Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Axolotl
|
188,694
|
6,289
|
C
|
High
|
2
|
Fibular hemimelia
|
133,448
|
4,448
|
Start
|
Low
|
3
|
DNA
|
88,232
|
2,941
|
FA
|
Top
|
4
|
Incest
|
82,924
|
2,764
|
C
|
Low
|
5
|
Eugenics
|
81,157
|
2,705
|
B
|
High
|
6
|
Prion
|
81,064
|
2,702
|
GA
|
Mid
|
7
|
Cancer
|
63,571
|
2,119
|
B
|
Top
|
8
|
Amino acid
|
61,474
|
2,049
|
GA
|
Top
|
9
|
Guinea pig
|
61,324
|
2,044
|
B
|
Low
|
10
|
Cystic fibrosis
|
56,635
|
1,887
|
B
|
High
|
11
|
Protein
|
53,979
|
1,799
|
GA
|
Top
|
12
|
Epigenetics
|
49,963
|
1,665
|
B
|
Top
|
13
|
Biodiversity
|
48,740
|
1,624
|
C
|
Mid
|
14
|
Blood type
|
47,159
|
1,571
|
B
|
High
|
15
|
Bayer
|
46,671
|
1,555
|
C
|
Low
|
16
|
Evolution
|
46,597
|
1,553
|
FA
|
Top
|
17
|
XY sex-determination system
|
46,355
|
1,545
|
C
|
High
|
18
|
Attachment theory
|
45,855
|
1,528
|
B
|
Mid
|
19
|
Enzyme
|
44,145
|
1,471
|
FA
|
Top
|
20
|
23andMe
|
44,135
|
1,471
|
C
|
Mid
|
21
|
Color blindness
|
43,266
|
1,442
|
B
|
Mid
|
22
|
Francis Collins
|
42,959
|
1,431
|
B
|
Mid
|
23
|
Gregor Mendel
|
41,879
|
1,395
|
B
|
High
|
24
|
Nicotinamide adenine dinucleotide
|
40,502
|
1,350
|
FA
|
Mid
|
25
|
Rosalind Franklin
|
38,952
|
1,298
|
B
|
High
|
26
|
Prader–Willi syndrome
|
38,748
|
1,291
|
B
|
Mid
|
27
|
Red hair
|
38,734
|
1,291
|
C
|
Mid
|
28
|
Chromosome
|
37,316
|
1,243
|
B
|
Top
|
29
|
Total fertility rate
|
37,258
|
1,241
|
C
|
Low
|
30
|
Adenosine triphosphate
|
37,214
|
1,240
|
C
|
High
|
31
|
Meiosis
|
36,975
|
1,232
|
C
|
Top
|
32
|
CRISPR
|
36,857
|
1,228
|
B
|
High
|
33
|
SARS-CoV-2
|
36,583
|
1,219
|
B
|
Top
|
34
|
Charcot–Marie–Tooth disease
|
36,403
|
1,213
|
C
|
Mid
|
35
|
Tetrasomy X
|
36,159
|
1,205
|
GA
|
Low
|
36
|
Scientific racism
|
34,367
|
1,145
|
C
|
Low
|
37
|
Cousin
|
31,855
|
1,061
|
Start
|
Low
|
38
|
Albinism
|
31,146
|
1,038
|
C
|
Low
|
39
|
Blue Fugates
|
30,921
|
1,030
|
Start
|
Low
|
40
|
Inbreeding
|
30,858
|
1,028
|
C
|
Low
|
41
|
Epicanthic fold
|
30,623
|
1,020
|
C
|
Low
|
42
|
Ribosome
|
30,433
|
1,014
|
B
|
Top
|
43
|
Last universal common ancestor
|
30,089
|
1,002
|
GA
|
Mid
|
44
|
Gigantism
|
29,842
|
994
|
B
|
High
|
45
|
Genetics
|
29,749
|
991
|
FA
|
Top
|
46
|
Human skin color
|
28,290
|
943
|
B
|
Mid
|
47
|
Polymerase chain reaction
|
28,260
|
942
|
B
|
High
|
48
|
Chimera (genetics)
|
28,158
|
938
|
B
|
Mid
|
49
|
James Watson
|
28,054
|
935
|
B
|
High
|
50
|
Consanguinity
|
27,912
|
930
|
C
|
Low
|
51
|
Birth defect
|
27,908
|
930
|
B
|
Mid
|
52
|
Nucleotide
|
27,451
|
915
|
C
|
Top
|
53
|
Gene
|
27,110
|
903
|
GA
|
Top
|
54
|
Wechsler Adult Intelligence Scale
|
26,773
|
892
|
C
|
Low
|
55
|
Lactose intolerance
|
26,743
|
891
|
B
|
Low
|
56
|
Cloning
|
26,700
|
890
|
B
|
Top
|
57
|
Pentasomy X
|
26,695
|
889
|
GA
|
Low
|
58
|
Blond
|
26,567
|
885
|
C
|
Low
|
59
|
RNA
|
26,316
|
877
|
GA
|
Top
|
60
|
Dominance (genetics)
|
26,238
|
874
|
C
|
Top
|
61
|
Svalbard Global Seed Vault
|
26,152
|
871
|
B
|
Mid
|
62
|
Early human migrations
|
25,875
|
862
|
B
|
Mid
|
63
|
Nucleic acid
|
25,790
|
859
|
C
|
Mid
|
64
|
Drosophila melanogaster
|
25,740
|
858
|
B
|
Top
|
65
|
XYY syndrome
|
25,577
|
852
|
B
|
Mid
|
66
|
Animal husbandry
|
25,498
|
849
|
GA
|
Mid
|
67
|
Friedreich's ataxia
|
25,494
|
849
|
GA
|
Mid
|
68
|
Hybrid (biology)
|
25,301
|
843
|
GA
|
High
|
69
|
Cleft lip and cleft palate
|
25,217
|
840
|
B
|
Low
|
70
|
Endogamy
|
24,685
|
822
|
Start
|
Low
|
71
|
Human Genome Project
|
24,495
|
816
|
B
|
Top
|
72
|
Estimates of historical world population
|
24,221
|
807
|
Start
|
Low
|
73
|
Japanese people
|
23,514
|
783
|
C
|
Low
|
74
|
RCCX
|
22,988
|
766
|
B
|
Mid
|
75
|
Jennifer Doudna
|
22,741
|
758
|
B
|
High
|
76
|
Genetic engineering
|
22,463
|
748
|
GA
|
Top
|
77
|
Mitochondrial Eve
|
22,179
|
739
|
B
|
Mid
|
78
|
DNA replication
|
22,155
|
738
|
B
|
Unknown
|
79
|
Genetically modified food
|
21,601
|
720
|
B
|
High
|
80
|
HeLa
|
21,484
|
716
|
C
|
Low
|
81
|
Leucism
|
21,256
|
708
|
Start
|
Low
|
82
|
Mutation
|
21,018
|
700
|
B
|
Top
|
83
|
Mendelian inheritance
|
20,524
|
684
|
C
|
High
|
84
|
Recent African origin of modern humans
|
20,149
|
671
|
C
|
Mid
|
85
|
Tuberous sclerosis
|
20,076
|
669
|
B
|
Mid
|
86
|
Human hair color
|
19,591
|
653
|
Start
|
Mid
|
87
|
Domesticated silver fox
|
19,541
|
651
|
C
|
Low
|
88
|
Sonic hedgehog protein
|
19,538
|
651
|
B
|
High
|
89
|
XX male syndrome
|
19,495
|
649
|
C
|
Low
|
90
|
Genetic studies of Jews
|
19,302
|
643
|
B
|
Mid
|
91
|
Francis Crick
|
19,172
|
639
|
B
|
High
|
92
|
Trisomy 18
|
18,785
|
626
|
B
|
Low
|
93
|
Phenotype
|
18,241
|
608
|
C
|
Top
|
94
|
Senescence
|
18,200
|
606
|
C
|
Low
|
95
|
XXXY syndrome
|
18,152
|
605
|
C
|
Low
|
96
|
Genetic disorder
|
18,006
|
600
|
B
|
Top
|
97
|
DNA and RNA codon tables
|
17,952
|
598
|
FL
|
High
|
98
|
M. S. Swaminathan
|
17,927
|
597
|
B
|
Low
|
99
|
Genetically modified organism
|
17,486
|
582
|
GA
|
Top
|
100
|
Y chromosome
|
17,480
|
582
|
B
|
High
|
101
|
CRISPR gene editing
|
17,300
|
576
|
B
|
Top
|
102
|
Haplogroup R1a
|
17,291
|
576
|
C
|
Low
|
103
|
Haplogroup R1b
|
17,276
|
575
|
C
|
Mid
|
104
|
Institutional racism
|
17,182
|
572
|
B
|
High
|
105
|
Messenger RNA
|
16,935
|
564
|
C
|
High
|
106
|
The Bell Curve
|
16,881
|
562
|
C
|
High
|
107
|
Cultivar
|
16,845
|
561
|
GA
|
Mid
|
108
|
Humanzee
|
16,712
|
557
|
C
|
Mid
|
109
|
Descent from Genghis Khan
|
16,697
|
556
|
C
|
Low
|
110
|
Mitochondrial DNA
|
16,421
|
547
|
B
|
High
|
111
|
William Shockley
|
15,902
|
530
|
B
|
Low
|
112
|
Landrace
|
15,673
|
522
|
C
|
Low
|
113
|
Allele
|
15,606
|
520
|
B
|
Top
|
114
|
Lectin
|
15,534
|
517
|
C
|
Mid
|
115
|
David Reich (geneticist)
|
15,496
|
516
|
C
|
Mid
|
116
|
Genetic code
|
15,445
|
514
|
GA
|
Top
|
117
|
Heredity
|
15,444
|
514
|
C
|
Top
|
118
|
Haplogroup
|
15,439
|
514
|
C
|
Mid
|
119
|
Brown hair
|
15,249
|
508
|
C
|
Mid
|
120
|
List of organisms by chromosome count
|
15,228
|
507
|
List
|
Low
|
121
|
Punnett square
|
15,134
|
504
|
C
|
Top
|
122
|
Human genome
|
15,113
|
503
|
C
|
High
|
123
|
Cat coat genetics
|
15,081
|
502
|
C
|
Mid
|
124
|
DNA methylation
|
14,889
|
496
|
B
|
High
|
125
|
Stephen Jay Gould
|
14,816
|
493
|
GA
|
Mid
|
126
|
Gamete
|
14,809
|
493
|
Start
|
Mid
|
127
|
Tay–Sachs disease
|
14,725
|
490
|
B
|
High
|
128
|
Population bottleneck
|
14,691
|
489
|
C
|
Mid
|
129
|
Transcription (biology)
|
14,671
|
489
|
B
|
Top
|
130
|
Incest taboo
|
14,668
|
488
|
C
|
Mid
|
131
|
DNA sequencing
|
14,639
|
487
|
C
|
Top
|
132
|
Phenylketonuria
|
14,576
|
485
|
B
|
Mid
|
133
|
Plasmid
|
14,533
|
484
|
C
|
High
|
134
|
Tetralogy of Fallot
|
14,532
|
484
|
C
|
Low
|
135
|
De-extinction
|
14,516
|
483
|
C
|
Low
|
136
|
Patau syndrome
|
14,091
|
469
|
C
|
Low
|
137
|
Plasmodium falciparum
|
13,849
|
461
|
B
|
Low
|
138
|
G. H. Hardy
|
13,751
|
458
|
C
|
Mid
|
139
|
Karyotype
|
13,531
|
451
|
C
|
Mid
|
140
|
Ploidy
|
13,456
|
448
|
C
|
High
|
141
|
Ronald Fisher
|
13,333
|
444
|
B
|
High
|
142
|
Homology (biology)
|
13,091
|
436
|
GA
|
High
|
143
|
Dravet syndrome
|
13,048
|
434
|
C
|
Low
|
144
|
Human Y-chromosome DNA haplogroup
|
12,989
|
432
|
C
|
Mid
|
145
|
DNA profiling
|
12,910
|
430
|
B
|
High
|
146
|
Genome
|
12,879
|
429
|
C
|
High
|
147
|
Telomere
|
12,822
|
427
|
C
|
Mid
|
148
|
Early European Farmers
|
12,810
|
427
|
C
|
Mid
|
149
|
Balaji Srinivasan
|
12,698
|
423
|
Start
|
Low
|
150
|
Domestic rabbit
|
12,661
|
422
|
GA
|
Low
|
151
|
Sex-determination system
|
12,605
|
420
|
C
|
Mid
|
152
|
Human–animal hybrid
|
12,520
|
417
|
C
|
Low
|
153
|
Nucleolus
|
12,299
|
409
|
Start
|
Mid
|
154
|
Von Hippel–Lindau disease
|
12,252
|
408
|
C
|
Mid
|
155
|
Polyploidy
|
12,236
|
407
|
B
|
High
|
156
|
Barbara McClintock
|
12,033
|
401
|
FA
|
High
|
157
|
Genetic drift
|
11,876
|
395
|
GA
|
High
|
158
|
Origin of SARS-CoV-2
|
11,870
|
395
|
C
|
Low
|
159
|
Atavism
|
11,852
|
395
|
C
|
Mid
|
160
|
Lactase
|
11,655
|
388
|
B
|
Mid
|
161
|
Ancient North Eurasian
|
11,619
|
387
|
C
|
Mid
|
162
|
Variants of SARS-CoV-2
|
11,552
|
385
|
C
|
Low
|
163
|
Hispanos of New Mexico
|
11,456
|
381
|
Start
|
Low
|
164
|
Selective breeding
|
11,427
|
380
|
C
|
Top
|
165
|
Gene therapy
|
11,219
|
373
|
B
|
High
|
166
|
Major histocompatibility complex
|
11,207
|
373
|
B
|
Mid
|
167
|
Freckle
|
11,147
|
371
|
Start
|
Low
|
168
|
Western Steppe Herders
|
11,136
|
371
|
C
|
Mid
|
169
|
Anthropometry
|
11,131
|
371
|
C
|
Low
|
170
|
Mosaic (genetics)
|
11,050
|
368
|
C
|
Mid
|
171
|
Hereditary haemochromatosis
|
10,894
|
363
|
B
|
Mid
|
172
|
Hardy–Weinberg principle
|
10,832
|
361
|
C
|
High
|
173
|
Citicoline
|
10,725
|
357
|
B
|
Low
|
174
|
Recombinant DNA
|
10,720
|
357
|
C
|
High
|
175
|
Haplogroup G-M201
|
10,716
|
357
|
Start
|
Low
|
176
|
Sexual selection
|
10,690
|
356
|
GA
|
Mid
|
177
|
Ventricular septal defect
|
10,689
|
356
|
C
|
Low
|
178
|
Exogamy
|
10,669
|
355
|
Start
|
Low
|
179
|
Congenital heart defect
|
10,669
|
355
|
C
|
Mid
|
180
|
Panthera hybrid
|
10,661
|
355
|
C
|
Mid
|
181
|
Western hunter-gatherer
|
10,643
|
354
|
C
|
Mid
|
182
|
Single-nucleotide polymorphism
|
10,381
|
346
|
C
|
High
|
183
|
Nazi eugenics
|
10,271
|
342
|
C
|
Mid
|
184
|
Impulsivity
|
10,155
|
338
|
B
|
Mid
|
185
|
Genotype
|
10,058
|
335
|
Start
|
Top
|
186
|
Biological engineering
|
10,058
|
335
|
C
|
High
|
187
|
Gene delivery
|
10,005
|
333
|
B
|
High
|
188
|
Heritability of IQ
|
9,987
|
332
|
C
|
Low
|
189
|
Genetics and archaeogenetics of South Asia
|
9,971
|
332
|
Start
|
Mid
|
190
|
He Jiankui affair
|
9,967
|
332
|
C
|
Low
|
191
|
Genetic testing
|
9,966
|
332
|
B
|
Top
|
192
|
Genentech
|
9,962
|
332
|
Start
|
Mid
|
193
|
HLA-B27
|
9,874
|
329
|
C
|
Low
|
194
|
Genetic history of Europe
|
9,821
|
327
|
Start
|
Low
|
195
|
Central dogma of molecular biology
|
9,783
|
326
|
C
|
Top
|
196
|
Base pair
|
9,728
|
324
|
C
|
Top
|
197
|
Eugenics in the United States
|
9,692
|
323
|
Start
|
Low
|
198
|
P53
|
9,683
|
322
|
B
|
High
|
199
|
Protein biosynthesis
|
9,542
|
318
|
B
|
Mid
|
200
|
Constriction ring syndrome
|
9,542
|
318
|
C
|
Low
|
201
|
Mebendazole
|
9,515
|
317
|
C
|
Mid
|
202
|
Chromosome abnormality
|
9,426
|
314
|
Start
|
High
|
203
|
Chédiak–Higashi syndrome
|
9,361
|
312
|
Start
|
Low
|
204
|
Transfer RNA
|
9,328
|
310
|
B
|
High
|
205
|
Auburn hair
|
9,292
|
309
|
Start
|
Low
|
206
|
Sanger sequencing
|
9,239
|
307
|
C
|
High
|
207
|
Hayflick limit
|
9,237
|
307
|
Start
|
Low
|
208
|
Hypoplastic left heart syndrome
|
9,206
|
306
|
C
|
Low
|
209
|
He Jiankui
|
9,178
|
305
|
B
|
Low
|
210
|
Sex chromosome
|
9,173
|
305
|
Start
|
High
|
211
|
Proteinogenic amino acid
|
9,145
|
304
|
C
|
High
|
212
|
Gene expression
|
9,140
|
304
|
B
|
Top
|
213
|
Black hair
|
9,108
|
303
|
Start
|
Mid
|
214
|
RNA world
|
9,077
|
302
|
C
|
Mid
|
215
|
Transgenesis
|
9,043
|
301
|
Redirect
|
Top
|
216
|
Nucleic acid double helix
|
8,949
|
298
|
C
|
Mid
|
217
|
Aneuploidy
|
8,891
|
296
|
B
|
High
|
218
|
Most recent common ancestor
|
8,870
|
295
|
B
|
Mid
|
219
|
X chromosome
|
8,838
|
294
|
B
|
Top
|
220
|
Single parent
|
8,836
|
294
|
B
|
Mid
|
221
|
Horizontal gene transfer
|
8,781
|
292
|
C
|
High
|
222
|
Translation (biology)
|
8,781
|
292
|
B
|
Top
|
223
|
Ectrodactyly
|
8,756
|
291
|
B
|
Mid
|
224
|
Ethnic groups of Japan
|
8,664
|
288
|
Start
|
Unknown
|
225
|
Transcription factor
|
8,660
|
288
|
B
|
High
|
226
|
Reverse transcription polymerase chain reaction
|
8,632
|
287
|
Start
|
Mid
|
227
|
Mitochondrial disease
|
8,549
|
284
|
C
|
Mid
|
228
|
Founder effect
|
8,548
|
284
|
C
|
High
|
229
|
Haplogroup H (mtDNA)
|
8,307
|
276
|
Start
|
Low
|
230
|
Stanley Norman Cohen
|
8,290
|
276
|
Start
|
Mid
|
231
|
Cyclic adenosine monophosphate
|
8,265
|
275
|
C
|
Mid
|
232
|
Synthetic biology
|
8,240
|
274
|
B
|
Mid
|
233
|
Lac operon
|
8,225
|
274
|
C
|
Mid
|
234
|
Telegony (inheritance)
|
8,141
|
271
|
C
|
Low
|
235
|
Data storage
|
8,131
|
271
|
Start
|
Low
|
236
|
NF-κB
|
8,111
|
270
|
C
|
High
|
237
|
Fertility
|
8,067
|
268
|
C
|
Mid
|
238
|
Chromatin
|
8,047
|
268
|
B
|
Mid
|
239
|
Blue rose
|
8,029
|
267
|
Start
|
Low
|
240
|
RNA splicing
|
8,023
|
267
|
C
|
Top
|
241
|
Atrial septal defect
|
7,950
|
265
|
B
|
Low
|
242
|
Zygosity
|
7,904
|
263
|
C
|
High
|
243
|
Nicotinamide adenine dinucleotide phosphate
|
7,710
|
257
|
Start
|
Mid
|
244
|
Genetic studies on Turkish people
|
7,630
|
254
|
Start
|
Low
|
245
|
Histone
|
7,621
|
254
|
C
|
Mid
|
246
|
Heterosis
|
7,615
|
253
|
C
|
High
|
247
|
Y-chromosomal Adam
|
7,603
|
253
|
C
|
High
|
248
|
Polymorphism (biology)
|
7,527
|
250
|
B
|
Low
|
249
|
Svante Pääbo
|
7,467
|
248
|
C
|
Low
|
250
|
Haplogroup J (Y-DNA)
|
7,464
|
248
|
Start
|
Low
|
251
|
Homologous chromosome
|
7,463
|
248
|
Start
|
High
|
252
|
Chin
|
7,447
|
248
|
C
|
Low
|
253
|
Error
|
7,441
|
248
|
Start
|
Mid
|
254
|
Leber's hereditary optic neuropathy
|
7,297
|
243
|
C
|
Mid
|
255
|
Dysgenics
|
7,267
|
242
|
Start
|
Low
|
256
|
Haplogroup J-M172
|
7,254
|
241
|
Start
|
Low
|
257
|
Methylation
|
7,214
|
240
|
C
|
Mid
|
258
|
Genomics
|
7,207
|
240
|
B
|
Top
|
259
|
Laboratory rat
|
7,190
|
239
|
C
|
Mid
|
260
|
Transposable element
|
7,124
|
237
|
C
|
High
|
261
|
Leigh syndrome
|
7,066
|
235
|
C
|
Low
|
262
|
Wnt signaling pathway
|
7,064
|
235
|
C
|
Mid
|
263
|
Haplogroup J-M267
|
7,007
|
233
|
C
|
Low
|
264
|
Somatic cell
|
6,986
|
232
|
Start
|
Mid
|
265
|
Real-time polymerase chain reaction
|
6,969
|
232
|
C
|
Mid
|
266
|
MicroRNA
|
6,932
|
231
|
B
|
Top
|
267
|
J. B. S. Haldane
|
6,913
|
230
|
C
|
Low
|
268
|
Hershey–Chase experiment
|
6,912
|
230
|
C
|
High
|
269
|
Designer baby
|
6,865
|
228
|
B
|
High
|
270
|
Autosome
|
6,852
|
228
|
Start
|
Top
|
271
|
Genetic recombination
|
6,843
|
228
|
C
|
High
|
272
|
Pedigree collapse
|
6,834
|
227
|
Start
|
Low
|
273
|
Sex-determining region Y protein
|
6,801
|
226
|
C
|
Low
|
274
|
Infantile epileptic spasms syndrome
|
6,756
|
225
|
C
|
Low
|
275
|
DNA polymerase
|
6,750
|
225
|
C
|
Top
|
276
|
Uterus didelphys
|
6,734
|
224
|
Start
|
Low
|
277
|
Monoamine oxidase A
|
6,733
|
224
|
C
|
Mid
|
278
|
DNA repair
|
6,715
|
223
|
C
|
High
|
279
|
Human mitochondrial DNA haplogroup
|
6,701
|
223
|
Start
|
Low
|
280
|
Whole genome sequencing
|
6,654
|
221
|
B
|
Top
|
281
|
Haplogroup E-M215
|
6,653
|
221
|
C
|
Low
|
282
|
Epistasis
|
6,609
|
220
|
B
|
High
|
283
|
Shyness
|
6,607
|
220
|
B
|
Low
|
284
|
Twin study
|
6,532
|
217
|
B
|
High
|
285
|
Webbed toes
|
6,515
|
217
|
Start
|
Low
|
286
|
Haplogroup L-M20
|
6,452
|
215
|
Start
|
Low
|
287
|
Phosphorylation
|
6,412
|
213
|
C
|
High
|
288
|
Chromosomal crossover
|
6,410
|
213
|
C
|
High
|
289
|
Haplogroup U
|
6,404
|
213
|
Start
|
Mid
|
290
|
List of genetic disorders
|
6,382
|
212
|
List
|
High
|
291
|
5α-Reductase 2 deficiency
|
6,371
|
212
|
B
|
Low
|
292
|
BRCA1
|
6,347
|
211
|
C
|
High
|
293
|
VACTERL association
|
6,307
|
210
|
Start
|
Mid
|
294
|
Laboratory mouse
|
6,289
|
209
|
B
|
Low
|
295
|
Patent ductus arteriosus
|
6,258
|
208
|
Start
|
Mid
|
296
|
HER2
|
6,255
|
208
|
C
|
Mid
|
297
|
Illumina, Inc.
|
6,224
|
207
|
C
|
Low
|
298
|
Eastern hunter-gatherer
|
6,204
|
206
|
C
|
Mid
|
299
|
Promoter (genetics)
|
6,203
|
206
|
Start
|
Mid
|
300
|
Genetically modified crops
|
6,200
|
206
|
B
|
High
|
301
|
Parent
|
6,129
|
204
|
C
|
High
|
302
|
Chargaff's rules
|
6,095
|
203
|
Start
|
Low
|
303
|
Reverse transcriptase
|
6,065
|
202
|
B
|
High
|
304
|
Telomerase
|
6,051
|
201
|
B
|
High
|
305
|
Neanderthal genetics
|
6,045
|
201
|
C
|
High
|
306
|
Non-Mendelian inheritance
|
6,012
|
200
|
C
|
Mid
|
307
|
16S ribosomal RNA
|
6,008
|
200
|
C
|
High
|
308
|
Purebred
|
6,002
|
200
|
C
|
Low
|
309
|
Coefficient of relationship
|
5,999
|
199
|
C
|
Low
|
310
|
Post-translational modification
|
5,990
|
199
|
Start
|
High
|
311
|
RNA polymerase
|
5,985
|
199
|
C
|
Top
|
312
|
CpG site
|
5,984
|
199
|
C
|
Mid
|
313
|
Griffith's experiment
|
5,975
|
199
|
Start
|
Mid
|
314
|
XXYY syndrome
|
5,970
|
199
|
Start
|
Low
|
315
|
List of redheads
|
5,967
|
198
|
List
|
Low
|
316
|
Photo 51
|
5,964
|
198
|
Start
|
Low
|
317
|
Heritability of autism
|
5,932
|
197
|
Start
|
Mid
|
318
|
Uracil
|
5,909
|
196
|
Start
|
Mid
|
319
|
Open reading frame
|
5,909
|
196
|
Start
|
Mid
|
320
|
Oncogene
|
5,894
|
196
|
C
|
High
|
321
|
Haplogroup N-M231
|
5,844
|
194
|
Start
|
Low
|
322
|
RNA interference
|
5,811
|
193
|
FA
|
Top
|
323
|
Trisomy
|
5,787
|
192
|
Start
|
High
|
324
|
MHC class I
|
5,773
|
192
|
C
|
Mid
|
325
|
Mathematical and theoretical biology
|
5,759
|
191
|
C
|
Low
|
326
|
Colour wheel theory of love
|
5,756
|
191
|
Stub
|
Low
|
327
|
Genetic history of Egypt
|
5,743
|
191
|
C
|
Low
|
328
|
DNA evidence in the O. J. Simpson murder case
|
5,726
|
190
|
B
|
Low
|
329
|
Zebrafish
|
5,712
|
190
|
B
|
Mid
|
330
|
George Church (geneticist)
|
5,711
|
190
|
C
|
Low
|
331
|
Genetic history of the British Isles
|
5,700
|
190
|
C
|
Low
|
332
|
Haplogroup I-M170
|
5,689
|
189
|
B
|
Low
|
333
|
The Population Bomb
|
5,672
|
189
|
B
|
Low
|
334
|
MHC class II
|
5,670
|
189
|
C
|
Mid
|
335
|
Phenotypic trait
|
5,658
|
188
|
Start
|
Mid
|
336
|
Genetic diversity
|
5,632
|
187
|
C
|
Mid
|
337
|
Okazaki fragments
|
5,631
|
187
|
B
|
High
|
338
|
Haplogroup I-M438
|
5,617
|
187
|
Start
|
Low
|
339
|
Sampling bias
|
5,591
|
186
|
C
|
Low
|
340
|
Oogenesis
|
5,587
|
186
|
C
|
High
|
341
|
Locus (genetics)
|
5,513
|
183
|
Start
|
Mid
|
342
|
Dwarf cat
|
5,508
|
183
|
Start
|
Low
|
343
|
Fitness (biology)
|
5,478
|
182
|
C
|
Mid
|
344
|
Maladaptation
|
5,474
|
182
|
Start
|
Low
|
345
|
Epidermal growth factor receptor
|
5,460
|
182
|
C
|
Mid
|
346
|
X-linked recessive inheritance
|
5,444
|
181
|
Start
|
Mid
|
347
|
GloFish
|
5,424
|
180
|
C
|
Mid
|
348
|
Ruth Benedict
|
5,393
|
179
|
C
|
Low
|
349
|
Disodium inosinate
|
5,364
|
178
|
Start
|
Low
|
350
|
Hox gene
|
5,349
|
178
|
C
|
High
|
351
|
Nucleic acid sequence
|
5,330
|
177
|
C
|
High
|
352
|
Flavin adenine dinucleotide
|
5,328
|
177
|
B
|
Low
|
353
|
Genealogical DNA test
|
5,301
|
176
|
C
|
Mid
|
354
|
Stop codon
|
5,239
|
174
|
Start
|
High
|
355
|
Haplogroup I-M253
|
5,231
|
174
|
B
|
Low
|
356
|
Chromosomal translocation
|
5,220
|
174
|
Start
|
High
|
357
|
Personalized medicine
|
5,209
|
173
|
B
|
Mid
|
358
|
Pleiotropy
|
5,192
|
173
|
C
|
High
|
359
|
Directionality (molecular biology)
|
5,189
|
172
|
Start
|
High
|
360
|
Model organism
|
5,188
|
172
|
B
|
Mid
|
361
|
Allopatric speciation
|
5,185
|
172
|
B
|
Low
|
362
|
Centromere
|
5,129
|
170
|
C
|
Mid
|
363
|
Modern synthesis (20th century)
|
5,105
|
170
|
GA
|
High
|
364
|
Plant breeding
|
5,089
|
169
|
C
|
High
|
365
|
Factor VIII
|
5,085
|
169
|
Start
|
Low
|
366
|
Sex linkage
|
5,072
|
169
|
Start
|
High
|
367
|
Isoelectric point
|
5,066
|
168
|
C
|
Mid
|
368
|
Regulation of gene expression
|
5,056
|
168
|
C
|
High
|
369
|
Sexual selection in humans
|
5,053
|
168
|
C
|
Low
|
370
|
Biopolymer
|
5,039
|
167
|
C
|
Mid
|
371
|
Transduction (genetics)
|
5,030
|
167
|
C
|
High
|
372
|
Racial hygiene
|
5,026
|
167
|
C
|
Low
|
373
|
Genetic memory (psychology)
|
5,000
|
166
|
Start
|
Low
|
374
|
Genomic imprinting
|
4,991
|
166
|
C
|
High
|
375
|
Aniridia
|
4,983
|
166
|
C
|
Low
|
376
|
Genome editing
|
4,970
|
165
|
C
|
High
|
377
|
Cre-Lox recombination
|
4,942
|
164
|
C
|
Mid
|
378
|
Inbreeding depression
|
4,914
|
163
|
C
|
Low
|
379
|
Causes of cancer
|
4,913
|
163
|
B
|
Mid
|
380
|
Haplogroup R (Y-DNA)
|
4,905
|
163
|
Start
|
Low
|
381
|
Fluorescence in situ hybridization
|
4,887
|
162
|
B
|
Mid
|
382
|
Bacterial conjugation
|
4,862
|
162
|
C
|
High
|
383
|
Cas9
|
4,816
|
160
|
C
|
Mid
|
384
|
Alternative splicing
|
4,805
|
160
|
B
|
High
|
385
|
ZW sex-determination system
|
4,796
|
159
|
C
|
Mid
|
386
|
Advanced maternal age
|
4,773
|
159
|
C
|
Mid
|
387
|
God gene
|
4,734
|
157
|
Start
|
Mid
|
388
|
Genetic history of the Iberian Peninsula
|
4,730
|
157
|
Start
|
Low
|
389
|
Medical genetics of Jews
|
4,722
|
157
|
Start
|
Low
|
390
|
MELAS syndrome
|
4,713
|
157
|
C
|
Low
|
391
|
Kozak consensus sequence
|
4,701
|
156
|
Start
|
Mid
|
392
|
46,XX/46,XY
|
4,692
|
156
|
C
|
Low
|
393
|
Systems biology
|
4,681
|
156
|
C
|
High
|
394
|
Biological determinism
|
4,661
|
155
|
GA
|
Mid
|
395
|
Heritability
|
4,655
|
155
|
C
|
High
|
396
|
Genetic counseling
|
4,616
|
153
|
C
|
Mid
|
397
|
Flavivirus
|
4,608
|
153
|
B
|
Mid
|
398
|
Chromosome 21
|
4,607
|
153
|
Start
|
Mid
|
399
|
Coefficient of inbreeding
|
4,600
|
153
|
Start
|
Low
|
400
|
Population genetics
|
4,591
|
153
|
C
|
Top
|
401
|
Adeno-associated virus
|
4,586
|
152
|
B
|
Low
|
402
|
Paternal age effect
|
4,578
|
152
|
C
|
Mid
|
403
|
Apomorphy and synapomorphy
|
4,569
|
152
|
C
|
Low
|
404
|
Myc
|
4,565
|
152
|
C
|
High
|
405
|
Hi-C (genomic analysis technique)
|
4,535
|
151
|
C
|
Low
|
406
|
Barr body
|
4,505
|
150
|
Start
|
High
|
407
|
Medical genetics
|
4,492
|
149
|
B
|
Mid
|
408
|
Genome-wide association study
|
4,489
|
149
|
GA
|
Top
|
409
|
Zellweger syndrome
|
4,487
|
149
|
Start
|
Low
|
410
|
Adenosine diphosphate
|
4,484
|
149
|
C
|
Mid
|
411
|
Eric Lander
|
4,458
|
148
|
C
|
Low
|
412
|
List of unusual biological names
|
4,436
|
147
|
List
|
Low
|
413
|
Breed
|
4,434
|
147
|
Start
|
Low
|
414
|
Homologous recombination
|
4,376
|
145
|
GA
|
High
|
415
|
X-inactivation
|
4,368
|
145
|
B
|
High
|
416
|
Endogeny (biology)
|
4,356
|
145
|
Stub
|
Low
|
417
|
Genetic variation
|
4,336
|
144
|
Start
|
High
|
418
|
List of haplogroups of historic people
|
4,332
|
144
|
List
|
Low
|
419
|
Human genetic variation
|
4,317
|
143
|
C
|
High
|
420
|
Janaki Ammal
|
4,305
|
143
|
B
|
Low
|
421
|
Introduction to evolution
|
4,295
|
143
|
B
|
High
|
422
|
Wiedemann–Steiner syndrome
|
4,288
|
142
|
Stub
|
Low
|
423
|
Haplotype
|
4,285
|
142
|
Start
|
High
|
424
|
F1 hybrid
|
4,279
|
142
|
Start
|
High
|
425
|
Y-DNA haplogroups in populations of Europe
|
4,259
|
141
|
List
|
Mid
|
426
|
Lydia Fairchild
|
4,250
|
141
|
Stub
|
Unknown
|
427
|
Adenosine monophosphate
|
4,224
|
140
|
Start
|
Low
|
428
|
JAK-STAT signaling pathway
|
4,222
|
140
|
B
|
Mid
|
429
|
Behavioural genetics
|
4,207
|
140
|
GA
|
High
|
430
|
Genetic transformation
|
4,185
|
139
|
B
|
Top
|
431
|
Maurice Wilkins
|
4,164
|
138
|
B
|
High
|
432
|
Haplogroup Q-M242
|
4,120
|
137
|
C
|
Low
|
433
|
Operon
|
4,108
|
136
|
B
|
Mid
|
434
|
Gene nomenclature
|
4,104
|
136
|
Start
|
Mid
|
435
|
Tongue rolling
|
4,079
|
135
|
Stub
|
Low
|
436
|
Haplogroup A (Y-DNA)
|
4,061
|
135
|
C
|
Low
|
437
|
Boar–pig hybrid
|
4,053
|
135
|
Stub
|
Low
|
438
|
Intron
|
4,039
|
134
|
C
|
High
|
439
|
Meselson–Stahl experiment
|
4,038
|
134
|
Start
|
Mid
|
440
|
Haplogroup R1
|
4,029
|
134
|
C
|
Low
|
441
|
Dun gene
|
4,028
|
134
|
C
|
Low
|
442
|
Ribozyme
|
4,020
|
134
|
Start
|
High
|
443
|
Bovine somatotropin
|
4,004
|
133
|
C
|
Low
|
444
|
SARS-CoV-2 Delta variant
|
3,982
|
132
|
C
|
Low
|
445
|
Haplogroup O-M175
|
3,970
|
132
|
Start
|
Low
|
446
|
Oligomer
|
3,957
|
131
|
Start
|
Low
|
447
|
Ancient DNA
|
3,949
|
131
|
C
|
Mid
|
448
|
Enzyme Commission number
|
3,877
|
129
|
Start
|
Low
|
449
|
Tumor suppressor gene
|
3,866
|
128
|
Start
|
High
|
450
|
Atomic gardening
|
3,857
|
128
|
C
|
Low
|
451
|
Haplogroup T-M184
|
3,837
|
127
|
B
|
Low
|
452
|
Microsatellite
|
3,820
|
127
|
C
|
Mid
|
453
|
Non-coding DNA
|
3,819
|
127
|
C
|
Mid
|
454
|
Kin selection
|
3,806
|
126
|
GA
|
Mid
|
455
|
Humanized mouse
|
3,806
|
126
|
Start
|
Low
|
456
|
Crossbreed
|
3,801
|
126
|
Start
|
Low
|
457
|
DNA extraction
|
3,797
|
126
|
Start
|
Mid
|
458
|
Hepatitis D
|
3,779
|
125
|
C
|
Low
|
459
|
Chromosome 2
|
3,769
|
125
|
C
|
Mid
|
460
|
Non-coding RNA
|
3,768
|
125
|
C
|
High
|
461
|
Phred quality score
|
3,766
|
125
|
Start
|
Low
|
462
|
Haplogroup E-M96
|
3,760
|
125
|
Start
|
Low
|
463
|
Sheep farming
|
3,739
|
124
|
C
|
Low
|
464
|
Biomaterial
|
3,737
|
124
|
C
|
Low
|
465
|
GC-content
|
3,735
|
124
|
C
|
Mid
|
466
|
Topoisomerase
|
3,731
|
124
|
C
|
High
|
467
|
Nucleoid
|
3,710
|
123
|
B
|
Mid
|
468
|
Penetrance
|
3,703
|
123
|
C
|
High
|
469
|
Single-cell sequencing
|
3,697
|
123
|
C
|
High
|
470
|
Cold Spring Harbor Laboratory
|
3,693
|
123
|
Start
|
Mid
|
471
|
Y-chromosomal Aaron
|
3,683
|
122
|
Start
|
Low
|
472
|
Taq polymerase
|
3,681
|
122
|
C
|
Mid
|
473
|
John Bell (physician)
|
3,667
|
122
|
C
|
Unknown
|
474
|
DNA supercoil
|
3,659
|
121
|
C
|
Mid
|
475
|
KRAS
|
3,658
|
121
|
C
|
Mid
|
476
|
Guanosine triphosphate
|
3,653
|
121
|
Start
|
Mid
|
477
|
Junk DNA
|
3,643
|
121
|
B
|
Mid
|
478
|
Cystic fibrosis transmembrane conductance regulator
|
3,641
|
121
|
C
|
Mid
|
479
|
Genetic history of the Middle East
|
3,632
|
121
|
C
|
Mid
|
480
|
Bcl-2
|
3,594
|
119
|
B
|
Mid
|
481
|
Haplogroup M (mtDNA)
|
3,591
|
119
|
Stub
|
Low
|
482
|
Pedigree chart
|
3,590
|
119
|
Start
|
Mid
|
483
|
Linkage disequilibrium
|
3,587
|
119
|
C
|
High
|
484
|
Exon
|
3,579
|
119
|
C
|
Top
|
485
|
Molecular cloning
|
3,576
|
119
|
C
|
High
|
486
|
45,X/46,XY mosaicism
|
3,573
|
119
|
C
|
Low
|
487
|
Heterochromatin
|
3,572
|
119
|
C
|
Mid
|
488
|
The Kallikak Family
|
3,549
|
118
|
C
|
Unknown
|
489
|
Genetically modified food controversies
|
3,547
|
118
|
C
|
Mid
|
490
|
Mutant
|
3,546
|
118
|
Start
|
Low
|
491
|
Preimplantation genetic diagnosis
|
3,539
|
117
|
B
|
Mid
|
492
|
TATA box
|
3,535
|
117
|
B
|
High
|
493
|
MERRF syndrome
|
3,530
|
117
|
C
|
Low
|
494
|
Sense (molecular biology)
|
3,528
|
117
|
C
|
High
|
495
|
Nucleoside triphosphate
|
3,526
|
117
|
Start
|
High
|
496
|
Oligonucleotide
|
3,508
|
116
|
Start
|
Mid
|
497
|
Gene flow
|
3,502
|
116
|
Start
|
High
|
498
|
History of eugenics
|
3,468
|
115
|
B
|
Low
|
499
|
Neo-Darwinism
|
3,466
|
115
|
Start
|
High
|
500
|
Ras GTPase
|
3,452
|
115
|
B
|
High
|