Most viewed articles last month
This is a list of pages in the scope of Wikipedia:WikiProject Genetics along with pageviews.
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Period: 2026-06-01 to 2026-06-30
Total views: 5,339,871
Updated: 15:44, 11 July 2026 (UTC)
| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
Axolotl
|
112,059
|
3,735
|
C
|
High
|
| 2
|
Charcot–Marie–Tooth disease
|
110,219
|
3,673
|
C
|
Mid
|
| 3
|
Incest
|
73,269
|
2,442
|
C
|
Low
|
| 4
|
Cystic fibrosis
|
54,602
|
1,820
|
B
|
High
|
| 5
|
Eugenics
|
53,872
|
1,795
|
B
|
High
|
| 6
|
Prion
|
51,079
|
1,702
|
GA
|
Mid
|
| 7
|
Guinea pig
|
50,507
|
1,683
|
B
|
Low
|
| 8
|
DNA
|
47,653
|
1,588
|
B
|
Top
|
| 9
|
Prader–Willi syndrome
|
44,185
|
1,472
|
B
|
Mid
|
| 10
|
Cancer
|
39,725
|
1,324
|
C
|
Top
|
| 11
|
Amino acid
|
33,994
|
1,133
|
GA
|
Top
|
| 12
|
Evolution
|
31,911
|
1,063
|
FA
|
Top
|
| 13
|
Red hair
|
31,307
|
1,043
|
C
|
Mid
|
| 14
|
Last universal common ancestor
|
29,900
|
996
|
GA
|
Mid
|
| 15
|
Bayer
|
28,933
|
964
|
C
|
Low
|
| 16
|
HeLa
|
28,218
|
940
|
C
|
Low
|
| 17
|
Color blindness
|
28,006
|
933
|
B
|
Mid
|
| 18
|
Rosalind Franklin
|
27,978
|
932
|
B
|
High
|
| 19
|
Attachment theory
|
27,744
|
924
|
B
|
Mid
|
| 20
|
Blue Fugates
|
26,362
|
878
|
Start
|
Low
|
| 21
|
Epicanthic fold
|
26,207
|
873
|
C
|
Low
|
| 22
|
Adenosine triphosphate
|
25,774
|
859
|
C
|
High
|
| 23
|
Consanguinity
|
24,725
|
824
|
C
|
Low
|
| 24
|
Scientific racism
|
24,107
|
803
|
C
|
Low
|
| 25
|
Protein
|
24,004
|
800
|
GA
|
Top
|
| 26
|
Blood type
|
23,983
|
799
|
B
|
High
|
| 27
|
XXYYY syndrome
|
23,746
|
791
|
Start
|
Unknown
|
| 28
|
Cleft lip and cleft palate
|
23,495
|
783
|
B
|
Low
|
| 29
|
Svalbard Global Seed Vault
|
23,486
|
782
|
B
|
Mid
|
| 30
|
Total fertility rate
|
23,444
|
781
|
C
|
Low
|
| 31
|
Inbreeding
|
23,046
|
768
|
C
|
Low
|
| 32
|
Cousin
|
22,334
|
744
|
Start
|
Low
|
| 33
|
Blond
|
22,220
|
740
|
C
|
Low
|
| 34
|
SARS-CoV-2
|
22,165
|
738
|
B
|
Top
|
| 35
|
Japanese people
|
21,304
|
710
|
C
|
Low
|
| 36
|
CRISPR
|
21,304
|
710
|
B
|
High
|
| 37
|
Gregor Mendel
|
20,854
|
695
|
B
|
High
|
| 38
|
Peppered moth evolution
|
20,349
|
678
|
GA
|
Mid
|
| 39
|
Endogamy
|
20,129
|
670
|
Start
|
Low
|
| 40
|
Human skin color
|
19,887
|
662
|
B
|
Mid
|
| 41
|
Hybrid (biology)
|
19,883
|
662
|
GA
|
High
|
| 42
|
Recent African origin of modern humans
|
19,870
|
662
|
C
|
Mid
|
| 43
|
Albinism
|
19,866
|
662
|
C
|
Low
|
| 44
|
Estimates of historical world population
|
19,412
|
647
|
Start
|
Low
|
| 45
|
Gigantism
|
19,247
|
641
|
B
|
High
|
| 46
|
Chimera (genetics)
|
18,944
|
631
|
B
|
Mid
|
| 47
|
Biodiversity
|
18,217
|
607
|
C
|
Mid
|
| 48
|
Epigenetics
|
18,113
|
603
|
B
|
Top
|
| 49
|
Jennifer Doudna
|
17,474
|
582
|
B
|
High
|
| 50
|
Early human migrations
|
17,408
|
580
|
B
|
Mid
|
| 51
|
Mitochondrial Eve
|
17,400
|
580
|
B
|
Mid
|
| 52
|
Birth defect
|
17,092
|
569
|
B
|
Mid
|
| 53
|
Landrace
|
17,070
|
569
|
C
|
Low
|
| 54
|
Nicotinamide adenine dinucleotide
|
16,282
|
542
|
FA
|
Mid
|
| 55
|
Chromosome
|
16,063
|
535
|
B
|
Top
|
| 56
|
James Watson
|
15,892
|
529
|
B
|
High
|
| 57
|
Enzyme
|
15,887
|
529
|
FA
|
Top
|
| 58
|
XYY syndrome
|
15,471
|
515
|
B
|
Mid
|
| 59
|
William Shockley
|
15,292
|
509
|
B
|
Low
|
| 60
|
Genetics
|
15,137
|
504
|
FA
|
Top
|
| 61
|
Animal husbandry
|
15,089
|
502
|
GA
|
Mid
|
| 62
|
Population bottleneck
|
15,041
|
501
|
C
|
Mid
|
| 63
|
Advanced maternal age
|
15,020
|
500
|
C
|
Mid
|
| 64
|
Domesticated silver fox
|
15,000
|
500
|
C
|
Low
|
| 65
|
Drosophila melanogaster
|
14,751
|
491
|
B
|
Top
|
| 66
|
G. H. Hardy
|
14,735
|
491
|
C
|
Mid
|
| 67
|
Meiosis
|
14,673
|
489
|
C
|
Top
|
| 68
|
Sonic hedgehog protein
|
14,584
|
486
|
B
|
High
|
| 69
|
Human hair color
|
14,539
|
484
|
Start
|
Mid
|
| 70
|
23andMe
|
14,537
|
484
|
C
|
Mid
|
| 71
|
De-extinction
|
14,376
|
479
|
C
|
Low
|
| 72
|
Dominance (genetics)
|
14,283
|
476
|
C
|
Top
|
| 73
|
Humanzee
|
14,269
|
475
|
C
|
Mid
|
| 74
|
Senescence
|
13,997
|
466
|
C
|
Low
|
| 75
|
Leucism
|
13,972
|
465
|
Start
|
Low
|
| 76
|
Genetic studies of Jews
|
13,762
|
458
|
C
|
Mid
|
| 77
|
Early European Farmers
|
13,242
|
441
|
C
|
Mid
|
| 78
|
Cat coat genetics
|
13,047
|
434
|
C
|
Mid
|
| 79
|
Gene
|
12,932
|
431
|
GA
|
Top
|
| 80
|
M. S. Swaminathan
|
12,814
|
427
|
B
|
Low
|
| 81
|
RNA
|
12,632
|
421
|
GA
|
Top
|
| 82
|
Cultivar
|
12,296
|
409
|
C
|
Mid
|
| 83
|
Phenotype
|
11,934
|
397
|
C
|
Top
|
| 84
|
XY sex-determination system
|
11,862
|
395
|
C
|
High
|
| 85
|
Mitochondrial DNA
|
11,799
|
393
|
B
|
High
|
| 86
|
Human Genome Project
|
11,667
|
388
|
B
|
Top
|
| 87
|
Lactose intolerance
|
11,619
|
387
|
B
|
Low
|
| 88
|
Haplogroup R1a
|
11,563
|
385
|
C
|
Low
|
| 89
|
Trisomy 18
|
11,422
|
380
|
B
|
Low
|
| 90
|
DNA and RNA codon tables
|
11,356
|
378
|
FL
|
High
|
| 91
|
Genetic engineering
|
11,346
|
378
|
GA
|
Top
|
| 92
|
Polymerase chain reaction
|
11,315
|
377
|
B
|
High
|
| 93
|
Francis Crick
|
11,252
|
375
|
B
|
High
|
| 94
|
XX male syndrome
|
11,198
|
373
|
C
|
Low
|
| 95
|
Pentasomy X
|
11,149
|
371
|
GA
|
Low
|
| 96
|
Tay–Sachs disease
|
11,113
|
370
|
B
|
High
|
| 97
|
Stephen Jay Gould
|
11,101
|
370
|
GA
|
Mid
|
| 98
|
Mutation
|
11,096
|
369
|
B
|
Top
|
| 99
|
Brooke Greenberg
|
10,863
|
362
|
Start
|
Mid
|
| 100
|
Haplogroup R1b
|
10,825
|
360
|
C
|
Mid
|
| 101
|
Human–animal hybrid
|
10,747
|
358
|
C
|
Low
|
| 102
|
Y chromosome
|
10,713
|
357
|
B
|
High
|
| 103
|
The Bell Curve
|
10,653
|
355
|
C
|
High
|
| 104
|
Domestic rabbit
|
10,651
|
355
|
GA
|
Low
|
| 105
|
New Order (Nazism)
|
10,566
|
352
|
C
|
Mid
|
| 106
|
Karyotype
|
10,544
|
351
|
C
|
Mid
|
| 107
|
CRISPR gene editing
|
10,447
|
348
|
B
|
Top
|
| 108
|
Origin of SARS-CoV-2
|
10,308
|
343
|
B
|
Low
|
| 109
|
Genetic disorder
|
10,119
|
337
|
B
|
Top
|
| 110
|
Cloning
|
10,099
|
336
|
B
|
Top
|
| 111
|
Eva Nogales
|
10,010
|
333
|
Start
|
Low
|
| 112
|
Brown hair
|
9,947
|
331
|
C
|
Mid
|
| 113
|
Nucleotide
|
9,943
|
331
|
C
|
Top
|
| 114
|
Gamete
|
9,871
|
329
|
Start
|
Mid
|
| 115
|
Chin
|
9,870
|
329
|
C
|
Low
|
| 116
|
Atavism
|
9,811
|
327
|
C
|
Mid
|
| 117
|
Ploidy
|
9,714
|
323
|
C
|
High
|
| 118
|
Freckle
|
9,708
|
323
|
Start
|
Low
|
| 119
|
Patau syndrome
|
9,649
|
321
|
C
|
Low
|
| 120
|
XXXY syndrome
|
9,603
|
320
|
C
|
Low
|
| 121
|
Incest pornography
|
9,546
|
318
|
Start
|
Mid
|
| 122
|
Friedreich's ataxia
|
9,500
|
316
|
GA
|
Mid
|
| 123
|
Mendelian inheritance
|
9,424
|
314
|
C
|
High
|
| 124
|
Photo 51
|
9,395
|
313
|
Start
|
Low
|
| 125
|
Panthera hybrid
|
9,186
|
306
|
C
|
Mid
|
| 126
|
Ribosome
|
9,163
|
305
|
B
|
Top
|
| 127
|
Genetic descent from Genghis Khan
|
9,129
|
304
|
C
|
Low
|
| 128
|
Homology (biology)
|
9,066
|
302
|
GA
|
High
|
| 129
|
Western hunter-gatherer
|
8,921
|
297
|
C
|
Mid
|
| 130
|
Haplogroup
|
8,814
|
293
|
C
|
Mid
|
| 131
|
Ronald Fisher
|
8,718
|
290
|
B
|
High
|
| 132
|
He Jiankui
|
8,703
|
290
|
B
|
Low
|
| 133
|
Western Steppe Herders
|
8,621
|
287
|
C
|
Mid
|
| 134
|
Incest taboo
|
8,454
|
281
|
C
|
Mid
|
| 135
|
Ancient North Eurasian
|
8,382
|
279
|
C
|
Mid
|
| 136
|
Human genome
|
8,294
|
276
|
C
|
High
|
| 137
|
Ethnic groups of Japan
|
8,279
|
275
|
Start
|
Unknown
|
| 138
|
Genetic code
|
8,258
|
275
|
GA
|
Top
|
| 139
|
Most recent common ancestor
|
8,252
|
275
|
B
|
Mid
|
| 140
|
Tetralogy of Fallot
|
8,223
|
274
|
C
|
Low
|
| 141
|
Francis Collins
|
8,153
|
271
|
B
|
Mid
|
| 142
|
Human Y-chromosome DNA haplogroup
|
8,148
|
271
|
C
|
Mid
|
| 143
|
Hereditary haemochromatosis
|
8,108
|
270
|
B
|
Mid
|
| 144
|
Sexual selection
|
8,067
|
268
|
GA
|
Mid
|
| 145
|
Genentech
|
7,995
|
266
|
Start
|
Mid
|
| 146
|
Polyploidy
|
7,949
|
264
|
B
|
High
|
| 147
|
Telomere
|
7,941
|
264
|
C
|
Mid
|
| 148
|
Selective breeding
|
7,916
|
263
|
C
|
Top
|
| 149
|
Nucleic acid double helix
|
7,828
|
260
|
C
|
Mid
|
| 150
|
Nucleic acid
|
7,825
|
260
|
C
|
Mid
|
| 151
|
Genetically modified organism
|
7,781
|
259
|
GA
|
Top
|
| 152
|
He Jiankui affair
|
7,774
|
259
|
C
|
Low
|
| 153
|
DNA profiling
|
7,743
|
258
|
B
|
High
|
| 154
|
Blue rose
|
7,653
|
255
|
Start
|
Low
|
| 155
|
Genetic history of Europe
|
7,640
|
254
|
Start
|
Low
|
| 156
|
Congenital heart defect
|
7,590
|
253
|
B
|
Mid
|
| 157
|
Ras GTPase
|
7,562
|
252
|
B
|
High
|
| 158
|
Mirror-image life
|
7,511
|
250
|
Start
|
Low
|
| 159
|
Phenylketonuria
|
7,447
|
248
|
B
|
Mid
|
| 160
|
Single parent
|
7,366
|
245
|
B
|
Mid
|
| 161
|
Black hair
|
7,249
|
241
|
Start
|
Mid
|
| 162
|
Mosaic (genetics)
|
7,230
|
241
|
C
|
Mid
|
| 163
|
Auburn hair
|
7,168
|
238
|
Start
|
Low
|
| 164
|
DNA replication
|
7,159
|
238
|
C
|
Unknown
|
| 165
|
Allele
|
7,140
|
238
|
B
|
Top
|
| 166
|
Zebrafish
|
7,094
|
236
|
B
|
Mid
|
| 167
|
Eugenics in the United States
|
7,054
|
235
|
C
|
Low
|
| 168
|
RNA world
|
6,907
|
230
|
C
|
Mid
|
| 169
|
List of organisms by chromosome count
|
6,903
|
230
|
List
|
Low
|
| 170
|
Heredity
|
6,902
|
230
|
C
|
Top
|
| 171
|
Inbreeding depression
|
6,816
|
227
|
C
|
Low
|
| 172
|
Fibular hemimelia
|
6,767
|
225
|
Start
|
Low
|
| 173
|
Ectrodactyly
|
6,734
|
224
|
B
|
Mid
|
| 174
|
Sex-determination system
|
6,650
|
221
|
C
|
Mid
|
| 175
|
Punnett square
|
6,647
|
221
|
C
|
Top
|
| 176
|
Nazi eugenics
|
6,628
|
220
|
C
|
Mid
|
| 177
|
Genome
|
6,578
|
219
|
C
|
High
|
| 178
|
Von Hippel–Lindau disease
|
6,537
|
217
|
C
|
Mid
|
| 179
|
Horizontal gene transfer
|
6,528
|
217
|
C
|
High
|
| 180
|
Heterosis
|
6,498
|
216
|
C
|
High
|
| 181
|
Neanderthal genetics
|
6,385
|
212
|
C
|
High
|
| 182
|
Base pair
|
6,375
|
212
|
C
|
Top
|
| 183
|
Polymorphism (biology)
|
6,370
|
212
|
B
|
Low
|
| 184
|
Genetic testing
|
6,347
|
211
|
B
|
Top
|
| 185
|
Heritability of IQ
|
6,292
|
209
|
B
|
Low
|
| 186
|
Colour wheel theory of love
|
6,282
|
209
|
Start
|
Low
|
| 187
|
Exogamy
|
6,264
|
208
|
Start
|
Low
|
| 188
|
Y-chromosomal Adam
|
6,178
|
205
|
C
|
High
|
| 189
|
Barbara McClintock
|
6,112
|
203
|
FA
|
High
|
| 190
|
Hayflick limit
|
6,098
|
203
|
Start
|
Low
|
| 191
|
J. B. S. Haldane
|
6,095
|
203
|
C
|
Low
|
| 192
|
Messenger RNA
|
6,081
|
202
|
C
|
High
|
| 193
|
5α-Reductase 2 deficiency
|
6,049
|
201
|
B
|
Low
|
| 194
|
P53
|
6,020
|
200
|
B
|
High
|
| 195
|
Laboratory rat
|
5,989
|
199
|
C
|
Mid
|
| 196
|
Sex-determining region Y protein
|
5,983
|
199
|
C
|
Low
|
| 197
|
Major histocompatibility complex
|
5,981
|
199
|
B
|
Mid
|
| 198
|
Hispanos of New Mexico
|
5,884
|
196
|
Start
|
Low
|
| 199
|
List of unusual biological names
|
5,853
|
195
|
List
|
Low
|
| 200
|
Impulsivity
|
5,812
|
193
|
B
|
Mid
|
| 201
|
Plasmodium falciparum
|
5,717
|
190
|
B
|
Low
|
| 202
|
Genetic studies on Turkish people
|
5,693
|
189
|
Start
|
Low
|
| 203
|
Transcription (biology)
|
5,686
|
189
|
B
|
Top
|
| 204
|
Chromosome abnormality
|
5,666
|
188
|
Start
|
High
|
| 205
|
Founder effect
|
5,628
|
187
|
C
|
High
|
| 206
|
Genetics and archaeogenetics of South Asia
|
5,467
|
182
|
Start
|
Mid
|
| 207
|
Hardy–Weinberg principle
|
5,437
|
181
|
C
|
High
|
| 208
|
The Population Bomb
|
5,418
|
180
|
B
|
Low
|
| 209
|
DNA sequencing
|
5,414
|
180
|
B
|
Top
|
| 210
|
List of genetic disorders
|
5,407
|
180
|
List
|
High
|
| 211
|
Shyness
|
5,390
|
179
|
B
|
Low
|
| 212
|
KRAS
|
5,376
|
179
|
C
|
Mid
|
| 213
|
Dysgenics
|
5,370
|
179
|
Start
|
Low
|
| 214
|
XXYY syndrome
|
5,364
|
178
|
Start
|
Low
|
| 215
|
Illumina, Inc.
|
5,318
|
177
|
C
|
Low
|
| 216
|
Genetic history of the British Isles
|
5,309
|
176
|
C
|
Low
|
| 217
|
Zygosity
|
5,275
|
175
|
C
|
High
|
| 218
|
Lydia Fairchild
|
5,233
|
174
|
Stub
|
Unknown
|
| 219
|
Error
|
5,212
|
173
|
C
|
Mid
|
| 220
|
X chromosome
|
5,190
|
173
|
B
|
Top
|
| 221
|
Anthropometry
|
5,189
|
172
|
C
|
Low
|
| 222
|
Institutional racism
|
5,138
|
171
|
B
|
High
|
| 223
|
Sex chromosome
|
5,087
|
169
|
Start
|
High
|
| 224
|
Gene therapy
|
5,063
|
168
|
B
|
High
|
| 225
|
HLA-B27
|
5,059
|
168
|
C
|
Low
|
| 226
|
George Church (geneticist)
|
5,051
|
168
|
C
|
Low
|
| 227
|
Central dogma of molecular biology
|
5,046
|
168
|
C
|
Top
|
| 228
|
Data storage
|
5,045
|
168
|
C
|
Low
|
| 229
|
Proteinogenic amino acid
|
5,037
|
167
|
C
|
High
|
| 230
|
Genetic drift
|
5,004
|
166
|
GA
|
High
|
| 231
|
Eastern hunter-gatherer
|
4,997
|
166
|
C
|
Mid
|
| 232
|
Plasmid
|
4,992
|
166
|
C
|
High
|
| 233
|
Tuberous sclerosis
|
4,942
|
164
|
C
|
Mid
|
| 234
|
Fertility
|
4,937
|
164
|
C
|
Mid
|
| 235
|
Ventricular septal defect
|
4,936
|
164
|
C
|
Low
|
| 236
|
Parent
|
4,922
|
164
|
C
|
High
|
| 237
|
Synthetic biology
|
4,914
|
163
|
B
|
Mid
|
| 238
|
NF-κB
|
4,896
|
163
|
C
|
High
|
| 239
|
Atrial septal defect
|
4,886
|
162
|
B
|
Low
|
| 240
|
Genetic history of the Middle East
|
4,873
|
162
|
C
|
Mid
|
| 241
|
Haplogroup J-M172
|
4,855
|
161
|
Start
|
Low
|
| 242
|
Boar–pig hybrid
|
4,842
|
161
|
Stub
|
Low
|
| 243
|
Single-nucleotide polymorphism
|
4,811
|
160
|
C
|
High
|
| 244
|
ZW sex-determination system
|
4,798
|
159
|
C
|
Mid
|
| 245
|
Webbed toes
|
4,751
|
158
|
Start
|
Low
|
| 246
|
Genetically modified food
|
4,743
|
158
|
B
|
High
|
| 247
|
Lactase
|
4,732
|
157
|
B
|
Mid
|
| 248
|
Genetic history of Egypt
|
4,613
|
153
|
C
|
Low
|
| 249
|
Genetic history of the Iberian Peninsula
|
4,606
|
153
|
Start
|
Low
|
| 250
|
Sexual selection in humans
|
4,599
|
153
|
C
|
Low
|
| 251
|
Dwarf cat
|
4,597
|
153
|
Start
|
Low
|
| 252
|
Biological engineering
|
4,590
|
153
|
C
|
High
|
| 253
|
DNA evidence in the O. J. Simpson murder trial
|
4,547
|
151
|
B
|
Low
|
| 254
|
Gene expression
|
4,524
|
150
|
B
|
Top
|
| 255
|
GloFish
|
4,510
|
150
|
C
|
Mid
|
| 256
|
Laboratory mouse
|
4,507
|
150
|
B
|
Low
|
| 257
|
Colossal Biosciences dire wolf project
|
4,506
|
150
|
B
|
High
|
| 258
|
Wnt signaling pathway
|
4,467
|
148
|
C
|
Mid
|
| 259
|
Tetrasomy X
|
4,452
|
148
|
GA
|
Low
|
| 260
|
Charles Epstein (geneticist)
|
4,423
|
147
|
Start
|
Mid
|
| 261
|
Haplogroup J-M267
|
4,411
|
147
|
C
|
Low
|
| 262
|
Haplogroup E-M215
|
4,396
|
146
|
C
|
Low
|
| 263
|
Coefficient of inbreeding
|
4,377
|
145
|
Start
|
Low
|
| 264
|
DNA methylation
|
4,332
|
144
|
B
|
High
|
| 265
|
Hox gene
|
4,312
|
143
|
C
|
High
|
| 266
|
Human mitochondrial DNA haplogroup
|
4,305
|
143
|
Start
|
Low
|
| 267
|
Protein biosynthesis
|
4,267
|
142
|
B
|
Mid
|
| 268
|
Neotenic complex syndrome
|
4,258
|
141
|
Start
|
Low
|
| 269
|
Recombinant DNA
|
4,238
|
141
|
C
|
High
|
| 270
|
Variants of SARS-CoV-2
|
4,235
|
141
|
C
|
Low
|
| 271
|
Mebendazole
|
4,224
|
140
|
C
|
Mid
|
| 272
|
Aneuploidy
|
4,209
|
140
|
B
|
High
|
| 273
|
Pedigree collapse
|
4,171
|
139
|
Start
|
Low
|
| 274
|
Sex selection
|
4,158
|
138
|
C
|
Low
|
| 275
|
Lectin
|
4,144
|
138
|
C
|
Mid
|
| 276
|
Haplogroup G-M201
|
4,141
|
138
|
Start
|
Low
|
| 277
|
David Reich (geneticist)
|
4,132
|
137
|
C
|
Mid
|
| 278
|
Monoamine oxidase A
|
4,129
|
137
|
C
|
Mid
|
| 279
|
Citicoline
|
4,107
|
136
|
B
|
Low
|
| 280
|
Haplogroup U
|
4,073
|
135
|
Start
|
Mid
|
| 281
|
Mitochondrial disease
|
4,034
|
134
|
C
|
Mid
|
| 282
|
Haplogroup H (mtDNA)
|
4,017
|
133
|
Start
|
Low
|
| 283
|
DNA repair
|
4,014
|
133
|
C
|
High
|
| 284
|
Fitness (biology)
|
4,010
|
133
|
C
|
Mid
|
| 285
|
Haplogroup J (Y-DNA)
|
3,974
|
132
|
Start
|
Low
|
| 286
|
Sexual differentiation in humans
|
3,959
|
131
|
C
|
Mid
|
| 287
|
Dun gene
|
3,958
|
131
|
C
|
Low
|
| 288
|
Chromosome 21
|
3,952
|
131
|
C
|
Mid
|
| 289
|
Sanger sequencing
|
3,946
|
131
|
C
|
High
|
| 290
|
Transposable element
|
3,936
|
131
|
C
|
High
|
| 291
|
Mathematical and theoretical biology
|
3,931
|
131
|
C
|
Low
|
| 292
|
Dravet syndrome
|
3,911
|
130
|
C
|
Low
|
| 293
|
Transfer RNA
|
3,903
|
130
|
B
|
High
|
| 294
|
Whole genome sequencing
|
3,875
|
129
|
B
|
Top
|
| 295
|
Haplogroup N-M231
|
3,862
|
128
|
Start
|
Low
|
| 296
|
Biological determinism
|
3,857
|
128
|
GA
|
Mid
|
| 297
|
New eugenics
|
3,823
|
127
|
Start
|
Mid
|
| 298
|
Haplogroup I-M253
|
3,804
|
126
|
B
|
Low
|
| 299
|
Telomerase
|
3,785
|
126
|
B
|
High
|
| 300
|
Haplogroup I-M170
|
3,748
|
124
|
B
|
Low
|
| 301
|
Cathy Tie
|
3,743
|
124
|
C
|
Low
|
| 302
|
Designer baby
|
3,703
|
123
|
B
|
High
|
| 303
|
Cyclic adenosine monophosphate
|
3,693
|
123
|
C
|
Mid
|
| 304
|
Genotype
|
3,682
|
122
|
Start
|
Top
|
| 305
|
Adeno-associated virus
|
3,661
|
122
|
B
|
Low
|
| 306
|
Somatic cell
|
3,645
|
121
|
Start
|
Mid
|
| 307
|
Uterus didelphys
|
3,635
|
121
|
Start
|
Low
|
| 308
|
Nicotinamide adenine dinucleotide phosphate
|
3,625
|
120
|
Start
|
Mid
|
| 309
|
Human genetic variation
|
3,624
|
120
|
C
|
High
|
| 310
|
Trisomy
|
3,621
|
120
|
Start
|
High
|
| 311
|
Twin study
|
3,607
|
120
|
B
|
High
|
| 312
|
Model organism
|
3,594
|
119
|
B
|
Mid
|
| 313
|
Coefficient of relationship
|
3,584
|
119
|
C
|
Low
|
| 314
|
Ghost population
|
3,577
|
119
|
Start
|
Low
|
| 315
|
Genomics
|
3,570
|
119
|
B
|
Top
|
| 316
|
BRCA1
|
3,564
|
118
|
C
|
High
|
| 317
|
Allopatric speciation
|
3,559
|
118
|
B
|
Low
|
| 318
|
Real-time polymerase chain reaction
|
3,552
|
118
|
C
|
Mid
|
| 319
|
Haplogroup I-M438
|
3,538
|
117
|
Start
|
Low
|
| 320
|
Transcription factor
|
3,530
|
117
|
B
|
High
|
| 321
|
Turi King
|
3,528
|
117
|
C
|
Low
|
| 322
|
Paternal age effect
|
3,527
|
117
|
C
|
Mid
|
| 323
|
Translation (biology)
|
3,515
|
117
|
B
|
Top
|
| 324
|
Uracil
|
3,476
|
115
|
B
|
Mid
|
| 325
|
Racial hygiene
|
3,476
|
115
|
C
|
Low
|
| 326
|
Modern synthesis (20th century)
|
3,475
|
115
|
GA
|
High
|
| 327
|
Heritability of autism
|
3,474
|
115
|
C
|
Mid
|
| 328
|
Non-paternity event
|
3,460
|
115
|
C
|
Low
|
| 329
|
Fisherian runaway
|
3,457
|
115
|
Start
|
Mid
|
| 330
|
MicroRNA
|
3,435
|
114
|
B
|
Top
|
| 331
|
Autosome
|
3,411
|
113
|
Start
|
Top
|
| 332
|
Purebred
|
3,403
|
113
|
C
|
Low
|
| 333
|
Gene drive
|
3,384
|
112
|
C
|
High
|
| 334
|
Ruth Benedict
|
3,354
|
111
|
C
|
Low
|
| 335
|
RNA splicing
|
3,343
|
111
|
C
|
Top
|
| 336
|
F1 hybrid
|
3,315
|
110
|
Start
|
High
|
| 337
|
Apomorphy and synapomorphy
|
3,298
|
109
|
C
|
Low
|
| 338
|
Genetic recombination
|
3,286
|
109
|
C
|
High
|
| 339
|
Kin selection
|
3,281
|
109
|
GA
|
Mid
|
| 340
|
46,XX/46,XY
|
3,270
|
109
|
C
|
Low
|
| 341
|
JAK-STAT signaling pathway
|
3,168
|
105
|
B
|
Mid
|
| 342
|
Histone
|
3,166
|
105
|
C
|
Mid
|
| 343
|
Hepatitis D
|
3,133
|
104
|
C
|
Low
|
| 344
|
Chromatin
|
3,129
|
104
|
B
|
Mid
|
| 345
|
Haplogroup A (Y-DNA)
|
3,121
|
104
|
C
|
Low
|
| 346
|
Methylation
|
3,113
|
103
|
C
|
Mid
|
| 347
|
Medical genetics of Jews
|
3,109
|
103
|
Start
|
Low
|
| 348
|
Patent ductus arteriosus
|
3,082
|
102
|
C
|
Mid
|
| 349
|
Nucleolus
|
3,057
|
101
|
Start
|
Mid
|
| 350
|
Genetic memory (psychology)
|
3,054
|
101
|
Start
|
Low
|
| 351
|
List of haplogroups of historic people
|
3,033
|
101
|
List
|
Low
|
| 352
|
Reverse transcription polymerase chain reaction
|
3,029
|
100
|
Start
|
Mid
|
| 353
|
Ancient DNA
|
3,027
|
100
|
C
|
Mid
|
| 354
|
Massimo Pigliucci
|
3,018
|
100
|
C
|
Unknown
|
| 355
|
RNA interference
|
3,011
|
100
|
FA
|
Top
|
| 356
|
Cas9
|
3,010
|
100
|
C
|
Mid
|
| 357
|
David Baulcombe
|
3,005
|
100
|
Start
|
Unknown
|
| 358
|
Factor VIII
|
2,996
|
99
|
Start
|
Low
|
| 359
|
Genome editing
|
2,996
|
99
|
C
|
High
|
| 360
|
Chromosome 2
|
2,992
|
99
|
C
|
Mid
|
| 361
|
Janaki Ammal
|
2,980
|
99
|
B
|
Low
|
| 362
|
Haplogroup R (Y-DNA)
|
2,977
|
99
|
Start
|
Low
|
| 363
|
Haplogroup Q-M242
|
2,955
|
98
|
C
|
Low
|
| 364
|
Y-chromosomal Aaron
|
2,952
|
98
|
Start
|
Low
|
| 365
|
Pleiotropy
|
2,951
|
98
|
C
|
High
|
| 366
|
Telegony (inheritance)
|
2,933
|
97
|
C
|
Low
|
| 367
|
Haplogroup E-V68
|
2,923
|
97
|
C
|
Low
|
| 368
|
Cold Spring Harbor Laboratory
|
2,914
|
97
|
Start
|
Mid
|
| 369
|
HER2
|
2,900
|
96
|
C
|
Mid
|
| 370
|
Bovine somatotropin
|
2,898
|
96
|
C
|
Low
|
| 371
|
Peopling of China
|
2,887
|
96
|
Start
|
Low
|
| 372
|
Genealogical DNA test
|
2,879
|
95
|
C
|
Mid
|
| 373
|
XXXYY syndrome
|
2,858
|
95
|
GA
|
Low
|
| 374
|
Flavin adenine dinucleotide
|
2,848
|
94
|
B
|
Low
|
| 375
|
Breed
|
2,840
|
94
|
C
|
Low
|
| 376
|
CpG site
|
2,826
|
94
|
C
|
Mid
|
| 377
|
Genomic imprinting
|
2,815
|
93
|
C
|
High
|
| 378
|
Epidermal growth factor receptor
|
2,802
|
93
|
C
|
Mid
|
| 379
|
Transgene
|
2,790
|
93
|
B
|
Mid
|
| 380
|
GEDmatch
|
2,775
|
92
|
Start
|
Mid
|
| 381
|
Svante Pääbo
|
2,771
|
92
|
C
|
Low
|
| 382
|
Maurice Wilkins
|
2,766
|
92
|
B
|
High
|
| 383
|
Aniridia
|
2,765
|
92
|
C
|
Low
|
| 384
|
Open reading frame
|
2,761
|
92
|
Start
|
Mid
|
| 385
|
Endogeny (biology)
|
2,753
|
91
|
Stub
|
Low
|
| 386
|
45,X/46,XY mosaicism
|
2,742
|
91
|
C
|
Low
|
| 387
|
Nucleic acid sequence
|
2,735
|
91
|
C
|
High
|
| 388
|
Genetically modified crops
|
2,712
|
90
|
B
|
High
|
| 389
|
Population genetics
|
2,710
|
90
|
C
|
Top
|
| 390
|
DNA polymerase
|
2,710
|
90
|
C
|
Top
|
| 391
|
Elizabeth Blackburn
|
2,708
|
90
|
C
|
Low
|
| 392
|
Haplogroup R1
|
2,685
|
89
|
C
|
Low
|
| 393
|
Stop codon
|
2,671
|
89
|
C
|
High
|
| 394
|
Fixation index
|
2,670
|
89
|
C
|
Low
|
| 395
|
Phenotypic trait
|
2,663
|
88
|
Start
|
Mid
|
| 396
|
Haplogroup T-M184
|
2,663
|
88
|
C
|
Low
|
| 397
|
Reverse transcriptase
|
2,655
|
88
|
B
|
High
|
| 398
|
Ursid hybrid
|
2,648
|
88
|
C
|
Low
|
| 399
|
Sampling bias
|
2,644
|
88
|
C
|
Low
|
| 400
|
Wild type
|
2,644
|
88
|
Start
|
Mid
|
| 401
|
Myc
|
2,635
|
87
|
C
|
High
|
| 402
|
Disodium inosinate
|
2,624
|
87
|
Start
|
Low
|
| 403
|
Humanized mouse
|
2,620
|
87
|
Start
|
Low
|
| 404
|
X-inactivation
|
2,612
|
87
|
B
|
High
|
| 405
|
FOXP2
|
2,601
|
86
|
B
|
Mid
|
| 406
|
Guanosine triphosphate
|
2,600
|
86
|
Start
|
Mid
|
| 407
|
Oogenesis
|
2,584
|
86
|
C
|
High
|
| 408
|
Post-translational modification
|
2,583
|
86
|
C
|
High
|
| 409
|
Eric Lander
|
2,582
|
86
|
C
|
Low
|
| 410
|
Pioneer Fund
|
2,564
|
85
|
B
|
Low
|
| 411
|
Transgenerational epigenetic inheritance
|
2,554
|
85
|
C
|
High
|
| 412
|
Maladaptation
|
2,534
|
84
|
Start
|
Low
|
| 413
|
Oncogene
|
2,529
|
84
|
C
|
High
|
| 414
|
Promoter (genetics)
|
2,529
|
84
|
Start
|
Mid
|
| 415
|
Behavioural genetics
|
2,529
|
84
|
GA
|
High
|
| 416
|
BRCA2
|
2,524
|
84
|
B
|
High
|
| 417
|
The Kallikak Family
|
2,515
|
83
|
C
|
Unknown
|
| 418
|
Somatic cell nuclear transfer
|
2,507
|
83
|
B
|
Mid
|
| 419
|
Haplodiploidy
|
2,496
|
83
|
C
|
Mid
|
| 420
|
Genetic and anthropology studies on Filipinos
|
2,496
|
83
|
C
|
Low
|
| 421
|
Genome-wide association study
|
2,491
|
83
|
GA
|
Top
|
| 422
|
16S ribosomal RNA
|
2,489
|
82
|
C
|
High
|
| 423
|
Locus (genetics)
|
2,488
|
82
|
Start
|
Mid
|
| 424
|
Directionality (molecular biology)
|
2,487
|
82
|
Start
|
High
|
| 425
|
Systems biology
|
2,479
|
82
|
C
|
High
|
| 426
|
Molecular clock
|
2,449
|
81
|
B
|
High
|
| 427
|
Jonathan Rothberg
|
2,448
|
81
|
C
|
Unknown
|
| 428
|
Tongue rolling
|
2,443
|
81
|
Stub
|
Low
|
| 429
|
Kozak consensus sequence
|
2,438
|
81
|
Start
|
Mid
|
| 430
|
SARS-CoV-2 Delta variant
|
2,430
|
81
|
C
|
Low
|
| 431
|
RNA polymerase
|
2,428
|
80
|
B
|
Top
|
| 432
|
Neo-Darwinism
|
2,403
|
80
|
Start
|
High
|
| 433
|
Crossbreed
|
2,402
|
80
|
Start
|
Low
|
| 434
|
Haplotype
|
2,389
|
79
|
Start
|
High
|
| 435
|
Gene-centered view of evolution
|
2,382
|
79
|
B
|
High
|
| 436
|
Intron
|
2,381
|
79
|
C
|
High
|
| 437
|
Medical genetics
|
2,378
|
79
|
B
|
Mid
|
| 438
|
Okazaki fragments
|
2,374
|
79
|
B
|
High
|
| 439
|
Fluorescence in situ hybridization
|
2,367
|
78
|
B
|
Mid
|
| 440
|
History of eugenics
|
2,366
|
78
|
B
|
Low
|
| 441
|
Feng Zhang
|
2,365
|
78
|
Start
|
Low
|
| 442
|
Scandinavian hunter-gatherer
|
2,350
|
78
|
C
|
Mid
|
| 443
|
Polygynandry
|
2,335
|
77
|
C
|
Low
|
| 444
|
Genetic studies on Arabs
|
2,321
|
77
|
C
|
Low
|
| 445
|
Lac operon
|
2,317
|
77
|
C
|
Mid
|
| 446
|
Haplogroup C-M217
|
2,317
|
77
|
B
|
Low
|
| 447
|
Broad Institute
|
2,313
|
77
|
Start
|
Mid
|
| 448
|
Galton–Watson process
|
2,312
|
77
|
B
|
Low
|
| 449
|
Southern dispersal
|
2,308
|
76
|
C
|
Low
|
| 450
|
Haldane's rule
|
2,303
|
76
|
C
|
Low
|
| 451
|
Haplogroup E-M96
|
2,302
|
76
|
Start
|
Low
|
| 452
|
Plant breeding
|
2,290
|
76
|
C
|
High
|
| 453
|
Constriction ring syndrome
|
2,289
|
76
|
C
|
Low
|
| 454
|
Sheep farming
|
2,287
|
76
|
C
|
Low
|
| 455
|
Vavilovian mimicry
|
2,278
|
75
|
GA
|
Low
|
| 456
|
Genetic history of Africa
|
2,276
|
75
|
B
|
Low
|
| 457
|
Haplogroup L-M20
|
2,264
|
75
|
Start
|
Low
|
| 458
|
Haplogroup O-M175
|
2,252
|
75
|
Start
|
Low
|
| 459
|
MELAS syndrome
|
2,250
|
75
|
C
|
Low
|
| 460
|
Orthoflavivirus
|
2,247
|
74
|
B
|
Mid
|
| 461
|
Epistasis
|
2,239
|
74
|
B
|
High
|
| 462
|
Haplogroup O-M122
|
2,237
|
74
|
Start
|
Low
|
| 463
|
Peter and Rosemary Grant
|
2,234
|
74
|
C
|
Unknown
|
| 464
|
Grandmother hypothesis
|
2,231
|
74
|
C
|
Mid
|
| 465
|
Genetic admixture
|
2,218
|
73
|
Start
|
Mid
|
| 466
|
Y-DNA haplogroups in populations of Europe
|
2,216
|
73
|
List
|
Mid
|
| 467
|
Zellweger syndrome
|
2,212
|
73
|
Start
|
Low
|
| 468
|
Heritability
|
2,205
|
73
|
C
|
High
|
| 469
|
Personalized medicine
|
2,201
|
73
|
B
|
Mid
|
| 470
|
Adenosine diphosphate
|
2,199
|
73
|
C
|
Mid
|
| 471
|
Chromosomal translocation
|
2,197
|
73
|
Start
|
High
|
| 472
|
Ancient Northern East Asian
|
2,192
|
73
|
B
|
Unknown
|
| 473
|
Y-DNA haplogroups by ethnic group
|
2,183
|
72
|
Start
|
Mid
|
| 474
|
FOSB
|
2,169
|
72
|
C
|
Mid
|
| 475
|
Leigh syndrome
|
2,168
|
72
|
C
|
Low
|
| 476
|
Haplogroup H (Y-DNA)
|
2,164
|
72
|
C
|
Low
|
| 477
|
Species distribution
|
2,155
|
71
|
C
|
High
|
| 478
|
Ribozyme
|
2,152
|
71
|
C
|
High
|
| 479
|
Sydney Brenner
|
2,148
|
71
|
B
|
Mid
|
| 480
|
Income and fertility
|
2,146
|
71
|
B
|
Low
|
| 481
|
Mutant
|
2,144
|
71
|
Start
|
Low
|
| 482
|
Knockout mouse
|
2,143
|
71
|
C
|
Mid
|
| 483
|
Epigenetic clock
|
2,141
|
71
|
C
|
Mid
|
| 484
|
Phred quality score
|
2,133
|
71
|
Start
|
Low
|
| 485
|
Homologous chromosome
|
2,128
|
70
|
Start
|
High
|
| 486
|
Genetic variation
|
2,127
|
70
|
Start
|
High
|
| 487
|
Genetic genealogy
|
2,125
|
70
|
C
|
Mid
|
| 488
|
Biomaterial
|
2,110
|
70
|
C
|
Low
|
| 489
|
Trisomy 16
|
2,108
|
70
|
Start
|
Low
|
| 490
|
Chédiak–Higashi syndrome
|
2,107
|
70
|
Start
|
Low
|
| 491
|
Hershey–Chase experiment
|
2,098
|
69
|
C
|
High
|
| 492
|
Genetic and anthropometric studies on Japanese people
|
2,095
|
69
|
Start
|
Low
|
| 493
|
Barr body
|
2,093
|
69
|
Start
|
High
|
| 494
|
Junk DNA
|
2,084
|
69
|
B
|
Mid
|
| 495
|
Sense (molecular biology)
|
2,079
|
69
|
C
|
High
|
| 496
|
Introgression
|
2,078
|
69
|
Start
|
High
|
| 497
|
Xenobiology
|
2,077
|
69
|
C
|
Low
|
| 498
|
C57BL/6
|
2,073
|
69
|
Start
|
Low
|
| 499
|
Nucleoid
|
2,057
|
68
|
B
|
Mid
|
| 500
|
Muller's ratchet
|
2,052
|
68
|
Start
|
Mid
|
|
Full category list
Categories within WP:GEN
|
Category WikiProject Genetics not found
|
Categories within Genetics
|
|
|
|