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Montenegrin People
Montenegrins ( cnr, Црногорци, Crnogorci, or ; lit. "Black Mountain People") are a South Slavic ethnic group that share a common Montenegrin culture, history, and language, identified with the country of Montenegro. Genetics According to one triple analysis – autosomal, mitochondrial and paternal — of available data from large-scale studies on Balto-Slavs and their proximal populations, the whole genome SNP data situates Montenegrins with Serbs in between two Balkan clusters. According to a 2020 autosomal marker analysis, Montenegrins are situated in-between Serbians and Kosovo Albanians. Y-DNA genetic study done in 2010 on 404 male individuals from Montenegro gave the following results: haplogroup I2a (29.7%), E-V13 (26.9%), R1b (9.4%), R1a (7.6%), I1 (6.1%), J2a1 (4.7%), J2b (4.4%), G2a (2.4%), Q (1.9%), I2b (1.7%), N (1.4%), H (1.4%), L (1.2%), and J1 (0.49%). A 2022 study on 267 samples from northeastern Montenegro found that the "most common h ...
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Serbs
The Serbs ( sr-Cyr, Срби, Srbi, ) are the most numerous South Slavic ethnic group native to the Balkans in Southeastern Europe, who share a common Serbian ancestry, culture, history and language. The majority of Serbs live in their nation state of Serbia, as well as in Bosnia and Herzegovina, Croatia, Montenegro, and Kosovo. They also form significant minorities in North Macedonia and Slovenia. There is a large Serb diaspora in Western Europe, and outside Europe and there are significant communities in North America and Australia. The Serbs share many cultural traits with the rest of the peoples of Southeast Europe. They are predominantly Eastern Orthodox Christians by religion. The Serbian language (a standardized version of Serbo-Croatian) is official in Serbia, co-official in Kosovo and Bosnia and Herzegovina, and is spoken by the plurality in Montenegro. Ethnology The identity of Serbs is rooted in Eastern Orthodoxy and traditions. In the 19th century, the Serbia ...
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Serbs Of Montenegro
Serbs of Montenegro ( sr, / ) or Montenegrin Serbs ( sr, / ),, meaning "Montenegrin Serbs", and meaning "Serbs Montenegrins". Specifically, Their regional autonym is simply , literal meaning "Montenegrins",Charles Seignobos, Political History of Europe, since 1814, ed. S. M. Macvane, H. Holt and Company, New York, 1900, pp. 663–664; excerpt from chapter XXI The Christian Nations of The Balkans, subchapter Servia and Montenegro, passages Montenegro the same as the ethnic group of ''Montenegrins''). In the early modern times, before the Kingdom of Montenegro, people iving within present-day borderswere divided by the identities of (; Brda), (; Old Herzegovina), (; Boka Kotorska) and (; Old Montenegro). , meaning "Serbs in Montenegro". compose native and the second largest ethnic group in Montenegro (28.7% of country's population), after the ethnic Montenegrins. Additional 0.64% of the population is made up of ''Serbs-Montenegrins'' () and ''Montenegrins-Serbs'' (). Hi ...
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Haplogroup R1b
Haplogroup R1b (R-M343), previously known as Hg1 and Eu18, is a human Y-chromosome haplogroup. It is the most frequently occurring paternal lineage in Western Europe, as well as some parts of Russia (e.g. the Bashkirs) and pockets of Central Africa (e.g. parts of Chad and among the Chadic-speaking minority ethnic groups of Cameroon). The clade is also present at lower frequencies throughout Eastern Europe, Western Asia, as well as parts of North Africa, South Asia and Central Asia. R1b has two primary branches: R1b1-L754 and R1b2-PH155. R1b1-L754 has two major subclades: R1b1a1b-M269, which predominates in Western Europe, and R1b1b-V88, which is today common in parts of Central Africa. The other branch, R1b2-PH155, is so rare and widely dispersed that it is difficult to draw any conclusions about its origins. It has been found in Bahrain, India, Nepal, Bhutan, Ladakh, Tajikistan, Turkey, and Western China. According to ancient DNA studies, most R1a and R1b lineages would hav ...
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Haplogroup E-V68
Haplogroup E-V68, also known as E1b1b1a, is a major human Y-chromosome DNA haplogroup found in North Africa, the Horn of Africa, Western Asia and Europe. It is a subclade of the larger and older haplogroup, known as E1b1b or E-M215 (also roughly equivalent to E-M35). The E1b1b1a lineage is identified by the presence of a single nucleotide polymorphism (SNP) mutation on the Y chromosome, which is known as V68. It is a subject of discussion and study in genetics as well as genetic genealogy, archaeology, and historical linguistics. E-V68 is dominated by its longer-known subclade E-M78. In various publications, both E-V68 and E-M78 have been referred to by other names, especially phylogenetic nomenclature such as "E3b1a" which are designed to show their place on the family tree of all human males. These various names change as new discoveries are made and are discussed below. Origins E-M78, like its parent clade E-V68, is thought to have an African origin. Based on genetic STR var ...
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Haplogroup I-M438
Haplogroup I-M438, also known as I2 (ISOGG 2019), is a human DNA Y-chromosome haplogroup, a subclade of Haplogroup I-M170. Haplogroup I-M438 originated some time around 26,000–31,000 BCE. It originated in Europe and developed into several main subgroups : I2-M438*, I2a-L460, I2b-L415 and I2c-L596. The haplogroup can be found all over Europe and reaches its maximum frequency in the Dinaric Alps (Balkans) via founder effect. Examples of basal I-M438* have been found in males from Crete and Sicily . Origin & prehistoric presence Haplogroup I2a was the most frequent Y-DNA among western European mesolithic hunter gatherers (WHG) belonging to Villabruna Cluster. A 2015 study found haplogroup I2a in 13,500 year old remains from the Azilian culture (from Grotte du Bichon, modern Switzerland). Subclades of I2a1 (I-P37.2), namely I-M423 and I-M26 have been found in remains of Western European Hunter-Gatherers dating from 10,000 to 8,000 years before present respectively. In a 201 ...
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Annals Of Human Biology
''Annals of Human Biology'' is a bimonthly academic journal that publishes review articles on human population biology, nature, development and causes of human variation. It is published by Taylor & Francis on behalf of the Society for the Study of Human Biology, of which it is the official journal. Coverage Includes * Global health * Ageing * Epidemiology * Ecology * Environmental physiology * Human genetics * Auxology * Population biology Society ''Annals of Human Biology'' is the official journal of the Society for the Study of Human Biology Editors-in-Chief Noël Cameron, Olga Rickards, and Babette Zemel are the Editors-in-Chief An editor-in-chief (EIC), also known as lead editor or chief editor, is a publication's editorial leader who has final responsibility for its operations and policies. The highest-ranking editor of a publication may also be titled editor, managing ... of ''Annals of Human Biology''. Publication Format ''Annals of Human Biology'' publishes si ...
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Kosovo Albanians
The Albanians of Kosovo ( sq, Shqiptarët e Kosovës, ), also commonly called Kosovo Albanians, Kosovar/Kosovan Albanians or Kosovars/Kosovans, constitute the largest ethnic group in Kosovo. Kosovo Albanians belong to the ethnic Albanian sub-group of Ghegs, who inhabit the north of Albania, north of the Shkumbin river, Kosovo, southern Serbia, and western parts of North Macedonia. They speak Gheg Albanian, more specifically the Northwestern and Northeastern Gheg variants. According to the 1991 Yugoslav census, boycotted by Albanians, there were 1,596,072 ethnic Albanians in Kosovo or 81.6% of population. By the estimation in the year 2000, there were between 1,584,000 and 1,733,600 Albanians in Kosovo or 88% of population; as of 2011, their population share is 92.93%. History Pre-7th century Toponymical evidence suggests that Albanian was spoken in western and eastern Kosovo and the Niš region before the Migration Period. In this era, Albanian in Kosovo was in linguistic ...
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Single Nucleotide Polymorphism
In genetics, a single-nucleotide polymorphism (SNP ; plural SNPs ) is a germline substitution of a single nucleotide at a specific position in the genome. Although certain definitions require the substitution to be present in a sufficiently large fraction of the population (e.g. 1% or more), many publications do not apply such a frequency threshold. For example, at a specific base position in the human genome, the G nucleotide may appear in most individuals, but in a minority of individuals, the position is occupied by an A. This means that there is a SNP at this specific position, and the two possible nucleotide variations – G or A – are said to be the alleles for this specific position. SNPs pinpoint differences in our susceptibility to a wide range of diseases, for example age-related macular degeneration (a common SNP in the CFH gene is associated with increased risk of the disease) or nonalcoholic fatty liver disease (a SNP in the PNPLA3 gene is associated with incr ...
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Balts
The Balts or Baltic peoples ( lt, baltai, lv, balti) are an ethno-linguistic group of peoples who speak the Baltic languages of the Balto-Slavic branch of the Indo-European languages. One of the features of Baltic languages is the number of conservative or archaic features retained. Among the Baltic peoples are modern-day Lithuanians and Latvians (including Latgalians) — all Eastern Balts — as well as the Old Prussians, Yotvingians and Galindians — the Western Balts — whose languages and cultures are now extinct. Etymology Medieval German chronicler Adam of Bremen in the latter part of the 11th century AD was the first writer to use the term "Baltic" in reference to the sea of that name.Bojtár page 9. Before him various ancient places names, such as Balcia, were used in reference to a supposed island in the Baltic Sea. Adam, a speaker of German, connected ''Balt-'' with ''belt'', a word with which he was familiar. In Germanic languages there was some form of t ...
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Y-DNA
The Y chromosome is one of two sex chromosomes (allosomes) in therian mammals, including humans, and many other animals. The other is the X chromosome. Y is normally the sex-determining chromosome in many species, since it is the presence or absence of Y that determines the male or female sex of offspring produced in sexual reproduction. In mammals, the Y chromosome contains the gene SRY, which triggers male development. The DNA in the human Y chromosome is composed of about 59 million base pairs, making it similar in size to chromosome 19. The Y chromosome is passed only from father to son. With a 30% difference between humans and chimpanzees, the Y chromosome is one of the fastest-evolving parts of the human genome. The human Y chromosome carries an estimated 100–200 genes, with between 45 and 73 of these being protein-coding. All single-copy Y-linked genes are hemizygous (present on only one chromosome) except in cases of aneuploidy such as XYY syndrome or XXYY syndrome. ...
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Mitochondrial
A mitochondrion (; ) is an organelle found in the cells of most Eukaryotes, such as animals, plants and fungi. Mitochondria have a double membrane structure and use aerobic respiration to generate adenosine triphosphate (ATP), which is used throughout the cell as a source of chemical energy. They were discovered by Albert von Kölliker in 1857 in the voluntary muscles of insects. The term ''mitochondrion'' was coined by Carl Benda in 1898. The mitochondrion is popularly nicknamed the "powerhouse of the cell", a phrase coined by Philip Siekevitz in a 1957 article of the same name. Some cells in some multicellular organisms lack mitochondria (for example, mature mammalian red blood cells). A large number of unicellular organisms, such as microsporidia, parabasalids and diplomonads, have reduced or transformed their mitochondria into other structures. One eukaryote, ''Monocercomonoides'', is known to have completely lost its mitochondria, and one multicellular organism, ...
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Autosome
An autosome is any chromosome that is not a sex chromosome. The members of an autosome pair in a diploid cell have the same morphology, unlike those in allosome, allosomal (sex chromosome) pairs, which may have different structures. The DNA in autosomes is collectively known as atDNA or auDNA. For example, humans have a diploid human genome, genome that usually contains 22 pairs of autosomes and one allosome pair (46 chromosomes total). The autosome pairs are labeled with numbers (1–22 in humans) roughly in order of their sizes in base pairs, while allosomes are labelled with their letters. By contrast, the allosome pair consists of two X chromosomes in females or one X and one Y chromosome in males. Unusual combinations of XYY syndrome, XYY, Klinefelter syndrome, XXY, Triple X syndrome, XXX, XXXX syndrome, XXXX, XXXXX syndrome, XXXXX or XXYY syndrome, XXYY, among Aneuploidy, other Salome combinations, are known to occur and usually cause developmental abnormalities. Autosomes ...
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