Haplogroup O-M117
Haplogroup O-M117 | |
---|---|
Possible time of origin | 18,203 [95% CI 16,626 <-> 19,783] years ago (Karmin 2015[2]) 17,430 ybp[3] 17,400 [95% CI 19,100 <-> 15,800] ybp (YFull[4]) |
Coalescence age | 13,750 ybp[3] 12,600 [95% CI 11,300 <-> 14,000] ybp (YFull[4]) |
Possible place of origin | probably East Asia or Southeast Asia[citation needed] |
Ancestor | O-M134 |
Descendants | O-M133 |
Defining mutations | M117, Page23, CTS899/M1531, CTS1275/M1536, CTS3251, CTS5128/M1619, CTS6623/M1638, CTS11742/M1720, F141/M1564, F144, F235/M1587, F342/M1627, F373/M1636, F476/M1671, F579/M1692, F581, F584, F613/M1702, F649[citation needed] |
Haplogroup O2a2b1a1-M117 or Haplogroup O2a2b1a1-M117 (also defined by the phylogenetically equivalent mutation Page23/F8/F42) is a subclade of O2a2b1-M134 (and also a subclade of haplogroup O2-M122) that occurs frequently in China and in neighboring countries like Bhutan, Nepal, and Korea, also found among Sino-Tibetan language speaking people.
O2-M117 has been detected in samples of Tamang (38/45 = 84.4%), Tibetans (45/156 = 28.8% or 13/35 = 37.1%), Tharus (57/171 = 33.3%), Han Taiwanese (40/183 = 21.9%), Newars (14/66 = 21.2%), the general population of Kathmandu, Nepal (13/77 = 16.9%), Han Chinese (5/34 = 14.7% Chengdu, 5/35 = 14.3% Harbin, 4/35 = 11.4% Meixian, 3/30 = 10.0% Lanzhou, 2/32 = 6.3% Yili), Tungusic peoples from the PRC (7/45 = 15.6% Hezhe, 4/26 = 15.4% Evenki, 5/35 = 14.3% Manchu, 2/41 = 4.9% Xibe, 1/31 = 3.2% Oroqen), and Uyghurs (2/39 = 5.1% Yili, 1/31 = 3.2% Ürümqi) (Xue et al. 2006, Gayden et al. 2007, and Fornarino et al. 2009).
Like O-M7, O-M117 has been found with greatly varying frequency in many samples of Hmong-Mien-speaking peoples, such as Mienic peoples (7/20 = 35.0% Mountain Straggler Mien, 9/28 = 32.1% Blue Kimmun, 6/19 = 31.6% Flower Head Mien, 3/11 = 27.3% Top Board Mien, 3/11 = 27.3% Thin Board Mien, 11/47 = 23.4% Western Mien, 6/33 = 18.2% Northern Mien, 5/31 = 16.1% Lowland Yao, 5/35 = 14.3% Yao from Liannan, Guangdong, 5/37 = 13.5% Zaomin, 5/41 = 12.2% Lowland Kimmun, 3/41 = 7.3% Native Mien, 2/31 = 6.5% Southern Mien, 2/32 = 6.3% Mountain Kimmun, but 0/35 Yao from Bama, Guangxi), She (6/34 = 17.6% She, 4/56 = 7.1% Northern She), and Hmongic peoples (9/100 = 9.0% Miao from Hunan, 4/51 = 7.8% Hmong Daw from northern Laos, 3/49 = 6.1% Miao from Yunnan, 1/49 = 2.0% Miao from Guizhou, but 0/36 Bunu from Guangxi) (Cai et al. 2011 and Xue et al. 2006).
In Meghalaya, a predominantly tribal state of Northeast India, O-M133 has been found in 19.7% (14/71) of a sample of the Tibeto-Burman-speaking Garos, but in only 6.2% (22/353, ranging from 0/32 Bhoi to 6/44 = 13.6% Pnar) of a pool of eight samples of the neighboring Khasian-speaking tribes (Reddy et al. 2007).
Origin
The earliest attested genealogical split within haplogroup O-M117, that between O-M133 and O-M117(xM133), is estimated to have occurred approximately 12,600 [95% CI 11,300 <-> 14,000] ybp.[4] However, members of O-M117(xM133) are quite rare among extant humans. O-M117(xM133) has been observed in 2.2% (1/46) of the CHB (Han Chinese in Beijing, China) sample of the 1000 Genomes Project.[4] In commercial testing, O-MF1380 or O-CTS4960, which belongs to O-M117(xM133), has been found in China (Beijing, Henan, Shandong, Jiangsu, Anhui, Chongqing, Guangdong), Singapore, Indonesia, Saudi Arabia, and Japan.[4][5] O-M117(xM133) also has been found in 1.5% (2/133) of a sample collected in Daejeon, South Korea and in 1.0% (6/573) of a sample collected in Seoul, South Korea.[6] According to 23mofang, members of O-M117(xM133) comprise a subclade called O-CTS4960 (TMRCA 8,570 ybp), which is relatively concentrated in central, eastern, and northeastern areas of China and currently accounts for approximately 0.51% of the total population of males in China.[7]
The most recent common ancestor of all extant members of the O-M133 subclade, which predominates among extant members of O-M117, is estimated to have lived in a significantly less ancient era: 7,600 [95% CI 6,400 <-> 8,900] ybp according to YFull,[4] 7,455 [95% CI 6,514 <-> 8,500] years ago according to Karmin et al. 2015,[2] or 7,500 or 6,400 years ago (depending on which estimate of the mutation rate is used) according to Poznik et al. 2016.[8]
Distribution
China
Haplogroup O-M117 or O-M133 has been found often in samples of Han Chinese from various parts of China: 10/34 = 29.4% O-M133 Hakka in Taiwan,[9] 57/258 = 22.1% O-M133 miscellaneous Han volunteers in Taiwan,[9] 4/19 = 21.1% Fujian (CHS),[4] 12/60 = 20.0% O-M133 Minnan in Taiwan,[9] 29/167 = 17.4% East China,[10] 21/129 = 16.3% North China,[10] 7/46 = 15.2% Beijing (CHB),[8] 5/34 = 14.7% Chengdu,[11] 5/35 = 14.3% Harbin,[11] 9/65 = 13.8% South China,[10] 7/55 = 12.7% O-M133 Fujian,[9] 4/35 = 11.4% Meixian,[11] 75/689 = 10.9% Pudong,[12] 3/30 = 10.0% Lanzhou,[11] 50/530 = 9.4% Chongming Island,[12] 2/32 = 6.3% Yili,[11] 1/37 = 2.7% Hunan (CHS).[4]
Members of haplogroup O-M117 also have been found among various ethnic minorities in China, such as Tibetans (13/35 = 37.1%,[11] 45/156 = 28.8%[13]), Dai (13/52 = 25.0% CDX, or Chinese Dai in Xishuangbanna),[4] She people (6/34 = 17.6%[11]), Koreans (4/25 = 16.0% Koreans in the PRC[11]), Hezhe (7/45 = 15.6%[11]), Evenks (4/26 = 15.4%[11]), Manchu (5/35 = 14.3%[11]), Yao in Liannan, Guangdong (5/35 = 14.3%[11]), Mongols (5/45 = 11.1% Inner Mongolian[11]), Qiang (3/33 = 9.1%[11]), Daurs (3/39 = 7.7% Daur[11]), Hani (2/34 = 5.9%[11]), Xibe (2/41 = 4.9%[11]), Uyghurs (3/70 = 4.3%[11]), Oroqen (1/31 = 3.2%[11]), Buyi (1/35 = 2.9%[11]), and Hui (1/35 = 2.9%[11]).
Yan et al. (2014) have estimated that 16% of the present Han Chinese should be patrilineal descendants of a certain ancestor belonging to haplogroup O-M117 who has initiated a star-like population expansion dated to the Late Neolithic (5,400 [95% CI 4,100 <-> 6,700] years before present), which the authors have dubbed "Oα."[14]
According to 23mofang, haplogroup O-M117 (TMRCA 13,750 years) accounts for about 16.27% of the total male population of China,[15] with most members of O-M117 belonging to its O-F8 subclade (TMRCA 7,280 years), this latter subclade accounting for the Y-DNA of about 15.71% of all present-day Chinese males.[3][16]
India
In a study of the DNA of Adivasi populations in the state of Meghalaya, Reddy et al. (2007) found O-M133 in 19.7% (14/71) Garo, 13.6% (6/44) Pnar, 11.1% (2/18) Nongtrai, 8.3% (5/60) Lyngngam, 6.9% (2/29) War-Khasi, 6.3% (4/64) Maram, 5.3% (1/19) War-Jaintia, 2.3% (2/87) Khynriam, and 0% (0/32) Bhoi. The Garo natively speak the Garo language, whereas all the other studied populations natively speak Khasic languages.[17]
In another study that included populations in Meghalaya, Kumar et al. (2007) found O-M133 in 9.8% (9/92) Khasi and 9.1% (3/33) Garo.[18]
A study of populations of northern West Bengal and Sikkim published in 2011 found O-M117 in 57.7% (15/26) Rabha, 47.4% (9/19) Mech, 43.1% (22/51) Rajbanshi, 41.7% (15/36) Dhimal, and 7.4% (4/54) Bengali from the northern panhandle of West Bengal and in 9.1% (1/11) of a sample of Lachungpa from Sikkim. O-M117 was not found in this study's samples of Kol (0/62), Santhal (0/51), Kharia (0/34), or Oraon (0/31) from the northern panhandle of West Bengal.[19]
Japan
A study published in the year 2000 found O-M117 in 4.3% (1/23) of a sample representing Japan.[20] In a study published by Chinese researchers in the year 2006, O-M117 was found with high frequency (8/47 = 17.0%) in a sample of Japanese that should be from Kagawa Prefecture according to the geographical coordinates (134.0°E, 34.2°N) that have been provided (Xue et al. 2006). However, in a study published by Japanese researchers in the year 2007, the same haplogroup was found with much lower frequency (11/263 = 4.2%) in a larger sample of Japanese from various regions of Japan (Nonaka et al. 2007). (More precisely, Nonaka et al. have found O-M117 in 1/12 = 8.3% of a sample from Shizuoka, 4/52 = 7.7% of a sample from Tokyo, 2/44 = 4.5% of a sample from Chiba, 1/2 of a sample from Gifu, 1/2 of a sample from Yamanashi, 1/3 of a sample from Hiroshima, and 1/6 of a sample from Aichi.) O-M117 has been found in 8.8% (5/57) of the JPT (Japanese in Tokyo, Japan) sample of the 1000 Genomes Project.[8][21]
Korea
Between 11% and 15% of males in samples collected in South Korea have been found to belong to haplogroup O-M117 or O-M133 (20/133 = 15.0% Koreans in Daejeon,[6] 70/573 = 12.2% Koreans in Seoul,[6] 5/43 = 11.6% Koreans in South Korea,[11] 33/300 = 11.0% O-M133 Koreans[22]).
Mongolia
Haplogroup O-M117 has been found in about 5% of samples of Mongols in Mongolia: 4/20 = 20.0% NE Mongolia,[23] 1/18 = 5.6% central Mongolia,[23] 3/65 = 4.6% Outer Mongolian,[11] 1/23 = 4.3% SE Mongolia,[23] 3/97 = 3.1% NW Mongolia.[23]
Nepal
Haplogroup O-M117 has been found in 84.4% (38/45) of a sample of Tamang, 33.3% of sample of Tharu of Chitwan and Morang, 21.2% (14/66) of a sample of Newar, and 16.9% (13/77) of a sample of the general population of Kathmandu.[13]
Laos
In a study published in 2011, haplogroup O-M117 has been found in 7.8% (4/51) of a sample of Hmong Daw in Laos and in 5.1% (37/728) of a set of ethnic minorities who speak various Austroasiatic languages: 32.1% (9/28) Bit, 16.2% (6/37) Kataang, 14.0% (7/50) Mal, 13.7% (7/51) Khmu, 6.9% (2/29) Xinhmul, 3.3% (1/30) Alak, 2.94% (1/34) Inh, 2.86% (1/35) Talieng, 2.0% (1/50) Laven, 2.0% (1/50) Oy, 2.0% (1/50) So, 0% (0/28) Bo, 0% (0/32) Brau, 0% (0/32) Jeh, 0% (0/35) Lamet, 0% (0/35) Ngeq, 0% (0/38) Aheu, 0% (0/39) Suy, and 0% (0/45) Katu.[24]
Kutanan et al. 2019 found O-F8/F42, which is currently considered to be phylogenetically equivalent to O-M133, in 25.0% (5/20) of a sample of Laotians from Luang Prabang and 5.0% (1/20) of a sample of Laotians from Vientiane.[25]
Thailand
In a study published in 2014, haplogroup O-M133 has been found in 13.3% (10/75) of a sample of the general population of Bangkok and in 3.7% (1/27) of a sample of Akka from Chiang Mai.[9]
Brunelli et al. (2017) have found O-M117 in 35.0% (7/20) of Shan, 22.4% (46/205) of Khon Mueang, 22.2% (4/18) of Mon, 20.0% (5/25) of Western Lawa, 17.6% (16/91) of Tai Lue, 16.7% (4/24) of Tai Khuen, 13.6% (9/66) of Tai Yuan, and 11.5% (3/26) of Tai Yong in Northern Thailand and in 31.6% (6/19) of Tai Yuan in Central Thailand.[26] However, in the same study, haplogroup O-M117 was not observed in a sample of 25 Eastern Lawa in Northern Thailand.[26]
Kutanan et al. (2019) have found O-F8/F42 (equivalent to O-M133) in 14.75% (131/888) of a pool of samples from Thailand, including 50.0% (9/18) Palaung in Northern Thailand, 38.9% (7/18) Shan in Northern Thailand, 33.3% (20/60) Khon Mueang in Northern Thailand, 31.0% (13/42) Karen in Northern Thailand, 28.6% (6/21) Nyahkur in Northeast Thailand, 23.5% (4/17) Kaleun, 17.1% (22/129) Thai (Siamese), 16.7% (5/30) Tai Lue in Northern Thailand, 16.7% (3/18) Nyaw in Northeast Thailand, 16.7% (3/18) Blang in Northern Thailand, 15.4% (4/26) Tai Yuan, 14.3% (15/105) Mon, 14.3% (5/35) Phuan, 11.8% (2/17) Soa, 11.8% (2/17) Tai Khün, 9.4% (3/32) Western Lawa, 8.3% (3/36) Black Tai, 6.5% (4/62) Lao Isan, and 5.6% (1/18) Khmu.[25]
Vietnam
Haplogroup O-M133 has been found in 4/46 = 8.7% of the KHV (Kinh in Ho Chi Minh City, Vietnam) sample of the 1000 Genomes Project.[8][4] Haplogroup O-M133 has been found in 1/24 = 4.17% of a sample of people in Hanoi, Vietnam.[9] A study published in 2011 found haplogroup O-M117 in 1/15 = 6.67% Kinh and 1/12 = 8.33% Muong.[24]
Macholdt et al. 2020 have found O-F8, which is currently considered to be phylogenetically equivalent to O-M1706 or O-M133, in 36.4% (12/33) of a sample of Hanhi from Mường Tè District, 22.2% (8/36) of a sample of Lachi from Hoàng Su Phì District, 14.9% (7/47) of a sample of Tay, 14.3% (3/21) of a sample of Phula from Xín Mần District, 12.9% (4/31) of a sample of Lahu from Mường Tè District, 8.3% (2/24) of a sample of Thai, 4.8% (2/42) of a sample of Kinh from Hanoi, 3.7% (1/27) of a sample of Giarai, 2.8% (1/36) of a sample of Pathen, and 2.7% (1/37) of a sample of Nung from Vietnam.[27] All members of O-F8 among the Hanhi and Lahu of Mường Tè District belonged to the O-F2137 subclade. One Tay individual from Mường Khương District belonged to the O-F155 subclade and one Tay individual from Tràng Định District belonged to the O-F317 subclade. All other members of O-F8 belonged to the O-F8(xF155, F2137, F317) paragroup. Only one individual in this study (a Tay from Đức Trọng District) has been assigned to O-P164(xF8, F46, F4110) and therefore potentially might belong to O-M117(xF8/M133).
Subclades
According to the ISOGG experiental tree, the subclades of O2ab1a1-M117 are shown below (Owen Lu et al. 2016):
- O2a2b1a1 (M117/Page23)
- O2a2b1a1a (M133)
- O2a2b1a1a1 (F438)
- O2a2b1a1a1a (Y17728)
- O2a2b1a1a1a1 (F155)
- O2a2b1a1a1a2 (F1754)
- O2a2b1a1a1a2a (F2137)
- O2a2b1a1a1a3 (Z25907)
- O2a2b1a1a2 (FGC23469)
- O2a2b1a1a2a (F310)
- O2a2b1a1a2a1 (F402)
- O2a2b1a1a2a1a (F1531)
- O2a2b1a1a2a1 (F402)
- O2a2b1a1a2a (F310)
- O2a2b1a1a1a (Y17728)
- O2a2b1a1a3 (CTS7634)
- O2a2b1a1a3a (F317)
- O2a2b1a1a3a1 (F3039)
- O2a2b1a1a3b (CTS5488)
- O2a2b1a1a3a (F317)
- O2a2b1a1a4 (Z25853)
- O2a2b1a1a4a (CTS5492)
- O2a2b1a1a4a1 (CTS6987)
- O2a2b1a1a4a (CTS5492)
- O2a2b1a1a5 (CTS10738/M1707)
- O2a2b1a1a5a (CTS9678)
- O2a2b1a1a5a1 (Z39663)
- O2a2b1a1a5b (A9457)
- O2a2b1a1a5a (CTS9678)
- O2a2b1a1a6 (CTS4658)
- O2a2b1a1a6a (CTS5308)
- O2a2b1a1a6b (Z25928)
- O2a2b1a1a6b1 (SK1730)
- O2a2b1a1a6b1a (Z26030)
- O2a2b1a1a6b1b (Z26010)
- O2a2b1a1a6b2 (A9462)
- O2a2b1a1a6b3 (B456)
- O2a2b1a1a6b1 (SK1730)
- O2a2b1a1a1 (F438)
- O2a2b1a1b (CTS4960)
- O2a2b1a1a (M133)
References
Citations
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- Journal articles
- Black, M. L.; Dufall, K.; Wise, C.; Sullivan, S.; Bittles, A. H. (2006). "Genetic ancestries in northwest Cambodia". Annals of Human Biology. 33 (5–6): 620–7. doi:10.1080/03014460600882561. PMID 17381059. S2CID 34579092.
- Cai, Xiaoyun; Qin, Zhendong; Wen, Bo; Xu, Shuhua; Wang, Yi; Lu, Yan; Wei, Lanhai; Wang, Chuanchao; et al. (2011). O'Rourke, Dennis (ed.). "Human Migration through Bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum Revealed by Y Chromosomes". PLOS ONE. 6 (8): e24282. Bibcode:2011PLoSO...624282C. doi:10.1371/journal.pone.0024282. PMC 3164178. PMID 21904623.
- Cordaux, R.; Weiss, G; Saha, N; Stoneking, M (2004). "The Northeast Indian Passageway: A Barrier or Corridor for Human Migrations?". Molecular Biology and Evolution. 21 (8): 1525–33. doi:10.1093/molbev/msh151. PMID 15128876.
- Gan, Rui-Jing; Pan, Shang-Ling; Mustavich, Laura F.; Qin, Zhen-Dong; Cai, Xiao-Yun; Qian, Ji; Liu, Cheng-Wu; Peng, Jun-Hua; et al. (2008). "Pinghua population as an exception of Han Chinese's coherent genetic structure". Journal of Human Genetics. 53 (4): 303–13. doi:10.1007/s10038-008-0250-x. PMID 18270655.
- Gayden, Tenzin; Cadenas, Alicia M.; Regueiro, Maria; Singh, Nanda B.; Zhivotovsky, Lev A.; Underhill, Peter A.; Cavalli-Sforza, Luigi L.; Herrera, Rene J. (2007). "The Himalayas as a Directional Barrier to Gene Flow". The American Journal of Human Genetics. 80 (5): 884–94. doi:10.1086/516757. PMC 1852741. PMID 17436243.
- Hammer, Michael F.; Karafet, Tatiana M.; Park, Hwayong; Omoto, Keiichi; Harihara, Shinji; Stoneking, Mark; Horai, Satoshi (2005). "Dual origins of the Japanese: Common ground for hunter-gatherer and farmer Y chromosomes". Journal of Human Genetics. 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082.
- He, Jun-Dong; Peng, Min-Sheng; Quang, Huy Ho; Dang, Khoa Pham; Trieu, An Vu; Wu, Shi-Fang; Jin, Jie-Qiong; Murphy, Robert W.; et al. (2012). Kayser, Manfred (ed.). "Patrilineal Perspective on the Austronesian Diffusion in Mainland Southeast Asia". PLOS ONE. 7 (5): e36437. Bibcode:2012PLoSO...736437H. doi:10.1371/journal.pone.0036437. PMC 3346718. PMID 22586471.
- Hurles, M; Sykes, B; Jobling, M; Forster, P (2005). "The Dual Origin of the Malagasy in Island Southeast Asia and East Africa: Evidence from Maternal and Paternal Lineages". The American Journal of Human Genetics. 76 (5): 894–901. doi:10.1086/430051. PMC 1199379. PMID 15793703.
- Jin, Han-Jun; Tyler-Smith, Chris; Kim, Wook (2009). Batzer, Mark A (ed.). "The Peopling of Korea Revealed by Analyses of Mitochondrial DNA and Y-Chromosomal Markers". PLOS ONE. 4 (1): e4210. Bibcode:2009PLoSO...4.4210J. doi:10.1371/journal.pone.0004210. PMC 2615218. PMID 19148289.
- Jing, Chen; Hui, LI; Zhen-Dong, QIN; Wen-Hong, LIU; Wei-Xiong, LIN; Rui-Xing, YIN; Li, JIN; Shang-Ling, PAN (2006). "Y-chromosome Genotyping and Genetic Structure of Zhuang Populations". Acta Genetica Sinica. 33 (12): 1060–72. CiteSeerX 10.1.1.602.5490. doi:10.1016/S0379-4172(06)60143-1. PMID 17185165.
- Karafet, Tatiana; Xu, Liping; Du, Ruofu; Wang, William; Feng, Shi; Wells, R.S.; Redd, Alan J.; Zegura, Stephen L.; Hammer, Michael F. (2001). "Paternal Population History of East Asia: Sources, Patterns, and Microevolutionary Processes". The American Journal of Human Genetics. 69 (3): 615–28. doi:10.1086/323299. PMC 1235490. PMID 11481588.
- Karafet, Tatiana M.; Lansing, J. S.; Redd, Alan J.; Watkins, Joseph C.; Surata, S. P. K.; Arthawiguna, W. A.; Mayer, Laura; Bamshad, Michael; et al. (2005). "Balinese Y-Chromosome Perspective on the Peopling of Indonesia: Genetic Contributions from Pre-Neolithic Hunter-Gatherers, Austronesian Farmers, and Indian Traders". Human Biology. 77 (1): 93–114. doi:10.1353/hub.2005.0030. hdl:1808/13586. PMID 16114819. S2CID 7953854.
- Katoh, Toru; Munkhbat, Batmunkh; Tounai, Kenichi; Mano, Shuhei; Ando, Harue; Oyungerel, Ganjuur; Chae, Gue-Tae; Han, Huun; Jia, Guan-Jun; Tokunaga, Katsushi; Munkhtuvshin, Namid; Tamiya, Gen; Inoko, Hidetoshi (2005). "Genetic features of Mongolian ethnic groups revealed by Y-chromosomal analysis". Gene. 346: 63–70. doi:10.1016/j.gene.2004.10.023. PMID 15716011.
- Kayser, M.; Brauer, S; Cordaux, R; Casto, A; Lao, O; Zhivotovsky, LA; Moyse-Faurie, C; Rutledge, RB; et al. (2006). "Melanesian and Asian Origins of Polynesians: MtDNA and Y Chromosome Gradients Across the Pacific". Molecular Biology and Evolution. 23 (11): 2234–44. doi:10.1093/molbev/msl093. hdl:11858/00-001M-0000-0010-0145-0. PMID 16923821.
- Kharkov, V. N.; Stepanov, V. A.; Medvedeva, O. F.; Spiridonova, M. G.; Voevoda, M. I.; Tadinova, V. N.; Puzyrev, V. P. (2007). "Gene pool differences between Northern and Southern Altaians inferred from the data on Y-chromosomal haplogroups". Russian Journal of Genetics. 43 (5): 551–562. doi:10.1134/S1022795407050110. PMID 17633562. S2CID 566825.
- Kim, Wook; Yoo, Tag-Keun; Kim, Sung-Joo; Shin, Dong-Jik; Tyler-Smith, Chris; Jin, Han-Jun; Kwak, Kyoung-Don; Kim, Eun-Tak; Bae, Yoon-Sun (2007). Blagosklonny, Mikhail (ed.). "Lack of Association between Y-Chromosomal Haplogroups and Prostate Cancer in the Korean Population". PLOS ONE. 2 (1): e172. Bibcode:2007PLoSO...2..172K. doi:10.1371/journal.pone.0000172. PMC 1766463. PMID 17245448.
- Kumar, Vikrant; Reddy, Arimanda NS; Babu, Jagedeesh P; Rao, Tipirisetti N; Langstieh, Banrida T; Thangaraj, Kumarasamy; Reddy, Alla G; Singh, Lalji; Reddy, Battini M (2007). "Y-chromosome evidence suggests a common paternal heritage of Austro-Asiatic populations". BMC Evolutionary Biology. 7 (1): 47. Bibcode:2007BMCEE...7...47K. doi:10.1186/1471-2148-7-47. PMC 1851701. PMID 17389048.
- Li, Hui; Wen, Bo; Chen, Shu-Juo; Su, Bing; Pramoonjago, Patcharin; Liu, Yangfan; Pan, Shangling; Qin, Zhendong; Liu, Wenhong; Cheng, Xu; Yang, Ningning; Li, Xin; Tran, Dinhbinh; Lu, Daru; Hsu, Mu-Tsu; Deka, Ranjan; Marzuki, Sangkot; Tan, Chia-Chen; Jin, Li (2008). "Paternal genetic affinity between western Austronesians and Daic populations". BMC Evolutionary Biology. 8 (1): 146. Bibcode:2008BMCEE...8..146L. doi:10.1186/1471-2148-8-146. PMC 2408594. PMID 18482451.
- Nonaka, I.; Minaguchi, K.; Takezaki, N. (2007). "Y-chromosomal Binary Haplogroups in the Japanese Population and their Relationship to 16 Y-STR Polymorphisms" (PDF). Annals of Human Genetics. 71 (4): 480–95. doi:10.1111/j.1469-1809.2006.00343.x. hdl:10130/491. PMID 17274803. S2CID 1041367.
- Reddy, B. Mohan; Langstieh, B. T.; Kumar, Vikrant; Nagaraja, T.; Reddy, A. N. S.; Meka, Aruna; Reddy, A. G.; Thangaraj, K.; Singh, Lalji (2007). Awadalla, Philip (ed.). "Austro-Asiatic Tribes of Northeast India Provide Hitherto Missing Genetic Link between South and Southeast Asia". PLOS ONE. 2 (11): e1141. Bibcode:2007PLoSO...2.1141R. doi:10.1371/journal.pone.0001141. PMC 2065843. PMID 17989774.
- Shi, Simona; Pala, Maria; Battaglia, Vincenza; Maranta, Ramona; Achilli, Alessandro; Modiano, Guido; Torroni, Antonio; Semino, Ornella; Santachiara-Benerecetti, Silvana A (2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): A reservoir of genetic variation". BMC Evolutionary Biology. 9 (1): 154. Bibcode:2009BMCEE...9..154F. doi:10.1186/1471-2148-9-154. PMC 2720951. PMID 19573232.
- Su, B.; Jin, L.; Underhill, P.; Martinson, J.; Saha, N.; McGarvey, S. T.; Shriver, M. D.; Chu, J.; et al. (2000). "Polynesian origins: Insights from the Y chromosome". Proceedings of the National Academy of Sciences. 97 (15): 8225–8228. Bibcode:2000PNAS...97.8225S. doi:10.1073/pnas.97.15.8225. PMC 26928. PMID 10899994.
*H6 (=O-M122(xO-M7, O-M134)) in 18/73=24.7% *H8 (=O-M134) in 2/73=2.7% for a total of 20/73=27.4% O-M122 in a pool of seven samples from Micronesia. *13/40=32.5% O-M122(xM7,M134) in a pool of three samples from Polynesia. *9/27=33.3% H6 (=O-M122(xM7,M134)) *6/27=22.2% H8 (=O-M134) for a total of 15/27=55.6% O-M122 in "Malay" sample *2/19=10.5% H6 (=O-M122(xM7,M134)) in "Kota Kinabalu" sample.
- Su, Bing; Xiao, Junhua; Underhill, Peter; Deka, Ranjan; Zhang, Weiling; Akey, Joshua; Huang, Wei; Shen, Di; et al. (1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". The American Journal of Human Genetics. 65 (6): 1718–24. doi:10.1086/302680. PMC 1288383. PMID 10577926.
- Tajima, Atsushi; Hayami, Masanori; Tokunaga, Katsushi; Juji, Takeo; Matsuo, Masafumi; Marzuki, Sangkot; Omoto, Keiichi; Horai, Satoshi (2004). "Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages". Journal of Human Genetics. 49 (4): 187–93. doi:10.1007/s10038-004-0131-x. PMID 14997363.
- Wang, Wei; Wise, Cheryl; Baric, Tom; Black, Michael L.; Bittles, Alan H. (August 1, 2003). "The origins and genetic structure of three co-resident Chinese Muslim populations: the Salar, Bo'an and Dongxiang". Human Genetics. 113 (3): 244–52. doi:10.1007/s00439-003-0948-y. ISSN 0340-6717. PMID 12759817. S2CID 11138499.
- Wells, R. S.; Yuldasheva, N.; Ruzibakiev, R.; Underhill, P. A.; Evseeva, I.; Blue-Smith, J.; Jin, L.; Su, B.; et al. (2001). "The Eurasian Heartland: A continental perspective on Y-chromosome diversity". Proceedings of the National Academy of Sciences. 98 (18): 10244–9. Bibcode:2001PNAS...9810244W. doi:10.1073/pnas.171305098. PMC 56946. PMID 11526236.
- Wen, Bo; Li, Hui; Lu, Daru; Song, Xiufeng; Zhang, Feng; He, Yungang; Li, Feng; Gao, Yang; et al. (2004). "Genetic evidence supports demic diffusion of Han culture". Nature. 431 (7006): 302–5. Bibcode:2004Natur.431..302W. doi:10.1038/nature02878. PMID 15372031. S2CID 4301581.
- Wen, Bo; Xie, Xuanhua; Gao, Song; Li, Hui; Shi, Hong; Song, Xiufeng; Qian, Tingzhi; Xiao, Chunjie; et al. (2004). "Analyses of Genetic Structure of Tibeto-Burman Populations Reveals Sex-Biased Admixture in Southern Tibeto-Burmans". The American Journal of Human Genetics. 74 (5): 856–865. doi:10.1086/386292. PMC 1181980. PMID 15042512.
- Wen, Bo; Hong, S; Ling, R; Huifeng, X; Kaiyuan, L; Wenyi, Z; Bing, S; Shiheng, S; et al. (2004). "The origin of Mosuo people as revealed by mtDNA and Y chromosome variation". Science China Life Sciences. 47 (1): 1–10. doi:10.1360/02yc0207. PMID 15382670. S2CID 7999778.
- Xie, Xuan-Hua (2004). "Genetic Structure of Tujia as Revealed by Y Chromosomes". Yi Chuan Xue Bao = Acta Genetica Sinica. 31 (10): 1023–9. PMID 15552034. Archived from the original on 2019-07-19. Retrieved 2016-05-04.
- Xue, Y.; Zerjal, T; Bao, W; Zhu, S; Shu, Q; Xu, J; Du, R; Fu, S; et al. (2005). "Male Demography in East Asia: A North-South Contrast in Human Population Expansion Times". Genetics. 172 (4): 2431–9. doi:10.1534/genetics.105.054270. PMC 1456369. PMID 16489223.
- Yang, Zhili; Dong, Yongli; Gao, Lu; Cheng, Baowen; Yang, Jie; Zeng, Weimin; Lu, Jing; Su, Yanhua; Xiao, Chunjie (2005). "The distribution of Y chromosome haplogroups in the nationalities from Yunnan Province of China". Annals of Human Biology. 32 (1): 80–7. doi:10.1080/03014460400027557. PMID 15788357. S2CID 39153696.
- Zhou, Ruixia; Yang, Daqun; Zhang, Hua; Yu, Weiping; An, Lizhe; Wang, Xilong; Li, Hong; Xu, Jiujin; Xie, Xiaodong (2008). "Origin and evolution of two Yugur sub-clans in Northwest China: A case study in paternal genetic landscape". Annals of Human Biology. 35 (2): 198–211. doi:10.1080/03014460801922927. PMID 18428013. S2CID 5453358.