Category:Human genetics

A

• Ancient DNA (human) (1 C, 9 P)

B

• Behavioural genetics (5 C, 51 P)

C

• Chromosomes (human) (1 C, 27 P)

E

• Estrogen regulation (3 P)
• Eugenics (8 C, 22 P)

G

• Genetic genealogy (7 C, 88 P)
• Genographic Project (2 P)

H

• Human genes (25 C, 491 P)
• Human genetic history (3 C, 8 P)
• Human geneticists (2 C, 62 P)
• Human haplotypes (2 C)
• Human mitochondrial genetics (2 C, 7 P)
• Human multigene haplotypes (2 P)

N

• National DNA databases (7 P)

P

• Paternity (1 C, 14 P)
• Human population genetics (7 C, 47 P)

T

• Twin studies (1 C, 19 P)

• Human genetics

-

• Template:Human genetics

0–9

• 1q21.1 copy number variations

A

• Adaptive evolution in the human genome
• Adoption study
• Alu element
• Archon X Prize

B

• Blood type distribution by country

C

• Choriogenesis
• Clinodactyly
• Common disease-common variant
• Consanguinity
• Genetic correlates of criminal behavior

D

• DEL17P13.1
• Disappearing blonde gene

E

• Exome

F

• Farming/language dispersal hypothesis
• Father tongue hypothesis
• FNAEG

G

• Gene–environment correlation
• Generalist Genes hypothesis
• GeneSweep
• Genetic discrimination
• Genetic epidemiology
• Genetic privacy
• Genetic reductionism
• Geneticization
• Human genome
• Genotype-first approach
• GIANT consortium
• GRAFS

H

• Haplarithm
• Haplarithmisis
• HCONDELs
• Human accelerated regions
• Human behaviour genetics
• Human evolutionary genetics
• Human interactome
• Human skin color
• HumHot

I

• Inflammatory bowel disease-22
• Isogenic human disease models

K

• Kinesiogenomics

L

• Lactase persistence
• List of human genetics conferences
• LZTFL1

M

• Mayan genetics
• Mendelian traits in humans
• Midphalangeal hair
• Mitochondrial replacement therapy
• MRC Human Genetics Unit

N

• Nature versus nurture

O

• Oxford Centre for Gene Function

P

• Phenylthiocarbamide

R

• Rare variant (genetics)
• Reference genome

S

• Secretor status
• Simple Mendelian genetics in humans
• Structural variation in the human genome

T

• Tc1/mariner

W

• WDR88
• Wellcome Centre for Human Genetics