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
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Period: 2024-05-01 to 2024-05-31
Total views: 9,799,561
Updated: 23:44, 8 June 2024 (UTC)
Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Axolotl
|
180,865
|
5,834
|
C
|
High
|
2
|
Prion
|
133,314
|
4,300
|
GA
|
Mid
|
3
|
Blue Fugates
|
104,573
|
3,373
|
Start
|
Low
|
4
|
Bayer
|
99,504
|
3,209
|
C
|
Low
|
5
|
Incest
|
90,061
|
2,905
|
C
|
Low
|
6
|
DNA
|
88,391
|
2,851
|
FA
|
Top
|
7
|
Eugenics
|
88,185
|
2,844
|
C
|
High
|
8
|
Amino acid
|
75,209
|
2,426
|
GA
|
Top
|
9
|
Guinea pig
|
73,974
|
2,386
|
B
|
Low
|
10
|
Cancer
|
73,166
|
2,360
|
B
|
Top
|
11
|
Protein
|
67,527
|
2,178
|
GA
|
Top
|
12
|
Cystic fibrosis
|
63,014
|
2,032
|
B
|
High
|
13
|
Meiosis
|
56,278
|
1,815
|
C
|
Top
|
14
|
Biodiversity
|
55,981
|
1,805
|
C
|
Mid
|
15
|
Evolution
|
55,978
|
1,805
|
FA
|
Top
|
16
|
Blood type
|
52,770
|
1,702
|
B
|
High
|
17
|
Enzyme
|
51,196
|
1,651
|
FA
|
Top
|
18
|
Gregor Mendel
|
49,615
|
1,600
|
B
|
High
|
19
|
Color blindness
|
49,181
|
1,586
|
B
|
Mid
|
20
|
CRISPR
|
45,978
|
1,483
|
B
|
High
|
21
|
Attachment theory
|
45,925
|
1,481
|
B
|
Mid
|
22
|
Epigenetics
|
45,319
|
1,461
|
B
|
Top
|
23
|
Red hair
|
44,931
|
1,449
|
C
|
Mid
|
24
|
Adenosine triphosphate
|
43,780
|
1,412
|
C
|
High
|
25
|
Prader–Willi syndrome
|
43,776
|
1,412
|
B
|
Mid
|
26
|
Total fertility rate
|
42,744
|
1,378
|
C
|
Low
|
27
|
XY sex-determination system
|
42,431
|
1,368
|
C
|
High
|
28
|
Chromosome
|
41,685
|
1,344
|
B
|
Top
|
29
|
Rosalind Franklin
|
40,786
|
1,315
|
B
|
High
|
30
|
Scientific racism
|
40,199
|
1,296
|
C
|
Low
|
31
|
SARS-CoV-2
|
39,200
|
1,264
|
B
|
Top
|
32
|
Human skin color
|
37,481
|
1,209
|
B
|
Mid
|
33
|
Svalbard Global Seed Vault
|
36,822
|
1,187
|
B
|
Mid
|
34
|
Polymerase chain reaction
|
36,662
|
1,182
|
B
|
High
|
35
|
Inbreeding
|
36,069
|
1,163
|
C
|
Low
|
36
|
Nicotinamide adenine dinucleotide
|
35,903
|
1,158
|
FA
|
Mid
|
37
|
Cousin
|
34,955
|
1,127
|
Start
|
Low
|
38
|
Ronald Plasterk
|
34,114
|
1,100
|
C
|
Unknown
|
39
|
Humanzee
|
34,045
|
1,098
|
C
|
Mid
|
40
|
Charcot–Marie–Tooth disease
|
33,577
|
1,083
|
C
|
Mid
|
41
|
Chimera (genetics)
|
33,345
|
1,075
|
B
|
Mid
|
42
|
Genetic engineering
|
33,315
|
1,074
|
GA
|
Top
|
43
|
Genetic studies of Jews
|
32,866
|
1,060
|
B
|
Mid
|
44
|
Genetics
|
32,651
|
1,053
|
FA
|
Top
|
45
|
Epicanthic fold
|
32,142
|
1,036
|
C
|
Low
|
46
|
Blond
|
31,698
|
1,022
|
C
|
Low
|
47
|
Consanguinity
|
30,551
|
985
|
C
|
Low
|
48
|
Mutation
|
30,540
|
985
|
B
|
Top
|
49
|
Hybrid (biology)
|
29,981
|
967
|
GA
|
High
|
50
|
Animal husbandry
|
29,387
|
947
|
GA
|
Mid
|
51
|
Nucleotide
|
28,762
|
927
|
C
|
Top
|
52
|
Cleft lip and cleft palate
|
28,616
|
923
|
B
|
Low
|
53
|
Birth defect
|
28,389
|
915
|
B
|
Mid
|
54
|
RNA
|
28,155
|
908
|
GA
|
Top
|
55
|
Estimates of historical world population
|
27,933
|
901
|
Start
|
Low
|
56
|
Japanese people
|
27,859
|
898
|
C
|
Low
|
57
|
Gigantism
|
27,548
|
888
|
B
|
High
|
58
|
Mitochondrial Eve
|
27,538
|
888
|
B
|
Mid
|
59
|
Wechsler Adult Intelligence Scale
|
27,433
|
884
|
C
|
Low
|
60
|
Gene
|
27,371
|
882
|
GA
|
Top
|
61
|
Albinism
|
27,323
|
881
|
C
|
Low
|
62
|
Human Genome Project
|
27,259
|
879
|
B
|
Top
|
63
|
Genetically modified food
|
27,183
|
876
|
B
|
High
|
64
|
DNA and RNA codon tables
|
27,155
|
875
|
FL
|
High
|
65
|
DNA replication
|
27,112
|
874
|
B
|
Unknown
|
66
|
Nucleic acid
|
26,811
|
864
|
C
|
Mid
|
67
|
Dominance (genetics)
|
26,304
|
848
|
C
|
Top
|
68
|
Lactose intolerance
|
26,062
|
840
|
B
|
Low
|
69
|
Last universal common ancestor
|
25,803
|
832
|
GA
|
Mid
|
70
|
Ribosome
|
24,922
|
803
|
B
|
Top
|
71
|
Early human migrations
|
24,503
|
790
|
B
|
Mid
|
72
|
Genetically modified organism
|
24,327
|
784
|
GA
|
Top
|
73
|
HeLa
|
23,508
|
758
|
C
|
Low
|
74
|
James Watson
|
23,348
|
753
|
B
|
High
|
75
|
Punnett square
|
23,232
|
749
|
C
|
Top
|
76
|
Genetic disorder
|
23,003
|
742
|
B
|
Top
|
77
|
CRISPR gene editing
|
22,741
|
733
|
B
|
Top
|
78
|
Mendelian inheritance
|
22,498
|
725
|
C
|
High
|
79
|
Drosophila melanogaster
|
22,324
|
720
|
B
|
Top
|
80
|
M. S. Swaminathan
|
22,277
|
718
|
B
|
Low
|
81
|
Senescence
|
22,190
|
715
|
C
|
Low
|
82
|
Endogamy
|
21,699
|
699
|
Start
|
Low
|
83
|
Phenotype
|
21,674
|
699
|
C
|
Top
|
84
|
Descent from Genghis Khan
|
21,336
|
688
|
C
|
Low
|
85
|
Cloning
|
21,045
|
678
|
B
|
Top
|
86
|
Domesticated silver fox
|
21,041
|
678
|
C
|
Low
|
87
|
Human hair color
|
21,012
|
677
|
Start
|
Mid
|
88
|
DNA sequencing
|
20,957
|
676
|
C
|
Top
|
89
|
XXXY syndrome
|
20,854
|
672
|
C
|
Low
|
90
|
Recent African origin of modern humans
|
20,819
|
671
|
C
|
Mid
|
91
|
Mitochondrial DNA
|
20,757
|
669
|
B
|
High
|
92
|
XYY syndrome
|
20,582
|
663
|
B
|
Mid
|
93
|
23andMe
|
20,554
|
663
|
C
|
Mid
|
94
|
Haplogroup R1b
|
20,304
|
654
|
C
|
Mid
|
95
|
Gene therapy
|
20,148
|
649
|
B
|
High
|
96
|
Pentasomy X
|
20,145
|
649
|
GA
|
Low
|
97
|
Transcription (biology)
|
19,982
|
644
|
B
|
Top
|
98
|
Messenger RNA
|
19,942
|
643
|
C
|
High
|
99
|
Plasmid
|
19,721
|
636
|
C
|
High
|
100
|
Haplogroup R1a
|
19,462
|
627
|
C
|
Low
|
101
|
Cultivar
|
19,324
|
623
|
GA
|
Mid
|
102
|
Gamete
|
19,258
|
621
|
Start
|
Mid
|
103
|
Haplogroup
|
19,128
|
617
|
C
|
Mid
|
104
|
Y chromosome
|
19,065
|
615
|
B
|
High
|
105
|
Sex-determination system
|
19,056
|
614
|
C
|
Mid
|
106
|
Human genome
|
18,787
|
606
|
C
|
High
|
107
|
Sonic hedgehog protein
|
18,636
|
601
|
B
|
High
|
108
|
Trisomy 18
|
18,407
|
593
|
B
|
Low
|
109
|
Institutional racism
|
18,010
|
580
|
B
|
High
|
110
|
Allele
|
17,933
|
578
|
B
|
Top
|
111
|
Karyotype
|
17,784
|
573
|
C
|
Mid
|
112
|
The Bell Curve
|
17,763
|
573
|
C
|
High
|
113
|
Incest taboo
|
17,567
|
566
|
C
|
Mid
|
114
|
Panthera hybrid
|
17,472
|
563
|
C
|
Mid
|
115
|
Landrace
|
17,173
|
553
|
C
|
Low
|
116
|
Polyploidy
|
17,020
|
549
|
B
|
High
|
117
|
Heredity
|
17,016
|
548
|
C
|
Top
|
118
|
Genome
|
17,006
|
548
|
C
|
High
|
119
|
Cat coat genetics
|
16,999
|
548
|
C
|
Mid
|
120
|
Population bottleneck
|
16,931
|
546
|
C
|
Mid
|
121
|
Origin of COVID-19
|
16,729
|
539
|
Start
|
Low
|
122
|
Francis Crick
|
16,698
|
538
|
B
|
High
|
123
|
Homology (biology)
|
16,638
|
536
|
GA
|
High
|
124
|
Hardy–Weinberg principle
|
16,467
|
531
|
C
|
High
|
125
|
Phenylketonuria
|
16,446
|
530
|
B
|
Mid
|
126
|
Major histocompatibility complex
|
16,246
|
524
|
B
|
Mid
|
127
|
DNA profiling
|
16,202
|
522
|
B
|
High
|
128
|
Ploidy
|
16,135
|
520
|
C
|
High
|
129
|
Genetic code
|
16,134
|
520
|
GA
|
Top
|
130
|
Recombinant DNA
|
16,089
|
519
|
C
|
High
|
131
|
DNA methylation
|
16,021
|
516
|
B
|
High
|
132
|
P53
|
15,964
|
514
|
B
|
High
|
133
|
Plasmodium falciparum
|
15,867
|
511
|
B
|
Low
|
134
|
De-extinction
|
15,831
|
510
|
C
|
Low
|
135
|
Human–animal hybrid
|
15,817
|
510
|
C
|
Low
|
136
|
Tetralogy of Fallot
|
15,816
|
510
|
C
|
Low
|
137
|
Nazi eugenics
|
15,787
|
509
|
C
|
Mid
|
138
|
Tay–Sachs disease
|
15,698
|
506
|
B
|
High
|
139
|
Stephen Jay Gould
|
15,595
|
503
|
GA
|
Mid
|
140
|
Selective breeding
|
15,434
|
497
|
C
|
Top
|
141
|
G. H. Hardy
|
15,367
|
495
|
C
|
Mid
|
142
|
Single-nucleotide polymorphism
|
15,336
|
494
|
C
|
High
|
143
|
Ancient North Eurasian
|
15,263
|
492
|
C
|
Mid
|
144
|
Eugenics in the United States
|
15,106
|
487
|
Start
|
Low
|
145
|
Freckle
|
15,077
|
486
|
Start
|
Low
|
146
|
Genotype
|
14,939
|
481
|
Start
|
Top
|
147
|
William Shockley
|
14,668
|
473
|
B
|
Low
|
148
|
List of organisms by chromosome count
|
14,583
|
470
|
List
|
Low
|
149
|
XX male syndrome
|
14,536
|
468
|
C
|
Low
|
150
|
Jennifer Doudna
|
14,430
|
465
|
B
|
High
|
151
|
Transfer RNA
|
14,343
|
462
|
B
|
High
|
152
|
Early European Farmers
|
14,144
|
456
|
C
|
Mid
|
153
|
Genetic drift
|
14,133
|
455
|
GA
|
High
|
154
|
Sexual selection
|
14,091
|
454
|
GA
|
Mid
|
155
|
Protein biosynthesis
|
13,977
|
450
|
B
|
Mid
|
156
|
Domestic rabbit
|
13,776
|
444
|
GA
|
Low
|
157
|
Gene expression
|
13,696
|
441
|
B
|
Top
|
158
|
Sanger sequencing
|
13,643
|
440
|
C
|
High
|
159
|
Brown hair
|
13,575
|
437
|
C
|
Mid
|
160
|
Leucism
|
13,519
|
436
|
Start
|
Low
|
161
|
Human Y-chromosome DNA haplogroup
|
13,452
|
433
|
C
|
Mid
|
162
|
DNA evidence in the O. J. Simpson murder case
|
13,264
|
427
|
B
|
Low
|
163
|
Lectin
|
13,177
|
425
|
C
|
Mid
|
164
|
Ronald Fisher
|
13,133
|
423
|
B
|
High
|
165
|
Reverse transcription polymerase chain reaction
|
13,116
|
423
|
Start
|
Mid
|
166
|
Factor VIII
|
13,009
|
419
|
Start
|
Low
|
167
|
Translation (biology)
|
12,773
|
412
|
B
|
Top
|
168
|
Ventricular septal defect
|
12,680
|
409
|
C
|
Low
|
169
|
Telomere
|
12,597
|
406
|
C
|
Mid
|
170
|
Blue rose
|
12,553
|
404
|
Start
|
Low
|
171
|
NF-κB
|
12,541
|
404
|
C
|
High
|
172
|
DNA repair
|
12,409
|
400
|
C
|
High
|
173
|
MicroRNA
|
12,360
|
398
|
B
|
Top
|
174
|
Atavism
|
12,210
|
393
|
C
|
Mid
|
175
|
Genetic history of Europe
|
12,156
|
392
|
Start
|
Low
|
176
|
Transcription factor
|
12,098
|
390
|
B
|
High
|
177
|
RNA splicing
|
12,048
|
388
|
C
|
Top
|
178
|
Hayflick limit
|
11,921
|
384
|
Start
|
Low
|
179
|
Patau syndrome
|
11,812
|
381
|
C
|
Low
|
180
|
Hereditary haemochromatosis
|
11,737
|
378
|
B
|
Mid
|
181
|
Genetically modified crops
|
11,714
|
377
|
B
|
High
|
182
|
Western Hunter-Gatherer
|
11,684
|
376
|
C
|
Mid
|
183
|
Variants of SARS-CoV-2
|
11,633
|
375
|
C
|
Low
|
184
|
Genetic testing
|
11,548
|
372
|
B
|
Top
|
185
|
Oogenesis
|
11,538
|
372
|
C
|
High
|
186
|
Mosaic (genetics)
|
11,504
|
371
|
C
|
Mid
|
187
|
Lac operon
|
11,497
|
370
|
C
|
Mid
|
188
|
Congenital heart defect
|
11,454
|
369
|
C
|
Mid
|
189
|
HLA-B27
|
11,447
|
369
|
C
|
Low
|
190
|
List of unusual biological names
|
11,424
|
368
|
List
|
Low
|
191
|
Anthropometry
|
11,321
|
365
|
C
|
Low
|
192
|
Real-time polymerase chain reaction
|
11,312
|
364
|
C
|
Mid
|
193
|
Western Steppe Herders
|
11,205
|
361
|
C
|
Mid
|
194
|
Biological engineering
|
11,180
|
360
|
C
|
High
|
195
|
Wnt signaling pathway
|
11,160
|
360
|
C
|
Mid
|
196
|
Single parent
|
11,102
|
358
|
B
|
Mid
|
197
|
Haplogroup H (mtDNA)
|
11,074
|
357
|
Start
|
Low
|
198
|
Neanderthal genetics
|
11,052
|
356
|
C
|
High
|
199
|
Ethnic groups of Japan
|
11,002
|
354
|
Start
|
Unknown
|
200
|
Founder effect
|
10,974
|
354
|
C
|
High
|
201
|
Genentech
|
10,971
|
353
|
Start
|
Mid
|
202
|
Balaji Srinivasan
|
10,897
|
351
|
Start
|
Low
|
203
|
Base pair
|
10,879
|
350
|
C
|
Top
|
204
|
Transposable element
|
10,833
|
349
|
C
|
High
|
205
|
Most recent common ancestor
|
10,797
|
348
|
B
|
Mid
|
206
|
Fertility
|
10,787
|
347
|
C
|
Mid
|
207
|
Black hair
|
10,746
|
346
|
Start
|
Mid
|
208
|
Central dogma of molecular biology
|
10,690
|
344
|
C
|
Top
|
209
|
Atrial septal defect
|
10,651
|
343
|
B
|
Low
|
210
|
Francis Collins
|
10,645
|
343
|
B
|
Mid
|
211
|
Genetics and archaeogenetics of South Asia
|
10,590
|
341
|
Start
|
Mid
|
212
|
X chromosome
|
10,569
|
340
|
B
|
Top
|
213
|
Lactase
|
10,555
|
340
|
B
|
Mid
|
214
|
DNA polymerase
|
10,545
|
340
|
C
|
Top
|
215
|
Polymorphism (biology)
|
10,497
|
338
|
B
|
Low
|
216
|
Homologous chromosome
|
10,491
|
338
|
Start
|
High
|
217
|
RNA interference
|
10,476
|
337
|
FA
|
Top
|
218
|
Citicoline
|
10,433
|
336
|
B
|
Low
|
219
|
Cyclic adenosine monophosphate
|
10,426
|
336
|
C
|
Mid
|
220
|
Heritability of IQ
|
10,326
|
333
|
C
|
Low
|
221
|
Auburn hair
|
10,256
|
330
|
Start
|
Low
|
222
|
Nucleic acid double helix
|
10,162
|
327
|
C
|
Mid
|
223
|
Zebrafish
|
10,117
|
326
|
B
|
Mid
|
224
|
Horizontal gene transfer
|
10,044
|
324
|
C
|
High
|
225
|
Synthetic biology
|
10,012
|
322
|
B
|
Mid
|
226
|
Chin
|
9,980
|
321
|
C
|
Low
|
227
|
Sex chromosome
|
9,977
|
321
|
Start
|
High
|
228
|
RNA world
|
9,792
|
315
|
C
|
Mid
|
229
|
Methylation
|
9,788
|
315
|
C
|
Mid
|
230
|
Ectrodactyly
|
9,746
|
314
|
B
|
Mid
|
231
|
Oncogene
|
9,732
|
313
|
C
|
High
|
232
|
Heterosis
|
9,725
|
313
|
C
|
High
|
233
|
Promoter (genetics)
|
9,670
|
311
|
Start
|
Mid
|
234
|
Nucleolus
|
9,627
|
310
|
Start
|
Mid
|
235
|
Genetic recombination
|
9,533
|
307
|
C
|
High
|
236
|
Proteinogenic amino acid
|
9,465
|
305
|
C
|
High
|
237
|
Nicotinamide adenine dinucleotide phosphate
|
9,458
|
305
|
Start
|
Mid
|
238
|
Tuberous sclerosis
|
9,449
|
304
|
B
|
Mid
|
239
|
He Jiankui affair
|
9,411
|
303
|
C
|
Low
|
240
|
Whole genome sequencing
|
9,374
|
302
|
B
|
Top
|
241
|
Impulsivity
|
9,322
|
300
|
B
|
Mid
|
242
|
Laboratory rat
|
9,277
|
299
|
C
|
Mid
|
243
|
Genomics
|
9,261
|
298
|
B
|
Top
|
244
|
Zygosity
|
9,215
|
297
|
C
|
High
|
245
|
Exogamy
|
9,152
|
295
|
Start
|
Low
|
246
|
Von Hippel–Lindau disease
|
9,099
|
293
|
C
|
Mid
|
247
|
MHC class I
|
9,037
|
291
|
C
|
Mid
|
248
|
Aneuploidy
|
9,022
|
291
|
B
|
High
|
249
|
Friedreich's ataxia
|
8,989
|
289
|
GA
|
Mid
|
250
|
Mathematical and theoretical biology
|
8,949
|
288
|
C
|
Low
|
251
|
Lydia Fairchild
|
8,902
|
287
|
Stub
|
Unknown
|
252
|
Post-translational modification
|
8,873
|
286
|
Start
|
High
|
253
|
Epistasis
|
8,858
|
285
|
B
|
High
|
254
|
MHC class II
|
8,844
|
285
|
C
|
Mid
|
255
|
Histone
|
8,826
|
284
|
C
|
Mid
|
256
|
Reverse transcriptase
|
8,771
|
282
|
B
|
High
|
257
|
Chromatin
|
8,742
|
282
|
B
|
Mid
|
258
|
List of genetic disorders
|
8,740
|
281
|
List
|
High
|
259
|
Chromosome abnormality
|
8,555
|
275
|
Start
|
High
|
260
|
Y-chromosomal Adam
|
8,382
|
270
|
C
|
High
|
261
|
X-linked recessive inheritance
|
8,339
|
269
|
Start
|
Mid
|
262
|
HER2
|
8,334
|
268
|
C
|
Mid
|
263
|
Regulation of gene expression
|
8,328
|
268
|
C
|
High
|
264
|
Haplogroup N-M231
|
8,304
|
267
|
Start
|
Low
|
265
|
Monoamine oxidase A
|
8,279
|
267
|
C
|
Mid
|
266
|
RNA polymerase
|
8,249
|
266
|
C
|
Top
|
267
|
Chromosomal crossover
|
8,227
|
265
|
C
|
High
|
268
|
Somatic cell
|
8,210
|
264
|
Start
|
Mid
|
269
|
Epidermal growth factor receptor
|
8,145
|
262
|
C
|
Mid
|
270
|
Genetic studies on Turkish people
|
8,103
|
261
|
Start
|
Low
|
271
|
Parent
|
8,096
|
261
|
C
|
High
|
272
|
Data storage
|
8,089
|
260
|
Start
|
Low
|
273
|
Klotho (biology)
|
8,057
|
259
|
Start
|
Low
|
274
|
Haplogroup U
|
8,047
|
259
|
Start
|
Mid
|
275
|
Twin study
|
8,034
|
259
|
B
|
High
|
276
|
Haplogroup E-M215
|
8,027
|
258
|
C
|
Low
|
277
|
Cas9
|
8,019
|
258
|
C
|
Mid
|
278
|
Genetic diversity
|
8,017
|
258
|
C
|
Mid
|
279
|
Mitochondrial disease
|
7,946
|
256
|
C
|
Mid
|
280
|
Open reading frame
|
7,930
|
255
|
Start
|
Mid
|
281
|
Photo 51
|
7,899
|
254
|
Start
|
Low
|
282
|
CpG site
|
7,898
|
254
|
C
|
Mid
|
283
|
BRCA1
|
7,866
|
253
|
C
|
High
|
284
|
Tumor suppressor gene
|
7,861
|
253
|
Start
|
High
|
285
|
Haplogroup J (Y-DNA)
|
7,815
|
252
|
Start
|
Low
|
286
|
Dysgenics
|
7,782
|
251
|
Start
|
Low
|
287
|
Biopolymer
|
7,735
|
249
|
C
|
Mid
|
288
|
Stop codon
|
7,690
|
248
|
Start
|
High
|
289
|
GloFish
|
7,672
|
247
|
C
|
Mid
|
290
|
Plant breeding
|
7,665
|
247
|
C
|
High
|
291
|
Heritability of autism
|
7,650
|
246
|
Start
|
Mid
|
292
|
Mebendazole
|
7,637
|
246
|
C
|
Mid
|
293
|
Designer baby
|
7,623
|
245
|
B
|
High
|
294
|
Fluorescence in situ hybridization
|
7,568
|
244
|
B
|
Mid
|
295
|
Haplogroup J-M172
|
7,561
|
243
|
Start
|
Low
|
296
|
Uracil
|
7,559
|
243
|
Start
|
Mid
|
297
|
Allopatric speciation
|
7,508
|
242
|
C
|
Low
|
298
|
Genetic transformation
|
7,359
|
237
|
B
|
Top
|
299
|
Chromosomal translocation
|
7,346
|
236
|
Start
|
High
|
300
|
Genome editing
|
7,343
|
236
|
C
|
High
|
301
|
Webbed toes
|
7,338
|
236
|
Start
|
Low
|
302
|
Haplogroup G-M201
|
7,337
|
236
|
Start
|
Low
|
303
|
Coefficient of relationship
|
7,328
|
236
|
C
|
Low
|
304
|
16S ribosomal RNA
|
7,285
|
235
|
C
|
High
|
305
|
J. B. S. Haldane
|
7,258
|
234
|
C
|
Low
|
306
|
Causes of cancer
|
7,223
|
233
|
B
|
Mid
|
307
|
Myc
|
7,220
|
232
|
C
|
High
|
308
|
Bacterial conjugation
|
7,216
|
232
|
C
|
High
|
309
|
Eastern Hunter-Gatherer
|
7,216
|
232
|
C
|
Mid
|
310
|
Human mitochondrial DNA haplogroup
|
7,168
|
231
|
Start
|
Low
|
311
|
Genetic history of Egypt
|
7,154
|
230
|
C
|
Low
|
312
|
Hispanos of New Mexico
|
7,140
|
230
|
Start
|
Low
|
313
|
Illumina, Inc.
|
7,131
|
230
|
C
|
Low
|
314
|
Autosome
|
7,125
|
229
|
Start
|
Top
|
315
|
5α-Reductase 2 deficiency
|
7,114
|
229
|
B
|
Low
|
316
|
Genomic imprinting
|
7,111
|
229
|
C
|
High
|
317
|
Barbara McClintock
|
7,097
|
228
|
FA
|
High
|
318
|
Fitness (biology)
|
7,097
|
228
|
C
|
Mid
|
319
|
Sex-determining region Y protein
|
7,082
|
228
|
C
|
Low
|
320
|
Cre-Lox recombination
|
7,075
|
228
|
C
|
Mid
|
321
|
Telomerase
|
7,053
|
227
|
B
|
High
|
322
|
Peppered moth evolution
|
7,051
|
227
|
GA
|
Mid
|
323
|
Locus (genetics)
|
7,026
|
226
|
Start
|
Mid
|
324
|
Patent ductus arteriosus
|
7,008
|
226
|
Start
|
Mid
|
325
|
Hox gene
|
6,997
|
225
|
C
|
High
|
326
|
Molecular cloning
|
6,997
|
225
|
C
|
High
|
327
|
Population genetics
|
6,981
|
225
|
C
|
Top
|
328
|
Okazaki fragments
|
6,962
|
224
|
B
|
High
|
329
|
Homologous recombination
|
6,916
|
223
|
GA
|
High
|
330
|
Inbreeding depression
|
6,871
|
221
|
C
|
Low
|
331
|
Pleiotropy
|
6,821
|
220
|
C
|
High
|
332
|
Laboratory mouse
|
6,799
|
219
|
B
|
Low
|
333
|
List of redheads
|
6,787
|
218
|
List
|
Low
|
334
|
Multiple sequence alignment
|
6,774
|
218
|
Unknown
|
Mid
|
335
|
Chromosome 21
|
6,711
|
216
|
Start
|
Mid
|
336
|
Phosphorylation
|
6,705
|
216
|
C
|
High
|
337
|
Isoelectric point
|
6,697
|
216
|
C
|
Mid
|
338
|
Flavin adenine dinucleotide
|
6,689
|
215
|
B
|
Low
|
339
|
Alternative splicing
|
6,636
|
214
|
B
|
High
|
340
|
Adeno-associated virus
|
6,590
|
212
|
B
|
Low
|
341
|
Colour wheel theory of love
|
6,564
|
211
|
Stub
|
Low
|
342
|
Racial hygiene
|
6,529
|
210
|
C
|
Low
|
343
|
Transduction (genetics)
|
6,506
|
209
|
C
|
High
|
344
|
Point mutation
|
6,500
|
209
|
C
|
High
|
345
|
JAK-STAT signaling pathway
|
6,442
|
207
|
B
|
Mid
|
346
|
XXYY syndrome
|
6,401
|
206
|
Start
|
Low
|
347
|
Shyness
|
6,399
|
206
|
B
|
Low
|
348
|
Brooke Greenberg
|
6,375
|
205
|
Start
|
Mid
|
349
|
Centromere
|
6,374
|
205
|
C
|
Mid
|
350
|
Nucleic acid sequence
|
6,357
|
205
|
C
|
High
|
351
|
Sex linkage
|
6,349
|
204
|
Start
|
High
|
352
|
Heritability
|
6,348
|
204
|
C
|
High
|
353
|
The Population Bomb
|
6,266
|
202
|
B
|
Low
|
354
|
Sampling bias
|
6,238
|
201
|
C
|
Low
|
355
|
Human genetic variation
|
6,171
|
199
|
C
|
High
|
356
|
God gene
|
6,144
|
198
|
Start
|
Mid
|
357
|
Genealogical DNA test
|
6,127
|
197
|
C
|
Mid
|
358
|
Genome-wide association study
|
6,122
|
197
|
GA
|
Top
|
359
|
Dravet syndrome
|
6,097
|
196
|
C
|
Low
|
360
|
Personalized medicine
|
6,074
|
195
|
B
|
Mid
|
361
|
Single-cell sequencing
|
6,056
|
195
|
C
|
High
|
362
|
Dwarf cat
|
6,042
|
194
|
Start
|
Low
|
363
|
Chargaff's rules
|
5,988
|
193
|
Start
|
Low
|
364
|
Gene mapping
|
5,985
|
193
|
Start
|
Low
|
365
|
Restriction fragment length polymorphism
|
5,954
|
192
|
Start
|
Mid
|
366
|
Operon
|
5,939
|
191
|
B
|
Mid
|
367
|
Microsatellite
|
5,914
|
190
|
C
|
Mid
|
368
|
Genetic variation
|
5,899
|
190
|
Start
|
High
|
369
|
Haplogroup I-M170
|
5,893
|
190
|
B
|
Low
|
370
|
Haplogroup J-M267
|
5,888
|
189
|
C
|
Low
|
371
|
Svante Pääbo
|
5,881
|
189
|
C
|
Low
|
372
|
Sexual selection in humans
|
5,881
|
189
|
C
|
Low
|
373
|
Haplogroup I-M438
|
5,873
|
189
|
Start
|
Low
|
374
|
Model organism
|
5,852
|
188
|
B
|
Mid
|
375
|
DNA extraction
|
5,804
|
187
|
Start
|
Mid
|
376
|
Genetic memory (psychology)
|
5,803
|
187
|
Start
|
Low
|
377
|
X-inactivation
|
5,792
|
186
|
B
|
High
|
378
|
ZW sex-determination system
|
5,768
|
186
|
C
|
Mid
|
379
|
Haplogroup I-M253
|
5,761
|
185
|
B
|
Low
|
380
|
Gene nomenclature
|
5,720
|
184
|
Start
|
Mid
|
381
|
Non-coding DNA
|
5,716
|
184
|
C
|
Mid
|
382
|
Kin selection
|
5,710
|
184
|
GA
|
Mid
|
383
|
Genetic linkage
|
5,684
|
183
|
Start
|
High
|
384
|
Non-coding RNA
|
5,668
|
182
|
C
|
High
|
385
|
KRAS
|
5,662
|
182
|
C
|
Mid
|
386
|
Oligonucleotide
|
5,648
|
182
|
Start
|
Mid
|
387
|
Systems biology
|
5,625
|
181
|
C
|
High
|
388
|
Genetically modified food controversies
|
5,604
|
180
|
C
|
Mid
|
389
|
Taq polymerase
|
5,576
|
179
|
C
|
Mid
|
390
|
Phenotypic trait
|
5,530
|
178
|
Start
|
Mid
|
391
|
He Jiankui
|
5,521
|
178
|
B
|
Low
|
392
|
Modern synthesis (20th century)
|
5,517
|
177
|
GA
|
High
|
393
|
Guanosine triphosphate
|
5,498
|
177
|
Start
|
Mid
|
394
|
Medical genetics of Jews
|
5,496
|
177
|
Start
|
Low
|
395
|
Ras GTPase
|
5,476
|
176
|
B
|
High
|
396
|
Hershey–Chase experiment
|
5,475
|
176
|
C
|
High
|
397
|
Neo-Darwinism
|
5,470
|
176
|
Start
|
High
|
398
|
Breed
|
5,460
|
176
|
Start
|
Low
|
399
|
Kozak consensus sequence
|
5,457
|
176
|
Start
|
Mid
|
400
|
Intron
|
5,453
|
175
|
C
|
High
|
401
|
Haplogroup K (mtDNA)
|
5,447
|
175
|
Start
|
Low
|
402
|
Biological determinism
|
5,438
|
175
|
B
|
Mid
|
403
|
Haplotype
|
5,424
|
174
|
Start
|
High
|
404
|
Introduction to evolution
|
5,422
|
174
|
B
|
High
|
405
|
Cystic fibrosis transmembrane conductance regulator
|
5,413
|
174
|
C
|
Mid
|
406
|
Haplogroup T-M184
|
5,362
|
172
|
B
|
Low
|
407
|
Reproductive isolation
|
5,357
|
172
|
C
|
High
|
408
|
Somatic cell nuclear transfer
|
5,354
|
172
|
C
|
Mid
|
409
|
Gene flow
|
5,346
|
172
|
Start
|
High
|
410
|
Purebred
|
5,335
|
172
|
C
|
Low
|
411
|
Ribozyme
|
5,332
|
172
|
Start
|
High
|
412
|
Haplogroup Q-M242
|
5,329
|
171
|
C
|
Low
|
413
|
Disodium inosinate
|
5,324
|
171
|
Start
|
Low
|
414
|
Biomaterial
|
5,322
|
171
|
C
|
Low
|
415
|
Barr body
|
5,320
|
171
|
Start
|
High
|
416
|
Haplogroup R (Y-DNA)
|
5,319
|
171
|
Start
|
Low
|
417
|
Transgene
|
5,302
|
171
|
B
|
Mid
|
418
|
Flavivirus
|
5,283
|
170
|
B
|
Mid
|
419
|
Genetic history of the British Isles
|
5,273
|
170
|
C
|
Low
|
420
|
Nucleoside triphosphate
|
5,248
|
169
|
Start
|
High
|
421
|
Chromosome 2
|
5,228
|
168
|
C
|
Mid
|
422
|
Y-chromosomal Aaron
|
5,220
|
168
|
Start
|
Low
|
423
|
Genetic history of the Iberian Peninsula
|
5,157
|
166
|
Start
|
Low
|
424
|
F1 hybrid
|
5,146
|
166
|
Start
|
High
|
425
|
Introgression
|
5,083
|
163
|
Start
|
High
|
426
|
Hi-C (genomic analysis technique)
|
5,076
|
163
|
C
|
Low
|
427
|
Flavr Savr
|
5,069
|
163
|
Start
|
Unknown
|
428
|
Non-homologous end joining
|
5,017
|
161
|
C
|
Mid
|
429
|
Haplogroup A (Y-DNA)
|
4,997
|
161
|
C
|
Low
|
430
|
Adenosine diphosphate
|
4,987
|
160
|
C
|
Mid
|
431
|
Viral vector vaccine
|
4,986
|
160
|
Start
|
Low
|
432
|
Endogeny (biology)
|
4,970
|
160
|
Stub
|
Low
|
433
|
Bcl-2
|
4,963
|
160
|
B
|
Mid
|
434
|
Topoisomerase
|
4,960
|
160
|
C
|
High
|
435
|
Sheep farming
|
4,947
|
159
|
C
|
Low
|
436
|
TATA box
|
4,944
|
159
|
B
|
High
|
437
|
SARS-CoV-2 Delta variant
|
4,923
|
158
|
C
|
Low
|
438
|
Linkage disequilibrium
|
4,909
|
158
|
C
|
High
|
439
|
Sequence homology
|
4,908
|
158
|
C
|
Top
|
440
|
Apomorphy and synapomorphy
|
4,878
|
157
|
C
|
Low
|
441
|
Long non-coding RNA
|
4,850
|
156
|
C
|
Mid
|
442
|
Hepatitis D
|
4,848
|
156
|
C
|
Low
|
443
|
Start codon
|
4,840
|
156
|
Start
|
Top
|
444
|
Allele frequency
|
4,837
|
156
|
Start
|
Mid
|
445
|
Haplogroup O-M175
|
4,799
|
154
|
Start
|
Low
|
446
|
Behavioural genetics
|
4,776
|
154
|
GA
|
High
|
447
|
Frameshift mutation
|
4,774
|
154
|
B
|
High
|
448
|
Trisomy
|
4,750
|
153
|
Start
|
High
|
449
|
Humanized mouse
|
4,746
|
153
|
Start
|
Low
|
450
|
Nettie Stevens
|
4,745
|
153
|
B
|
Mid
|
451
|
Gene knockout
|
4,742
|
152
|
Start
|
Mid
|
452
|
Paternal age effect
|
4,742
|
152
|
C
|
Mid
|
453
|
Penetrance
|
4,715
|
152
|
C
|
High
|
454
|
Crossbreed
|
4,715
|
152
|
Start
|
Low
|
455
|
Directionality (molecular biology)
|
4,707
|
151
|
Start
|
High
|
456
|
Adenosine monophosphate
|
4,704
|
151
|
Start
|
Low
|
457
|
Sexual differentiation in humans
|
4,701
|
151
|
C
|
Mid
|
458
|
Haplogroup M (mtDNA)
|
4,700
|
151
|
Stub
|
Low
|
459
|
Molecular clock
|
4,696
|
151
|
C
|
High
|
460
|
Complementary DNA
|
4,689
|
151
|
Start
|
Mid
|
461
|
Genetic counseling
|
4,689
|
151
|
C
|
Mid
|
462
|
Sense (molecular biology)
|
4,687
|
151
|
C
|
High
|
463
|
Junk DNA
|
4,668
|
150
|
B
|
Mid
|
464
|
Maladaptation
|
4,667
|
150
|
Start
|
Low
|
465
|
History of eugenics
|
4,666
|
150
|
B
|
Low
|
466
|
Genetic history of the Middle East
|
4,653
|
150
|
C
|
Mid
|
467
|
Griffith's experiment
|
4,644
|
149
|
Start
|
Mid
|
468
|
Polytene chromosome
|
4,639
|
149
|
Start
|
Mid
|
469
|
Ancient DNA
|
4,631
|
149
|
C
|
Mid
|
470
|
Haplogroup R1
|
4,628
|
149
|
C
|
Low
|
471
|
Advanced maternal age
|
4,621
|
149
|
C
|
Mid
|
472
|
George Church (geneticist)
|
4,617
|
148
|
C
|
Low
|
473
|
Leigh syndrome
|
4,611
|
148
|
C
|
Low
|
474
|
Knockout mouse
|
4,595
|
148
|
C
|
Mid
|
475
|
Tongue rolling
|
4,592
|
148
|
Stub
|
Low
|
476
|
List of haplogroups of historic people
|
4,578
|
147
|
List
|
Low
|
477
|
Gene set enrichment analysis
|
4,569
|
147
|
C
|
Mid
|
478
|
Exome sequencing
|
4,563
|
147
|
C
|
High
|
479
|
STR analysis
|
4,554
|
146
|
Start
|
Low
|
480
|
Medical genetics
|
4,538
|
146
|
B
|
Mid
|
481
|
Bovine somatotropin
|
4,498
|
145
|
C
|
Low
|
482
|
Enhancer (genetics)
|
4,493
|
144
|
C
|
High
|
483
|
Phred quality score
|
4,477
|
144
|
Start
|
Low
|
484
|
Pedigree chart
|
4,457
|
143
|
Start
|
Mid
|
485
|
Dun gene
|
4,421
|
142
|
C
|
Low
|
486
|
Oligomer
|
4,418
|
142
|
Start
|
Low
|
487
|
Eric Lander
|
4,413
|
142
|
C
|
Low
|
488
|
Maurice Wilkins
|
4,403
|
142
|
B
|
High
|
489
|
Chromosome 1
|
4,395
|
141
|
Start
|
Low
|
490
|
Trp operon
|
4,358
|
140
|
C
|
Mid
|
491
|
Semiconservative replication
|
4,353
|
140
|
C
|
High
|
492
|
Pharmacogenomics
|
4,347
|
140
|
B
|
Mid
|
493
|
Signal peptide
|
4,346
|
140
|
Start
|
Mid
|
494
|
Preimplantation genetic diagnosis
|
4,342
|
140
|
B
|
Mid
|
495
|
Janaki Ammal
|
4,323
|
139
|
B
|
Low
|
496
|
Telegony (inheritance)
|
4,313
|
139
|
C
|
Low
|
497
|
GC-content
|
4,295
|
138
|
C
|
Mid
|
498
|
C57BL/6
|
4,285
|
138
|
Start
|
Low
|
499
|
Quantitative trait locus
|
4,282
|
138
|
C
|
High
|
500
|
Enzyme Commission number
|
4,279
|
138
|
Start
|
Low
|
|
Full category list
Categories within Genetics
|
|
|