RESEARCH BASE

Search 3,721 documents across 34 fields — every claim tier-rated by evidence

3,721 Documents 34 Sections 43,625 Citations 34,852 Keywords Indexed 4 Evidence Tiers

3,633 are the core, quality-scored corpus (34 lettered sections — see How We Work); the remaining 88 are cross-corpus synthesis documents (68 InterDocs, 12 Connections, 8 Theories) also indexed here.

3,436 results for "mtDNA haplogroup B" — page 139 of 172

L_2_15 Verified Genetics & Origins

L_2_15 — Population Structure of the Ancient Near East: Farming Spread Genetics

The Neolithic Revolution — the independent invention of agriculture in the Fertile Crescent (~10,000-8,000 BCE) — was one of the most consequential transformations in human history, and ancient DNA has revealed that the

Neolithic farming Near East Fertile Crescent Anatolia Levant
L_2_18 Verified Genetics & Origins

L_2_18 — Archaic Admixture in Africa (Ghost Populations)

While Neanderthal and Denisovan admixture in non-African populations has been well-documented since Svante Pääbo's landmark 2010 Neanderthal genome paper, evidence for archaic admixture within Africa represents a more re

archaic admixture ghost population African genetics ancient DNA introgression archaic hominin
L_3_16 Verified Genetics & Origins

L_3_16 — Genomic Imprinting & Evolutionary Conflict

Genomic imprinting — the epigenetic phenomenon in which a subset of genes (~100–200 in mammals) are expressed from only one parental allele, with the other allele silenced by DNA methylation and histone modification esta

genomic imprinting parent-of-origin expression epigenetics kinship theory parental conflict IGF2
L_3_06 Credible Genetics & Origins

L_3_06 — Genetics of Intelligence and Cognition

The genetics of intelligence — one of the most studied yet contentious areas in behavioral genetics — has established that cognitive ability, as measured by standardized tests, has a substantial heritable component (~50–

intelligence genetics cognitive ability IQ heritability GWAS intelligence polygenic score educational attainment
L_3_17 Verified Genetics & Origins

L_3_17 — Endogenous Retroviruses (HERVs) in the Human Genome

Human endogenous retroviruses (HERVs) — remnants of ancient retroviral infections that integrated into the germline DNA of human ancestors and have been vertically transmitted through the host genome for millions of year

endogenous retroviruses HERVs HERV-K HERV-W syncytin retroviral integration
L_3_09 Verified Genetics & Origins

L_3_09 — HLA Diversity and Immune System Evolution

The Human Leukocyte Antigen (HLA) system — the human version of the Major Histocompatibility Complex (MHC) found in all jawed vertebrates — is the most polymorphic gene region in the entire human genome. Located on chrom

HLA MHC major histocompatibility complex immune diversity balancing selection antigen presentation
L_3_00 Genetics & Origins

L_3_00 — Adaptation Traits: Subfolder Summary

L_3_18 Verified Genetics & Origins

L_3_18 — Horizontal Gene Transfer in Eukaryotes

Horizontal gene transfer (HGT) — the movement of genetic material between organisms through mechanisms other than vertical parent-to-offspring inheritance — was long considered a predominantly prokaryotic phenomenon, cen

horizontal gene transfer lateral gene transfer HGT LGT eukaryotes introgression
L_3_03 Verified Genetics & Origins

L_3_03 — Lactase Persistence and Gene-Culture Coevolution

Lactase persistence — the ability of adults to digest the milk sugar lactose — is the most thoroughly documented case of gene-culture coevolution in the human species. The ancestral mammalian condition is lactase non-per

lactase persistence lactose intolerance LCT gene gene-culture coevolution pastoralism dairy farming
L_3_08 Verified Genetics & Origins

L_3_08 — Genetics of Skin, Hair, and Eye Color

Human pigmentation — skin, hair, and eye color — is one of the best-understood complex traits in human genetics, with a relatively modest number of genes explaining a large proportion of variation compared to most polyge

pigmentation genetics melanin eumelanin pheomelanin MC1R OCA2
L_5_10 Verified Genetics & Origins

L_5_10 — Neandertal Introgression: Which Genes and Why They Persisted

When modern humans (Homo sapiens) migrated out of Africa ~60,000-70,000 years ago and encountered Neanderthals (Homo neanderthalensis) in western Asia and Europe, the two species interbred — and the genetic legacy of tha

Neandertal introgression admixture adaptive introgression purifying selection immune genes
L_5_03 Verified Genetics & Origins

L_5_03 — Pharmacogenomics and Ancestral Medicine

Pharmacogenomics — the study of how genetic variation influences individual responses to drugs — bridges genetics, pharmacology, and clinical medicine. Humans carry extensive polymorphism in genes encoding drug-metaboliz

pharmacogenomics CYP2D6 CYP2C_5_04 drug metabolism personalized medicine warfarin
L_5_16 Verified Genetics & Origins

L_5_16 — Archaeogenetics: Ancient DNA and the Human Past

Archaeogenetics — the extraction and analysis of DNA from ancient human, animal, and plant remains — has transformed our understanding of human history since the field's breakthrough in 2010. Advances in next-generation

archaeogenetics ancient DNA aDNA paleogenomics Svante Pääbo David Reich
L_5_08 Verified Genetics & Origins

L_5_08 — Ancient DNA from Sediments: Cave Dirt Genomics

One of the most revolutionary methodological advances in ancient DNA (aDNA) research has been the recovery of hominin DNA directly from cave sediments — without any bones or teeth. This technique, pioneered by Matthias M

sediment DNA environmental DNA eDNA cave sediment ancient DNA metagenomic
L_5_00 Genetics & Origins

L_5_00 — Health Microbiome Applied: Subfolder Summary

L_5_02 Verified Genetics & Origins

L_5_02 — Genetic Diseases and Founder Effect Populations

When a small group founds a new population and subsequently expands in relative isolation, genetic drift can amplify alleles that were rare in the ancestral population — including deleterious recessive disease alleles. T

founder effect genetic disease Tay-Sachs sickle cell cystic fibrosis Ashkenazi
Y_4_08 Verified Altered States

Y_4_08 — Sleep Science — REM, NREM, and the Ancient Understanding of Sleep

Sleep science has undergone a revolution in the 21st century, fundamentally altering our understanding of why humans sleep. The landmark 2012 discovery of the glymphatic system by Maiken Nedergaard revealed that the brai

sleep REM NREM glymphatic system slow-wave sleep dreams
Y_4_06 Verified Altered States

Y_4_06 — Synesthesia and Cross-Modal Perception

Synesthesia — the involuntary, consistent experience of one sensory modality triggering perception in another (e.g., hearing colors, tasting shapes) — affects roughly 4% of the general population when broad subtype defin

synesthesia cross-modal perception chromesthesia grapheme-color sound-color mirror-touch
Y_4_02 Verified Altered States

Y_4_02 — Savant Syndrome and Acquired Genius

Savant syndrome — extraordinary ability coexisting with significant cognitive disability — affects roughly 1 in 10 people with autism and ~1 in 2,000 people with other developmental disabilities or brain injuries. What m

savant syndrome acquired savant traumatic brain injury autistic savant Kim Peek Daniel Tammet
Y_4_17 Verified Altered States

Y_4_17 — Sleep Disorders & Parasomnias

Sleep disorders affect an estimated 50–70 million Americans and up to 45% of the global population, encompassing over 80 distinct conditions classified by the International Classification of Sleep Disorders (ICSD-3, 2014

sleep disorders parasomnias narcolepsy sleepwalking REM behavior disorder sleep terrors