1st row: Masinissa • Hanibal • Victor I • Septimius Severus • Caracalla • Juba I 2nd row: Ibn Arabi • Augustine • Apuleius • Tertullian • Tarik ibn Ziyad • Leo Africanus 3rd row: Ibn Khaldoun • Dihya • Abd ar-Rahman I • Ibn al-Jazzar • Ibn Battuta • Averroes 4th row: Omar Mukhtar • Kateb Yacine • Mustapha Benboulaïd • Ibn Badis • Moufdi Zakaria • Aboul-Qacem Echebbi5th row: Hindi Zahra • Idir • Assia Djebar • Tahar Ben Jelloun • Yasmina Khadra • Zidane
|Regions with significant populations|
|Europe (mostly France)||~10 million|
Predominantly Sunni IslamChristian and Jewish minorities
|Related ethnic groups|
|Population statistics from the world factbook (July 2011 pop est.)|
Maghrebis or Maghrebian people or Maghrebians (or North Africans) are the inhabitants of the Maghreb countries (Algeria, Morocco, Tunisia, Libya, Mauritania). During Al-Andalus, Maghrebis were known as Moors.
- 1 Origins
- 2 Religion
- 3 Culture
- 4 Diaspora
- 5 Anthropology, genetics and linguistics
- 6 See also
- 7 References and notes
- 8 External links
The inhabitants of the region are predominantly "Berber And Arab-Berber" but this term implies a complete fusion of the two groups which is not the case. Whereas Arabs and Berbers, united through Islam are the main ethnic and cultural elements, it is important to bear in mind that over the centuries the Maghreb has been a melting-pot of many other ethnic groups and cultures. Before the Arab conquest Carthagenns, Greeks, Romans, Vandals, and Byzantines colonized the Maghreb and contributed to the development of its culture. Later, moriscos and muladies, that is, Iberian who had earlier converted to the Muslim faith and were fleeing, together with ethnic Arab and Berber Muslims, from the Christian Reconquista settled to the Maghreb. Among are Turks who came over with the expansion of the Ottoman Empire. A small Turkish descended population exists, particularly in Tunisia and Algeria. Other European contributions included French, Italians, and others captured by the corsairs and then turned into slaves.
Nowadays, a majority of the current population in the Maghreb consider themselves generally Arab in identity, regardless of mixed ethnic or linguistic heritage. There are significant non-Arab or non-Arab identifying populations in the region and most important of the non-Arab populations found throughout the Maghreb, particularly in Morocco and Algeria, are the Berbers. They represented the majority of the pre-Islamic population. After the arrival of Islamic Arabs, Berbers assimilated in large numbers to Arab or mixed Arab-Berber ethnic identities.
Historically the Maghreb was also home to significant Jewish communities, including the Maghrebim Jews, who predated the 7th century introduction and conversion of the majority of Berbers to Islam. Later largely augmented by Iberian Sephardi Jews, fleeing the Iberian Catholic Reconquista, established a presence in North Africa, chiefly in the urban trading centers. Many Sephardic Jews emigrated to North America in the early 19th century or to France and Israel later in the 20th century.
On the Saharan southern edge of the Maghreb are large communities of black populations, sometimes called Haratin, who orally identify themselves as the original inhabitants of southern oasis.
|This section does not cite any references or sources. (September 2009)|
Historic records of religion in the Maghreb region show its gradual inclusion in the Classical World, with coastal colonies established first by Phoenicians, some Greeks, and later extensive conquest and colonization by the Romans. By the 2nd century common era, the area had become a center of Latin-speaking Christianity. Both Roman settlers and Romanized populations converted to Christianity. The region produced figures such as Christian Church writer Tertullian (c. 155 – c. 202); and Christian Church martyrs or leading figures such as St Cyprian of Carthage (+ 258); Saint Monica; her son the philosopher St. Augustine, Bishop of Hippo I (+ 430) (1); and St Julia of Carthage (5th century). The region was a birthplace of many Christians movements like arianism and donatism, now casted-off.
The domination of Christianity ended when Arab invasions brought Islam in 647. Carthage fell in 698 and the remainder of the region followed in subsequent decades. Gradual Islamization proceeded, although surviving letters showed correspondence from regional Christians to Rome up until the 9th century. Christianity was still a living faith. Christian bishoprics and dioceses continued to be active, with relations continuing with Rome. As late as Pope Benedict VII (974-983) reign, a new Archbishop of Carthage was consecrated. Evidence of Christianity in the region then faded through the 10th century.
During the 7th century, the region's peoples began their nearly total conversion to Islam. There is a small but thriving Jewish community, as well as a small Christian community. Most Muslims follow the Sunni Maliki school. Small Ibadi communities remain in some areas. A strong tradition of venerating marabouts and saints' tombs is found throughout regions inhabited by Berbers. Any map of the region demonstrates the tradition by the proliferation of "Sidi"s, showing places named after the marabouts. Like some other religious traditions, this has substantially decreased over the 20th century. A network of zaouias traditionally helped proliferate basic literacy and knowledge of Islam in rural regions.
According to Michel Tribalat, a researcher at INED, there were 3.5 million people of Maghrebi origin (with at least one grandparent from Algeria, Morocco or Tunisia) living in France in 2005 corresponding to 5.8% of the total French metropolitan population (60.7 millions in 2005). Maghrebis have settled mainly in the industrial regions in France, especially in the Paris region. Many famous French people like Edith Piaf, Isabelle Adjani, Arnaud Montebourg, Alain Bashung, Dany Boon and many others have Maghrebi ancestry.
Below is a table of population of Maghrebi origin in France, numbers are in thousands:
|Country||1999||2005||% 1999/2005||% French population
(60.7 millions in 2005)
|Born in France||1,003||1,186|
|Born in France||482||576|
|Born in France||215||236|
|Immigrants||1 299||1 526||2.5%|
|Born in France||1 700||1 998||3.3%|
In 2005, the percentage of young people under 18 of maghrebi origin (at least one immigrant parent) were about 7% in Metropolitan France, 12% in Greater Paris, 13% in Lyon, 21% in Perpignan, 22% in French département of Seine-Saint-Denis, 37% in 18th arrondissement of Paris and 40% in several arrondissements of Marseilles.
Anthropology, genetics and linguistics
Various disciplines shed light on the origin of the Northwest-Africans (Berbers and Arabs).
The genetic proximity observed between the Northwest-Africans and Southern Europeans is due to the fact that both these groups shared a common ancestor either in the Upper Paleolithic, in the Neolithic or alternatively during history with the invasion and the occupation during nearly seven centuries of the Iberian Peninsula by Moorish troops. A genetic study published in January 2012 stated that the indigenous North African ancestry appears most closely related to populations outside of Africa but "divergence between Maghrebi peoples and Near Eastern/Europeans likely precedes the Holocene (>12,000 ya)."
The Y-chromosome genetic structure of the Maghreb population seems to be mainly Modulated by geography, The Y-DNA Haplogroups E3b and J, which are so common among the population of North African and the Middle East, Haplogroups E3b and J, are the most widespread among North African groups especially E1b1b1b (E-M81, formerly E3b1b) which is typical of the indigenous Berbers of North-West Africa. In some parts of Tunisia E1b1b1b can peak at 100% of the population. Followed by Haplogroup J especially J1 , which is typically Middle Eastern which can reach frequencies of 40% in the region, and has its highest density founded in the Southwestern Arabian Peninsula, Followed by Haplogroup R1 which has been observed in North African though with lower frequency. The Y-DNA Haplogroups shown above are observed in both Arab and Berber-speakers.
The Northwest-African Y chromosome pool (including both Berber and Arab populations) may be summarized as follows where only two haplogroups E1b1b and J comprise generally more than 80% of the total chromosomes:
- E1b1b (mainly E-M81) (50-100%)
- J (mainly J1-M267) (0-45%)
- R1b (0-15%)
- Sub-Saharan and other haplogroups (0-8%)
E1b1b1b (E-M81) is the most common Y haplogroup among North African Arabs and Berbers dominated by its sub-clade E-M183. It is thought to have originated in North Africa 5,600 years ago. Colloquially referred to as the "Berber marker" for its prevalence among Mozabite, Middle Atlas, Kabyle and other Berber groups, E-M81 is also quite common among North African Arab groups (45% in Oran). It can reach frequencies of up to 100% in the Maghreb.
Regarding J1-M267, according to a recent study in 2011 about Tunisia, it is significantly more abundant in the urban (31.3%) than in the rural total population (2.5%). According to the authors, these results could be explained supposing that Arabization in Tunisia was a military enterprise, therefore, mainly driven by men that displaced native Berbers to geographically marginal areas but that frequently married Berber women.
|Population||Nb||A/B||E(xE1b1b)||E1b1b1 (M35)||E1b1b1a (M78)||E1b1b1b (M81)||E1b1b1c (M123)||F||K||G||I||J1||J2||R1a||R1b||Other||Study|
|1 Algeria/Oran||102||0||7.9%||0||5.9%||45.1%||0||0||0||0||0||22.5%||4.9%||1%||11.8%||1%||Robino et al. (2008)|
|2 Algeria/Algiers||35||0||2.9%||0||11.4%||42.9%||0||11.8%||2.9%||0||0||22.9%||5.7%||0||0||0||Arredi et al. (2004)|
|3 Algeria/Kabyles/Tizi Ouzou||19||0||0||0||0||47.4%||10.5%||10.5%||0||0||0||15.8%||0||0||15.8%||0||Arredi et al. (2004)|
|4 Algeria/Mozabites||67||0||4.5%||0||1.5%||86.6%||1.5%||0||0||1.5%||0||1.5%||0||0||3%||0||Dugoujon et al. (2009)|
|5 Tunisia/Tunis||148||0||2%||3.4%||5.4%||37.8%||2.7%||4.7%||0.7%||0||0||32.4%||3.4%||0.7%||6.1%||0.7%||Arredi et al. (2004)|
|6 Tunisia||52||0||0||9.6%||15.4%||32.7%||0||1.9%||1.9%||0||0||34.6%||3.8%||0||0||0||Onofri et al. (2008)|
|7 Tunisia/Bou Omrane||40||0||5%||0||5%||87.5%||0||2.5%||0||0||0||0||0||0||0||0||Ennafaa et al. (2011)|
|8 Tunisia/Bou Saad||40||0||0||0||0||92.5%||0||0||0||0||0||5%||0||0||0||2.5%||Ennafaa et al. (2011)|
|9 Tunisia/Jerbian Arabs||46||2.2%||0||0||15.2%||60.9%||4.3%||0||0||0||0||8.7%||2.2%||4.3%||2.2%||0||Ennafaa et al. (2011)|
|10 Tunisia/Jerbian Berbers||47||0||0||0||17%||76.6%||0||4.25%||2.1%||0||0||0||0||0||0||0||Ennafaa et al. (2011)|
|11 Tunisia/Chenini–Douiret Berbers||27||0||0||0||0||100%||0||0||0||0||0||0||0||0||0||0||Karima Fadhlaoui-Zid et al. (2011)|
|12 Tunisia/Sened Berbers||35||0||0||0||0||65.7%||0||2.9%||0||0||0||31.4%||0||0||0||0||Karima Fadhlaoui-Zid et al. (2011)|
|13 Tunisia/Jradou Berbers||32||0||0||0||0||100%||0||0||0||0||0||0||0||0||0||0||Karima Fadhlaoui-Zid et al. (2011)|
|14 Tunisia/Andalusian Zaghouan||32||0||0||0||3.1%||40.6%||0||9.4%||0||0||0||43.8%||3.1%||0||0||0||Karima Fadhlaoui-Zid et al. (2011)|
|15 Tunisia/Cosmopolitan Tunis||33||0||0||3.0%||6.0%||54.5%||3.0%||6.0%||0||3.0%||0||24.2%||0||0||0||0||Karima Fadhlaoui-Zid et al. (2011)|
|16 Morocco||221||0||6.4%||4.1%||6.8%||65%||0||0.9%||1.8%||0.9%||0.5%||5%||4.1%||0||4.1%||0||Fregel et al. (2009)|
|17 Morocco||51||3.9%||5.9%||5.9%||5.9%||54.9%||0||0||0||0||0||19.6%||0||0||3.9%||0||Onofri et al. (2008)|
|18 Morocco/Amizmiz Valley||33||3%||6.1%||0||3%||84.8%||3%||0||0||0||0||0||0||0||0||0||Alvarez et al. (2009)|
|19 Sahrawi||89||0||20.2%||0||0||59.6%||0||0||0||0||0||20.2%||0||0||0||0||Fregel et al. (2009)|
|20 Libya/Tuaregs from Fezzan||47||0||42.5%||0||0||48.9%||0||0||0||0||0||0||0||0||6.4%||2.1%||Ottoni et al. (2011)|
Many studies have attempted to describe the genetic diversity of Northwest-African populations, evaluating mitochondrial DNA (mtDNA) sequence variation and the results may be summarized as follows (data for 536 individuals from 9 populations : Morocco (Asni, Bouhria, Figuig, Souss), Algeria (Mozabites), Tunisia (Chenini-Douiret, Sened, Matmata, Jerba)):
- Total Eurasian lineages (H, HV0, HV, R0, J, T, U (without U6), K, N1, N2, X) : 50-90% with an average of about 5/8
- Total sub-Saharan lineages (L0, L1, L2, L3, L4-L5) : 3-50% with an average of about 2/8
- Total North African lineages (U6, M1) : 0-35% with an average of about 1/8
The Northwest-African mtDna pool is characterized by an "overall high frequency of Western Eurasian haplogroups, a somehow lower frequency of sub-Saharan L lineages, and a significant (but differential) presence of North African haplogroups U6 and M1." According to Cherni et al. 2009 "the post-Last glacial maximum expansion originating in Iberia not only led to the resettlement of Europe but also of North Africa".
According to an Ottoni et al. 2010, besides the "autochthonous" South-Saharan component, the maternal pool of Northern Africa appears to be characterized by at least two other major components: (i) a Levantine contribution (i.e. haplogroups U6 and M1), associated with the return to Africa around 45 kya, and (ii) a more recent West European input associated with the postglacial expansion.
Until recently, some papers suggested that the distribution of the main L haplogroups in North Africa was mainly due to trans-Saharan slave trade. However in September 2010, a thorough study about Berber mtDNA by Frigi et al. concluded that most of L haplogroups were much older and introduced by an ancient African gene flow around 20,000 years ago.
In an autosomal study in 2012 by Henn et al., the authors conclude that North African populations retain a unique signature of early "Maghrebi" ancestry, but are not a homogenous group and most display varying combinations of five distinct ancestries (Maghrebi, European, Near Eastern, eastern and western sub-Saharan Africa). The majority of their ancestry derives from populations outside of Africa and is the result of at least three distinct episodes:
- ancient "back-to-Africa" gene flow prior to the Holocene
- more recent gene flow from the Near East resulting in a longitudinal gradient
- limited but very recent migrations from sub-Saharan Africa.
They observed two distinct, opposite gradients of ancestry : an east-to-west increase in likely autochthonous North African ancestry likely derived from "back-to-Africa" gene flow more than 12,000 years ago and an east-to-west decrease in likely Near Eastern Arabic ancestry. The indigenous North African ancestry is more frequent in populations with historical Berber ethnicity. They also find significant signatures of sub-Saharan African ancestry that vary substantially among populations. According to the authors "these sub-Saharan ancestries appear to be a recent introduction into North African populations, dating to about 1,200 years ago in southern Morocco and about 750 years ago into Egypt, possibly reflecting the patterns of the trans-Saharan slave trade that occurred during this period".
Recent genetic analysis of North African populations have found that, despite the complex admixture genetic background, there is an autochthonous genomic component which is likely derived from “back-to-Africa” gene flow older than 12,000 years ago (ya) (i.e., prior to the Neolithic migrations). This local population substratum seems to represent a genetic discontinuity with the earliest modern human settlers of North Africa (those with the Aterian industry) given the estimated ancestry is younger than 40,000 years ago. North Morocco, Libya and Egypt carry high proportions of European and Near Eastern ancestral components, whereas Tunisia and Saharawi are those populations with highest autochthonous North African component.
- Average ancestry proportions in North African populations estimated by ADMIXTURE for k = 4 different ancestries (October 2012)
|Population||N||Maghreb||Europe||Near East||Sub-Saharan Africa|
According to a recent study in 2013 by Botigué et al using genome-wide SNP data from over 2,000 individuals, "southwestern European populations averaged between 4% and 20% of their genomes assigned to a North African ancestral cluster, whereas this value did not exceed 2% in southeastern European populations". The highest North African admixture (20%) was found into Canarians while in the Iberian peninsula, the average was 10-12%.
In the Iberian Peninsula, North African male haplogroups, especially E1b1b1b (E-M81), E1b1b1a-b (M78 derived chromosomes showing the rare DYS439 allele 10 or E-V65) and a subset of J1 (M267 derived), are found in significant amounts with an average frequency of about 7-8% in the peninsula with frequencies surpassing 10% in some regions, like 18.6% in Cantabria.
- Historically introduced NW African types in Italy and Iberia (Capelli et al. (2009))
|J1 (subset)||Total %|
Concerning the level of male genetic admixture in Iberia, an important study by Adams et al. 2008 that analysed 1140 individuals in Iberia found a mean North African admixture of 10.6%, with wide geographical variation, ranging from 2.5% in Catalonia, 11.8% in North Portugal, 16.1% in South Portugal, 20.8% in Galicia to 21.7% in Northwest Castile.
|Iberian region||%NW African
MtDna (female lineages) genetic studies on Iberian populations also show that North African mitochondrial DNA sequences (haplogroup U6) are found at much higher levels than those generally observed elsewhere in Europe. Although the overall absolute frequency of U6 is low (2.4%), this signals a possible current North African ancestry proportion of 8%–9%, because U6 is not a common lineage in North Africa itself. U6 reaches its highest frequency in North Portugal at about 4-6% where Gonzalez et al. 2003 estimated a possible North African ancestry proportion of 27%.
Iberia is also the region in Europe with the highest frequency of the female mediated mtDNA haplogroup L of Sub-Saharan origin, likely a result of Berber and Arab colonization or African slave trade. Pereira et al. 2005, who analysed 1045 Iberian individuals, found sub-Saharan mtDNA L haplogroups at rates of 11.38% in south Portugal, 5.02% in Center Portugal, 3.21% in North Portugal and 3.26% in Galicia. According to Alvarez et al. 2010 who found L haplogroups at a rate of 4.70% in the Spanish province of Zamora, "as the Hts found in the area are also shared with North African populations, we cannot discard the possibility that these lineages derived from the North African Muslim permanence in the Iberian Peninsula". In another study, Casas et al. 2006 extracted DNA from human remains that were exhumed from historic burial sites in Al-Andalus, Spain (between 12th-13th century). The frequency of Sub-Saharan lineages detected in the medieval samples was 14.6% and 8.3% in the present population of Priego de Cordoba. The authors suggest both the Muslim occupation, and prehistoric migrations before the Muslim occupation would have been the source of these lineages. Brehm at al. 2003 also found a significant Sub-Saharan imprint in the Autonomous regions of Portugal, with L haplogroups constituting about 13% of the lineages in Madeira and 3.4% in the Azores.
|Iberian region/NW African mtDna > 2%||N||%U6||%L||Total||Study|
|Portugal, Alcacer do Sal||50||6.00%||22.00%||28.00%||Pereira 2010|
|Spain, Canary islands (Avg)||300||14.00%||6.60%||20.60%||Brehm 2003|
|Portugal, Madeira||155||3.90%||12.90%||16.80%||Brehm 2003|
|Spain, Huelva (Andalusia)||135||8.86%||5.70%||14.56%||Hernandez 2014|
|Portugal, South||123||1.63%||11.38%||13.01%||Pereira 2005|
|Portugal, South||203||0.49%||10.84%||11.33%||Achilli 2007|
|Portugal, Coruche||160||0.62%||8.7%||9.32%||Pereira 2010|
|Spain, Priego de Cordoba||108||0.93%||8.33%||9.26%||Casas 2006|
|Portugal, Center||203||2.46%||6.40%||8.87%||Achilli 2007|
|Portugal, North||187||5.35%||3.21%||8.56%||Pereira 2005|
|South Iberian Peninsula||310||0.65%||7.42%||8.07%||Casas 2006|
|Portugal, Center||239||2.51%||5.02%||7.53%||Pereira 2005|
|Portugal, North||188||4.26%||3.19%||7.45%||Achilli 2007|
|Spain, Galicia||92||2.17%||3.26%||5.43%||Pereira 2005|
|Spain, Zamora||214||0.47%||4.67%||5.14%||Alvarez 2010|
|Portugal, Açores||179||1.70%||3.40%||5.10%||Brehm 2003|
|Spain, NorthWest||216||1.39%||3.70%||5.09%||Achilli 2007|
|Spain, Center||148||4.05%||0.68%||4.73%||Achilli 2007|
|Spain, NorthEast||118||1.69%||2.54%||4.24%||Pereira 2005|
|Spain, multiple regions||312||1.28%||2.88%||4.16%||CarlosAlvarez 2007|
|Portugal, Pias||75||0.00%||3.9%||3.9%||Pereira 2010|
|Spain, Andalusia||114||1.75%||1.75%||3.51%||Achilli 2007|
|Spain, Granada (Andalusia)||117||2.48%||0.83%||3.31%||Hernandez 2014|
|Spain, Leon||61||1.64%||1.64%||3.28%||Pereira 2005|
|Spain, Andalusia||65||1.54%||1.54%||3.08%||Pereira 2005|
|Spain, NorthEast||179||1.12%||1.68%||2.79%||Achilli 2007|
|Spain, Castile||38||2.63%||0.00%||2.63%||Pereira 2005|
|Spain, Balearic islands||231||0.00%||2.16%||2.16%||Picornell 2005|
In Canary Islands, a study by Nicole Maca-Meyer in 2003 found mtDna haplogroup U6 at rate of 14% in the present-day Canary Islands populations reflecting the Berber origin of the Guanches, the aboriginal population of the Canary Islands. In this study they compared aboriginal Guanche mtDNA (collected from Canarian archaeological sites) to that of today's Canarians and concluded that, "despite the continuous changes suffered by the population (Spanish colonization, slave trade), aboriginal mtDNA lineages constitute a considerable proportion [42–73%] of the Canarian gene pool". MtDNA haplogroup L were also found at rate of 6.6% and E-M81 at a rate of 8.28% with frequencies over 10% in the three largest islands of Tenerife (10.68%), Gran Canaria (11.54%) and Fuerteventura (13.33%). According to Fregel et al. 2009 the presence of autochthonous North African E-M81 lineages, and also other relatively abundant markers (E-M78 and J-M267) from the same region in the indigenous Guanche population, "strongly points to that area [North Africa] as the most probable origin of the Guanche ancestors". In this study, they estimated that, based on Y-chromosome and mtDNA haplogroup frequencies, the relative female and male indigenous Guanche contributions to the present-day Canary Islands populations were respectively of 41.8% and 16.1%.
NW African mtDna
|La Gomera||46||50.01%||10.86%||60.87%||Fregel 2009|
|El Hierro||32||21.88%||12.49%||34.37%||Fregel 2009|
|Gran Canaria||80||11.25%||10%||21.25%||Fregel 2009|
|La Palma||68||17.65%||1.47%||19.12%||Fregel 2009|
An autosomal study in 2011 found an average Northwest African influence of about 17% in Canary Islanders with a wide interindividual variation ranging from 0% to 96%. According to the authors, the substantial Northwest African ancestry found for Canary Islanders supports that, despite the aggressive conquest by the Spanish in the 15th century and the subsequent immigration, genetic footprints of the first settlers of the Canary Islands persist in the current inhabitants. Paralleling mtDNA findings, the largest average Northwest African contribution was found for the samples from La Gomera.
|Total Canary Islanders||104||17.40%|
In Sicily, the contribution of North African populations is estimated to be about 6%-8% which shows a "genetic affinity between Sicily and North Africa". In Italy, North African haplogroups were found especially in a region of Southern Italy (East Campania, Northwest Apulia, Lucera) at frequency of 4.7% due to Frederick II’s relocation of Sicilian Muslims in the city of Lucera in the 13th century. Haplogroup U6 have also been detected in Sicily and Southern Italy at very low levels.
Haplogroup E-M81 is also found in some regions of France (excluding recent immigration as only men with French surname were analysed). 2.70% (15/555) overall with frequencies surpassing 5% in Auvergne (5/89) and Île-de-France (5/91).
According to a genetic study in 2000 based on HLA, French from Marseille "are more or less isolated from the other western European populations. They are in an intermediate position between the North Africans (Algerians from Algiers and Oran; Tunisians) and the western Europeans populations (France, Spain, and Portugal)". According to the authors "these results cannot be attributed to recent events because of the knowledge of the grandparents’ origin" in the sample. This study reveals "that the southern French population from Marseilles is related genetically to the southwestern Europeans and North Africans, who are geographically close" and that "a substantial gene flow has thus probably been present among the populations of these neighboring areas".
As a consequence of Spanish and Portuguese colonization of Latin America, North African haplogroups are also found throughout Latin America especially in Brazil and Cuba where frequencies surpass generally 5%. and among Hispanic men in USA.
According to Fregel et al. (2009), the fact that male North African E-M81 and female U6 lineages from the Canaries have been detected in Cuba and Iberoamerica, demonstrates that Canary Islanders with indigenous Guanche ancestors actively participated in the American colonization.
The Maghreb have hosted several languages. Berber or also known as Amazigh is the indigenous language family of the region, belonging to the greater Afro-Asiatic family. Two thousand years ago, Punic, Berber and Latin would have alternated in communication among the populations of the Western parts of North Africa and the rest of the Mediterranean basin. The Arabic language as known throughout the region nowadays arrived later in the Maghreb with the historical Arab conquest and Islam. This language ousted the Berber languages in its various variants, although the process was a long time one, Berber has long been a very prominent language in Algeria and Morocco till our contemporary era. Romance language itself might still have existed in the Maghreb in the 12th century. The Maghreb once again became partly Romance with colonisation. From the 1830s, the French began by conquering Algeria, where French was declared the official language of the country. It also obtains the position of highly placed languages of local elites.
In today's Maghreb, only Modern Standard Arabic possesses the status of official language, despite Maghrebi Arabic and Berber being the languages of most people. In spite of that, French is doing well in the region at the start of the 21st century.
English is becoming quite popular as a second language subject at schools across the Maghreb.
- Maghrebi Jews
- Northwest Africa
- List of Maghrebis
- E1b1b1b (Y-DNA)
- Berber Revolt
- Berber Spring
- Muslim conquest of North Africa
- Berbers and Islam
- Berber Jews
- Christian Berbers
- Arabized Berber
- Kabylism, Algerianism, Berberism
- Barbary Coast
References and notes
||This 2 lacks information such as ISBNs for the books listed in it.|
- Population of Algeria exceeds 37M in 2012
- without Ceuta and Melilla
- "Estimé à six millions d'individus, l'histoire de leur enracinement, processus toujours en devenir, suscite la mise en avant de nombreuses problématiques...", « Être Maghrébins en France » in Les Cahiers de l’Orient, n° 71, troisième trimestre 2003
- Maghreb people represent 45% of people born in Arab countries who emigrated to Europe and N.America, they are 41% of the all Immigrants in Europe
- "The Moors were simply Maghrebis, inhabitants of the maghreb, the western part of the Islamic world, that extends from Spain to Tunisia, and represents a homogeneous cultural entity", Titus Burckhardt, "Moorish culture in Spain". Suhail Academy. 1997, p.7
- Smail Chadli, Afrique du Nord: Anthropologie Génétique et Histoire du peuplement Humain, Anthropologie Génétique et Histoire du peuplement Humain. Antropo, 20, 41-48
- Michèle Tribalat , « Mariages « mixtes » et immigration en France », Espace populations sociétés [En ligne] , 2009/2 | 2009 , mis en ligne le 01 avril 2011
- Carolyn Burke. No Regrets: The Life of Edith Piaf, Bloomsbury Publishing, 2011, p.5
- Les immigrés, les descendants d'immigrés et leurs enfants, Pascale Breuil-Genier, Catherine Borrel, Bertrand Lhommeau, Insee 2011
- Michèle Tribalat, Revue Commentaire, juin 2009, n°126, p.436
- Michèle Tribalat, Les yeux grands fermés, Denoël, 2010
- Robert Castel, La discrimination négative, Paris, La République des idées/Seuil, 2007
- Drouet, Jean-Baptiste; Alex Masson (December 2008). "Culture Le cinéma français est-il raciste ?". Première (in French): 75–78.
- Marie-Claude Chamla in Physical Anthropology of European Populations, Mouton, 1980, p.264: "Basically, there are three main types to be found (...). The Mediterranean element is always the major one making up about three-quarters of the population , and it appears to have three recognizable variants: (1) an Ibero-insular type (...); (2) an Atlanto-Mediterranean type (...); (3) finally, a type called "Saharan", rather infrequent (...). A second element which is fundamental but not widespread has been classed as Alpine by certain authors. (...) They constitute about one-tenth of the population, but it does not seem that they can be confused with the European Alpine type (...). A third element with Armenoid ties characterizes less than ten percent of the subjects (...). Beside these classes, some traces of the ancient Mechta-Afalou type can be found (...)."
- Marie-Claude Chamla in Physical Anthropology of European Populations, Mouton, 1980, p.265-66 :"Green or light chestnut-colored eyes can frequently be found in the mountains areas (Kabylie and especially aures) and in the high plains of the east. This relative frequency of "mixed" colored eyes is not peculiar to Algerians but is apparent in other countries of North Africa as well, especially in Morocco (...) The frequency of pale-colored eyes (blue and gray), varies from two to fifteen percent according the region concerned"
- Coudray C, Olivieri A, Achilli A et al. (March 2009). "The Complex and Diversified Mitochondrial Gene Pool of Berber Populations". Annals of Human Genetics 73 (2): 196–214. doi:10.1111/j.1469-1809.2008.00493.x. ISSN 0003-4800. PMID 19053990.
- Henn BM, Botigué LR, Gravel S, Wang W, Brisbin A et al. (January 2012). "Genomic Ancestry of North Africans Supports Back-to-Africa Migrations". In Schierup, Mikkel H. PLOS Genetics 8 (1): e1002397. doi:10.1371/journal.pgen.1002397. PMC 3257290. PMID 22253600.
- combined (Semino et al. 2004 30%) & (Arredi et al. 2004 32%)
- Alshamali F, Pereira L, Budowle B, Poloni ES, Currat M (2009). "Local population structure in Arabian Peninsula revealed by Y-STR diversity". Hum. Hered. 68 (1): 45–54. doi:10.1159/000210448. PMID 19339785.
- *Alshamali et al. 2009 81% (84/104) *Malouf et al. 2008: 70% (28/40) *Cadenas et al. 2008:45/62 = 72.6% J1-M267
- Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample
- Bosch E, Calafell F, Comas D et al. (April 2001). "High-Resolution Analysis of Human Y-Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula". The American Journal of Human Genetics 68 (4): 1019–29. doi:10.1086/319521. ISSN 0002-9297. PMC 1275654. PMID 11254456.
- Nebel A, Landau-Tasseron E, Filon D et al. (June 2002). "Genetic Evidence for the Expansion of Arabian Tribes into the Southern Levant and North Africa". The American Journal of Human Genetics 70 (6): 1594–6. doi:10.1086/340669. ISSN 0002-9297. PMC 379148. PMID 11992266.
- Semino O, Magri C, Benuzzi G et al. (May 2004). "Origin, Diffusion, and Differentiation of Y-Chromosome Haplogroups E and J: Inferences on the Neolithization of Europe and Later Migratory Events in the Mediterranean Area". The American Journal of Human Genetics 74 (5): 1023–34. doi:10.1086/386295. ISSN 0002-9297. PMC 1181965. PMID 15069642.
- Arredi B, Poloni ES, Paracchini S et al. (August 2004). "A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa". The American Journal of Human Genetics 75 (2): 338–345. doi:10.1086/423147. ISSN 0002-9297. PMC 1216069. PMID 15202071.
- Cruciani F, La Fratta R, Santolamazza P et al. (May 2004). "Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa". The American Journal of Human Genetics 74 (5): 1014–22. doi:10.1086/386294. ISSN 0002-9297. PMC 1181964. PMID 15042509.
- Robino C, Crobu F, Di Gaetano C et al. (May 2008). "Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample". International Journal of Legal Medicine 122 (3): 251–5. doi:10.1007/s00414-007-0203-5. ISSN 0937-9827. PMID 17909833.
- Onofri V, Alessandrini F, Turchi C et al. (August 2008). "Y-chromosome markers distribution in Northern Africa: High-resolution SNP and STR analysis in Tunisia and Morocco populations". Forensic Science International Genetics Supplement Series 1 (1): 235–6. doi:10.1016/j.fsigss.2007.10.173.
- Ennafaa et al. (2011)
- Robino C, Crobu F, Di Gaetano C, et al. (May 2008). "Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample". International Journal of Legal Medicine 122 (3): 251–5. doi:10.1007/s00414-007-0203-5. PMID 17909833.
- Arredi B, Poloni ES, Paracchini S, et al. (August 2004). "A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa". American Journal of Human Genetics 75 (2): 338–45. doi:10.1086/423147. PMC 1216069. PMID 15202071.
- Dugoujon J.M., Coudray C., Torroni A., Cruciani F., Scozzari F., Moral P., Louali N., Kossmann M. The Berber and the Berbers: Genetic and linguistic diversities. In: Become Eloquent. Edited by J.M. Hombert and F. d’Errico. Ed. John Benjamins. pp 123-146; 2009
- Ennafaa; Fregel; Khodjet-el-khil; Gonzalez (2011), "Mitochondrial DNA and Y-chromosome microstructure in Tunisia", European Journal of Human Genetics, doi:10.1038/jhg.2011.92, PMID 21833004
- Fadhlaoui-Zid, K., Martinez-Cruz, B., Khodjet-el-khil, H., Mendizabal, I., Benammar-Elgaaied, A. and Comas, D. (2011), Genetic structure of Tunisian ethnic groups revealed by paternal lineages. American Journal of Physical Anthropology. doi:10.1002/ajpa.21581 PMID 21915847
- Ottoni C, Larmuseau MH, Vanderheyden N, Martínez-Labarga C, Primativo G, Biondi G, Decorte R, Rickards O (May 2011). "Deep into the roots of the Libyan Tuareg: a genetic survey of their paternal heritage". Am J Phys Anthropol 145 (1): 118–24. doi:10.1002/ajpa.21473. PMID 21312181.
- Achilli A, Rengo C, Battaglia V et al. (May 2005). "Saami and Berbers—An Unexpected Mitochondrial DNA Link". The American Journal of Human Genetics 76 (5): 883–6. doi:10.1086/430073. ISSN 0002-9297. PMC 1199377. PMID 15791543.
- Brakez Z, Bosch E, Izaabel H et al. (May–June 2001). "Human mitochondrial DNA sequence variation in the Moroccan population of the Souss area". Annals of Human Biology 28 (3): 295–307. doi:10.1080/030144601300119106. ISSN 0301-4460. PMID 11393336.
- Cherni L, Loueslati BY, Pereira L et al. (February 2005). "Female Gene Pools of Berber and Arab Neighboring Communities in Central Tunisia: Microstructure of mtDNA Variation in North Africa". Human Biology 77 (1): 61–70. doi:10.1353/hub.2005.0028. ISSN 0018-7143. PMID 16114817.
- Fadhlaoui-Zid, K; Plaza, S; Calafell, F; Ben Amor, M; Comas, D; Bennamar El Gaaied, A; Gaaied, El (May 2004). "Mitochondrial DNA Heterogeneity in Tunisian Berbers". Annals of Human Genetics 68 (Pt 3): 222–33. doi:10.1046/j.1529-8817.2004.00096.x. ISSN 0003-4800. PMID 15180702.
- Krings, M; Salem, A; Bauer, K; Geisert, H; Malek, A; Chaix, L; Simon, C; Welsby, D; Dirienzo, A (1999). "mtDNA Analysis of Nile River Valley Populations: A Genetic Corridor or a Barrier to Migration?". The American Journal of Human Genetics 64 (4): 1166–76. doi:10.1086/302314. PMC 1377841. PMID 10090902.
- Loueslati et al. 2006[verification needed]
- Macaulay, V; Richards, M; Hickey, E; Vega, E; Cruciani, F; Guida, V; Scozzari, R; Bonné-Tamir, B; Sykes, B (Jan 1999). "The Emerging Tree of West Eurasian mtDNAs: A Synthesis of Control-Region Sequences and RFLPs". The American Journal of Human Genetics 64 (1): 232–49. doi:10.1086/302204. ISSN 0002-9297. PMC 1377722. PMID 9915963.
- Olivieri, A.; Achilli, A; Pala, M; Battaglia, V; Fornarino, S; Al-Zahery, N; Scozzari, R; Cruciani, F; Behar, DM (Dec 2006). "The mtDNA Legacy of the Levantine Early Upper Palaeolithic in Africa". Science 314 (5806): 1767–70. Bibcode:2006Sci...314.1767O. doi:10.1126/science.1135566. ISSN 0036-8075. PMID 17170302.
- Plaza, S.; Calafell, F; Helal, A; Bouzerna, N; Lefranc, G; Bertranpetit, J; Comas, D (2003). "Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean". Annals of Human Genetics 67 (Pt 4): 312–28. doi:10.1046/j.1469-1809.2003.00039.x. PMID 12914566.
- Rando, JC; Pinto, F; González, AM; Hernández, M; Larruga, JM; Cabrera, VM; Bandelt, HJ (Nov 1998). "Mitochondrial DNA analysis of Northwest African populations reveals genetic exchanges with European, Near-Eastern, and sub-Saharan populations". Annals of Human Genetics 62 (Pt 6): 531–50. doi:10.1046/j.1469-1809.1998.6260531.x. ISSN 0003-4800. PMID 10363131.
- Stevanovitch, A.; Gilles, A; Bouzaid, E; Kefi, R; Paris, F; Gayraud, RP; Spadoni, JL; El-Chenawi, F; Béraud-Colomb, E (2004). "Mitochondrial DNA Sequence Diversity in a Sedentary Population from Egypt". Annals of Human Genetics 68 (Pt 1): 23–39. doi:10.1046/j.1529-8817.2003.00057.x. PMID 14748828.
- Coudray, C; Olivieri, A; Achilli, A; Pala, M; Melhaoui, M; Cherkaoui, M; El-Chennawi, F; Kossmann, M; Torroni, A (Mar 2009). "The Complex and Diversified Mitochondrial Gene Pool of Berber Populations". Annals of Human Genetics 73 (2): 196–214. doi:10.1111/j.1469-1809.2008.00493.x. ISSN 0003-4800. PMID 19053990.
- Cherni, L; Fernandes, V; Pereira, JB; Costa, MD; Goios, A; Frigi, S; Yacoubi-Loueslati, B; Amor, MB; Slama, A (Jun 2009). "Post-last glacial maximum expansion from Iberia to North Africa revealed by fine characterization of mtDNA H haplogroup in Tunisia". American Journal of Physical Anthropology 139 (2): 253–60. doi:10.1002/ajpa.20979. ISSN 0002-9483. PMID 19090581.
- Ottoni C, Primativo G, Hooshiar Kashani B, Achilli A, Martínez-Labarga C et al. (2010). "Mitochondrial Haplogroup H1 in North Africa: An Early Holocene Arrival from Iberia". In Kayser, Manfred. PLoS ONE 5 (10): e13378. Bibcode:2010PLoSO...513378O. doi:10.1371/journal.pone.0013378.
- Harich et al 2010, The trans-Saharan slave trade - clues from interpolation analyses and high-resolution characterization of mitochondrial DNA lineages
- Frigi et. al 2010, Ancient Local Evolution of African mtDNA Haplogroups in Tunisian Berber Populations, Human Biology, Volume 82, Number 4, August 2010
- Henn BM, Botigué LR, Gravel S, Wang W, Brisbin A et al. (2012). "Genomic Ancestry of North Africans Supports Back-to-Africa Migrations". PLoS Genet 8 (1): e1002397. doi:10.1371/journal.pgen.1002397. PMC 3257290. PMID 22253600.
- Sánchez-Quinto F, Botigué LR, Civit S, Arenas C, Ávila-Arcos MC et al. (2012). "North African Populations Carry the Signature of Admixture with Neandertals". PLoS ONE 7 (10): e47765. Bibcode:2012PLoSO...747765S. doi:10.1371/journal.pone.0047765. PMC 3474783. PMID 23082212.
- Sánchez-Quinto F et al. 2012
- "With the reassuring exception of the Basque population isolate, the Iberian Peninsula showed the greatest imprint. Specifically, southwestern European populations averaged between 4% and 20% of their genomes assigned to a North African ancestral cluster, whereas this value did not exceed 2% in southeastern European populations. " Karl Skorecki and Doron M. Behar, North Africans traveling north PNAS July 16, 2013 vol. 110 no. 29 Karl Skorecki, 11668–11669
- Botigué LR, et al. (2013) Gene flow from North Africa contributes to differential human genetic diversity in southern Europe. Proc Natl Acad Sci USA 110:11791–11796
- David Comas, one of the authors of the study : "La cifra del 20% sólo se da en Canarias, para el resto del país oscila entre el 10% y 12%", Los españoles somos los europeos con más genes magrebíes, Huffington post, 3rd June 2013
- Capelli et al. 2008
- Flores, C; Maca-Meyer, N; González, AM; Oefner, PJ; Shen, P; Pérez, JA; Rojas, A; Larruga, JM; Underhill, PA (October 2004). "Reduced genetic structure of the Iberian peninsula revealed by Y-chromosome analysis: implications for population demography" (Free full text). European Journal of Human Genetics 12 (10): 855–63. doi:10.1038/sj.ejhg.5201225. ISSN 1018-4813. PMID 15280900. Retrieved 26 February 2014.
- Beleza, S; Gusmão, L; Lopes, A; Alves, C; Gomes, I; Giouzeli, M; Calafell, F; Carracedo, A; Amorim, A (Mar 2006). "Micro-Phylogeographic and Demographic History of Portuguese Male Lineages". Annals of Human Genetics 70 (Pt 2): 181–94. doi:10.1111/j.1529-8817.2005.00221.x. ISSN 0003-4800. PMID 16626329.
- Adams, SM; Bosch, E; Balaresque, PL; Ballereau, SJ; Lee, AC; Arroyo, E; López-Parra, AM; Aler, M; Grifo, MS (Dec 2008). "The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula". The American Journal of Human Genetics 83 (6): 725–36. doi:10.1016/j.ajhg.2008.11.007. ISSN 0002-9297. PMC 2668061. PMID 19061982.
- Capelli, C; Onofri, V; Brisighelli, F; Boschi, I; Scarnicci, F; Masullo, M; Ferri, G; Tofanelli, S; Tagliabracci, A (Jun 2009). "Moors and Saracens in Europe: estimating the medieval North African male legacy in southern Europe". European Journal of Human Genetics 17 (6): 848–52. doi:10.1038/ejhg.2008.258. ISSN 1018-4813. PMC 2947089. PMID 19156170.
- Cruciani, F; La Fratta, R; Santolamazza, P; Sellitto, D; Pascone, R; Moral, P; Watson, E; Guida, V; Colomb, EB (May 2004). "Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa". The American Journal of Human Genetics 74 (5): 1014–22. doi:10.1086/386294. ISSN 0002-9297. PMC 1181964. PMID 15042509.
- "The study shows that religious conversions and the subsequent marriages between people of different lineage had a relevant impact on modern populations both in Spain, especially in the Balearic Islands, and in Portugal", The religious conversions of Jews and Muslims have had a profound impact on the population of the Iberian Peninsula, Elena Bosch, 2008
- Pereira, Luisa; Cunha, Carla; Alves, Cintia; Amorim, Antonio (2005). "African Female Heritage in Iberia: A Reassessment of mtDNA Lineage Distribution in Present Times". Human Biology 77 (2): 213–29. doi:10.1353/hub.2005.0041. PMID 16201138.
- Plaza, S.; Calafell, F; Helal, A; Bouzerna, N; Lefranc, G; Bertranpetit, J; Comas, D (2003). "Joining the Pillars of Hercules: mtDNA Sequences Show Multidirectional Gene Flow in the Western Mediterranean". Annals of Human Genetics 67 (Pt 4): 312–28. doi:10.1046/j.1469-1809.2003.00039.x. PMID 12914566.
- González, AM; Brehm, A; Pérez, JA; Maca-Meyer, N; Flores, C; Cabrera, VM (Apr 2003). "Mitochondrial DNA affinities at the Atlantic fringe of Europe". American Journal of Physical Anthropology 120 (4): 391–404. doi:10.1002/ajpa.10168. ISSN 0002-9483. PMID 12627534.
- Alvarez L, Santos C, Ramos A, Pratdesaba R, Francalacci P, Aluja MP (February 2010). "Mitochondrial DNA patterns in the Iberian Northern plateau: Population dynamics and substructure of the Zamora province". American Journal of Physical Anthropology 142 (4): 531–9. doi:10.1002/ajpa.21252. PMID 20127843.
- Casas MJ, Hagelberg E, Fregel R, Larruga JM, González AM (December 2006). "Human mitochondrial DNA diversity in an archaeological site in al-Andalus: genetic impact of migrations from North Africa in medieval Spain". American Journal of Physical Anthropology 131 (4): 539–51. doi:10.1002/ajpa.20463. PMID 16685727.
- Pereira, V. N.; Gomes, V. N.; Amorim, A. N.; Gusmão, L.; João Prata, M. (September–October 2010). "Genetic characterization of uniparental lineages in populations from Southwest Iberia with past malaria endemicity". American Journal of Human Biology 22 (5): 588–595. doi:10.1002/ajhb.21049. PMID 20737604.
- Brehm A., Pereira L., Kivisild T., Amorim A. (2003). "Mitochondrial portraits of the madeira and açores archipelagos witness different genetic pools of its settlers.". Hum Genet 114 (1): 77–86. doi:10.1007/s00439-003-1024-3. PMID 14513360.
- Hernandez et al. 2014, 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
- Pereira, Luisa. Cunha, Carla. Alves, Cintia. Amorim, António, African Female Heritage in Iberia: A Reassessment of mtDNA Lineage Distribution in Present Times. Human Biology — Volume 77, Number 2, April 2005, pp. 213-229
- Achilli, A; Olivieri, A, Pala, M, Metspalu, E, Fornarino, S, Battaglia, V, Accetturo, M, Kutuev, I, Khusnutdinova, E, Pennarun, E, Cerutti, N, Di Gaetano, C, Crobu, F, Palli, D, Matullo, G, Santachiara-Benerecetti, AS, Cavalli-Sforza, LL, Semino, O, Villems, R, Bandelt, HJ, Piazza, A, Torroni, A (April 2007). "Mitochondrial DNA variation of modern Tuscans supports the near eastern origin of Etruscans". American Journal of Human Genetics 80 (4): 759–68. doi:10.1086/512822. PMC 1852723. PMID 17357081.
- Casas MJ, Hagelberg E, Fregel R, Larruga JM, Gonzalez AM (2006). "Human mitochondrial DNA diversity in an archaeological site in al-Andalus: genetic impact of migrations from North Africa in medieval Spain.". Am J Phys Anthropol 131 (4): 539–551. doi:10.1002/ajpa.20463. PMID 16685727.
- Alvarez L, Santos C, Ramos A, Pratdesaba R, Francalacci P, Aluja MP (Aug 2010). "Mitochondrial DNA patterns in the Iberian Northern plateau: population dynamics and substructure of the Zamora province.". Am J Phys Anthropol 142 (4): 531–9. doi:10.1002/ajpa.21252. PMID 20127843.
- Alvarez JC, Johnson DL, Lorente JA, Martinez-Espin E, Martinez-Gonzalez LJ, Allard M, Wilson MR, Budowle B.Characterization of human control region sequences for Spanish individuals in a forensic mtDNA data set. Leg Med (Tokyo). 2007 Nov;9(6) 293-304
- Picornell A, Gómez-Barbeito L, Tomàs C, Castro JA, Ramon MM (Sep 2005). "Mitochondrial DNA HVRI variation in Balearic populations.". Am J Phys Anthropol 128 (1): 119–30. doi:10.1002/ajpa.10423.
- Maca-Meyer, N; Arnay, M; Rando, JC; Flores, C; González, AM; Cabrera, VM; Larruga, JM (Feb 2004). "Ancient mtDNA analysis and the origin of the Guanches" (Free full text). European Journal of Human Genetics 12 (2): 155–62. doi:10.1038/sj.ejhg.5201075. ISSN 1018-4813. PMID 14508507.
- Brehm, A; Pereira, L; Kivisild, T; Amorim, A (Dec 2003). "Mitochondrial portraits of the Madeira and Açores archipelagos witness different genetic pools of its settlers". Human Genetics 114 (1): 77–86. doi:10.1007/s00439-003-1024-3. ISSN 0340-6717. PMID 14513360.
- Fregel R, Gomes V, Gusmão L et al. (2009). "Demographic history of Canary Islands male gene-pool: replacement of native lineages by European". BMC Evolutionary Biology 9: 181. doi:10.1186/1471-2148-9-181. PMC 2728732. PMID 19650893.
- Fregel et al. (2009). "The maternal aborigine colonization of La Palma (Canary Islands)". Euro J Hum Gen 17 (10): 1314–1324. doi:10.1038/ejhg.2009.46. PMC 2986650. PMID 19337312.
- Pino-Yanes M, Corrales A, Basaldúa S, Hernández A, Guerra L et al. (2011). "North African Influences and Potential Bias in Case-Control Association Studies in the Spanish Population". In O'Rourke, Dennis. PLoS ONE 6 (3): e18389. Bibcode:2011PLoSO...6E8389P. doi:10.1371/journal.pone.0018389. PMC 3068190. PMID 21479138.
- Di Gaetano, C; Cerutti, N; Crobu, F; Robino, C; Inturri, S; Gino, S; Guarrera, S; Underhill, PA; King, RJ (Jan 2009). "Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome". European Journal of Human Genetics 17 (1): 91–9. doi:10.1038/ejhg.2008.120. ISSN 1018-4813. PMC 2985948. PMID 18685561.
- Cruciani, F.; La Fratta, R; Trombetta, B; Santolamazza, P; Sellitto, D; Colomb, EB; Dugoujon, JM; Crivellaro, F; Benincasa, T (Jun 2007). "Tracing Past Human Male Movements in Northern/Eastern Africa and Western Eurasia: New Clues from Y-Chromosomal Haplogroups E-M78 and J-M12" (Free full text). Molecular Biology and Evolution 24 (6): 1300–11. doi:10.1093/molbev/msm049. ISSN 0737-4038. PMID 17351267.
- Pertovaara, Antti; Kauppila, Timo; Mecke, Ernst (1991). "An Attempted Reversal of Cocaine-Induced Analgesia by Dexamethasone". Pharmacology & Toxicology 68 (2): 93. doi:10.1111/j.1600-0773.1991.tb02042.x.
- Ramos-Luisa et al. (2009)
- Gibert M, Reviron D, Mercier P, Chiaroni J, Boetsch G (Sep 2000). "HLA-DRB1 and DQB1 polymorphisms in southern France and genetic relationships with other Mediterranean populations". Hum Immunol 61 (9): 930–6. doi:10.1016/S0198-8859(00)00158-0. PMID 11053637.
- See the remarks of genetic genealogist Robert Tarín for example. We can add 6.1% (8 out of 132) in Cuba[unreliable source?]
- Sener, S. F.; Imperato, JP; Chmiel, J; Fremgen, A; Sylvester, J (Jan 1989). "The Use of Cancer Registry Data to Study Preoperative Carcinoembryonic Antigen Level as an Indicator of Survival in Colorectal Cancer" (Free full text). CA – A Cancer Journal for Clinicians 39 (1): 50–7. doi:10.3322/canjclin.39.1.50. ISSN 0007-9235. PMID 2492877.
- Silva, DA; Carvalho, E; Costa, G; Tavares, L; Amorim, A; Gusmão, L (Nov 2006). "Y-chromosome genetic variation in Rio De Janeiro population". American Journal of Human Biology 18 (6): 829–37. doi:10.1002/ajhb.20567. ISSN 1042-0533. PMID 17039481.
- Paracchini, S; Pearce, CL; Kolonel, LN; Altshuler, D; Henderson, BE; Tyler-Smith, C (Nov 2003). "A Y chromosomal influence on prostate cancer risk: the multi-ethnic cohort study". Journal of Medical Genetics 40 (11): 815–9. doi:10.1136/jmg.40.11.815. ISSN 0022-2593. PMC 1735314. PMID 14627670.
- Rosa Fregel, Verónica Gomes, Leonor Gusmão, Ana M González , Vicente M Cabrera1 , António Amorim, Jose M Larruga et al. (2009) Demographic history of Canary Islands male gene-pool: replacement of native lineages by European BMC Evolutionary Biology 2009, 9:181 doi:10.1186/1471-2148-9-181
- Flores, C; Maca-Meyer, N; Larruga, JM; Cabrera, VM; Karadsheh, N; Gonzalez, AM (2005). "Isolates in a corridor of migrations: a high-resolution analysis of Y-chromosome variation in Jordan". Journal of Human Genetics 50 (9): 435–41. doi:10.1007/s10038-005-0274-4. ISSN 1434-5161. PMID 16142507.
- The African roots of Latin Christianity by Henri Teissier, Regional Bishop of North Africa