Genetic affinities among the historical provinces of Romania and Central Europe as revealed by an mtDNA analysis
© The Author(s). 2017
Received: 3 August 2016
Accepted: 2 March 2017
Published: 7 March 2017
As a major crossroads between Asia and Europe, Romania has experienced continuous migration and invasion episodes. The precise routes may have been shaped by the topology of the territory and had diverse impacts on the genetic structure of mitochondrial DNA (mtDNA) in historical Romanian provinces. We studied 714 Romanians from all historical provinces, Wallachia, Dobrudja, Moldavia, and Transylvania, by analyzing the mtDNA control region and coding markers to encompass the complete landscape of mtDNA haplogroups.
We observed a homogenous distribution of the majority of haplogroups among the Romanian provinces and a clear association with the European populations. A principal component analysis and multidimensional scaling analysis supported the genetic similarity of the Wallachia, Moldavia, and Dobrudja groups with the Balkans, while the Transylvania population was closely related to Central European groups. These findings could be explained by the topology of the Romanian territory, where the Carpathian Arch played an important role in migration patterns. Signals of Asian maternal lineages were observed in all Romanian historical provinces, indicating gene flow along the migration routes through East Asia and Europe.
Our current findings based on the mtDNA analysis of populations in historical provinces of Romania suggest similarity between populations in Transylvania and Central Europe, supported both by the observed clines in haplogroup frequencies for several European and Asian maternal lineages and MDS analyses.
KeywordsMitochondrial DNA Romanian provinces Genetic diversity Transylvania
Romania is located in Southeastern Europe as part of the Central basin of the Black Sea and lower Danube basin, and the country is divided in the center by the orographic Carpathian-Balkan system. As a segment of the Danube basin, this territory was a major crossroads between Asia and Southeastern, Central, and North Europe and one of the direct eastward routes linking to the North Pontic steppe. The Romanian language is a part of the Eastern Romance languages that evolved from spoken Latin during the process of Romanization followed by a period of Slavic influence at the beginning of the sixth century .
The earliest anatomically modern human fossils in Europe attributed to the end of the Upper Paleolithic period were found in Romania in the Peştera cu Oase (the cave with bones) dated ~35 ka 14C BP  and Peștera Muierii (~30 ka 14C BP) .
Population movement during the Neolithic and Bronze Age shaped genetic variation in the present-day Romanian population, especially during the Middle Neolithic . During the Iron Age, in the territory defined by the Danube Basin and Carpathian Arch, archaeological records and historical sources have revealed the presence of Indo-European populations close to Thracians who probably arrived during the second millennium BC named Dacians in Transylvania and Getae in Wallachia, Dobrudja, and Bessarabia .
The partial conquest of Dacia by Romans (1st to 2nd centuries AD), with the exception of current regions of Moldavia, northeastern Transylvania, and eastern Wallachia, was followed by a period of colonization by various groups from the Roman Empire (Italians, Illyrians, Thracians, Greeks, Celts, Germans, and Eastern or North Africans) who settled mostly in Transylvania .
Starting in the 6th century, the Slavs extensively penetrated the present-day territory of Romania and were eventually assimilated into Daco-Romanian, proto-Romanian, and Romanian populations by the end of the 12th century .
The current territory of Romania was divided in the Middle Ages (ca. 14th century AD) into three different political structures: Wallachia, Moldavia, and Transylvania. Dobrudja was, during most of its medieval history, under Ottoman rule. During the next several centuries, the historical provinces of Romania were continuously under the suzerainty of the Byzantine, Austro-Hungarian, Habsburg, Ottoman, and Russian Empires. However, these empires had no major demographic impact, except in Transylvania, which underwent a massive colonization by Székelys, Saxons, and Hungarians under the domination of the Kingdom of Hungary between the 10th and 13th centuries .
The historical provinces evolved more or less separately for over 500 years under different political and religious influences, until the unification into a single country officially named Romania in the 19th century.
At present, few studies have assessed the genetic composition of Romanian populations based on mitochondrial DNA (mtDNA) haplogroups. MtDNA variation in Romanian populations has mainly been analyzed in multinational studies characterized by a relatively small number of samples collected over the entire Romanian territory to encompass the complete mtDNA haplogroup landscape. Previous studies have revealed that Romanian populations exhibit genetic similarity with other Europeans [8–11], while another study pointed to possible segregation within the Middle East populations . MtDNA variation in Romania was examined in a recent study, but the sample size was small, especially for the Dobrudja and Transylvania regions, and a detailed comparison of historical regions was not performed . Other studies have focused on the mtDNA diversity of various minority groups, such as Aromanian, Hungarian, and Roma populations [10, 14–16].
The maternal lineages of Balkan Peninsula populations exhibit genetic uniformity, with region-specific characteristics . It is worth noting that the resemblance between Western Balkan populations follows a nearest neighbor-based model that is in concordance with the geographical distribution .
To address the scarcity of information and to improve our understanding of mtDNA variation in the context of European and Middle East populations, we analyzed 714 Romanians belonging to the four historical provinces. We purpose to reveal the specific genetic differences between populations from the historical provinces that could experience demographic combinations as a consequences of past migrations, local admixture and colonization events in their past.
Written informed consent was obtained for the collection of samples and subsequent analyses before patients were entered in the study, in accordance with protocols that comply with the Declaration of Helsinki, and the study was approved by the ethics committee of the “Carol Davila” University of Medicine and Pharmacy in Bucharest, Romania.
Population data set
The samples analyzed in this study originated from the main historical provinces, Wallachia (n = 226), Dobrudja (n = 46), Moldavia (n = 235), and Transylvania (n = 207). The samples were randomly collected from maternally unrelated subjects with known genealogical information for at least three generations (parents and grandparents). For all samples, the precise affiliations to the Romanian counties (n = 41) that constitute the administrative divisions of present-day Romania were known (Additional file 1: Table S1).
Mitochondrial DNA sequencing and haplotype identification
Genomic DNA was extracted from 200 μL of whole blood in EDTA or buccal swabs using the PureLink Genomic DNA Mini Kit (Invitrogen, Carlsbad, CA, USA). For all samples, the hypervariable segments HVS I (positions 16024–16416) and HVS II (positions 1–410) of the mtDNA control region were sequenced using two pairs of primers, as previously described .
PCRs were performed in 25 μL of reaction mixture including 1× PCR buffer (15 mM Tris–HCl, pH 8.0, and 50 mM KCl), 200 μM each dNTP, 2.5 mM MgCl2, 0.2 μM each primer, 0.2 U of AmpliTaq Gold DNA Polymerase (Life Technologies, Carlsbad, CA, USA), and approximately 30 ng of DNA. The amplification products were purified using the QIAquick PCR Purification Kit (Qiagen, Hilden, Germany) and sequenced with the Big Dye Terminator v3.1 Cycle Sequencing Kit using the ABI 3130XL Genetic Analyzer (Applied Biosystems, Waltham, MA, USA). To resolve the ambiguously classified samples, a hierarchical system based on a PCR restriction fragment length polymorphism (PCR-RFLP) protocol using 18 coding region positions was used for haplogroup assignment, as described elsewhere .
The sequences were edited using ABI PRISM SeqScape v.2.5. The sequences of the HVS I and HVS II regions for each individual were aligned manually using MEGA 6 and compared with the revised Cambridge Reference Sequence rCRS [19, 20].
We amplified the two HVSI and HVSII segments in different PCRs (thermal cyclers) and corroborated the haplogroup assignation of two researchers to reduce the probability of the artificial recombination. The sequences were corroborated based on the forward and reverse sequencing results.
Haplogroup assignments were based on the HVS I and HVS II sequences of all samples in this study and were determined using online programs, i.e., HaploGrep , Mitomap , and Phylotree (mtDNA tree Build 16) .
The control region sequences of the 714 subjects in this study are available at GenBank under the following accession numbers: KT945272–KT945497 (Wallachia group), KT945940–KT945993 (Dobrudja group), KT945705–KT945939 (Moldavia group), and KT945498–KT945704 (Transylvania group).
Gene diversity parameters, including the number of sequences, haplotype diversity, nucleotide diversity, number of polymorphic sites, and mean number of pairwise differences, were estimated using DnaSP version 5. To assess neutrality, Tajima’s D  and Fu’s  were calculated using ARLEQUIN version 188.8.131.52 .
The distance matrix generated by pairwise F ST values between populations was calculated with ARLEQUIN version 184.108.40.206 (based on mtDNA haplogroup frequencies) and visualized by a multidimensional scaling (MDS) plot using SPSS 17.0 (SPSS Inc., Chicago, IL, USA). Statistical significance of F ST values was assessed using 10000 permutations.
Romanian populations were compared with published data for two groups corresponding to European and Middle East populations (data included in Additional file 2: Table S3).
A principal component analysis (PCA) was performed based on mtDNA haplogroup frequencies using the same software for comparisons among populations. A median joining network (MJN) for certain haplogroups was generated to infer phylogenetic relationships among the populations from the four Romanian provinces using Network v220.127.116.11 (available at http://www.fluxus-engineering.com). The MJN was obtained to better differentiate the haplotype frequencies among the Romanian provinces. Different mutation weights were applied in accordance with the previous papers [27–29], and point insertions and deletions were excluded from the analysis.
Lastly, the Surfer 9.0 application (Golden Software Inc., Golden, CO, USA) was used to graphically represent the geographical distribution of haplogroup frequencies (H, U, HV, T, J, K, X, N, M, V, and W) in the European region by applying the Kriging algorithm for the surface interpolation map.
We analyzed 714 samples to estimate genetic diversity in each of the four Romanian provinces (Additional file 1: Table S1). We observed high mtDNA haplotype diversity in the Wallachian population. Analyzing the control region, we detected 189 haplotypes and k = 4.530 nucleotide differences, on average. The results are summarized in Additional file 3: Table S2.
We observed similar haplotype and nucleotide diversity values for all Romanian provinces, with a slightly lower nucleotide diversity in the Dobrudja population and higher haplotype diversity in Transylvania. We observed significant deviations from neutrality tests according to Tajima’s D and Fu’s  for all Romanian provinces (Additional file 3: Table S2).
We observed length heteroplasmy in HVSI generated by a T to C transition in the poly-C tract between nucleotide positions 16184 and 16193 in 82 individuals (11.48%). In addition to length heteroplasmy, we found two sequence heteroplasmies in HVSI at position 16084 T/C in one sample and at position 16237 T/C in a second sample.
The resampling analysis for the Dobrudja sample using a 1000 replicate bootstrap indicated that the mean statistics for our data in the vector that we analyzed was 3.833. The bootstrap bias was only -0,0152 and its standard error was about 1.1364. The 95% confidence for mean statistic: the lower bound was 2.08 and the upper bound was 6. The histogram of men of bootstrap samples was nearly normal considering the great number of bootstrap replications, as depicted in the Additional file 4: Figure S4.
As expected, we were able to classify the huge majority of individuals from the four Romanian populations into nine Eurasian mitochondrial haplogroups (H, U, K, T, J, HV, V, W, and X). All mtDNA data are summarized in Additional file 1: Table S1.
The Romanian populations also exhibited sequences that belonged to the most frequent Asian haplogroups (haplogroups A, C, D, I, M, and N) and African haplogroup L. We detected haplogroups A, C, D, and I in the Romanian sample, with an overall frequency of 2.24%, consistent with the frequency in other European populations. We observed a relatively high frequency of Asian haplogroups M and N in Wallachia, Dobrudja, and Moldavia, but not in Transylvania, which also lacked the M haplogroup. The haplogroup X, entirely represented by subhaplogroup X2, was present at the highest frequency in Transylvania.
Our data indicated that haplogroup U is the second most frequent in all analyzed populations but is noticeably less frequent in Transylvania than in other areas (Fig. 1). In our sample, we detected the subhaplogroups U1, U6, and U7 at a general frequency of 1.4%, 0.14% and 0.14%, respectively. Within haplogroup U, the most ancient and prevalent subhaplogroup in Europe , U5 had the highest frequency (47.94% within haplogroup U) in all four provinces.
In Walachia, Moldavia, and Transylvania, we detected similar HV haplogroup frequencies to those observed in other European countries, but we observed the highest frequency in the Dobrudja population. With respect to haplogroups N, M, X, and V, we found different frequency distributions between Transylvania and the other three provinces, as depicted in Additional file 2: Table S3 and Fig. 1.
The high frequencies of the haplogroup M (excepting Transylvania) and U5, as well as the lower frequencies of subhaplogroup U1 reveal a pattern that could explain the distribution of Romanian populations on the PCA plot. Component loadings of PC2 indicated a high correlation coefficient for X, which is consistent with the observed high frequencies of the haplogroup X in the Wallachian, Dobrudjan, and Moldavian provinces.
To further visualize the relationships among Romanian populations analyzed here and European and Near Eastern populations, we estimated pairwise F ST based on the mitochondrial haplogroup frequencies for 19 neighboring populations, including Romanian mtDNA data from previous studies, or 41 populations from all of Europe and the Near East (data shown in Additional file 2: Table S3). For both analyses, the pairwise population F ST values were not statistically significant (p = 0.00000 ± 0.0000, F ST test), indicating no differentiation among Romanian provinces (Additional file 5: Table S4). In a statistical analysis, we only found statistically significant differentiation (p = 0.00000) between these provinces and the Caucasus, Egypt, or Turkey populations.
As anticipated, a substantial number of haplotypes observed in all Romanian provinces generated a main haplogroup H cluster with a star-like shape. In general, we detected a large number of haplotypes that were shared among Wallachia, Moldavia, and Transylvania populations. In particular, we detected haplotypes that were shared between Moldavia and Wallachia as well as between Moldavia and Transylvania. We observed high sequence diversity within haplogroup U and no star-like topology; the haplotypes were mostly shared between Moldavia and Transylvania and between Moldavia and Wallachia according to the majority of the networks. For Dobrudja, we observed shared haplotypes with Moldavia and Wallachia.
Our analysis of mitochondrial DNA control region variation for 714 samples confirmed the genetic affinity of all historical provinces to Southeastern European populations and demonstrated that Transylvania samples were most closely related to those from central Europe.
We observed similar frequency distributions for the majority of mitochondrial haplogroups among the four Romanian provinces. For other haplogroups, we detected a variation in frequencies, with overall values within the range for central and Southeastern European populations.
As highlighted by their spatial frequency distribution, we detected differences in mtDNA haplogroup frequencies among the populations of these four Romanian provinces. We observed general genetic differentiation of the Transylvania population as a whole, considering some haplogroups had higher or lower frequencies in this region than in the other three provinces (Fig. 5 and Additional file 8: Figure S3). Geographical position and proximity to Central European populations, together with historical gene flow determined by the topology of Romania could explain these data.
The genetic affinities, illustrated by the mtDNA haplogroup frequencies, among the four Romanian provinces were supported by a PCA plot in which these populations formed a clustered, and Transylvania was slightly detached from this cluster. The location of this cluster in the PCA analysis, i.e., separated from the other European populations, is in line with the results of an important study based on SNP markers showing that Romanians cluster with other Eastern European populations and providing evidence for complex admixture from Southwestern Asia .
The location of Transylvania in the European space was more evident in both MDS analyses, which are based on pairwise F ST, indicating a noticeable genetic proximity of this province to Central European populations, in contrast to the other three provinces, which show spatial integration within the Balkan populations.
These observations are consistent with previous analyses of the non-recombining region of the Y chromosome (NRY), suggesting that the Carpathians correspond with a genetic boundary, as evidenced by a discontinuity of NRY markers between the East and West of the Carpathian ridge, highlighted by the peculiarities of samples from Central Transylvania compared to Moldavia [35, 36].
The networks that show the general topology of control sequences of Romanian samples mainly indicate overlapping haplotypes between Moldavia-Wallachia and Moldavia-Transylvania, suggesting gene flow between these provinces. The substantial workforce movement from Moldavia towards these two provinces throughout the communist period supports these observations. The geographic proximity and recent population movement explain the common haplotypes observed in Dobrudja, Moldavia, and Wallachia.
The differences in the haplogroup frequency distributions and haplotype diversity in Dobrudja can also be explained by its smaller sample size compared to that of the other populations included in the study.
The presence of Asian mtDNA lineages among Romanian populations, albeit at low frequencies, indicates the flow of maternal lineages along migration routes through East Asia and Europe during different time periods, namely, the Upper Paleolithic period and/or, with a likely greater preponderance, the Middle Ages [37, 38]. It is worth mentioning that a higher frequency value of these lineages (7.9%) was earlier reported in two Hungarian ethnic groups in Transylvania, and this was attributed to their genetic proximity to west Eurasian populations . This clear discrepancy between Romanian populations and Hungarian minority groups could reflect a reduction in admixture, as was historically documented later for the Saxons in Romania . This contribution of genes from Southwestern Asia is not supported by our pairwise F ST values, which indicate statistically significant differentiation between Wallachian, Moldavian, and Transylvanian populations and the Asian population included in the analysis. The Dobrudjan population did not show the same patterns; a larger Asian influence shaped genetic variation in this province during its history.
As for haplogroup L, we found two samples with L3, one in Wallachia and the other in Dobrudja (0.28%), consistent with the low frequencies found in European populations , except in the Iberian Peninsula, where Western Andalusians have high frequencies of African lineages . The occurrence of the African haplogroup L might be the result of colonists from African provinces during the Roman period or the recent slave trade that generated movements of African people from the Ottoman Empire to East Europe at the beginning of the 17th century.
The different genetic affinities observed here could be explained by the topology of the Romanian territory, which influenced admixture among the Transylvania population and neighboring populations over time, together with the distinct historically attested migration  and colonization events , which were likely the main determinants of the close genetic resemblance of Transylvania and Central European populations. In this scenario, the Carpathian Arch could have played a defining role for the major three migration routes that were apparently used throughout history, since the Neolithic period to the Middle Ages. One route was to the Baltic region and the Northern Pontic steppe and, from there, through the Trans-Carpathian passes in the present-day Ukrainian Carpathians, towards the Tisza plain and Transylvania. The second route crossed Wallachia, Dobruja, and Moldavia, and was related to the lower Danube River basin and Black Sea, which connected the basins of the Prut, Dniester, and lower Danube to northern Europe, the Northern Pontic steppes, and the Balkan Peninsula. The third was through the passes of the Eastern and Southern Carpathians (Fig. 1). The first two routes were highly active during prehistory, the Roman period, Migration period, and Middle Ages, as evidenced by archaeological findings, and the Carpathians passes were rarely exploited for large-scale population movements.
In our mtDNA analysis, we observed a uniform distribution of the majority of haplogroups among Romanian provinces with the populations in the Wallachia, Moldavia, and Dobrudja provinces tended to cluster together within the Slav population based on the MDS scatterplots, while Transylvania was more closely related to Central European populations. We confirmed gene flow from Southwestern Asia based on pairwise population F ST values strictly in the case of Dobrudja, and this result could be easily explained by the greater Asian influence in this area throughout history.
Our findings suggesting a closer affinity of Transylvania to central Europe are supported by the observed haplogroup frequency clines for several European and Asian maternal lineages and could be attributed to different migratory routes shaped by the Carpathian Arch.
The mitochondrial DNA data in this study and the analysis of differentiation among historical regions represent a considerable extension of our knowledge of mitochondrial diversity in Romania.
Thousand years ago
Last glacial maximum
Median joining network
Non-recombining part of the Y chromosome
Principal component analysis
Polymerase chain reaction-restriction fragment length polymorphism
Cambridge reference sequence
Single nucleotide polymorphism
We acknowledge and thank all participants for their cooperation and sample contribution.
This work was supported by grants two grants of the Romanian National Authority for Scientific Research, CNCS-UEFISCDI, project numbers PN-II-RU-TE-2014-4-0527 and PN-II-ID-PCCE 2011-2-0013; and by the Spanish Ministry of Science and Innovation (GCL2016-79093/P, Basque Government to Research Groups (IT1138-16) and University of the Basque Country-UPV/EHU (UFI 11/09). The funders had no role in the study design, collection, analysis and interpretation of data, or in the writing of the report or decision to submit the article for publication.
Availability of data and material
The control region sequences of the 714 subjects generated in this study are available at GenBank through the following accession numbers: KT945272-KT945497 Wallachia group), KT945940-KT945993 (Dobrudja group), KT945705-KT945939 (Moldavia group) and KT945498-KT945704 (Transylvania group).
RC and FR conceived and designed the experiments; RC, FR, SS, PC, RP, CB and AM collected and provided the samples; RC, FR and SS performed the experiments; RC, FR, MH and SS analyzed the data; RC and MH performed the statistical analysis; RC and FR wrote the original draft; RC, FR, SS, PC MH and MC wrote the paper. All authors read and approved the final version of the manuscript.
The authors declare that they have no competing interests.
Consent for publication
Consent for publication is not applicable in this study.
Ethics approval and consent to participate
Informed written consent was obtained in accordance with protocols that comply with the Declaration of Helsinki, approved by ethical committee of “Carol Davila” University of Medicine and Pharmacy in Bucharest, Romania. The methods were carried out in accordance with the approved guidelines.
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- Mihaescu H, Creteanu R, editors. La langue latine dans le sud-est de l’Europe. Bucuresti : Editura Academiei. Paris: les Belles lettres; 1978.Google Scholar
- Trinkaus E, Moldovan O, Milota S, Bilgar A, Sarcina L, Athreya S, Bailey SE, Rodrigo R, Mircea G, Higham T, Ramsey CB, van der Plicht J. An early modern human from the Pestera cu Oase, Romania. Proc Natl Acad Sci U S A. 2003;20:11231.View ArticleGoogle Scholar
- Soficaru A, Dobos A, Trinkaus E. Early modern humans from the Pestera Muierii, Baia de Fier, Romania. Proc Natl Acad Sci U S A. 2006;46:17196.View ArticleGoogle Scholar
- Hervella M, Rotea M, Izagirre N, Constantinescu M, Alonso S, Ioana M, Lazăr C, Ridiche F, Soficaru AD, Netea MG, De-la-Rua C. Ancient DNA from South-East Europe reveals different events during early and middle neolithic influencing the European genetic heritage. PLoS One. 2015;10:6.View ArticleGoogle Scholar
- Djuvara N. A brief illustrated history of Romanians. Bucuresti: Humanitas; 2014.Google Scholar
- Protase D, Suceveanu A, Academia Română. Secţia de Ştiinţe Istorice şi Arheologice, Daco-romani, romanici, alogeni, in Istoria Romanilor, vol. 02. Bucuresti: Editura Enciclopedică; 2001. p. 21–38. 137–158; 693–737 (in Romanian).Google Scholar
- Pascu S, Theodorescu R, Academia Română. Secţia de Ştiinţe Istorice şi Arheologice, Genezele româneşti, in Istoria Romanilor, vol. 03. Bucuresti: Editura Enciclopedică; 2001. p. 412–38. in Romanian.Google Scholar
- Richards M, Macaulay V, Hickey E, Vega E, Sykes B, Guida V, Rengo C, Sellitto D, Cruciani F, Kivisild T, Villems R, Thomas M, Rychkov S, Rychkov O, Rychkov Y, Gölge M, Dimitrov D, Hill E, Bradley D, Romano V, Calì F, Vona G, Demaine, Papiha S, Triantaphyllidis C, Stefanescu G, Hatina J, Belledi M, Di R, Novelletto, Oppenheim, Nørby S, Al-Zaheri N, Santachiara-Benerecetti S, Scozari R, Torroni, Bandelt HJ. Tracing European founder lineages in the Near Eastern mtDNA pool. Am J Hum Genet. 2000;67:1251.View ArticlePubMedPubMed CentralGoogle Scholar
- Pereira L, Richards M, Goios A, Alonso A, Albarrán C, Garcia O, Behar DM, Gölge M, Hatina J, Al-Gazali L, et al. High-resolution mtDNA evidence for the late-glacial resettlement of Europe from an Iberian refugium. Genome Res. 2005;15:19.View ArticlePubMedPubMed CentralGoogle Scholar
- Bosch E, Calafell F, Gonzalez-Neira A, Flaiz C, Mateu E, Scheil HG, Huckenbeck W, Efremovska L, Mikerezi I, Xirotiris N, Grasa C, Schmidt H, Comas D. Paternal and maternal lineages in the Balkans show a homogeneous landscape over linguistic barriers, except for the isolated Aromuns. Ann Hum Genet. 2006;70:459.View ArticlePubMedGoogle Scholar
- Hervella M, Izagirre N, Alonso S, Ioana M, Netea MG, De-la-Rua C. The Carpathian range represents a weak genetic barrier in South-East Europe. BMC Genet. 2014;15:1.View ArticleGoogle Scholar
- Der Sarkissian C, Balanovsky O, Brandt G, Khartanovich V, Buzhilova A, Koshel S, Zaporozhchenko V, Gronenborn D, Moiseyev V, Kolpakov E, Shumkin V, Alt KW, Balanovska E, Cooper A, Haak W. Ancient DNA reveals prehistoric gene-flow from Siberia in the complex human population history of North East Europe. PLoS Genet. 2013;9:2.Google Scholar
- Turchi C, Stanciu F, Paselli G, Buscemi L, Parson W, Tagliabracci A. The mitochondrial DNA makeup of Romanians: a forensic mtDNA control region database and phylogenetic characterization. Forensic Sci Int Genet. 2016;24:136.View ArticlePubMedGoogle Scholar
- Egyed B, Brandstätter AA, Irwin JA, Padar Z, Parsons TJ, Parson W. Mitochondrial control region sequence variations in the Hungarian population: analysis of population samples from Hungary and from Transylvania (Romania). Forensic Sci Int Genet. 2007;1:158.View ArticlePubMedGoogle Scholar
- Brandstätter A, Egyed B, Zimmermann B, Duftner N, Padar Z, Parson W. Migration rates and genetic structure of two Hungarian ethnic groups in Transylvania, Romania. Ann Hum Genet. 2007;6:803.Google Scholar
- Mendizabal I, Lao O, Marigorta UM, Wollstein A, Gusmão L, Ferak V, Ioana M, Jordanova A, Kaneva R, Kouvatsi A, Kučinskas V, Makukh H, Metspalu A, Netea MG, de Pablo R, Pamjav H, Radojkovic D, Rolleston SJH, Sertic J, Macek M, Comas D, Kayser M. Reconstructing the population history of European Romani from genome-wide data. Curr Biol. 2012;22:2342.View ArticlePubMedGoogle Scholar
- Kovacevic L, Tambets K, Ilumäe A-M, Kushniarevich A, Yunusbayev B, Solnik A, Bego T, Primorac D, Skaro V, Leskovac A, Jakovski Z, Drobnic K, Tolk HV, Kovacevic S, Rudan P, Metspalu E, Marjanovic D. Standing at the gateway to Europe - The genetic structure of Western Balkan populations based on autosomal and haploid markers. PLoS One. 2014;9:8.View ArticleGoogle Scholar
- Santos C, Montiel R, Angles N, Lima M, Francalacci P, Malgosa A, Abade A, Aluja. Determination of human caucasian mitochondrial DNA haplogroups by means of a hierarchical approach. Hum Biol. 2004;76:431.View ArticlePubMedGoogle Scholar
- Anderson S, Bankier AT, Barrell BG, de Bruijn MHL, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJH, Staden R, Young IG. Sequence and organization of the human mitochondrial genome. Nature. 1981;290:457.View ArticlePubMedGoogle Scholar
- Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet. 1999;23:147.View ArticlePubMedGoogle Scholar
- Kloss-Brandstätter A, Pacher D, Schönherr S, Weissensteiner H, Binna R, Specht G, Kronenberg F, HaploGrep. A fast and reliable algorithm for automatic classification of mitochondrial DNA haplogroups. Hum Mutat. 2011;32:25.View ArticlePubMedGoogle Scholar
- Brandon MC, Lott MT, Nguyen KC, Spolim S, Navathe SB, Baldi P, Wallace DC. MITOMAP: a human mitochondrial genome database--2004 update. Nucleic Acids Res. 2005;33:611.View ArticleGoogle Scholar
- van Oven M, Kayser M. Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation. Hum Mutat. 2009;30:386.View ArticleGoogle Scholar
- Tajima F. Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics. 1989;123:585.PubMedPubMed CentralGoogle Scholar
- Fu YX. Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics. 1997;147:925.Google Scholar
- Excoffier L, Lischer HEL. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Mol Ecol Resour. 2010;10:564.View ArticlePubMedGoogle Scholar
- Meyer S, Weiss G, Von Haeseler A. Pattern of nucleotide substitution and rate heterogeneity in the hypervariable regions I and II of human mtDNA. Genetics. 1999;152:1103.PubMedPubMed CentralGoogle Scholar
- Allard MW, Miller K, Wilson M, Monson K, Budowle B. Characterization of the Caucasian haplogroups present in the SWGDAM forensic mtDNA dataset for 1771 human control region sequences. Scientific Working Group on DNA Analysis Methods. J Forensic Sci. 2002;47:1215.View ArticlePubMedGoogle Scholar
- Santos C, Montiel R, Sierra B, Bettencourt C, Fernandez E, Alvarez L, Lima M, Abade A, Aluja MP. Understanding differences between phylogenetic and pedigree-derived mtDNA mutation rate: a model using families from the Azores Islands (Portugal). Mol Biol Evol. 2005;22:1490.View ArticlePubMedGoogle Scholar
- Schneider S, Excoffier L. Estimation of past demographic parameters from the distribution of pairwise differences when the mutation rates vary among sites: application to human mitochondrial DNA. Genetics. 1999;152:1079.PubMedPubMed CentralGoogle Scholar
- Richards M, Macaulay V, Torroni A, Bandelt H-J. In search of geographical patterns in European mitochondrial DNA. Am J Hum Genet. 2002;71:1168.View ArticlePubMedPubMed CentralGoogle Scholar
- Brandstätter A, Zimmermann B, Wagner J, Göbel T, Röck AW, Salas A, Carracedo A, Parson W. Timing and deciphering mitochondrial DNA macro-haplogroup R0 variability in Central Europe and Middle East. BMC Evol Biol. 2008;8:191.View ArticlePubMedPubMed CentralGoogle Scholar
- Malyarchuk B, Derenko M, Grzybowski T, Perkova M, Rogalla U, Vanecek T, Tsybovsky I. The peopling of Europe from the mitochondrial haplogroup U5 perspective. PLoS One. 2010;5:6.View ArticleGoogle Scholar
- Hellenthal G, Busby GBJ, Band G, Wilson JF, Capelli C, Falush D, Myers S. A genetic atlas of human admixture history. Science. 2014;343:747.View ArticlePubMedPubMed CentralGoogle Scholar
- Stefan M, Stefanescu G, Gavrila L, Terrenato L, Jobling MA, Malaspina P, Novelletto A. Y chromosome analysis reveals a sharp genetic boundary in the Carpathian region. Eur J Hum Genet. 2001;9:27.View ArticlePubMedGoogle Scholar
- Varzari A, Kharkov V, Nikitin AG, Raicu F, Simonova K, Stephan W, Weiss EH, Stepanov V. Paleo-Balkan and Slavic contributions to the genetic pool of Moldavians: insights from the Y chromosome. PLoS One. 2013;8:1.View ArticleGoogle Scholar
- Derenko M, Malyarchuk B, Grzybowski T, Denisova G, Dambueva I, Perkova M, Dorzhu C, Luzina F, Lee HK, Vanecek T, Villems R, Zakharov I. Phylogeographic analysis of mitochondrial DNA in northern Asian populations. Am J Hum Genet. 2007;81:1025.View ArticlePubMedPubMed CentralGoogle Scholar
- Mielnik-Sikorska M, Daca P, Malyarchuk B, Derenko M, Skonieczna K, Perkova M, Dobosz T, Grzybowski T. The history of Slavs inferred from complete mitochondrial genome sequences. PLoS One. 2013;8:1.View ArticleGoogle Scholar
- Salas A, Richards M, De la Fe T, Lareu M-V, Sobrino B, Sánchez-Diz P, Macaulay V, Carracedo A. The making of the African mtDNA landscape. Am J Hum Genet. 2002;71:1082.View ArticlePubMedPubMed CentralGoogle Scholar
- Hernández CL, Reales G, Dugoujon J-M, Novelletto A, Rodríguez JN, Cuesta P, Calderón R. Human maternal heritage in Andalusia (Spain): its composition reveals high internal complexity and distinctive influences of mtDNA haplogroups U6 and L in the western and eastern side of region. BMC Genet. 2014;15:1.View ArticleGoogle Scholar