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This is a list of pages in the scope of Wikipedia:WikiProject Genetics along with their pageviews, including all redirects.
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Period: 2022-06-01 to 2022-06-30
Total views: 8,458,954
Updated: 20:07, 6 July 2022 (UTC)
| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
Axolotl
|
114,371
|
3,812
|
C
|
High
|
| 2
|
DNA
|
102,983
|
3,432
|
FA
|
Top
|
| 3
|
Eugenics
|
92,916
|
3,097
|
C
|
High
|
| 4
|
Incest
|
87,716
|
2,923
|
C
|
Low
|
| 5
|
Cancer
|
80,227
|
2,674
|
B
|
Top
|
| 6
|
Guinea pig
|
71,982
|
2,399
|
B
|
Low
|
| 7
|
Cystic fibrosis
|
65,603
|
2,186
|
B
|
High
|
| 8
|
Amino acid
|
63,627
|
2,120
|
GA
|
Top
|
| 9
|
XY sex-determination system
|
61,711
|
2,057
|
C
|
High
|
| 10
|
Prion
|
60,650
|
2,021
|
GA
|
Mid
|
| 11
|
SARS-CoV-2
|
57,283
|
1,909
|
B
|
Top
|
| 12
|
Blood type
|
52,917
|
1,763
|
B
|
High
|
| 13
|
Protein
|
52,531
|
1,751
|
GA
|
Top
|
| 14
|
Color blindness
|
48,810
|
1,627
|
C
|
Mid
|
| 15
|
Polymerase chain reaction
|
47,859
|
1,595
|
B
|
High
|
| 16
|
Evolution
|
46,984
|
1,566
|
FA
|
Top
|
| 17
|
Inbreeding
|
44,264
|
1,475
|
C
|
Low
|
| 18
|
CRISPR
|
43,873
|
1,462
|
B
|
High
|
| 19
|
Attachment theory
|
43,788
|
1,459
|
B
|
Mid
|
| 20
|
Enzyme
|
42,934
|
1,431
|
FA
|
Top
|
| 21
|
Biodiversity
|
42,793
|
1,426
|
B
|
High
|
| 22
|
Red hair
|
42,136
|
1,404
|
C
|
Mid
|
| 23
|
Blue Fugates
|
41,286
|
1,376
|
Start
|
Low
|
| 24
|
Prader–Willi syndrome
|
40,537
|
1,351
|
B
|
Mid
|
| 25
|
Bayer
|
38,894
|
1,296
|
C
|
Low
|
| 26
|
Cousin
|
38,331
|
1,277
|
Start
|
Low
|
| 27
|
Chromosome
|
36,482
|
1,216
|
B
|
Top
|
| 28
|
Svalbard Global Seed Vault
|
35,721
|
1,190
|
B
|
Mid
|
| 29
|
Charcot–Marie–Tooth disease
|
34,929
|
1,164
|
C
|
Mid
|
| 30
|
Human skin color
|
34,699
|
1,156
|
B
|
Mid
|
| 31
|
Genetics
|
33,233
|
1,107
|
FA
|
Top
|
| 32
|
Genetic engineering
|
33,189
|
1,106
|
GA
|
Top
|
| 33
|
Gregor Mendel
|
33,094
|
1,103
|
B
|
High
|
| 34
|
Adenosine triphosphate
|
32,453
|
1,081
|
C
|
High
|
| 35
|
Rosalind Franklin
|
32,084
|
1,069
|
B
|
High
|
| 36
|
Meiosis
|
31,872
|
1,062
|
C
|
Top
|
| 37
|
Epicanthic fold
|
31,797
|
1,059
|
Start
|
Low
|
| 38
|
Estimates of historical world population
|
31,426
|
1,047
|
Start
|
Low
|
| 39
|
Epigenetics
|
31,338
|
1,044
|
B
|
Top
|
| 40
|
Scientific racism
|
30,367
|
1,012
|
C
|
Low
|
| 41
|
Y chromosome
|
29,243
|
974
|
B
|
High
|
| 42
|
Japanese people
|
28,887
|
962
|
C
|
Low
|
| 43
|
Transcription (biology)
|
28,820
|
960
|
B
|
Top
|
| 44
|
Albinism
|
28,498
|
949
|
Start
|
Low
|
| 45
|
Gigantism
|
27,507
|
916
|
Start
|
High
|
| 46
|
RNA
|
27,317
|
910
|
GA
|
Top
|
| 47
|
Total fertility rate
|
27,215
|
907
|
C
|
Low
|
| 48
|
De-extinction
|
27,050
|
901
|
C
|
Low
|
| 49
|
Lactose intolerance
|
26,916
|
897
|
B
|
Low
|
| 50
|
Nucleic acid
|
26,744
|
891
|
C
|
Mid
|
| 51
|
Nicotinamide adenine dinucleotide
|
26,694
|
889
|
FA
|
Mid
|
| 52
|
Blond
|
26,694
|
889
|
C
|
Low
|
| 53
|
Animal husbandry
|
26,680
|
889
|
GA
|
Mid
|
| 54
|
Atrial septal defect
|
26,239
|
874
|
B
|
Low
|
| 55
|
Dominance (genetics)
|
26,218
|
873
|
C
|
Top
|
| 56
|
Birth defect
|
26,149
|
871
|
B
|
Mid
|
| 57
|
Genetic disorder
|
25,933
|
864
|
B
|
Top
|
| 58
|
Mutation
|
25,918
|
863
|
B
|
Top
|
| 59
|
Consanguinity
|
25,362
|
845
|
C
|
Low
|
| 60
|
Chimera (genetics)
|
25,203
|
840
|
B
|
Mid
|
| 61
|
DNA replication
|
25,023
|
834
|
Unknown
|
Unknown
|
| 62
|
Mendelian inheritance
|
24,623
|
820
|
C
|
High
|
| 63
|
DNA sequencing
|
24,536
|
817
|
C
|
Top
|
| 64
|
Human Genome Project
|
24,162
|
805
|
B
|
Top
|
| 65
|
Congenital heart defect
|
23,061
|
768
|
C
|
Mid
|
| 66
|
Wechsler Adult Intelligence Scale
|
22,710
|
757
|
C
|
Low
|
| 67
|
Nucleotide
|
22,562
|
752
|
C
|
Top
|
| 68
|
Genetically modified organism
|
22,543
|
751
|
GA
|
Top
|
| 69
|
Combined DNA Index System
|
22,404
|
746
|
GA
|
Low
|
| 70
|
Hybrid (biology)
|
22,129
|
737
|
GA
|
High
|
| 71
|
Ribosome
|
21,679
|
722
|
B
|
Top
|
| 72
|
Cleft lip and cleft palate
|
21,391
|
713
|
B
|
Low
|
| 73
|
HeLa
|
21,212
|
707
|
C
|
Low
|
| 74
|
XYY syndrome
|
21,075
|
702
|
B
|
Mid
|
| 75
|
Variants of SARS-CoV-2
|
20,489
|
682
|
C
|
Low
|
| 76
|
Endogamy
|
20,327
|
677
|
Start
|
Low
|
| 77
|
Early human migrations
|
20,005
|
666
|
C
|
Mid
|
| 78
|
Messenger RNA
|
19,970
|
665
|
C
|
High
|
| 79
|
Phenotype
|
19,931
|
664
|
C
|
Mid
|
| 80
|
James Watson
|
19,916
|
663
|
B
|
High
|
| 81
|
XX male syndrome
|
19,511
|
650
|
C
|
Low
|
| 82
|
Mitochondrial Eve
|
19,276
|
642
|
C
|
Mid
|
| 83
|
Tay–Sachs disease
|
18,992
|
633
|
B
|
High
|
| 84
|
Cloning
|
18,943
|
631
|
B
|
Top
|
| 85
|
M. S. Swaminathan
|
18,930
|
631
|
B
|
Low
|
| 86
|
Human hair color
|
18,890
|
629
|
Start
|
Mid
|
| 87
|
Mitochondrial DNA
|
18,831
|
627
|
B
|
High
|
| 88
|
XXXY syndrome
|
18,830
|
627
|
C
|
Low
|
| 89
|
Heredity
|
18,764
|
625
|
C
|
Top
|
| 90
|
Pentasomy X
|
18,699
|
623
|
GA
|
Low
|
| 91
|
23andMe
|
18,182
|
606
|
C
|
Mid
|
| 92
|
Gamete
|
18,081
|
602
|
Start
|
Mid
|
| 93
|
Humanzee
|
17,949
|
598
|
C
|
Mid
|
| 94
|
Senescence
|
17,633
|
587
|
C
|
Low
|
| 95
|
Lectin
|
17,585
|
586
|
Start
|
Mid
|
| 96
|
Eugenics in the United States
|
17,575
|
585
|
Start
|
Low
|
| 97
|
Gene therapy
|
17,413
|
580
|
B
|
High
|
| 98
|
Genome
|
17,269
|
575
|
C
|
High
|
| 99
|
Cultivar
|
17,161
|
572
|
GA
|
Mid
|
| 100
|
Human genome
|
17,073
|
569
|
B
|
High
|
| 101
|
G. H. Hardy
|
17,066
|
568
|
C
|
Mid
|
| 102
|
CRISPR gene editing
|
16,877
|
562
|
B
|
Top
|
| 103
|
Recent African origin of modern humans
|
16,725
|
557
|
C
|
Mid
|
| 104
|
Plasmid
|
16,562
|
552
|
C
|
High
|
| 105
|
Translation (biology)
|
16,522
|
550
|
B
|
Top
|
| 106
|
The Bell Curve
|
16,507
|
550
|
C
|
High
|
| 107
|
Major histocompatibility complex
|
16,409
|
546
|
B
|
Mid
|
| 108
|
Sex-determination system
|
16,386
|
546
|
C
|
Mid
|
| 109
|
Sonic hedgehog protein
|
16,328
|
544
|
B
|
High
|
| 110
|
Uterus didelphys
|
16,166
|
538
|
Start
|
Low
|
| 111
|
DNA and RNA codon tables
|
16,151
|
538
|
FL
|
High
|
| 112
|
Single-nucleotide polymorphism
|
15,753
|
525
|
C
|
High
|
| 113
|
Reverse transcription polymerase chain reaction
|
15,722
|
524
|
Start
|
Mid
|
| 114
|
Allele
|
15,618
|
520
|
B
|
Top
|
| 115
|
Genetic code
|
15,544
|
518
|
GA
|
Top
|
| 116
|
Landrace
|
15,293
|
509
|
C
|
Low
|
| 117
|
Karyotype
|
15,080
|
502
|
C
|
Mid
|
| 118
|
Jennifer Doudna
|
14,927
|
497
|
B
|
High
|
| 119
|
Haplogroup
|
14,851
|
495
|
C
|
Mid
|
| 120
|
Stephen Jay Gould
|
14,729
|
490
|
GA
|
Mid
|
| 121
|
Institutional racism
|
14,670
|
489
|
B
|
High
|
| 122
|
Genetically modified food
|
14,646
|
488
|
B
|
High
|
| 123
|
Gene expression
|
14,521
|
484
|
B
|
Top
|
| 124
|
Haplogroup R1a
|
14,412
|
480
|
C
|
Low
|
| 125
|
DNA profiling
|
14,368
|
478
|
B
|
High
|
| 126
|
Edwards syndrome
|
14,288
|
476
|
B
|
Low
|
| 127
|
Haplogroup R1b
|
14,225
|
474
|
C
|
Mid
|
| 128
|
Ploidy
|
14,200
|
473
|
C
|
High
|
| 129
|
Sexual selection
|
13,894
|
463
|
GA
|
Mid
|
| 130
|
Recombinant DNA
|
13,891
|
463
|
C
|
High
|
| 131
|
Francis Crick
|
13,877
|
462
|
B
|
High
|
| 132
|
Tetralogy of Fallot
|
13,760
|
458
|
C
|
High
|
| 133
|
Polyploidy
|
13,681
|
456
|
B
|
High
|
| 134
|
Sanger sequencing
|
13,667
|
455
|
C
|
High
|
| 135
|
Brown hair
|
13,554
|
451
|
Start
|
Mid
|
| 136
|
Domesticated silver fox
|
13,531
|
451
|
C
|
Low
|
| 137
|
Population bottleneck
|
13,501
|
450
|
C
|
Mid
|
| 138
|
Selective breeding
|
13,339
|
444
|
C
|
Top
|
| 139
|
Punnett square
|
13,251
|
441
|
C
|
Top
|
| 140
|
Protein biosynthesis
|
13,233
|
441
|
C
|
Mid
|
| 141
|
Orange petunia
|
13,232
|
441
|
C
|
Low
|
| 142
|
Plasmodium falciparum
|
12,985
|
432
|
B
|
Low
|
| 143
|
Hardy–Weinberg principle
|
12,981
|
432
|
C
|
High
|
| 144
|
Freckle
|
12,901
|
430
|
Start
|
Low
|
| 145
|
Strømme syndrome
|
12,876
|
429
|
B
|
Low
|
| 146
|
Real-time polymerase chain reaction
|
12,872
|
429
|
C
|
Mid
|
| 147
|
Domestic rabbit
|
12,750
|
425
|
C
|
Low
|
| 148
|
Transgene
|
12,615
|
420
|
B
|
Mid
|
| 149
|
List of organisms by chromosome count
|
12,479
|
415
|
List
|
Low
|
| 150
|
Ronald Fisher
|
12,422
|
414
|
B
|
High
|
| 151
|
Cat coat genetics
|
12,361
|
412
|
C
|
Mid
|
| 152
|
DNA methylation
|
12,354
|
411
|
B
|
High
|
| 153
|
Leucism
|
12,257
|
408
|
Start
|
Low
|
| 154
|
Telomere
|
12,200
|
406
|
C
|
Mid
|
| 155
|
Central dogma of molecular biology
|
12,198
|
406
|
C
|
Top
|
| 156
|
P53
|
12,012
|
400
|
B
|
High
|
| 157
|
Epidermal growth factor receptor
|
11,853
|
395
|
C
|
Mid
|
| 158
|
Transposable element
|
11,773
|
392
|
C
|
High
|
| 159
|
Transcription factor
|
11,737
|
391
|
B
|
High
|
| 160
|
SARS-CoV-2 Delta variant
|
11,640
|
388
|
C
|
Low
|
| 161
|
Data storage
|
11,583
|
386
|
Start
|
Low
|
| 162
|
Descent from Genghis Khan
|
11,582
|
386
|
C
|
Low
|
| 163
|
Oogenesis
|
11,578
|
385
|
C
|
High
|
| 164
|
Transfer RNA
|
11,520
|
384
|
B
|
High
|
| 165
|
Lac operon
|
11,510
|
383
|
C
|
Mid
|
| 166
|
Human–animal hybrid
|
11,307
|
376
|
C
|
Low
|
| 167
|
Genotype
|
11,025
|
367
|
Start
|
Top
|
| 168
|
NF-κB
|
10,957
|
365
|
B
|
High
|
| 169
|
RNA splicing
|
10,949
|
364
|
C
|
Top
|
| 170
|
Biological engineering
|
10,942
|
364
|
C
|
High
|
| 171
|
Aneuploidy
|
10,907
|
363
|
B
|
High
|
| 172
|
X chromosome
|
10,873
|
362
|
B
|
Top
|
| 173
|
Homology (biology)
|
10,768
|
358
|
GA
|
High
|
| 174
|
Nazi eugenics
|
10,691
|
356
|
C
|
Mid
|
| 175
|
Wnt signaling pathway
|
10,642
|
354
|
C
|
Mid
|
| 176
|
Post-translational modification
|
10,632
|
354
|
Start
|
High
|
| 177
|
Fertility
|
10,618
|
353
|
C
|
Mid
|
| 178
|
William Shockley
|
10,560
|
352
|
B
|
Low
|
| 179
|
RNA interference
|
10,553
|
351
|
FA
|
Top
|
| 180
|
Genetic drift
|
10,504
|
350
|
GA
|
High
|
| 181
|
MicroRNA
|
10,456
|
348
|
B
|
Top
|
| 182
|
Base pair
|
10,452
|
348
|
C
|
Top
|
| 183
|
Cyclic adenosine monophosphate
|
10,343
|
344
|
C
|
Mid
|
| 184
|
Reverse transcriptase
|
10,329
|
344
|
B
|
High
|
| 185
|
DNA polymerase
|
10,311
|
343
|
C
|
Top
|
| 186
|
Black hair
|
10,207
|
340
|
Start
|
Mid
|
| 187
|
Founder effect
|
10,203
|
340
|
C
|
High
|
| 188
|
Most recent common ancestor
|
10,103
|
336
|
B
|
Mid
|
| 189
|
Polymorphism (biology)
|
10,101
|
336
|
B
|
Low
|
| 190
|
Chin
|
10,077
|
335
|
C
|
Low
|
| 191
|
Genetically modified crops
|
10,014
|
333
|
B
|
High
|
| 192
|
Sex linkage
|
10,013
|
333
|
Start
|
High
|
| 193
|
MHC class I
|
9,976
|
332
|
C
|
Mid
|
| 194
|
Chromosome abnormality
|
9,902
|
330
|
Start
|
High
|
| 195
|
Zebrafish
|
9,844
|
328
|
B
|
Mid
|
| 196
|
Zygosity
|
9,834
|
327
|
C
|
High
|
| 197
|
Turi King
|
9,832
|
327
|
C
|
Low
|
| 198
|
HLA-B27
|
9,805
|
326
|
C
|
Low
|
| 199
|
Francis Collins
|
9,767
|
325
|
B
|
Mid
|
| 200
|
XXYY syndrome
|
9,733
|
324
|
Start
|
Low
|
| 201
|
Parent
|
9,726
|
324
|
C
|
High
|
| 202
|
Sex chromosome
|
9,686
|
322
|
Start
|
High
|
| 203
|
Genetic testing
|
9,673
|
322
|
B
|
Top
|
| 204
|
Anthropometry
|
9,670
|
322
|
C
|
Low
|
| 205
|
Ventricular septal defect
|
9,633
|
321
|
C
|
Low
|
| 206
|
Tuberous sclerosis
|
9,629
|
320
|
B
|
Mid
|
| 207
|
Open reading frame
|
9,542
|
318
|
Start
|
Mid
|
| 208
|
Genomics
|
9,514
|
317
|
B
|
Top
|
| 209
|
Promoter (genetics)
|
9,465
|
315
|
Start
|
Mid
|
| 210
|
MHC class II
|
9,423
|
314
|
C
|
Mid
|
| 211
|
Nicotinamide adenine dinucleotide phosphate
|
9,347
|
311
|
Start
|
Mid
|
| 212
|
Friedreich's ataxia
|
9,312
|
310
|
GA
|
Mid
|
| 213
|
Whole genome sequencing
|
9,273
|
309
|
B
|
Top
|
| 214
|
Mitochondrial disease
|
9,247
|
308
|
C
|
Mid
|
| 215
|
Illumina, Inc.
|
9,227
|
307
|
C
|
Low
|
| 216
|
Genentech
|
9,216
|
307
|
Start
|
Mid
|
| 217
|
Ectrodactyly
|
9,188
|
306
|
B
|
Mid
|
| 218
|
Fluorescence in situ hybridization
|
9,135
|
304
|
B
|
Mid
|
| 219
|
Incest taboo
|
9,106
|
303
|
C
|
Mid
|
| 220
|
Panthera hybrid
|
9,084
|
302
|
C
|
Mid
|
| 221
|
Nucleic acid double helix
|
9,083
|
302
|
C
|
Mid
|
| 222
|
Oncogene
|
8,912
|
297
|
C
|
High
|
| 223
|
Synthetic biology
|
8,852
|
295
|
B
|
Mid
|
| 224
|
RNA world
|
8,845
|
294
|
C
|
Mid
|
| 225
|
Ethnic groups of Japan
|
8,775
|
292
|
Start
|
Unknown
|
| 226
|
Mosaic (genetics)
|
8,747
|
291
|
C
|
Mid
|
| 227
|
Histone
|
8,709
|
290
|
C
|
Mid
|
| 228
|
Auburn hair
|
8,697
|
289
|
Stub
|
Low
|
| 229
|
Genetic history of Europe
|
8,635
|
287
|
Start
|
Low
|
| 230
|
Heterosis
|
8,617
|
287
|
C
|
High
|
| 231
|
Horizontal gene transfer
|
8,572
|
285
|
C
|
High
|
| 232
|
Molecular cloning
|
8,568
|
285
|
C
|
High
|
| 233
|
Causes of cancer
|
8,554
|
285
|
B
|
Mid
|
| 234
|
He Jiankui affair
|
8,483
|
282
|
C
|
Low
|
| 235
|
List of genetic disorders
|
8,329
|
277
|
List
|
High
|
| 236
|
CpG site
|
8,327
|
277
|
C
|
Mid
|
| 237
|
Genetic recombination
|
8,323
|
277
|
C
|
High
|
| 238
|
Genetic linkage
|
8,188
|
272
|
Start
|
High
|
| 239
|
RNA polymerase
|
8,187
|
272
|
C
|
Top
|
| 240
|
Plant breeding
|
8,136
|
271
|
C
|
High
|
| 241
|
Exogamy
|
8,113
|
270
|
Start
|
Low
|
| 242
|
Reference genome
|
8,099
|
269
|
Start
|
Mid
|
| 243
|
Chromatin
|
8,051
|
268
|
B
|
Mid
|
| 244
|
Heritability of IQ
|
8,008
|
266
|
C
|
Low
|
| 245
|
HER2/neu
|
7,906
|
263
|
C
|
Mid
|
| 246
|
Haplogroup E-M215 (Y-DNA)
|
7,877
|
262
|
C
|
Low
|
| 247
|
Nucleolus
|
7,867
|
262
|
Start
|
Mid
|
| 248
|
Isoelectric point
|
7,819
|
260
|
C
|
Mid
|
| 249
|
Patent ductus arteriosus
|
7,816
|
260
|
Start
|
Mid
|
| 250
|
Hereditary haemochromatosis
|
7,808
|
260
|
B
|
Mid
|
| 251
|
Stop codon
|
7,717
|
257
|
Start
|
High
|
| 252
|
Genetic diversity
|
7,710
|
257
|
C
|
Mid
|
| 253
|
Epistasis
|
7,704
|
256
|
B
|
High
|
| 254
|
Transformation (genetics)
|
7,696
|
256
|
B
|
Top
|
| 255
|
Mathematical and theoretical biology
|
7,633
|
254
|
C
|
Low
|
| 256
|
Blue rose
|
7,609
|
253
|
Start
|
Low
|
| 257
|
Dysgenics
|
7,593
|
253
|
Start
|
Low
|
| 258
|
Y-chromosomal Adam
|
7,566
|
252
|
C
|
High
|
| 259
|
Monoamine oxidase A
|
7,532
|
251
|
C
|
Mid
|
| 260
|
Laboratory rat
|
7,499
|
249
|
C
|
Mid
|
| 261
|
Regulation of gene expression
|
7,478
|
249
|
C
|
High
|
| 262
|
Sex-determining region Y protein
|
7,446
|
248
|
C
|
Low
|
| 263
|
Dravet syndrome
|
7,440
|
248
|
C
|
Low
|
| 264
|
Citicoline
|
7,380
|
246
|
B
|
Low
|
| 265
|
Myc
|
7,359
|
245
|
C
|
High
|
| 266
|
Introduction to evolution
|
7,273
|
242
|
B
|
High
|
| 267
|
Genetics and archaeogenetics of South Asia
|
7,251
|
241
|
Start
|
Mid
|
| 268
|
Genomic imprinting
|
7,225
|
240
|
C
|
High
|
| 269
|
Hershey–Chase experiment
|
7,175
|
239
|
C
|
High
|
| 270
|
Homologous recombination
|
7,108
|
236
|
GA
|
High
|
| 271
|
Genetic studies on Turkish people
|
7,092
|
236
|
Start
|
Low
|
| 272
|
Barbara McClintock
|
7,062
|
235
|
FA
|
High
|
| 273
|
Haplogroup H (mtDNA)
|
7,061
|
235
|
Start
|
Low
|
| 274
|
Lactase
|
7,040
|
234
|
B
|
Mid
|
| 275
|
Chromosomal crossover
|
7,034
|
234
|
C
|
High
|
| 276
|
Homologous chromosome
|
6,993
|
233
|
Start
|
High
|
| 277
|
Color wheel theory of love
|
6,937
|
231
|
Stub
|
Low
|
| 278
|
JAK-STAT signaling pathway
|
6,936
|
231
|
B
|
Mid
|
| 279
|
Ancient North Eurasian
|
6,919
|
230
|
C
|
Mid
|
| 280
|
Western Hunter-Gatherer
|
6,852
|
228
|
C
|
Mid
|
| 281
|
X-linked recessive inheritance
|
6,849
|
228
|
Start
|
Mid
|
| 282
|
Restriction fragment length polymorphism
|
6,847
|
228
|
Start
|
Mid
|
| 283
|
Biopolymer
|
6,838
|
227
|
C
|
Mid
|
| 284
|
BRCA1
|
6,837
|
227
|
C
|
High
|
| 285
|
Transduction (genetics)
|
6,820
|
227
|
C
|
High
|
| 286
|
Population genetics
|
6,800
|
226
|
C
|
Top
|
| 287
|
16S ribosomal RNA
|
6,778
|
225
|
C
|
High
|
| 288
|
Cas9
|
6,756
|
225
|
C
|
Mid
|
| 289
|
Eukaryotic transcription
|
6,719
|
223
|
B
|
High
|
| 290
|
Inbreeding depression
|
6,687
|
222
|
C
|
Low
|
| 291
|
DNA history of Egypt
|
6,677
|
222
|
C
|
Low
|
| 292
|
Trisomy
|
6,652
|
221
|
Start
|
High
|
| 293
|
Uracil
|
6,648
|
221
|
C
|
Mid
|
| 294
|
Allopatric speciation
|
6,637
|
221
|
C
|
Low
|
| 295
|
Genomic library
|
6,596
|
219
|
C
|
Mid
|
| 296
|
Designer baby
|
6,581
|
219
|
B
|
High
|
| 297
|
Adeno-associated virus
|
6,578
|
219
|
B
|
Low
|
| 298
|
Griffith's experiment
|
6,572
|
219
|
Start
|
Mid
|
| 299
|
Neanderthal genetics
|
6,535
|
217
|
C
|
High
|
| 300
|
Chromosomal translocation
|
6,535
|
217
|
Start
|
High
|
| 301
|
Haplotype
|
6,534
|
217
|
Start
|
High
|
| 302
|
Non-coding DNA
|
6,531
|
217
|
C
|
Mid
|
| 303
|
Webbed toes
|
6,530
|
217
|
Start
|
Low
|
| 304
|
Complementary DNA
|
6,518
|
217
|
Start
|
Mid
|
| 305
|
Impulsivity
|
6,514
|
217
|
B
|
Mid
|
| 306
|
Mebendazole
|
6,440
|
214
|
C
|
Mid
|
| 307
|
Flavin adenine dinucleotide
|
6,413
|
213
|
B
|
Low
|
| 308
|
Genetic counseling
|
6,355
|
211
|
C
|
Mid
|
| 309
|
Western Steppe Herders
|
6,321
|
210
|
C
|
Mid
|
| 310
|
Bacterial conjugation
|
6,308
|
210
|
C
|
High
|
| 311
|
Heritability of autism
|
6,287
|
209
|
Start
|
Mid
|
| 312
|
SARS-CoV-2 Alpha variant
|
6,275
|
209
|
C
|
Low
|
| 313
|
KRAS
|
6,264
|
208
|
C
|
Mid
|
| 314
|
Early European Farmers
|
6,224
|
207
|
C
|
Mid
|
| 315
|
J. B. S. Haldane
|
6,216
|
207
|
C
|
Low
|
| 316
|
ZW sex-determination system
|
6,198
|
206
|
Start
|
Mid
|
| 317
|
Autosome
|
6,175
|
205
|
Start
|
Top
|
| 318
|
Tumor suppressor gene
|
6,121
|
204
|
Start
|
High
|
| 319
|
Sampling bias
|
6,116
|
203
|
C
|
Low
|
| 320
|
Somatic cell
|
6,114
|
203
|
Start
|
Mid
|
| 321
|
Laboratory mouse
|
6,074
|
202
|
B
|
Low
|
| 322
|
Pleiotropy
|
6,061
|
202
|
C
|
High
|
| 323
|
Microsatellite
|
6,054
|
201
|
C
|
Mid
|
| 324
|
Methylation
|
6,035
|
201
|
C
|
Mid
|
| 325
|
Shyness
|
6,015
|
200
|
B
|
Low
|
| 326
|
Locus (genetics)
|
6,008
|
200
|
Start
|
Mid
|
| 327
|
Hayflick limit
|
6,007
|
200
|
Start
|
Low
|
| 328
|
Factor VIII
|
5,997
|
199
|
Start
|
Low
|
| 329
|
Sexual differentiation in humans
|
5,950
|
198
|
C
|
Mid
|
| 330
|
Ribozyme
|
5,916
|
197
|
Start
|
High
|
| 331
|
Bcl-2
|
5,915
|
197
|
B
|
Mid
|
| 332
|
Ras GTPase
|
5,873
|
195
|
B
|
High
|
| 333
|
Telomerase
|
5,857
|
195
|
B
|
High
|
| 334
|
Sexual selection in humans
|
5,844
|
194
|
C
|
Low
|
| 335
|
Alternative splicing
|
5,828
|
194
|
B
|
High
|
| 336
|
Haplogroup J-M172
|
5,825
|
194
|
Start
|
Low
|
| 337
|
Linkage disequilibrium
|
5,821
|
194
|
C
|
High
|
| 338
|
Genetic variation
|
5,801
|
193
|
Start
|
High
|
| 339
|
Flavivirus
|
5,798
|
193
|
B
|
Mid
|
| 340
|
Gene mapping
|
5,763
|
192
|
Stub
|
Low
|
| 341
|
Phosphorylation
|
5,757
|
191
|
B
|
High
|
| 342
|
Proteinogenic amino acid
|
5,739
|
191
|
C
|
High
|
| 343
|
Okazaki fragments
|
5,728
|
190
|
B
|
High
|
| 344
|
Hox gene
|
5,711
|
190
|
C
|
High
|
| 345
|
Von Hippel–Lindau disease
|
5,697
|
189
|
C
|
Mid
|
| 346
|
Genome editing
|
5,687
|
189
|
C
|
High
|
| 347
|
Genealogical DNA test
|
5,674
|
189
|
C
|
Mid
|
| 348
|
Biological determinism
|
5,653
|
188
|
B
|
Mid
|
| 349
|
Nucleic acid sequence
|
5,641
|
188
|
C
|
High
|
| 350
|
Anonychia
|
5,638
|
187
|
Stub
|
Low
|
| 351
|
PBR322
|
5,622
|
187
|
Start
|
Low
|
| 352
|
The Population Bomb
|
5,604
|
186
|
B
|
Low
|
| 353
|
X-inactivation
|
5,537
|
184
|
B
|
High
|
| 354
|
Intron
|
5,514
|
183
|
C
|
High
|
| 355
|
Hispanos of New Mexico
|
5,513
|
183
|
Start
|
Low
|
| 356
|
Chargaff's rules
|
5,502
|
183
|
Start
|
Low
|
| 357
|
GloFish
|
5,490
|
183
|
C
|
Mid
|
| 358
|
Semiconservative replication
|
5,465
|
182
|
C
|
High
|
| 359
|
5α-Reductase 2 deficiency
|
5,453
|
181
|
B
|
Low
|
| 360
|
Eric Lander
|
5,444
|
181
|
C
|
Low
|
| 361
|
Crossbreed
|
5,398
|
179
|
Start
|
Low
|
| 362
|
TATA box
|
5,344
|
178
|
B
|
High
|
| 363
|
Haplogroup I-M170
|
5,291
|
176
|
Start
|
Low
|
| 364
|
The Passing of the Great Race
|
5,280
|
176
|
C
|
Unknown
|
| 365
|
Disodium inosinate
|
5,278
|
175
|
Start
|
Low
|
| 366
|
Gene nomenclature
|
5,276
|
175
|
B
|
Mid
|
| 367
|
Point mutation
|
5,248
|
174
|
C
|
High
|
| 368
|
Kin selection
|
5,245
|
174
|
GA
|
Mid
|
| 369
|
Model organism
|
5,236
|
174
|
B
|
Mid
|
| 370
|
Heritability
|
5,234
|
174
|
C
|
High
|
| 371
|
Sequence homology
|
5,218
|
173
|
C
|
Top
|
| 372
|
Breed
|
5,204
|
173
|
Start
|
Low
|
| 373
|
Barr body
|
5,204
|
173
|
Start
|
High
|
| 374
|
Topoisomerase
|
5,186
|
172
|
C
|
High
|
| 375
|
Taq polymerase
|
5,161
|
172
|
C
|
Mid
|
| 376
|
Behavioural genetics
|
5,157
|
171
|
GA
|
High
|
| 377
|
Polytene chromosome
|
5,069
|
168
|
Start
|
Mid
|
| 378
|
Photo 51
|
5,052
|
168
|
Start
|
Low
|
| 379
|
Phenotypic trait
|
5,036
|
167
|
Start
|
Mid
|
| 380
|
Genetically modified animal
|
5,027
|
167
|
C
|
High
|
| 381
|
Oligomer
|
5,026
|
167
|
Start
|
Low
|
| 382
|
Oligonucleotide
|
4,987
|
166
|
Start
|
Mid
|
| 383
|
Medical genetics
|
4,982
|
166
|
B
|
Mid
|
| 384
|
Systems biology
|
4,977
|
165
|
Start
|
High
|
| 385
|
Haplogroup G-M201
|
4,958
|
165
|
Start
|
Low
|
| 386
|
Human genetic variation
|
4,956
|
165
|
C
|
High
|
| 387
|
Ames test
|
4,956
|
165
|
C
|
Low
|
| 388
|
Sheep farming
|
4,955
|
165
|
C
|
Low
|
| 389
|
Start codon
|
4,949
|
164
|
Start
|
Top
|
| 390
|
Single cell sequencing
|
4,943
|
164
|
C
|
High
|
| 391
|
Exome sequencing
|
4,926
|
164
|
C
|
High
|
| 392
|
Heterochromatin
|
4,914
|
163
|
C
|
Mid
|
| 393
|
Racial hygiene
|
4,893
|
163
|
C
|
Low
|
| 394
|
Gene flow
|
4,892
|
163
|
Start
|
High
|
| 395
|
George Church (geneticist)
|
4,887
|
162
|
C
|
Low
|
| 396
|
DNA vaccine
|
4,879
|
162
|
B
|
High
|
| 397
|
Centromere
|
4,863
|
162
|
C
|
Mid
|
| 398
|
Biomaterial
|
4,849
|
161
|
C
|
Low
|
| 399
|
Molecular clock
|
4,837
|
161
|
C
|
High
|
| 400
|
Sex selection
|
4,837
|
161
|
C
|
Low
|
| 401
|
Phred quality score
|
4,795
|
159
|
Start
|
Low
|
| 402
|
Hepatitis D
|
4,792
|
159
|
C
|
Low
|
| 403
|
Genetic memory (psychology)
|
4,767
|
158
|
Start
|
Low
|
| 404
|
Chromosome 21
|
4,767
|
158
|
Start
|
Mid
|
| 405
|
Capillary electrophoresis
|
4,749
|
158
|
B
|
Mid
|
| 406
|
Sense (molecular biology)
|
4,734
|
157
|
C
|
High
|
| 407
|
Nucleoside triphosphate
|
4,719
|
157
|
Start
|
High
|
| 408
|
Wobble base pair
|
4,714
|
157
|
Start
|
Mid
|
| 409
|
Monohybrid cross
|
4,709
|
156
|
C
|
Mid
|
| 410
|
Flavr Savr
|
4,693
|
156
|
Start
|
Unknown
|
| 411
|
Cis-regulatory element
|
4,688
|
156
|
C
|
High
|
| 412
|
Expression vector
|
4,677
|
155
|
C
|
Mid
|
| 413
|
Quantitative trait locus
|
4,673
|
155
|
C
|
High
|
| 414
|
Copy number variation
|
4,668
|
155
|
B
|
High
|
| 415
|
Haplogroup I-M253
|
4,656
|
155
|
Start
|
Low
|
| 416
|
Modern synthesis (20th century)
|
4,638
|
154
|
GA
|
High
|
| 417
|
Paternal age effect
|
4,618
|
153
|
C
|
Low
|
| 418
|
Frameshift mutation
|
4,601
|
153
|
B
|
High
|
| 419
|
DNA evidence in the O. J. Simpson murder case
|
4,581
|
152
|
B
|
Low
|
| 420
|
Retrotransposon
|
4,574
|
152
|
C
|
High
|
| 421
|
Cytogenetics
|
4,561
|
152
|
B
|
Mid
|
| 422
|
CDNA library
|
4,560
|
152
|
Start
|
Low
|
| 423
|
Molecular marker
|
4,559
|
151
|
Start
|
Low
|
| 424
|
Genetic genealogy
|
4,543
|
151
|
C
|
Mid
|
| 425
|
Pharmacogenomics
|
4,540
|
151
|
B
|
Mid
|
| 426
|
Advanced maternal age
|
4,534
|
151
|
C
|
Mid
|
| 427
|
Dihybrid cross
|
4,519
|
150
|
Start
|
Mid
|
| 428
|
Cystic fibrosis transmembrane conductance regulator
|
4,505
|
150
|
C
|
Mid
|
| 429
|
Boar–pig hybrid
|
4,496
|
149
|
Stub
|
Low
|
| 430
|
Electroporation
|
4,494
|
149
|
C
|
High
|
| 431
|
Viral vector
|
4,481
|
149
|
B
|
Mid
|
| 432
|
Apomorphy and synapomorphy
|
4,472
|
149
|
C
|
Low
|
| 433
|
He Jiankui
|
4,468
|
148
|
C
|
Unknown
|
| 434
|
Adenosine diphosphate
|
4,456
|
148
|
C
|
Mid
|
| 435
|
Neo-Darwinism
|
4,446
|
148
|
Start
|
High
|
| 436
|
Homeobox
|
4,436
|
147
|
C
|
Mid
|
| 437
|
Janaki Ammal
|
4,427
|
147
|
B
|
Low
|
| 438
|
Endogeny (biology)
|
4,426
|
147
|
Stub
|
Low
|
| 439
|
Long non-coding RNA
|
4,417
|
147
|
C
|
Mid
|
| 440
|
GC-content
|
4,402
|
146
|
C
|
Mid
|
| 441
|
Exon
|
4,382
|
146
|
C
|
Top
|
| 442
|
Chromosome 8
|
4,364
|
145
|
Start
|
Mid
|
| 443
|
Peppered moth evolution
|
4,363
|
145
|
B
|
Mid
|
| 444
|
Haplogroup I-M438
|
4,360
|
145
|
Start
|
Low
|
| 445
|
Trp operon
|
4,353
|
145
|
C
|
Mid
|
| 446
|
DNA extraction
|
4,348
|
144
|
Start
|
Mid
|
| 447
|
Enhancer (genetics)
|
4,347
|
144
|
C
|
High
|
| 448
|
F1 hybrid
|
4,340
|
144
|
Start
|
High
|
| 449
|
Cosmid
|
4,336
|
144
|
Start
|
Mid
|
| 450
|
History of eugenics
|
4,334
|
144
|
B
|
Low
|
| 451
|
Coalescent theory
|
4,310
|
143
|
C
|
Mid
|
| 452
|
Charles Epstein (geneticist)
|
4,273
|
142
|
Start
|
Mid
|
| 453
|
Eastern Hunter-Gatherer
|
4,263
|
142
|
C
|
Mid
|
| 454
|
Purebred
|
4,253
|
141
|
C
|
Low
|
| 455
|
Blue–white screen
|
4,244
|
141
|
Start
|
Mid
|
| 456
|
Maxam–Gilbert sequencing
|
4,239
|
141
|
Start
|
Low
|
| 457
|
Penetrance
|
4,230
|
141
|
C
|
High
|
| 458
|
Gene duplication
|
4,221
|
140
|
C
|
High
|
| 459
|
Site-directed mutagenesis
|
4,212
|
140
|
C
|
Mid
|
| 460
|
Twin study
|
4,202
|
140
|
B
|
High
|
| 461
|
Proto-oncogene tyrosine-protein kinase Src
|
4,168
|
138
|
C
|
Mid
|
| 462
|
Gene knockout
|
4,167
|
138
|
Start
|
Mid
|
| 463
|
Illumina dye sequencing
|
4,115
|
137
|
C
|
High
|
| 464
|
DNA supercoil
|
4,112
|
137
|
C
|
Mid
|
| 465
|
ChIP sequencing
|
4,106
|
136
|
C
|
Mid
|
| 466
|
Nondisjunction
|
4,105
|
136
|
B
|
High
|
| 467
|
Feed conversion ratio
|
4,104
|
136
|
Start
|
Unknown
|
| 468
|
Nanopore sequencing
|
4,102
|
136
|
C
|
Low
|
| 469
|
Adenosine monophosphate
|
4,078
|
135
|
Start
|
Low
|
| 470
|
Translational research
|
4,072
|
135
|
C
|
Mid
|
| 471
|
Ruth Benedict
|
4,063
|
135
|
C
|
Low
|
| 472
|
Knockout mouse
|
4,061
|
135
|
C
|
Mid
|
| 473
|
Genetic marker
|
4,049
|
134
|
Start
|
Mid
|
| 474
|
Zellweger syndrome
|
4,038
|
134
|
Start
|
Low
|
| 475
|
Genetic history of the Iberian Peninsula
|
4,017
|
133
|
Start
|
Low
|
| 476
|
Brooke Greenberg
|
4,005
|
133
|
Start
|
Mid
|
| 477
|
Korean ethnic nationalism
|
4,005
|
133
|
C
|
Low
|
| 478
|
Coefficient of relationship
|
3,999
|
133
|
C
|
Low
|
| 479
|
Personalized medicine
|
3,986
|
132
|
B
|
Mid
|
| 480
|
Introduction to genetics
|
3,966
|
132
|
B
|
High
|
| 481
|
Pedigree chart
|
3,962
|
132
|
Start
|
Mid
|
| 482
|
Microsatellite instability
|
3,957
|
131
|
C
|
Mid
|
| 483
|
45,X/46,XY mosaicism
|
3,944
|
131
|
Stub
|
Low
|
| 484
|
Genotoxicity
|
3,932
|
131
|
C
|
High
|
| 485
|
Gene set enrichment analysis
|
3,931
|
131
|
C
|
Mid
|
| 486
|
Introgression
|
3,925
|
130
|
Start
|
High
|
| 487
|
Sticky and blunt ends
|
3,919
|
130
|
Start
|
Low
|
| 488
|
Viral vector vaccine
|
3,899
|
129
|
Start
|
Low
|
| 489
|
Transcriptome
|
3,898
|
129
|
B
|
High
|
| 490
|
Signal peptide
|
3,886
|
129
|
Start
|
Mid
|
| 491
|
Balaji Srinivasan
|
3,861
|
128
|
Start
|
Low
|
| 492
|
Non-Mendelian inheritance
|
3,837
|
127
|
C
|
Mid
|
| 493
|
Missense mutation
|
3,801
|
126
|
Start
|
Mid
|
| 494
|
Genetic history of the British Isles
|
3,798
|
126
|
C
|
Low
|
| 495
|
God gene
|
3,770
|
125
|
Start
|
Mid
|
| 496
|
Z-DNA
|
3,766
|
125
|
C
|
High
|
| 497
|
Lysis buffer
|
3,763
|
125
|
Start
|
Low
|
| 498
|
Lethal allele
|
3,762
|
125
|
Start
|
Mid
|
| 499
|
Chromosome 1
|
3,756
|
125
|
Start
|
Low
|
| 500
|
Dwarf cat
|
3,723
|
124
|
Start
|
Low
|
