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This is a list of pages in the scope of Wikipedia:WikiProject Genetics along with pageviews.
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Period: 2024-08-01 to 2024-08-31
Total views: 9,160,480
Updated: 16:10, 8 September 2024 (UTC)
| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
Fibular hemimelia
|
369,090
|
11,906
|
Start
|
Low
|
| 2
|
XY sex-determination system
|
273,487
|
8,822
|
C
|
High
|
| 3
|
Axolotl
|
215,975
|
6,966
|
C
|
High
|
| 4
|
Tetrasomy X
|
166,051
|
5,356
|
GA
|
Low
|
| 5
|
Prion
|
114,814
|
3,703
|
GA
|
Mid
|
| 6
|
5α-Reductase 2 deficiency
|
90,220
|
2,910
|
B
|
Low
|
| 7
|
Eugenics
|
87,861
|
2,834
|
B
|
High
|
| 8
|
Incest
|
87,762
|
2,831
|
C
|
Low
|
| 9
|
XX male syndrome
|
82,714
|
2,668
|
C
|
Low
|
| 10
|
Red hair
|
77,182
|
2,489
|
C
|
Mid
|
| 11
|
DNA
|
73,154
|
2,359
|
FA
|
Top
|
| 12
|
Guinea pig
|
62,555
|
2,017
|
B
|
Low
|
| 13
|
Cancer
|
61,855
|
1,995
|
B
|
Top
|
| 14
|
Prader–Willi syndrome
|
59,875
|
1,931
|
B
|
Mid
|
| 15
|
XYY syndrome
|
58,495
|
1,886
|
B
|
Mid
|
| 16
|
Cystic fibrosis
|
55,591
|
1,793
|
B
|
High
|
| 17
|
Bayer
|
53,290
|
1,719
|
C
|
Low
|
| 18
|
Chromosome
|
52,809
|
1,703
|
B
|
Top
|
| 19
|
Amino acid
|
52,350
|
1,688
|
GA
|
Top
|
| 20
|
Protein
|
51,149
|
1,649
|
GA
|
Top
|
| 21
|
Blood type
|
48,791
|
1,573
|
B
|
High
|
| 22
|
Attachment theory
|
46,055
|
1,485
|
B
|
Mid
|
| 23
|
Evolution
|
44,125
|
1,423
|
FA
|
Top
|
| 24
|
Color blindness
|
43,817
|
1,413
|
B
|
Mid
|
| 25
|
Y chromosome
|
43,089
|
1,389
|
B
|
High
|
| 26
|
SARS-CoV-2
|
41,699
|
1,345
|
B
|
Top
|
| 27
|
Biodiversity
|
41,287
|
1,331
|
C
|
Mid
|
| 28
|
Epicanthic fold
|
41,234
|
1,330
|
C
|
Low
|
| 29
|
Pentasomy X
|
40,834
|
1,317
|
GA
|
Low
|
| 30
|
Nicotinamide adenine dinucleotide
|
40,719
|
1,313
|
FA
|
Mid
|
| 31
|
Epigenetics
|
40,418
|
1,303
|
B
|
Top
|
| 32
|
Cousin
|
39,946
|
1,288
|
Start
|
Low
|
| 33
|
Enzyme
|
39,595
|
1,277
|
FA
|
Top
|
| 34
|
Blue Fugates
|
38,336
|
1,236
|
Start
|
Low
|
| 35
|
Inbreeding
|
36,440
|
1,175
|
C
|
Low
|
| 36
|
Total fertility rate
|
36,114
|
1,164
|
C
|
Low
|
| 37
|
Human skin color
|
35,208
|
1,135
|
B
|
Mid
|
| 38
|
Scientific racism
|
35,190
|
1,135
|
C
|
Low
|
| 39
|
23andMe
|
35,013
|
1,129
|
C
|
Mid
|
| 40
|
Gregor Mendel
|
34,659
|
1,118
|
B
|
High
|
| 41
|
XXXY syndrome
|
32,729
|
1,055
|
C
|
Low
|
| 42
|
Charcot–Marie–Tooth disease
|
32,601
|
1,051
|
C
|
Mid
|
| 43
|
CRISPR
|
32,590
|
1,051
|
B
|
High
|
| 44
|
Chimera (genetics)
|
32,242
|
1,040
|
B
|
Mid
|
| 45
|
Albinism
|
32,199
|
1,038
|
C
|
Low
|
| 46
|
Consanguinity
|
32,163
|
1,037
|
C
|
Low
|
| 47
|
Adenosine triphosphate
|
31,833
|
1,026
|
C
|
High
|
| 48
|
Meiosis
|
31,571
|
1,018
|
C
|
Top
|
| 49
|
Genetics
|
30,925
|
997
|
FA
|
Top
|
| 50
|
Last universal common ancestor
|
30,121
|
971
|
GA
|
Mid
|
| 51
|
Rosalind Franklin
|
29,976
|
966
|
B
|
High
|
| 52
|
Sex-determination system
|
29,601
|
954
|
C
|
Mid
|
| 53
|
Birth defect
|
29,437
|
949
|
B
|
Mid
|
| 54
|
Svalbard Global Seed Vault
|
28,759
|
927
|
B
|
Mid
|
| 55
|
Blond
|
28,727
|
926
|
C
|
Low
|
| 56
|
Friedreich's ataxia
|
28,672
|
924
|
GA
|
Mid
|
| 57
|
Lactose intolerance
|
27,721
|
894
|
B
|
Low
|
| 58
|
Sex-determining region Y protein
|
27,635
|
891
|
C
|
Low
|
| 59
|
Karyotype
|
27,311
|
881
|
C
|
Mid
|
| 60
|
Hybrid (biology)
|
26,889
|
867
|
GA
|
High
|
| 61
|
Drosophila melanogaster
|
26,643
|
859
|
B
|
Top
|
| 62
|
Endogamy
|
26,347
|
849
|
Start
|
Low
|
| 63
|
Dominance (genetics)
|
26,303
|
848
|
C
|
Top
|
| 64
|
Gigantism
|
25,932
|
836
|
B
|
High
|
| 65
|
Cleft lip and cleft palate
|
25,526
|
823
|
B
|
Low
|
| 66
|
Mitochondrial Eve
|
24,742
|
798
|
B
|
Mid
|
| 67
|
Animal husbandry
|
24,472
|
789
|
GA
|
Mid
|
| 68
|
Japanese people
|
24,336
|
785
|
C
|
Low
|
| 69
|
Gene
|
24,218
|
781
|
GA
|
Top
|
| 70
|
Polymerase chain reaction
|
24,010
|
774
|
B
|
High
|
| 71
|
Wechsler Adult Intelligence Scale
|
23,568
|
760
|
C
|
Low
|
| 72
|
Early human migrations
|
23,118
|
745
|
B
|
Mid
|
| 73
|
RNA
|
22,815
|
735
|
GA
|
Top
|
| 74
|
Estimates of historical world population
|
22,136
|
714
|
Start
|
Low
|
| 75
|
Trisomy 18
|
22,024
|
710
|
B
|
Low
|
| 76
|
M. S. Swaminathan
|
21,899
|
706
|
B
|
Low
|
| 77
|
Phenotype
|
21,884
|
705
|
C
|
Top
|
| 78
|
Mutation
|
21,809
|
703
|
B
|
Top
|
| 79
|
Sex chromosome
|
21,748
|
701
|
Start
|
High
|
| 80
|
Human hair color
|
21,650
|
698
|
Start
|
Mid
|
| 81
|
James Watson
|
21,274
|
686
|
B
|
High
|
| 82
|
Ribosome
|
21,207
|
684
|
B
|
Top
|
| 83
|
Nucleotide
|
21,098
|
680
|
C
|
Top
|
| 84
|
Recent African origin of modern humans
|
20,861
|
672
|
C
|
Mid
|
| 85
|
HeLa
|
20,365
|
656
|
C
|
Low
|
| 86
|
Genetic studies of Jews
|
20,281
|
654
|
B
|
Mid
|
| 87
|
Genetic engineering
|
20,176
|
650
|
GA
|
Top
|
| 88
|
Human Genome Project
|
19,805
|
638
|
B
|
Top
|
| 89
|
Tuberous sclerosis
|
19,780
|
638
|
B
|
Mid
|
| 90
|
Mosaic (genetics)
|
19,333
|
623
|
C
|
Mid
|
| 91
|
Genetic disorder
|
19,178
|
618
|
B
|
Top
|
| 92
|
Gamete
|
19,076
|
615
|
Start
|
Mid
|
| 93
|
Senescence
|
18,920
|
610
|
C
|
Low
|
| 94
|
Nucleic acid
|
18,651
|
601
|
C
|
Mid
|
| 95
|
Haplogroup R1a
|
18,638
|
601
|
C
|
Low
|
| 96
|
The Bell Curve
|
18,363
|
592
|
C
|
High
|
| 97
|
Charis Eng
|
18,269
|
589
|
Start
|
Low
|
| 98
|
Humanzee
|
18,203
|
587
|
C
|
Mid
|
| 99
|
Mendelian inheritance
|
18,036
|
581
|
C
|
High
|
| 100
|
Genetically modified food
|
17,686
|
570
|
B
|
High
|
| 101
|
Haplogroup R1b
|
17,592
|
567
|
C
|
Mid
|
| 102
|
DNA replication
|
17,182
|
554
|
B
|
Unknown
|
| 103
|
Haplogroup
|
16,632
|
536
|
C
|
Mid
|
| 104
|
Mitochondrial DNA
|
16,584
|
534
|
B
|
High
|
| 105
|
Cultivar
|
16,398
|
528
|
GA
|
Mid
|
| 106
|
Cat coat genetics
|
16,346
|
527
|
C
|
Mid
|
| 107
|
Descent from Genghis Khan
|
16,211
|
522
|
C
|
Low
|
| 108
|
Cloning
|
15,930
|
513
|
B
|
Top
|
| 109
|
Incest taboo
|
15,867
|
511
|
C
|
Mid
|
| 110
|
Sonic hedgehog protein
|
15,843
|
511
|
B
|
High
|
| 111
|
Genetically modified organism
|
15,827
|
510
|
GA
|
Top
|
| 112
|
Heredity
|
15,775
|
508
|
C
|
Top
|
| 113
|
Landrace
|
15,729
|
507
|
C
|
Low
|
| 114
|
Francis Crick
|
15,576
|
502
|
B
|
High
|
| 115
|
Phenylketonuria
|
15,433
|
497
|
B
|
Mid
|
| 116
|
Balaji Srinivasan
|
15,398
|
496
|
Start
|
Low
|
| 117
|
William Shockley
|
15,077
|
486
|
B
|
Low
|
| 118
|
Messenger RNA
|
15,055
|
485
|
C
|
High
|
| 119
|
Punnett square
|
15,044
|
485
|
C
|
Top
|
| 120
|
XXYY syndrome
|
14,978
|
483
|
Start
|
Low
|
| 121
|
Population bottleneck
|
14,940
|
481
|
C
|
Mid
|
| 122
|
Leucism
|
14,937
|
481
|
Start
|
Low
|
| 123
|
Brown hair
|
14,908
|
480
|
C
|
Mid
|
| 124
|
X chromosome
|
14,897
|
480
|
B
|
Top
|
| 125
|
Domesticated silver fox
|
14,892
|
480
|
C
|
Low
|
| 126
|
Tay–Sachs disease
|
14,704
|
474
|
B
|
High
|
| 127
|
46,XX/46,XY
|
14,506
|
467
|
C
|
Low
|
| 128
|
Allele
|
14,392
|
464
|
B
|
Top
|
| 129
|
Ploidy
|
14,347
|
462
|
C
|
High
|
| 130
|
Institutional racism
|
14,344
|
462
|
B
|
High
|
| 131
|
De-extinction
|
13,907
|
448
|
C
|
Low
|
| 132
|
Chromosome abnormality
|
13,825
|
445
|
Start
|
High
|
| 133
|
CRISPR gene editing
|
13,736
|
443
|
B
|
Top
|
| 134
|
Early European Farmers
|
13,530
|
436
|
C
|
Mid
|
| 135
|
Atavism
|
13,494
|
435
|
C
|
Mid
|
| 136
|
Stephen Jay Gould
|
13,468
|
434
|
GA
|
Mid
|
| 137
|
Human–animal hybrid
|
13,450
|
433
|
C
|
Low
|
| 138
|
Genetic code
|
13,405
|
432
|
GA
|
Top
|
| 139
|
Plasmodium falciparum
|
13,384
|
431
|
B
|
Low
|
| 140
|
Human Y-chromosome DNA haplogroup
|
13,353
|
430
|
C
|
Mid
|
| 141
|
Genetic testing
|
13,275
|
428
|
B
|
Top
|
| 142
|
Telomere
|
13,274
|
428
|
C
|
Mid
|
| 143
|
Hayflick limit
|
13,272
|
428
|
Start
|
Low
|
| 144
|
Tetralogy of Fallot
|
13,210
|
426
|
C
|
Low
|
| 145
|
Barr body
|
13,160
|
424
|
Start
|
High
|
| 146
|
Human genome
|
13,124
|
423
|
C
|
High
|
| 147
|
Dravet syndrome
|
12,980
|
418
|
C
|
Low
|
| 148
|
Patau syndrome
|
12,929
|
417
|
C
|
Low
|
| 149
|
Homology (biology)
|
12,825
|
413
|
GA
|
High
|
| 150
|
Lectin
|
12,632
|
407
|
C
|
Mid
|
| 151
|
Ancient North Eurasian
|
12,457
|
401
|
C
|
Mid
|
| 152
|
DNA and RNA codon tables
|
12,342
|
398
|
FL
|
High
|
| 153
|
List of organisms by chromosome count
|
12,281
|
396
|
List
|
Low
|
| 154
|
Genome
|
12,129
|
391
|
C
|
High
|
| 155
|
Genotype
|
12,016
|
387
|
Start
|
Top
|
| 156
|
DNA sequencing
|
11,986
|
386
|
C
|
Top
|
| 157
|
Von Hippel–Lindau disease
|
11,969
|
386
|
C
|
Mid
|
| 158
|
Transcription (biology)
|
11,902
|
383
|
B
|
Top
|
| 159
|
Plasmid
|
11,863
|
382
|
C
|
High
|
| 160
|
Ventricular septal defect
|
11,809
|
380
|
C
|
Low
|
| 161
|
Freckle
|
11,778
|
379
|
Start
|
Low
|
| 162
|
G. H. Hardy
|
11,776
|
379
|
C
|
Mid
|
| 163
|
Exogamy
|
11,701
|
377
|
Start
|
Low
|
| 164
|
Western Steppe Herders
|
11,687
|
377
|
C
|
Mid
|
| 165
|
Francis Collins
|
11,623
|
374
|
B
|
Mid
|
| 166
|
Jennifer Doudna
|
11,515
|
371
|
B
|
High
|
| 167
|
Polyploidy
|
11,427
|
368
|
B
|
High
|
| 168
|
Ronald Fisher
|
11,416
|
368
|
B
|
High
|
| 169
|
45,X/46,XY mosaicism
|
11,390
|
367
|
C
|
Low
|
| 170
|
Domestic rabbit
|
11,190
|
360
|
GA
|
Low
|
| 171
|
Origin of SARS-CoV-2
|
11,049
|
356
|
C
|
Low
|
| 172
|
Congenital heart defect
|
11,003
|
354
|
C
|
Mid
|
| 173
|
Aneuploidy
|
10,952
|
353
|
B
|
High
|
| 174
|
Selective breeding
|
10,911
|
351
|
C
|
Top
|
| 175
|
Western hunter-gatherer
|
10,813
|
348
|
C
|
Mid
|
| 176
|
Hereditary haemochromatosis
|
10,811
|
348
|
B
|
Mid
|
| 177
|
Sexual selection
|
10,710
|
345
|
GA
|
Mid
|
| 178
|
DNA profiling
|
10,679
|
344
|
B
|
High
|
| 179
|
Gene therapy
|
10,493
|
338
|
B
|
High
|
| 180
|
Haplodiploidy
|
10,438
|
336
|
C
|
Mid
|
| 181
|
Nazi eugenics
|
10,380
|
334
|
C
|
Mid
|
| 182
|
Citicoline
|
10,352
|
333
|
B
|
Low
|
| 183
|
HLA-B27
|
10,255
|
330
|
C
|
Low
|
| 184
|
Heritability of IQ
|
10,195
|
328
|
C
|
Low
|
| 185
|
Lactase
|
10,123
|
326
|
B
|
Mid
|
| 186
|
Horizontal gene transfer
|
10,113
|
326
|
C
|
High
|
| 187
|
Panthera hybrid
|
9,949
|
320
|
C
|
Mid
|
| 188
|
Genentech
|
9,896
|
319
|
Start
|
Mid
|
| 189
|
Genetic history of Europe
|
9,777
|
315
|
Start
|
Low
|
| 190
|
Auburn hair
|
9,770
|
315
|
Start
|
Low
|
| 191
|
Ectrodactyly
|
9,766
|
315
|
B
|
Mid
|
| 192
|
Mebendazole
|
9,744
|
314
|
C
|
Mid
|
| 193
|
Biological engineering
|
9,656
|
311
|
C
|
High
|
| 194
|
Impulsivity
|
9,614
|
310
|
B
|
Mid
|
| 195
|
Most recent common ancestor
|
9,601
|
309
|
B
|
Mid
|
| 196
|
Eugenics in the United States
|
9,600
|
309
|
Start
|
Low
|
| 197
|
Major histocompatibility complex
|
9,599
|
309
|
B
|
Mid
|
| 198
|
DNA methylation
|
9,550
|
308
|
B
|
High
|
| 199
|
Anthropometry
|
9,493
|
306
|
C
|
Low
|
| 200
|
Variants of SARS-CoV-2
|
9,444
|
304
|
C
|
Low
|
| 201
|
Single-nucleotide polymorphism
|
9,326
|
300
|
C
|
High
|
| 202
|
Genetic drift
|
9,249
|
298
|
GA
|
High
|
| 203
|
Black hair
|
9,177
|
296
|
Start
|
Mid
|
| 204
|
The Code Breaker
|
9,068
|
292
|
Stub
|
Low
|
| 205
|
VACTERL association
|
9,007
|
290
|
Start
|
Mid
|
| 206
|
Genetics and archaeogenetics of South Asia
|
9,004
|
290
|
Start
|
Mid
|
| 207
|
Ethnic groups of Japan
|
8,955
|
288
|
Start
|
Unknown
|
| 208
|
Haplogroup H (mtDNA)
|
8,937
|
288
|
Start
|
Low
|
| 209
|
Base pair
|
8,885
|
286
|
C
|
Top
|
| 210
|
P53
|
8,800
|
283
|
B
|
High
|
| 211
|
Atrial septal defect
|
8,761
|
282
|
B
|
Low
|
| 212
|
Founder effect
|
8,759
|
282
|
C
|
High
|
| 213
|
Y-chromosomal Adam
|
8,687
|
280
|
C
|
High
|
| 214
|
He Jiankui affair
|
8,523
|
274
|
C
|
Low
|
| 215
|
Genetic studies on Turkish people
|
8,469
|
273
|
Start
|
Low
|
| 216
|
Data storage
|
8,465
|
273
|
Start
|
Low
|
| 217
|
RNA world
|
8,453
|
272
|
C
|
Mid
|
| 218
|
Gene expression
|
8,401
|
271
|
B
|
Top
|
| 219
|
Single parent
|
8,374
|
270
|
B
|
Mid
|
| 220
|
Hardy–Weinberg principle
|
8,247
|
266
|
C
|
High
|
| 221
|
Zygosity
|
8,224
|
265
|
C
|
High
|
| 222
|
Recombinant DNA
|
8,149
|
262
|
C
|
High
|
| 223
|
Haplogroup G-M201
|
8,136
|
262
|
Start
|
Low
|
| 224
|
Hypoplastic left heart syndrome
|
8,093
|
261
|
C
|
Low
|
| 225
|
Nucleolus
|
8,038
|
259
|
Start
|
Mid
|
| 226
|
Central dogma of molecular biology
|
8,028
|
258
|
C
|
Top
|
| 227
|
Chédiak–Higashi syndrome
|
7,996
|
257
|
Start
|
Low
|
| 228
|
Heterosis
|
7,977
|
257
|
C
|
High
|
| 229
|
Fertility
|
7,900
|
254
|
C
|
Mid
|
| 230
|
Epileptic spasms
|
7,900
|
254
|
C
|
Low
|
| 231
|
Reverse transcription polymerase chain reaction
|
7,830
|
252
|
Start
|
Mid
|
| 232
|
Synthetic biology
|
7,820
|
252
|
B
|
Mid
|
| 233
|
Protein biosynthesis
|
7,812
|
252
|
B
|
Mid
|
| 234
|
Polymorphism (biology)
|
7,810
|
251
|
B
|
Low
|
| 235
|
Blue rose
|
7,793
|
251
|
Start
|
Low
|
| 236
|
Constriction ring syndrome
|
7,773
|
250
|
C
|
Low
|
| 237
|
Dysgenics
|
7,771
|
250
|
Start
|
Low
|
| 238
|
NF-κB
|
7,740
|
249
|
C
|
High
|
| 239
|
Hispanos of New Mexico
|
7,740
|
249
|
Start
|
Low
|
| 240
|
Haplogroup E-M215
|
7,701
|
248
|
C
|
Low
|
| 241
|
Genomics
|
7,676
|
247
|
B
|
Top
|
| 242
|
Haplogroup J (Y-DNA)
|
7,627
|
246
|
Start
|
Low
|
| 243
|
Proteinogenic amino acid
|
7,603
|
245
|
C
|
High
|
| 244
|
Haplogroup J-M172
|
7,547
|
243
|
Start
|
Low
|
| 245
|
Chin
|
7,540
|
243
|
C
|
Low
|
| 246
|
Monoamine oxidase A
|
7,430
|
239
|
C
|
Mid
|
| 247
|
Mitochondrial disease
|
7,395
|
238
|
C
|
Mid
|
| 248
|
Cyclic adenosine monophosphate
|
7,384
|
238
|
C
|
Mid
|
| 249
|
Advanced maternal age
|
7,371
|
237
|
C
|
Mid
|
| 250
|
Haplogroup U
|
7,342
|
236
|
Start
|
Mid
|
| 251
|
Methylation
|
7,290
|
235
|
C
|
Mid
|
| 252
|
Autosome
|
7,258
|
234
|
Start
|
Top
|
| 253
|
Sexual differentiation in humans
|
7,217
|
232
|
C
|
Mid
|
| 254
|
Nucleic acid double helix
|
7,161
|
231
|
C
|
Mid
|
| 255
|
Error
|
7,147
|
230
|
Start
|
Mid
|
| 256
|
Transfer RNA
|
7,138
|
230
|
B
|
High
|
| 257
|
Transcription factor
|
7,132
|
230
|
B
|
High
|
| 258
|
Haplogroup I-M438
|
7,061
|
227
|
Start
|
Low
|
| 259
|
Translation (biology)
|
6,933
|
223
|
B
|
Top
|
| 260
|
J. B. S. Haldane
|
6,851
|
221
|
C
|
Low
|
| 261
|
Sanger sequencing
|
6,810
|
219
|
C
|
High
|
| 262
|
Human mitochondrial DNA haplogroup
|
6,806
|
219
|
Start
|
Low
|
| 263
|
Laboratory rat
|
6,722
|
216
|
C
|
Mid
|
| 264
|
Heritability of autism
|
6,655
|
214
|
Start
|
Mid
|
| 265
|
Webbed toes
|
6,624
|
213
|
Start
|
Low
|
| 266
|
Transposable element
|
6,595
|
212
|
C
|
High
|
| 267
|
Chromatin
|
6,569
|
211
|
B
|
Mid
|
| 268
|
Humanized mouse
|
6,567
|
211
|
Start
|
Low
|
| 269
|
Phenotypic trait
|
6,551
|
211
|
Start
|
Mid
|
| 270
|
BRCA1
|
6,495
|
209
|
C
|
High
|
| 271
|
RNA splicing
|
6,485
|
209
|
C
|
Top
|
| 272
|
Coefficient of relationship
|
6,466
|
208
|
C
|
Low
|
| 273
|
Genetic history of the British Isles
|
6,380
|
205
|
C
|
Low
|
| 274
|
Eastern hunter-gatherer
|
6,376
|
205
|
C
|
Mid
|
| 275
|
Nicotinamide adenine dinucleotide phosphate
|
6,348
|
204
|
Start
|
Mid
|
| 276
|
Leber's hereditary optic neuropathy
|
6,333
|
204
|
C
|
Mid
|
| 277
|
Wnt signaling pathway
|
6,331
|
204
|
C
|
Mid
|
| 278
|
Genetic history of Egypt
|
6,309
|
203
|
C
|
Low
|
| 279
|
Barbara McClintock
|
6,303
|
203
|
FA
|
High
|
| 280
|
Genomic imprinting
|
6,259
|
201
|
C
|
High
|
| 281
|
ZW sex-determination system
|
6,254
|
201
|
C
|
Mid
|
| 282
|
Genetic recombination
|
6,236
|
201
|
C
|
High
|
| 283
|
Real-time polymerase chain reaction
|
6,219
|
200
|
C
|
Mid
|
| 284
|
Shyness
|
6,215
|
200
|
B
|
Low
|
| 285
|
MicroRNA
|
6,195
|
199
|
B
|
Top
|
| 286
|
Whole genome sequencing
|
6,168
|
198
|
B
|
Top
|
| 287
|
DNA repair
|
6,137
|
197
|
C
|
High
|
| 288
|
Illumina, Inc.
|
6,094
|
196
|
C
|
Low
|
| 289
|
Chromosomal crossover
|
6,074
|
195
|
C
|
High
|
| 290
|
Haplogroup N-M231
|
6,067
|
195
|
Start
|
Low
|
| 291
|
Telegony (inheritance)
|
6,057
|
195
|
C
|
Low
|
| 292
|
GloFish
|
6,036
|
194
|
C
|
Mid
|
| 293
|
Parent
|
6,016
|
194
|
C
|
High
|
| 294
|
Patent ductus arteriosus
|
6,009
|
193
|
Start
|
Mid
|
| 295
|
Somatic cell
|
5,961
|
192
|
Start
|
Mid
|
| 296
|
HER2
|
5,961
|
192
|
C
|
Mid
|
| 297
|
MHC class II
|
5,948
|
191
|
C
|
Mid
|
| 298
|
Genetic memory (psychology)
|
5,948
|
191
|
Start
|
Low
|
| 299
|
Detasseling
|
5,947
|
191
|
B
|
Low
|
| 300
|
X-inactivation
|
5,934
|
191
|
B
|
High
|
| 301
|
Haplogroup I-M170
|
5,920
|
190
|
B
|
Low
|
| 302
|
List of genetic disorders
|
5,915
|
190
|
List
|
High
|
| 303
|
Leigh syndrome
|
5,882
|
189
|
C
|
Low
|
| 304
|
Zebrafish
|
5,868
|
189
|
B
|
Mid
|
| 305
|
Colour wheel theory of love
|
5,865
|
189
|
Stub
|
Low
|
| 306
|
List of redheads
|
5,818
|
187
|
List
|
Low
|
| 307
|
Histone
|
5,781
|
186
|
C
|
Mid
|
| 308
|
Oogenesis
|
5,771
|
186
|
C
|
High
|
| 309
|
Biological determinism
|
5,737
|
185
|
GA
|
Mid
|
| 310
|
Dwarf cat
|
5,708
|
184
|
Start
|
Low
|
| 311
|
Haplogroup J-M267
|
5,687
|
183
|
C
|
Low
|
| 312
|
Telomerase
|
5,677
|
183
|
B
|
High
|
| 313
|
Genealogical DNA test
|
5,670
|
182
|
C
|
Mid
|
| 314
|
Lac operon
|
5,669
|
182
|
C
|
Mid
|
| 315
|
The Population Bomb
|
5,651
|
182
|
B
|
Low
|
| 316
|
Uterus didelphys
|
5,636
|
181
|
Start
|
Low
|
| 317
|
Allopatric speciation
|
5,630
|
181
|
B
|
Low
|
| 318
|
Haplogroup I-M253
|
5,615
|
181
|
B
|
Low
|
| 319
|
Genetically modified crops
|
5,608
|
180
|
B
|
High
|
| 320
|
Disodium inosinate
|
5,597
|
180
|
Start
|
Low
|
| 321
|
Maladaptation
|
5,550
|
179
|
Start
|
Low
|
| 322
|
Homologous chromosome
|
5,546
|
178
|
Start
|
High
|
| 323
|
Laboratory mouse
|
5,522
|
178
|
B
|
Low
|
| 324
|
Twin study
|
5,486
|
176
|
B
|
High
|
| 325
|
Paternal age effect
|
5,478
|
176
|
C
|
Mid
|
| 326
|
Reverse transcriptase
|
5,477
|
176
|
B
|
High
|
| 327
|
Chromosome 21
|
5,475
|
176
|
Start
|
Mid
|
| 328
|
Epistasis
|
5,472
|
176
|
B
|
High
|
| 329
|
Grandmother hypothesis
|
5,440
|
175
|
C
|
Mid
|
| 330
|
Oncogene
|
5,408
|
174
|
C
|
High
|
| 331
|
Mathematical and theoretical biology
|
5,390
|
173
|
C
|
Low
|
| 332
|
Non-Mendelian inheritance
|
5,385
|
173
|
C
|
Mid
|
| 333
|
Causes of cancer
|
5,372
|
173
|
B
|
Mid
|
| 334
|
Factor VIII
|
5,369
|
173
|
Start
|
Low
|
| 335
|
Designer baby
|
5,359
|
172
|
B
|
High
|
| 336
|
Inbreeding depression
|
5,320
|
171
|
C
|
Low
|
| 337
|
Zellweger syndrome
|
5,283
|
170
|
Start
|
Low
|
| 338
|
Racial hygiene
|
5,257
|
169
|
C
|
Low
|
| 339
|
Haplogroup R (Y-DNA)
|
5,239
|
169
|
Start
|
Low
|
| 340
|
DNA polymerase
|
5,228
|
168
|
C
|
Top
|
| 341
|
Purebred
|
5,174
|
166
|
C
|
Low
|
| 342
|
Promoter (genetics)
|
5,167
|
166
|
Start
|
Mid
|
| 343
|
MHC class I
|
5,107
|
164
|
C
|
Mid
|
| 344
|
Sexual selection in humans
|
5,096
|
164
|
C
|
Low
|
| 345
|
Fitness (biology)
|
5,079
|
163
|
C
|
Mid
|
| 346
|
Medical genetics of Jews
|
5,078
|
163
|
Start
|
Low
|
| 347
|
XO sex-determination system
|
5,074
|
163
|
Start
|
Mid
|
| 348
|
Pleiotropy
|
5,065
|
163
|
C
|
High
|
| 349
|
Chromosomal translocation
|
5,037
|
162
|
Start
|
High
|
| 350
|
Trisomy
|
5,034
|
162
|
Start
|
High
|
| 351
|
God gene
|
5,028
|
162
|
Start
|
Mid
|
| 352
|
Plant breeding
|
4,974
|
160
|
C
|
High
|
| 353
|
Sampling bias
|
4,970
|
160
|
C
|
Low
|
| 354
|
X-linked recessive inheritance
|
4,968
|
160
|
Start
|
Mid
|
| 355
|
Genetic diversity
|
4,950
|
159
|
C
|
Mid
|
| 356
|
Genetic history of the Iberian Peninsula
|
4,950
|
159
|
Start
|
Low
|
| 357
|
Epidermal growth factor receptor
|
4,947
|
159
|
C
|
Mid
|
| 358
|
Hershey–Chase experiment
|
4,935
|
159
|
C
|
High
|
| 359
|
RNA interference
|
4,926
|
158
|
FA
|
Top
|
| 360
|
Medical genetics
|
4,924
|
158
|
B
|
Mid
|
| 361
|
Flavivirus
|
4,920
|
158
|
B
|
Mid
|
| 362
|
Hox gene
|
4,889
|
157
|
C
|
High
|
| 363
|
16S ribosomal RNA
|
4,857
|
156
|
C
|
High
|
| 364
|
CpG site
|
4,852
|
156
|
C
|
Mid
|
| 365
|
Aniridia
|
4,839
|
156
|
C
|
Low
|
| 366
|
Uracil
|
4,798
|
154
|
Start
|
Mid
|
| 367
|
Model organism
|
4,781
|
154
|
B
|
Mid
|
| 368
|
RNA polymerase
|
4,777
|
154
|
C
|
Top
|
| 369
|
Phosphorylation
|
4,774
|
154
|
C
|
High
|
| 370
|
Genetic counseling
|
4,761
|
153
|
C
|
Mid
|
| 371
|
Post-translational modification
|
4,739
|
152
|
Start
|
High
|
| 372
|
Human genetic variation
|
4,730
|
152
|
C
|
High
|
| 373
|
Locus (genetics)
|
4,681
|
151
|
Start
|
Mid
|
| 374
|
Nucleic acid sequence
|
4,671
|
150
|
C
|
High
|
| 375
|
Neanderthal genetics
|
4,664
|
150
|
C
|
High
|
| 376
|
Repository for Germinal Choice
|
4,649
|
149
|
Start
|
Unknown
|
| 377
|
Breed
|
4,647
|
149
|
Start
|
Low
|
| 378
|
Haplogroup T-M184
|
4,646
|
149
|
B
|
Low
|
| 379
|
David Reich (geneticist)
|
4,641
|
149
|
Start
|
Mid
|
| 380
|
Haplogroup A (Y-DNA)
|
4,639
|
149
|
C
|
Low
|
| 381
|
Chargaff's rules
|
4,627
|
149
|
Start
|
Low
|
| 382
|
Modern synthesis (20th century)
|
4,626
|
149
|
GA
|
High
|
| 383
|
Endogeny (biology)
|
4,613
|
148
|
Stub
|
Low
|
| 384
|
He Jiankui
|
4,610
|
148
|
B
|
Low
|
| 385
|
Personalized medicine
|
4,608
|
148
|
B
|
Mid
|
| 386
|
Haplogroup Q-M242
|
4,607
|
148
|
C
|
Low
|
| 387
|
Lydia Fairchild
|
4,587
|
147
|
Stub
|
Unknown
|
| 388
|
List of haplogroups of historic people
|
4,561
|
147
|
List
|
Low
|
| 389
|
XXXYY syndrome
|
4,542
|
146
|
GA
|
Low
|
| 390
|
Photo 51
|
4,534
|
146
|
Start
|
Low
|
| 391
|
Janaki Ammal
|
4,507
|
145
|
B
|
Low
|
| 392
|
Systems biology
|
4,506
|
145
|
C
|
High
|
| 393
|
MELAS syndrome
|
4,504
|
145
|
C
|
Low
|
| 394
|
Myc
|
4,493
|
144
|
C
|
High
|
| 395
|
Tongue rolling
|
4,477
|
144
|
Stub
|
Low
|
| 396
|
George Church (geneticist)
|
4,467
|
144
|
C
|
Low
|
| 397
|
Population genetics
|
4,464
|
144
|
C
|
Top
|
| 398
|
Stop codon
|
4,459
|
143
|
Start
|
High
|
| 399
|
Fluorescence in situ hybridization
|
4,449
|
143
|
B
|
Mid
|
| 400
|
Open reading frame
|
4,445
|
143
|
Start
|
Mid
|
| 401
|
Flavin adenine dinucleotide
|
4,423
|
142
|
B
|
Low
|
| 402
|
Biopolymer
|
4,409
|
142
|
C
|
Mid
|
| 403
|
Heritability
|
4,324
|
139
|
C
|
High
|
| 404
|
JAK-STAT signaling pathway
|
4,293
|
138
|
B
|
Mid
|
| 405
|
Haplogroup R1
|
4,290
|
138
|
C
|
Low
|
| 406
|
F1 hybrid
|
4,276
|
137
|
Start
|
High
|
| 407
|
Haplotype
|
4,262
|
137
|
Start
|
High
|
| 408
|
Genome editing
|
4,227
|
136
|
C
|
High
|
| 409
|
XYYY syndrome
|
4,223
|
136
|
GA
|
Low
|
| 410
|
Isoelectric point
|
4,219
|
136
|
C
|
Mid
|
| 411
|
Centromere
|
4,218
|
136
|
C
|
Mid
|
| 412
|
Sex linkage
|
4,191
|
135
|
Start
|
High
|
| 413
|
Genetic variation
|
4,189
|
135
|
Start
|
High
|
| 414
|
Dun gene
|
4,180
|
134
|
C
|
Low
|
| 415
|
Kozak consensus sequence
|
4,172
|
134
|
Start
|
Mid
|
| 416
|
Gene nomenclature
|
4,171
|
134
|
Start
|
Mid
|
| 417
|
Haplogroup L-M20
|
4,159
|
134
|
Start
|
Low
|
| 418
|
Modified vaccinia Ankara
|
4,140
|
133
|
Start
|
Mid
|
| 419
|
Adeno-associated virus
|
4,139
|
133
|
B
|
Low
|
| 420
|
SARS-CoV-2 Delta variant
|
4,124
|
133
|
C
|
Low
|
| 421
|
Introduction to evolution
|
4,119
|
132
|
B
|
High
|
| 422
|
Haplogroup M (mtDNA)
|
4,112
|
132
|
Stub
|
Low
|
| 423
|
Griffith's experiment
|
4,100
|
132
|
Start
|
Mid
|
| 424
|
Haplogroup O-M175
|
4,100
|
132
|
Start
|
Low
|
| 425
|
Haplogroup E-M96
|
4,092
|
132
|
Start
|
Low
|
| 426
|
Cre-Lox recombination
|
4,074
|
131
|
C
|
Mid
|
| 427
|
Eric Lander
|
4,073
|
131
|
C
|
Low
|
| 428
|
Intron
|
4,050
|
130
|
C
|
High
|
| 429
|
Y-chromosomal Aaron
|
4,028
|
129
|
Start
|
Low
|
| 430
|
Hybrid fruit
|
3,994
|
128
|
Stub
|
Unknown
|
| 431
|
Genetic history of the Middle East
|
3,993
|
128
|
C
|
Mid
|
| 432
|
Ruth Benedict
|
3,983
|
128
|
C
|
Low
|
| 433
|
Cas9
|
3,975
|
128
|
C
|
Mid
|
| 434
|
List of unusual biological names
|
3,956
|
127
|
List
|
Low
|
| 435
|
Boar–pig hybrid
|
3,933
|
126
|
Stub
|
Low
|
| 436
|
Sheep farming
|
3,923
|
126
|
C
|
Low
|
| 437
|
Crossbreed
|
3,920
|
126
|
Start
|
Low
|
| 438
|
DNA evidence in the O. J. Simpson murder case
|
3,913
|
126
|
B
|
Low
|
| 439
|
Hi-C (genomic analysis technique)
|
3,899
|
125
|
C
|
Low
|
| 440
|
Mutant
|
3,898
|
125
|
Start
|
Low
|
| 441
|
Bovine somatotropin
|
3,883
|
125
|
C
|
Low
|
| 442
|
FOXP2
|
3,882
|
125
|
B
|
Mid
|
| 443
|
Pedigree collapse
|
3,874
|
124
|
Start
|
Low
|
| 444
|
Regulation of gene expression
|
3,864
|
124
|
C
|
High
|
| 445
|
Apomorphy and synapomorphy
|
3,853
|
124
|
C
|
Low
|
| 446
|
Svante Pääbo
|
3,806
|
122
|
C
|
Low
|
| 447
|
Kin selection
|
3,792
|
122
|
GA
|
Mid
|
| 448
|
Okazaki fragments
|
3,778
|
121
|
B
|
High
|
| 449
|
Homologous recombination
|
3,767
|
121
|
GA
|
High
|
| 450
|
Chromosome 2
|
3,767
|
121
|
C
|
Mid
|
| 451
|
Alternative splicing
|
3,755
|
121
|
B
|
High
|
| 452
|
Neo-Darwinism
|
3,741
|
120
|
Start
|
High
|
| 453
|
Junk DNA
|
3,734
|
120
|
B
|
Mid
|
| 454
|
Cold Spring Harbor Laboratory
|
3,731
|
120
|
Start
|
Mid
|
| 455
|
Behavioural genetics
|
3,714
|
119
|
GA
|
High
|
| 456
|
Y-DNA haplogroups in populations of Europe
|
3,695
|
119
|
List
|
Mid
|
| 457
|
Biomaterial
|
3,690
|
119
|
C
|
Low
|
| 458
|
Adenosine monophosphate
|
3,688
|
118
|
Start
|
Low
|
| 459
|
Genetic studies on Arabs
|
3,681
|
118
|
C
|
Low
|
| 460
|
Transduction (genetics)
|
3,663
|
118
|
C
|
High
|
| 461
|
Hepatitis D
|
3,656
|
117
|
C
|
Low
|
| 462
|
Transgene
|
3,655
|
117
|
B
|
Mid
|
| 463
|
Haplogroup C-M217
|
3,638
|
117
|
Start
|
Low
|
| 464
|
Genome-wide association study
|
3,622
|
116
|
GA
|
Top
|
| 465
|
Epigenetic clock
|
3,605
|
116
|
C
|
Mid
|
| 466
|
The Seven Daughters of Eve
|
3,592
|
115
|
Start
|
Unknown
|
| 467
|
Haplogroup E-V68
|
3,590
|
115
|
C
|
Low
|
| 468
|
Adenosine diphosphate
|
3,565
|
115
|
C
|
Mid
|
| 469
|
Oligomer
|
3,557
|
114
|
Start
|
Low
|
| 470
|
Ancient DNA
|
3,550
|
114
|
C
|
Mid
|
| 471
|
Non-coding RNA
|
3,543
|
114
|
C
|
High
|
| 472
|
Genetic transformation
|
3,542
|
114
|
B
|
Top
|
| 473
|
Non-coding DNA
|
3,517
|
113
|
C
|
Mid
|
| 474
|
DNA extraction
|
3,503
|
113
|
Start
|
Mid
|
| 475
|
Haplogroup K (mtDNA)
|
3,500
|
112
|
Start
|
Low
|
| 476
|
Haplogroup H (Y-DNA)
|
3,497
|
112
|
C
|
Low
|
| 477
|
Bacterial conjugation
|
3,486
|
112
|
C
|
High
|
| 478
|
Tumor suppressor gene
|
3,457
|
111
|
Start
|
High
|
| 479
|
Haplogroup C-M130
|
3,441
|
111
|
Start
|
Low
|
| 480
|
Ribozyme
|
3,416
|
110
|
Start
|
High
|
| 481
|
Phred quality score
|
3,411
|
110
|
Start
|
Low
|
| 482
|
Single-cell sequencing
|
3,391
|
109
|
C
|
High
|
| 483
|
Muller's morphs
|
3,390
|
109
|
C
|
Low
|
| 484
|
Chromosome 15
|
3,385
|
109
|
Start
|
Mid
|
| 485
|
Human Microbiome Project
|
3,374
|
108
|
B
|
Low
|
| 486
|
History of eugenics
|
3,373
|
108
|
B
|
Low
|
| 487
|
Maurice Wilkins
|
3,371
|
108
|
B
|
High
|
| 488
|
KRAS
|
3,358
|
108
|
C
|
Mid
|
| 489
|
Genetically modified food controversies
|
3,330
|
107
|
C
|
Mid
|
| 490
|
Bcl-2
|
3,323
|
107
|
B
|
Mid
|
| 491
|
Microsatellite
|
3,322
|
107
|
C
|
Mid
|
| 492
|
Translational research
|
3,282
|
105
|
C
|
Mid
|
| 493
|
Fixation index
|
3,272
|
105
|
C
|
Low
|
| 494
|
Pedigree chart
|
3,264
|
105
|
Start
|
Mid
|
| 495
|
AquAdvantage salmon
|
3,264
|
105
|
C
|
Low
|
| 496
|
XYYYY syndrome
|
3,251
|
104
|
Start
|
Low
|
| 497
|
Penetrance
|
3,241
|
104
|
C
|
High
|
| 498
|
Coefficient of inbreeding
|
3,230
|
104
|
Start
|
Low
|
| 499
|
Introgression
|
3,227
|
104
|
Start
|
High
|
| 500
|
C57BL/6
|
3,211
|
103
|
Start
|
Low
|
