markers (AIMs) are human polymorphisms that exhibit substantially allele frequency differences among populations. These markers can be useful to provide information about ancestry of samples which may be useful in predicting a perpetrator’s ethnic origin to aid criminal investigations. Variations in human pigmentation are the most obvious phenotypes to distinguish individuals. It has been recently shown that the variation of a G in an A allele of the coding single-nucleotide polymorphism (SNP) rs1426654 within SLC24A5 gene varies in frequency among several population samples according to skin pigmentation. Because of these observations, the SLC24A5 locus has been evaluated as Ancestry Informative Region (AIR) by typing rs1426654 together with two additional intragenic markers (rs2555364 and rs16960620) in 471 unrelated individuals originating from three different continents (Africa, Asia and Europe). This study further supports the role of human SLC24A5 gene in skin pigmentation suggesting that variations in SLC24A5 haplotypes can correlate with human migration and ancestry. Furthermore, our data do reveal the utility of haplotype and combined unphased genotype analysis of SLC24A5 in predicting ancestry and provide a good example of usefulness of genetic characterization of larger regions, in addition to single polymorphisms, as candidates for population-specific sweeps in the ancestral population.


American Journal of Physical Anthropology | 2011

Deep Into the Roots of the Libyan Tuareg: A Genetic Survey of Their Paternal Heritage.

Claudio Ottoni; Maarten Larmuseau; Nancy Vanderheyden; Cristina Martínez-Labarga; Giuseppina Primativo; Gianfranco Biondi; Ronny Decorte; Olga Rickards

Recent genetic studies of the Tuareg have begun to uncover the origin of this semi-nomadic northwest African people and their relationship with African populations. For centuries they were caravan traders plying the trade routes between the Mediterranean coast and south-Saharan Africa. Their origin most likely coincides with the fall of the Garamantes who inhabited the Fezzan (Libya) between the 1st millennium BC and the 5th century AD. In this study we report novel data on the Y-chromosome variation in the Libyan Tuareg from Al Awaynat and Tahala, two villages in Fezzan, whose maternal genetic pool was previously characterized. High-resolution investigation of 37 Y-chromosome STR loci and analysis of 35 bi-allelic markers in 47 individuals revealed a predominant northwest African component (E-M81, haplogroup E1b1b1b) which likely originated in the second half of the Holocene in the same ancestral population that contributed to the maternal pool of the Libyan Tuareg. A significant paternal contribution from south-Saharan Africa (E-U175, haplogroup E1b1a8) was also detected, which may likely be due to recent secondary introduction, possibly through slavery practices or fusion between different tribal groups. The difference in haplogroup composition between the villages of Al Awaynat and Tahala suggests that founder effects and drift played a significant role in shaping the genetic pool of the Libyan Tuareg.

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Olga Rickards

University of Rome Tor Vergata

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Gianfranco Biondi

Sapienza University of Rome

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Gabriele Scorrano

University of Rome Tor Vergata

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Giuseppina Scano

University of Rome Tor Vergata

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Roberta Lelli

University of Rome Tor Vergata

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Carla Babalini

University of Rome Tor Vergata

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Flavio De Angelis

University of Rome Tor Vergata

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Irene Contini

University of Rome Tor Vergata

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G.F. De Stefano

University of Rome Tor Vergata

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