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: 2024-10-01 to 2024-10-31
Total views: 9,317,149
Updated: 10:00, 8 November 2024 (UTC)
Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Axolotl
|
191,043
|
6,162
|
C
|
High
|
2
|
Victor Ambros
|
183,526
|
5,920
|
C
|
Low
|
3
|
Gary Ruvkun
|
181,353
|
5,850
|
C
|
Low
|
4
|
Eugenics
|
101,460
|
3,272
|
B
|
High
|
5
|
DNA
|
96,889
|
3,125
|
FA
|
Top
|
6
|
Incest
|
95,109
|
3,068
|
C
|
Low
|
7
|
MicroRNA
|
86,620
|
2,794
|
B
|
Top
|
8
|
Cancer
|
73,003
|
2,354
|
B
|
Top
|
9
|
Prion
|
69,829
|
2,252
|
GA
|
Mid
|
10
|
Protein
|
68,097
|
2,196
|
GA
|
Top
|
11
|
Amino acid
|
66,969
|
2,160
|
GA
|
Top
|
12
|
Guinea pig
|
60,769
|
1,960
|
B
|
Low
|
13
|
Cystic fibrosis
|
58,627
|
1,891
|
B
|
High
|
14
|
Enzyme
|
51,853
|
1,672
|
FA
|
Top
|
15
|
Nicotinamide adenine dinucleotide
|
49,747
|
1,604
|
FA
|
Mid
|
16
|
Attachment theory
|
49,429
|
1,594
|
B
|
Mid
|
17
|
Biodiversity
|
49,112
|
1,584
|
C
|
Mid
|
18
|
Evolution
|
49,049
|
1,582
|
FA
|
Top
|
19
|
Meiosis
|
48,860
|
1,576
|
C
|
Top
|
20
|
Color blindness
|
48,202
|
1,554
|
B
|
Mid
|
21
|
Blood type
|
47,609
|
1,535
|
B
|
High
|
22
|
Bayer
|
47,076
|
1,518
|
C
|
Low
|
23
|
Adenosine triphosphate
|
42,009
|
1,355
|
C
|
High
|
24
|
Epigenetics
|
41,676
|
1,344
|
B
|
Top
|
25
|
Rosalind Franklin
|
41,514
|
1,339
|
B
|
High
|
26
|
23andMe
|
41,260
|
1,330
|
C
|
Mid
|
27
|
Total fertility rate
|
40,027
|
1,291
|
C
|
Low
|
28
|
Chromosome
|
39,496
|
1,274
|
B
|
Top
|
29
|
Red hair
|
39,359
|
1,269
|
C
|
Mid
|
30
|
CRISPR
|
39,210
|
1,264
|
B
|
High
|
31
|
Cousin
|
39,072
|
1,260
|
Start
|
Low
|
32
|
Prader–Willi syndrome
|
39,020
|
1,258
|
B
|
Mid
|
33
|
Gregor Mendel
|
38,443
|
1,240
|
B
|
High
|
34
|
Scientific racism
|
37,129
|
1,197
|
C
|
Low
|
35
|
SARS-CoV-2
|
37,010
|
1,193
|
B
|
Top
|
36
|
Mitochondrial Eve
|
36,365
|
1,173
|
B
|
Mid
|
37
|
James Watson
|
35,562
|
1,147
|
B
|
High
|
38
|
XY sex-determination system
|
35,401
|
1,141
|
C
|
High
|
39
|
Endogamy
|
34,489
|
1,112
|
Start
|
Low
|
40
|
Ribosome
|
33,824
|
1,091
|
B
|
Top
|
41
|
Albinism
|
33,274
|
1,073
|
C
|
Low
|
42
|
Epicanthic fold
|
33,176
|
1,070
|
C
|
Low
|
43
|
RNA
|
33,164
|
1,069
|
GA
|
Top
|
44
|
Birth defect
|
32,078
|
1,034
|
B
|
Mid
|
45
|
Blue Fugates
|
32,002
|
1,032
|
Start
|
Low
|
46
|
Charcot–Marie–Tooth disease
|
30,636
|
988
|
C
|
Mid
|
47
|
Tay–Sachs disease
|
30,107
|
971
|
B
|
High
|
48
|
Last universal common ancestor
|
30,049
|
969
|
GA
|
Mid
|
49
|
Genetics
|
29,906
|
964
|
FA
|
Top
|
50
|
Polymerase chain reaction
|
29,286
|
944
|
B
|
High
|
51
|
Inbreeding
|
29,257
|
943
|
C
|
Low
|
52
|
Svalbard Global Seed Vault
|
28,819
|
929
|
B
|
Mid
|
53
|
Gigantism
|
28,742
|
927
|
B
|
High
|
54
|
Wechsler Adult Intelligence Scale
|
28,532
|
920
|
C
|
Low
|
55
|
Pentasomy X
|
28,519
|
919
|
GA
|
Low
|
56
|
Human skin color
|
28,486
|
918
|
B
|
Mid
|
57
|
Blond
|
28,306
|
913
|
C
|
Low
|
58
|
Gene
|
28,196
|
909
|
GA
|
Top
|
59
|
Animal husbandry
|
28,089
|
906
|
GA
|
Mid
|
60
|
Drosophila melanogaster
|
28,011
|
903
|
B
|
Top
|
61
|
Consanguinity
|
27,553
|
888
|
C
|
Low
|
62
|
Genetic engineering
|
27,458
|
885
|
GA
|
Top
|
63
|
Hybrid (biology)
|
27,424
|
884
|
GA
|
High
|
64
|
Chimera (genetics)
|
27,188
|
877
|
B
|
Mid
|
65
|
Nucleotide
|
27,146
|
875
|
C
|
Top
|
66
|
Cleft lip and cleft palate
|
27,136
|
875
|
B
|
Low
|
67
|
Lactose intolerance
|
27,117
|
874
|
B
|
Low
|
68
|
Human Genome Project
|
26,612
|
858
|
B
|
Top
|
69
|
Dominance (genetics)
|
26,003
|
838
|
C
|
Top
|
70
|
HeLa
|
25,959
|
837
|
C
|
Low
|
71
|
Genetic studies of Jews
|
25,415
|
819
|
B
|
Mid
|
72
|
Early human migrations
|
25,368
|
818
|
B
|
Mid
|
73
|
Nucleic acid
|
25,277
|
815
|
C
|
Mid
|
74
|
M. S. Swaminathan
|
25,213
|
813
|
B
|
Low
|
75
|
DNA replication
|
24,684
|
796
|
B
|
Unknown
|
76
|
Japanese people
|
24,567
|
792
|
C
|
Low
|
77
|
XYY syndrome
|
24,391
|
786
|
B
|
Mid
|
78
|
DNA and RNA codon tables
|
24,139
|
778
|
FL
|
High
|
79
|
Estimates of historical world population
|
23,291
|
751
|
Start
|
Low
|
80
|
Karyotype
|
22,966
|
740
|
C
|
Mid
|
81
|
Friedreich's ataxia
|
22,454
|
724
|
GA
|
Mid
|
82
|
Mutation
|
22,093
|
712
|
B
|
Top
|
83
|
Francis Crick
|
22,019
|
710
|
B
|
High
|
84
|
Cloning
|
21,905
|
706
|
B
|
Top
|
85
|
Messenger RNA
|
21,546
|
695
|
C
|
High
|
86
|
Recent African origin of modern humans
|
21,501
|
693
|
C
|
Mid
|
87
|
Mendelian inheritance
|
21,120
|
681
|
C
|
High
|
88
|
Human hair color
|
20,263
|
653
|
Start
|
Mid
|
89
|
Humanzee
|
20,067
|
647
|
C
|
Mid
|
90
|
XX male syndrome
|
19,625
|
633
|
C
|
Low
|
91
|
List of organisms by chromosome count
|
19,226
|
620
|
List
|
Low
|
92
|
Genetic code
|
18,994
|
612
|
GA
|
Top
|
93
|
Genetically modified organism
|
18,960
|
611
|
GA
|
Top
|
94
|
Genetic disorder
|
18,828
|
607
|
B
|
Top
|
95
|
Haplogroup R1b
|
18,753
|
604
|
C
|
Mid
|
96
|
Francis Collins
|
18,752
|
604
|
B
|
Mid
|
97
|
Cultivar
|
18,703
|
603
|
GA
|
Mid
|
98
|
Domesticated silver fox
|
18,639
|
601
|
C
|
Low
|
99
|
Phenotype
|
18,591
|
599
|
C
|
Top
|
100
|
Incest taboo
|
18,501
|
596
|
C
|
Mid
|
101
|
Genetically modified food
|
18,415
|
594
|
B
|
High
|
102
|
Descent from Genghis Khan
|
18,390
|
593
|
C
|
Low
|
103
|
Senescence
|
18,296
|
590
|
C
|
Low
|
104
|
Human genome
|
18,141
|
585
|
C
|
High
|
105
|
Trisomy 18
|
18,065
|
582
|
B
|
Low
|
106
|
Sonic hedgehog protein
|
17,987
|
580
|
B
|
High
|
107
|
Haplogroup R1a
|
17,934
|
578
|
C
|
Low
|
108
|
CRISPR gene editing
|
17,588
|
567
|
B
|
Top
|
109
|
Heredity
|
17,568
|
566
|
C
|
Top
|
110
|
Punnett square
|
17,517
|
565
|
C
|
Top
|
111
|
Tuberous sclerosis
|
17,368
|
560
|
B
|
Mid
|
112
|
Mitochondrial DNA
|
17,365
|
560
|
B
|
High
|
113
|
Cat coat genetics
|
17,152
|
553
|
C
|
Mid
|
114
|
The Bell Curve
|
16,999
|
548
|
C
|
High
|
115
|
Institutional racism
|
16,943
|
546
|
B
|
High
|
116
|
William Shockley
|
16,930
|
546
|
B
|
Low
|
117
|
Jennifer Doudna
|
16,832
|
542
|
B
|
High
|
118
|
De-extinction
|
16,691
|
538
|
C
|
Low
|
119
|
Plasmid
|
16,673
|
537
|
C
|
High
|
120
|
Gamete
|
16,615
|
535
|
Start
|
Mid
|
121
|
Tetralogy of Fallot
|
16,511
|
532
|
C
|
Low
|
122
|
Gene therapy
|
16,385
|
528
|
B
|
High
|
123
|
Transcription (biology)
|
16,332
|
526
|
B
|
Top
|
124
|
Leucism
|
16,255
|
524
|
Start
|
Low
|
125
|
G. H. Hardy
|
16,251
|
524
|
C
|
Mid
|
126
|
Phenylketonuria
|
16,195
|
522
|
B
|
Mid
|
127
|
Brown hair
|
16,014
|
516
|
C
|
Mid
|
128
|
Landrace
|
15,869
|
511
|
C
|
Low
|
129
|
XXXY syndrome
|
15,869
|
511
|
C
|
Low
|
130
|
Y chromosome
|
15,765
|
508
|
B
|
High
|
131
|
Allele
|
15,571
|
502
|
B
|
Top
|
132
|
DNA sequencing
|
15,015
|
484
|
C
|
Top
|
133
|
Plasmodium falciparum
|
14,826
|
478
|
B
|
Low
|
134
|
Haplogroup
|
14,720
|
474
|
C
|
Mid
|
135
|
Stephen Jay Gould
|
14,655
|
472
|
GA
|
Mid
|
136
|
Ronald Fisher
|
14,576
|
470
|
B
|
High
|
137
|
Patau syndrome
|
14,358
|
463
|
C
|
Low
|
138
|
Lectin
|
14,310
|
461
|
C
|
Mid
|
139
|
Von Hippel–Lindau disease
|
14,222
|
458
|
C
|
Mid
|
140
|
Atavism
|
14,061
|
453
|
C
|
Mid
|
141
|
Sex-determination system
|
13,850
|
446
|
C
|
Mid
|
142
|
Genome
|
13,793
|
444
|
C
|
High
|
143
|
Telomere
|
13,690
|
441
|
C
|
Mid
|
144
|
Ploidy
|
13,417
|
432
|
C
|
High
|
145
|
Homology (biology)
|
13,387
|
431
|
GA
|
High
|
146
|
Nucleolus
|
13,322
|
429
|
Start
|
Mid
|
147
|
DNA profiling
|
13,244
|
427
|
B
|
High
|
148
|
Population bottleneck
|
13,127
|
423
|
C
|
Mid
|
149
|
Selective breeding
|
12,897
|
416
|
C
|
Top
|
150
|
Early European Farmers
|
12,842
|
414
|
C
|
Mid
|
151
|
Tetrasomy X
|
12,725
|
410
|
GA
|
Low
|
152
|
Ventricular septal defect
|
12,346
|
398
|
C
|
Low
|
153
|
Lactase
|
12,324
|
397
|
B
|
Mid
|
154
|
Human–animal hybrid
|
12,261
|
395
|
C
|
Low
|
155
|
Ancient North Eurasian
|
12,242
|
394
|
C
|
Mid
|
156
|
Nazi eugenics
|
12,192
|
393
|
C
|
Mid
|
157
|
RNA world
|
12,169
|
392
|
C
|
Mid
|
158
|
Major histocompatibility complex
|
12,078
|
389
|
B
|
Mid
|
159
|
Congenital heart defect
|
12,014
|
387
|
C
|
Mid
|
160
|
Transfer RNA
|
12,003
|
387
|
B
|
High
|
161
|
Hardy–Weinberg principle
|
11,939
|
385
|
C
|
High
|
162
|
Exogamy
|
11,893
|
383
|
Start
|
Low
|
163
|
Polyploidy
|
11,866
|
382
|
B
|
High
|
164
|
He Jiankui affair
|
11,836
|
381
|
C
|
Low
|
165
|
Protein biosynthesis
|
11,720
|
378
|
B
|
Mid
|
166
|
Human Y-chromosome DNA haplogroup
|
11,695
|
377
|
C
|
Mid
|
167
|
Western Steppe Herders
|
11,637
|
375
|
C
|
Mid
|
168
|
Hereditary haemochromatosis
|
11,500
|
370
|
B
|
Mid
|
169
|
Single-nucleotide polymorphism
|
11,490
|
370
|
C
|
High
|
170
|
Freckle
|
11,479
|
370
|
Start
|
Low
|
171
|
Impulsivity
|
11,473
|
370
|
B
|
Mid
|
172
|
Anthropometry
|
11,466
|
369
|
C
|
Low
|
173
|
Recombinant DNA
|
11,280
|
363
|
C
|
High
|
174
|
Heritability of IQ
|
11,194
|
361
|
C
|
Low
|
175
|
Sexual selection
|
11,151
|
359
|
GA
|
Mid
|
176
|
DNA methylation
|
11,151
|
359
|
B
|
High
|
177
|
Sanger sequencing
|
11,082
|
357
|
C
|
High
|
178
|
Domestic rabbit
|
11,025
|
355
|
GA
|
Low
|
179
|
Citicoline
|
10,977
|
354
|
B
|
Low
|
180
|
Base pair
|
10,968
|
353
|
C
|
Top
|
181
|
Biological engineering
|
10,886
|
351
|
C
|
High
|
182
|
Genetic drift
|
10,856
|
350
|
GA
|
High
|
183
|
Genentech
|
10,847
|
349
|
Start
|
Mid
|
184
|
Mosaic (genetics)
|
10,834
|
349
|
C
|
Mid
|
185
|
Gene expression
|
10,820
|
349
|
B
|
Top
|
186
|
Western hunter-gatherer
|
10,790
|
348
|
C
|
Mid
|
187
|
Eugenics in the United States
|
10,752
|
346
|
Start
|
Low
|
188
|
Genotype
|
10,713
|
345
|
Start
|
Top
|
189
|
Origin of SARS-CoV-2
|
10,702
|
345
|
C
|
Low
|
190
|
P53
|
10,697
|
345
|
B
|
High
|
191
|
Hayflick limit
|
10,552
|
340
|
Start
|
Low
|
192
|
Central dogma of molecular biology
|
10,487
|
338
|
C
|
Top
|
193
|
Mebendazole
|
10,421
|
336
|
C
|
Mid
|
194
|
Dravet syndrome
|
10,327
|
333
|
C
|
Low
|
195
|
Nucleic acid double helix
|
10,219
|
329
|
C
|
Mid
|
196
|
David Reich (geneticist)
|
10,053
|
324
|
C
|
Mid
|
197
|
Lac operon
|
9,978
|
321
|
C
|
Mid
|
198
|
Aneuploidy
|
9,969
|
321
|
B
|
High
|
199
|
HLA-B27
|
9,944
|
320
|
C
|
Low
|
200
|
Chromosome abnormality
|
9,889
|
319
|
Start
|
High
|
201
|
Panthera hybrid
|
9,884
|
318
|
C
|
Mid
|
202
|
Translation (biology)
|
9,858
|
318
|
B
|
Top
|
203
|
Horizontal gene transfer
|
9,804
|
316
|
C
|
High
|
204
|
Reverse transcription polymerase chain reaction
|
9,773
|
315
|
Start
|
Mid
|
205
|
RNA interference
|
9,711
|
313
|
FA
|
Top
|
206
|
Balaji Srinivasan
|
9,669
|
311
|
Start
|
Low
|
207
|
Genetic history of Europe
|
9,651
|
311
|
Start
|
Low
|
208
|
Genetics and archaeogenetics of South Asia
|
9,648
|
311
|
Start
|
Mid
|
209
|
Genetic testing
|
9,619
|
310
|
B
|
Top
|
210
|
Black hair
|
9,521
|
307
|
Start
|
Mid
|
211
|
RNA splicing
|
9,507
|
306
|
C
|
Top
|
212
|
Single parent
|
9,478
|
305
|
B
|
Mid
|
213
|
Nicotinamide adenine dinucleotide phosphate
|
9,398
|
303
|
Start
|
Mid
|
214
|
Proteinogenic amino acid
|
9,379
|
302
|
C
|
High
|
215
|
Auburn hair
|
9,377
|
302
|
Start
|
Low
|
216
|
NF-κB
|
9,330
|
300
|
C
|
High
|
217
|
Chédiak–Higashi syndrome
|
9,327
|
300
|
Start
|
Low
|
218
|
Homologous chromosome
|
9,292
|
299
|
Start
|
High
|
219
|
He Jiankui
|
9,261
|
298
|
B
|
Low
|
220
|
Transcription factor
|
9,202
|
296
|
B
|
High
|
221
|
Ethnic groups of Japan
|
9,164
|
295
|
Start
|
Unknown
|
222
|
Chromatin
|
9,026
|
291
|
B
|
Mid
|
223
|
X chromosome
|
8,978
|
289
|
B
|
Top
|
224
|
Founder effect
|
8,888
|
286
|
C
|
High
|
225
|
Cyclic adenosine monophosphate
|
8,872
|
286
|
C
|
Mid
|
226
|
Sex chromosome
|
8,806
|
284
|
Start
|
High
|
227
|
Synthetic biology
|
8,805
|
284
|
B
|
Mid
|
228
|
Most recent common ancestor
|
8,774
|
283
|
B
|
Mid
|
229
|
Baldwin effect
|
8,694
|
280
|
GA
|
Low
|
230
|
Variants of SARS-CoV-2
|
8,643
|
278
|
C
|
Low
|
231
|
RCCX
|
8,607
|
277
|
B
|
Mid
|
232
|
Zygosity
|
8,589
|
277
|
C
|
High
|
233
|
Transposable element
|
8,588
|
277
|
C
|
High
|
234
|
Mitochondrial disease
|
8,487
|
273
|
C
|
Mid
|
235
|
Fertility
|
8,482
|
273
|
C
|
Mid
|
236
|
Wnt signaling pathway
|
8,454
|
272
|
C
|
Mid
|
237
|
Data storage
|
8,428
|
271
|
Start
|
Low
|
238
|
Haplogroup H (mtDNA)
|
8,368
|
269
|
Start
|
Low
|
239
|
Atrial septal defect
|
8,337
|
268
|
B
|
Low
|
240
|
Autosome
|
8,328
|
268
|
Start
|
Top
|
241
|
Chin
|
8,284
|
267
|
C
|
Low
|
242
|
Ectrodactyly
|
8,271
|
266
|
B
|
Mid
|
243
|
Svante Pääbo
|
8,261
|
266
|
C
|
Low
|
244
|
Polymorphism (biology)
|
8,159
|
263
|
B
|
Low
|
245
|
Chromosomal crossover
|
8,089
|
260
|
C
|
High
|
246
|
Histone
|
8,028
|
258
|
C
|
Mid
|
247
|
Barbara McClintock
|
8,025
|
258
|
FA
|
High
|
248
|
Hypoplastic left heart syndrome
|
8,022
|
258
|
C
|
Low
|
249
|
Haplogroup J-M172
|
8,016
|
258
|
Start
|
Low
|
250
|
Real-time polymerase chain reaction
|
7,966
|
256
|
C
|
Mid
|
251
|
Heterosis
|
7,781
|
251
|
C
|
High
|
252
|
Hispanos of New Mexico
|
7,770
|
250
|
Start
|
Low
|
253
|
DNA repair
|
7,742
|
249
|
C
|
High
|
254
|
DNA polymerase
|
7,731
|
249
|
C
|
Top
|
255
|
Genetic studies on Turkish people
|
7,698
|
248
|
Start
|
Low
|
256
|
Photo 51
|
7,650
|
246
|
Start
|
Low
|
257
|
J. B. S. Haldane
|
7,646
|
246
|
C
|
Low
|
258
|
Laboratory rat
|
7,639
|
246
|
C
|
Mid
|
259
|
DNA evidence in the O. J. Simpson murder case
|
7,619
|
245
|
B
|
Low
|
260
|
Error
|
7,616
|
245
|
Start
|
Mid
|
261
|
Whole genome sequencing
|
7,549
|
243
|
B
|
Top
|
262
|
Regulation of gene expression
|
7,544
|
243
|
C
|
High
|
263
|
Leigh syndrome
|
7,539
|
243
|
C
|
Low
|
264
|
Phosphorylation
|
7,496
|
241
|
C
|
High
|
265
|
Promoter (genetics)
|
7,487
|
241
|
Start
|
Mid
|
266
|
Methylation
|
7,467
|
240
|
C
|
Mid
|
267
|
The Population Bomb
|
7,466
|
240
|
B
|
Low
|
268
|
List of genetic disorders
|
7,392
|
238
|
List
|
High
|
269
|
Open reading frame
|
7,361
|
237
|
Start
|
Mid
|
270
|
RNA polymerase
|
7,354
|
237
|
C
|
Top
|
271
|
Monoamine oxidase A
|
7,345
|
236
|
C
|
Mid
|
272
|
Boar–pig hybrid
|
7,266
|
234
|
Stub
|
Low
|
273
|
Haplogroup J (Y-DNA)
|
7,261
|
234
|
Start
|
Low
|
274
|
BRCA1
|
7,197
|
232
|
C
|
High
|
275
|
Genomics
|
7,172
|
231
|
B
|
Top
|
276
|
Y-chromosomal Adam
|
7,171
|
231
|
C
|
High
|
277
|
Uterus didelphys
|
7,160
|
230
|
Start
|
Low
|
278
|
Designer baby
|
7,135
|
230
|
B
|
High
|
279
|
Dysgenics
|
7,135
|
230
|
Start
|
Low
|
280
|
Haplogroup J-M267
|
7,134
|
230
|
C
|
Low
|
281
|
Genetically modified crops
|
7,076
|
228
|
B
|
High
|
282
|
HER2
|
7,071
|
228
|
C
|
Mid
|
283
|
VACTERL association
|
7,060
|
227
|
Start
|
Mid
|
284
|
Genetic recombination
|
7,058
|
227
|
C
|
High
|
285
|
Blue rose
|
7,050
|
227
|
Start
|
Low
|
286
|
Haplogroup G-M201
|
7,038
|
227
|
Start
|
Low
|
287
|
Haplogroup E-M215
|
7,034
|
226
|
C
|
Low
|
288
|
CpG site
|
6,975
|
225
|
C
|
Mid
|
289
|
Chargaff's rules
|
6,971
|
224
|
Start
|
Low
|
290
|
Okazaki fragments
|
6,953
|
224
|
B
|
High
|
291
|
Human mitochondrial DNA haplogroup
|
6,940
|
223
|
Start
|
Low
|
292
|
Post-translational modification
|
6,939
|
223
|
Start
|
High
|
293
|
Patent ductus arteriosus
|
6,917
|
223
|
Start
|
Mid
|
294
|
Parent
|
6,887
|
222
|
C
|
High
|
295
|
Disodium inosinate
|
6,883
|
222
|
Start
|
Low
|
296
|
Colour wheel theory of love
|
6,873
|
221
|
Stub
|
Low
|
297
|
Illumina, Inc.
|
6,850
|
220
|
C
|
Low
|
298
|
Reverse transcriptase
|
6,844
|
220
|
B
|
High
|
299
|
Shyness
|
6,841
|
220
|
B
|
Low
|
300
|
Coefficient of relationship
|
6,821
|
220
|
C
|
Low
|
301
|
Neanderthal genetics
|
6,757
|
217
|
C
|
High
|
302
|
Flavin adenine dinucleotide
|
6,729
|
217
|
B
|
Low
|
303
|
Haplogroup U
|
6,724
|
216
|
Start
|
Mid
|
304
|
MHC class I
|
6,674
|
215
|
C
|
Mid
|
305
|
Fibular hemimelia
|
6,665
|
215
|
Start
|
Low
|
306
|
Telomerase
|
6,622
|
213
|
B
|
High
|
307
|
Oogenesis
|
6,607
|
213
|
C
|
High
|
308
|
16S ribosomal RNA
|
6,605
|
213
|
C
|
High
|
309
|
Stop codon
|
6,573
|
212
|
Start
|
High
|
310
|
Causes of cancer
|
6,565
|
211
|
B
|
Mid
|
311
|
Haplogroup I-M438
|
6,526
|
210
|
Start
|
Low
|
312
|
Laboratory mouse
|
6,524
|
210
|
B
|
Low
|
313
|
Medical genetics of Jews
|
6,516
|
210
|
Start
|
Low
|
314
|
MHC class II
|
6,513
|
210
|
C
|
Mid
|
315
|
Oncogene
|
6,486
|
209
|
C
|
High
|
316
|
Somatic cell
|
6,450
|
208
|
Start
|
Mid
|
317
|
Eastern hunter-gatherer
|
6,359
|
205
|
C
|
Mid
|
318
|
Epistasis
|
6,358
|
205
|
B
|
High
|
319
|
Peppered moth evolution
|
6,339
|
204
|
GA
|
Mid
|
320
|
List of redheads
|
6,310
|
203
|
List
|
Low
|
321
|
Uracil
|
6,307
|
203
|
Start
|
Mid
|
322
|
Twin study
|
6,299
|
203
|
B
|
High
|
323
|
Isoelectric point
|
6,269
|
202
|
C
|
Mid
|
324
|
Mathematical and theoretical biology
|
6,268
|
202
|
C
|
Low
|
325
|
XXYY syndrome
|
6,257
|
201
|
Start
|
Low
|
326
|
Bacterial conjugation
|
6,244
|
201
|
C
|
High
|
327
|
Sex-determining region Y protein
|
6,227
|
200
|
C
|
Low
|
328
|
Heritability of autism
|
6,187
|
199
|
Start
|
Mid
|
329
|
Zebrafish
|
6,173
|
199
|
B
|
Mid
|
330
|
Hershey–Chase experiment
|
6,120
|
197
|
C
|
High
|
331
|
Cre-Lox recombination
|
6,112
|
197
|
C
|
Mid
|
332
|
Hox gene
|
6,103
|
196
|
C
|
High
|
333
|
Trisomy
|
6,006
|
193
|
Start
|
High
|
334
|
Genealogical DNA test
|
6,003
|
193
|
C
|
Mid
|
335
|
Phenotypic trait
|
5,990
|
193
|
Start
|
Mid
|
336
|
Epidermal growth factor receptor
|
5,954
|
192
|
C
|
Mid
|
337
|
Genetic history of the British Isles
|
5,945
|
191
|
C
|
Low
|
338
|
Plant breeding
|
5,923
|
191
|
C
|
High
|
339
|
Haplogroup N-M231
|
5,904
|
190
|
Start
|
Low
|
340
|
Pioneer Fund
|
5,875
|
189
|
B
|
Low
|
341
|
Ruth Benedict
|
5,859
|
189
|
C
|
Low
|
342
|
Fitness (biology)
|
5,840
|
188
|
C
|
Mid
|
343
|
Dwarf cat
|
5,833
|
188
|
Start
|
Low
|
344
|
Centromere
|
5,820
|
187
|
C
|
Mid
|
345
|
Griffith's experiment
|
5,806
|
187
|
Start
|
Mid
|
346
|
Infantile epileptic spasms syndrome
|
5,796
|
186
|
C
|
Low
|
347
|
Locus (genetics)
|
5,775
|
186
|
Start
|
Mid
|
348
|
Webbed toes
|
5,771
|
186
|
Start
|
Low
|
349
|
X-linked recessive inheritance
|
5,758
|
185
|
Start
|
Mid
|
350
|
Maladaptation
|
5,755
|
185
|
Start
|
Low
|
351
|
Kozak consensus sequence
|
5,748
|
185
|
Start
|
Mid
|
352
|
Haplogroup I-M170
|
5,692
|
183
|
B
|
Low
|
353
|
Genome editing
|
5,660
|
182
|
C
|
High
|
354
|
Chromosomal translocation
|
5,656
|
182
|
Start
|
High
|
355
|
Myc
|
5,645
|
182
|
C
|
High
|
356
|
Non-coding RNA
|
5,633
|
181
|
C
|
High
|
357
|
Genetic diversity
|
5,632
|
181
|
C
|
Mid
|
358
|
Personalized medicine
|
5,629
|
181
|
B
|
Mid
|
359
|
Haplogroup I-M253
|
5,621
|
181
|
B
|
Low
|
360
|
Hi-C (genomic analysis technique)
|
5,620
|
181
|
C
|
Low
|
361
|
Heritability
|
5,603
|
180
|
C
|
High
|
362
|
Homologous recombination
|
5,588
|
180
|
GA
|
High
|
363
|
GloFish
|
5,576
|
179
|
C
|
Mid
|
364
|
Cas9
|
5,569
|
179
|
C
|
Mid
|
365
|
Genetic history of Egypt
|
5,565
|
179
|
C
|
Low
|
366
|
Racial hygiene
|
5,558
|
179
|
C
|
Low
|
367
|
Sampling bias
|
5,547
|
178
|
C
|
Low
|
368
|
Fluorescence in situ hybridization
|
5,540
|
178
|
B
|
Mid
|
369
|
Factor VIII
|
5,509
|
177
|
Start
|
Low
|
370
|
George Church (geneticist)
|
5,485
|
176
|
C
|
Low
|
371
|
Purebred
|
5,447
|
175
|
C
|
Low
|
372
|
Adenosine diphosphate
|
5,401
|
174
|
C
|
Mid
|
373
|
Alternative splicing
|
5,380
|
173
|
B
|
High
|
374
|
Gene delivery
|
5,328
|
171
|
B
|
High
|
375
|
Model organism
|
5,325
|
171
|
B
|
Mid
|
376
|
Genomic imprinting
|
5,264
|
169
|
C
|
High
|
377
|
Adeno-associated virus
|
5,254
|
169
|
B
|
Low
|
378
|
Guanosine triphosphate
|
5,253
|
169
|
Start
|
Mid
|
379
|
Eric Lander
|
5,228
|
168
|
C
|
Low
|
380
|
Allopatric speciation
|
5,226
|
168
|
B
|
Low
|
381
|
Ribozyme
|
5,213
|
168
|
Start
|
High
|
382
|
Genetic history of the Iberian Peninsula
|
5,213
|
168
|
Start
|
Low
|
383
|
Nucleic acid sequence
|
5,204
|
167
|
C
|
High
|
384
|
Maurice Wilkins
|
5,168
|
166
|
B
|
High
|
385
|
5α-Reductase 2 deficiency
|
5,166
|
166
|
B
|
Low
|
386
|
Inbreeding depression
|
5,124
|
165
|
C
|
Low
|
387
|
Modern synthesis (20th century)
|
5,123
|
165
|
GA
|
High
|
388
|
Operon
|
5,105
|
164
|
B
|
Mid
|
389
|
JAK-STAT signaling pathway
|
5,092
|
164
|
B
|
Mid
|
390
|
ZW sex-determination system
|
5,069
|
163
|
C
|
Mid
|
391
|
Chromosome 21
|
5,012
|
161
|
Start
|
Mid
|
392
|
Population genetics
|
5,010
|
161
|
C
|
Top
|
393
|
Biopolymer
|
5,001
|
161
|
C
|
Mid
|
394
|
Constriction ring syndrome
|
4,992
|
161
|
C
|
Low
|
395
|
Genetic memory (psychology)
|
4,974
|
160
|
Start
|
Low
|
396
|
Intron
|
4,966
|
160
|
C
|
High
|
397
|
Telegony (inheritance)
|
4,964
|
160
|
C
|
Low
|
398
|
Sydney Brenner
|
4,960
|
160
|
B
|
Mid
|
399
|
Sex linkage
|
4,954
|
159
|
Start
|
High
|
400
|
Pleiotropy
|
4,933
|
159
|
C
|
High
|
401
|
Nucleoside triphosphate
|
4,916
|
158
|
Start
|
High
|
402
|
MELAS syndrome
|
4,908
|
158
|
C
|
Low
|
403
|
Apomorphy and synapomorphy
|
4,905
|
158
|
C
|
Low
|
404
|
Transduction (genetics)
|
4,891
|
157
|
C
|
High
|
405
|
Sexual selection in humans
|
4,876
|
157
|
C
|
Low
|
406
|
F1 hybrid
|
4,875
|
157
|
Start
|
High
|
407
|
Directionality (molecular biology)
|
4,860
|
156
|
Start
|
High
|
408
|
Haplotype
|
4,799
|
154
|
Start
|
High
|
409
|
Flavivirus
|
4,786
|
154
|
B
|
Mid
|
410
|
X-inactivation
|
4,786
|
154
|
B
|
High
|
411
|
Zellweger syndrome
|
4,772
|
153
|
Start
|
Low
|
412
|
Haplogroup R (Y-DNA)
|
4,751
|
153
|
Start
|
Low
|
413
|
Advanced maternal age
|
4,748
|
153
|
C
|
Mid
|
414
|
Janaki Ammal
|
4,740
|
152
|
B
|
Low
|
415
|
Systems biology
|
4,737
|
152
|
C
|
High
|
416
|
Genome-wide association study
|
4,724
|
152
|
GA
|
Top
|
417
|
Genetic counseling
|
4,681
|
151
|
C
|
Mid
|
418
|
Wiedemann–Steiner syndrome
|
4,666
|
150
|
Stub
|
Low
|
419
|
Non-coding DNA
|
4,656
|
150
|
C
|
Mid
|
420
|
Breed
|
4,649
|
149
|
Start
|
Low
|
421
|
Phred quality score
|
4,641
|
149
|
Start
|
Low
|
422
|
DNA extraction
|
4,595
|
148
|
Start
|
Mid
|
423
|
List of unusual biological names
|
4,590
|
148
|
List
|
Low
|
424
|
Biological determinism
|
4,587
|
147
|
GA
|
Mid
|
425
|
Medical genetics
|
4,550
|
146
|
B
|
Mid
|
426
|
Hepatitis D
|
4,535
|
146
|
C
|
Low
|
427
|
Genetic transformation
|
4,528
|
146
|
B
|
Top
|
428
|
Barr body
|
4,507
|
145
|
Start
|
High
|
429
|
Cystic fibrosis transmembrane conductance regulator
|
4,488
|
144
|
C
|
Mid
|
430
|
Adenosine monophosphate
|
4,468
|
144
|
Start
|
Low
|
431
|
Endogeny (biology)
|
4,450
|
143
|
Stub
|
Low
|
432
|
Human genetic variation
|
4,449
|
143
|
C
|
High
|
433
|
Transgenesis
|
4,440
|
143
|
Redirect
|
Top
|
434
|
Gene nomenclature
|
4,434
|
143
|
Start
|
Mid
|
435
|
Ras GTPase
|
4,399
|
141
|
B
|
High
|
436
|
Oligomer
|
4,359
|
140
|
Start
|
Low
|
437
|
Haplogroup L-M20
|
4,328
|
139
|
Start
|
Low
|
438
|
Pedigree collapse
|
4,298
|
138
|
Start
|
Low
|
439
|
Sheep farming
|
4,293
|
138
|
C
|
Low
|
440
|
Tumor suppressor gene
|
4,281
|
138
|
Start
|
High
|
441
|
Y-DNA haplogroups in populations of Europe
|
4,280
|
138
|
List
|
Mid
|
442
|
KRAS
|
4,263
|
137
|
C
|
Mid
|
443
|
Paternal age effect
|
4,237
|
136
|
C
|
Mid
|
444
|
Taq polymerase
|
4,220
|
136
|
C
|
Mid
|
445
|
Haplogroup Q-M242
|
4,215
|
135
|
C
|
Low
|
446
|
Topoisomerase
|
4,190
|
135
|
C
|
High
|
447
|
Single-cell sequencing
|
4,187
|
135
|
C
|
High
|
448
|
Genetic variation
|
4,185
|
135
|
Start
|
High
|
449
|
Biomaterial
|
4,175
|
134
|
C
|
Low
|
450
|
Crossbreed
|
4,173
|
134
|
Start
|
Low
|
451
|
History of eugenics
|
4,163
|
134
|
B
|
Low
|
452
|
Bovine somatotropin
|
4,160
|
134
|
C
|
Low
|
453
|
Elizabeth Blackburn
|
4,134
|
133
|
C
|
Low
|
454
|
Non-homologous end joining
|
4,132
|
133
|
C
|
Mid
|
455
|
Humanized mouse
|
4,131
|
133
|
Start
|
Low
|
456
|
Genetic history of the Middle East
|
4,121
|
132
|
C
|
Mid
|
457
|
TATA box
|
4,116
|
132
|
B
|
High
|
458
|
Tauros Programme
|
4,112
|
132
|
C
|
Mid
|
459
|
List of haplogroups of historic people
|
4,100
|
132
|
List
|
Low
|
460
|
Ancient DNA
|
4,098
|
132
|
C
|
Mid
|
461
|
Exon
|
4,068
|
131
|
C
|
Top
|
462
|
Haplogroup A (Y-DNA)
|
4,066
|
131
|
C
|
Low
|
463
|
Chromosome 2
|
4,055
|
130
|
C
|
Mid
|
464
|
Haplogroup R1
|
4,052
|
130
|
C
|
Low
|
465
|
Penetrance
|
4,050
|
130
|
C
|
High
|
466
|
Kin selection
|
4,045
|
130
|
GA
|
Mid
|
467
|
Geneticist
|
4,043
|
130
|
Start
|
High
|
468
|
Lydia Fairchild
|
4,034
|
130
|
Stub
|
Unknown
|
469
|
Microsatellite
|
4,032
|
130
|
C
|
Mid
|
470
|
C57BL/6
|
4,020
|
129
|
Start
|
Low
|
471
|
Junk DNA
|
4,015
|
129
|
B
|
Mid
|
472
|
Cold Spring Harbor Laboratory
|
4,008
|
129
|
Start
|
Mid
|
473
|
Introduction to evolution
|
4,008
|
129
|
B
|
High
|
474
|
Gene flow
|
4,005
|
129
|
Start
|
High
|
475
|
Sense (molecular biology)
|
3,998
|
128
|
C
|
High
|
476
|
Y-chromosomal Aaron
|
3,993
|
128
|
Start
|
Low
|
477
|
Bcl-2
|
3,986
|
128
|
B
|
Mid
|
478
|
God gene
|
3,981
|
128
|
Start
|
Mid
|
479
|
Sexual differentiation in humans
|
3,940
|
127
|
C
|
Mid
|
480
|
Heterochromatin
|
3,939
|
127
|
C
|
Mid
|
481
|
Fixation index
|
3,918
|
126
|
C
|
Low
|
482
|
STR analysis
|
3,903
|
125
|
Start
|
Low
|
483
|
Dun gene
|
3,892
|
125
|
C
|
Low
|
484
|
Identical ancestors point
|
3,890
|
125
|
Start
|
Low
|
485
|
Behavioural genetics
|
3,876
|
125
|
GA
|
High
|
486
|
Haplogroup T-M184
|
3,846
|
124
|
B
|
Low
|
487
|
46,XX/46,XY
|
3,845
|
124
|
C
|
Low
|
488
|
Introgression
|
3,832
|
123
|
Start
|
High
|
489
|
DNA supercoil
|
3,828
|
123
|
C
|
Mid
|
490
|
Meselson–Stahl experiment
|
3,816
|
123
|
Start
|
Mid
|
491
|
Genetic linkage
|
3,813
|
123
|
Start
|
High
|
492
|
Somatic cell nuclear transfer
|
3,806
|
122
|
C
|
Mid
|
493
|
Nanopore sequencing
|
3,805
|
122
|
C
|
Low
|
494
|
Aniridia
|
3,799
|
122
|
C
|
Low
|
495
|
Linkage disequilibrium
|
3,791
|
122
|
C
|
High
|
496
|
Oligonucleotide
|
3,786
|
122
|
Start
|
Mid
|
497
|
Chromosome 1
|
3,782
|
122
|
Start
|
Low
|
498
|
Enzyme Commission number
|
3,776
|
121
|
Start
|
Low
|
499
|
Haplogroup M (mtDNA)
|
3,775
|
121
|
Stub
|
Low
|
500
|
Nucleoid
|
3,771
|
121
|
B
|
Mid
|
|
Full category list
Categories within WP:GEN
|
Category WikiProject Genetics not found
|
Categories within Genetics
|
|
|