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Juan L. Rodriguez-Flores, Khalid Fakhro, Francisco Agosto-Perez, Monica D. Ramstetter, Leonardo Arbiza, Thomas L. Vincent1, Amal Robay, Joel A. Malek, Karsten Suhre, Lotfi Chouchane, Ramin Badii, Ajayeb Al-Nabet Al-Marri, Charbel Abi Khalil, Mahmoud Zirie, Amin Jayyousi, Jacqueline Salit, Alon Keinan, Andrew G. Clark, Ronald G. Crystal and Jason G. Mezey
An open question in the history of human migration is the identity of the earliest Eurasian populations that have left contemporary descendants. The Arabian Peninsula was the initial site of the out-of-Africa migrations that occurred between 125,000 and 60,000 yr ago, leading to the hypothesis that the first Eurasian populations were established on the Peninsula and that contemporary indigenous Arabs are direct descendants of these ancient peoples...
Samples
ID: 1
Francalacci P, Morelli L, Angius A, Berutti R, Reinier F, Atzeni R, Pilu R, Busonero F, Maschio A, Zara I, Sanna D, Useli A, Urru MF, Marcelli M, Cusano R, Oppo M, Zoledziewska M, Pitzalis M, Deidda F, Porcu E, Poddie F, Kang HM, Lyons R, Tarrier B, Gresham JB, Li B, Tofanelli S, Alonso S, Dei M, Lai S, Mulas A, Whalen MB, Uzzau S, Jones C, Schlessinger D, Abecasis GR, Sanna S, Sidore C, Cucca F.
Genetic variation within the male-specific portion of the Y chromosome (MSY) can clarify the origins of contemporary populations, but previous studies were hampered by partial genetic information. Population sequencing of 1204 Sardinian males identified 11,763 MSY single-nucleotide polymorphisms, 6751 of which have not previously been observed. We constructed a MSY phylogenetic tree containing all main haplogroups found in Europe, along with many Sardinian-specific lineage clusters within each haplogroup...
Samples
ID: 2
Swapan Mallick, Heng Li, Mark Lipson, Iain Mathieson, Melissa Gymrek, Fernando Racimo, Mengyao Zhao, Niru Chennagiri, Susanne Nordenfelt, Arti Tandon, Pontus Skoglund, Iosif Lazaridis, Sriram Sankararaman, Qiaomei Fu, Nadin Rohland, Gabriel Renaud, Yaniv Erlich, Thomas Willems, Carla Gallo, Jeffrey P. Spence, Yun S. Song, Giovanni Poletti, Francois Balloux, George van Driem, Peter de Knijff, Irene Gallego Romero, Aashish R. Jha, Doron M. Behar, Claudio M. Bravi, Cristian Capelli, Tor Hervig, Andres Moreno-Estrada, Olga L. Posukh, Elena Balanovska, Oleg Balanovsky, Sena Karachanak-Yankova, Hovhannes Sahakyan, Draga Toncheva, Levon Yepiskoposyan, Chris Tyler-Smith, Yali Xue, M. Syafiq Abdullah, Andres Ruiz-Linares, Cynthia M. Beall, Anna Di Rienzo, Choongwon Jeong, Elena B. Starikovskaya, Ene Metspalu, Jüri Parik, Richard Villems, Brenna M. Henn, Ugur Hodoglugil, Robert Mahley, Antti Sajantila, George Stamatoyannopoulos, Joseph T. S. Wee, Rita Khusainova, Elza Khusnutdinova, Sergey Litvinov, George Ayodo, David Comas, Michael F. Hammer, Toomas Kivisild, William Klitz, Cheryl A. Winkler, Damian Labuda, Michael Bamshad, Lynn B. Jorde, Sarah A. Tishkoff, W. Scott Watkins, Mait Metspalu, Stanislav Dryomov, Rem Sukernik, Lalji Singh, Kumarasamy Thangaraj, Svante Pääbo, Janet Kelso, Nick Patterson & David Reich- Show fewer authors
Here we report the Simons Genome Diversity Project data set: high quality genomes from 300 individuals from 142 diverse populations. These genomes include at least 5.8 million base pairs that are not present in the human reference genome. Our analysis reveals key features of the landscape of human genome variation, including that the rate of accumulation of mutations has accelerated by about 5% in non-Africans compared to Africans since divergence...
Samples
ID: 3
1000 Genomes Project
The International Genome Sample Resource (IGSR) was established to ensure the ongoing usability of data generated by the 1000 Genomes Project and to extend the data set.
Samples
ID: 4
Doron M. Behar, Lauri Saag, Monika Karmin, Meir G. Gover, Jeffrey D. Wexler, Luisa Fernanda Sanchez, Elliott Greenspan, Alena Kushniarevich, Oleg Davydenko, Hovhannes Sahakyan, Levon Yepiskoposyan, Alessio Boattini, Stefania Sarno, Luca Pagani, Shai Carmi, Shay Tzur, Ene Metspalu, Concetta Bormans, Karl Skorecki, Mait Metspalu, Siiri Rootsi & Richard Villems
Approximately 300,000 men around the globe self-identify as Ashkenazi Levites, of whom two thirds were previously shown to descend from a single male. The paucity of whole Y-chromosome sequences precluded conclusive identification of this ancestor’s age, geographic origin and migration patterns. Here, we report the variation of 486 Y-chromosomes within the Ashkenazi and non-Ashkenazi Levite R1a clade, other Ashkenazi Jewish paternal lineages, as well as non-Levite Jewish and non-Jewish R1a samples...
Samples
ID: 5
Ilumäe AM, Reidla M, Chukhryaeva M, Järve M, Post H, Karmin M, Saag L, Agdzhoyan A, Kushniarevich A, Litvinov S, Ekomasova N, Tambets K, Metspalu E, Khusainova R, Yunusbayev B, Khusnutdinova EK, Osipova LP, Fedorova S, Utevska O, Koshel S, Balanovska E, Behar DM, Balanovsky O, Kivisild T, Underhill PA, Villems R, Rootsi S.
The paternal haplogroup (hg) N is distributed from southeast Asia to eastern Europe. The demographic processes that have shaped the vast extent of this major Y chromosome lineage across numerous linguistically and autosomally divergent populations have previously been unresolved. On the basis of 94 high-coverage re-sequenced Y chromosomes, we establish and date a detailed hg N phylogeny...
Samples
ID: 6
Andrey V. Khrunin, Denis V. Khokhrin, Irina N. Filippova, Tõnu Esko, Mari Nelis, Natalia A. Bebyakova, Natalia L. Bolotova, Janis Klovins, Liene Nikitina-Zake, Karola Rehnström, Samuli Ripatti, Stefan Schreiber, Andre Franke, Milan Macek, Veronika Krulišová, Jan Lubinski, Andres Metspalu and Svetlana A. Limborska
Several studies examined the fine-scale structure of human genetic variation in Europe. However, the European sets analyzed represent mainly northern, western, central, and southern Europe. Here, we report an analysis of approximately 166,000 single nucleotide polymorphisms in populations from eastern (northeastern) Europe: four Russian populations from European Russia, and three populations from the northernmost Finno-Ugric ethnicities (Veps and two contrast groups of Komi people)...
Samples
ID: 7
John C. Chambers, James Abbott, Weihua Zhang, Ernest Turro, William R. Scott, Sian-Tsung Tan, Uzma Afzal, Saima Afaq, Marie Loh, Benjamin Lehne, Paul O'Reilly, Kyle J. Gaulton, Richard D. Pearson, Xinzhong Li, Anita Lavery, Jana Vandrovcova, Mark N. Wass, Kathryn Miller, Joban Sehmi, Laticia Oozageer, Ishminder K. Kooner, Abtehale Al-Hussaini, Rebecca Mills, Jagvir Grewal, Vasileios Panoulas, Alexandra M. Lewin, Korrinne Northwood, Gurpreet S. Wander, Frank Geoghegan, Yingrui Li, Jun Wang, Timothy J. Aitman, Mark I. McCarthy, James Scott, Sarah Butcher, Paul Elliott and Jaspal S. Kooner
The genetic sequence variation of people from the Indian subcontinent who comprise one-quarter of the world's population, is not well described. We carried out whole genome sequencing of 168 South Asians, along with whole-exome sequencing of 147 South Asians to provide deeper characterisation of coding regions. We identify 12,962,155 autosomal sequence variants, including 2,946,861 new SNPs and 312,738 novel indels...
Samples
ID: 8
Mondal M., Casals F., Xu T., Dall'Olio GM., Pybus M., Netea MG., Comas D., Laayouni H., Li Q., Majumder PP., Bertranpetit J. Institut de Biologia Evolutiva (UPF-CSIC), Universitat Pompeu Fabra, Barcelona, Spain.
To shed light on the peopling of South Asia and the origins of the morphological adaptations found there, we analyzed whole-genome sequences from 10 Andamanese individuals and compared them with sequences for 60 individuals from mainland Indian populations with different ethnic histories and with publicly available data from other populations...
Samples
ID: 9
Peter de Barros Damgaard, Nina Marchi, Simon Rasmussen, Michaël Peyrot, Gabriel Renaud, Thorfinn Korneliussen, J. Víctor Moreno-Mayar, Mikkel Winther Pedersen, Amy Goldberg, Emma Usmanova, Nurbol Baimukhanov, Valeriy Loman, Lotte Hedeager, Anders Gorm Pedersen, Kasper Nielsen, Gennady Afanasiev, Kunbolot Akmatov, Almaz Aldashev, Ashyk Alpaslan, Gabit Baimbetov, Vladimir I. Bazaliiskii, Arman Beisenov, Bazartseren Boldbaatar, Bazartseren Boldgiv, Choduraa Dorzhu, Sturla Ellingvag, Diimaajav Erdenebaatar, Rana Dajani, Evgeniy Dmitriev, Valeriy Evdokimov, Karin M. Frei, Andrey Gromov, Alexander Goryachev, Hakon Hakonarson, Tatyana Hegay, Zaruhi Khachatryan, Ruslan Khaskhanov, Egor Kitov, Alina Kolbina, Tabaldiev Kubatbek, Alexey Kukushkin, Igor Kukushkin, Nina Lau, Ashot Margaryan, Inga Merkyte, Ilya V. Mertz, Viktor K. Mertz, Enkhbayar Mijiddorj, Vyacheslav Moiyesev, Gulmira Mukhtarova, Bekmukhanbet Nurmukhanbetov, Z. Orozbekova, Irina Panyushkina, Karol Pieta, Václav Smrčka, Irina Shevnina, Andrey Logvin, Karl-Göran Sjögren, Tereza Štolcová, Kadicha Tashbaeva, Alexander Tkachev, Turaly Tulegenov, Dmitriy Voyakin, Levon Yepiskoposyan, Sainbileg Undrakhbold, Victor Varfolomeev, Andrzej Weber, Nikolay Kradin, Morten E. Allentoft, Ludovic Orlando, Rasmus Nielsen, Martin Sikora, Evelyne Heyer, Kristian Kristiansen & Eske Willerslev
For thousands of years the Eurasian steppes have been a centre of human migrations and cultural change. Here we sequence the genomes of 137 ancient humans (about 1× average coverage), covering a period of 4,000 years, to understand the population history of the Eurasian steppes after the Bronze Age migrations. We find that the genetics of the Scythian groups that dominated the Eurasian steppes throughout the Iron Age were highly structured...
Samples
ID: 10
Peter de Barros Damgaard, Rui Martiniano, Jack Kamm, J. Víctor Moreno-Mayar, Guus Kroonen, Michaël Peyrot, Gojko Barjamovic, Simon Rasmussen, Claus Zacho, Nurbol Baimukhanov, Victor Zaibert, Victor Merz, Arjun Biddanda, Ilja Merz, Valeriy Loman, Valeriy Evdokimov, Emma Usmanova, Brian Hemphill, Andaine Seguin-Orlando, Fulya Eylem Yediay, Inam Ullah, Karl-Göran Sjögren, Katrine Højholt Iversen, Jeremy Choin, Constanza de la Fuente, Melissa Ilardo, Hannes Schroeder, Vyacheslav Moiseyev, Andrey Gromov, Andrei Polyakov, Sachihiro Omura, Süleyman Yücel Senyurt, Habib Ahmad, Catriona McKenzie, Ashot Margaryan, Abdul Hameed, Abdul Samad, Nazish Gul, Muhammad Hassan Khokhar, O. I. Goriunova, Vladimir I. Bazaliiskii, John Novembre, Andrzej W. Weber, Ludovic Orlando, Morten E. Allentoft, Rasmus Nielsen, Kristian Kristiansen, Martin Sikora, Alan K. Outram, Richard Durbin, Eske Willerslev
The Yamnaya expansions from the western steppe into Europe and Asia during the Early Bronze Age (~3000 BCE) are believed to have brought with them Indo-European languages and possibly horse husbandry. We analyze 74 ancient whole-genome sequences from across Inner Asia and Anatolia and show that the Botai people associated with...
Samples
ID: 11
O. Balanovsky, M. Chukhryaeva, V. Zaporozhchenko, V. Urasin, M. Zhabagin, A. Hovhannisyan, A. Agdzhoyan, K. Dibirova, M. Kuznetsova, S. Koshel, E. Pocheshkhova, I. Alborova, R. Skhalyakho, O. Utevska, The Genographic Consortium, Kh. Mustafin, L. Yepiskoposyan, C. Tyler‑Smith, E. Balanovska
Y-chromosomal variation in West Asian populations has so far been studied in less detail than in the neighboring Europe. Here, we analyzed 598 Y-chromosomes from two West Asian subregions—Transcaucasia and the Armenian plateau—using 40 Y-SNPs and 17 Y-STRs and combined them with previously published data from the region. The West Asian populations fell into two clusters: upland populations from the Anatolian, Armenian and Iranian plateaus, and lowland populations from the Levant, Mesopotamia and the Arabian Peninsula...
Samples
ID: 12
Oleg Balanovsky, Maxat Zhabagin, Anastasiya Agdzhoyan, Marina Chukhryaeva, Valery Zaporozhchenko, Olga Utevska, Gareth Highnam, Zhaxylyk Sabitov, Elliott Greenspan, Khadizhat Dibirova, Roza Skhalyakho, Marina Kuznetsova, Sergey Koshel, Yuldash Yusupov, Pagbajabyn Nymadawa, Zhaxybay Zhumadilov, Elvira Pocheshkhova, Marc Haber, Pierre A. Zalloua, Levon Yepiskoposyan, Anna Dybo, Chris Tyler-Smith, Elena Balanovska
Y-chromosomal haplogroup G1 is a minor component of the overall gene pool of South-West and Central Asia but reaches up to 80% frequency in some populations scattered within this area. We have genotyped the G1-defining marker M285 in 27 Eurasian populations (n= 5,346), analyzed 367 M285-positive samples using 17 Y-STRs, and sequenced ~11 Mb of the Y-chromosome in 20 of these samples to an average coverage of 67X. This allowed detailed phylogenetic reconstruction...
Samples
ID: 13
S. Sunna Ebenesersdóttir, Marcela Sandoval-Velasco, Ellen D. Gunnarsdóttir, Anuradha Jagadeesan, Valdís B. Guðmundsdóttir, Elísabet L. Thordardóttir, Margrét S. Einarsdóttir, Kristjan H. S. Moore, Ásgeir Sigurðsson, Droplaug N. Magnúsdóttir, Hákon Jónsson, Steinunn Snorradóttir, Eivind Hovig, Pål Møller, Ingrid Kockum, Tomas Olsson, Lars Alfredsson, Thomas F. Hansen, Thomas Werge, Gianpiero L. Cavalleri, Edmund Gilbert, Carles Lalueza-Fox, Joe W. Walser III, Steinunn Kristjánsdóttir, Shyam Gopalakrishnan, Lilja Árnadóttir, Ólafur Þ. Magnússon, M. Thomas P. Gilbert, Kári Stefánsson, Agnar Helgason
Abstract Opportunities to directly study the founding of a human population and its subsequent evolutionary history are rare. Using genome sequence data from 27 ancient Icelanders, we demonstrate that they are a combination of Norse, Gaelic, and admixed individuals. We further show that these ancient Icelanders are markedly more similar to their source populations in Scandinavia and the British-Irish Isles than to contemporary Icelanders, who have been shaped by 1100 years of extensive genetic drift. Finally, we report evidence of unequal contributions from the ancient founders to the contemporary Icelandic gene pool. These results provide detailed insights into the making of a human population that has proven extraordinarily useful for the discovery of genotype-phenotype associations.
Samples
ID: 14
Maja Krzewińska, Anna Kjellström, Torsten Günther, Charlotte Hedenstierna-Jonson, Torun Zachrisson, Ayça Omrak, Reyhan Yaka, Gülşah Merve Kılınç, Mehmet Somel, Veronica Sobrado, Jane Evans, Corina Knipper, Mattias Jakobsson, Jan Storå, Anders Götherström, Show less, Show footnotes
The impact of human mobility on the northern European urban populations during the Viking and Early Middle Ages and its repercussions in Scandinavia itself are still largely unexplored. Our study of the demographics in the final phase of the Viking era is the first comprehensive multidisciplinary investigation that includes genetics, isotopes, archaeology, and osteology on a larger scale. This early Christian dataset is particularly important as the earlier common pagan burial tradition during the Iron Age was cremation, hindering large-scale DNA analyses. We present genome-wide sequence data from 23 individuals from the 10th to 12th century Swedish town of Sigtuna. The data revealed high genetic diversity among the early urban residents. The observed variation exceeds the genetic diversity in distinct modern-day and Iron Age groups of central and northern Europe. Strontium isotope data suggest mixed local and non-local origin of the townspeople. Our results uncover the social system underlying the urbanization process of the Viking World of which mobility was an intricate part and was comparable between males and females. The inhabitants of Sigtuna were heterogeneous in their genetic affinities, probably reflecting both close and distant connections through an established network, confirming that early urbanization processes in northern Europe were driven by migration.
Samples
ID: 15
Eugenia D’Atanasio, Beniamino Trombetta, Maria Bonito, Andrea Finocchio, Genny Di Vito, Mara Seghizzi, Rita Romano, Gianluca Russo, Giacomo Maria Paganotti, Elizabeth Watson, Alfredo Coppa, Paolo Anagnostou, Jean-Michel Dugoujon, Pedro Moral, Daniele Sellitto, Andrea Novelletto and Fulvio CrucianiEmail
Background Little is known about the peopling of the Sahara during the Holocene climatic optimum, when the desert was replaced by a fertile environment. Results In order to investigate the role of the last Green Sahara in the peopling of Africa, we deep-sequence the whole non-repetitive portion of the Y chromosome in 104 males selected as representative of haplogroups which are currently found to the north and to the south of the Sahara. We identify 5,966 mutations, from which we extract 142 informative markers then genotyped in about 8,000 subjects from 145 African, Eurasian and African American populations. We find that the coalescence age of the trans-Saharan haplogroups dates back to the last Green Sahara, while most northern African or sub-Saharan clades expanded locally in the subsequent arid phase. Conclusions Our findings suggest that the Green Sahara promoted human movements and demographic expansions, possibly linked to the adoption of pastoralism. Comparing our results with previously reported genome-wide data, we also find evidence for a sex-biased sub-Saharan contribution to northern Africans, suggesting that historical events such as the trans-Saharan slave trade mainly contributed to the mtDNA and autosomal gene pool, whereas the northern African paternal gene pool was mainly shaped by more ancient events.
Samples
ID: 16
Can Alkan, Pinar Kavak, Mehmet Somel, Omer Gokcumen, Serkan Ugurlu, Ceren Saygi, Elif Dal, Kuyas Bugra, Tunga Güngör, S Cenk Sahinalp, Nesrin Özören and Cemalettin Bekpen
Turkey is a crossroads of major population movements throughout history and has been a hotspot of cultural interactions. Several studies have investigated the complex population history of Turkey through a limited set of genetic markers. However, to date, there have been no studies to assess the genetic variation at the whole genome level using whole genome sequencing. Here, we present whole genome sequences of 16 Turkish individuals resequenced at high coverage (32 × -48×).
Samples
ID: 17
Carlos Eduardo G. Amorim, Stefania Vai, Cosimo Posth, Alessandra Modi, István Koncz, Susanne Hakenbeck, Maria Cristina La Rocca, Balazs Mende, Dean Bobo, Walter Pohl, Luisella Pejrani Baricco, Elena Bedini, Paolo Francalacci, Caterina Giostra, Tivadar Vida, Daniel Winger, Uta von Freeden, Silvia Ghirotto, Martina Lari, Guido Barbujani, Johannes Krause, David Caramelli, Patrick J. Geary & Krishna R. Veeramah
Despite centuries of research, much about the barbarian migrations that took place between the fourth and sixth centuries in Europe remains hotly debated. To better understand this key era that marks the dawn of modern European societies, we obtained ancient genomic DNA from 63 samples from two cemeteries (from Hungary and Northern Italy) that have been previously associated with the Longobards, a barbarian people that ruled large parts of Italy for over 200 years after invading from Pannonia in 568 CE. Our dense cemetery-based sampling revealed that each cemetery was primarily organized around one large pedigree, suggesting that biological relationships played an important role in these early medieval societies. Moreover, we identified genetic structure in each cemetery involving at least two groups with different ancestry that were very distinct in terms of their funerary customs. Finally, our data are consistent with the proposed long-distance migration from Pannonia to Northern Italy.
Samples
ID: 18
Viola Grugni†, Alessandro Raveane†, Linda Ongaro, Vincenza Battaglia, Beniamino Trombetta, Giulia Colombo, Marco Rosario Capodiferro, Anna Olivieri, Alessandro Achilli, Ugo A. Perego, Jorge Motta, Maribel Tribaldos, Scott R. Woodward, Luca Ferretti, Fulvio Cruciani, Antonio Torroni and Ornella Semino
Recent genome studies of modern and ancient samples have proposed that Native Americans derive from a subset of the Eurasian gene pool carried to America by an ancestral Beringian population, from which two well-differentiated components originated and subsequently mixed in different proportion during their spread in the Americas. To assess the timing, places of origin and extent of admixture between these components, we performed an analysis of the Y-chromosome haplogroup Q, which is the only Pan-American haplogroup and accounts for virtually all Native American Y chromosomes in Mesoamerica and South America.
Samples
ID: 19
KPGP
Korean Personal Genome Project (KPGP) is a participative research project established by Genome Research Foundation(GRF).
Samples
ID: 20
Thomaz Pinotti, Anders Bergström, Maria Geppert, Matt Bawn, Dominique Ohasi, Wentao Shi, Daniela R. Lacerda, Arne Solli, Jakob Norstedt, Kate Reed, Kim Dawtry, Fabricio González-Andrade, Cesar Paz-y-Miño, Susana Revollo, Cinthia Cuellar, Marilza S. Jota, José E. Santos Jr., Qasim Ayub, Toomas Kivisild, José R. Sandoval, Ricardo Fujita, Yali Xue, Lutz Roewer, Fabrício R. Santos, Chris Tyler-Smith
The Americas were the last inhabitable continents to be occupied by humans, with a growing multidisciplinary consensus for entry 15–25 thousand years ago (kya) from northeast Asia via the former Beringia land bridge. Autosomal DNA analyses have dated the separation of Native American ancestors from the Asian gene pool to 23 kya or later and mtDNA analyses to ∼25 kya, followed by isolation (“Beringian Standstill”) for 2.4–9 ky and then a rapid expansion throughout the Americas. Here, we present a calibrated sequence-based analysis of 222 Native American and relevant Eurasian Y chromosomes (24 new) from haplogroups Q and C, with four major conclusions. First, we identify three to four independent lineages as autochthonous and likely founders: the major Q-M3 and rarer Q-CTS1780 present throughout the Americas, the very rare C3-MPB373 in South America, and possibly the C3-P39/Z30536 in North America. Second, from the divergence times and Eurasian/American distribution of lineages, we estimate a Beringian Standstill duration of 2.7 ky or 4.6 ky, according to alternative models, and entry south of the ice sheet after 19.5 kya. Third, we describe the star-like expansion of Q-M848 (within Q-M3) starting at 15 kya in the Americas, followed by establishment of substantial spatial structure in South America by 12 kya. Fourth, the deep branches of the Q-CTS1780 lineage present at low frequencies throughout the Americas today may reflect a separate out-of-Beringia dispersal after the melting of the glaciers at the end of the Pleistocene.
Samples
ID: 21
Behar,D.M., van Oven,M., Rosset,S., Metspalu,M., Loogvali,E.L., Silva,N.M., Kivisild,T., Torroni,A. and Villems,R.
Am. J. Hum. Genet. 90 (4), 675-684 (2012) Erratum:[Am J Hum Genet. 2012 May 4;90(5):936]
Samples
ID: 22
Maca-Meyer,N., Gonzalez,A.M., Pestano,J., Flores,C., Larruga,J.M. and Cabrera,V.M.
BMC Genet. 4, 15 (2003) Publication Status: Online-Only
Samples
ID: 23
Bodner,M., Perego,U.A., Huber,G., Fendt,L., Rock,A.W., Zimmermann,B., Olivieri,A., Gomez-Carballa,A., Lancioni,H., Angerhofer,N., Bobillo,M.C., Corach,D., Woodward,S.R., Salas,A., Achilli,A., Torroni,A., Bandelt,H.J. and Parson,W.
Genome Res. 22 (5), 811-820 (2012)
Samples
ID: 24
Fraumene,C., Belle,E.M., Castri,L., Sanna,S., Mancosu,G., Cosso,M., Marras,F., Barbujani,G., Pirastu,M. and Angius,A.
Mol. Biol. Evol. 23 (11), 2101-2111 (2006)
Samples
ID: 25
Kazuno,A.A., Munakata,K., Mori,K., Tanaka,M., Nanko,S., Kunugi,H., Umekage,T., Tochigi,M., Kohda,K., Sasaki,T., Akiyama,T., Washizuka,S., Kato,N. and Kato,T.
Psychiatry Clin. Neurosci. 59 (4), 497-503 (2005) Publication_Status: Available-Online
Samples
ID: 26
Kazuno,A.A., Munakata,K., Nagai,T., Shimozono,S., Tanaka,M., Yoneda,M., Kato,N., Miyawaki,A. and Kato,T.
PLoS Genet. 2 (8), E128 (2006) Publication_Status: Available-Online
Samples
ID: 27
Kazuno,A.A., Munakata,K., Kato,N. and Kato,T.
Int. J. Neuropsychopharmacol. 11 (1), 71-78 (2008) Publication_Status: Available-Online
Samples
ID: 28
Kazuno,A.A., Munakata,K., Tanaka,M., Kato,N. and Kato,T.
Mitochondrion 8 (2), 164-169 (2008) Publication_Status: Available-Online
Samples
ID: 29
Pierson,M.J., Martinez-Arias,R., Holland,B.R., Gemmell,N.J., Hurles,M.E. and Penny,D.
Mol. Biol. Evol. 23 (10), 1966-1975 (2006)
Samples
ID: 30
Friedlaender,J.S., Friedlaender,F.R., Hodgson,J.A., Stoltz,M., Koki,G., Horvat,G., Zhadanov,S., Schurr,T.G. and Merriwether,D.A.
PLoS ONE 2, E248 (2007) Publication Status: Online-Only
Samples
ID: 31
Thangaraj,K., Chaubey,G., Kivisild,T., Reddy,A.G., Singh,V.K., Rasalkar,A.A. and Singh,L.
Science 308 (5724), 996 (2005)
Samples
ID: 32
Tanaka,M., Cabrera,V.M., Gonzalez,A.M., Larruga,J.M., Takeyasu,T., Fuku,N., Guo,L.J., Hirose,R., Fujita,Y., Kurata,M., Shinoda,K., Umetsu,K., Yamada,Y., Oshida,Y., Sato,Y., Hattori,N., Mizuno,Y., Arai,Y., Hirose,N., Ohta,S., Ogawa,O., Tanaka,Y., Kawamori,R., Shamoto-Nagai,M., Maruyama,W., Shimokata,H., Suzuki,R. and Shimodaira,H.
Genome Res. 14 (10A), 1832-1850 (2004)
Samples
ID: 33
Fu,Q., Rudan,P., Paabo,S. and Krause,J.
PLoS ONE 7 (3), E32473 (2012) Publication Status: Online-Only
Samples
ID: 34
Hudjashov,G., Kivisild,T., Underhill,P.A., Endicott,P., Sanchez,J.J., Lin,A.A., Shen,P., Oefner,P., Renfrew,C., Villems,R. and Forster,P.
Proc. Natl. Acad. Sci. U.S.A. 104 (21), 8726-8730 (2007)
Samples
ID: 35
Soares,P., Rito,T., Trejaut,J.A., Mormina,M., Hill,C., Tinkler-Hundel,E., Braid,M., Clarke,D.J., Loo,J.-H., Thomson,N., Denham,T., Donohue,M., Macaulay,V., Lin,M., Oppenheimer,S. and Richards,M.B.
Am. J. Hum. Genet. 88 (2), 239-247 (2011)
Samples
ID: 36
Derenko,M., Malyarchuk,B., Grzybowski,T., Denisova,G., Dambueva,I., Perkova,M., Dorzhu,C., Luzina,F., Lee,H.K., Vanecek,T., Villems,R. and Zakharov,I.
Am. J. Hum. Genet. 81 (5), 1025-1041 (2007)
Samples
ID: 37
Palanichamy,M.G., Sun,C., Agrawal,S., Bandelt,H.J., Kong,Q.P., Khan,F., Wang,C.Y., Chaudhuri,T.K., Palla,V. and Zhang,Y.P.
Am. J. Hum. Genet. 75 (6), 966-978 (2004)
Samples
ID: 38
Ingman,M. and Gyllensten,U.
Genome Res. 13 (7), 1600-1606 (2003)
Samples
ID: 39
Ingman,M. and Gyllensten,U.
Eur. J. Hum. Genet. 15 (1), 115-120 (2007)
Samples
ID: 40
Achilli,A., Rengo,C., Battaglia,V., Pala,M., Olivieri,A., Fornarino,S., Magri,C., Scozzari,R., Babudri,N., Santachiara-Benerecetti,A.S., Bandelt,H.J., Semino,O. and Torroni,A.
Am. J. Hum. Genet. 76 (5), 883-886 (2005)
Samples
ID: 41
Gonder,M.K., Mortensen,H.M., Reed,F.A., de Sousa,A. and Tishkoff,S.A.
Mol. Biol. Evol. 24 (3), 757-768 (2007)
Samples
ID: 42
Pereira,L., Silva,N.M., Franco-Duarte,R., Fernandes,V., Pereira,J.B., Costa,M.D., Martins,H., Soares,P., Behar,D.M., Richards,M.B. and Macaulay,V.
BMC Evol. Biol. 10 (1), 390 (2010) Publication Status: Online-Only
Samples
ID: 43
Soares,P., Alshamali,F., Pereira,J.B., Fernandes,V., Silva,N.M., Afonso,C., Costa,M.D., Musilova,E., Macaulay,V., Richards,M.B., Cerny,V. and Pereira,L.
Mol. Biol. Evol. 29 (3), 915-927 (2012)
Samples
ID: 44
Gunnarsdottir,E.D., Li,M., Bauchet,M., Finstermeier,K. and Stoneking,M.
Genome Res. 21 (1), 1-11 (2011)
Samples
ID: 45
Malyarchuk,B., Derenko,M., Denisova,G. and Kravtsova,O.
Mol. Biol. Evol. 27 (10), 2220-2226 (2010)
Samples
ID: 46
Jinam,T.A., Hong,L.C., Phipps,M.E., Stoneking,M., Ameen,M., Edo,J. and Saitou,N.
Mol. Biol. Evol. 29 (11), 3513-3527 (2012) DOI:10.1093/molbev/mss169
Samples
ID: 47
Pala,M., Achilli,A., Olivieri,A., Hooshiar Kashani,B., Perego,U.A., Sanna,D., Metspalu,E., Tambets,K., Tamm,E., Accetturo,M., Carossa,V., Lancioni,H., Panara,F., Zimmermann,B., Huber,G., Al-Zahery,N., Brisighelli,F., Woodward,S.R., Francalacci,P., Parson,W., Salas,A., Behar,D.M., Villems,R., Semino,O., Bandelt,H.J. and Torroni,A.
Am. J. Hum. Genet. 84 (6), 814-821 (2009)
Samples
ID: 48
Olivieri,A., Achilli,A., Pala,M., Battaglia,V., Fornarino,S., Al-Zahery,N., Scozzari,R., Cruciani,F., Behar,D.M., Dugoujon,J.M., Coudray,C., Santachiara-Benerecetti,A.S., Semino,O., Bandelt,H.J. and Torroni,A.
Science 314 (5806), 1767-1770 (2006)
Samples
ID: 49
Achilli,A., Rengo,C., Magri,C., Battaglia,V., Olivieri,A., Scozzari,R., Cruciani,F., Zeviani,M., Briem,E., Carelli,V., Moral,P., Dugoujon,J.M., Roostalu,U., Loogvali,E.L., Kivisild,T., Bandelt,H.J., Richards,M., Villems,R., Santachiara-Benerecetti,A.S., Semino,O. and Torroni,A.
Am. J. Hum. Genet. 75 (5), 910-918 (2004)
Samples
ID: 50
Perego,U.A., Achilli,A., Angerhofer,N., Accetturo,M., Pala,M., Olivieri,A., Kashani,B.H., Ritchie,K.H., Scozzari,R., Kong,Q.P., Myres,N.M., Salas,A., Semino,O., Bandelt,H.J., Woodward,S.R. and Torroni,A.
Curr. Biol. 19 (1), 1-8 (2009)
Samples
ID: 51
Torroni,A., Achilli,A., Macaulay,V., Richards,M. and Bandelt,H.J.
Trends Genet. 22 (6), 339-345 (2006)
Samples
ID: 52
Ingman,M., Kaessmann,H., Paabo,S. and Gyllensten,U.
Nature 408 (6813), 708-713 (2000) Erratum:[Nature 2001 Mar 29;410(6828):611]
Samples
ID: 53
Mishmar,D., Ruiz-Pesini,E., Golik,P., Macaulay,V., Clark,A.G., Hosseini,S., Brandon,M., Easley,K., Chen,E., Brown,M.D., Sukernik,R.I., Olckers,A. and Wallace,D.C.
Proc. Natl. Acad. Sci. U.S.A. 100 (1), 171-176 (2003)
Samples
ID: 54
Kong,Q.P., Sun,C., Wang,H.W., Zhao,M., Wang,W.Z., Zhong,L., Hao,X.D., Pan,H., Wang,S.Y., Cheng,Y.T., Zhu,C.L., Wu,S.F., Liu,L.N., Jin,J.Q., Yao,Y.G. and Zhang,Y.P.
Mol. Biol. Evol. 28 (1), 513-522 (2011)
Samples
ID: 55
Fagundes,N.J., Kanitz,R., Eckert,R., Valls,A.C., Bogo,M.R., Salzano,F.M., Smith,D.G., Silva,W.A. Jr., Zago,M.A., Ribeiro-dos-Santos,A.K., Santos,S.E., Petzl-Erler,M.L. and Bonatto,S.L.
Am. J. Hum. Genet. 82 (3), 583-592 (2008)
Samples
ID: 56
Gilbert,M.T., Kivisild,T., Gronnow,B., Andersen,P.K., Metspalu,E., Reidla,M., Tamm,E., Axelsson,E., Gotherstrom,A., Campos,P.F., Rasmussen,M., Metspalu,M., Higham,T.F., Schwenninger,J.L., Nathan,R., De Hoog,C.J., Koch,A., Moller,L.N., Andreasen,C., Meldgaard,M., Villems,R., Bendixen,C. and Willerslev,E.
Science 320 (5884), 1787-1789 (2008)
Samples
ID: 57
Fernandes,V., Alshamali,F., Alves,M., Costa,M.D., Pereira,J.B., Silva,N.M., Cherni,L., Harich,N., Cerny,V., Soares,P., Richards,M.B. and Pereira,L.
Am. J. Hum. Genet. 90 (2), 347-355 (2012)
Samples
ID: 58
van Holst Pellekaan,S.M., Ingman,M., Roberts-Thomson,J. and Harding,R.M.
Am. J. Phys. Anthropol. 131 (2), 282-294 (2006)
Samples
ID: 59
Tamm,E., Kivisild,T., Reidla,M., Metspalu,M., Smith,D.G., Mulligan,C.J., Bravi,C.M., Rickards,O., Martinez-Labarga,C., Khusnutdinova,E.K., Fedorova,S.A., Golubenko,M.V., Stepanov,V.A., Gubina,M.A., Zhadanov,S.I., Ossipova,L.P., Damba,L., Voevoda,M.I., Dipierri,J.E., Villems,R. and Malhi,R.S.
PLoS ONE 2 (9), E829 (2007) Publication Status: Online-Only
Samples
ID: 60
Nohira,C., Maruyama,S. and Minaguchi,K.
Int. J. Legal Med. 124 (1), 7-12 (2010) DOI:10.1007/s00414-008-0308-5
Samples
ID: 61
Andrews,R.M., Kubacka,I., Chinnery,P.F., Lightowlers,R.N., Turnbull,D.M. and Howell,N.
Nat. Genet. 23 (2), 147 (1999)
Samples
ID: 62
Anderson,S., Bankier,A.T., Barrell,B.G., de Bruijn,M.H., Coulson,A.R., Drouin,J., Eperon,I.C., Nierlich,D.P., Roe,B.A., Sanger,F., Schreier,P.H., Smith,A.J., Staden,R. and Young,I.G.
Nature 290 (5806), 457-465 (1981)
Samples
ID: 63
Achilli,A., Perego,U.A., Bravi,C.M., Coble,M.D., Kong,Q.P., Woodward,S.R., Salas,A., Torroni,A. and Bandelt,H.J.
PLoS ONE 3 (3), E1764 (2008) Publication Status: Online-Only
Samples
ID: 64
Behar,D.M., Villems,R., Soodyall,H., Blue-Smith,J., Pereira,L., Metspalu,E., Scozzari,R., Makkan,H., Tzur,S., Comas,D., Bertranpetit,J., Quintana-Murci,L., Tyler-Smith,C., Wells,R.S. and Rosset,S.
Am. J. Hum. Genet. 82 (5), 1130-1140 (2008)
Samples
ID: 65
Trejaut,J.A., Kivisild,T., Loo,J.H., Lee,C.L., He,C.L., Hsu,C.J., Lee,Z.Y. and Lin,M.
PLoS Biol. 3 (8), E247 (2005) Erratum:[PLoS Biol. 2005 Oct;3(10):e376. Li, Zheng Yuan [corrected to Lee, Zheng Yuan]]
Samples
ID: 66
Derbeneva,O.A., Starikovskaia,E.B., Volod'ko,N.V., Wallace,D.C. and Sukernik,R.I.
Genetika 38 (11), 1554-1560 (2002)
Samples
ID: 67
Ji,F., Sharpley,M.S., Derbeneva,O., Alves,L.S., Qian,P., Wang,Y., Chalkia,D., Lvova,M., Xu,J., Yao,W., Simon,M., Platt,J., Xu,S., Angelin,A., Davila,A., Huang,T., Wang,P.H., Chuang,L.M., Moore,L.G., Qian,G. and Wallace,D.C.
Proc. Natl. Acad. Sci. U.S.A. 109 (19), 7391-7396 (2012)
Samples
ID: 68
Bollongino,R., Nehlich,O., Richards,M.P., Orschiedt,J., Thomas,M.G., Sell,C., Fajkosova,Z., Powell,A. and Burger,J.
Science 342 (6157), 479-481 (2013)
Samples
ID: 69
Fu,Q., Mittnik,A., Johnson,P.L., Bos,K., Lari,M., Bollongino,R., Sun,C., Giemsch,L., Schmitz,R., Burger,J., Ronchitelli,A.M., Martini,F., Cremonesi,R.G., Svoboda,J., Bauer,P., Caramelli,D., Castellano,S., Reich,D., Paabo,S. and Krause,J.
Curr. Biol. 23 (7), 553-559 (2013)
Samples
ID: 70
Cui,Y., Lindo,J., Hughes,C.E., Johnson,J.W., Hernandez,A.G., Kemp,B.M., Ma,J., Cunningham,R., Petzelt,B., Mitchell,J., Archer,D., Cybulski,J.S. and Malhi,R.S.
PLoS ONE 8 (7), E66948 (2013) Publication Status: Online-Only
Samples
ID: 71
Krause,J., Briggs,A.W., Kircher,M., Maricic,T., Zwyns,N., Derevianko,A. and Paabo,S.
Curr. Biol. 20 (3), 231-236 (2010)
Samples
ID: 72
Sanchez-Quinto,F., Schroeder,H., Ramirez,O., Avila-Arcos,M.C., Pybus,M., Olalde,I., Velazquez,A.M., Marcos,M.E., Encinas,J.M., Bertranpetit,J., Orlando,L., Gilbert,M.T. and Lalueza-Fox,C.
Curr. Biol. 22 (16), 1494-1499 (2012)
Samples
ID: 73
Ermini,L., Olivieri,C., Rizzi,E., Corti,G., Bonnal,R., Soares,P., Luciani,S., Marota,I., De Bellis,G., Richards,M.B. and Rollo,F.
Curr. Biol. 18 (21), 1687-1693 (2008)
Samples
ID: 74
Fu,Q., Meyer,M., Gao,X., Stenzel,U., Burbano,H.A., Kelso,J. and Paabo,S.
Proc. Natl. Acad. Sci. U.S.A. 110 (6), 2223-2227 (2013)
Samples
ID: 75
Rieux,A., Eriksson,A., Li,M., Sobkowiak,B., Weinert,L.A., Warmuth,V., Ruiz-Linares,A., Manica,A. and Balloux,F.
Mol. Biol. Evol. 31 (10), 2780-2792 (2014)
Samples
ID: 76
Lippold,S., Xu,H., Ko,A., Li,M., Renaud,G., Butthof,A., Schroder,R. and Stoneking,M.
Investig Genet 5, 13 (2014) Publication Status: Online-Only
Samples
ID: 77
Miles Benton, Donia Macartney-Coxson, David Eccles, Lyn Griffiths, Geoff Chambers, Rod Lea
The high risk of metabolic disease traits in Polynesians may be partly explained by elevated prevalence of genetic variants involved in energy metabolism. The genetics of Polynesian populations has been shaped by island hoping migration events which have possibly favoured thrifty genes. The aim of this study was to sequence the mitochondrial genome in a group of Maoris in an effort to characterise genome variation in this Polynesian population for use in future disease association studies. We sequenced the complete mitochondrial genomes of 20 non-admixed Maori subjects using Affymetrix technology. DNA diversity analyses showed the Maori group exhibited reduced mitochondrial genome diversity compared to other worldwide populations, which is consistent with historical bottleneck and founder effects. Global phylogenetic analysis positioned these Maori subjects specifically within mitochondrial haplogroup - B4a1a1. Interestingly, we identified several novel variants that collectively form new and unique Maori motifs – B4a1a1c, B4a1a1a3 and B4a1a1a5. Compared to ancestral populations we observed an increased frequency of non-synonymous coding variants of several mitochondrial genes in the Maori group, which may be a result of positive selection and/or genetic drift effects. In conclusion, this study reports the first complete mitochondrial genome sequence data for a Maori population. Overall, these new data reveal novel mitochondrial genome signatures in this Polynesian population and enhance the phylogenetic picture of maternal ancestry in Oceania. The increased frequency of several mitochondrial coding variants makes them good candidates for future studies aimed at assessment of metabolic disease risk in Polynesian populations.
Samples
ID: 78
Maca-Meyer,N., Gonzalez,A.M., Larruga,J.M., Flores,C. and Cabrera,V.M.
BMC Genet. 2 (1), 13 (2001)
Samples
ID: 79
Zalloua,P., Collins,C.J., Gosling,A., Biagini,S.A., Costa,B., Kardailsky,O., Nigro,L., Khalil,W., Calafell,F. and Matisoo-Smith,E.
Sci Rep 8 (1), 17567 (2018) Publication Status: Online-Only
Samples
ID: 80
Kang,L., Zheng,H.X., Chen,F., Yan,S., Liu,K., Qin,Z., Liu,L., Zhao,Z., Li,L., Wang,X., He,Y. and Jin,L.
Mol. Biol. Evol. 30 (12), 2579-2587 (2013)
Samples
ID: 81
Olivieri,A., Sidore,C., Achilli,A., Angius,A., Posth,C., Furtwangler,A., Brandini,S., Rosario Capodiferro,M., Gandini,F., Zoledziewska,M., Pitzalis,M., Maschio,A., Busonero,F., Lai,L., Skeates,R., Giuseppina Gradoli,M., Beckett,J., Marongiu,M., Mazzarello,V., Marongiu,P., Rubino,S., Rito,T., Macaulay,V., Semino,O., Pala,M., Abecasis,G.R., Schlessinger,D., Conde-Sousa,E., Soares,P., Richards,M.B., Cucca,F. and Torroni,A.
Mol. Biol. Evol. (2017) In press Publication Status: Available-Online prior to print
Samples
ID: 82
Kutanan,W., Kampuansai,J., Brunelli,A., Ghirotto,S., Pittayaporn,P., Ruangchai,S., Schroder,R., Macholdt,E., Srikummool,M., Kangwanpong,D., Hubner,A., Arias,L. and Stoneking,M.
Eur. J. Hum. Genet. (2018) In press Publication Status: Available-Online prior to print
Samples
ID: 83
Govindaraj,P., Khan,N.A., Gopalakrishna,P., Chandra,R.V., Vanniarajan,A., Reddy,A.A., Singh,S., Kumaresan,R., Srinivas,G., Singh,L. and Thangaraj,K.
Mitochondrion 11 (3), 504-512 (2011)
Samples
ID: 84
Palanichamy,M.G., Mitra,B., Zhang,C.L., Debnath,M., Li,G.M., Wang,H.W., Agrawal,S., Chaudhuri,T.K. and Zhang,Y.P.
Hum. Genet. (2015) In press Publication Status: Available-Online prior to print
Samples
ID: 85
Sequeira,A., Rollins,B., Magnan,C., van Oven,M., Baldi,P., Myers,R.M., Barchas,J.D., Schatzberg,A.F., Watson,S.J., Akil,H., Bunney,W.E. and Vawter,M.P.
PLoS ONE 10 (5), E0127280 (2015) Publication Status: Online-Only
Samples
ID: 86
Derenko,M., Malyarchuk,B., Denisova,G., Perkova,M., Litvinov,A., Grzybowski,T., Dambueva,I., Skonieczna,K., Rogalla,U., Tsybovsky,I. and Zakharov,I.
BMC Evol. Biol. 14 (1), 217 (2014) Publication Status: Online-Only
Samples
ID: 87
Simao,F., Strobl,C., Vullo,C., Catelli,L., Machado,P., Huber,N., Schnaller,L., Huber,G., Xavier,C., Carvalho,E.F., Gusmao,L. and Parson,W.
Forensic Sci Int Genet 39, 66-72 (2018)
Samples
ID: 88
Derenko,M., Malyarchuk,B., Bahmanimehr,A., Denisova,G., Perkova,M., Farjadian,S. and Yepiskoposyan,L.
PLoS ONE 8 (11), E80673 (2013) Publication Status: Online-Only
Samples
ID: 89
Malyarchuk,B., Derenko,M., Denisova,G., Litvinov,A., Rogalla,U., Skonieczna,K., Grzybowski,T., Pentelenyi,K., Guba,Z., Zeke,T. and Molnar,M.J.
Mol. Genet. Genomics (2018) In press Publication Status: Available-Online prior to print
Samples
ID: 90
Larruga,J.M., Marrero,P., Abu-Amero,K.K., Golubenko,M.V. and Cabrera,V.M.
BMC Evol. Biol. 17 (1), 115 (2017) Publication Status: Online-Only
Samples
ID: 91
Matisoo-Smith,E., Gosling,A.L., Platt,D., Kardailsky,O., Prost,S., Cameron-Christie,S., Collins,C.J., Boocock,J., Kurumilian,Y., Guirguis,M., Pla Orquin,R., Khalil,W., Genz,H., Abou Diwan,G., Nassar,J. and Zalloua,P.
PLoS ONE 13 (1), e0190169 (2018) Publication Status: Online-Only
Samples
ID: 92
Margaryan,A., Derenko,M., Hovhannisyan,H., Malyarchuk,B., Heller,R., Khachatryan,Z., Avetisyan,P., Badalyan,R., Bobokhyan,A., Melikyan,V., Sargsyan,G., Piliposyan,A., Simonyan,H., Mkrtchyan,R., Denisova,G., Yepiskoposyan,L., Willerslev,E. and Allentoft,M.E.
Curr. Biol. 27 (13), 2023-2028 (2017)
Samples
ID: 93
Skonieczna,K., Malyarchuk,B., Jawien,A., Marszalek,A., Banaszkiewicz,Z., Jarmocik,P. and Grzybowski,T.
Hum. Mutat. (2018) In press Publication Status: Available-Online prior to print
Samples
ID: 94
Malyarchuk,B., Grzybowski,T., Derenko,M., Perkova,M., Vanecek,T., Lazur,J., Gomolcak,P. and Tsybovsky,I.
Mol. Biol. Evol. 25 (8), 1651-1658 (2008)
Samples
ID: 95
Davidovic,S., Malyarchuk,B., Aleksic,J.M., Derenko,M., Topalovic,V., Litvinov,A., Stevanovic,M. and Kovacevic-Grujicic,N.
Am. J. Phys. Anthropol. (2014) In press Publication Status: Available-Online prior to print
Samples
ID: 96
Sukernik,R.I., Volodko,N.V., Mazunin,I.O., Eltsov,N.P., Dryomov,S.V. and Starikovskaya,E.B.
Am. J. Phys. Anthropol. 148 (1), 123-138 (2012)
Samples
ID: 97
Raule,N., Sevini,F., Li,S., Barbieri,A., Tallaro,F., Lomartire,L., Vianello,D., Montesanto,A., Moilanen,J.S., Bezrukov,V., Blanche,H., Hervonen,A., Christensen,K., Deiana,L., Gonos,E.S., Kirkwood,T.B., Kristensen,P., Leon,A., Pelicci,P.G., Poulain,M., Rea,I.M., Remacle,J., Robine,J.M., Schreiber,S., Sikora,E., Eline Slagboom,P., Spazzafumo,L., Antonietta Stazi,M., Toussaint,O., Vaupel,J.W., Rose,G., Majamaa,K., Perola,M., Johnson,T.E., Bolund,L., Yang,H., Passarino,G. and Franceschi,C.
Aging Cell 13 (3), 401-407 (2014)
Samples
ID: 98
Kloss-Brandstatter,A., Schafer,G., Erhart,G., Huttenhofer,A., Coassin,S., Seifarth,C., Summerer,M., Bektic,J., Klocker,H. and Kronenberg,F.
Am. J. Hum. Genet. 87 (6), 802-812 (2010)
Samples
ID: 99
Malyarchuk,B., Litvinov,A., Derenko,M., Skonieczna,K., Grzybowski,T., Grosheva,A., Shneider,Y., Rychkov,S. and Zhukova,O.
Forensic Sci Int Genet 30, 51-56 (2017)
Samples
ID: 100