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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: 2024-04-01 to 2024-04-30
Total views: 9,648,560
Updated: 15:59, 25 May 2024 (UTC)
| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
Axolotl
|
185,341
|
6,178
|
C
|
High
|
| 2
|
Bayer
|
112,248
|
3,741
|
C
|
Low
|
| 3
|
Incest
|
105,820
|
3,527
|
C
|
Low
|
| 4
|
Prion
|
96,056
|
3,201
|
GA
|
Mid
|
| 5
|
DNA
|
91,682
|
3,056
|
FA
|
Top
|
| 6
|
DNA evidence in the O. J. Simpson murder case
|
91,366
|
3,045
|
B
|
Low
|
| 7
|
Eugenics
|
88,164
|
2,938
|
C
|
High
|
| 8
|
Guinea pig
|
82,081
|
2,736
|
B
|
Low
|
| 9
|
Amino acid
|
78,878
|
2,629
|
GA
|
Top
|
| 10
|
Cancer
|
72,403
|
2,413
|
B
|
Top
|
| 11
|
Cystic fibrosis
|
67,510
|
2,250
|
B
|
High
|
| 12
|
Protein
|
65,969
|
2,198
|
GA
|
Top
|
| 13
|
Meiosis
|
62,758
|
2,091
|
C
|
Top
|
| 14
|
Evolution
|
57,794
|
1,926
|
FA
|
Top
|
| 15
|
XY sex-determination system
|
57,036
|
1,901
|
C
|
High
|
| 16
|
Blood type
|
51,232
|
1,707
|
B
|
High
|
| 17
|
Attachment theory
|
50,159
|
1,671
|
B
|
Mid
|
| 18
|
Color blindness
|
49,924
|
1,664
|
B
|
Mid
|
| 19
|
Enzyme
|
49,561
|
1,652
|
FA
|
Top
|
| 20
|
Red hair
|
49,243
|
1,641
|
C
|
Mid
|
| 21
|
Biodiversity
|
48,987
|
1,632
|
C
|
Mid
|
| 22
|
Blue Fugates
|
45,295
|
1,509
|
Start
|
Low
|
| 23
|
Epigenetics
|
44,916
|
1,497
|
B
|
Top
|
| 24
|
Adenosine triphosphate
|
44,894
|
1,496
|
C
|
High
|
| 25
|
Gregor Mendel
|
43,880
|
1,462
|
B
|
High
|
| 26
|
Scientific racism
|
41,943
|
1,398
|
C
|
Low
|
| 27
|
CRISPR
|
41,811
|
1,393
|
B
|
High
|
| 28
|
Rosalind Franklin
|
40,552
|
1,351
|
B
|
High
|
| 29
|
Chromosome
|
40,480
|
1,349
|
B
|
Top
|
| 30
|
Total fertility rate
|
40,320
|
1,344
|
C
|
Low
|
| 31
|
Cousin
|
38,823
|
1,294
|
Start
|
Low
|
| 32
|
Prader–Willi syndrome
|
37,874
|
1,262
|
B
|
Mid
|
| 33
|
SARS-CoV-2
|
37,412
|
1,247
|
B
|
Top
|
| 34
|
Estimates of historical world population
|
37,285
|
1,242
|
Start
|
Low
|
| 35
|
Human skin color
|
36,566
|
1,218
|
B
|
Mid
|
| 36
|
Nicotinamide adenine dinucleotide
|
35,889
|
1,196
|
FA
|
Mid
|
| 37
|
Epicanthic fold
|
35,465
|
1,182
|
C
|
Low
|
| 38
|
DNA and RNA codon tables
|
35,432
|
1,181
|
FL
|
High
|
| 39
|
Polymerase chain reaction
|
35,136
|
1,171
|
B
|
High
|
| 40
|
Blond
|
33,795
|
1,126
|
C
|
Low
|
| 41
|
Inbreeding
|
33,767
|
1,125
|
C
|
Low
|
| 42
|
Genetics
|
33,597
|
1,119
|
FA
|
Top
|
| 43
|
Genetic engineering
|
32,874
|
1,095
|
GA
|
Top
|
| 44
|
Mutation
|
31,991
|
1,066
|
B
|
Top
|
| 45
|
Consanguinity
|
31,431
|
1,047
|
C
|
Low
|
| 46
|
Nucleotide
|
30,443
|
1,014
|
C
|
Top
|
| 47
|
Albinism
|
29,820
|
994
|
C
|
Low
|
| 48
|
Gene
|
29,765
|
992
|
GA
|
Top
|
| 49
|
Gigantism
|
29,712
|
990
|
B
|
High
|
| 50
|
Animal husbandry
|
29,000
|
966
|
GA
|
Mid
|
| 51
|
Galton–Watson process
|
28,623
|
954
|
B
|
Low
|
| 52
|
Wechsler Adult Intelligence Scale
|
28,333
|
944
|
C
|
Low
|
| 53
|
Genetically modified food
|
28,090
|
936
|
B
|
High
|
| 54
|
Genetic studies of Jews
|
27,823
|
927
|
B
|
Mid
|
| 55
|
Japanese people
|
27,765
|
925
|
C
|
Low
|
| 56
|
RNA
|
27,739
|
924
|
GA
|
Top
|
| 57
|
James Watson
|
27,720
|
924
|
B
|
High
|
| 58
|
Charcot–Marie–Tooth disease
|
27,455
|
915
|
C
|
Mid
|
| 59
|
DNA replication
|
27,154
|
905
|
B
|
Unknown
|
| 60
|
Chimera (genetics)
|
27,109
|
903
|
B
|
Mid
|
| 61
|
Human Genome Project
|
27,099
|
903
|
B
|
Top
|
| 62
|
Hybrid (biology)
|
27,068
|
902
|
GA
|
High
|
| 63
|
Nucleic acid
|
26,294
|
876
|
C
|
Mid
|
| 64
|
CC (cat)
|
26,112
|
870
|
Start
|
Mid
|
| 65
|
Punnett square
|
25,813
|
860
|
C
|
Top
|
| 66
|
Last universal common ancestor
|
25,529
|
850
|
GA
|
Mid
|
| 67
|
Cleft lip and cleft palate
|
25,216
|
840
|
B
|
Low
|
| 68
|
Dominance (genetics)
|
25,170
|
839
|
C
|
Top
|
| 69
|
Senescence
|
25,096
|
836
|
C
|
Low
|
| 70
|
Birth defect
|
25,040
|
834
|
B
|
Mid
|
| 71
|
Svalbard Global Seed Vault
|
24,920
|
830
|
B
|
Mid
|
| 72
|
Mitochondrial Eve
|
24,596
|
819
|
B
|
Mid
|
| 73
|
Lactose intolerance
|
24,196
|
806
|
B
|
Low
|
| 74
|
Ribosome
|
24,183
|
806
|
B
|
Top
|
| 75
|
Drosophila melanogaster
|
23,587
|
786
|
B
|
Top
|
| 76
|
Genetically modified organism
|
23,408
|
780
|
GA
|
Top
|
| 77
|
Phenotype
|
23,180
|
772
|
C
|
Top
|
| 78
|
Early human migrations
|
23,165
|
772
|
B
|
Mid
|
| 79
|
M. S. Swaminathan
|
22,831
|
761
|
B
|
Low
|
| 80
|
Pentasomy X
|
22,681
|
756
|
GA
|
Low
|
| 81
|
HeLa
|
22,661
|
755
|
C
|
Low
|
| 82
|
Gamete
|
22,412
|
747
|
Start
|
Mid
|
| 83
|
Human hair color
|
22,223
|
740
|
Start
|
Mid
|
| 84
|
XYY syndrome
|
22,114
|
737
|
B
|
Mid
|
| 85
|
Endogamy
|
21,707
|
723
|
Start
|
Low
|
| 86
|
Cloning
|
21,073
|
702
|
B
|
Top
|
| 87
|
Messenger RNA
|
20,830
|
694
|
C
|
High
|
| 88
|
Mendelian inheritance
|
20,786
|
692
|
C
|
High
|
| 89
|
Plasmid
|
20,554
|
685
|
C
|
High
|
| 90
|
Recent African origin of modern humans
|
20,448
|
681
|
C
|
Mid
|
| 91
|
Population bottleneck
|
20,241
|
674
|
C
|
Mid
|
| 92
|
Genome
|
20,081
|
669
|
C
|
High
|
| 93
|
Cultivar
|
20,050
|
668
|
GA
|
Mid
|
| 94
|
Genetic disorder
|
20,032
|
667
|
B
|
Top
|
| 95
|
Francis Crick
|
19,833
|
661
|
B
|
High
|
| 96
|
Human genome
|
19,830
|
661
|
C
|
High
|
| 97
|
Y chromosome
|
19,644
|
654
|
B
|
High
|
| 98
|
Haplogroup R1a
|
19,555
|
651
|
C
|
Low
|
| 99
|
CRISPR gene editing
|
19,452
|
648
|
B
|
Top
|
| 100
|
DNA sequencing
|
19,295
|
643
|
C
|
Top
|
| 101
|
Haplogroup R1b
|
19,145
|
638
|
C
|
Mid
|
| 102
|
Transcription (biology)
|
18,945
|
631
|
B
|
Top
|
| 103
|
Sex-determination system
|
18,790
|
626
|
C
|
Mid
|
| 104
|
Mitochondrial DNA
|
18,784
|
626
|
B
|
High
|
| 105
|
Descent from Genghis Khan
|
18,718
|
623
|
C
|
Low
|
| 106
|
23andMe
|
18,686
|
622
|
C
|
Mid
|
| 107
|
Allele
|
18,499
|
616
|
B
|
Top
|
| 108
|
Institutional racism
|
17,942
|
598
|
B
|
High
|
| 109
|
Karyotype
|
17,894
|
596
|
C
|
Mid
|
| 110
|
Haplogroup
|
17,721
|
590
|
C
|
Mid
|
| 111
|
Stephen Jay Gould
|
17,647
|
588
|
GA
|
Mid
|
| 112
|
The Bell Curve
|
17,561
|
585
|
C
|
High
|
| 113
|
Gene therapy
|
17,534
|
584
|
B
|
High
|
| 114
|
Heredity
|
17,347
|
578
|
C
|
Top
|
| 115
|
Phenylketonuria
|
17,284
|
576
|
B
|
Mid
|
| 116
|
Humanzee
|
17,246
|
574
|
C
|
Mid
|
| 117
|
Trisomy 18
|
17,216
|
573
|
B
|
Low
|
| 118
|
Domesticated silver fox
|
17,059
|
568
|
C
|
Low
|
| 119
|
Sonic hedgehog protein
|
16,993
|
566
|
B
|
High
|
| 120
|
Homology (biology)
|
16,900
|
563
|
GA
|
High
|
| 121
|
Genetic code
|
16,882
|
562
|
GA
|
Top
|
| 122
|
Tay–Sachs disease
|
16,783
|
559
|
B
|
High
|
| 123
|
Jennifer Doudna
|
16,676
|
555
|
B
|
High
|
| 124
|
Landrace
|
16,652
|
555
|
C
|
Low
|
| 125
|
List of organisms by chromosome count
|
16,455
|
548
|
List
|
Low
|
| 126
|
Incest taboo
|
15,998
|
533
|
C
|
Mid
|
| 127
|
Nazi eugenics
|
15,744
|
524
|
C
|
Mid
|
| 128
|
XX male syndrome
|
15,736
|
524
|
C
|
Low
|
| 129
|
XXXY syndrome
|
15,703
|
523
|
C
|
Low
|
| 130
|
Ploidy
|
15,642
|
521
|
C
|
High
|
| 131
|
De-extinction
|
15,639
|
521
|
C
|
Low
|
| 132
|
Freckle
|
15,634
|
521
|
Start
|
Low
|
| 133
|
DNA methylation
|
15,503
|
516
|
B
|
High
|
| 134
|
Hardy–Weinberg principle
|
15,439
|
514
|
C
|
High
|
| 135
|
Major histocompatibility complex
|
15,386
|
512
|
B
|
Mid
|
| 136
|
Genotype
|
15,257
|
508
|
Start
|
Top
|
| 137
|
Cat coat genetics
|
14,990
|
499
|
C
|
Mid
|
| 138
|
Origin of COVID-19
|
14,958
|
498
|
Start
|
Low
|
| 139
|
Plasmodium falciparum
|
14,897
|
496
|
B
|
Low
|
| 140
|
DNA profiling
|
14,884
|
496
|
B
|
High
|
| 141
|
Balaji Srinivasan
|
14,812
|
493
|
Start
|
Low
|
| 142
|
Selective breeding
|
14,807
|
493
|
C
|
Top
|
| 143
|
Tetralogy of Fallot
|
14,773
|
492
|
C
|
Low
|
| 144
|
William Shockley
|
14,647
|
488
|
B
|
Low
|
| 145
|
Polyploidy
|
14,596
|
486
|
B
|
High
|
| 146
|
Leucism
|
14,536
|
484
|
Start
|
Low
|
| 147
|
Brown hair
|
14,419
|
480
|
C
|
Mid
|
| 148
|
Single-nucleotide polymorphism
|
14,078
|
469
|
C
|
High
|
| 149
|
G. H. Hardy
|
14,066
|
468
|
C
|
Mid
|
| 150
|
Sexual selection
|
14,033
|
467
|
GA
|
Mid
|
| 151
|
Ronald Fisher
|
13,911
|
463
|
B
|
High
|
| 152
|
Transfer RNA
|
13,883
|
462
|
B
|
High
|
| 153
|
Domestic rabbit
|
13,851
|
461
|
B
|
Low
|
| 154
|
Genetic drift
|
13,828
|
460
|
GA
|
High
|
| 155
|
Early European Farmers
|
13,659
|
455
|
C
|
Mid
|
| 156
|
Central dogma of molecular biology
|
13,559
|
451
|
C
|
Top
|
| 157
|
Blue rose
|
13,539
|
451
|
Start
|
Low
|
| 158
|
Recombinant DNA
|
13,501
|
450
|
C
|
High
|
| 159
|
Zebrafish
|
13,499
|
449
|
B
|
Mid
|
| 160
|
Sanger sequencing
|
13,483
|
449
|
C
|
High
|
| 161
|
Chin
|
13,470
|
449
|
C
|
Low
|
| 162
|
Ancient North Eurasian
|
13,450
|
448
|
C
|
Mid
|
| 163
|
Eugenics in the United States
|
13,221
|
440
|
Start
|
Low
|
| 164
|
P53
|
13,172
|
439
|
B
|
High
|
| 165
|
Telomere
|
13,135
|
437
|
C
|
Mid
|
| 166
|
Atavism
|
12,800
|
426
|
C
|
Mid
|
| 167
|
Founder effect
|
12,666
|
422
|
C
|
High
|
| 168
|
Ventricular septal defect
|
12,609
|
420
|
C
|
Low
|
| 169
|
Human Y-chromosome DNA haplogroup
|
12,603
|
420
|
C
|
Mid
|
| 170
|
Lectin
|
12,581
|
419
|
C
|
Mid
|
| 171
|
Protein biosynthesis
|
12,527
|
417
|
B
|
Mid
|
| 172
|
Reverse transcription polymerase chain reaction
|
12,507
|
416
|
Start
|
Mid
|
| 173
|
Patau syndrome
|
12,461
|
415
|
C
|
Low
|
| 174
|
Human–animal hybrid
|
12,425
|
414
|
C
|
Low
|
| 175
|
Gene expression
|
12,300
|
410
|
B
|
Top
|
| 176
|
RNA splicing
|
12,254
|
408
|
C
|
Top
|
| 177
|
Francis Collins
|
12,251
|
408
|
B
|
Mid
|
| 178
|
Panthera hybrid
|
12,101
|
403
|
C
|
Mid
|
| 179
|
Fertility
|
12,031
|
401
|
C
|
Mid
|
| 180
|
Single parent
|
11,928
|
397
|
B
|
Mid
|
| 181
|
Homologous chromosome
|
11,792
|
393
|
Start
|
High
|
| 182
|
Translation (biology)
|
11,718
|
390
|
B
|
Top
|
| 183
|
Anthropometry
|
11,639
|
387
|
C
|
Low
|
| 184
|
Black hair
|
11,542
|
384
|
Start
|
Mid
|
| 185
|
Auburn hair
|
11,492
|
383
|
Start
|
Low
|
| 186
|
Genentech
|
11,478
|
382
|
Start
|
Mid
|
| 187
|
X chromosome
|
11,461
|
382
|
B
|
Top
|
| 188
|
He Jiankui affair
|
11,376
|
379
|
C
|
Low
|
| 189
|
Lactase
|
11,319
|
377
|
B
|
Mid
|
| 190
|
Base pair
|
11,235
|
374
|
C
|
Top
|
| 191
|
Mosaic (genetics)
|
11,133
|
371
|
C
|
Mid
|
| 192
|
Congenital heart defect
|
11,083
|
369
|
C
|
Mid
|
| 193
|
Oogenesis
|
10,968
|
365
|
C
|
High
|
| 194
|
Ethnic groups of Japan
|
10,942
|
364
|
Start
|
Unknown
|
| 195
|
Heritability of IQ
|
10,807
|
360
|
C
|
Low
|
| 196
|
Citicoline
|
10,806
|
360
|
B
|
Low
|
| 197
|
NF-κB
|
10,791
|
359
|
Unknown
|
High
|
| 198
|
Cyclic adenosine monophosphate
|
10,761
|
358
|
C
|
Mid
|
| 199
|
Lac operon
|
10,684
|
356
|
C
|
Mid
|
| 200
|
Transposable element
|
10,636
|
354
|
C
|
High
|
| 201
|
Genetic testing
|
10,635
|
354
|
B
|
Top
|
| 202
|
Transcription factor
|
10,615
|
353
|
B
|
High
|
| 203
|
Chromatin
|
10,602
|
353
|
B
|
Mid
|
| 204
|
Real-time polymerase chain reaction
|
10,526
|
350
|
C
|
Mid
|
| 205
|
Parent
|
10,470
|
349
|
C
|
High
|
| 206
|
Y-chromosomal Adam
|
10,469
|
348
|
C
|
High
|
| 207
|
Exogamy
|
10,373
|
345
|
Start
|
Low
|
| 208
|
Nicotinamide adenine dinucleotide phosphate
|
10,281
|
342
|
Start
|
Mid
|
| 209
|
Most recent common ancestor
|
10,191
|
339
|
B
|
Mid
|
| 210
|
DNA polymerase
|
10,170
|
339
|
C
|
Top
|
| 211
|
Western Steppe Herders
|
10,169
|
338
|
C
|
Mid
|
| 212
|
Methylation
|
10,159
|
338
|
C
|
Mid
|
| 213
|
Aneuploidy
|
10,119
|
337
|
B
|
High
|
| 214
|
Sex chromosome
|
10,105
|
336
|
Start
|
High
|
| 215
|
Polymorphism (biology)
|
10,103
|
336
|
B
|
Low
|
| 216
|
Proteinogenic amino acid
|
10,096
|
336
|
C
|
High
|
| 217
|
RNA interference
|
10,094
|
336
|
FA
|
Top
|
| 218
|
RNA world
|
10,081
|
336
|
C
|
Mid
|
| 219
|
Horizontal gene transfer
|
10,066
|
335
|
C
|
High
|
| 220
|
MicroRNA
|
9,945
|
331
|
B
|
Top
|
| 221
|
Hereditary haemochromatosis
|
9,893
|
329
|
B
|
Mid
|
| 222
|
List of genetic disorders
|
9,850
|
328
|
List
|
High
|
| 223
|
HLA-B27
|
9,788
|
326
|
C
|
Low
|
| 224
|
Biological engineering
|
9,757
|
325
|
C
|
High
|
| 225
|
DNA repair
|
9,741
|
324
|
C
|
High
|
| 226
|
Somatic cell
|
9,645
|
321
|
Start
|
Mid
|
| 227
|
Haplogroup H (mtDNA)
|
9,634
|
321
|
Start
|
Low
|
| 228
|
Hayflick limit
|
9,595
|
319
|
Start
|
Low
|
| 229
|
Friedreich's ataxia
|
9,549
|
318
|
GA
|
Mid
|
| 230
|
Photo 51
|
9,534
|
317
|
Start
|
Low
|
| 231
|
Synthetic biology
|
9,515
|
317
|
B
|
Mid
|
| 232
|
Western Hunter-Gatherer
|
9,484
|
316
|
C
|
Mid
|
| 233
|
Epistasis
|
9,400
|
313
|
B
|
High
|
| 234
|
Genetically modified crops
|
9,375
|
312
|
B
|
High
|
| 235
|
Nucleic acid double helix
|
9,330
|
311
|
C
|
Mid
|
| 236
|
Genomics
|
9,242
|
308
|
B
|
Top
|
| 237
|
Nucleolus
|
9,237
|
307
|
Start
|
Mid
|
| 238
|
Wnt signaling pathway
|
9,221
|
307
|
C
|
Mid
|
| 239
|
Genetic history of Europe
|
9,158
|
305
|
Start
|
Low
|
| 240
|
Promoter (genetics)
|
9,154
|
305
|
Start
|
Mid
|
| 241
|
Monoamine oxidase A
|
9,137
|
304
|
C
|
Mid
|
| 242
|
Genetic recombination
|
9,104
|
303
|
C
|
High
|
| 243
|
Tuberous sclerosis
|
9,104
|
303
|
B
|
Mid
|
| 244
|
Heterosis
|
8,961
|
298
|
C
|
High
|
| 245
|
Histone
|
8,913
|
297
|
C
|
Mid
|
| 246
|
Impulsivity
|
8,904
|
296
|
B
|
Mid
|
| 247
|
Barbara McClintock
|
8,816
|
293
|
FA
|
High
|
| 248
|
MHC class II
|
8,699
|
289
|
C
|
Mid
|
| 249
|
Whole genome sequencing
|
8,690
|
289
|
B
|
Top
|
| 250
|
Zygosity
|
8,689
|
289
|
C
|
High
|
| 251
|
MHC class I
|
8,666
|
288
|
C
|
Mid
|
| 252
|
Laboratory rat
|
8,591
|
286
|
C
|
Mid
|
| 253
|
He Jiankui
|
8,564
|
285
|
B
|
Low
|
| 254
|
Ectrodactyly
|
8,560
|
285
|
B
|
Mid
|
| 255
|
Reverse transcriptase
|
8,535
|
284
|
B
|
High
|
| 256
|
Stop codon
|
8,395
|
279
|
Start
|
High
|
| 257
|
Post-translational modification
|
8,388
|
279
|
Start
|
High
|
| 258
|
Dysgenics
|
8,336
|
277
|
Start
|
Low
|
| 259
|
Open reading frame
|
8,297
|
276
|
Start
|
Mid
|
| 260
|
J. B. S. Haldane
|
8,294
|
276
|
C
|
Low
|
| 261
|
Genetic diversity
|
8,220
|
274
|
C
|
Mid
|
| 262
|
Allopatric speciation
|
8,155
|
271
|
C
|
Low
|
| 263
|
Chromosome abnormality
|
8,145
|
271
|
Start
|
High
|
| 264
|
Genetic studies on Turkish people
|
8,118
|
270
|
Start
|
Low
|
| 265
|
RNA polymerase
|
8,045
|
268
|
C
|
Top
|
| 266
|
Mitochondrial disease
|
8,032
|
267
|
C
|
Mid
|
| 267
|
Genetics and archaeogenetics of South Asia
|
7,934
|
264
|
Start
|
Mid
|
| 268
|
Data storage
|
7,916
|
263
|
Start
|
Low
|
| 269
|
Factor VIII
|
7,894
|
263
|
Start
|
Low
|
| 270
|
Atrial septal defect
|
7,883
|
262
|
B
|
Low
|
| 271
|
CpG site
|
7,876
|
262
|
C
|
Mid
|
| 272
|
Designer baby
|
7,846
|
261
|
B
|
High
|
| 273
|
Oncogene
|
7,808
|
260
|
C
|
High
|
| 274
|
Haplogroup E-M215
|
7,801
|
260
|
C
|
Low
|
| 275
|
Von Hippel–Lindau disease
|
7,795
|
259
|
C
|
Mid
|
| 276
|
Chromosomal crossover
|
7,741
|
258
|
C
|
High
|
| 277
|
Isoelectric point
|
7,740
|
258
|
C
|
Mid
|
| 278
|
Fluorescence in situ hybridization
|
7,731
|
257
|
B
|
Mid
|
| 279
|
Mebendazole
|
7,684
|
256
|
C
|
Mid
|
| 280
|
Coefficient of relationship
|
7,674
|
255
|
C
|
Low
|
| 281
|
16S ribosomal RNA
|
7,667
|
255
|
C
|
High
|
| 282
|
Okazaki fragments
|
7,614
|
253
|
B
|
High
|
| 283
|
XXYY syndrome
|
7,599
|
253
|
Start
|
Low
|
| 284
|
Genetic history of Egypt
|
7,579
|
252
|
C
|
Low
|
| 285
|
Haplogroup J-M172
|
7,535
|
251
|
Start
|
Low
|
| 286
|
Hershey–Chase experiment
|
7,521
|
250
|
C
|
High
|
| 287
|
Fitness (biology)
|
7,508
|
250
|
C
|
Mid
|
| 288
|
Haplogroup J (Y-DNA)
|
7,503
|
250
|
Start
|
Low
|
| 289
|
Telomerase
|
7,496
|
249
|
B
|
High
|
| 290
|
Hox gene
|
7,468
|
248
|
C
|
High
|
| 291
|
BRCA1
|
7,453
|
248
|
C
|
High
|
| 292
|
HER2
|
7,444
|
248
|
C
|
Mid
|
| 293
|
X-linked recessive inheritance
|
7,435
|
247
|
Start
|
Mid
|
| 294
|
Flavin adenine dinucleotide
|
7,431
|
247
|
B
|
Low
|
| 295
|
Uracil
|
7,425
|
247
|
Start
|
Mid
|
| 296
|
Autosome
|
7,413
|
247
|
Start
|
Top
|
| 297
|
Haplogroup G-M201
|
7,307
|
243
|
Start
|
Low
|
| 298
|
Phosphorylation
|
7,288
|
242
|
C
|
High
|
| 299
|
Twin study
|
7,283
|
242
|
B
|
High
|
| 300
|
Heritability of autism
|
7,279
|
242
|
Start
|
Mid
|
| 301
|
Human mitochondrial DNA haplogroup
|
7,272
|
242
|
Start
|
Low
|
| 302
|
Webbed toes
|
7,134
|
237
|
Start
|
Low
|
| 303
|
Cre-Lox recombination
|
7,073
|
235
|
C
|
Mid
|
| 304
|
Chargaff's rules
|
7,043
|
234
|
Start
|
Low
|
| 305
|
Chromosomal translocation
|
7,030
|
234
|
Start
|
High
|
| 306
|
Genome editing
|
7,027
|
234
|
C
|
High
|
| 307
|
GloFish
|
6,977
|
232
|
C
|
Mid
|
| 308
|
Regulation of gene expression
|
6,962
|
232
|
C
|
High
|
| 309
|
List of redheads
|
6,913
|
230
|
List
|
Low
|
| 310
|
Cas9
|
6,878
|
229
|
C
|
Mid
|
| 311
|
Transformation (genetics)
|
6,864
|
228
|
B
|
Top
|
| 312
|
Colour wheel theory of love
|
6,824
|
227
|
Stub
|
Low
|
| 313
|
Guanosine triphosphate
|
6,810
|
227
|
Start
|
Mid
|
| 314
|
5α-Reductase 2 deficiency
|
6,809
|
226
|
B
|
Low
|
| 315
|
Shyness
|
6,789
|
226
|
B
|
Low
|
| 316
|
Sex-determining region Y protein
|
6,789
|
226
|
C
|
Low
|
| 317
|
Locus (genetics)
|
6,779
|
225
|
Start
|
Mid
|
| 318
|
Causes of cancer
|
6,766
|
225
|
B
|
Mid
|
| 319
|
Plant breeding
|
6,758
|
225
|
C
|
High
|
| 320
|
Epidermal growth factor receptor
|
6,749
|
224
|
C
|
Mid
|
| 321
|
Haplogroup U
|
6,746
|
224
|
Start
|
Mid
|
| 322
|
Myc
|
6,740
|
224
|
C
|
High
|
| 323
|
Homologous recombination
|
6,729
|
224
|
GA
|
High
|
| 324
|
Illumina, Inc.
|
6,709
|
223
|
C
|
Low
|
| 325
|
Laboratory mouse
|
6,703
|
223
|
B
|
Low
|
| 326
|
Variants of SARS-CoV-2
|
6,665
|
222
|
C
|
Low
|
| 327
|
Disodium inosinate
|
6,620
|
220
|
Start
|
Low
|
| 328
|
Transduction (genetics)
|
6,606
|
220
|
C
|
High
|
| 329
|
Patent ductus arteriosus
|
6,585
|
219
|
Start
|
Mid
|
| 330
|
Eastern Hunter-Gatherer
|
6,560
|
218
|
C
|
Mid
|
| 331
|
Tumor suppressor gene
|
6,543
|
218
|
Start
|
High
|
| 332
|
Mathematical and theoretical biology
|
6,519
|
217
|
C
|
Low
|
| 333
|
Pleiotropy
|
6,471
|
215
|
C
|
High
|
| 334
|
Hispanos of New Mexico
|
6,417
|
213
|
Start
|
Low
|
| 335
|
Bacterial conjugation
|
6,355
|
211
|
C
|
High
|
| 336
|
Genetic memory (psychology)
|
6,330
|
211
|
Start
|
Low
|
| 337
|
Alternative splicing
|
6,293
|
209
|
B
|
High
|
| 338
|
Medical genetics of Jews
|
6,291
|
209
|
Start
|
Low
|
| 339
|
Inbreeding depression
|
6,279
|
209
|
C
|
Low
|
| 340
|
Dwarf cat
|
6,272
|
209
|
Start
|
Low
|
| 341
|
Point mutation
|
6,260
|
208
|
C
|
High
|
| 342
|
Taq polymerase
|
6,235
|
207
|
C
|
Mid
|
| 343
|
JAK-STAT signaling pathway
|
6,228
|
207
|
B
|
Mid
|
| 344
|
Gene flow
|
6,215
|
207
|
Start
|
High
|
| 345
|
Centromere
|
6,182
|
206
|
C
|
Mid
|
| 346
|
Ribozyme
|
6,152
|
205
|
Start
|
High
|
| 347
|
Operon
|
6,134
|
204
|
B
|
Mid
|
| 348
|
The Population Bomb
|
6,121
|
204
|
B
|
Low
|
| 349
|
Sex linkage
|
6,112
|
203
|
Start
|
High
|
| 350
|
Paternal age effect
|
6,080
|
202
|
C
|
Mid
|
| 351
|
Haplogroup J-M267
|
6,060
|
202
|
C
|
Low
|
| 352
|
Haplogroup N-M231
|
5,999
|
199
|
Start
|
Low
|
| 353
|
Racial hygiene
|
5,994
|
199
|
C
|
Low
|
| 354
|
Adeno-associated virus
|
5,994
|
199
|
B
|
Low
|
| 355
|
Molecular cloning
|
5,968
|
198
|
C
|
High
|
| 356
|
Haplogroup I-M170
|
5,963
|
198
|
B
|
Low
|
| 357
|
Population genetics
|
5,947
|
198
|
C
|
Top
|
| 358
|
Genetic variation
|
5,937
|
197
|
Start
|
High
|
| 359
|
Chromosome 21
|
5,933
|
197
|
Start
|
Mid
|
| 360
|
Human genetic variation
|
5,908
|
196
|
C
|
High
|
| 361
|
Neanderthal genetics
|
5,892
|
196
|
C
|
High
|
| 362
|
Sampling bias
|
5,889
|
196
|
C
|
Low
|
| 363
|
X-inactivation
|
5,806
|
193
|
B
|
High
|
| 364
|
Phenotypic trait
|
5,795
|
193
|
Start
|
Mid
|
| 365
|
Biological determinism
|
5,789
|
192
|
B
|
Mid
|
| 366
|
Topoisomerase
|
5,780
|
192
|
C
|
High
|
| 367
|
Barr body
|
5,762
|
192
|
Start
|
High
|
| 368
|
Nucleic acid sequence
|
5,760
|
192
|
C
|
High
|
| 369
|
Introduction to evolution
|
5,744
|
191
|
B
|
High
|
| 370
|
Genomic imprinting
|
5,733
|
191
|
C
|
High
|
| 371
|
Genetic linkage
|
5,716
|
190
|
Start
|
High
|
| 372
|
Griffith's experiment
|
5,710
|
190
|
Start
|
Mid
|
| 373
|
Intron
|
5,707
|
190
|
C
|
High
|
| 374
|
Microsatellite
|
5,705
|
190
|
C
|
Mid
|
| 375
|
Model organism
|
5,695
|
189
|
B
|
Mid
|
| 376
|
ZW sex-determination system
|
5,642
|
188
|
Start
|
Mid
|
| 377
|
Restriction fragment length polymorphism
|
5,637
|
187
|
Start
|
Mid
|
| 378
|
Identical Strangers
|
5,609
|
186
|
Start
|
Low
|
| 379
|
Breed
|
5,586
|
186
|
Start
|
Low
|
| 380
|
Heritability
|
5,580
|
186
|
C
|
High
|
| 381
|
PBR322
|
5,550
|
185
|
Start
|
Low
|
| 382
|
Biopolymer
|
5,543
|
184
|
C
|
Mid
|
| 383
|
Peppered moth evolution
|
5,504
|
183
|
GA
|
Mid
|
| 384
|
Haplogroup I-M438
|
5,500
|
183
|
Start
|
Low
|
| 385
|
Haplogroup I-M253
|
5,495
|
183
|
B
|
Low
|
| 386
|
Start codon
|
5,480
|
182
|
Start
|
Top
|
| 387
|
Dravet syndrome
|
5,464
|
182
|
C
|
Low
|
| 388
|
KRAS
|
5,464
|
182
|
C
|
Mid
|
| 389
|
Directionality (molecular biology)
|
5,429
|
180
|
Start
|
High
|
| 390
|
Flavivirus
|
5,420
|
180
|
B
|
Mid
|
| 391
|
Ras GTPase
|
5,413
|
180
|
B
|
High
|
| 392
|
Sexual selection in humans
|
5,375
|
179
|
C
|
Low
|
| 393
|
Modern synthesis (20th century)
|
5,373
|
179
|
GA
|
High
|
| 394
|
Trisomy
|
5,353
|
178
|
Start
|
High
|
| 395
|
Single-cell sequencing
|
5,346
|
178
|
C
|
High
|
| 396
|
Korean ethnic nationalism
|
5,343
|
178
|
C
|
Low
|
| 397
|
Genetic history of the Iberian Peninsula
|
5,313
|
177
|
Start
|
Low
|
| 398
|
Hi-C (genomic analysis technique)
|
5,300
|
176
|
C
|
Low
|
| 399
|
Haplogroup R (Y-DNA)
|
5,299
|
176
|
Start
|
Low
|
| 400
|
Personalized medicine
|
5,290
|
176
|
B
|
Mid
|
| 401
|
Multiple sequence alignment
|
5,259
|
175
|
Unknown
|
Mid
|
| 402
|
Gene nomenclature
|
5,251
|
175
|
Start
|
Mid
|
| 403
|
Non-coding RNA
|
5,247
|
174
|
C
|
High
|
| 404
|
Oligonucleotide
|
5,246
|
174
|
Start
|
Mid
|
| 405
|
Haplotype
|
5,236
|
174
|
Start
|
High
|
| 406
|
George Church (geneticist)
|
5,232
|
174
|
C
|
Low
|
| 407
|
Svante Pääbo
|
5,197
|
173
|
C
|
Low
|
| 408
|
Apomorphy and synapomorphy
|
5,187
|
172
|
C
|
Low
|
| 409
|
Systems biology
|
5,176
|
172
|
C
|
High
|
| 410
|
Tongue rolling
|
5,167
|
172
|
Stub
|
Low
|
| 411
|
Reproductive isolation
|
5,164
|
172
|
C
|
High
|
| 412
|
Adenosine monophosphate
|
5,158
|
171
|
Start
|
Low
|
| 413
|
F1 hybrid
|
5,158
|
171
|
Start
|
High
|
| 414
|
Genome-wide association study
|
5,137
|
171
|
GA
|
Top
|
| 415
|
Genealogical DNA test
|
5,111
|
170
|
C
|
Mid
|
| 416
|
Flavr Savr
|
5,055
|
168
|
Start
|
Unknown
|
| 417
|
Non-homologous end joining
|
5,054
|
168
|
C
|
Mid
|
| 418
|
TATA box
|
5,045
|
168
|
B
|
High
|
| 419
|
DNA extraction
|
5,023
|
167
|
Start
|
Mid
|
| 420
|
Lydia Fairchild
|
4,988
|
166
|
Stub
|
Unknown
|
| 421
|
Purebred
|
4,954
|
165
|
C
|
Low
|
| 422
|
Endogeny (biology)
|
4,953
|
165
|
Stub
|
Low
|
| 423
|
Uterus didelphys
|
4,937
|
164
|
Start
|
Low
|
| 424
|
Adenosine diphosphate
|
4,935
|
164
|
C
|
Mid
|
| 425
|
Pedigree chart
|
4,935
|
164
|
Start
|
Mid
|
| 426
|
Maladaptation
|
4,889
|
162
|
Start
|
Low
|
| 427
|
Bcl-2
|
4,879
|
162
|
B
|
Mid
|
| 428
|
Directional selection
|
4,876
|
162
|
Start
|
Low
|
| 429
|
Genetic history of the British Isles
|
4,866
|
162
|
C
|
Low
|
| 430
|
Jefferson–Hemings controversy
|
4,848
|
161
|
B
|
Low
|
| 431
|
Kozak consensus sequence
|
4,844
|
161
|
Start
|
Mid
|
| 432
|
Gene delivery
|
4,827
|
160
|
B
|
High
|
| 433
|
Transgene
|
4,811
|
160
|
B
|
Mid
|
| 434
|
Frameshift mutation
|
4,760
|
158
|
B
|
High
|
| 435
|
Telegony (inheritance)
|
4,755
|
158
|
C
|
Low
|
| 436
|
Non-coding DNA
|
4,754
|
158
|
C
|
Mid
|
| 437
|
Somatic cell nuclear transfer
|
4,745
|
158
|
C
|
Mid
|
| 438
|
Bovine somatotropin
|
4,738
|
157
|
C
|
Low
|
| 439
|
Maurice Wilkins
|
4,728
|
157
|
B
|
High
|
| 440
|
Crossbreed
|
4,720
|
157
|
Start
|
Low
|
| 441
|
Phred quality score
|
4,716
|
157
|
Start
|
Low
|
| 442
|
Kin selection
|
4,714
|
157
|
GA
|
Mid
|
| 443
|
Mutant
|
4,711
|
157
|
Start
|
Low
|
| 444
|
Chromosome 2
|
4,707
|
156
|
C
|
Mid
|
| 445
|
Polytene chromosome
|
4,684
|
156
|
Start
|
Mid
|
| 446
|
Complementary DNA
|
4,663
|
155
|
Start
|
Mid
|
| 447
|
Haplogroup Q-M242
|
4,656
|
155
|
C
|
Low
|
| 448
|
God gene
|
4,653
|
155
|
Start
|
Mid
|
| 449
|
STR analysis
|
4,618
|
153
|
Start
|
Low
|
| 450
|
Leigh syndrome
|
4,601
|
153
|
C
|
Low
|
| 451
|
Fisherian runaway
|
4,598
|
153
|
Start
|
Mid
|
| 452
|
Nucleoside triphosphate
|
4,591
|
153
|
Start
|
High
|
| 453
|
Oligomer
|
4,590
|
153
|
Start
|
Low
|
| 454
|
List of haplogroups of historic people
|
4,537
|
151
|
List
|
Low
|
| 455
|
Peter and Rosemary Grant
|
4,533
|
151
|
C
|
Unknown
|
| 456
|
Y-chromosomal Aaron
|
4,525
|
150
|
Start
|
Low
|
| 457
|
Missense mutation
|
4,523
|
150
|
Start
|
Mid
|
| 458
|
DNA supercoil
|
4,517
|
150
|
C
|
Mid
|
| 459
|
Haplogroup A (Y-DNA)
|
4,516
|
150
|
C
|
Low
|
| 460
|
Chromosome 1
|
4,515
|
150
|
Start
|
Low
|
| 461
|
Molecular clock
|
4,512
|
150
|
C
|
High
|
| 462
|
Gene mapping
|
4,509
|
150
|
Start
|
Low
|
| 463
|
Nucleoid
|
4,504
|
150
|
B
|
Mid
|
| 464
|
Enhancer (genetics)
|
4,500
|
150
|
C
|
High
|
| 465
|
List of unusual biological names
|
4,494
|
149
|
List
|
Low
|
| 466
|
C57BL/6
|
4,492
|
149
|
Start
|
Low
|
| 467
|
Hepatitis D
|
4,484
|
149
|
C
|
Low
|
| 468
|
Sense (molecular biology)
|
4,482
|
149
|
C
|
High
|
| 469
|
Ruth Benedict
|
4,453
|
148
|
C
|
Low
|
| 470
|
Exon
|
4,433
|
147
|
C
|
Top
|
| 471
|
Sheep farming
|
4,431
|
147
|
C
|
Low
|
| 472
|
Exome sequencing
|
4,426
|
147
|
C
|
High
|
| 473
|
Neo-Darwinism
|
4,403
|
146
|
Start
|
High
|
| 474
|
SARS-CoV-2 Delta variant
|
4,382
|
146
|
C
|
Low
|
| 475
|
Biomaterial
|
4,361
|
145
|
C
|
Low
|
| 476
|
Haplogroup X (mtDNA)
|
4,359
|
145
|
Start
|
Mid
|
| 477
|
Haplogroup H (Y-DNA)
|
4,320
|
144
|
C
|
Low
|
| 478
|
Genetically modified food controversies
|
4,314
|
143
|
C
|
Mid
|
| 479
|
Haplogroup R1
|
4,301
|
143
|
C
|
Low
|
| 480
|
Haplogroup E-M96
|
4,293
|
143
|
Start
|
Low
|
| 481
|
Genetic history of the Middle East
|
4,287
|
142
|
C
|
Mid
|
| 482
|
Sequence homology
|
4,269
|
142
|
C
|
Top
|
| 483
|
Gene knockout
|
4,261
|
142
|
Start
|
Mid
|
| 484
|
Eric Lander
|
4,261
|
142
|
C
|
Low
|
| 485
|
Retrotransposon
|
4,250
|
141
|
C
|
High
|
| 486
|
History of eugenics
|
4,249
|
141
|
B
|
Low
|
| 487
|
Penetrance
|
4,248
|
141
|
C
|
High
|
| 488
|
Ancient DNA
|
4,239
|
141
|
C
|
Mid
|
| 489
|
Sexual differentiation in humans
|
4,239
|
141
|
C
|
Mid
|
| 490
|
Linkage disequilibrium
|
4,237
|
141
|
C
|
High
|
| 491
|
Combined DNA Index System
|
4,234
|
141
|
GA
|
Low
|
| 492
|
Electroporation
|
4,229
|
140
|
C
|
High
|
| 493
|
Nondisjunction
|
4,223
|
140
|
B
|
High
|
| 494
|
Haplogroup E-V68
|
4,222
|
140
|
C
|
Low
|
| 495
|
Hypoplastic left heart syndrome
|
4,204
|
140
|
C
|
Low
|
| 496
|
Copy number variation
|
4,201
|
140
|
B
|
High
|
| 497
|
Dun gene
|
4,200
|
140
|
C
|
Low
|
| 498
|
Fixation index
|
4,199
|
139
|
C
|
Low
|
| 499
|
Pedigree collapse
|
4,181
|
139
|
Start
|
Low
|
| 500
|
Translational research
|
4,158
|
138
|
C
|
Mid
|
