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List
Period: 2024-07-01 to 2024-07-31
Total views: 8,345,711
Updated: 17:39, 8 August 2024 (UTC)
Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Axolotl
|
185,108
|
5,971
|
C
|
High
|
2
|
Rosalind Franklin
|
91,539
|
2,952
|
B
|
High
|
3
|
Incest
|
88,430
|
2,852
|
C
|
Low
|
4
|
Eugenics
|
87,009
|
2,806
|
B
|
High
|
5
|
Prion
|
78,739
|
2,539
|
GA
|
Mid
|
6
|
DNA
|
68,164
|
2,198
|
FA
|
Top
|
7
|
Mitochondrial Eve
|
66,766
|
2,153
|
B
|
Mid
|
8
|
Guinea pig
|
65,033
|
2,097
|
B
|
Low
|
9
|
Cystic fibrosis
|
64,233
|
2,072
|
B
|
High
|
10
|
Cancer
|
61,066
|
1,969
|
B
|
Top
|
11
|
Bayer
|
54,890
|
1,770
|
C
|
Low
|
12
|
Amino acid
|
51,765
|
1,669
|
GA
|
Top
|
13
|
Blood type
|
50,505
|
1,629
|
B
|
High
|
14
|
Prader–Willi syndrome
|
50,342
|
1,623
|
B
|
Mid
|
15
|
Protein
|
48,622
|
1,568
|
GA
|
Top
|
16
|
Color blindness
|
45,283
|
1,460
|
B
|
Mid
|
17
|
Attachment theory
|
44,644
|
1,440
|
B
|
Mid
|
18
|
Epigenetics
|
42,448
|
1,369
|
B
|
Top
|
19
|
Meiosis
|
40,539
|
1,307
|
C
|
Top
|
20
|
Evolution
|
40,266
|
1,298
|
FA
|
Top
|
21
|
Red hair
|
40,001
|
1,290
|
C
|
Mid
|
22
|
XY sex-determination system
|
39,815
|
1,284
|
C
|
High
|
23
|
Nicotinamide adenine dinucleotide
|
38,364
|
1,237
|
FA
|
Mid
|
24
|
Enzyme
|
37,381
|
1,205
|
FA
|
Top
|
25
|
SARS-CoV-2
|
37,266
|
1,202
|
B
|
Top
|
26
|
Chimera (genetics)
|
36,727
|
1,184
|
B
|
Mid
|
27
|
Cousin
|
36,695
|
1,183
|
Start
|
Low
|
28
|
Fibular hemimelia
|
36,510
|
1,177
|
Start
|
Low
|
29
|
Total fertility rate
|
36,020
|
1,161
|
C
|
Low
|
30
|
Consanguinity
|
35,473
|
1,144
|
C
|
Low
|
31
|
Biodiversity
|
35,088
|
1,131
|
C
|
Mid
|
32
|
Blue Fugates
|
34,581
|
1,115
|
Start
|
Low
|
33
|
Inbreeding
|
34,366
|
1,108
|
C
|
Low
|
34
|
Human skin color
|
34,316
|
1,106
|
B
|
Mid
|
35
|
Scientific racism
|
33,243
|
1,072
|
C
|
Low
|
36
|
Albinism
|
32,751
|
1,056
|
C
|
Low
|
37
|
Last universal common ancestor
|
32,688
|
1,054
|
GA
|
Mid
|
38
|
Svalbard Global Seed Vault
|
32,646
|
1,053
|
B
|
Mid
|
39
|
Adenosine triphosphate
|
32,551
|
1,050
|
C
|
High
|
40
|
CRISPR
|
32,127
|
1,036
|
B
|
High
|
41
|
Friedreich's ataxia
|
31,815
|
1,026
|
GA
|
Mid
|
42
|
Chromosome
|
31,147
|
1,004
|
B
|
Top
|
43
|
Epicanthic fold
|
31,046
|
1,001
|
C
|
Low
|
44
|
Charcot–Marie–Tooth disease
|
29,956
|
966
|
C
|
Mid
|
45
|
Genetics
|
29,489
|
951
|
FA
|
Top
|
46
|
James Watson
|
29,484
|
951
|
B
|
High
|
47
|
Gregor Mendel
|
29,456
|
950
|
B
|
High
|
48
|
XYY syndrome
|
28,356
|
914
|
B
|
Mid
|
49
|
Blond
|
27,110
|
874
|
C
|
Low
|
50
|
Lactose intolerance
|
26,910
|
868
|
B
|
Low
|
51
|
Polymerase chain reaction
|
26,687
|
860
|
B
|
High
|
52
|
Endogamy
|
26,360
|
850
|
Start
|
Low
|
53
|
Cleft lip and cleft palate
|
26,188
|
844
|
B
|
Low
|
54
|
Estimates of historical world population
|
25,721
|
829
|
Start
|
Low
|
55
|
Birth defect
|
25,307
|
816
|
B
|
Mid
|
56
|
Dominance (genetics)
|
25,150
|
811
|
C
|
Top
|
57
|
Animal husbandry
|
25,100
|
809
|
GA
|
Mid
|
58
|
Gigantism
|
25,024
|
807
|
B
|
High
|
59
|
Hybrid (biology)
|
24,950
|
804
|
GA
|
High
|
60
|
Gene
|
23,951
|
772
|
GA
|
Top
|
61
|
Japanese people
|
23,563
|
760
|
C
|
Low
|
62
|
Genetic studies of Jews
|
22,957
|
740
|
B
|
Mid
|
63
|
Pentasomy X
|
22,872
|
737
|
GA
|
Low
|
64
|
Genetically modified food
|
22,802
|
735
|
B
|
High
|
65
|
Drosophila melanogaster
|
22,321
|
720
|
B
|
Top
|
66
|
M. S. Swaminathan
|
22,239
|
717
|
B
|
Low
|
67
|
Wechsler Adult Intelligence Scale
|
22,060
|
711
|
C
|
Low
|
68
|
Human Genome Project
|
21,833
|
704
|
B
|
Top
|
69
|
Early human migrations
|
21,616
|
697
|
B
|
Mid
|
70
|
Sonic hedgehog protein
|
21,601
|
696
|
B
|
High
|
71
|
Cat coat genetics
|
21,566
|
695
|
C
|
Mid
|
72
|
Recent African origin of modern humans
|
21,162
|
682
|
C
|
Mid
|
73
|
RNA
|
20,852
|
672
|
GA
|
Top
|
74
|
Human hair color
|
20,330
|
655
|
Start
|
Mid
|
75
|
Ribosome
|
20,071
|
647
|
B
|
Top
|
76
|
HeLa
|
19,962
|
643
|
C
|
Low
|
77
|
Genetic engineering
|
19,676
|
634
|
GA
|
Top
|
78
|
Mutation
|
19,498
|
628
|
B
|
Top
|
79
|
Senescence
|
19,303
|
622
|
C
|
Low
|
80
|
Nucleotide
|
19,250
|
620
|
C
|
Top
|
81
|
Population bottleneck
|
19,124
|
616
|
C
|
Mid
|
82
|
Y chromosome
|
18,680
|
602
|
B
|
High
|
83
|
Haplogroup R1a
|
18,664
|
602
|
C
|
Low
|
84
|
Haplogroup R1b
|
18,655
|
601
|
C
|
Mid
|
85
|
Trisomy 18
|
18,467
|
595
|
B
|
Low
|
86
|
DNA replication
|
18,436
|
594
|
B
|
Unknown
|
87
|
Mitochondrial DNA
|
18,346
|
591
|
B
|
High
|
88
|
Descent from Genghis Khan
|
18,229
|
588
|
C
|
Low
|
89
|
XX male syndrome
|
18,074
|
583
|
C
|
Low
|
90
|
Aniridia
|
18,071
|
582
|
C
|
Low
|
91
|
Genetic disorder
|
17,937
|
578
|
B
|
Top
|
92
|
Humanzee
|
17,813
|
574
|
C
|
Mid
|
93
|
Cultivar
|
17,229
|
555
|
GA
|
Mid
|
94
|
Phenotype
|
16,985
|
547
|
C
|
Top
|
95
|
Balaji Srinivasan
|
16,646
|
536
|
Start
|
Low
|
96
|
The Bell Curve
|
16,594
|
535
|
C
|
High
|
97
|
Haplogroup
|
16,583
|
534
|
C
|
Mid
|
98
|
23andMe
|
16,332
|
526
|
C
|
Mid
|
99
|
Genetically modified organism
|
16,167
|
521
|
GA
|
Top
|
100
|
Mendelian inheritance
|
16,117
|
519
|
C
|
High
|
101
|
XXXY syndrome
|
16,103
|
519
|
C
|
Low
|
102
|
Francis Crick
|
16,053
|
517
|
B
|
High
|
103
|
Landrace
|
15,892
|
512
|
C
|
Low
|
104
|
Nucleic acid
|
15,783
|
509
|
C
|
Mid
|
105
|
Leucism
|
15,777
|
508
|
Start
|
Low
|
106
|
Cloning
|
15,745
|
507
|
B
|
Top
|
107
|
Sex-determination system
|
15,736
|
507
|
C
|
Mid
|
108
|
Domesticated silver fox
|
15,670
|
505
|
C
|
Low
|
109
|
Incest taboo
|
15,618
|
503
|
C
|
Mid
|
110
|
Ancient North Eurasian
|
15,232
|
491
|
C
|
Mid
|
111
|
Tuberous sclerosis
|
15,165
|
489
|
B
|
Mid
|
112
|
CRISPR gene editing
|
15,002
|
483
|
B
|
Top
|
113
|
Gamete
|
14,930
|
481
|
Start
|
Mid
|
114
|
DNA profiling
|
14,533
|
468
|
B
|
High
|
115
|
Plasmodium falciparum
|
14,485
|
467
|
B
|
Low
|
116
|
Messenger RNA
|
14,175
|
457
|
C
|
High
|
117
|
DNA sequencing
|
14,116
|
455
|
C
|
Top
|
118
|
Human genome
|
14,028
|
452
|
C
|
High
|
119
|
Allele
|
13,929
|
449
|
B
|
Top
|
120
|
Origin of SARS-CoV-2
|
13,854
|
446
|
C
|
Low
|
121
|
Lectin
|
13,768
|
444
|
C
|
Mid
|
122
|
Tetralogy of Fallot
|
13,760
|
443
|
C
|
Low
|
123
|
Transcription (biology)
|
13,696
|
441
|
B
|
Top
|
124
|
Punnett square
|
13,691
|
441
|
C
|
Top
|
125
|
DNA and RNA codon tables
|
13,656
|
440
|
FL
|
High
|
126
|
Heredity
|
13,631
|
439
|
C
|
Top
|
127
|
DNA methylation
|
13,578
|
438
|
B
|
High
|
128
|
Phenylketonuria
|
13,534
|
436
|
B
|
Mid
|
129
|
Human Y-chromosome DNA haplogroup
|
13,468
|
434
|
C
|
Mid
|
130
|
Hereditary haemochromatosis
|
13,429
|
433
|
B
|
Mid
|
131
|
Plasmid
|
13,369
|
431
|
C
|
High
|
132
|
Early European Farmers
|
13,082
|
422
|
C
|
Mid
|
133
|
Human–animal hybrid
|
13,066
|
421
|
C
|
Low
|
134
|
William Shockley
|
12,976
|
418
|
B
|
Low
|
135
|
X chromosome
|
12,965
|
418
|
B
|
Top
|
136
|
Stephen Jay Gould
|
12,944
|
417
|
GA
|
Mid
|
137
|
Karyotype
|
12,847
|
414
|
C
|
Mid
|
138
|
Brown hair
|
12,838
|
414
|
C
|
Mid
|
139
|
Institutional racism
|
12,746
|
411
|
B
|
High
|
140
|
Freckle
|
12,737
|
410
|
Start
|
Low
|
141
|
Tay–Sachs disease
|
12,695
|
409
|
B
|
High
|
142
|
De-extinction
|
12,664
|
408
|
C
|
Low
|
143
|
Ploidy
|
12,645
|
407
|
C
|
High
|
144
|
Patau syndrome
|
12,628
|
407
|
C
|
Low
|
145
|
Major histocompatibility complex
|
12,410
|
400
|
B
|
Mid
|
146
|
Homology (biology)
|
12,406
|
400
|
GA
|
High
|
147
|
G. H. Hardy
|
12,252
|
395
|
C
|
Mid
|
148
|
Atavism
|
12,250
|
395
|
C
|
Mid
|
149
|
Genome
|
12,178
|
392
|
C
|
High
|
150
|
Panthera hybrid
|
12,172
|
392
|
C
|
Mid
|
151
|
Jennifer Doudna
|
12,144
|
391
|
B
|
High
|
152
|
Genetic code
|
11,962
|
385
|
GA
|
Top
|
153
|
Domestic rabbit
|
11,891
|
383
|
GA
|
Low
|
154
|
Mosaic (genetics)
|
11,855
|
382
|
C
|
Mid
|
155
|
Western Steppe Herders
|
11,849
|
382
|
C
|
Mid
|
156
|
Western hunter-gatherer
|
11,700
|
377
|
C
|
Mid
|
157
|
5α-Reductase 2 deficiency
|
11,651
|
375
|
B
|
Low
|
158
|
Nazi eugenics
|
11,628
|
375
|
C
|
Mid
|
159
|
Polyploidy
|
11,569
|
373
|
B
|
High
|
160
|
Sexual selection
|
11,500
|
370
|
GA
|
Mid
|
161
|
Telomere
|
11,451
|
369
|
C
|
Mid
|
162
|
P53
|
11,445
|
369
|
B
|
High
|
163
|
Single-nucleotide polymorphism
|
11,443
|
369
|
C
|
High
|
164
|
Y-chromosomal Adam
|
11,280
|
363
|
C
|
High
|
165
|
Genetic history of Europe
|
11,229
|
362
|
Start
|
Low
|
166
|
Heritability of IQ
|
11,176
|
360
|
C
|
Low
|
167
|
Von Hippel–Lindau disease
|
11,121
|
358
|
C
|
Mid
|
168
|
Gene therapy
|
11,050
|
356
|
B
|
High
|
169
|
Lydia Fairchild
|
11,044
|
356
|
Stub
|
Unknown
|
170
|
Eugenics in the United States
|
10,945
|
353
|
Start
|
Low
|
171
|
Ronald Fisher
|
10,940
|
352
|
B
|
High
|
172
|
Congenital heart defect
|
10,934
|
352
|
C
|
Mid
|
173
|
List of organisms by chromosome count
|
10,876
|
350
|
List
|
Low
|
174
|
Ventricular septal defect
|
10,745
|
346
|
C
|
Low
|
175
|
Genetic testing
|
10,723
|
345
|
B
|
Top
|
176
|
Francis Collins
|
10,698
|
345
|
B
|
Mid
|
177
|
Selective breeding
|
10,692
|
344
|
C
|
Top
|
178
|
Citicoline
|
10,682
|
344
|
B
|
Low
|
179
|
Gene expression
|
10,665
|
344
|
B
|
Top
|
180
|
Genotype
|
10,345
|
333
|
Start
|
Top
|
181
|
Most recent common ancestor
|
10,172
|
328
|
B
|
Mid
|
182
|
Genetic studies on Turkish people
|
10,071
|
324
|
Start
|
Low
|
183
|
Variants of SARS-CoV-2
|
10,037
|
323
|
C
|
Low
|
184
|
Recombinant DNA
|
10,019
|
323
|
C
|
High
|
185
|
NF-κB
|
9,991
|
322
|
C
|
High
|
186
|
Auburn hair
|
9,991
|
322
|
Start
|
Low
|
187
|
Dysgenics
|
9,990
|
322
|
Start
|
Low
|
188
|
HLA-B27
|
9,937
|
320
|
C
|
Low
|
189
|
Haplogroup G-M201
|
9,836
|
317
|
Start
|
Low
|
190
|
Chromosome abnormality
|
9,833
|
317
|
Start
|
High
|
191
|
Sex chromosome
|
9,827
|
317
|
Start
|
High
|
192
|
Genetics and archaeogenetics of South Asia
|
9,819
|
316
|
Start
|
Mid
|
193
|
Black hair
|
9,764
|
314
|
Start
|
Mid
|
194
|
Aneuploidy
|
9,755
|
314
|
B
|
High
|
195
|
Genentech
|
9,748
|
314
|
Start
|
Mid
|
196
|
VACTERL association
|
9,737
|
314
|
Start
|
Mid
|
197
|
Exogamy
|
9,711
|
313
|
Start
|
Low
|
198
|
Sanger sequencing
|
9,608
|
309
|
C
|
High
|
199
|
Reverse transcription polymerase chain reaction
|
9,595
|
309
|
Start
|
Mid
|
200
|
Dravet syndrome
|
9,453
|
304
|
C
|
Low
|
201
|
Haplogroup H (mtDNA)
|
9,408
|
303
|
Start
|
Low
|
202
|
Ethnic groups of Japan
|
9,376
|
302
|
Start
|
Unknown
|
203
|
RNA world
|
9,326
|
300
|
C
|
Mid
|
204
|
Hardy–Weinberg principle
|
9,258
|
298
|
C
|
High
|
205
|
Lactase
|
9,194
|
296
|
B
|
Mid
|
206
|
Biological engineering
|
9,169
|
295
|
C
|
High
|
207
|
Blue rose
|
9,165
|
295
|
Start
|
Low
|
208
|
Anthropometry
|
9,092
|
293
|
C
|
Low
|
209
|
Error
|
9,009
|
290
|
Start
|
Mid
|
210
|
Real-time polymerase chain reaction
|
8,949
|
288
|
C
|
Mid
|
211
|
Protein biosynthesis
|
8,891
|
286
|
B
|
Mid
|
212
|
Transcription factor
|
8,862
|
285
|
B
|
High
|
213
|
Detasseling
|
8,840
|
285
|
B
|
Low
|
214
|
Wnt signaling pathway
|
8,821
|
284
|
C
|
Mid
|
215
|
Single parent
|
8,817
|
284
|
B
|
Mid
|
216
|
Genetic drift
|
8,794
|
283
|
GA
|
High
|
217
|
Nucleic acid double helix
|
8,786
|
283
|
C
|
Mid
|
218
|
Impulsivity
|
8,781
|
283
|
B
|
Mid
|
219
|
Hayflick limit
|
8,757
|
282
|
Start
|
Low
|
220
|
Leigh syndrome
|
8,729
|
281
|
C
|
Low
|
221
|
Founder effect
|
8,693
|
280
|
C
|
High
|
222
|
Polymorphism (biology)
|
8,445
|
272
|
B
|
Low
|
223
|
Fertility
|
8,416
|
271
|
C
|
Mid
|
224
|
Base pair
|
8,385
|
270
|
C
|
Top
|
225
|
Ectrodactyly
|
8,366
|
269
|
B
|
Mid
|
226
|
Zygosity
|
8,357
|
269
|
C
|
High
|
227
|
Cyclic adenosine monophosphate
|
8,292
|
267
|
C
|
Mid
|
228
|
Atrial septal defect
|
8,231
|
265
|
B
|
Low
|
229
|
DNA repair
|
8,218
|
265
|
C
|
High
|
230
|
Proteinogenic amino acid
|
8,201
|
264
|
C
|
High
|
231
|
Heterosis
|
8,166
|
263
|
C
|
High
|
232
|
Lac operon
|
7,967
|
257
|
C
|
Mid
|
233
|
Translation (biology)
|
7,964
|
256
|
B
|
Top
|
234
|
Data storage
|
7,903
|
254
|
Start
|
Low
|
235
|
Oogenesis
|
7,850
|
253
|
C
|
High
|
236
|
RNA splicing
|
7,838
|
252
|
C
|
Top
|
237
|
Hispanos of New Mexico
|
7,792
|
251
|
Start
|
Low
|
238
|
Haplogroup J (Y-DNA)
|
7,789
|
251
|
Start
|
Low
|
239
|
Methylation
|
7,770
|
250
|
C
|
Mid
|
240
|
DNA polymerase
|
7,732
|
249
|
C
|
Top
|
241
|
Heritability of autism
|
7,709
|
248
|
Start
|
Mid
|
242
|
MicroRNA
|
7,700
|
248
|
B
|
Top
|
243
|
Haplogroup E-M215
|
7,697
|
248
|
C
|
Low
|
244
|
Mebendazole
|
7,671
|
247
|
C
|
Mid
|
245
|
Transposable element
|
7,642
|
246
|
C
|
High
|
246
|
Human mitochondrial DNA haplogroup
|
7,640
|
246
|
Start
|
Low
|
247
|
Horizontal gene transfer
|
7,629
|
246
|
C
|
High
|
248
|
Central dogma of molecular biology
|
7,612
|
245
|
C
|
Top
|
249
|
Transfer RNA
|
7,597
|
245
|
B
|
High
|
250
|
Genetic history of Egypt
|
7,585
|
244
|
C
|
Low
|
251
|
Nucleolus
|
7,534
|
243
|
Start
|
Mid
|
252
|
Chin
|
7,534
|
243
|
C
|
Low
|
253
|
Photo 51
|
7,504
|
242
|
Start
|
Low
|
254
|
Genomics
|
7,476
|
241
|
B
|
Top
|
255
|
He Jiankui affair
|
7,466
|
240
|
C
|
Low
|
256
|
Uterus didelphys
|
7,444
|
240
|
Start
|
Low
|
257
|
Haplogroup U
|
7,440
|
240
|
Start
|
Mid
|
258
|
Whole genome sequencing
|
7,438
|
239
|
B
|
Top
|
259
|
Laboratory rat
|
7,396
|
238
|
C
|
Mid
|
260
|
Telegony (inheritance)
|
7,368
|
237
|
C
|
Low
|
261
|
BRCA1
|
7,350
|
237
|
C
|
High
|
262
|
Haplogroup J-M172
|
7,325
|
236
|
Start
|
Low
|
263
|
Eastern hunter-gatherer
|
7,287
|
235
|
C
|
Mid
|
264
|
Chromatin
|
7,268
|
234
|
B
|
Mid
|
265
|
Mitochondrial disease
|
7,252
|
233
|
C
|
Mid
|
266
|
Promoter (genetics)
|
7,240
|
233
|
Start
|
Mid
|
267
|
Synthetic biology
|
7,157
|
230
|
B
|
Mid
|
268
|
The Population Bomb
|
7,145
|
230
|
B
|
Low
|
269
|
Nicotinamide adenine dinucleotide phosphate
|
7,109
|
229
|
Start
|
Mid
|
270
|
Constriction ring syndrome
|
7,046
|
227
|
C
|
Low
|
271
|
Monoamine oxidase A
|
7,020
|
226
|
C
|
Mid
|
272
|
Sex-determining region Y protein
|
7,005
|
225
|
C
|
Low
|
273
|
Epileptic spasms
|
6,887
|
222
|
C
|
Low
|
274
|
MHC class II
|
6,798
|
219
|
C
|
Mid
|
275
|
Genetic recombination
|
6,769
|
218
|
C
|
High
|
276
|
XXYY syndrome
|
6,755
|
217
|
Start
|
Low
|
277
|
Webbed toes
|
6,755
|
217
|
Start
|
Low
|
278
|
Epidermal growth factor receptor
|
6,754
|
217
|
C
|
Mid
|
279
|
Genetically modified crops
|
6,723
|
216
|
B
|
High
|
280
|
Oncogene
|
6,714
|
216
|
C
|
High
|
281
|
Parent
|
6,642
|
214
|
C
|
High
|
282
|
Coefficient of relationship
|
6,636
|
214
|
C
|
Low
|
283
|
HER2
|
6,608
|
213
|
C
|
Mid
|
284
|
Histone
|
6,606
|
213
|
C
|
Mid
|
285
|
Dwarf cat
|
6,534
|
210
|
Start
|
Low
|
286
|
Tetrasomy X
|
6,503
|
209
|
GA
|
Low
|
287
|
List of redheads
|
6,492
|
209
|
List
|
Low
|
288
|
Reverse transcriptase
|
6,389
|
206
|
B
|
High
|
289
|
RNA interference
|
6,366
|
205
|
FA
|
Top
|
290
|
Autosome
|
6,295
|
203
|
Start
|
Top
|
291
|
Chromosomal crossover
|
6,263
|
202
|
C
|
High
|
292
|
Illumina, Inc.
|
6,262
|
202
|
C
|
Low
|
293
|
Post-translational modification
|
6,242
|
201
|
Start
|
High
|
294
|
Inbreeding depression
|
6,238
|
201
|
C
|
Low
|
295
|
Genetic history of the British Isles
|
6,231
|
201
|
C
|
Low
|
296
|
Shyness
|
6,198
|
199
|
B
|
Low
|
297
|
Genetic diversity
|
6,198
|
199
|
C
|
Mid
|
298
|
Regulation of gene expression
|
6,194
|
199
|
C
|
High
|
299
|
Telomerase
|
6,106
|
196
|
B
|
High
|
300
|
Patent ductus arteriosus
|
6,101
|
196
|
Start
|
Mid
|
301
|
Hypoplastic left heart syndrome
|
6,083
|
196
|
C
|
Low
|
302
|
Genetic history of the Iberian Peninsula
|
6,079
|
196
|
Start
|
Low
|
303
|
CpG site
|
6,077
|
196
|
C
|
Mid
|
304
|
Haplogroup I-M170
|
6,077
|
196
|
B
|
Low
|
305
|
MHC class I
|
6,061
|
195
|
C
|
Mid
|
306
|
Homologous chromosome
|
6,025
|
194
|
Start
|
High
|
307
|
J. B. S. Haldane
|
5,939
|
191
|
C
|
Low
|
308
|
Haplogroup N-M231
|
5,931
|
191
|
Start
|
Low
|
309
|
Causes of cancer
|
5,921
|
191
|
B
|
Mid
|
310
|
Twin study
|
5,912
|
190
|
B
|
High
|
311
|
Pleiotropy
|
5,897
|
190
|
C
|
High
|
312
|
Somatic cell
|
5,880
|
189
|
Start
|
Mid
|
313
|
16S ribosomal RNA
|
5,877
|
189
|
C
|
High
|
314
|
God gene
|
5,853
|
188
|
Start
|
Mid
|
315
|
Fluorescence in situ hybridization
|
5,845
|
188
|
B
|
Mid
|
316
|
Genomic imprinting
|
5,838
|
188
|
C
|
High
|
317
|
Haplogroup C-M217
|
5,820
|
187
|
Start
|
Low
|
318
|
Epistasis
|
5,810
|
187
|
B
|
High
|
319
|
Genealogical DNA test
|
5,773
|
186
|
C
|
Mid
|
320
|
Barbara McClintock
|
5,728
|
184
|
FA
|
High
|
321
|
Haplogroup J-M267
|
5,705
|
184
|
C
|
Low
|
322
|
Cre-Lox recombination
|
5,684
|
183
|
C
|
Mid
|
323
|
Zebrafish
|
5,670
|
182
|
B
|
Mid
|
324
|
Fitness (biology)
|
5,660
|
182
|
C
|
Mid
|
325
|
Colour wheel theory of love
|
5,652
|
182
|
Stub
|
Low
|
326
|
Haplogroup I-M438
|
5,604
|
180
|
Start
|
Low
|
327
|
JAK-STAT signaling pathway
|
5,601
|
180
|
B
|
Mid
|
328
|
GloFish
|
5,560
|
179
|
C
|
Mid
|
329
|
Medical genetics of Jews
|
5,549
|
179
|
Start
|
Low
|
330
|
X-linked recessive inheritance
|
5,544
|
178
|
Start
|
Mid
|
331
|
Laboratory mouse
|
5,531
|
178
|
B
|
Low
|
332
|
Cas9
|
5,501
|
177
|
C
|
Mid
|
333
|
RNA polymerase
|
5,485
|
176
|
C
|
Top
|
334
|
Heritability
|
5,480
|
176
|
C
|
High
|
335
|
Genome editing
|
5,459
|
176
|
C
|
High
|
336
|
Racial hygiene
|
5,453
|
175
|
C
|
Low
|
337
|
Adeno-associated virus
|
5,436
|
175
|
B
|
Low
|
338
|
Mathematical and theoretical biology
|
5,424
|
174
|
C
|
Low
|
339
|
Factor VIII
|
5,422
|
174
|
Start
|
Low
|
340
|
Haplogroup I-M253
|
5,389
|
173
|
B
|
Low
|
341
|
Single-cell sequencing
|
5,378
|
173
|
C
|
High
|
342
|
Maladaptation
|
5,369
|
173
|
Start
|
Low
|
343
|
Stop codon
|
5,342
|
172
|
Start
|
High
|
344
|
Neanderthal genetics
|
5,333
|
172
|
C
|
High
|
345
|
Biological determinism
|
5,331
|
171
|
GA
|
Mid
|
346
|
Locus (genetics)
|
5,330
|
171
|
Start
|
Mid
|
347
|
Chromosomal translocation
|
5,306
|
171
|
Start
|
High
|
348
|
Jefferson–Hemings controversy
|
5,283
|
170
|
B
|
Low
|
349
|
Human genetic variation
|
5,277
|
170
|
C
|
High
|
350
|
Phosphorylation
|
5,271
|
170
|
C
|
High
|
351
|
Barr body
|
5,268
|
169
|
Start
|
High
|
352
|
Personalized medicine
|
5,260
|
169
|
B
|
Mid
|
353
|
Sexual selection in humans
|
5,252
|
169
|
C
|
Low
|
354
|
Haplogroup M (mtDNA)
|
5,242
|
169
|
Stub
|
Low
|
355
|
Biopolymer
|
5,233
|
168
|
C
|
Mid
|
356
|
Myc
|
5,232
|
168
|
C
|
High
|
357
|
Hox gene
|
5,222
|
168
|
C
|
High
|
358
|
Purebred
|
5,221
|
168
|
C
|
Low
|
359
|
Kin selection
|
5,179
|
167
|
GA
|
Mid
|
360
|
Haplogroup T-M184
|
5,170
|
166
|
B
|
Low
|
361
|
Advanced maternal age
|
5,168
|
166
|
C
|
Mid
|
362
|
Flavin adenine dinucleotide
|
5,161
|
166
|
B
|
Low
|
363
|
Chargaff's rules
|
5,131
|
165
|
Start
|
Low
|
364
|
Endogeny (biology)
|
5,105
|
164
|
Stub
|
Low
|
365
|
Chromosome 21
|
5,104
|
164
|
Start
|
Mid
|
366
|
Haplogroup R (Y-DNA)
|
5,092
|
164
|
Start
|
Low
|
367
|
The Gene: An Intimate History
|
5,084
|
164
|
Start
|
Unknown
|
368
|
Genetic memory (psychology)
|
5,078
|
163
|
Start
|
Low
|
369
|
Bacterial conjugation
|
5,074
|
163
|
C
|
High
|
370
|
Disodium inosinate
|
5,067
|
163
|
Start
|
Low
|
371
|
Hi-C (genomic analysis technique)
|
4,998
|
161
|
C
|
Low
|
372
|
Phenotypic trait
|
4,977
|
160
|
Start
|
Mid
|
373
|
Open reading frame
|
4,964
|
160
|
Start
|
Mid
|
374
|
Breed
|
4,952
|
159
|
Start
|
Low
|
375
|
List of haplogroups of historic people
|
4,936
|
159
|
List
|
Low
|
376
|
List of genetic disorders
|
4,910
|
158
|
List
|
High
|
377
|
ZW sex-determination system
|
4,906
|
158
|
C
|
Mid
|
378
|
Uracil
|
4,880
|
157
|
Start
|
Mid
|
379
|
Hershey–Chase experiment
|
4,840
|
156
|
C
|
High
|
380
|
Population genetics
|
4,833
|
155
|
C
|
Top
|
381
|
Haplogroup Q-M242
|
4,833
|
155
|
C
|
Low
|
382
|
Gene nomenclature
|
4,832
|
155
|
Start
|
Mid
|
383
|
X-inactivation
|
4,822
|
155
|
B
|
High
|
384
|
Tumor suppressor gene
|
4,818
|
155
|
Start
|
High
|
385
|
Paternal age effect
|
4,818
|
155
|
C
|
Mid
|
386
|
Genetic transformation
|
4,815
|
155
|
B
|
Top
|
387
|
Flavivirus
|
4,797
|
154
|
B
|
Mid
|
388
|
Medical genetics
|
4,771
|
153
|
B
|
Mid
|
389
|
Genome-wide association study
|
4,705
|
151
|
GA
|
Top
|
390
|
Haplogroup A (Y-DNA)
|
4,704
|
151
|
C
|
Low
|
391
|
Sampling bias
|
4,702
|
151
|
C
|
Low
|
392
|
Haplotype
|
4,696
|
151
|
Start
|
High
|
393
|
Griscelli syndrome
|
4,695
|
151
|
Start
|
Low
|
394
|
Nucleic acid sequence
|
4,668
|
150
|
C
|
High
|
395
|
Zellweger syndrome
|
4,665
|
150
|
Start
|
Low
|
396
|
Alternative splicing
|
4,651
|
150
|
B
|
High
|
397
|
George Church (geneticist)
|
4,636
|
149
|
C
|
Low
|
398
|
Designer baby
|
4,635
|
149
|
B
|
High
|
399
|
Isoelectric point
|
4,628
|
149
|
C
|
Mid
|
400
|
Okazaki fragments
|
4,604
|
148
|
B
|
High
|
401
|
Plant breeding
|
4,604
|
148
|
C
|
High
|
402
|
He Jiankui
|
4,600
|
148
|
B
|
Low
|
403
|
Homologous recombination
|
4,598
|
148
|
GA
|
High
|
404
|
Chillingham cattle
|
4,583
|
147
|
B
|
Low
|
405
|
Eric Lander
|
4,579
|
147
|
C
|
Low
|
406
|
Kozak consensus sequence
|
4,557
|
147
|
Start
|
Mid
|
407
|
Trisomy
|
4,538
|
146
|
Start
|
High
|
408
|
Modern synthesis (20th century)
|
4,497
|
145
|
GA
|
High
|
409
|
SARS-CoV-2 Delta variant
|
4,497
|
145
|
C
|
Low
|
410
|
Model organism
|
4,481
|
144
|
B
|
Mid
|
411
|
Non-coding DNA
|
4,456
|
143
|
C
|
Mid
|
412
|
Haplogroup R1
|
4,443
|
143
|
C
|
Low
|
413
|
Allopatric speciation
|
4,435
|
143
|
C
|
Low
|
414
|
F1 hybrid
|
4,413
|
142
|
Start
|
High
|
415
|
Tongue rolling
|
4,403
|
142
|
Stub
|
Low
|
416
|
Epigenetic clock
|
4,388
|
141
|
C
|
Mid
|
417
|
Multiple sequence alignment
|
4,341
|
140
|
Unknown
|
Mid
|
418
|
DNA evidence in the O. J. Simpson murder case
|
4,331
|
139
|
B
|
Low
|
419
|
Oligonucleotide
|
4,323
|
139
|
Start
|
Mid
|
420
|
Systems biology
|
4,317
|
139
|
C
|
High
|
421
|
DNA extraction
|
4,292
|
138
|
Start
|
Mid
|
422
|
Gene set enrichment analysis
|
4,272
|
137
|
C
|
Mid
|
423
|
Genetic counseling
|
4,265
|
137
|
C
|
Mid
|
424
|
Transduction (genetics)
|
4,259
|
137
|
C
|
High
|
425
|
Non-coding RNA
|
4,250
|
137
|
C
|
High
|
426
|
Pedigree collapse
|
4,237
|
136
|
Start
|
Low
|
427
|
Molecular cloning
|
4,223
|
136
|
C
|
High
|
428
|
Genetic variation
|
4,215
|
135
|
Start
|
High
|
429
|
Haplogroup E-V38
|
4,173
|
134
|
C
|
Mid
|
430
|
Sheep farming
|
4,172
|
134
|
C
|
Low
|
431
|
MELAS syndrome
|
4,171
|
134
|
C
|
Low
|
432
|
Centromere
|
4,141
|
133
|
C
|
Mid
|
433
|
KRAS
|
4,141
|
133
|
C
|
Mid
|
434
|
Operon
|
4,130
|
133
|
B
|
Mid
|
435
|
Chromosome 2
|
4,122
|
132
|
C
|
Mid
|
436
|
Microsatellite
|
4,113
|
132
|
C
|
Mid
|
437
|
Hepatitis D
|
4,111
|
132
|
C
|
Low
|
438
|
Bovine somatotropin
|
4,100
|
132
|
C
|
Low
|
439
|
Haplogroup E-M96
|
4,083
|
131
|
Start
|
Low
|
440
|
Haplogroup O-M175
|
4,083
|
131
|
Start
|
Low
|
441
|
Gene mapping
|
4,060
|
130
|
Start
|
Low
|
442
|
Crossbreed
|
4,059
|
130
|
Start
|
Low
|
443
|
Boar–pig hybrid
|
4,019
|
129
|
Stub
|
Low
|
444
|
Peter and Rosemary Grant
|
4,009
|
129
|
C
|
Unknown
|
445
|
Restriction fragment length polymorphism
|
4,004
|
129
|
Start
|
Mid
|
446
|
Apomorphy and synapomorphy
|
4,001
|
129
|
C
|
Low
|
447
|
Haplogroup E-V68
|
3,999
|
129
|
C
|
Low
|
448
|
Y-chromosomal Aaron
|
3,986
|
128
|
Start
|
Low
|
449
|
Genetic history of the Middle East
|
3,985
|
128
|
C
|
Mid
|
450
|
Janaki Ammal
|
3,976
|
128
|
B
|
Low
|
451
|
Adenosine monophosphate
|
3,975
|
128
|
Start
|
Low
|
452
|
Ancient DNA
|
3,967
|
127
|
C
|
Mid
|
453
|
Haplogroup L-M20
|
3,948
|
127
|
Start
|
Low
|
454
|
Humanized mouse
|
3,947
|
127
|
Start
|
Low
|
455
|
Adenosine diphosphate
|
3,946
|
127
|
C
|
Mid
|
456
|
Ras GTPase
|
3,942
|
127
|
B
|
High
|
457
|
Introduction to evolution
|
3,918
|
126
|
B
|
High
|
458
|
Dun gene
|
3,908
|
126
|
C
|
Low
|
459
|
Genetic studies on Arabs
|
3,908
|
126
|
C
|
Low
|
460
|
Neo-Darwinism
|
3,906
|
126
|
Start
|
High
|
461
|
Atomic gardening
|
3,899
|
125
|
C
|
Low
|
462
|
Phred quality score
|
3,890
|
125
|
Start
|
Low
|
463
|
Bcl-2
|
3,877
|
125
|
B
|
Mid
|
464
|
List of unusual biological names
|
3,875
|
125
|
List
|
Low
|
465
|
Klotho (biology)
|
3,866
|
124
|
Start
|
Low
|
466
|
Exome sequencing
|
3,862
|
124
|
C
|
High
|
467
|
Maurice Wilkins
|
3,850
|
124
|
B
|
High
|
468
|
Biomaterial
|
3,846
|
124
|
C
|
Low
|
469
|
46,XX/46,XY
|
3,846
|
124
|
C
|
Low
|
470
|
History of eugenics
|
3,841
|
123
|
B
|
Low
|
471
|
Sexual differentiation in humans
|
3,838
|
123
|
C
|
Mid
|
472
|
Transgene
|
3,837
|
123
|
B
|
Mid
|
473
|
Intron
|
3,819
|
123
|
C
|
High
|
474
|
Chédiak–Higashi syndrome
|
3,815
|
123
|
Start
|
Low
|
475
|
Svante Pääbo
|
3,813
|
123
|
C
|
Low
|
476
|
Haplogroup H (Y-DNA)
|
3,783
|
122
|
C
|
Low
|
477
|
Aryl hydrocarbon receptor
|
3,777
|
121
|
B
|
Mid
|
478
|
Cold Spring Harbor Laboratory
|
3,745
|
120
|
Start
|
Mid
|
479
|
Point mutation
|
3,716
|
119
|
C
|
High
|
480
|
Haplogroup K (mtDNA)
|
3,686
|
118
|
Start
|
Low
|
481
|
Behavioural genetics
|
3,682
|
118
|
GA
|
High
|
482
|
Translational research
|
3,661
|
118
|
C
|
Mid
|
483
|
Taq polymerase
|
3,656
|
117
|
C
|
Mid
|
484
|
Leber's hereditary optic neuropathy
|
3,654
|
117
|
C
|
Mid
|
485
|
Y-DNA haplogroups in populations of Europe
|
3,637
|
117
|
List
|
Mid
|
486
|
Copy number variation
|
3,627
|
117
|
B
|
High
|
487
|
Genetic linkage
|
3,609
|
116
|
Start
|
High
|
488
|
Oligomer
|
3,605
|
116
|
Start
|
Low
|
489
|
Cystic fibrosis transmembrane conductance regulator
|
3,592
|
115
|
C
|
Mid
|
490
|
Penetrance
|
3,582
|
115
|
C
|
High
|
491
|
Junk DNA
|
3,581
|
115
|
B
|
Mid
|
492
|
Gene delivery
|
3,561
|
114
|
B
|
High
|
493
|
Ribozyme
|
3,539
|
114
|
Start
|
High
|
494
|
Griffith's experiment
|
3,534
|
114
|
Start
|
Mid
|
495
|
Weaver syndrome
|
3,511
|
113
|
Start
|
Low
|
496
|
Gene knockout
|
3,510
|
113
|
Start
|
Mid
|
497
|
Guanosine triphosphate
|
3,509
|
113
|
Start
|
Mid
|
498
|
Ronald Plasterk
|
3,491
|
112
|
C
|
Unknown
|
499
|
Pharmacogenomics
|
3,490
|
112
|
B
|
Mid
|
500
|
Mendelian randomization
|
3,490
|
112
|
Start
|
Low
|