Haplogroup J-M267
Interpolated geographical frequency distribution.[1]
Possible time of origin17,000[2]–24,000 years before present (Di Giacomo 2004)
Possible place of originWestern Asia[3][4]
AncestorJ-P209
DescendantsJ-M62, J-M365.1, J-L136, J-Z1828
Defining mutationsM267, L255, L321, L765, L814, L827, L1030

Haplogroup J-M267, also commonly known as Haplogroup J1, is a subclade (branch) of Y-DNA haplogroup J-P209 (commonly known as haplogroup J) along with its sibling clade haplogroup J-M172 (commonly known as haplogroup J2). (All these haplogroups have had other historical names listed below.[Phylogenetics 1][Phylogenetics 2])

Men from this lineage share a common paternal ancestor, which is demonstrated and defined by the presence of the single nucleotide polymorphism (SNP) mutation referred to as M267, which was announced in (Cinnioğlu 2004). This haplogroup is found today in significant frequencies in many areas in or near the Arabian Peninsula and Western Asia. Out of its native Asian Continent, it is found at very high frequencies in Sudan. It is also found at very high but lesser extent in parts of the Caucasus, Ethiopia and parts of North Africa and amongst most Levant peoples, incl. Jewish groups, especially those with Cohen surnames. It can also be found much less commonly, but still occasionally in significant amounts, in parts of southern Europe and as far east as Central Asia.

Origins

Since the discovery of haplogroup J-P209 it has generally been recognized that it shows signs of having evolved ~ 20,000 years ago somewhere in northwestern Iran, the Caucasus, the Armenian Highlands, and northern Mesopotamia.[5][6][3] The frequency and diversity of both its major branches, J-M267 and J-M172, in that region makes them candidates as genetic markers of the spread of farming technology during the Neolithic, which is proposed to have had a major impact upon human populations.

J-M267 has several recognized subclades, some of which were recognized before J-M267 itself was recognized, for example J-M62 Y Chromosome Consortium "YCC" 2002. With one notable exception, J-P58, most of these are not common (Tofanelli 2009). Because of the dominance of J-P58 in J-M267 populations in many areas, discussion of J-M267's origins require a discussion of J-P58 at the same time.

Distribution

Africa

North Africa and Horn of Africa

North Africa received Semitic migrations, according to some studies it may have been diffused in recent time by Arabs who, mainly from the 7th century A.D., expanded to northern Africa (Arredi 2004 and Semino 2004). However the Canary Islands is not known to have had any Semitic language. In North Africa J-M267 is dominated by J-P58, and dispersed in a very uneven manner according to studies so far, often but not always being lower among Berber and/or non-urban populations. In Ethiopia there are signs of older movements of J-M267 into Africa across the Red Sea, not only in the J-P58 form. This also appears to be associated with Semitic languages. According to a study in 2011, in Tunisia, J-M267 is significantly more abundant in the urban (31.3%) than in the rural total population (2.5%) (Ennafaa 2011).

Population Sample size J*(xJ-M172) total J-M267 J-M267(xP58) J-P58 publication previous research on same samples
Algeria (Arabs from Oran)102NA22.5%NANARobino 2007
Algeria20NA35%NANASemino 2004
Egypt147NA21.1%1.4%19.7%Chiaroni 2009Luis 2004
Egypt124NA19.8%NANAEl-Sibai 2009
Egypt (Siwa, Western Desert)35NA31.4%NANAKujanová 2009
Libya (Tuareg)47NA0%NANAOttoni 2011
Libya (Benghazi)238NA39.5%NANAAlvarez 2014[7]Elmrghni 2012
Morocco (Arabs)87NA26.4%NANAFadhlaoui-Zid 2013[8]
Morocco (Arabs)49NA20.4%NANASemino 2004
Morocco (Arabs) 28 NA 60.7% NA NA Underhill 2000[9]
Morocco (Arabs) 19 NA 31.5% NA NA Francalacci 2008[10]
Morocco (Berbers)64NA6.3%NANASemino 2004
Morocco (Berbers)103NA10.7%NANASemino 2004
Morocco (Rabat)267NA21.3%NANAAlvarez 2014Aboukhalid 2010
Morocco (Casablanca)166NA15.7%NANAAlvarez 2014Laouina 2011
Morocco (Figuig)96NA29.2%NANAAlvarez 2014Palet 2010
Morocco (El Jadida)49NA8.2%NANAAlvarez 2014
Morocco (Fes)108NA16.7%0.0%16.7%Regueiro 2015
Tunisia73NA34.2%NANASemino 2004
Tunisia 601 Na 16.64% NA NA Pestano J, et al. (2013)[11]
Tunisia (Sousse)220NA25.9%0.0%25.9%Fadhlaoui-Zid 2015[12]
Tunisia (Tunis)148NA32.4%1.3%31.1%Grugni 2012Arredi 2004
Tunisia52NA34.6%NANAOnofri 2008
Tunisia (Bou Omran Berbers)40NA0%NANAEnnafaa 2011
Tunisia (Bou Saad Berbers)40NA5%0%5%Ennafaa 2011
Tunisia (Jerbian Arabs)46NA8.7%NANAEnnafaa 2011
Tunisia (Jerbian Berbers)47NA0%NANAEnnafaa 2011
Tunisia (Sened Berbers)35NA31.4%0%31.4%Fadhlaoui-Zid 2011
Tunisia (Andalusi Zaghouan)32NA43.8%0%43.8%Fadhlaoui-Zid 2011
Tunisia (Cosmopolitan Tunis)33NA24.20%24.2%Fadhlaoui-Zid 2011
Tunisia (Sejenane)47NA34.0%NANAAlvarez 2014Frigi 2011
Tunisia (Sfax)56NA25%0.0%25%Regueiro 2015
Tunisia (Beja)72NA15.3%0.0%15.3%Regueiro 2015
Canary Islands (pre-Hispanic)30NA16.7%NANAFregel 2009
Canary Islands (17th-18th c)42NA11.9%NANAFregel 2009
Canary Islands652NA3.5%NANAFregel 2009
Sahrawis89NA20.2%NANAFregel 2009Bosch 2001 and Flores 2001
Sudan (Khartoum)35NA74.3%0.0%74.3%Chiaroni 2009Tofanelli 2009 and Hassan 2008
Sudan (Sudanese Arabs)35NA17.1%0.0%17.1%Chiaroni 2009Hassan 2008
Sudan (Nilo-Saharans)61NA4.9%3.3%1.6%Chiaroni 2009Hassan 2008
Ethiopia (Oromo)78NA2.6%2.6%0.0%Chiaroni 2009Semino 2004
Ethiopia (Amhara)48NA29.2%8.3%20.8%Chiaroni 2009Semino 2004
Ethiopia (Arsi)8522%NANANAMoran 2004
Ethiopia9521%NANANAMoran 2004
Somalis 201 0.5% 2.5% NA 2.5% Sanchez 2005 J-P58 might be 5% in upcoming study
Comoros293NA5.0%NANAMsaidie 2011
South Africa (Lemba) 76 NA 39.5% 26.3% 13.2% Soodyall 2011
Zimbabwe (Lemba) 54 NA 9.3% 9.3% NA Soodyall 2011

Asia

South Asia

J*(xJ-M172) was found in India among Indian Muslims.[13]

Population Sample size J*(xJ-M172) total J-M267 J-M267(xP58) J-P58 Publication
India (Shia)16110.6%NANANAEaaswarkhanth 2009
India (Sunni)1292.3%NANANAEaaswarkhanth 2009
India (Mappla)4010%NANANAEaaswarkhanth 2009

West Asia

The area including eastern Turkey and the Zagros and Taurus mountains, has been identified as a likely area of ancient J-M267 diversity. Both J-P58 and other types of J-M267 are present, sometimes with similar frequencies.

Population Sample size Total J-M267 J-M267(xP58) J-P58 Publication Previous research on same samples
Turkey5239.0%3.1%5.9%Chiaroni 2009Cinnioğlu 2004
Iran15011.3%2.7%8.7%Chiaroni 2009Regueiro 2006
Iran (Khuzestan) NA 33.4% NA NA Kivisild 2012[14]
Iraq (Kurds)9311.8%4.3%7.5%Chiaroni 2009
Iraq (Assyrians)2828.6%17.9%10.7%Chiaroni 2009
Iraq (Arabs)5664.1%1.8%62.3%Chiaroni 2009Tofanelli 2009
Iran (Assyrians)3116.1%9.7%6.5%Chiaroni 2009
Iran923.2%NANAEl-Sibai 2009
Turkey (Assyrians)2520.0%16.0%4.0%Chiaroni 2009

Levant and Semitic populations

J-M267 is very common throughout this region, dominated by J-P58, but some specific sub-populations have notably low frequencies.

Population Sample size Total J-M267 J-M267(xP58) J-P58 Publication Previous research on same samples
Syria55433.6%NANAEl-Sibai 2009Zalloua 2008a
Syria (Jabel Druze)3414.7%2.9%11.8%Chiaroni 2009
Syria (Hama Sunnis)3647.2%2.8%44.4%Chiaroni 2009
Syria (Ma'loula Aramaeans)446.8%4.5%2.3%Chiaroni 2009
Syria (Sednaya Syriac Catholic)1414.3%0.0%14.3%Chiaroni 2009
Syria (Damascus Syriac Catholic)429.5%0.0%9.5%Chiaroni 2009
Syria (Alawites)4526.7%0.0%26.7%Chiaroni 2009
Syria (North-east Assyrians)303.3%0.0%3.3%Chiaroni 2009
Syria (Damascus Ismailis)5158.8%0.0%58.8%Chiaroni 2009
Lebanon95125%NANAZalloua 2008a
Galilee Druze17213.4%1.2%12.2%Chiaroni 2009Shlush 2008
Palestinians (Akka)10139.2%NANAZalloua 2008b
Palestinians4932.7%0.0%32.7%Chiaroni 2009
Jordan7648.7%0.0%48.7%Chiaroni 2009
Jordan27335.5%NANAEl-Sibai 2009
Jordan (Amman)10140.6%NANAFlores 2005
Jordan (Dead Sea)458.9%NANAFlores 2005
Jews (Trás-os-Montes, Portugal)5712.3%NANANogueiro 2009
Jews (Cohanim)21546.0%0.0%46.0%Hammer 2009
Jews (non-Cohanim Ashkenazi)1,36014.9%0.9%14.0%Hammer 2009
Bedouin (Negev)2867.9%3.6%64.3%Chiaroni 2009Cann 2002

Arabian peninsula

J-P58 is the most common Y-Chromosome haplogroup among men from all of this region.

Population Sample size Total J-M267 J-M267(xP58) J-P58 Publication Previous research on same samples
Saudi Arabia15740.1%NANAAbu-Amero 2009
Qatar7258.3%1.4%56.9%Chiaroni 2009Cadenas 2008
United Arab Emirates16434.8%0.0%34.8%Chiaroni 2009Cadenas 2008
Yemen6272.6%4.8%67.7%Chiaroni 2009Cadenas 2008
Kuwait11745.2%NANA[15]
Oman12138.0%0.8%37.2%Chiaroni 2009Luis 2004

Europe

J-M267 is uncommon in most of Northern and Central Europe. It is, however, found in significant pockets at levels of 5–10% among many populations in southern Europe. A recent study with the extant variation concludes that the Caucasus is likely to be the source of the Greek and Italian haplogroup J1-M267 chromosomes.[16]

Population Sample size Total J-M267 J-M267(xP58) J-P58 publication
Albania563.6%NANASemino 2004
North Macedonia (Albanian speakers)646.3%NANABattaglia 2008
Malta907.8%NANAEl-Sibai 2009[17]
Greece (Crete)1938.3%NANAKing 2008
Greece (mainland)1714.7%NANAKing 2008
Greece (Macedonia)561.8%NANASemino 2004
Greece2491.6%NANADi Giacomo 2004
Bulgaria8083.4%NANAKarachanak 2013
Romania1301.5%NANADi Giacomo 2004
Russia2230.4%NANADi Giacomo 2004
Croatia (Osijek Croats)290%NANABattaglia 2008
Slovenia751.3%NANABattaglia 2008
Italy (northeast Italians)670%NANABattaglia 2008
Italy (Italians)9150.7%NANACapelli 2009
Italy (Sicily)2363.8%NANADi Gaetano 2008
France (Provence)512%NANAKing 2011
Portugal (North)1011%NANAGonçalves 2005
Portugal (Centre)1024.9%NANAGonçalves 2005
Portugal (South)1007%NANAGonçalves 2005
Portugal (Açores)1212.5%NANAGonçalves 2005
Portugal (Madeira)1290%NANAGonçalves 2005

Caucasus

The Caucasus has areas of both high and low J-M267 frequency. The J-M267 in the Caucasus is also notable because most of it is not within the J-P58 subclade.

Population Sample size Total J-M267 J-M267(xP58) J-P58 Publication
Avars11559%58%1%Balanovsky 2011
Dargins10170%69%1%Balanovsky 2011
Kubachi6599%99%0%Balanovsky 2011
Kaitak3385%85%0%Balanovsky 2011
Lezghins8144.4%44.4%0%Balanovsky 2011
Shapsug1000%0%0%Balanovsky 2011
Abkhaz580%0%0%Balanovsky 2011
Circassians14211.9%4.9%7%Balanovsky 2011
Ingush1432.8%2.8%0%Balanovsky 2011
Ossetians3571.3%1.3%0.0%Balanovsky 2011
Chechens (Ingushetia)11221%21%0%Balanovsky 2011
Chechens (Chechnya)11825%25%0%Balanovsky 2011
Chechens (Dagestan)10016%16%0%Balanovsky 2011
Azerbaijan4615.2%NANADi Giacomo 2004

Subclade Distribution

J-P58

The P58 marker which defines subgroup J1c3 was announced in (Karafet 2008), but had been announced earlier under the name Page08 in (Repping 2006 and called that again in Chiaroni 2009). It is very prevalent in many areas where J-M267 is common, especially in parts of North Africa and throughout the Arabian peninsula. It also makes up approximately 70% of the J-M267 among the Amhara of Ethiopia. Notably, it is not common among the J-M267 of the Caucasus.

Chiaroni 2009 proposed that J-P58 (that they refer to as J1e) might have first dispersed during the Pre-Pottery Neolithic B period, "from a geographical zone, including northeast Syria, northern Iraq and eastern Turkey toward Mediterranean Anatolia, Ismaili from southern Syria, Jordan, Palestine and northern Egypt." They further propose that the Zarzian material culture may be ancestral. They also propose that this movement of people may also be linked to the dispersal of Semitic languages by hunter-herders, who moved into arid areas during periods known to have had low rainfall. Thus, while other haplogroups including J-M267 moved out of the area with agriculturalists who followed the rainfall, populations carrying J-M267 remained with their flocks (King 2002 and Chiaroni 2008).

According to this scenario, after the initial neolithic expansion involving Semitic languages, which possibly reached as far as Yemen, a more recent dispersal occurred during the Chalcolithic or Early Bronze Age (approximately 3000–5000 BCE), and this involved the branch of Semitic which leads to the Arabic language. The authors propose that this involved a spread of some J-P58 from the direction of Syria towards Arab populations of the Arabian Peninsula and Negev.

On the other hand, the authors agree that later waves of dispersion in and around this area have also had complex effects upon the distributions of some types of J-P58 in some regions. They list three regions which are particularly important to their proposal:

  1. The Levant (Syria, Jordan, Israel and Palestine). In this area, Chiaroni 2009 note a "patchy distribution of J1c3 or J-P58 frequency" which is difficult to interpret, and which "may reflect the complex demographic dynamics of religion and ethnicity in the region".
  2. The Eastern Anatolia, northern Iraq and western Iran. In this area, Chiaroni 2009 recognize signs that J-M267 might have an older presence, and on balance they accept the evidence but note that it could be in error.
  3. The southern area of Oman, Yemen and Ethiopia. In this area, Chiaroni 2009 recognize similar signs, but reject it as possibly a result of "either sampling variability and/or demographic complexity associated with multiple founders and multiple migrations."

The "YCAII=22-22 and DYS388≥15" cluster

Studies show that J-P58 group is not only in itself very dominant in many areas where J-M267 or J1 are common, but it also contains a large cluster which had been recognized before the discovery of P58. It is still a subject of research though.

This relatively young cluster, compared to J-M267 overall, was identified by STR markers haplotypes - specifically YCAII as 22-22, and DYS388 having unusual repeat values of 15 or higher, instead of more typical 13 (Chiaroni 2009) This cluster was found to be relevant in some well-publicized studies of Jewish and Palestinian populations (Nebel 2000 and Hammer 2009). More generally, since then this cluster has been found to be frequent among men in the Middle East and North Africa, but less frequent in areas of Ethiopia and Europe where J-M267 is nevertheless common. The genetical pattern is therefore similar to the pattern of J-P58 generally, described above, and may be caused by the same movements/migration of people (Chiaroni 2009).

Tofanelli 2009 refers to this overall cluster with YCAII=22-22 and high DYS388 values as an "Arabic" as opposed to a "Eurasian" type of J-M267. This Arabic type includes Arabic speakers from Maghreb, Sudan, Iraq and Qatar, and it is a relatively homogeneous group, implying that it might have dispersed relatively recently compared to J-M267 generally. The more diverse "Eurasian" group includes Europeans, Kurds, Iranians and Ethiopians (despite Ethiopia being outside of Eurasia), and is much more diverse. The authors also say that "Omanis show a mix of Eurasian pool-like and typical Arabic haplotypes as expected, considering the role of corridor played at different times by the Gulf of Oman in the dispersal of Asian and East African genes." Chiaroni 2009 also noted the anomalously high apparent age of Omani J-M267 when looking more generally at J-P58 and J-M267 more generally.

This cluster in turn contains three well-known related sub-clusters. First, it contains the majority of the Jewish "Cohen modal haplotype", found among Jewish populations, but especially in men with surnames related to Cohen. It also contains the "Galilee modal haplotype" (GMH) and "Palestinian & Israeli Arab modal haplotype", both of which are associated with Palestinian/Israeli Arabs by Nebel 2000 and Hammer 2009. Nebel 2002 then pointed out that the GMH is also the most frequent type of J-P209 haplotype found in north-west Africans and Yemenis, so it is not restricted to Israel and Palestine. However, this particular variant "is absent" from two particular "non-Arab Middle Eastern populations", namely "Jews and Muslim Kurds" (even though both of these populations do have high levels of J-P209). Nebel 2002 noted not only the presence of the GMH in the Maghreb but also that J-M267 in this region had very little diversity. They concluded that J-M267 in this region is a result of two distinct migration events: "early Neolithic dispersion" and "expansions from the Arabian peninsula" during the 7th century.Semino 2004 later agreed that this seemed consistent with the evidence and generalized from this that distribution of the entire YCAII=22-22 cluster of J-M267 in the Arabic-speaking areas of the Middle East and North Africa might in fact mainly have an origin in historical times.

More recent studies have emphasized doubt that the Islamic expansions are old enough to completely explain the major patterns of J-M267 frequencies. Chiaroni 2009 rejected this for J-P58 as a whole, but accepted that "some of the populations with low diversity, such as Bedouins from Israel, Qatar, Sudan and UAE, are tightly clustered near high-frequency haplotypes suggesting founder effects with star burst expansion in the Arabian Desert". They did not comment on the Maghreb.

Tofanelli 2009 take a stronger position of rejecting any strong correlation between the Arab expansion and either the YCAII=22-22 STR-defined sub-cluster as discussed by Semino 2004 or the smaller "Galilee modal haplotype" as discussed by (Nebel 2002). They also estimate that the Cohen modal haplotype must be older than 4500 years old, and maybe as much as 8600 years old - well before the supposed origin of the Cohanim. Only the "Palestinian & Israeli Arab" modal had a strong correlation to an ethnic group, but it was also rare. In conclusion, the authors were negative about the usefulness of STR defined modals for any "forensic or genealogical purposes" because "they were found across ethnic groups with different cultural or geographic affiliation".

Hammer 2009 disagreed, at least concerning the Cohen modal haplotype. They said that it was necessary to look at a more detailed STR haplotype in order to define a new "Extended Cohen Modal Haplotype" which is extremely rare outside Jewish populations, and even within Jewish populations is mainly only found in Cohanim. They also said that by using more markers and a more restrictive definition, the estimated age of the Cohanim lineage is lower than the estimates of Tofanelli 2009, and it is consistent with a common ancestor at the approximate time of founding of the priesthood which is the source of Cohen surnames.

Tofanelli et al. 2014 responded by saying: "In conclusion, while the observed distribution of sub-clades of haplotypes at mitochondrial and Y chromosome non-recombinant genomes might be compatible with founder events in recent times at the origin of Jewish groups as Cohenite, Levite, Ashkenazite, the overall substantial polyphyletism as well as their systematic occurrence in non-Jewish groups highlights the lack of support for using them either as markers of Jewish ancestry or Biblical tales."[18]

J-M368

The correspondence between P58 and high DYS388 values, and YCAII=22-22 is not perfect. For example the J-M267 subclade of J-P58 defined by SNP M368 has DYS388=13 and YCAII=19-22, like other types of J-M267 outside the "Arabic" type of J-M267, and it is therefore believed to be a relatively old offshoot of J-P58, that did not take part in the most recent waves of J-M267 expansion in the Middle East (Chiaroni 2009). These DYS388=13 haplotypes are most common in the Caucasus and Anatolia, but also found in Ethiopia (Tofanelli 2009).

Phylogenetics and distribution

There are several confirmed and proposed phylogenetic trees available for haplogroup J-M267. The following phylogeny or family tree of J-M267 haplogroup subclades is based on the ISOGG (2012) tree, which is in turn based upon the YCC 2008 tree and subsequent published research.

J1 (L255, L321, M267)

  • J1* J1* clusters are found in Eastern Anatolia and parts of the Caucasus.
  • J1a (M62) Found at very low frequency in Britain.
  • J1b (M365.1) Found at low frequency in Eastern Anatolia, Iran and parts of Europe.
  • J1c (L136)
    • J1c* Found at low frequency in Europe.
    • J1c1 (M390)
    • J1c2 (P56) Found sporadically in Anatolia, East Africa, the Arabian Peninsula and Europe.
    • J1c3
      • J1c3* Found at low frequency in the Levant and the Arabian Peninsula.
      • J1c3a (M367.1, M368.1) Previously known as J1e1.
      • J1c3b (M369) Previously known as J1e2.
      • J1c3c (L92, L93) Found at low frequency in South Arabia.
      • J1c3d (L147.1) Accounts for the majority of J1, the predominant haplogroup in the Arabian peninsula.
        • J1c3d* Accounts for the majority of J1 in Yemen, Cohen Jews (both Rabbinical and Karaitic),[19] but missing from Quraysh including Sharif of Makkah of Banu Hashem clan.
        • J1c3d1 (L174.1)
        • J1c3d2 (L222.2) Accounts for the majority of J1c3d in Saudi Arabia. An important element of J1c3d in North Africa.
          • J1c3d2*
            • J1c3d2a (L65.2/S159.2)

Ancient DNA

Alalakh Amorite city-state

Five out 12 male individuals from Alalakh who lived between 1930-1325 BC, belonged to haplogroup J1-P58.[20][21]

Arslantepe archaeological complex

One out of 18 male individuals from Arslantepe who lived c. 3491-3122 BC, belonged to haplogroup J1-Z1824.[22][23]

Ancient city of Ebla

Three out of 6 individuals from Ebla who lived between 2565-1896 BC, belonged to J1-P58.[24][25] Ebla was an ancient East Semitic-speaking city and kingdom in Syria in the early Bronze age that was destroyed by the Akkadians.

Karelia

A member of haplogroup J1-M267 is found among eastern hunter-gatherers from Karelia, Northeast Europe living ~ 8.3 kya. This branch is absent in other ancient European hunter-gatherers. Unfortunately, it is not possible to put this sample in the context of the current haplogroup J1-M267 variation because of the poor quality of the DNA sequence.[3]

Sardinia

Olivieri et al. found a J1c3 haplotype in one of their ancient samples from Sardinia, dated to 6190–6000 calBP.[26]

Satsurblia

An ancient sample of J1 was found at Satsurblia Cave circa 11,000 BC, specifically belonging to the rare J1-FT34521 subclade.[27] The ancient individual from Satsurblia was male with black hair, brown eyes, and light skin.

Tell Kurdu

One out of 4 male individuals from Tell Kurdu who lived circa 5706-5622 BC, belonged to J1-L620.[28][29]

See also

Genetics

Y-DNA J Subclades

Y-DNA Backbone Tree

References

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  2. J1
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  4. Rebai, Ahmed. "Synthetic review on the genetic relatedness between North Africa and Arabia deduced from paternal lineage distributions".
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  7. Alvarez, Luis; Ciria, Estela; Marques, Sofia L.; Santos, Cristina; Aluja, Maria Pilar (2014). "Y-chromosome analysis in a Northwest Iberian population: Unraveling the impact of Northern African lineages". American Journal of Human Biology. 26 (6): 740–746. doi:10.1002/ajhb.22602. PMID 25123837. S2CID 205303372.
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  14. Grugni, Viola; Battaglia, Vincenza; Hooshiar Kashani, Baharak; Parolo, Silvia; Al-Zahery, Nadia; Achilli, Alessandro; Olivieri, Anna; Gandini, Francesca; Houshmand, Massoud; Sanati, Mohammad Hossein; Torroni, Antonio; Semino, Ornella (2012-07-18). "Ancient Migratory Events in the Middle East: New Clues from the Y-Chromosome Variation of Modern Iranians". PLOS ONE. 7 (7): e41252. Bibcode:2012PLoSO...741252G. doi:10.1371/journal.pone.0041252. ISSN 1932-6203. PMC 3399854. PMID 22815981.
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  17. El-Sibai et al.,2009, Percentage of haplogroups
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  20. "J-P58 YTree".
  21. Skourtanioti, Eirini; Erdal, Yilmaz S.; Frangipane, Marcella; Balossi Restelli, Francesca; Yener, K. Aslıhan; Pinnock, Frances; Matthiae, Paolo; Özbal, Rana; Schoop, Ulf-Dietrich; Guliyev, Farhad; Akhundov, Tufan; Lyonnet, Bertille; Hammer, Emily L.; Nugent, Selin E.; Burri, Marta; Neumann, Gunnar U.; Penske, Sandra; Ingman, Tara; Akar, Murat; Shafiq, Rula; Palumbi, Giulio; Eisenmann, Stefanie; d'Andrea, Marta; Rohrlach, Adam B.; Warinner, Christina; Jeong, Choongwon; Stockhammer, Philipp W.; Haak, Wolfgang; Krause, Johannes (2020). "Genomic History of Neolithic to Bronze Age Anatolia, Northern Levant, and Southern Caucasus". Cell. 181 (5): 1158–1175.e28. doi:10.1016/j.cell.2020.04.044. hdl:20.500.12154/1254. PMID 32470401. S2CID 219105572.
  22. "J-Z1842 YTree".
  23. Skourtanioti, Eirini; Erdal, Yilmaz S.; Frangipane, Marcella; Balossi Restelli, Francesca; Yener, K. Aslıhan; Pinnock, Frances; Matthiae, Paolo; Özbal, Rana; Schoop, Ulf-Dietrich; Guliyev, Farhad; Akhundov, Tufan; Lyonnet, Bertille; Hammer, Emily L.; Nugent, Selin E.; Burri, Marta; Neumann, Gunnar U.; Penske, Sandra; Ingman, Tara; Akar, Murat; Shafiq, Rula; Palumbi, Giulio; Eisenmann, Stefanie; d'Andrea, Marta; Rohrlach, Adam B.; Warinner, Christina; Jeong, Choongwon; Stockhammer, Philipp W.; Haak, Wolfgang; Krause, Johannes (2020). "Genomic History of Neolithic to Bronze Age Anatolia, Northern Levant, and Southern Caucasus". Cell. 181 (5): 1158–1175.e28. doi:10.1016/j.cell.2020.04.044. hdl:20.500.12154/1254. PMID 32470401. S2CID 219105572.
  24. "J-P58 YTree".
  25. Skourtanioti, Eirini; Erdal, Yilmaz S.; Frangipane, Marcella; Balossi Restelli, Francesca; Yener, K. Aslıhan; Pinnock, Frances; Matthiae, Paolo; Özbal, Rana; Schoop, Ulf-Dietrich; Guliyev, Farhad; Akhundov, Tufan; Lyonnet, Bertille; Hammer, Emily L.; Nugent, Selin E.; Burri, Marta; Neumann, Gunnar U.; Penske, Sandra; Ingman, Tara; Akar, Murat; Shafiq, Rula; Palumbi, Giulio; Eisenmann, Stefanie; d'Andrea, Marta; Rohrlach, Adam B.; Warinner, Christina; Jeong, Choongwon; Stockhammer, Philipp W.; Haak, Wolfgang; Krause, Johannes (2020). "Genomic History of Neolithic to Bronze Age Anatolia, Northern Levant, and Southern Caucasus". Cell. 181 (5): 1158–1175.e28. doi:10.1016/j.cell.2020.04.044. hdl:20.500.12154/1254. PMID 32470401. S2CID 219105572.
  26. Olivieri, A.; Sidore, C.; Achilli, A.; Angius, A.; Posth, C.; Furtwängler, A.; Brandini, S.; Rosario Capodiferro, M.; Gandini, F.; Zoledziewska, M.; Pitzalis, M.; Maschio, A.; Busonero, F.; Lai, L.; Skeates, R. (2017-05-01). "Mitogenome diversity in Sardinians : a genetic window onto an island's past". Molecular Biology and Evolution. 34 (5): 1230–1239. doi:10.1093/molbev/msx082. ISSN 0737-4038. PMC 5400395. PMID 28177087.
  27. "J-Y6313 YTree".
  28. "J-L620 YTree".
  29. Skourtanioti, Eirini; Erdal, Yilmaz S.; Frangipane, Marcella; Balossi Restelli, Francesca; Yener, K. Aslıhan; Pinnock, Frances; Matthiae, Paolo; Özbal, Rana; Schoop, Ulf-Dietrich; Guliyev, Farhad; Akhundov, Tufan; Lyonnet, Bertille; Hammer, Emily L.; Nugent, Selin E.; Burri, Marta; Neumann, Gunnar U.; Penske, Sandra; Ingman, Tara; Akar, Murat; Shafiq, Rula; Palumbi, Giulio; Eisenmann, Stefanie; d'Andrea, Marta; Rohrlach, Adam B.; Warinner, Christina; Jeong, Choongwon; Stockhammer, Philipp W.; Haak, Wolfgang; Krause, Johannes (2020). "Genomic History of Neolithic to Bronze Age Anatolia, Northern Levant, and Southern Caucasus". Cell. 181 (5): 1158–1175.e28. doi:10.1016/j.cell.2020.04.044. hdl:20.500.12154/1254. PMID 32470401. S2CID 219105572.

Footnotes

    Works cited

    Journals

    • Onofri, Valerio; Alessandrini, Federica; Turchi, Chiara; Pesaresi, Mauro; Tagliabracci, Adriano (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: 235–236. doi:10.1016/j.fsigss.2007.10.173.
    • Ottoni, Claudio; Larmuseau, Maarten H.D.; Vanderheyden, Nancy; Martínez-Labarga, Cristina; Primativo, Giuseppina; Biondi, Gianfranco; Decorte, Ronny; Rickards, Olga (2011). "Deep into the roots of the Libyan Tuareg: A genetic survey of their paternal heritage". American Journal of Physical Anthropology. 145 (1): 118–124. doi:10.1002/ajpa.21473. PMID 21312181.
    • Regueiro, M.; Cadenas, A.M.; Gayden, T.; Underhill, P.A.; Herrera, R.J. (2006). "Iran: tricontinental nexus for Y-chromosome driven migration". Human Heredity. 61 (3): 132–143. doi:10.1159/000093774. PMID 16770078. S2CID 7017701.
    • Repping, S; van Daalen, SK; Brown, LG; Korver, Cindy M; Lange, Julian; Marszalek, Janet D; Pyntikova, Tatyana; van der Veen, Fulco; et al. (2006). "High mutation rates have driven extensive structural polymorphism among human Y chromosomes". Nat Genet. 38 (4): 463–467. CiteSeerX 10.1.1.537.1822. doi:10.1038/ng1754. PMID 16501575. S2CID 17083896.
    • Robino, C.; Crobu, F.; Di Gaetano, C.; Bekada, A.; Benhamamouch, S.; Cerutti, N.; Piazza, A.; Inturri, S.; Torre, C. (2008). "Analysis of Y-chromosomal SNP haplogroups and STR haplotypes in an Algerian population sample". International Journal of Legal Medicine. 122 (3): 251–255. doi:10.1007/s00414-007-0203-5. PMID 17909833. S2CID 11556974.
    • Shen, Peidong; Lavi, Tal; Kivisild, Toomas; Chou, Vivian; Sengun, Deniz; Gefel, Dov; Shpirer, Issac; Woolf, Eilon; et al. (2004). "Reconstruction of patrilineages and matrilineages of Samaritans and other Israeli populations from Y-chromosome and mitochondrial DNA sequence variation". Human Mutation. 24 (3): 248–260. doi:10.1002/humu.20077. PMID 15300852. S2CID 1571356.

    Websites

    Haplogroups/Phylogeny

    Haplotype/SNP research Projects. See also Y-DNA haplogroup projects (ISOGG Wiki)

    • Schrack; Janzen; Rottensteiner; Ricci; Mas (2013). "Y-DNA J Haplogroup Project". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 2300 members.
      • Givargidze; Hrechdakian (2013). "J1* Y-DNA Project". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 150 members.
      • Al Haddad (2013). "J1c3 (J-L147)". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 550 members.
      • Cone; Al Gazzah; Sanders (2013). "J-M172 Y-DNA Project (J2)". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 1050 members.
      • Aburto; Katz; Al Gazzah; Janzen (2013). "J-L24-Y-DNA Haplogroup Project (J2a1h)". Family Tree DNA. This is an ongoing research project by citizen scientists. Over 450 members.

    Haplogroup-Specific Ethnic/Geographical Group Projects

    Further reading

    Phylogenetic Notes

    1. This table shows the historic names for J-M267 and its earlier discovered and named subclade J-M62 in published peer reviewed literature.
      YCC 2002/2008 (Shorthand) J-M267 J-M62
      Jobling and Tyler-Smith 2000-9
      Underhill 2000-VI
      Hammer 2001-Med
      Karafet 2001-23
      Semino 2000-Eu10
      Su 1999-H4
      Capelli 2001-B
      YCC 2002 (Longhand)-J1
      YCC 2005 (Longhand)J1J1a
      YCC 2008 (Longhand)J1J1a
      YCC 2010r (Longhand)J1J1a
    2. This table shows the historic names for J-P209 (AKA J-12f2.1 or J-M304) in published peer reviewed literature. Note that in Semino 2000 Eu09 is a subclade of Eu10 and in Karafet 2001 24 is a subclade of 23.
      YCC 2002/2008 (Shorthand) J-P209
      (AKA J-12f2.1 or J-M304)
      Jobling and Tyler-Smith 20009
      Underhill 2000VI
      Hammer 2001Med
      Karafet 200123
      Semino 2000Eu10
      Su 1999H4
      Capelli 2001B
      YCC 2002 (Longhand)J*
      YCC 2005 (Longhand)J
      YCC 2008 (Longhand)J
      YCC 2010r (Longhand)J
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