Haplogroup E-Z827 Explained
E-Z827 |
Origin-Date: | 24,100 BP[1] |
Tmrca: | 23,500 BP |
Descendants: | E-L19, E-Z830 |
Mutations: | Z827 |
E-Z827, also known as E1b1b1b,[2] is a major human Y-chromosome DNA haplogroup. It is the parent lineage to the E-Z830 and E-V257 subclades, and defines their common phylogeny. The former is predominantly found in the Middle East; the latter is most frequently observed in North Africa, with its E-M81 subclade observed among the ancient Guanche natives of the Canary Islands. E-Z827 is also found at lower frequencies in Europe, and in isolated parts of Southeast Africa.
Subclades of E-Z827 and Distribution
Family Tree
The following phylogeny is based on the YCC 2008 tree and subsequent published research as summarized by ISOGG.[3] [4]
- E-Z827 (Z827) - E1b1b1b[5]
- E-V257/L19 (L19, V257) - E1b1b1b1[5]
- E-PF2431 (PF2431)[6]
- E-PF2438
- E-Y10561
- E-FGC18981
- E-FGC38527
- E-Y35933
- E-FGC18960
- E-PF2440
- E-M81 (M81)[7]
- E-M81*
- E-PF2546
- E-PF2546*
- E-CTS12227
- E-A929
- E-Z5009
- E-A2227
- E-PF6794
- E-A930
- E-Z2198/E-MZ46
- E-Z830 (Z830) - E1b1b1b2[5]
- E-M123 (M123)
- E-M34 (M34)
- E-M84 (M84)
- E-M290 (M290)
- E-V23 (V23)
- E-L791 (L791,L792)
- E-V1515
- E-V1515*
- E-V1486
- E-V1486*
- E-V2881
- E-M293 (M293)
- E-M293*
- E-P72 (P72)
- E-V3065*
- E-V1700
E-V257/L19 (E1b1b1b1)
- "E-V257/L19*" individuals were found in published samples who were E-V257/L19, but not E-M81. several Middle Easterners and northafricans, a Corsican, a Sardinian, a Borana from Kenya, a southern Spaniard and a Cantabrian.[8]
E-PF2431
PF2431 is the sister branch of M81 which was discovered in Paolo Francalacci (2011). Previously, it was designated L19*/V257*. This mutation has been discovered in North Africa (in Souss in Morocco, in central and eastern Algeria, West Nile in Egypt), the Sahel (Chad, Gambia), Western Europe (United Kingdom (Derbyshire), Germany, Switzerland, Spain, Italy) and Near Eastern (Turkey, Karabakh and Urmia).It would have formed 13800 years ago and is thought to originate from the "green" Sahara. Its TMRCA is estimated at 10600 years by yfull.
Archeology unearthed the remains of a member of the Hungarian conquering elite was analyzed from branch E-FGC19010, it had been discovered in Sandorfalva in Hungary and is dated to the second half of the tenth century.[9] A skeleton was discovered at the Monastery of San Pietro, Villa Magna in Italy, whose DNA belongs to the same branch and lived around 1180CE.[10] Scientists have examined the DNA of a mass grave of victims of the bubonic plague in Ellwangen in Germany, this one dates from the 16th century and belongs to another branch E-FGC18981.[11]
E-M81
E-V257's dominant sub-clade E-M81 is thought to have originated in the area of the northwest of Africa 7,000 years ago,[12] but all Yfull members are M183 and have a TMRCA just 2700 years ago.[13] E-M81 is the most common subclade of haplogroup E-L19/V257. It is concentrated in North Africa, and is dominated by its E-M183 subclade. E-M183 is believed to have originated in the Northwest of Africa, and has an estimated age of 2284-2984 ybp.[14]
The E-M183 sub haplogroup reaches a mean frequency of 42% in North Africa. It decreases in frequency from 100% in some populations to approximately 28.6% to the east of this range in Egypt.[15] [16] The E-M81 subclade is predominant among North African Berber-speaking populations. In Tunisia, it reached 100% frequency among a sample of Arabs from Zriba,[17] 89.5% in Andalusians (Qalaat-al-Andalous), and 100% in Berbers from Chenini-Douiret, Jradou and Takrouna. It is generally found at frequencies around 45% in coastal cities of the Maghreb (Oran, Tunis, Algiers).It is also prevalent among other Berber populations and reaches frequency of 72.4% in Marrakesh Berbers,[18] 80% in Mozabite, and 71% in Middle Atlas Berbers (Moyen). It also reaches high levels (77.8%) among the Tuareg population inhabiting the Sahara in Burkina Faso, near Gor it reaches a much lower frequency of 11.1% in the vicinity of Tanut in the Republic of Niger.
In this key area from Egypt to the Atlantic Ocean, report a pattern of decreasing STR haplotype variation (implying decreasing lineage age in those areas) from East to West (but[19] reports West to East for M183), accompanied by a substantial increasing frequency. At the eastern extreme of this core range, M81 is found in 28.6% (10 out of 35 men) in El-Hayez in the Western desert in Egypt
The pattern of distribution and variance to be consistent with the hypothesis of a post Paleolithic "demic diffusion" from the Middle East. The ancestral lineage of E-M81 in their hypothesis could have been linked with the spread of Neolithic food-producing technologies from the Fertile Crescent via the Nile, although pastoralism rather than agriculture. E-M81 and possibly proto-Afroasiatic language may have been carried either all the way from Asia, or they may represent a "local contribution to the North African Neolithic transition".
The E-M81 subclade has been found in ancient Guanche (Bimbapes) fossils excavated in Punta Azul, El Hierro, Canary Islands, which are dated to the 10th century (~44%).[20] Also found in ifri n'ammar that makes the Northwest African origin the likely origin of where it expanded, and not the Middle East.
Europe
In Europe, E-M81 has a widespread distribution at very low frequencies but is common mostly in the Iberian Peninsula, where unlike in the rest of Europe,[21] shows an average frequency of 4.3% (49/1140) in the Iberian Peninsula with frequencies reaching 4% and 9% in two separate surveys of Galicia, 10% in Western Andalusia and Northwest Castile. However this study also includes 153 individuals from Majorca, Minorca and Ibiza islands as well as 24 individuals from Gascony which are not in the Iberian Peninsula. Without these 177 individuals, real average for Iberian Peninsula is 4.9% (47/963) it is more common than E-M78, with an average frequency around 5%. Its frequencies are higher in the western half of the peninsula with frequencies reaching 8% in Extremadura and South Portugal, 4% in one study and 9% in another in Galicia, 10% in Western Andalusia and Northwest Castile and 9% to 17% in Cantabria.[22] [23] [24] The highest frequencies of this clade found so far in Europe were observed in the Pasiegos from Cantabria, ranging from 18% (8/45)[25] to 41% (23/56). An average frequency of 8.28% (54/652) has also been reported in the Spanish Canary Islands with frequencies over 10% in the three largest islands of Tenerife (10.68%), Gran Canaria (11.54%) and Fuerteventura (13.33%).[26]
E-M81 is also found in other parts of Europe, such as Britain – especially Wales and Scotland – and France, where it has an overall incidence of 2.7% (15/555), with frequencies surpassing 5.0% in Auvergne (5/89) and Île-de-France (5/91).[27] [28] [29] E-M81 was also observed in Italy with frequencies of 0,7% to 5,8% in Sardinia,[30] [31] approximately 2.12% overall in Sicily (but up to 7.14% in Piazza Armerina), and in very much lower frequency near Lucera (1.7%), in continental Italy, possibly due to ancient migrations during the Islamic, Roman, and Carthaginian empires. In a 2014 study by Stefania Sarno et al. with 326 samples from Cosenza, Reggio Calabria, Lecce and five Sicilian provinces, E-M81 shows an average frequency of 1.53%, but the typical Maghrebin core haplotype 13-14-30-24-9-11-13 has been found in only two out of the five E-M81 individuals. These results, along with the negligible contribution from North-African populations revealed by the admixture-like plot analysis, suggest only a marginal impact of trans-Mediterranean gene flows on the current SSI genetic pool.[32]
Latin America
As a result of Spanish and Portuguese colonization of the Americas, this sub-clade is found throughout Latin America, for example 6.1% in Cuba, (8 out of 132),[33] 5.4% in Brazil (Rio de Janeiro) (6 out of 112), "The presence of chromosomes of North African origin (E3b1b-M81; can also be explained by a Portuguese-mediated influx, since this haplogroup reaches a frequency of 5.6% in Portugal, quite similar to the frequency found in Rio de Janeiro (5.4%) among European contributors."[34] and among Hispanic men from California and Hawaii 2.4% (7 out of 295),[35]
Others
In smaller numbers, E-M81 men can be found in areas in contact with the Maghreb, both around the Sahara, in places like Sudan, and around the Mediterranean in places like Lebanon, Turkey, and amongst Sephardic Jews.
Distribution
The following gives a summary of most of the studies which specifically tested for E-M81, showing where its distribution is greater than 1% in Europe, North Africa, the Middle East and Latin America.
Country/Region | Sampling | n | %E-M81 | Source |
---|
Mauretania | Arabs | 17 | 94 | [36] |
Algeria | Arabs | 60 | 80 | [37] |
Tunisia | Arabs from Zriba | 32 | 100 | [38] |
Tunisia | Arabs from Djerba | 47 | 93.7 | [39] |
Algeria | Mozabite Berbers | 67 | 86.6 | [40] |
Algeria | Mozabite Berbers | 20 | 80 | |
Algeria | Oran | 102 | 45.1 | [41] |
Algeria | Algiers | 35 | 42.9 | [42] |
Algeria | Kabyles from Tizi Ouzou | 19 | 47.4 | |
Algeria | Arabs and Berbers | 156 | 44.2 | [43] |
Algeria | Zenata | 35 | 48.6 | [44] |
Brazil | Rio de Janeiro | 112 | 5.4 | |
Burkina Faso | Tuaregs | 38 | 77.8 | [45] |
Canary Islands | Fuerteventura | 75 | 13.3 | |
Canary Islands | Gran Canaria | 78 | 11.5 | |
Canary Islands | Tenerife | 178 | 10.7 | |
Canary Islands | Lanzarote | 97 | 6.2 | |
Canary Islands | La Palma | 85 | 5.9 | |
Canary Islands | Gomera | 92 | 4.4 | |
Canary Islands | Hierro | 47 | 2.1 | |
Cuba | | 132 | 6.1 | |
Cyprus | Turkish Cypriots | 46 | 8.7 | |
Egypt | Northern Egyptians | 21 | 4.8 | |
Egypt | Western Desert | 35 | 28.6 | |
Egypt | | 147 | 8.2 | |
Egypt | Arabs | 370 | 11.8 | |
France | | 85 | 3.5 | |
France | Auvergne | 89 | 5.6 | |
France | Île-de-France | 91 | 5.5 | |
France | Nord-Pas-de-Calais | 68 | 4.4 | |
France | Provence-Alpes-Côte d'Azur | 45 | 2.2 | |
France | Midi-Pyrénées | 67 | 1.5 | |
France | Béarnais | 56 | 1.8 | |
France | Bigorre | 44 | 2.3 | |
Iberia | Spain, Portugal | 655 | 5.2 | |
Iberia | Spain, Portugal | 1140 | 4.3 | |
Israel | Bedouins | 28 | 3.6 | |
Italy | Central Italians | 89 | 2.2 | |
Italy | Northern Italians | 67 | 1.5 | |
Italy | East Campania | 84 | 1.2 | |
Italy | Lucera | 60 | 1.7 | |
Italy | Peninsular Italy | 915 | 0.3 | |
Italy | Sicily | 236 | 2.1 | [46] |
Italy | Sicilians | 136 | 0.7 | |
Italy | Sardinians | 367 | 0.3 | |
Italy | Sardinia | 1204 | 5.8 | |
Jordan | Arabs | 101 | 4 | |
Lebanon | Arabs | 104 | 1.9 | |
Lebanon | Arabs | 914 | 1.2 | [47] |
Libya | Tuaregs | 47 | 48.9 | [48] |
Libya | Arabs | 215 | 35.9 | [49] |
Libya | Arabs and Berbers | 83 | 45.7 | |
Mauritania | Arabs and Berbers | 189 | 55.5 | |
Morocco | Marrakesh Berbers | 29 | 72.4 | |
Morocco | Southern Moroccan Berbers | 187 | 98.5 | [50] |
Morocco | Moyen Atlas Berbers | 69 | 71 | |
Morocco | Moroccan Arabs | 54 | 31.5 | |
Morocco | Marrakesh (Amizmiz Valley) | 33 | 84.8 | |
Morocco | Northern Moroccans (Beni Snassen) | 67 | 79.1 | |
Morocco | Northern Moroccans (Rhiraya) | 54 | 79.6 | |
Morocco | Immigrants resident in Italy | 51 | 54.9 | [51] |
Morocco | Arabs and Berbers | 221 | 65 | |
Morocco | Arabs and Berbers | 760 | 67.3 | |
Morocco | Saharawi | 29 | 76 | [52] |
Niger | Tuaregs | 22 | 9.1 | |
Niger | Tuaregs | 31 | 11.1 | |
North Africa | Sahara | 89 | 59.6 | |
North Africa | Algeria, Tunisia | 202 | 39.1 | |
Portugal | North | 109 | 5.5 | [53] |
Portugal | South | 49 | 12.2 | |
Portugal | North | 50 | 4 | |
Portugal | South | 78 | 7.7 | |
Portugal | North | 60 | 3.3 | |
Portugal | | 303 | 5.6 | [54] |
Portugal | North | 101 | 6 | |
Portugal | Center | 102 | 4.9 | |
Portugal | South | 100 | 6 | |
Portugal | Madeira | 129 | 5.4 | |
Portugal | Açores | 121 | 5 | |
Portugal | | 657 | 5.6 | |
Portugal | Entre Douro e Minho | 228 | 6.6 | |
Portugal | Tras os Montes | 64 | 3.1 | |
Portugal | Beira Litoral | 116 | 5.2 | |
Portugal | Beira Interior | 58 | 5.3 | |
Portugal | Estremadura | 43 | 4.6 | |
Portugal | Lisboa e Setubal | 62 | 6.5 | |
Portugal | Alentejo | 65 | 7.7 | |
Portugal | Coruche | 64 | 9.4 | |
Portugal | Pias | 46 | 4.3 | |
Portugal | Alcacer do Sal | 21 | 4.8 | |
Portugal | Tras-os-Montes (Jews) | 57 | 5.3 | [55] |
Portugal | Tras-os-Montes (Non Jews) | 30 | 10 | |
Somalia | | 201 | 1.5 | |
Spain | Pasiegos from Cantabria | 19 | 36.8 | [56] |
Spain | Pasiegos from Cantabria | 56 | 41.1 | |
Spain | Pasiegos from Cantabria | 45 | 17.8 | |
Spain | Spanish Basques | 55 | 3.6 | |
Spain | Asturians | 90 | 2.2 | |
Spain | Southern Spaniards | 62 | 1.6 | |
Spain | Castile, NorthWest | 100 | 10 | |
Spain | Andalucia, West | 73 | 9.6 | |
Spain | Galicia | 19 | 10.5 | |
Spain | Galicia | 292 | 4.1 | [57] |
Spain | Galicia | 88 | 9.1 | |
Spain | Galicia | 44 | 9.1 | [58] |
Spain | Galicia | 164 | 9.1 | [59] |
Spain | Extremadura | 52 | 7.7 | |
Spain | Valencia | 73 | 4.1 | |
Spain | Castile, NorthEast | 31 | 3.2 | |
Spain | Aragon | 34 | 2.9 | |
Spain | Minorca | 37 | 2.7 | |
Spain | Andalucia, East | 95 | 2.1 | |
Spain | Majorca | 62 | 1.6 | |
Spain | Castile, La Mancha | 63 | 1.6 | |
Spain | Catalonia | 80 | 1.3 | |
Spain | Catalonia | 111 | 3.6 | |
Spain | Cantabria | 161 | 13 | |
Spain | Malaga | 26 | 11.5 | |
Spain | Cantabria | 70 | 8.6 | |
Spain | Cordoba | 27 | 7.4 | |
Spain | Valencia | 31 | 6.5 | |
Spain | Valencia | 59 | 5.1 | |
Spain | Almeria | 36 | 5.6 | |
Spain | Leon | 60 | 5 | |
Spain | Castile | 21 | 4.8 | |
Spain | Seville | 155 | 4.5 | |
Spain | Huelva | 22 | 4.5 | |
Spain | Basques | 45 | 2.2 | |
Spain | Huelva | 167 | 3 | [60] |
Spain | Granada | 250 | 3.6 | |
Spain | Pedroches Valley | 68 | 1.5 | |
Spain | Andalucia | 94 | 2.1 | |
Spain | Zamora | 235 | 5.5 | [61] |
Tunisia | Tunis | 148 | 37.9 | |
Tunisia | Immigrants resident in Italy | 52 | 32.7 | |
Tunisia | Berbers from Bou Omrane | 40 | 87.5 | [62] |
Tunisia | Berbers from Bou Saad | 40 | 92.5 | |
Tunisia | Arabs from Djerba | 46 | 60.8 | |
Tunisia | Berbers from Djerba | 47 | 76.6 | |
Tunisia | Berbers from Chenini–Douiret | 27 | 100 | [63] |
Tunisia | Berbers from Sened | 35 | 65.7 | |
Tunisia | Arabs from Jradou | 32 | 100 | |
Tunisia | Andalusians from Zaghouan | 32 | 40.6 | |
Tunisia | Cosmopolitan Tunis | 33 | 54.4 | |
Tunisia | Arabs | 601 | 62.7 | |
Turkey | Istanbul Turkish | 35 | 5.7 | |
Turkey | Sephardi Turkish | 19 | 5.3 | |
Turkey | Southwestern Turkish | 40 | 2.5 | |
Turkey | Northeastern Turkish | 41 | 2.4 | |
Egypt | Berbers | 93 | 1.1 | |
|
E-Z830 (E1b1b1b2)
A recently confirmed sub-clade of E-Z827, Z830, includes the confirmed sub-clades of E-M123, E-M293, and E-V42, and is a sibling clade to E-L19. Currently, the E-M35 phylogeny project recognizes four distinct clusters of Z830* carriers, two of which are exclusively Jewish in origin. The remaining two are significantly smaller, and include scattered individuals in Germany, Spain, Latin America, Egypt, and Ethiopia.[64] [65] [66] [67]
E-M123
See main article: Haplogroup E-M123 (Y-DNA). E-M123 is mostly known for its major subclade E-M34, which dominates this clade.[68]
E-V1515
A new clade (E-V1515) was defined by Trombetta et al. 2015, which originated about 12 kya (95% CI 8.6-16.4) in eastern Africa where it is currently mainly distributed. This clade includes all the sub-Saharan haplogroups (E-V42, E-M293, E-V92, E-V6) reported as E-M35 basal clades in a previous phylogeny.[69]
We observed the highest frequency and diversity of this haplogroup in the northern part of the Horn of Africa (present day Eritrea and northern Ethiopia), where the majority of the deepest E-V1515 subhaplogroups and paragroups were found. In the southern part of the Horn (southern Ethiopia, Somalia and northern Kenya), haplogroup E-V1515 is almost exclusively represented by the recent (3.5 ka; 95% CI: 1.7–5.9 ka) subhaplogroup E-V1486. Further south, in southern Kenya and southern Africa, a single E-V1486 terminal clade, known as E-M293 (Henn et al. 2008), was found (fig. 3). This phylogeographic pattern is strongly suggestive of human movements from the northern part of the Horn to the Ethiopian/Kenyan borders between 12 ka (the coalescence of E-V1515) and 3.5 ka (the coalescence of E-V1486), and from here toward southern Africa across the equatorial belt in more recent times.[69]
Multiple instances of commercially observed E-V1515 have also been detected in Arabia.[70]
E-M293
E-M293 is a subclade of E-V1515. It was identified by ISOGG as the second clade within E-Z830. It was discovered before E-Z830 and is associated with the spread of pastoralism from Eastern Africa by South Cushites into Southern Africa.[71] So far high levels have been found in specific ethnic groups in Tanzania and Southern Africa. Highest were the Datog (43%), Khwe (Kxoe) (31%), Burunge (28%), and Sandawe (24%). Two Bantu-speaking Kenyan males were found with the M293 mutation.Other E-M215 subclades are rare in Southern Africa. The authors state...
Without information about M293 in the Maasai, Hema, and other populations in Kenya, Sudan, and Ethiopia, we cannot pinpoint the precise geographic source of M293 with greater confidence. However, the available evidence points to present-day Tanzania as an early and important geographic locus of M293 evolution.
They also say that "M293 is only found in sub-Saharan Africa, indicating a separate phylogenetic history for M35.1 * (former) samples further north".
E-P72.
[72] This is a subclade of E-M293.
[73]
E-V42
E-V42 was discovered in two Ethiopian Jews. It was suggested that it may be restricted to the region around Ethiopia. However, further testing by commercial DNA testing companies confirmed positive results for this subclade in Arabia as well.[74]
E-V6
The E-V6 subclade of E-V1515 is defined by V6 and has been identified a significant presence of these lineages in Ethiopia, and also some in the neighboring Somali population. Among the Ethiopian and Somali samples, the highest were 14.7% among the Ethiopian Amhara, and 16.7% among the Ethiopian Wolayta.
E-V92
E-V92 was discovered in two Ethiopian Amhara. Like E-V6 and E-V42 it possibly only exists in the area of Ethiopia.
Phylogenetics
Phylogenetic History
See main article: Conversion table for Y chromosome haplogroups.
Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.
YCC 2002/2008 (Shorthand) | (α) | (β) | (γ) | (δ) | (ε) | (ζ) | (η) | YCC 2002 (Longhand) | YCC 2005 (Longhand) | YCC 2008 (Longhand) | YCC 2010r (Longhand) | ISOGG 2006 | ISOGG 2007 | ISOGG 2008 | ISOGG 2009 | ISOGG 2010 | ISOGG 2011 | ISOGG 2012 |
---|
E-P29 | 21 | III | 3A | 13 | Eu3 | H2 | B | E* | E | E | E | E | E | E | E | E | E | E |
E-M33 | 21 | III | 3A | 13 | Eu3 | H2 | B | E1* | E1 | E1a | E1a | E1 | E1 | E1a | E1a | E1a | E1a | E1a |
E-M44 | 21 | III | 3A | 13 | Eu3 | H2 | B | E1a | E1a | E1a1 | E1a1 | E1a | E1a | E1a1 | E1a1 | E1a1 | E1a1 | E1a1 |
E-M75 | 21 | III | 3A | 13 | Eu3 | H2 | B | E2a | E2 | E2 | E2 | E2 | E2 | E2 | E2 | E2 | E2 | E2 |
E-M54 | 21 | III | 3A | 13 | Eu3 | H2 | B | E2b | E2b | E2b | E2b1 | - | - | - | - | - | - | - |
E-P2 | 25 | III | 4 | 14 | Eu3 | H2 | B | E3* | E3 | E1b | E1b1 | E3 | E3 | E1b1 | E1b1 | E1b1 | E1b1 | E1b1 |
E-M2 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a* | E3a | E1b1 | E1b1a | E3a | E3a | E1b1a | E1b1a | E1b1a | E1b1a1 | E1b1a1 |
E-M58 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a1 | E3a1 | E1b1a1 | E1b1a1 | E3a1 | E3a1 | E1b1a1 | E1b1a1 | E1b1a1 | E1b1a1a1a | E1b1a1a1a |
E-M116.2 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a2 | E3a2 | E1b1a2 | E1b1a2 | E3a2 | E3a2 | E1b1a2 | E1b1a2 | E1ba12 | removed | removed |
E-M149 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a3 | E3a3 | E1b1a3 | E1b1a3 | E3a3 | E3a3 | E1b1a3 | E1b1a3 | E1b1a3 | E1b1a1a1c | E1b1a1a1c |
E-M154 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a4 | E3a4 | E1b1a4 | E1b1a4 | E3a4 | E3a4 | E1b1a4 | E1b1a4 | E1b1a4 | E1b1a1a1g1c | E1b1a1a1g1c |
E-M155 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a5 | E3a5 | E1b1a5 | E1b1a5 | E3a5 | E3a5 | E1b1a5 | E1b1a5 | E1b1a5 | E1b1a1a1d | E1b1a1a1d |
E-M10 | 8 | III | 5 | 15 | Eu2 | H2 | B | E3a6 | E3a6 | E1b1a6 | E1b1a6 | E3a6 | E3a6 | E1b1a6 | E1b1a6 | E1b1a6 | E1b1a1a1e | E1b1a1a1e |
E-M35 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b* | E3b | E1b1b1 | E1b1b1 | E3b1 | E3b1 | E1b1b1 | E1b1b1 | E1b1b1 | removed | removed |
E-M78 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b1* | E3b1 | E1b1b1a | E1b1b1a1 | E3b1a | E3b1a | E1b1b1a | E1b1b1a | E1b1b1a | E1b1b1a1 | E1b1b1a1 |
E-M148 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b1a | E3b1a | E1b1b1a3a | E1b1b1a1c1 | E3b1a3a | E3b1a3a | E1b1b1a3a | E1b1b1a3a | E1b1b1a3a | E1b1b1a1c1 | E1b1b1a1c1 |
E-M81 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b2* | E3b2 | E1b1b1b | E1b1b1b1 | E3b1b | E3b1b | E1b1b1b | E1b1b1b | E1b1b1b | E1b1b1b1 | E1b1b1b1a |
E-M107 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b2a | E3b2a | E1b1b1b1 | E1b1b1b1a | E3b1b1 | E3b1b1 | E1b1b1b1 | E1b1b1b1 | E1b1b1b1 | E1b1b1b1a | E1b1b1b1a1 |
E-M165 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b2b | E3b2b | E1b1b1b2 | E1b1b1b1b1 | E3b1b2 | E3b1b2 | E1b1b1b2a | E1b1b1b2a | E1b1b1b2a | E1b1b1b2a | E1b1b1b1a2a |
E-M123 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b3* | E3b3 | E1b1b1c | E1b1b1c | E3b1c | E3b1c | E1b1b1c | E1b1b1c | E1b1b1c | E1b1b1c | E1b1b1b2a |
E-M34 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3b3a* | E3b3a | E1b1b1c1 | E1b1b1c1 | E3b1c1 | E3b1c1 | E1b1b1c1 | E1b1b1c1 | E1b1b1c1 | E1b1b1c1 | E1b1b1b2a1 |
E-M136 | 25 | III | 4 | 14 | Eu4 | H2 | B | E3ba1 | E3b3a1 | E1b1b1c1a | E1b1b1c1a1 | E3b1c1a | E3b1c1a | E1b1b1c1a1 | E1b1b1c1a1 | E1b1b1c1a1 | E1b1b1c1a1 | E1b1b1b2a1a1 |
|
Original Research Publications
The following research teams per their publications were represented in the creation of the YCC Tree.
See also
Y-DNA Backbone Tree
Further reading
- Battaglia V, Fornarino S, Al-Zahery N, Olivieri A, Pala M, Myres NM, King RJ, Rootsi S, Marjanovic D, Primorac D, Hadziselimovic R, Vidovic S, Drobnic K, Durmishi N, Torroni A, Santachiara-Benerecetti AS, Underhill PA, Semino O . Y-chromosomal evidence of the cultural diffusion of agriculture in Southeast Europe . European Journal of Human Genetics . 17 . 6 . 820–30 . June 2009 . 19107149 . 2947100 . 10.1038/ejhg.2008.249 .
- Bird S . Haplogroup E3b1a2 as a Possible Indicator of Settlement in Roman Britain by Soldiers of Balkan Origin . Journal of Genetic Genealogy . 2007 . 3 . 2 . 2011-06-17 . 2016-04-22 . https://web.archive.org/web/20160422005652/http://www.jogg.info/32/bird.htm . dead .
- Bosch E, Calafell F, González-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 . Annals of Human Genetics . 70 . Pt 4 . 459–87 . July 2006 . 16759179 . 10.1111/j.1469-1809.2005.00251.x . 23156886 . https://archive.today/20121210100310/http://www3.interscience.wiley.com/journal/118548826/abstract?CRETRY=1&SRETRY=0 . dead . 2012-12-10 . .
- Cadenas AM, Zhivotovsky LA, Cavalli-Sforza LL, Underhill PA, Herrera RJ . Y-chromosome diversity characterizes the Gulf of Oman . European Journal of Human Genetics . 16 . 3 . 374–86 . March 2008 . 17928816 . 10.1038/sj.ejhg.5201934 . . free .
- Capelli C, Redhead N, Abernethy JK, Gratrix F, Wilson JF, Moen T, Hervig T, Richards M, Stumpf MP, Underhill PA, Bradshaw P, Shaha A, Thomas MG, Bradman N, Goldstein DB . 6 . A Y chromosome census of the British Isles . Current Biology . 13 . 11 . 979–84 . May 2003 . 12781138 . 10.1016/S0960-9822(03)00373-7 . 526263 . .
- Caratti S, Gino S, Torre C, Robino C . Subtyping of Y-chromosomal haplogroup E-M78 (E1b1b1a) by SNP assay and its forensic application . International Journal of Legal Medicine . 123 . 4 . 357–60 . July 2009 . 19430804 . 10.1007/s00414-009-0350-y . 5657112 . .
- Cruciani F, Santolamazza P, Shen P, Macaulay V, Moral P, Olckers A, Modiano D, Holmes S, Destro-Bisol G, Coia V, Wallace DC, Oefner PJ, Torroni A, Cavalli-Sforza LL, Scozzari R, Underhill PA . A back migration from Asia to sub-Saharan Africa is supported by high-resolution analysis of human Y-chromosome haplotypes . American Journal of Human Genetics . 70 . 5 . 1197–214 . May 2002 . 11910562 . 447595 . 10.1086/340257 . .
- Cruciani F, La Fratta R, Torroni A, Underhill PA, Scozzari R . Molecular dissection of the Y chromosome haplogroup E-M78 (E3b1a): a posteriori evaluation of a microsatellite-network-based approach through six new biallelic markers . Human Mutation . 27 . 8 . 831–2 . August 2006 . 16835895 . 10.1002/humu.9445 . 26886757 . .
- Cruciani F, La Fratta R, Trombetta B, Santolamazza P, Sellitto D, Colomb EB, Dugoujon JM, Crivellaro F, Benincasa T, Pascone R, Moral P, Watson E, Melegh B, Barbujani G, Fuselli S, Vona G, Zagradisnik B, Assum G, Brdicka R, Kozlov AI, Efremov GD, Coppa A, Novelletto A, Scozzari R . 6 . Tracing past human male movements in northern/eastern Africa and western Eurasia: new clues from Y-chromosomal haplogroups E-M78 and J-M12 . Molecular Biology and Evolution . 24 . 6 . 1300–11 . June 2007 . 17351267 . 10.1093/molbev/msm049 . . free .
- Di Giacomo F, Luca F, Anagnou N, Ciavarella G, Corbo RM, Cresta M, Cucci F, Di Stasi L, Agostiano V, Giparaki M, Loutradis A, Mammi' C, Michalodimitrakis EN, Papola F, Pedicini G, Plata E, Terrenato L, Tofanelli S, Malaspina P, Novelletto A . Clinal patterns of human Y chromosomal diversity in continental Italy and Greece are dominated by drift and founder effects . Molecular Phylogenetics and Evolution . 28 . 3 . 387–95 . September 2003 . 12927125 . 10.1016/S1055-7903(03)00016-2 . . 2011-06-17 . https://web.archive.org/web/20090305052003/http://www.familytreedna.com/pdf/italy.pdf . 2009-03-05 . dead .
- Firasat S, Khaliq S, Mohyuddin A, Papaioannou M, Tyler-Smith C, Underhill PA, Ayub Q . Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan . European Journal of Human Genetics . 15 . 1 . 121–6 . January 2007 . 17047675 . 2588664 . 10.1038/sj.ejhg.5201726 . .
- Hassan HY, Underhill PA, Cavalli-Sforza LL, Ibrahim ME . Y-chromosome variation among Sudanese: restricted gene flow, concordance with language, geography, and history . American Journal of Physical Anthropology . 137 . 3 . 316–23 . November 2008 . 18618658 . 10.1002/ajpa.20876 . .
- King RJ, Ozcan SS, Carter T, Kalfoğlu E, Atasoy S, Triantaphyllidis C, Kouvatsi A, Lin AA, Chow CE, Zhivotovsky LA, Michalodimitrakis M, Underhill PA . Differential Y-chromosome Anatolian influences on the Greek and Cretan Neolithic . Annals of Human Genetics . 72 . Pt 2 . 205–14 . March 2008 . 18269686 . 10.1111/j.1469-1809.2007.00414.x . 22406638 . .
- Congruent distribution of Neolithic painted pottery and ceramic figurines with Y-chromosome lineages. Antiquity. 2002. 76. 293. 707–14. King R, Underhill PA . 10.1017/s0003598x00091158 . 160359661 .
- Lancaster A. 2009. Y Haplogroups, Archaeological Cultures and Language Families: a Review of the Multidisciplinary Comparisons using the case of E-M35. Journal of Genetic Genealogy. 5. 1. 2011-06-17. 2016-05-06. https://web.archive.org/web/20160506150956/http://www.jogg.info/51/files/Lancaster.pdf. dead.
- Onofri V, Alessandrini F, Turchi C, Pesaresi M, Buscemi L, Tagliabracci A . Development of multiplex PCRs for evolutionary and forensic applications of 37 human Y chromosome SNPs . Forensic Science International . 157 . 1 . 23–35 . February 2006 . 15896936 . 10.1016/j.forsciint.2005.03.014 . .
- Pelotti S, Ceccardi S, Lugaresi F, Trane R, Falconi M, Bini C, Willuweit S, Roewer L . Microgeographic genetic variation of Y chromosome in a population sample of Ravenna's area in the Emilia-Romagna region (North of Italy) . Forensic Science International: Genetics Supplement Series . 1 . 1 . 242–243 . 2008 . 10.1016/j.fsigss.2007.10.025 .
- Pericić M, Lauc LB, Klarić IM, Rootsi S, Janićijevic B, Rudan I, Terzić R, Colak I, Kvesić A, Popović D, Sijacki A, Behluli I, Dordevic D, Efremovska L, Bajec DD, Stefanović BD, Villems R, Rudan P . High-resolution phylogenetic analysis of southeastern Europe traces major episodes of paternal gene flow among Slavic populations . Molecular Biology and Evolution . 22 . 10 . 1964–75 . October 2005 . 15944443 . 10.1093/molbev/msi185 . . free .
- Pontikos D. "Phylogeographic refinement of haplogroup E" http://dienekes.blogspot.ru/2015/07/phylogeographic-refinement-of.html
- Rosa A, Ornelas C, Jobling MA, Brehm A, Villems R . Y-chromosomal diversity in the population of Guinea-Bissau: a multiethnic perspective . BMC Evolutionary Biology . 7 . 1 . 124 . July 2007 . 17662131 . 1976131 . 10.1186/1471-2148-7-124 . . free .
- Rosser ZH, Zerjal T, Hurles ME, Adojaan M, Alavantic D, Amorim A, Amos W, Armenteros M, Arroyo E, Barbujani G, Beckman G, Beckman L, Bertranpetit J, Bosch E, Bradley DG, Brede G, Cooper G, Côrte-Real HB, de Knijff P, Decorte R, Dubrova YE, Evgrafov O, Gilissen A, Glisic S, Gölge M, Hill EW, Jeziorowska A, Kalaydjieva L, Kayser M, Kivisild T, Kravchenko SA, Krumina A, Kucinskas V, Lavinha J, Livshits LA, Malaspina P, Maria S, McElreavey K, Meitinger TA, Mikelsaar AV, Mitchell RJ, Nafa K, Nicholson J, Nørby S, Pandya A, Parik J, Patsalis PC, Pereira L, Peterlin B, Pielberg G, Prata MJ, Previderé C, Roewer L, Rootsi S, Rubinsztein DC, Saillard J, Santos FR, Stefanescu G, Sykes BC, Tolun A, Villems R, Tyler-Smith C, Jobling MA . 6 . Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language . American Journal of Human Genetics . 67 . 6 . 1526–43 . December 2000 . 11078479 . 1287948 . 10.1086/316890 .
- Sanchez JJ, Hallenberg C, Børsting C, Hernandez A, Morling N . High frequencies of Y chromosome lineages characterized by E3b1, DYS19-11, DYS392-12 in Somali males . European Journal of Human Genetics . 13 . 7 . 856–66 . July 2005 . 15756297 . 10.1038/sj.ejhg.5201390 . . free .
- Semino O, Santachiara-Benerecetti AS, Falaschi F, Cavalli-Sforza LL, Underhill PA . Ethiopians and Khoisan share the deepest clades of the human Y-chromosome phylogeny . American Journal of Human Genetics . 70 . 1 . 265–8 . January 2002 . 11719903 . 384897 . 10.1086/338306 . . dead . https://web.archive.org/web/20060315210510/http://hpgl.stanford.edu/publications/AJHG_2002_v70_p265-268.pdf . 2006-03-15 .
- Semino O, Magri C, Benuzzi G, Lin AA, Al-Zahery N, Battaglia V, Maccioni L, Triantaphyllidis C, Shen P, Oefner PJ, Zhivotovsky LA, King R, Torroni A, Cavalli-Sforza LL, Underhill PA, Santachiara-Benerecetti AS . 6 . 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 . American Journal of Human Genetics . 74 . 5 . 1023–34 . May 2004 . 15069642 . 1181965 . 10.1086/386295 . .
- Shen P, Lavi T, Kivisild T, Chou V, Sengun D, Gefel D, Shpirer I, Woolf E, Hillel J, Feldman MW, Oefner PJ . Reconstruction of patrilineages and matrilineages of Samaritans and other Israeli populations from Y-chromosome and mitochondrial DNA sequence variation . Human Mutation . 24 . 3 . 248–60 . September 2004 . 15300852 . 10.1002/humu.20077 . 1571356 . . 2011-06-17 . https://wayback.archive-it.org/all/20090305052143/http://www.ebc.ee/EVOLUTSIOON/publications/Shen2004.pdf . 2009-03-05 . dead .
- Thomas MG, Stumpf MP, Härke H . Evidence for an apartheid-like social structure in early Anglo-Saxon England . Proceedings. Biological Sciences . 273 . 1601 . 2651–7 . October 2006 . 17002951 . 1635457 . 10.1098/rspb.2006.3627 . . dead . https://web.archive.org/web/20090305052141/http://publishing.royalsociety.org/media/proceedings_b/papers/RSPB20063627.pdf . 2009-03-05 .
- Hassan HY, Underhill PA, Cavalli-Sforza LL, Ibrahim ME . Y-chromosome variation among Sudanese: restricted gene flow, concordance with language, geography, and history . American Journal of Physical Anthropology . 137 . 3 . 316–23 . November 2008 . 18618658 . 10.1002/ajpa.20876 . .
- Underhill PA, Passarino G, Lin AA, Shen P, Mirazón Lahr M, Foley RA, Oefner PJ, Cavalli-Sforza LL . The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations . Annals of Human Genetics . 65 . Pt 1 . 43–62 . January 2001 . 11415522 . 10.1046/j.1469-1809.2001.6510043.x . 9441236 . . free .
- Book: Underhill PA . 2002. Inference of Neolithic Population Histories using Y-chromosome Haplotypes. Bellwood PS, Renfrew C. Examining the farming/language dispersal hypothesis, McDonald Institute for Archaeological Research. 978-1-902937-20-5. McDonald Institute for Archaeological Research. Cambridge.
- Underhill PA, Kivisild T . Use of y chromosome and mitochondrial DNA population structure in tracing human migrations . Annual Review of Genetics . 41 . 1 . 539–64 . 2007 . 18076332 . 10.1146/annurev.genet.41.110306.130407 .
- Weale ME, Weiss DA, Jager RF, Bradman N, Thomas MG . Y chromosome evidence for Anglo-Saxon mass migration . Molecular Biology and Evolution . 19 . 7 . 1008–21 . July 2002 . 12082121 . 10.1093/oxfordjournals.molbev.a004160 . . free .
- Weale . . September 1, 2003 . Rare Deep-Rooting Y Chromosome Lineages in Humans: Lessons for Phylogeography . Genetics . 165 . 229–234 . 1 . 10.1093/genetics/165.1.229 . 14504230 . 1462739 .
External links
Notes and References
- Web site: YFull YTree v6.02 . YFull: Y-Chr Sequence Interpretation Service .
- ISOGG (2015), Y-DNA Haplogroup E and its Subclades - 2015
- Web site: ISOGG . ISOGG . Y-DNA Haplogroup E and its Subclades - 2008 . International Society of Genetic Genealogists "ISOGG" . 2008 .
- Y Chromosome Consortium "YCC" . A nomenclature system for the tree of human Y-chromosomal binary haplogroups . Genome Research . 12 . 2 . 339–48 . February 2002 . 11827954 . 155271 . 10.1101/gr.217602 .
- ISOGG 2015
- Web site: E-PF2431 YTree.
- Web site: E-M81 YTree. www.yfull.com. 2016-07-09.
- Web site: E-L19 YTree . 2023-07-24 . www.yfull.com.
- Maroti at al. 2022, Whole genome analysis sheds light on the genetic origin of Huns, Avars and conquering Hungarians https://www.biorxiv.org/content/10.1101/2022.01.19.476915v1
- Antonio et al. 2019, Ancient Rome: A genetic crossroads of Europe and the Mediterranean
- Immel et al. 2021, Analysis of Genomic DNA from Medieval Plague Victims Suggests Long-Term Effect of Yersinia pestis on Human Immunity Genes
- Arredi . Barbara . Poloni . Estella S. . Paracchini . Silvia . Zerjal . Tatiana . Fathallah . Dahmani M. . Makrelouf . Mohamed . Pascali . Vincenzo L. . Novelletto . Andrea . Tyler-Smith . Chris . August 2004 . A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa . American Journal of Human Genetics . 75 . 2 . 338–345 . 10.1086/423147 . 0002-9297 . 1216069 . 15202071.
- Web site: E-M81 YTree. www.yfull.com. 2016-07-10.
- Solé-Morata N, García-Fernández C, Urasin V, Bekada A, Fadhlaoui-Zid K, Zalloua P, Comas D, Calafell F . Whole Y-chromosome sequences reveal an extremely recent origin of the most common North African paternal lineage E-M183 (M81) . Scientific Reports . 7 . 1 . 15941 . November 2017 . 29162904 . 5698413 . 10.1038/s41598-017-16271-y . 2017NatSR...715941S .
- Alvarez L, Santos C, Montiel R, Caeiro B, Baali A, Dugoujona JM, Dugoujon JM, Aluja MP . Y-chromosome variation in South Iberia: insights into the North African contribution . American Journal of Human Biology . 21 . 3 . 407–9 . 2009 . 19213004 . 10.1002/ajhb.20888 . 7041905 . free .
- Kujanová M, Pereira L, Fernandes V, Pereira JB, Cerný V . Near eastern neolithic genetic input in a small oasis of the Egyptian Western Desert . American Journal of Physical Anthropology . 140 . 2 . 336–46 . October 2009 . 19425100 . 10.1002/ajpa.21078 .
- Elkamel . Sarra . Marques . Sofia L. . Alvarez . Luis . Gomes . Veronica . Boussetta . Sami . Mourali-Chebil . Soufia . Khodjet-El-Khil . Houssein . Cherni . Lotfi . Benammar-Elgaaied . Amel . Prata . Maria J. . 2021-08-03 . Insights into the Middle Eastern paternal genetic pool in Tunisia: high prevalence of T-M70 haplogroup in an Arab population . Scientific Reports . 11 . 1 . 15728 . 10.1038/s41598-021-95144-x . 2045-2322 . 8333252 . 34344940. 2021NatSR..1115728E .
- Cruciani F, La Fratta R, Santolamazza P, Sellitto D, Pascone R, Moral P, Watson E, Guida V, Colomb EB, Zaharova B, Lavinha J, Vona G, Aman R, Cali F, Akar N, Richards M, Torroni A, Novelletto A, Scozzari R . May 2004 . Phylogeographic analysis of haplogroup E3b (E-M215) y chromosomes reveals multiple migratory events within and out of Africa . American Journal of Human Genetics . 74 . 5 . 1014–22 . 10.1086/386294 . 1181964 . 15042509.
- Solé-Morata N, García-Fernández C, Urasin V, Bekada A, Fadhlaoui-Zid K, Zalloua P, Comas D, Calafell F . 6 . Whole Y-chromosome sequences reveal an extremely recent origin of the most common North African paternal lineage E-M183 (M81) . Scientific Reports . 7 . 1 . 15941 . November 2017 . 29162904 . 5698413 . 10.1038/s41598-017-16271-y . 2017NatSR...715941S .
- Ordóñez AC, Fregel R, Trujillo-Mederos A, Hervella M, de-la-Rúa C, Arnay-de-la-Rosa M . Genetic studies on the prehispanic population buried in Punta Azul cave (El Hierro, Canary Islands). Journal of Archaeological Science. 2017. 78. 20–28 . 10.1016/j.jas.2016.11.004. 2017JArSc..78...20O .
- Adams SM, Bosch E, Balaresque PL, Ballereau SJ, Lee AC, Arroyo E, López-Parra AM, Aler M, Grifo MS, Brion M, Carracedo A, Lavinha J, Martínez-Jarreta B, Quintana-Murci L, Picornell A, Ramon M, Skorecki K, Behar DM, Calafell F, Jobling MA . The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian Peninsula . American Journal of Human Genetics . 83 . 6 . 725–36 . December 2008 . 19061982 . 2668061 . 10.1016/j.ajhg.2008.11.007 .
- Flores C, Maca-Meyer N, Larruga JM, Cabrera VM, Karadsheh N, Gonzalez AM . Isolates in a corridor of migrations: a high-resolution analysis of Y-chromosome variation in Jordan . Journal of Human Genetics . 50 . 9 . 435–41 . 2005 . 16142507 . 10.1007/s10038-005-0274-4 . free .
- Beleza S, Gusmão L, Lopes A, Alves C, Gomes I, Giouzeli M, Calafell F, Carracedo A, Amorim A . Micro-phylogeographic and demographic history of Portuguese male lineages . Annals of Human Genetics . 70 . Pt 2 . 181–94 . March 2006 . 16626329 . 10.1111/j.1529-8817.2005.00221.x . 4652154 .
- Capelli C, Onofri V, Brisighelli F, Boschi I, Scarnicci F, Masullo M, Ferri G, Tofanelli S, Tagliabracci A, Gusmao L, Amorim A, Gatto F, Kirin M, Merlitti D, Brion M, Verea AB, Romano V, Cali F, Pascali V . 6 . Moors and Saracens in Europe: estimating the medieval North African male legacy in southern Europe . European Journal of Human Genetics . 17 . 6 . 848–52 . June 2009 . 19156170 . 2947089 . 10.1038/ejhg.2008.258 .
- Maca-Meyer N, Sánchez-Velasco P, Flores C, Larruga JM, González AM, Oterino A, Leyva-Cobián F . Y chromosome and mitochondrial DNA characterization of Pasiegos, a human isolate from Cantabria (Spain) . Annals of Human Genetics . 67 . Pt 4 . 329–39 . July 2003 . 12914567 . 10.1046/j.1469-1809.2003.00045.x . 10.1.1.584.4253 . 40355653 .
- Fregel R, Gomes V, Gusmão L, González AM, Cabrera VM, Amorim A, Larruga JM . Demographic history of Canary Islands male gene-pool: replacement of native lineages by European . BMC Evolutionary Biology . 9 . 181 . August 2009 . 19650893 . 2728732 . 10.1186/1471-2148-9-181 . free .
- Ramos-Luis E, Blanco-Verea A, Brión M, Van Huffel V, Carracedo A, Sánchez-Diz P . Phylogeography of French male lineages . Forensic Science International: Genetics Supplement Series . December 2009 . 2 . 1 . 439–441 . 10.1016/j.fsigss.2009.09.026 . free .
- Martínez-Cruz B, Harmant C, Platt DE, Haak W, Manry J, Ramos-Luis E, Soria-Hernanz DF, Bauduer F, Salaberria J, Oyharçabal B. Evidence of Pre-Roman Tribal Genetic Structure in Basques from Uniparentally Inherited Markers. Molecular Biology and Evolution . 29. 9 . 2211–2222 . March 2012 . 22411853 . 10.1093/molbev/mss091 . free . 10261/112478 . free .
- Only men with French surname were analysed, in order to try to exclude more recent immigrants.
- Grugni V, Raveane A, Colombo G, Nici C, Crobu F, Ongaro L, Battaglia V, Sanna D, Al-Zahery N, Fiorani O, Lisa A, Ferretti L, Achilli A, Olivieri A, Francalacci P, Piazza A, Torroni A, Semino O . 6 . Y-chromosome and Surname Analyses for Reconstructing Past Population Structures: The Sardinian Population as a Test Case . International Journal of Molecular Sciences . 20 . 22 . 5763 . November 2019 . 31744094 . 6888588 . 10.3390/ijms20225763 . free .
- Francalacci et al. (2013), Low-Pass DNA Sequencing of 1200 Sardinians Reconstructs European Y-Chromosome Phylogeny
- Sarno S, Boattini A, Carta M, Ferri G, Alù M, Yao DY, Ciani G, Pettener D, Luiselli D . 6 . An ancient Mediterranean melting pot: investigating the uniparental genetic structure and population history of sicily and southern Italy . PLOS ONE . 9 . 4 . e96074 . 2014 . 24788788 . 4005757 . 10.1371/journal.pone.0096074 . free . 2014PLoSO...996074S . This article contains quotations from this source, which is available under a Creative Commons Attribution 4.0 International (CC BY 4.0) license.
- Mendizabal I, Sandoval K, Berniell-Lee G, Calafell F, Salas A, Martínez-Fuentes A, Comas D . Genetic origin, admixture, and asymmetry in maternal and paternal human lineages in Cuba . BMC Evolutionary Biology . 8 . 213 . July 2008 . 18644108 . 2492877 . 10.1186/1471-2148-8-213 . free .
- Silva DA, Carvalho E, Costa G, Tavares L, Amorim A, Gusmão L . Y-chromosome genetic variation in Rio de Janeiro population . American Journal of Human Biology . 18 . 6 . 829–37 . 2006 . 17039481 . 10.1002/ajhb.20567 . 23778828 .
- Paracchini S, Pearce CL, Kolonel LN, Altshuler D, Henderson BE, Tyler-Smith C . A Y chromosomal influence on prostate cancer risk: the multi-ethnic cohort study . Journal of Medical Genetics . 40 . 11 . 815–9 . November 2003 . 14627670 . 1735314 . 10.1136/jmg.40.11.815.
- Web site: E-M81 YTree . 2023-07-16 . www.yfull.com.
- Bekada A, Arauna LR, Deba T, Calafell F, Benhamamouch S, Comas D . Genetic Heterogeneity in Algerian Human Populations . PLOS ONE . 10 . 9 . e0138453 . 2015-09-24 . 26402429 . 4581715 . 10.1371/journal.pone.0138453 . 2015PLoSO..1038453B . free .
- Cherni L, Pereira L, Goios A, Loueslati BY, Khodjet el Khil H, Gomes I, Gusmão L, Alves C, Slama A, Amorim A, Elgaaied AB . 6 . Y-chromosomal STR haplotypes in three ethnic groups and one cosmopolitan population from Tunisia . Forensic Science International . 152 . 1 . 95–99 . August 2005 . 15939181 . 10.1016/j.forsciint.2005.02.007 .
- Manni F, Leonardi P, Patin É, Berrebi A, Khodjet el Khil H, Skorecki K, Rosengarten D, Rouba H, Heyer E, Fellous M . 6 . June 2005 . A Y-chromosome portrait of the population of Jerba (Tunisia) to elucidate its complex demographic history . Bulletins et mémoires de la Société d'Anthropologie de Paris . en . 17 . 1–2 . 103–114 . 10.4000/bmsap.956 . 0037-8984.
- Web site: The Berbers: Linguistic and genetic diversity . https://web.archive.org/web/20120325132014/http://www.ddl.ish-lyon.cnrs.fr/Fulltext/philippson/AUSSOIS_2005_final.pdf . dead . 2012-03-25 . Dugoujon JM, Philippson G . 2005 .
- Robino C, Crobu F, Di Gaetano C, Bekada A, Benhamamouch S, Cerutti N, Piazza A, Inturri S, Torre C . Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample . International Journal of Legal Medicine . 122 . 3 . 251–5 . May 2008 . 17909833 . 10.1007/s00414-007-0203-5 . 11556974 .
- Arredi B, Poloni ES, Paracchini S, Zerjal T, Fathallah DM, Makrelouf M, Pascali VL, Novelletto A, Tyler-Smith C . A predominantly neolithic origin for Y-chromosomal DNA variation in North Africa . American Journal of Human Genetics . 75 . 2 . 338–45 . August 2004 . 15202071 . 1216069 . 10.1086/423147 .
- Bekada A, Fregel R, Cabrera VM, Larruga JM, Pestano J, Benhamamouch S, González AM . Introducing the Algerian mitochondrial DNA and Y-chromosome profiles into the North African landscape . PLOS ONE . 8 . 2 . e56775 . February 2013 . 23431392 . 3576335 . 10.1371/journal.pone.0056775 . 2013PLoSO...856775B . free .
- Bekada . Asmahan . Arauna . Lara R. . Deba . Tahria . Calafell . Francesc . Benhamamouch . Soraya . Comas . David . 2015-09-24 . Genetic Heterogeneity in Algerian Human Populations . PLOS ONE . 10 . 9 . e0138453 . 10.1371/journal.pone.0138453 . 1932-6203 . 4581715 . 26402429 . free .
- Pereira L, Cerný V, Cerezo M, Silva NM, Hájek M, Vasíková A, Kujanová M, Brdicka R, Salas A . Linking the sub-Saharan and West Eurasian gene pools: maternal and paternal heritage of the Tuareg nomads from the African Sahel . European Journal of Human Genetics . 18 . 8 . 915–23 . August 2010 . 20234393 . 2987384 . 10.1038/ejhg.2010.21 .
- Di Gaetano C, Cerutti N, Crobu F, Robino C, Inturri S, Gino S, Guarrera S, Underhill PA, King RJ, Romano V, Cali F, Gasparini M, Matullo G, Salerno A, Torre C, Piazza A . 6 . 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 . January 2009 . 18685561 . 2985948 . 10.1038/ejhg.2008.120 .
- ((Genographic Consortium)), Zalloua PA, Platt DE, El Sibai M, Khalife J, Makhoul N, Haber M, Xue Y, Izaabel H, Bosch E, Adams SM, Arroyo E, López-Parra AM, Aler M, Picornell A, Ramon M, Jobling MA, Comas D, Bertranpetit J, Wells RS, Tyler-Smith C . 6 . Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean . American Journal of Human Genetics . 83 . 5 . 633–42 . November 2008 . 18976729 . 2668035 . 10.1016/j.ajhg.2008.10.012 .
- Ottoni C, Larmuseau MH, Vanderheyden N, Martínez-Labarga C, Primativo G, Biondi G, Decorte R, Rickards O . Deep into the roots of the Libyan Tuareg: a genetic survey of their paternal heritage . American Journal of Physical Anthropology . 145 . 1 . 118–24 . May 2011 . 21312181 . 10.1002/ajpa.21473 .
- Fadhlaoui-Zid K, Haber M, Martínez-Cruz B, Zalloua P, Benammar Elgaaied A, Comas D . Genome-wide and paternal diversity reveal a recent origin of human populations in North Africa . PLOS ONE . 8 . 11 . e80293 . 2013 . 24312208 . 3842387 . 10.1371/journal.pone.0080293 . 2013PLoSO...880293F . free .
- Reguig A, Harich N, Barakat A, Rouba H . Phylogeography of E1b1b1b-M81 haplogroup and analysis of its subclades in Morocco . Human Biology . 86 . 2 . 105–12 . 2014 . 25397701 . 10.3378/027.086.0204 . 11334895 .
- Onofri V, Alessandrini F, Turchi C, Pesaresi M, Tagliabracci A . Y-chromosome markers distribution in Northern Africa: High-resolution SNP and STR analysis in Tunisia and Morocco populations. Forensic Science International: Genetics Supplement Series . August 2008 . 1 . 1 . 235–236. 10.1016/j.fsigss.2007.10.173 .
- Bosch . Elena . Calafell . Francesc . Comas . David . Oefner . Peter J. . Underhill . Peter A. . Bertranpetit . Jaume . 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 . American Journal of Human Genetics . 68 . 4 . 1019–1029 . 10.1086/319521 . 0002-9297 . 1275654 . 11254456.
- Flores C, Maca-Meyer N, González AM, Oefner PJ, Shen P, Pérez JA, Rojas A, Larruga JM, Underhill PA . Reduced genetic structure of the Iberian peninsula revealed by Y-chromosome analysis: implications for population demography . European Journal of Human Genetics . 12 . 10 . 855–63 . October 2004 . 15280900 . 10.1038/sj.ejhg.5201225 . free .
- Gonçalves R, Freitas A, Branco M, Rosa A, Fernandes AT, Zhivotovsky LA, Underhill PA, Kivisild T, Brehm A . Y-chromosome lineages from Portugal, Madeira and Açores record elements of Sephardim and Berber ancestry . Annals of Human Genetics . 69 . Pt 4 . 443–54 . July 2005 . 15996172 . 10.1111/j.1529-8817.2005.00161.x . 3229760 . 10400.13/3018 . free .
- Nogueiro I, Manco L, Gomes V, Amorim A, Gusmão L . Phylogeographic analysis of paternal lineages in NE Portuguese Jewish communities . American Journal of Physical Anthropology . 141 . 3 . 373–81 . March 2010 . 19918998 . 10.1002/ajpa.21154 . free .
- Scozzari R, Cruciani F, Pangrazio A, Santolamazza P, Vona G, Moral P, Latini V, Varesi L, Memmi MM, Romano V, De Leo G, Gennarelli M, Jaruzelska J, Villems R, Parik J, Macaulay V, Torroni A . Human Y-chromosome variation in the western Mediterranean area: implications for the peopling of the region . Human Immunology . 62 . 9 . 871–84 . September 2001 . 11543889 . 10.1016/S0198-8859(01)00286-5 . 10.1.1.408.4857 . 2011-06-17 . 2012-12-17 . https://web.archive.org/web/20121217135021/http://evolutsioon.ut.ee/publications/Scozzari2001.pdf . dead .
- Brion M, Quintans B, Zarrabeitia M, Gonzalez-Neira A, Salas A, Lareu V, Tyler-Smith C, Carracedo A . Micro-geographical differentiation in Northern Iberia revealed by Y-chromosomal DNA analysis . Gene . 329 . 17–25 . March 2004 . 15033525 . 10.1016/j.gene.2003.12.035 .
- Santos C, Fregel R, Cabrera VM, Alvarez L, Larruga JM, Ramos A, López MA, Pilar Aluja M, González AM . Mitochondrial DNA and Y-chromosome structure at the Mediterranean and Atlantic façades of the Iberian Peninsula . American Journal of Human Biology . 26 . 2 . 130–41 . 2014 . 24375863 . 10.1002/ajhb.22497 . 205303141 .
- Regueiro M, Garcia-Bertrand R, Fadhlaoui-Zid K, Álvarez J, Herrera RJ . From Arabia to Iberia: A Y chromosome perspective . Gene . 564 . 2 . 141–52 . June 2015 . 25701402 . 10.1016/j.gene.2015.02.042 .
- Ambrosio B, Dugoujon JM, Hernández C, De La Fuente D, González-Martín A, Fortes-Lima CA, Novelletto A, Rodríguez JN, Calderón R . The Andalusian population from Huelva reveals a high diversification of Y-DNA paternal lineages from haplogroup E: Identifying human male movements within the Mediterranean space . Annals of Human Biology . 37 . 1 . 86–107 . 2010 . 19939195 . 10.3109/03014460903229155 . 1667431 .
- Alvarez L, Ciria E, Marques SL, Santos C, Aluja MP . Y-chromosome analysis in a Northwest Iberian population: unraveling the impact of Northern African lineages . American Journal of Human Biology . 26 . 6 . 740–6 . 2014 . 25123837 . 10.1002/ajhb.22602 . 205303372 .
- Ennafaa H, Fregel R, Khodjet-El-Khil H, González AM, Mahmoudi HA, Cabrera VM, Larruga JM, Benammar-Elgaaïed A . Mitochondrial DNA and Y-chromosome microstructure in Tunisia . Journal of Human Genetics . 56 . 10 . 734–41 . October 2011 . 21833004 . 10.1038/jhg.2011.92 . free .
- Fadhlaoui-Zid K, Martinez-Cruz B, Khodjet-el-khil H, Mendizabal I, Benammar-Elgaaied A, Comas D . Genetic structure of Tunisian ethnic groups revealed by paternal lineages . American Journal of Physical Anthropology . 146 . 2 . 271–80 . October 2011 . 21915847 . 10.1002/ajpa.21581 .
- Web site: E-M35 Project Data. haplozone.net. 2012-05-22. https://web.archive.org/web/20150924024908/http://www.haplozone.net/e3b/project/cluster/3. 2015-09-24. dead.
- Web site: E-M35 Project Data. haplozone.net. 2012-05-22. https://web.archive.org/web/20150924024910/http://www.haplozone.net/e3b/project/cluster/4. 2015-09-24. dead.
- Web site: E-M35 Project Data. haplozone.net. 2012-05-22. https://web.archive.org/web/20150924024913/http://www.haplozone.net/e3b/project/cluster/81. 2015-09-24. dead.
- Web site: E-M35 Project Data. haplozone.net. 2012-05-22. https://web.archive.org/web/20150924024912/http://www.haplozone.net/e3b/project/cluster/72. 2015-09-24. dead.
- Web site: E-M35 phylogeny project . As of 11 November 2008 for example, the E-M35 phylogeny project had records of four E-M123* tests, compared to 93 test results with E-M34. .
- Trombetta B, D'Atanasio E, Massaia A, Ippoliti M, Coppa A, Candilio F, Coia V, Russo G, Dugoujon JM, Moral P, Akar N, Sellitto D, Valesini G, Novelletto A, Scozzari R, Cruciani F . 6 . Phylogeographic Refinement and Large Scale Genotyping of Human Y Chromosome Haplogroup E Provide New Insights into the Dispersal of Early Pastoralists in the African Continent . Genome Biology and Evolution . 7 . 7 . 1940–50 . June 2015 . 26108492 . 4524485 . 10.1093/gbe/evv118 .
- Web site: E-CTS10880 YTree.
- Henn BM, Gignoux C, Lin AA, Oefner PJ, Shen P, Scozzari R, Cruciani F, Tishkoff SA, Mountain JL, Underhill PA . Y-chromosomal evidence of a pastoralist migration through Tanzania to southern Africa . Proceedings of the National Academy of Sciences of the United States of America . 105 . 31 . 10693–8 . August 2008 . 18678889 . 2504844 . 10.1073/pnas.0801184105 . 2008PNAS..10510693H . free .
- Karafet TM, Mendez FL, Meilerman MB, Underhill PA, Zegura SL, Hammer MF . New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree . Genome Research . 18 . 5 . 830–8 . May 2008 . 18385274 . 2336805 . 10.1101/gr.7172008 .
- Trombetta B, Cruciani F, Sellitto D, Scozzari R . A new topology of the human Y chromosome haplogroup E1b1 (E-P2) revealed through the use of newly characterized binary polymorphisms . PLOS ONE . 6 . 1 . e16073 . January 2011 . 21253605 . 3017091 . 10.1371/journal.pone.0016073 . MacAulay V . 2011PLoSO...616073T . free .
- Web site: E-M35 Project Data. haplozone.net. 2013-01-16. https://web.archive.org/web/20150924024911/http://www.haplozone.net/e3b/project/cluster/60. 2015-09-24. dead.