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: 2024-06-01 to 2024-06-30
Total views: 8,228,839
Updated: 04:17, 9 July 2024 (UTC)
Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Axolotl
|
168,869
|
5,628
|
C
|
High
|
2
|
Error
|
108,030
|
3,601
|
Start
|
Mid
|
3
|
Prion
|
87,342
|
2,911
|
GA
|
Mid
|
4
|
Eugenics
|
82,173
|
2,739
|
B
|
High
|
5
|
Incest
|
77,906
|
2,596
|
C
|
Low
|
6
|
DNA
|
69,685
|
2,322
|
FA
|
Top
|
7
|
Guinea pig
|
64,860
|
2,162
|
B
|
Low
|
8
|
Cancer
|
59,377
|
1,979
|
B
|
Top
|
9
|
Cystic fibrosis
|
55,070
|
1,835
|
B
|
High
|
10
|
Amino acid
|
54,260
|
1,808
|
GA
|
Top
|
11
|
Bayer
|
54,256
|
1,808
|
C
|
Low
|
12
|
Blood type
|
50,997
|
1,699
|
B
|
High
|
13
|
Protein
|
49,027
|
1,634
|
GA
|
Top
|
14
|
Epigenetics
|
44,497
|
1,483
|
B
|
Top
|
15
|
Meiosis
|
41,997
|
1,399
|
C
|
Top
|
16
|
Attachment theory
|
41,424
|
1,380
|
B
|
Mid
|
17
|
Color blindness
|
41,247
|
1,374
|
B
|
Mid
|
18
|
Evolution
|
41,219
|
1,373
|
FA
|
Top
|
19
|
Red hair
|
40,431
|
1,347
|
C
|
Mid
|
20
|
Total fertility rate
|
39,556
|
1,318
|
C
|
Low
|
21
|
Biodiversity
|
39,380
|
1,312
|
C
|
Mid
|
22
|
Cousin
|
38,560
|
1,285
|
Start
|
Low
|
23
|
XY sex-determination system
|
37,801
|
1,260
|
C
|
High
|
24
|
Blue Fugates
|
37,022
|
1,234
|
Start
|
Low
|
25
|
CRISPR
|
36,840
|
1,228
|
B
|
High
|
26
|
Enzyme
|
36,798
|
1,226
|
FA
|
Top
|
27
|
Gregor Mendel
|
36,569
|
1,218
|
B
|
High
|
28
|
SARS-CoV-2
|
35,243
|
1,174
|
B
|
Top
|
29
|
Chromosome
|
35,130
|
1,171
|
B
|
Top
|
30
|
Prader–Willi syndrome
|
34,900
|
1,163
|
B
|
Mid
|
31
|
Charcot–Marie–Tooth disease
|
34,251
|
1,141
|
C
|
Mid
|
32
|
Adenosine triphosphate
|
33,788
|
1,126
|
C
|
High
|
33
|
Scientific racism
|
33,155
|
1,105
|
C
|
Low
|
34
|
Human skin color
|
32,491
|
1,083
|
B
|
Mid
|
35
|
Nicotinamide adenine dinucleotide
|
32,305
|
1,076
|
FA
|
Mid
|
36
|
Inbreeding
|
30,519
|
1,017
|
C
|
Low
|
37
|
Chimera (genetics)
|
30,452
|
1,015
|
B
|
Mid
|
38
|
Rosalind Franklin
|
29,928
|
997
|
B
|
High
|
39
|
Consanguinity
|
29,873
|
995
|
C
|
Low
|
40
|
Epicanthic fold
|
29,546
|
984
|
C
|
Low
|
41
|
Polymerase chain reaction
|
28,108
|
936
|
B
|
High
|
42
|
Blond
|
27,414
|
913
|
C
|
Low
|
43
|
Genetics
|
26,318
|
877
|
FA
|
Top
|
44
|
Animal husbandry
|
25,576
|
852
|
GA
|
Mid
|
45
|
Lactose intolerance
|
25,357
|
845
|
B
|
Low
|
46
|
Hybrid (biology)
|
25,090
|
836
|
GA
|
High
|
47
|
Japanese people
|
24,878
|
829
|
C
|
Low
|
48
|
Humanzee
|
24,876
|
829
|
C
|
Mid
|
49
|
Mitochondrial Eve
|
24,742
|
824
|
B
|
Mid
|
50
|
Estimates of historical world population
|
24,737
|
824
|
Start
|
Low
|
51
|
Genetic engineering
|
24,205
|
806
|
GA
|
Top
|
52
|
Genetic studies of Jews
|
23,958
|
798
|
B
|
Mid
|
53
|
Albinism
|
23,952
|
798
|
C
|
Low
|
54
|
Gigantism
|
23,882
|
796
|
B
|
High
|
55
|
Gene
|
23,660
|
788
|
GA
|
Top
|
56
|
Human Genome Project
|
23,391
|
779
|
B
|
Top
|
57
|
Wechsler Adult Intelligence Scale
|
23,306
|
776
|
C
|
Low
|
58
|
RNA
|
23,207
|
773
|
GA
|
Top
|
59
|
Birth defect
|
23,091
|
769
|
B
|
Mid
|
60
|
Sonic hedgehog protein
|
22,977
|
765
|
B
|
High
|
61
|
Dominance (genetics)
|
22,934
|
764
|
C
|
Top
|
62
|
Cleft lip and cleft palate
|
22,877
|
762
|
B
|
Low
|
63
|
M. S. Swaminathan
|
22,595
|
753
|
B
|
Low
|
64
|
Nucleotide
|
21,850
|
728
|
C
|
Top
|
65
|
Svalbard Global Seed Vault
|
21,441
|
714
|
B
|
Mid
|
66
|
Last universal common ancestor
|
21,386
|
712
|
GA
|
Mid
|
67
|
Genetically modified food
|
21,379
|
712
|
B
|
High
|
68
|
XYY syndrome
|
21,253
|
708
|
B
|
Mid
|
69
|
Endogamy
|
20,729
|
690
|
Start
|
Low
|
70
|
Origin of COVID-19
|
20,644
|
688
|
Start
|
Low
|
71
|
Mutation
|
20,530
|
684
|
B
|
Top
|
72
|
Early human migrations
|
20,427
|
680
|
B
|
Mid
|
73
|
Ribosome
|
20,312
|
677
|
B
|
Top
|
74
|
Human hair color
|
19,697
|
656
|
Start
|
Mid
|
75
|
Drosophila melanogaster
|
19,638
|
654
|
B
|
Top
|
76
|
DNA replication
|
19,503
|
650
|
B
|
Unknown
|
77
|
Genetic disorder
|
19,373
|
645
|
B
|
Top
|
78
|
Cultivar
|
18,883
|
629
|
GA
|
Mid
|
79
|
HeLa
|
18,693
|
623
|
C
|
Low
|
80
|
Senescence
|
18,620
|
620
|
C
|
Low
|
81
|
James Watson
|
18,496
|
616
|
B
|
High
|
82
|
Phenotype
|
18,396
|
613
|
C
|
Top
|
83
|
Recent African origin of modern humans
|
18,353
|
611
|
C
|
Mid
|
84
|
Mendelian inheritance
|
18,315
|
610
|
C
|
High
|
85
|
Pentasomy X
|
18,210
|
607
|
GA
|
Low
|
86
|
Haplogroup R1b
|
17,995
|
599
|
C
|
Mid
|
87
|
Sex-determination system
|
17,875
|
595
|
C
|
Mid
|
88
|
Descent from Genghis Khan
|
17,830
|
594
|
C
|
Low
|
89
|
Mitochondrial DNA
|
17,710
|
590
|
B
|
High
|
90
|
Genetically modified organism
|
17,625
|
587
|
GA
|
Top
|
91
|
Domesticated silver fox
|
17,537
|
584
|
C
|
Low
|
92
|
Nucleic acid
|
17,495
|
583
|
C
|
Mid
|
93
|
Haplogroup R1a
|
17,424
|
580
|
C
|
Low
|
94
|
CRISPR gene editing
|
17,154
|
571
|
B
|
Top
|
95
|
Y chromosome
|
17,137
|
571
|
B
|
High
|
96
|
Trisomy 18
|
16,455
|
548
|
B
|
Low
|
97
|
The Bell Curve
|
16,150
|
538
|
C
|
High
|
98
|
Francis Crick
|
16,125
|
537
|
B
|
High
|
99
|
DNA and RNA codon tables
|
15,989
|
532
|
FL
|
High
|
100
|
Landrace
|
15,939
|
531
|
C
|
Low
|
101
|
Messenger RNA
|
15,906
|
530
|
C
|
High
|
102
|
Punnett square
|
15,802
|
526
|
C
|
Top
|
103
|
Cloning
|
15,743
|
524
|
B
|
Top
|
104
|
Cat coat genetics
|
15,725
|
524
|
C
|
Mid
|
105
|
DNA sequencing
|
15,710
|
523
|
C
|
Top
|
106
|
Allele
|
15,370
|
512
|
B
|
Top
|
107
|
Gamete
|
15,329
|
510
|
Start
|
Mid
|
108
|
Population bottleneck
|
15,309
|
510
|
C
|
Mid
|
109
|
Haplogroup
|
15,170
|
505
|
C
|
Mid
|
110
|
23andMe
|
15,162
|
505
|
C
|
Mid
|
111
|
Leucism
|
15,139
|
504
|
Start
|
Low
|
112
|
Incest taboo
|
15,003
|
500
|
C
|
Mid
|
113
|
Human genome
|
14,835
|
494
|
C
|
High
|
114
|
Ancient North Eurasian
|
14,780
|
492
|
C
|
Mid
|
115
|
Transcription (biology)
|
14,543
|
484
|
B
|
Top
|
116
|
XXXY syndrome
|
14,443
|
481
|
C
|
Low
|
117
|
Plasmid
|
14,362
|
478
|
C
|
High
|
118
|
DNA methylation
|
14,123
|
470
|
B
|
High
|
119
|
Institutional racism
|
14,112
|
470
|
B
|
High
|
120
|
Genetic code
|
14,073
|
469
|
GA
|
Top
|
121
|
Selective breeding
|
14,045
|
468
|
C
|
Top
|
122
|
Genome
|
13,939
|
464
|
C
|
High
|
123
|
Human–animal hybrid
|
13,928
|
464
|
C
|
Low
|
124
|
G. H. Hardy
|
13,910
|
463
|
C
|
Mid
|
125
|
Lectin
|
13,796
|
459
|
C
|
Mid
|
126
|
Heredity
|
13,665
|
455
|
C
|
Top
|
127
|
XX male syndrome
|
13,649
|
454
|
C
|
Low
|
128
|
Stephen Jay Gould
|
13,605
|
453
|
GA
|
Mid
|
129
|
Fibular hemimelia
|
13,601
|
453
|
Start
|
Low
|
130
|
Phenylketonuria
|
13,582
|
452
|
B
|
Mid
|
131
|
Ectrodactyly
|
13,555
|
451
|
B
|
Mid
|
132
|
DNA profiling
|
13,427
|
447
|
B
|
High
|
133
|
Major histocompatibility complex
|
13,424
|
447
|
B
|
Mid
|
134
|
Single-nucleotide polymorphism
|
13,302
|
443
|
C
|
High
|
135
|
Brown hair
|
13,238
|
441
|
C
|
Mid
|
136
|
Tay–Sachs disease
|
13,222
|
440
|
B
|
High
|
137
|
Telomere
|
13,187
|
439
|
C
|
Mid
|
138
|
Ploidy
|
13,140
|
438
|
C
|
High
|
139
|
Karyotype
|
13,070
|
435
|
C
|
Mid
|
140
|
William Shockley
|
13,020
|
434
|
B
|
Low
|
141
|
Plasmodium falciparum
|
12,968
|
432
|
B
|
Low
|
142
|
Tetralogy of Fallot
|
12,963
|
432
|
C
|
Low
|
143
|
Jennifer Doudna
|
12,881
|
429
|
B
|
High
|
144
|
Haplogroup G-M201
|
12,744
|
424
|
Start
|
Low
|
145
|
Gene therapy
|
12,726
|
424
|
B
|
High
|
146
|
Human Y-chromosome DNA haplogroup
|
12,724
|
424
|
C
|
Mid
|
147
|
Early European Farmers
|
12,669
|
422
|
C
|
Mid
|
148
|
Homology (biology)
|
12,567
|
418
|
GA
|
High
|
149
|
Polyploidy
|
12,355
|
411
|
B
|
High
|
150
|
Heritability of IQ
|
12,354
|
411
|
C
|
Low
|
151
|
Sexual selection
|
12,330
|
411
|
GA
|
Mid
|
152
|
God gene
|
12,218
|
407
|
Start
|
Mid
|
153
|
Friedreich's ataxia
|
12,128
|
404
|
GA
|
Mid
|
154
|
De-extinction
|
12,118
|
403
|
C
|
Low
|
155
|
Eugenics in the United States
|
12,044
|
401
|
Start
|
Low
|
156
|
Mosaic (genetics)
|
11,996
|
399
|
C
|
Mid
|
157
|
Genotype
|
11,863
|
395
|
Start
|
Top
|
158
|
Domestic rabbit
|
11,734
|
391
|
GA
|
Low
|
159
|
Freckle
|
11,678
|
389
|
Start
|
Low
|
160
|
Western Steppe Herders
|
11,644
|
388
|
C
|
Mid
|
161
|
Gene expression
|
11,507
|
383
|
B
|
Top
|
162
|
List of organisms by chromosome count
|
11,179
|
372
|
List
|
Low
|
163
|
Ronald Fisher
|
11,177
|
372
|
B
|
High
|
164
|
Genetic history of Europe
|
11,141
|
371
|
Start
|
Low
|
165
|
Atavism
|
11,084
|
369
|
C
|
Mid
|
166
|
Western hunter-gatherer
|
11,025
|
367
|
C
|
Mid
|
167
|
Nazi eugenics
|
11,023
|
367
|
C
|
Mid
|
168
|
He Jiankui affair
|
10,977
|
365
|
C
|
Low
|
169
|
P53
|
10,965
|
365
|
B
|
High
|
170
|
Sanger sequencing
|
10,937
|
364
|
C
|
High
|
171
|
Biological engineering
|
10,911
|
363
|
C
|
High
|
172
|
Recombinant DNA
|
10,797
|
359
|
C
|
High
|
173
|
Genentech
|
10,726
|
357
|
Start
|
Mid
|
174
|
Ventricular septal defect
|
10,698
|
356
|
C
|
Low
|
175
|
Genetic drift
|
10,687
|
356
|
GA
|
High
|
176
|
Reverse transcription polymerase chain reaction
|
10,663
|
355
|
Start
|
Mid
|
177
|
Hardy–Weinberg principle
|
10,612
|
353
|
C
|
High
|
178
|
Panthera hybrid
|
10,512
|
350
|
C
|
Mid
|
179
|
Protein biosynthesis
|
10,457
|
348
|
B
|
Mid
|
180
|
Patau syndrome
|
10,338
|
344
|
C
|
Low
|
181
|
Black hair
|
10,086
|
336
|
Start
|
Mid
|
182
|
Real-time polymerase chain reaction
|
10,070
|
335
|
C
|
Mid
|
183
|
HLA-B27
|
10,028
|
334
|
C
|
Low
|
184
|
Anthropometry
|
9,955
|
331
|
C
|
Low
|
185
|
NF-κB
|
9,936
|
331
|
C
|
High
|
186
|
RNA splicing
|
9,874
|
329
|
C
|
Top
|
187
|
Hereditary haemochromatosis
|
9,763
|
325
|
B
|
Mid
|
188
|
Congenital heart defect
|
9,757
|
325
|
C
|
Mid
|
189
|
X chromosome
|
9,610
|
320
|
B
|
Top
|
190
|
Citicoline
|
9,596
|
319
|
B
|
Low
|
191
|
Lactase
|
9,590
|
319
|
B
|
Mid
|
192
|
Founder effect
|
9,589
|
319
|
C
|
High
|
193
|
Genetic testing
|
9,550
|
318
|
B
|
Top
|
194
|
He Jiankui
|
9,533
|
317
|
B
|
Low
|
195
|
Auburn hair
|
9,530
|
317
|
Start
|
Low
|
196
|
Transfer RNA
|
9,513
|
317
|
B
|
High
|
197
|
DNA evidence in the O. J. Simpson murder case
|
9,471
|
315
|
B
|
Low
|
198
|
Most recent common ancestor
|
9,433
|
314
|
B
|
Mid
|
199
|
Base pair
|
9,387
|
312
|
C
|
Top
|
200
|
Transcription factor
|
9,336
|
311
|
B
|
High
|
201
|
Blue rose
|
9,317
|
310
|
Start
|
Low
|
202
|
Haplogroup H (mtDNA)
|
9,281
|
309
|
Start
|
Low
|
203
|
Sex chromosome
|
9,129
|
304
|
Start
|
High
|
204
|
Francis Collins
|
9,018
|
300
|
B
|
Mid
|
205
|
Methylation
|
8,953
|
298
|
C
|
Mid
|
206
|
Haplogroup C-M217
|
8,906
|
296
|
Start
|
Low
|
207
|
Lac operon
|
8,886
|
296
|
C
|
Mid
|
208
|
DNA repair
|
8,845
|
294
|
C
|
High
|
209
|
Wnt signaling pathway
|
8,842
|
294
|
C
|
Mid
|
210
|
Hayflick limit
|
8,831
|
294
|
Start
|
Low
|
211
|
Polymorphism (biology)
|
8,807
|
293
|
B
|
Low
|
212
|
Nucleolus
|
8,784
|
292
|
Start
|
Mid
|
213
|
RNA world
|
8,767
|
292
|
C
|
Mid
|
214
|
Exogamy
|
8,725
|
290
|
Start
|
Low
|
215
|
Proteinogenic amino acid
|
8,721
|
290
|
C
|
High
|
216
|
Ethnic groups of Japan
|
8,676
|
289
|
Start
|
Unknown
|
217
|
Genetics and archaeogenetics of South Asia
|
8,646
|
288
|
Start
|
Mid
|
218
|
Translation (biology)
|
8,595
|
286
|
B
|
Top
|
219
|
Central dogma of molecular biology
|
8,588
|
286
|
C
|
Top
|
220
|
MicroRNA
|
8,581
|
286
|
B
|
Top
|
221
|
Variants of SARS-CoV-2
|
8,581
|
286
|
C
|
Low
|
222
|
Single parent
|
8,573
|
285
|
B
|
Mid
|
223
|
Genetic studies on Turkish people
|
8,535
|
284
|
Start
|
Low
|
224
|
Zygosity
|
8,490
|
283
|
C
|
High
|
225
|
Cyclic adenosine monophosphate
|
8,480
|
282
|
C
|
Mid
|
226
|
Transposable element
|
8,461
|
282
|
C
|
High
|
227
|
Tuberous sclerosis
|
8,419
|
280
|
B
|
Mid
|
228
|
Heterosis
|
8,383
|
279
|
C
|
High
|
229
|
Nucleic acid double helix
|
8,306
|
276
|
C
|
Mid
|
230
|
Humanized mouse
|
8,304
|
276
|
Start
|
Low
|
231
|
Haplogroup I-M170
|
8,279
|
275
|
B
|
Low
|
232
|
Monoamine oxidase A
|
8,217
|
273
|
C
|
Mid
|
233
|
Fertility
|
8,191
|
273
|
C
|
Mid
|
234
|
DNA polymerase
|
8,179
|
272
|
C
|
Top
|
235
|
Impulsivity
|
8,166
|
272
|
B
|
Mid
|
236
|
Telegony (inheritance)
|
8,148
|
271
|
C
|
Low
|
237
|
Medical genetics of Jews
|
8,014
|
267
|
Start
|
Low
|
238
|
Genomics
|
7,973
|
265
|
B
|
Top
|
239
|
Atrial septal defect
|
7,920
|
264
|
B
|
Low
|
240
|
Nicotinamide adenine dinucleotide phosphate
|
7,889
|
262
|
Start
|
Mid
|
241
|
Chromosome abnormality
|
7,880
|
262
|
Start
|
High
|
242
|
Promoter (genetics)
|
7,875
|
262
|
Start
|
Mid
|
243
|
Whole genome sequencing
|
7,863
|
262
|
B
|
Top
|
244
|
Phenotypic disparity
|
7,836
|
261
|
C
|
Low
|
245
|
Horizontal gene transfer
|
7,790
|
259
|
C
|
High
|
246
|
Reverse transcriptase
|
7,677
|
255
|
B
|
High
|
247
|
Chin
|
7,669
|
255
|
C
|
Low
|
248
|
Dysgenics
|
7,668
|
255
|
Start
|
Low
|
249
|
Oogenesis
|
7,653
|
255
|
C
|
High
|
250
|
Synthetic biology
|
7,603
|
253
|
B
|
Mid
|
251
|
Oncogene
|
7,565
|
252
|
C
|
High
|
252
|
Aneuploidy
|
7,547
|
251
|
B
|
High
|
253
|
Chromatin
|
7,530
|
251
|
B
|
Mid
|
254
|
Sex-determining region Y protein
|
7,522
|
250
|
C
|
Low
|
255
|
Balaji Srinivasan
|
7,440
|
248
|
Start
|
Low
|
256
|
RNA interference
|
7,421
|
247
|
FA
|
Top
|
257
|
Eastern hunter-gatherer
|
7,367
|
245
|
C
|
Mid
|
258
|
Haplogroup U
|
7,362
|
245
|
Start
|
Mid
|
259
|
Genetic recombination
|
7,305
|
243
|
C
|
High
|
260
|
Genetically modified crops
|
7,300
|
243
|
B
|
High
|
261
|
Photo 51
|
7,292
|
243
|
Start
|
Low
|
262
|
Haplogroup E-M215
|
7,278
|
242
|
C
|
Low
|
263
|
Y-chromosomal Adam
|
7,269
|
242
|
C
|
High
|
264
|
Regulation of gene expression
|
7,238
|
241
|
C
|
High
|
265
|
Data storage
|
7,216
|
240
|
Start
|
Low
|
266
|
Laboratory rat
|
7,142
|
238
|
C
|
Mid
|
267
|
Homologous chromosome
|
7,139
|
237
|
Start
|
High
|
268
|
Haplogroup J (Y-DNA)
|
7,116
|
237
|
Start
|
Low
|
269
|
Post-translational modification
|
7,112
|
237
|
Start
|
High
|
270
|
Genetic history of Egypt
|
7,093
|
236
|
C
|
Low
|
271
|
Haplogroup J-M172
|
7,090
|
236
|
Start
|
Low
|
272
|
Illumina, Inc.
|
7,052
|
235
|
C
|
Low
|
273
|
MHC class II
|
7,046
|
234
|
C
|
Mid
|
274
|
Mitochondrial disease
|
7,030
|
234
|
C
|
Mid
|
275
|
Von Hippel–Lindau disease
|
7,014
|
233
|
C
|
Mid
|
276
|
Histone
|
6,939
|
231
|
C
|
Mid
|
277
|
Chromosomal crossover
|
6,855
|
228
|
C
|
High
|
278
|
Human mitochondrial DNA haplogroup
|
6,838
|
227
|
Start
|
Low
|
279
|
MHC class I
|
6,789
|
226
|
C
|
Mid
|
280
|
5α-Reductase 2 deficiency
|
6,721
|
224
|
B
|
Low
|
281
|
Epistasis
|
6,717
|
223
|
B
|
High
|
282
|
HER2
|
6,700
|
223
|
C
|
Mid
|
283
|
Dwarf cat
|
6,667
|
222
|
Start
|
Low
|
284
|
List of redheads
|
6,663
|
222
|
List
|
Low
|
285
|
Webbed toes
|
6,633
|
221
|
Start
|
Low
|
286
|
Hispanos of New Mexico
|
6,626
|
220
|
Start
|
Low
|
287
|
BRCA1
|
6,622
|
220
|
C
|
High
|
288
|
Heritability of autism
|
6,588
|
219
|
Start
|
Mid
|
289
|
CpG site
|
6,579
|
219
|
C
|
Mid
|
290
|
J. B. S. Haldane
|
6,562
|
218
|
C
|
Low
|
291
|
Twin study
|
6,538
|
217
|
B
|
High
|
292
|
X-linked recessive inheritance
|
6,524
|
217
|
Start
|
Mid
|
293
|
Barbara McClintock
|
6,411
|
213
|
FA
|
High
|
294
|
Fluorescence in situ hybridization
|
6,337
|
211
|
B
|
Mid
|
295
|
Telomerase
|
6,331
|
211
|
B
|
High
|
296
|
Coefficient of relationship
|
6,331
|
211
|
C
|
Low
|
297
|
Mebendazole
|
6,320
|
210
|
C
|
Mid
|
298
|
Neanderthal genetics
|
6,286
|
209
|
C
|
High
|
299
|
XXYY syndrome
|
6,237
|
207
|
Start
|
Low
|
300
|
Parent
|
6,225
|
207
|
C
|
High
|
301
|
Somatic cell
|
6,206
|
206
|
Start
|
Mid
|
302
|
Autosome
|
6,175
|
205
|
Start
|
Top
|
303
|
Colour wheel theory of love
|
6,170
|
205
|
Stub
|
Low
|
304
|
Causes of cancer
|
6,147
|
204
|
B
|
Mid
|
305
|
Mathematical and theoretical biology
|
6,128
|
204
|
C
|
Low
|
306
|
16S ribosomal RNA
|
6,126
|
204
|
C
|
High
|
307
|
Lydia Fairchild
|
6,122
|
204
|
Stub
|
Unknown
|
308
|
Sexual selection in humans
|
6,122
|
204
|
C
|
Low
|
309
|
Cre-Lox recombination
|
6,116
|
203
|
C
|
Mid
|
310
|
ZW sex-determination system
|
6,115
|
203
|
C
|
Mid
|
311
|
Open reading frame
|
6,100
|
203
|
Start
|
Mid
|
312
|
Inbreeding depression
|
6,062
|
202
|
C
|
Low
|
313
|
Biopolymer
|
6,018
|
200
|
C
|
Mid
|
314
|
Shyness
|
6,012
|
200
|
B
|
Low
|
315
|
Locus (genetics)
|
5,998
|
199
|
Start
|
Mid
|
316
|
Pleiotropy
|
5,953
|
198
|
C
|
High
|
317
|
Chromosome 21
|
5,945
|
198
|
Start
|
Mid
|
318
|
Cas9
|
5,912
|
197
|
C
|
Mid
|
319
|
Fitness (biology)
|
5,911
|
197
|
C
|
Mid
|
320
|
Epidermal growth factor receptor
|
5,864
|
195
|
C
|
Mid
|
321
|
Haplogroup N-M231
|
5,860
|
195
|
Start
|
Low
|
322
|
GloFish
|
5,824
|
194
|
C
|
Mid
|
323
|
Chromosome 2
|
5,805
|
193
|
C
|
Mid
|
324
|
Genome editing
|
5,788
|
192
|
C
|
High
|
325
|
Factor VIII
|
5,767
|
192
|
Start
|
Low
|
326
|
Stop codon
|
5,755
|
191
|
Start
|
High
|
327
|
Tumor suppressor gene
|
5,738
|
191
|
Start
|
High
|
328
|
Genetic diversity
|
5,738
|
191
|
C
|
Mid
|
329
|
RNA polymerase
|
5,724
|
190
|
C
|
Top
|
330
|
JAK-STAT signaling pathway
|
5,719
|
190
|
B
|
Mid
|
331
|
Patent ductus arteriosus
|
5,712
|
190
|
Start
|
Mid
|
332
|
Heritability
|
5,705
|
190
|
C
|
High
|
333
|
Dravet syndrome
|
5,700
|
190
|
C
|
Low
|
334
|
Isoelectric point
|
5,689
|
189
|
C
|
Mid
|
335
|
Genomic imprinting
|
5,674
|
189
|
C
|
High
|
336
|
Flavin adenine dinucleotide
|
5,658
|
188
|
B
|
Low
|
337
|
Chromosomal translocation
|
5,647
|
188
|
Start
|
High
|
338
|
Chargaff's rules
|
5,642
|
188
|
Start
|
Low
|
339
|
Haplogroup J-M267
|
5,630
|
187
|
C
|
Low
|
340
|
Sampling bias
|
5,572
|
185
|
C
|
Low
|
341
|
Genetic history of the British Isles
|
5,555
|
185
|
C
|
Low
|
342
|
Laboratory mouse
|
5,527
|
184
|
B
|
Low
|
343
|
Single-cell sequencing
|
5,521
|
184
|
C
|
High
|
344
|
Modern synthesis (20th century)
|
5,475
|
182
|
GA
|
High
|
345
|
Myc
|
5,465
|
182
|
C
|
High
|
346
|
Alternative splicing
|
5,464
|
182
|
B
|
High
|
347
|
Allopatric speciation
|
5,460
|
182
|
C
|
Low
|
348
|
Racial hygiene
|
5,440
|
181
|
C
|
Low
|
349
|
Zebrafish
|
5,408
|
180
|
B
|
Mid
|
350
|
Genetic memory (psychology)
|
5,398
|
179
|
Start
|
Low
|
351
|
Okazaki fragments
|
5,366
|
178
|
B
|
High
|
352
|
Designer baby
|
5,365
|
178
|
B
|
High
|
353
|
Ruth Benedict
|
5,360
|
178
|
C
|
Low
|
354
|
Hox gene
|
5,330
|
177
|
C
|
High
|
355
|
Phosphorylation
|
5,310
|
177
|
C
|
High
|
356
|
Purebred
|
5,302
|
176
|
C
|
Low
|
357
|
Phenotypic trait
|
5,292
|
176
|
Start
|
Mid
|
358
|
Genetic history of the Iberian Peninsula
|
5,270
|
175
|
Start
|
Low
|
359
|
Genealogical DNA test
|
5,262
|
175
|
C
|
Mid
|
360
|
Haplogroup R (Y-DNA)
|
5,255
|
175
|
Start
|
Low
|
361
|
Homologous recombination
|
5,219
|
173
|
GA
|
High
|
362
|
Uracil
|
5,217
|
173
|
Start
|
Mid
|
363
|
Adeno-associated virus
|
5,212
|
173
|
B
|
Low
|
364
|
Multiple sequence alignment
|
5,212
|
173
|
Unknown
|
Mid
|
365
|
Paternal age effect
|
5,211
|
173
|
C
|
Mid
|
366
|
Haplogroup I-M438
|
5,207
|
173
|
Start
|
Low
|
367
|
Nucleic acid sequence
|
5,187
|
172
|
C
|
High
|
368
|
Centromere
|
5,159
|
171
|
C
|
Mid
|
369
|
Haplogroup I-M253
|
5,147
|
171
|
B
|
Low
|
370
|
Bacterial conjugation
|
5,143
|
171
|
C
|
High
|
371
|
Genetic transformation
|
5,116
|
170
|
B
|
Top
|
372
|
Junk DNA
|
5,086
|
169
|
B
|
Mid
|
373
|
The Population Bomb
|
5,082
|
169
|
B
|
Low
|
374
|
Personalized medicine
|
5,061
|
168
|
B
|
Mid
|
375
|
List of genetic disorders
|
5,028
|
167
|
List
|
High
|
376
|
Human genetic variation
|
4,992
|
166
|
C
|
High
|
377
|
Genome-wide association study
|
4,961
|
165
|
GA
|
Top
|
378
|
Plant breeding
|
4,953
|
165
|
C
|
High
|
379
|
Restriction fragment length polymorphism
|
4,938
|
164
|
Start
|
Mid
|
380
|
Barr body
|
4,889
|
162
|
Start
|
High
|
381
|
Population genetics
|
4,874
|
162
|
C
|
Top
|
382
|
Model organism
|
4,845
|
161
|
B
|
Mid
|
383
|
Genetic variation
|
4,845
|
161
|
Start
|
High
|
384
|
Hi-C (genomic analysis technique)
|
4,811
|
160
|
C
|
Low
|
385
|
George Church (geneticist)
|
4,788
|
159
|
C
|
Low
|
386
|
Gene mapping
|
4,768
|
158
|
Start
|
Low
|
387
|
Brooke Greenberg
|
4,757
|
158
|
Start
|
Mid
|
388
|
Microsatellite
|
4,746
|
158
|
C
|
Mid
|
389
|
Oligonucleotide
|
4,743
|
158
|
Start
|
Mid
|
390
|
Operon
|
4,742
|
158
|
B
|
Mid
|
391
|
Gene nomenclature
|
4,733
|
157
|
Start
|
Mid
|
392
|
Systems biology
|
4,732
|
157
|
C
|
High
|
393
|
Non-coding DNA
|
4,728
|
157
|
C
|
Mid
|
394
|
Transduction (genetics)
|
4,728
|
157
|
C
|
High
|
395
|
Ronald Plasterk
|
4,727
|
157
|
C
|
Unknown
|
396
|
Non-coding RNA
|
4,711
|
157
|
C
|
High
|
397
|
X-inactivation
|
4,703
|
156
|
B
|
High
|
398
|
Flavivirus
|
4,700
|
156
|
B
|
Mid
|
399
|
Molecular cloning
|
4,633
|
154
|
C
|
High
|
400
|
Advanced maternal age
|
4,632
|
154
|
C
|
Mid
|
401
|
Haplotype
|
4,623
|
154
|
Start
|
High
|
402
|
Dun gene
|
4,605
|
153
|
C
|
Low
|
403
|
Hershey–Chase experiment
|
4,570
|
152
|
C
|
High
|
404
|
Kin selection
|
4,567
|
152
|
GA
|
Mid
|
405
|
Pedigree chart
|
4,552
|
151
|
Start
|
Mid
|
406
|
KRAS
|
4,530
|
151
|
C
|
Mid
|
407
|
Maladaptation
|
4,516
|
150
|
Start
|
Low
|
408
|
F1 hybrid
|
4,514
|
150
|
Start
|
High
|
409
|
Kozak consensus sequence
|
4,503
|
150
|
Start
|
Mid
|
410
|
Endogeny (biology)
|
4,497
|
149
|
Stub
|
Low
|
411
|
Biological determinism
|
4,478
|
149
|
GA
|
Mid
|
412
|
Trisomy
|
4,470
|
149
|
Start
|
High
|
413
|
Sheep farming
|
4,456
|
148
|
C
|
Low
|
414
|
Janaki Ammal
|
4,421
|
147
|
B
|
Low
|
415
|
Frameshift mutation
|
4,413
|
147
|
B
|
High
|
416
|
Point mutation
|
4,398
|
146
|
C
|
High
|
417
|
Neo-Darwinism
|
4,392
|
146
|
Start
|
High
|
418
|
Disodium inosinate
|
4,391
|
146
|
Start
|
Low
|
419
|
Taq polymerase
|
4,382
|
146
|
C
|
Mid
|
420
|
Breed
|
4,372
|
145
|
Start
|
Low
|
421
|
Leigh syndrome
|
4,359
|
145
|
C
|
Low
|
422
|
Svante Pääbo
|
4,357
|
145
|
C
|
Low
|
423
|
List of unusual biological names
|
4,350
|
145
|
List
|
Low
|
424
|
Haplogroup R1
|
4,347
|
144
|
C
|
Low
|
425
|
Haplogroup Q-M242
|
4,338
|
144
|
C
|
Low
|
426
|
Introduction to evolution
|
4,303
|
143
|
B
|
High
|
427
|
List of haplogroups of historic people
|
4,291
|
143
|
List
|
Low
|
428
|
Transgene
|
4,282
|
142
|
B
|
Mid
|
429
|
Haplogroup M (mtDNA)
|
4,276
|
142
|
Stub
|
Low
|
430
|
Sex linkage
|
4,250
|
141
|
Start
|
High
|
431
|
Jefferson–Hemings controversy
|
4,245
|
141
|
B
|
Low
|
432
|
Sexual differentiation in humans
|
4,234
|
141
|
C
|
Mid
|
433
|
Haplogroup A (Y-DNA)
|
4,224
|
140
|
C
|
Low
|
434
|
Genetic linkage
|
4,217
|
140
|
Start
|
High
|
435
|
Gene set enrichment analysis
|
4,194
|
139
|
C
|
Mid
|
436
|
Ribozyme
|
4,179
|
139
|
Start
|
High
|
437
|
Guanosine triphosphate
|
4,177
|
139
|
Start
|
Mid
|
438
|
Y-chromosomal Aaron
|
4,160
|
138
|
Start
|
Low
|
439
|
DNA extraction
|
4,125
|
137
|
Start
|
Mid
|
440
|
Ras GTPase
|
4,124
|
137
|
B
|
High
|
441
|
Crossbreed
|
4,111
|
137
|
Start
|
Low
|
442
|
Genetic history of the Middle East
|
4,107
|
136
|
C
|
Mid
|
443
|
Medical genetics
|
4,082
|
136
|
B
|
Mid
|
444
|
Haplogroup T-M184
|
4,061
|
135
|
B
|
Low
|
445
|
Intron
|
4,057
|
135
|
C
|
High
|
446
|
Apomorphy and synapomorphy
|
4,039
|
134
|
C
|
Low
|
447
|
Klotho (biology)
|
4,033
|
134
|
Start
|
Low
|
448
|
Bcl-2
|
4,025
|
134
|
B
|
Mid
|
449
|
Phred quality score
|
4,025
|
134
|
Start
|
Low
|
450
|
Tongue rolling
|
4,024
|
134
|
Stub
|
Low
|
451
|
Exome sequencing
|
4,018
|
133
|
C
|
High
|
452
|
Non-homologous end joining
|
4,007
|
133
|
C
|
Mid
|
453
|
Hepatitis D
|
4,002
|
133
|
C
|
Low
|
454
|
Heterochromatin
|
3,999
|
133
|
C
|
Mid
|
455
|
Enzyme Commission number
|
3,965
|
132
|
Start
|
Low
|
456
|
Peppered moth evolution
|
3,952
|
131
|
GA
|
Mid
|
457
|
Constriction ring syndrome
|
3,951
|
131
|
C
|
Low
|
458
|
TATA box
|
3,941
|
131
|
B
|
High
|
459
|
GC-content
|
3,936
|
131
|
C
|
Mid
|
460
|
Detasseling
|
3,927
|
130
|
B
|
Low
|
461
|
Ancient DNA
|
3,911
|
130
|
C
|
Mid
|
462
|
Adenosine diphosphate
|
3,893
|
129
|
C
|
Mid
|
463
|
Boar–pig hybrid
|
3,884
|
129
|
Stub
|
Low
|
464
|
Topoisomerase
|
3,855
|
128
|
C
|
High
|
465
|
Biomaterial
|
3,831
|
127
|
C
|
Low
|
466
|
Genetic counseling
|
3,810
|
127
|
C
|
Mid
|
467
|
Cystic fibrosis transmembrane conductance regulator
|
3,810
|
127
|
C
|
Mid
|
468
|
Haplogroup H (Y-DNA)
|
3,807
|
126
|
C
|
Low
|
469
|
Linkage disequilibrium
|
3,805
|
126
|
C
|
High
|
470
|
Complementary DNA
|
3,799
|
126
|
Start
|
Mid
|
471
|
Haplogroup E-M96
|
3,797
|
126
|
Start
|
Low
|
472
|
Uterus didelphys
|
3,797
|
126
|
Start
|
Low
|
473
|
Molecular clock
|
3,795
|
126
|
C
|
High
|
474
|
Gene flow
|
3,779
|
125
|
Start
|
High
|
475
|
Long non-coding RNA
|
3,770
|
125
|
C
|
Mid
|
476
|
Adenosine monophosphate
|
3,754
|
125
|
Start
|
Low
|
477
|
SARS-CoV-2 Delta variant
|
3,753
|
125
|
C
|
Low
|
478
|
Copy number variation
|
3,733
|
124
|
B
|
High
|
479
|
Eric Lander
|
3,732
|
124
|
C
|
Low
|
480
|
Gene knockout
|
3,726
|
124
|
Start
|
Mid
|
481
|
Enhancer (genetics)
|
3,710
|
123
|
C
|
High
|
482
|
Oligomer
|
3,702
|
123
|
Start
|
Low
|
483
|
Start codon
|
3,671
|
122
|
Start
|
Top
|
484
|
Combined DNA Index System
|
3,670
|
122
|
GA
|
Low
|
485
|
Prime editing
|
3,669
|
122
|
Stub
|
Low
|
486
|
Maurice Wilkins
|
3,656
|
121
|
B
|
High
|
487
|
Bovine somatotropin
|
3,636
|
121
|
C
|
Low
|
488
|
Sequence homology
|
3,633
|
121
|
C
|
Top
|
489
|
Gene polymorphism
|
3,632
|
121
|
Start
|
High
|
490
|
Haplogroup E-V68
|
3,629
|
120
|
C
|
Low
|
491
|
Directionality (molecular biology)
|
3,598
|
119
|
Start
|
High
|
492
|
Retrotransposon
|
3,593
|
119
|
C
|
High
|
493
|
Penetrance
|
3,589
|
119
|
C
|
High
|
494
|
Griffith's experiment
|
3,587
|
119
|
Start
|
Mid
|
495
|
Haplogroup K (mtDNA)
|
3,579
|
119
|
Start
|
Low
|
496
|
Somatic cell nuclear transfer
|
3,576
|
119
|
C
|
Mid
|
497
|
Haplogroup O-M175
|
3,571
|
119
|
Start
|
Low
|
498
|
Knockout mouse
|
3,562
|
118
|
C
|
Mid
|
499
|
Cold Spring Harbor Laboratory
|
3,554
|
118
|
Start
|
Mid
|
500
|
Transgenerational epigenetic inheritance
|
3,548
|
118
|
C
|
High
|
|
Full category list
Categories within Genetics
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