Most viewed articles last month
This is a list of pages in the scope of Wikipedia:WikiProject Genetics along with pageviews.
To report bugs, please write on the Community tech bot talk page on Meta.
Period: 2025-02-01 to 2025-02-28
Total views: 7,611,667
Updated: 18:42, 9 March 2025 (UTC)
Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Axolotl
|
189,362
|
6,762
|
C
|
High
|
2
|
Eugenics
|
137,606
|
4,914
|
B
|
High
|
3
|
Incest
|
82,447
|
2,944
|
C
|
Low
|
4
|
DNA
|
71,687
|
2,560
|
FA
|
Top
|
5
|
Cancer
|
62,741
|
2,240
|
B
|
Top
|
6
|
Guinea pig
|
60,203
|
2,150
|
B
|
Low
|
7
|
Prion
|
60,023
|
2,143
|
GA
|
Mid
|
8
|
Cystic fibrosis
|
57,493
|
2,053
|
B
|
High
|
9
|
Amino acid
|
49,790
|
1,778
|
GA
|
Top
|
10
|
Attachment theory
|
47,263
|
1,687
|
B
|
Mid
|
11
|
Nicotinamide adenine dinucleotide
|
47,019
|
1,679
|
FA
|
Mid
|
12
|
Bayer
|
43,835
|
1,565
|
C
|
Low
|
13
|
Prader–Willi syndrome
|
42,348
|
1,512
|
B
|
Mid
|
14
|
Evolution
|
41,331
|
1,476
|
FA
|
Top
|
15
|
Protein
|
41,193
|
1,471
|
GA
|
Top
|
16
|
Blood type
|
40,572
|
1,449
|
B
|
High
|
17
|
SARS-CoV-2
|
39,808
|
1,421
|
B
|
Top
|
18
|
Color blindness
|
38,964
|
1,391
|
B
|
Mid
|
19
|
Scientific racism
|
37,726
|
1,347
|
C
|
Low
|
20
|
Gregor Mendel
|
37,445
|
1,337
|
B
|
High
|
21
|
Rosalind Franklin
|
36,555
|
1,305
|
B
|
High
|
22
|
CRISPR
|
35,195
|
1,256
|
B
|
High
|
23
|
Red hair
|
35,105
|
1,253
|
C
|
Mid
|
24
|
Meiosis
|
34,238
|
1,222
|
C
|
Top
|
25
|
DNA and RNA codon tables
|
33,751
|
1,205
|
FL
|
High
|
26
|
Pentasomy X
|
33,219
|
1,186
|
GA
|
Low
|
27
|
Epigenetics
|
32,212
|
1,150
|
B
|
Top
|
28
|
Adenosine triphosphate
|
31,252
|
1,116
|
C
|
High
|
29
|
Enzyme
|
30,322
|
1,082
|
FA
|
Top
|
30
|
Biodiversity
|
29,746
|
1,062
|
C
|
Mid
|
31
|
Blue Fugates
|
29,735
|
1,061
|
Start
|
Low
|
32
|
Jennifer Doudna
|
29,599
|
1,057
|
B
|
High
|
33
|
Last universal common ancestor
|
28,379
|
1,013
|
GA
|
Mid
|
34
|
Genetic engineering
|
28,274
|
1,009
|
GA
|
Top
|
35
|
Epicanthic fold
|
28,274
|
1,009
|
C
|
Low
|
36
|
XY sex-determination system
|
27,819
|
993
|
C
|
High
|
37
|
Cousin
|
27,580
|
985
|
Start
|
Low
|
38
|
Total fertility rate
|
27,492
|
981
|
C
|
Low
|
39
|
Svalbard Global Seed Vault
|
27,389
|
978
|
B
|
Mid
|
40
|
Cleft lip and cleft palate
|
27,190
|
971
|
B
|
Low
|
41
|
Chimera (genetics)
|
27,161
|
970
|
B
|
Mid
|
42
|
Chromosome
|
27,091
|
967
|
B
|
Top
|
43
|
Consanguinity
|
26,608
|
950
|
C
|
Low
|
44
|
HeLa
|
26,131
|
933
|
C
|
Low
|
45
|
James Watson
|
25,644
|
915
|
B
|
High
|
46
|
Charcot–Marie–Tooth disease
|
25,545
|
912
|
C
|
Mid
|
47
|
Balaji Srinivasan
|
25,363
|
905
|
Start
|
Low
|
48
|
Inbreeding
|
25,253
|
901
|
C
|
Low
|
49
|
Polymerase chain reaction
|
25,159
|
898
|
B
|
High
|
50
|
DNA evidence in the O. J. Simpson murder case
|
25,151
|
898
|
B
|
Low
|
51
|
Gigantism
|
24,798
|
885
|
B
|
High
|
52
|
Wechsler Adult Intelligence Scale
|
24,566
|
877
|
C
|
Low
|
53
|
Twinless twin
|
24,424
|
872
|
Start
|
Low
|
54
|
Hybrid (biology)
|
24,226
|
865
|
GA
|
High
|
55
|
Birth defect
|
24,071
|
859
|
B
|
Mid
|
56
|
Albinism
|
23,647
|
844
|
C
|
Low
|
57
|
Endogamy
|
23,445
|
837
|
Start
|
Low
|
58
|
Animal husbandry
|
23,440
|
837
|
GA
|
Mid
|
59
|
RNA
|
23,396
|
835
|
GA
|
Top
|
60
|
Human skin color
|
23,121
|
825
|
B
|
Mid
|
61
|
Lactose intolerance
|
22,574
|
806
|
B
|
Low
|
62
|
Genetics
|
22,400
|
800
|
FA
|
Top
|
63
|
Blond
|
22,315
|
796
|
C
|
Low
|
64
|
XYY syndrome
|
21,189
|
756
|
B
|
Mid
|
65
|
Dominance (genetics)
|
21,150
|
755
|
C
|
Top
|
66
|
Estimates of historical world population
|
21,039
|
751
|
Start
|
Low
|
67
|
Japanese people
|
21,033
|
751
|
C
|
Low
|
68
|
XXXY syndrome
|
20,853
|
744
|
C
|
Low
|
69
|
XX male syndrome
|
20,464
|
730
|
C
|
Low
|
70
|
Sonic hedgehog protein
|
20,303
|
725
|
B
|
High
|
71
|
Mutation
|
20,159
|
719
|
B
|
Top
|
72
|
Early human migrations
|
19,817
|
707
|
B
|
Mid
|
73
|
Gene
|
19,723
|
704
|
GA
|
Top
|
74
|
Origin of SARS-CoV-2
|
18,628
|
665
|
C
|
Low
|
75
|
Genetic studies of Jews
|
18,349
|
655
|
B
|
Mid
|
76
|
Eugenics in the United States
|
18,336
|
654
|
Start
|
Low
|
77
|
Mitochondrial Eve
|
18,317
|
654
|
B
|
Mid
|
78
|
DNA replication
|
18,234
|
651
|
C
|
Unknown
|
79
|
Mendelian inheritance
|
18,021
|
643
|
C
|
High
|
80
|
Human Genome Project
|
17,967
|
641
|
B
|
Top
|
81
|
Ribosome
|
17,594
|
628
|
B
|
Top
|
82
|
Recent African origin of modern humans
|
17,537
|
626
|
C
|
Mid
|
83
|
De-extinction
|
17,512
|
625
|
C
|
Low
|
84
|
Human genome
|
17,433
|
622
|
C
|
High
|
85
|
Phenotype
|
17,271
|
616
|
C
|
Top
|
86
|
William Shockley
|
17,131
|
611
|
B
|
Low
|
87
|
Francis Crick
|
17,095
|
610
|
B
|
High
|
88
|
Nucleotide
|
17,005
|
607
|
C
|
Top
|
89
|
Humanzee
|
16,902
|
603
|
C
|
Mid
|
90
|
Cloning
|
16,862
|
602
|
B
|
Top
|
91
|
Nucleic acid
|
16,622
|
593
|
C
|
Mid
|
92
|
Genetic descent from Genghis Khan
|
16,512
|
589
|
C
|
Low
|
93
|
Human hair color
|
16,294
|
581
|
Start
|
Mid
|
94
|
Friedreich's ataxia
|
16,241
|
580
|
GA
|
Mid
|
95
|
Genetic disorder
|
16,206
|
578
|
B
|
Top
|
96
|
Haplogroup R1a
|
16,098
|
574
|
C
|
Low
|
97
|
Haplogroup R1b
|
16,090
|
574
|
C
|
Mid
|
98
|
Ventricular septal defect
|
15,820
|
565
|
C
|
Low
|
99
|
M. S. Swaminathan
|
15,538
|
554
|
B
|
Low
|
100
|
Trisomy 18
|
15,444
|
551
|
B
|
Low
|
101
|
Domesticated silver fox
|
15,386
|
549
|
C
|
Low
|
102
|
Gamete
|
15,198
|
542
|
Start
|
Mid
|
103
|
Punnett square
|
15,134
|
540
|
C
|
Top
|
104
|
Dravet syndrome
|
15,104
|
539
|
C
|
Low
|
105
|
Senescence
|
15,098
|
539
|
C
|
Low
|
106
|
23andMe
|
15,069
|
538
|
C
|
Mid
|
107
|
Nazi eugenics
|
15,049
|
537
|
C
|
Mid
|
108
|
CRISPR gene editing
|
14,895
|
531
|
B
|
Top
|
109
|
Drosophila melanogaster
|
14,805
|
528
|
B
|
Top
|
110
|
Population bottleneck
|
14,770
|
527
|
C
|
Mid
|
111
|
The Bell Curve
|
14,743
|
526
|
C
|
High
|
112
|
List of organisms by chromosome count
|
14,684
|
524
|
List
|
Low
|
113
|
Cultivar
|
14,533
|
519
|
GA
|
Mid
|
114
|
Leucism
|
14,443
|
515
|
Start
|
Low
|
115
|
Landrace
|
14,328
|
511
|
C
|
Low
|
116
|
Mitochondrial DNA
|
14,310
|
511
|
B
|
High
|
117
|
Tay–Sachs disease
|
14,273
|
509
|
B
|
High
|
118
|
Messenger RNA
|
13,966
|
498
|
C
|
High
|
119
|
Tetralogy of Fallot
|
13,954
|
498
|
C
|
Low
|
120
|
Y chromosome
|
13,864
|
495
|
B
|
High
|
121
|
Stephen Jay Gould
|
13,716
|
489
|
GA
|
Mid
|
122
|
Mirror life
|
13,672
|
488
|
Start
|
Low
|
123
|
Incest taboo
|
13,632
|
486
|
C
|
Mid
|
124
|
Genetically modified organism
|
13,548
|
483
|
GA
|
Top
|
125
|
G. H. Hardy
|
13,313
|
475
|
C
|
Mid
|
126
|
Human–animal hybrid
|
13,251
|
473
|
C
|
Low
|
127
|
Heredity
|
13,065
|
466
|
C
|
Top
|
128
|
Tetrasomy X
|
13,032
|
465
|
GA
|
Low
|
129
|
Cat coat genetics
|
12,969
|
463
|
C
|
Mid
|
130
|
Genetic code
|
12,810
|
457
|
GA
|
Top
|
131
|
Phenylketonuria
|
12,773
|
456
|
B
|
Mid
|
132
|
He Jiankui affair
|
12,737
|
454
|
C
|
Low
|
133
|
Ronald Fisher
|
12,711
|
453
|
B
|
High
|
134
|
Hardy–Weinberg principle
|
12,683
|
452
|
C
|
High
|
135
|
Illumina, Inc.
|
12,580
|
449
|
C
|
Low
|
136
|
Patau syndrome
|
12,476
|
445
|
C
|
Low
|
137
|
Early European Farmers
|
12,476
|
445
|
C
|
Mid
|
138
|
Karyotype
|
12,453
|
444
|
C
|
Mid
|
139
|
NUBPL
|
12,345
|
440
|
Start
|
Low
|
140
|
Francis Collins
|
12,285
|
438
|
B
|
Mid
|
141
|
DNA profiling
|
12,255
|
437
|
B
|
High
|
142
|
Homology (biology)
|
12,251
|
437
|
GA
|
High
|
143
|
Institutional racism
|
11,989
|
428
|
B
|
High
|
144
|
Incest pornography
|
11,938
|
426
|
Start
|
Mid
|
145
|
Selective breeding
|
11,894
|
424
|
C
|
Top
|
146
|
Haplogroup
|
11,889
|
424
|
C
|
Mid
|
147
|
Sex-determination system
|
11,642
|
415
|
C
|
Mid
|
148
|
Allele
|
11,629
|
415
|
B
|
Top
|
149
|
Telomere
|
11,599
|
414
|
C
|
Mid
|
150
|
Brown hair
|
11,406
|
407
|
C
|
Mid
|
151
|
Transcription (biology)
|
11,070
|
395
|
B
|
Top
|
152
|
Blue rose
|
11,062
|
395
|
Start
|
Low
|
153
|
He Jiankui
|
10,982
|
392
|
B
|
Low
|
154
|
Sexual selection
|
10,951
|
391
|
GA
|
Mid
|
155
|
Von Hippel–Lindau disease
|
10,918
|
389
|
C
|
Mid
|
156
|
Ancient North Eurasian
|
10,909
|
389
|
C
|
Mid
|
157
|
Atavism
|
10,843
|
387
|
C
|
Mid
|
158
|
Hereditary haemochromatosis
|
10,839
|
387
|
B
|
Mid
|
159
|
Ploidy
|
10,625
|
379
|
C
|
High
|
160
|
Congenital heart defect
|
10,601
|
378
|
C
|
Mid
|
161
|
Human Y-chromosome DNA haplogroup
|
10,529
|
376
|
C
|
Mid
|
162
|
Genetically modified food
|
10,495
|
374
|
B
|
High
|
163
|
DNA sequencing
|
10,442
|
372
|
C
|
Top
|
164
|
Tuberous sclerosis
|
10,376
|
370
|
C
|
Mid
|
165
|
Western Steppe Herders
|
10,371
|
370
|
C
|
Mid
|
166
|
Genome
|
10,369
|
370
|
C
|
High
|
167
|
Polyploidy
|
10,347
|
369
|
B
|
High
|
168
|
Plasmodium falciparum
|
10,224
|
365
|
B
|
Low
|
169
|
Plasmid
|
10,165
|
363
|
C
|
High
|
170
|
Domestic rabbit
|
10,142
|
362
|
GA
|
Low
|
171
|
Mosaic (genetics)
|
10,066
|
359
|
C
|
Mid
|
172
|
Panthera hybrid
|
9,954
|
355
|
C
|
Mid
|
173
|
Western hunter-gatherer
|
9,933
|
354
|
C
|
Mid
|
174
|
Heritability of IQ
|
9,876
|
352
|
C
|
Low
|
175
|
Ethnic groups of Japan
|
9,845
|
351
|
Start
|
Unknown
|
176
|
RNA world
|
9,810
|
350
|
C
|
Mid
|
177
|
Gene therapy
|
9,659
|
344
|
B
|
High
|
178
|
Genentech
|
9,525
|
340
|
Start
|
Mid
|
179
|
Central dogma of molecular biology
|
9,164
|
327
|
C
|
Top
|
180
|
Lectin
|
9,162
|
327
|
C
|
Mid
|
181
|
Major histocompatibility complex
|
9,131
|
326
|
B
|
Mid
|
182
|
Most recent common ancestor
|
9,018
|
322
|
B
|
Mid
|
183
|
Genetic testing
|
8,987
|
320
|
B
|
Top
|
184
|
Base pair
|
8,903
|
317
|
C
|
Top
|
185
|
Recombinant DNA
|
8,874
|
316
|
C
|
High
|
186
|
Transfer RNA
|
8,868
|
316
|
B
|
High
|
187
|
Chromosome abnormality
|
8,795
|
314
|
Start
|
High
|
188
|
Single-nucleotide polymorphism
|
8,758
|
312
|
C
|
High
|
189
|
Impulsivity
|
8,726
|
311
|
B
|
Mid
|
190
|
Mitochondrial disease
|
8,647
|
308
|
C
|
Mid
|
191
|
Auburn hair
|
8,601
|
307
|
Start
|
Low
|
192
|
P53
|
8,531
|
304
|
B
|
High
|
193
|
List of genetic disorders
|
8,509
|
303
|
List
|
High
|
194
|
Genetic drift
|
8,456
|
302
|
GA
|
High
|
195
|
Sanger sequencing
|
8,456
|
302
|
C
|
High
|
196
|
Freckle
|
8,339
|
297
|
Start
|
Low
|
197
|
DNA methylation
|
8,297
|
296
|
B
|
High
|
198
|
Protein biosynthesis
|
8,274
|
295
|
B
|
Mid
|
199
|
Founder effect
|
8,266
|
295
|
C
|
High
|
200
|
Gene expression
|
8,146
|
290
|
B
|
Top
|
201
|
Mebendazole
|
8,140
|
290
|
C
|
Mid
|
202
|
Genetic history of Europe
|
8,064
|
288
|
Start
|
Low
|
203
|
HLA-B27
|
8,048
|
287
|
C
|
Low
|
204
|
5α-Reductase 2 deficiency
|
8,043
|
287
|
B
|
Low
|
205
|
Uterus didelphys
|
8,034
|
286
|
Start
|
Low
|
206
|
X chromosome
|
8,015
|
286
|
B
|
Top
|
207
|
MicroRNA
|
7,989
|
285
|
B
|
Top
|
208
|
Sex chromosome
|
7,925
|
283
|
Start
|
High
|
209
|
Exogamy
|
7,915
|
282
|
Start
|
Low
|
210
|
Hayflick limit
|
7,818
|
279
|
Start
|
Low
|
211
|
Brooke Greenberg
|
7,718
|
275
|
Start
|
Mid
|
212
|
Reverse transcription polymerase chain reaction
|
7,691
|
274
|
Start
|
Mid
|
213
|
Dysgenics
|
7,678
|
274
|
Start
|
Low
|
214
|
Genetics and archaeogenetics of South Asia
|
7,665
|
273
|
Start
|
Mid
|
215
|
Black hair
|
7,621
|
272
|
Start
|
Mid
|
216
|
Synthetic biology
|
7,552
|
269
|
B
|
Mid
|
217
|
Genetic studies on Turkish people
|
7,551
|
269
|
Start
|
Low
|
218
|
Proteinogenic amino acid
|
7,522
|
268
|
C
|
High
|
219
|
Biological engineering
|
7,511
|
268
|
C
|
High
|
220
|
Translation (biology)
|
7,484
|
267
|
B
|
Top
|
221
|
Anthropometry
|
7,475
|
266
|
C
|
Low
|
222
|
Citicoline
|
7,468
|
266
|
B
|
Low
|
223
|
NF-κB
|
7,369
|
263
|
C
|
High
|
224
|
Fertility
|
7,362
|
262
|
C
|
Mid
|
225
|
Hispanos of New Mexico
|
7,320
|
261
|
Start
|
Low
|
226
|
Haplogroup H (mtDNA)
|
7,318
|
261
|
Start
|
Low
|
227
|
Horizontal gene transfer
|
7,225
|
258
|
C
|
High
|
228
|
Genotype
|
7,222
|
257
|
Start
|
Top
|
229
|
Polymorphism (biology)
|
7,199
|
257
|
B
|
Low
|
230
|
Atrial septal defect
|
7,197
|
257
|
B
|
Low
|
231
|
Data storage
|
7,177
|
256
|
Start
|
Low
|
232
|
Lactase
|
7,158
|
255
|
B
|
Mid
|
233
|
Barbara McClintock
|
7,153
|
255
|
FA
|
High
|
234
|
Nucleic acid double helix
|
7,112
|
254
|
C
|
Mid
|
235
|
Colour wheel theory of love
|
7,099
|
253
|
Stub
|
Low
|
236
|
Haplogroup J-M172
|
6,993
|
249
|
Start
|
Low
|
237
|
RNA splicing
|
6,974
|
249
|
C
|
Top
|
238
|
Photo 51
|
6,969
|
248
|
Start
|
Low
|
239
|
Pleiotropy
|
6,938
|
247
|
C
|
High
|
240
|
Zygosity
|
6,937
|
247
|
C
|
High
|
241
|
Zebrafish
|
6,936
|
247
|
B
|
Mid
|
242
|
Haplogroup J-M267
|
6,932
|
247
|
C
|
Low
|
243
|
Haplogroup E-M215
|
6,920
|
247
|
C
|
Low
|
244
|
Sex-determining region Y protein
|
6,834
|
244
|
C
|
Low
|
245
|
Nucleolus
|
6,830
|
243
|
Start
|
Mid
|
246
|
Single parent
|
6,830
|
243
|
B
|
Mid
|
247
|
XXYY syndrome
|
6,816
|
243
|
Start
|
Low
|
248
|
J. B. S. Haldane
|
6,786
|
242
|
C
|
Low
|
249
|
Aneuploidy
|
6,764
|
241
|
B
|
High
|
250
|
Lac operon
|
6,737
|
240
|
C
|
Mid
|
251
|
Chin
|
6,735
|
240
|
C
|
Low
|
252
|
Designer baby
|
6,734
|
240
|
B
|
High
|
253
|
Genetic history of Egypt
|
6,729
|
240
|
C
|
Low
|
254
|
Transcription factor
|
6,696
|
239
|
B
|
High
|
255
|
Variants of SARS-CoV-2
|
6,678
|
238
|
C
|
Low
|
256
|
Wnt signaling pathway
|
6,656
|
237
|
C
|
Mid
|
257
|
Ectrodactyly
|
6,603
|
235
|
B
|
Mid
|
258
|
Laboratory rat
|
6,565
|
234
|
C
|
Mid
|
259
|
Cyclic adenosine monophosphate
|
6,554
|
234
|
C
|
Mid
|
260
|
Haplogroup G-M201
|
6,404
|
228
|
Start
|
Low
|
261
|
Heterosis
|
6,388
|
228
|
C
|
High
|
262
|
Constriction ring syndrome
|
6,386
|
228
|
C
|
Low
|
263
|
Chromosomal crossover
|
6,372
|
227
|
C
|
High
|
264
|
Nicotinamide adenine dinucleotide phosphate
|
6,339
|
226
|
Start
|
Mid
|
265
|
Chromatin
|
6,300
|
225
|
B
|
Mid
|
266
|
Y-chromosomal Adam
|
6,248
|
223
|
C
|
High
|
267
|
Chargaff's rules
|
6,247
|
223
|
Start
|
Low
|
268
|
Transposable element
|
6,186
|
220
|
C
|
High
|
269
|
DNA repair
|
6,179
|
220
|
C
|
High
|
270
|
Haplogroup J (Y-DNA)
|
6,150
|
219
|
Start
|
Low
|
271
|
Methylation
|
6,115
|
218
|
C
|
Mid
|
272
|
Uracil
|
6,114
|
218
|
B
|
Mid
|
273
|
BRCA1
|
6,092
|
217
|
C
|
High
|
274
|
Pedigree collapse
|
6,084
|
217
|
Start
|
Low
|
275
|
Eastern hunter-gatherer
|
6,084
|
217
|
C
|
Mid
|
276
|
Twin study
|
6,058
|
216
|
B
|
High
|
277
|
Real-time polymerase chain reaction
|
6,053
|
216
|
C
|
Mid
|
278
|
Heritability of autism
|
6,042
|
215
|
C
|
Mid
|
279
|
Coefficient of inbreeding
|
6,022
|
215
|
Start
|
Low
|
280
|
Webbed toes
|
5,933
|
211
|
Start
|
Low
|
281
|
Coefficient of relationship
|
5,929
|
211
|
C
|
Low
|
282
|
Genetically modified crops
|
5,929
|
211
|
B
|
High
|
283
|
Histone
|
5,881
|
210
|
C
|
Mid
|
284
|
Haplogroup U
|
5,879
|
209
|
Start
|
Mid
|
285
|
Haplogroup I-M253
|
5,871
|
209
|
B
|
Low
|
286
|
Mathematical and theoretical biology
|
5,784
|
206
|
C
|
Low
|
287
|
Racial hygiene
|
5,768
|
206
|
C
|
Low
|
288
|
Genetic history of the British Isles
|
5,765
|
205
|
C
|
Low
|
289
|
Human mitochondrial DNA haplogroup
|
5,763
|
205
|
Start
|
Low
|
290
|
Error
|
5,739
|
204
|
Start
|
Mid
|
291
|
Chromosome 8
|
5,739
|
204
|
Start
|
Mid
|
292
|
Patent ductus arteriosus
|
5,701
|
203
|
C
|
Mid
|
293
|
VACTERL association
|
5,698
|
203
|
Start
|
Mid
|
294
|
DNA polymerase
|
5,691
|
203
|
C
|
Top
|
295
|
Gene delivery
|
5,660
|
202
|
B
|
High
|
296
|
Monoamine oxidase A
|
5,654
|
201
|
C
|
Mid
|
297
|
Hox gene
|
5,639
|
201
|
C
|
High
|
298
|
Promoter (genetics)
|
5,631
|
201
|
Start
|
Mid
|
299
|
Genomics
|
5,612
|
200
|
B
|
Top
|
300
|
Laboratory mouse
|
5,606
|
200
|
B
|
Low
|
301
|
Lydia Fairchild
|
5,603
|
200
|
Stub
|
Unknown
|
302
|
Polar body biopsy
|
5,599
|
199
|
Start
|
Low
|
303
|
Haplogroup N-M231
|
5,597
|
199
|
Start
|
Low
|
304
|
HER2
|
5,595
|
199
|
C
|
Mid
|
305
|
Oogenesis
|
5,592
|
199
|
C
|
High
|
306
|
Leigh syndrome
|
5,588
|
199
|
C
|
Low
|
307
|
Modern synthesis (20th century)
|
5,580
|
199
|
GA
|
High
|
308
|
Homologous chromosome
|
5,523
|
197
|
Start
|
High
|
309
|
RNA interference
|
5,517
|
197
|
FA
|
Top
|
310
|
Parent
|
5,386
|
192
|
C
|
High
|
311
|
Autosome
|
5,349
|
191
|
Start
|
Top
|
312
|
Personalized medicine
|
5,334
|
190
|
B
|
Mid
|
313
|
Whole genome sequencing
|
5,333
|
190
|
B
|
Top
|
314
|
GloFish
|
5,327
|
190
|
C
|
Mid
|
315
|
Janaki Ammal
|
5,314
|
189
|
B
|
Low
|
316
|
Shyness
|
5,281
|
188
|
B
|
Low
|
317
|
Hershey–Chase experiment
|
5,236
|
187
|
C
|
High
|
318
|
Haplogroup I-M438
|
5,219
|
186
|
Start
|
Low
|
319
|
Genetic recombination
|
5,181
|
185
|
C
|
High
|
320
|
New eugenics
|
5,180
|
185
|
Start
|
Mid
|
321
|
Fitness (biology)
|
5,177
|
184
|
C
|
Mid
|
322
|
Okazaki fragments
|
5,169
|
184
|
B
|
High
|
323
|
The Population Bomb
|
5,153
|
184
|
B
|
Low
|
324
|
Transgene
|
5,141
|
183
|
B
|
Mid
|
325
|
Neanderthal genetics
|
5,134
|
183
|
C
|
High
|
326
|
Open reading frame
|
5,123
|
182
|
Start
|
Mid
|
327
|
Haplogroup I-M170
|
5,086
|
181
|
B
|
Low
|
328
|
Sexual differentiation in humans
|
5,074
|
181
|
C
|
Mid
|
329
|
Locus (genetics)
|
5,069
|
181
|
Start
|
Mid
|
330
|
George Church (geneticist)
|
5,067
|
180
|
C
|
Low
|
331
|
Cold Spring Harbor Laboratory
|
5,051
|
180
|
Start
|
Mid
|
332
|
16S ribosomal RNA
|
5,035
|
179
|
C
|
High
|
333
|
Chromosome 21
|
5,031
|
179
|
C
|
Mid
|
334
|
Dwarf cat
|
5,006
|
178
|
Start
|
Low
|
335
|
Genealogical DNA test
|
4,964
|
177
|
C
|
Mid
|
336
|
CpG site
|
4,962
|
177
|
C
|
Mid
|
337
|
List of people with red hair
|
4,954
|
176
|
List
|
Low
|
338
|
Telomerase
|
4,946
|
176
|
B
|
High
|
339
|
Phenotypic trait
|
4,928
|
176
|
Start
|
Mid
|
340
|
Inbreeding depression
|
4,910
|
175
|
C
|
Low
|
341
|
Griffith's experiment
|
4,906
|
175
|
Start
|
Mid
|
342
|
History of eugenics
|
4,904
|
175
|
B
|
Low
|
343
|
Trisomy
|
4,899
|
174
|
Start
|
High
|
344
|
Transgenesis
|
4,887
|
174
|
Redirect
|
Top
|
345
|
Reverse transcriptase
|
4,873
|
174
|
B
|
High
|
346
|
MHC class I
|
4,854
|
173
|
C
|
Mid
|
347
|
X-linked recessive inheritance
|
4,833
|
172
|
Start
|
Mid
|
348
|
Fluorescence in situ hybridization
|
4,799
|
171
|
B
|
Mid
|
349
|
Cas9
|
4,789
|
171
|
C
|
Mid
|
350
|
MHC class II
|
4,784
|
170
|
C
|
Mid
|
351
|
Allopatric speciation
|
4,762
|
170
|
B
|
Low
|
352
|
Causes of cancer
|
4,761
|
170
|
B
|
Mid
|
353
|
Post-translational modification
|
4,754
|
169
|
Start
|
High
|
354
|
Flavin adenine dinucleotide
|
4,748
|
169
|
B
|
Low
|
355
|
ZW sex-determination system
|
4,698
|
167
|
C
|
Mid
|
356
|
Stop codon
|
4,692
|
167
|
Start
|
High
|
357
|
List of haplogroups of historic people
|
4,660
|
166
|
List
|
Low
|
358
|
Genetic diversity
|
4,632
|
165
|
C
|
Mid
|
359
|
Model organism
|
4,631
|
165
|
B
|
Mid
|
360
|
Phosphorylation
|
4,630
|
165
|
C
|
High
|
361
|
Oncogene
|
4,624
|
165
|
C
|
High
|
362
|
Cre-Lox recombination
|
4,578
|
163
|
C
|
Mid
|
363
|
Sampling bias
|
4,519
|
161
|
C
|
Low
|
364
|
Nucleic acid sequence
|
4,484
|
160
|
C
|
High
|
365
|
Purebred
|
4,476
|
159
|
C
|
Low
|
366
|
Heritability
|
4,474
|
159
|
C
|
High
|
367
|
Epistasis
|
4,457
|
159
|
B
|
High
|
368
|
Adeno-associated virus
|
4,452
|
159
|
B
|
Low
|
369
|
MELAS syndrome
|
4,443
|
158
|
C
|
Low
|
370
|
Genomic imprinting
|
4,439
|
158
|
C
|
High
|
371
|
Sexual selection in humans
|
4,421
|
157
|
C
|
Low
|
372
|
Eric Lander
|
4,405
|
157
|
C
|
Low
|
373
|
Humanized mouse
|
4,398
|
157
|
Start
|
Low
|
374
|
Epidermal growth factor receptor
|
4,377
|
156
|
C
|
Mid
|
375
|
RNA polymerase
|
4,372
|
156
|
C
|
Top
|
376
|
List of unusual biological names
|
4,332
|
154
|
List
|
Low
|
377
|
Boar–pig hybrid
|
4,298
|
153
|
Stub
|
Low
|
378
|
Advanced maternal age
|
4,271
|
152
|
C
|
Mid
|
379
|
46,XX/46,XY
|
4,270
|
152
|
C
|
Low
|
380
|
F1 hybrid
|
4,265
|
152
|
Start
|
High
|
381
|
Hi-C (genomic analysis technique)
|
4,255
|
151
|
C
|
Low
|
382
|
Genetic memory (psychology)
|
4,242
|
151
|
Start
|
Low
|
383
|
Fibular hemimelia
|
4,224
|
150
|
Start
|
Low
|
384
|
Bacterial conjugation
|
4,185
|
149
|
C
|
High
|
385
|
The Mismeasure of Man
|
4,185
|
149
|
B
|
Mid
|
386
|
Population genetics
|
4,182
|
149
|
C
|
Top
|
387
|
Sex linkage
|
4,167
|
148
|
Start
|
High
|
388
|
Genome-wide association study
|
4,165
|
148
|
GA
|
Top
|
389
|
Weaver syndrome
|
4,162
|
148
|
Start
|
Low
|
390
|
Ribozyme
|
4,161
|
148
|
Start
|
High
|
391
|
Apomorphy and synapomorphy
|
4,160
|
148
|
C
|
Low
|
392
|
Genome editing
|
4,143
|
147
|
C
|
High
|
393
|
Haplogroup A (Y-DNA)
|
4,126
|
147
|
C
|
Low
|
394
|
Regulation of gene expression
|
4,114
|
146
|
C
|
High
|
395
|
Aniridia
|
4,110
|
146
|
C
|
Low
|
396
|
Zellweger syndrome
|
4,093
|
146
|
Start
|
Low
|
397
|
Phred quality score
|
4,093
|
146
|
Start
|
Low
|
398
|
Ancient DNA
|
4,089
|
146
|
C
|
Mid
|
399
|
Plant breeding
|
4,083
|
145
|
C
|
High
|
400
|
Maurice Wilkins
|
4,078
|
145
|
B
|
High
|
401
|
Victor Ambros
|
4,062
|
145
|
B
|
Low
|
402
|
Genetic history of the Iberian Peninsula
|
4,060
|
145
|
Start
|
Low
|
403
|
Factor VIII
|
4,058
|
144
|
Start
|
Low
|
404
|
Taq polymerase
|
4,058
|
144
|
C
|
Mid
|
405
|
Biological determinism
|
4,045
|
144
|
GA
|
Mid
|
406
|
Myc
|
4,031
|
143
|
C
|
High
|
407
|
Haplogroup R (Y-DNA)
|
4,015
|
143
|
Start
|
Low
|
408
|
Haplogroup Q-M242
|
4,011
|
143
|
C
|
Low
|
409
|
Maladaptation
|
3,988
|
142
|
Start
|
Low
|
410
|
Somatic cell
|
3,966
|
141
|
Start
|
Mid
|
411
|
45,X/46,XY mosaicism
|
3,951
|
141
|
C
|
Low
|
412
|
Paternal age effect
|
3,950
|
141
|
C
|
Mid
|
413
|
JAK-STAT signaling pathway
|
3,947
|
140
|
B
|
Mid
|
414
|
Isoelectric point
|
3,934
|
140
|
C
|
Mid
|
415
|
Disodium inosinate
|
3,932
|
140
|
Start
|
Low
|
416
|
Sense (molecular biology)
|
3,929
|
140
|
C
|
High
|
417
|
Human genetic variation
|
3,899
|
139
|
C
|
High
|
418
|
Medical genetics of Jews
|
3,899
|
139
|
Start
|
Low
|
419
|
Haplogroup R1
|
3,886
|
138
|
C
|
Low
|
420
|
Kin selection
|
3,881
|
138
|
GA
|
Mid
|
421
|
X-inactivation
|
3,875
|
138
|
B
|
High
|
422
|
Barr body
|
3,870
|
138
|
Start
|
High
|
423
|
Haplotype
|
3,865
|
138
|
Start
|
High
|
424
|
Introgression
|
3,864
|
138
|
Start
|
High
|
425
|
Hepatitis D
|
3,860
|
137
|
C
|
Low
|
426
|
Directionality (molecular biology)
|
3,853
|
137
|
Start
|
High
|
427
|
Chromosomal translocation
|
3,839
|
137
|
Start
|
High
|
428
|
Crossbreed
|
3,839
|
137
|
Start
|
Low
|
429
|
KRAS
|
3,831
|
136
|
C
|
Mid
|
430
|
David Reich (geneticist)
|
3,793
|
135
|
C
|
Mid
|
431
|
Ruth Benedict
|
3,792
|
135
|
C
|
Low
|
432
|
GEDmatch
|
3,778
|
134
|
Start
|
Mid
|
433
|
Systems biology
|
3,730
|
133
|
C
|
High
|
434
|
Chromosome 2
|
3,722
|
132
|
C
|
Mid
|
435
|
Operon
|
3,711
|
132
|
B
|
Mid
|
436
|
Medical genetics
|
3,709
|
132
|
B
|
Mid
|
437
|
Gary Ruvkun
|
3,700
|
132
|
B
|
Low
|
438
|
Adenosine diphosphate
|
3,681
|
131
|
C
|
Mid
|
439
|
Homologous recombination
|
3,668
|
131
|
GA
|
High
|
440
|
Dun gene
|
3,660
|
130
|
C
|
Low
|
441
|
Haplogroup E-M96
|
3,632
|
129
|
Start
|
Low
|
442
|
Kozak consensus sequence
|
3,631
|
129
|
Start
|
Mid
|
443
|
Svante Pääbo
|
3,621
|
129
|
C
|
Low
|
444
|
Pioneer Fund
|
3,614
|
129
|
B
|
Low
|
445
|
SARS-CoV-2 Delta variant
|
3,605
|
128
|
C
|
Low
|
446
|
Intron
|
3,604
|
128
|
C
|
High
|
447
|
Endogeny (biology)
|
3,585
|
128
|
Stub
|
Low
|
448
|
Centromere
|
3,583
|
127
|
C
|
Mid
|
449
|
Flavivirus
|
3,582
|
127
|
B
|
Mid
|
450
|
Breed
|
3,572
|
127
|
Start
|
Low
|
451
|
Guanosine triphosphate
|
3,564
|
127
|
Start
|
Mid
|
452
|
Tongue rolling
|
3,557
|
127
|
Stub
|
Low
|
453
|
Gene nomenclature
|
3,553
|
126
|
Start
|
Mid
|
454
|
Gene flow
|
3,538
|
126
|
Start
|
High
|
455
|
Alternative splicing
|
3,521
|
125
|
B
|
High
|
456
|
Y-DNA haplogroups in populations of Europe
|
3,508
|
125
|
List
|
Mid
|
457
|
Genetic history of the Middle East
|
3,506
|
125
|
C
|
Mid
|
458
|
Genetically modified food controversies
|
3,478
|
124
|
C
|
Mid
|
459
|
Elizabeth Blackburn
|
3,470
|
123
|
C
|
Low
|
460
|
Haplogroup L-M20
|
3,468
|
123
|
Start
|
Low
|
461
|
C57BL/6
|
3,465
|
123
|
Start
|
Low
|
462
|
Telegony (inheritance)
|
3,423
|
122
|
C
|
Low
|
463
|
Pedigree chart
|
3,415
|
121
|
Start
|
Mid
|
464
|
Peppered moth evolution
|
3,408
|
121
|
GA
|
Mid
|
465
|
Haplogroup O-M175
|
3,397
|
121
|
Start
|
Low
|
466
|
Haplogroup T-M184
|
3,361
|
120
|
B
|
Low
|
467
|
Cystic fibrosis transmembrane conductance regulator
|
3,358
|
119
|
C
|
Mid
|
468
|
Infantile epileptic spasms syndrome
|
3,351
|
119
|
C
|
Low
|
469
|
Introduction to evolution
|
3,349
|
119
|
B
|
High
|
470
|
Fisherian runaway
|
3,345
|
119
|
Start
|
Mid
|
471
|
Single-cell sequencing
|
3,345
|
119
|
C
|
High
|
472
|
Neo-Darwinism
|
3,344
|
119
|
Start
|
High
|
473
|
Oligomer
|
3,344
|
119
|
Start
|
Low
|
474
|
Molecular cloning
|
3,342
|
119
|
C
|
High
|
475
|
Biopolymer
|
3,322
|
118
|
C
|
Mid
|
476
|
MERRF syndrome
|
3,318
|
118
|
C
|
Low
|
477
|
Sheep farming
|
3,312
|
118
|
C
|
Low
|
478
|
Geneticist
|
3,304
|
118
|
Start
|
High
|
479
|
Ras GTPase
|
3,297
|
117
|
B
|
High
|
480
|
Nondisjunction
|
3,267
|
116
|
B
|
High
|
481
|
Adenosine monophosphate
|
3,263
|
116
|
Start
|
Low
|
482
|
Genetic variation
|
3,259
|
116
|
Start
|
High
|
483
|
Somatic cell nuclear transfer
|
3,258
|
116
|
C
|
Mid
|
484
|
TATA box
|
3,251
|
116
|
B
|
High
|
485
|
Nucleoside triphosphate
|
3,247
|
115
|
Start
|
High
|
486
|
FOXP2
|
3,242
|
115
|
B
|
Mid
|
487
|
XXXYY syndrome
|
3,238
|
115
|
GA
|
Low
|
488
|
DNA extraction
|
3,237
|
115
|
Start
|
Mid
|
489
|
Junk DNA
|
3,227
|
115
|
B
|
Mid
|
490
|
Tumor suppressor gene
|
3,221
|
115
|
Start
|
High
|
491
|
Behavioural genetics
|
3,214
|
114
|
GA
|
High
|
492
|
Microsatellite
|
3,209
|
114
|
C
|
Mid
|
493
|
Genetic studies on Arabs
|
3,206
|
114
|
C
|
Low
|
494
|
Leber's hereditary optic neuropathy
|
3,203
|
114
|
C
|
Mid
|
495
|
Genetic transformation
|
3,197
|
114
|
B
|
Top
|
496
|
Chédiak–Higashi syndrome
|
3,182
|
113
|
Start
|
Low
|
497
|
Nanopore sequencing
|
3,174
|
113
|
C
|
Low
|
498
|
Linkage disequilibrium
|
3,173
|
113
|
C
|
High
|
499
|
Haplogroup K (mtDNA)
|
3,124
|
111
|
Start
|
Low
|
500
|
Haplogroup E-V68
|
3,119
|
111
|
C
|
Low
|
|
Full category list
Categories within WP:GEN
|
Category WikiProject Genetics not found
|
Categories within Genetics
|
|
|