-
1
-
-
78650895972
-
Loss-of-function variants in the genomes of healthy humans
-
MacArthur D.G., Tyler-Smith C. Loss-of-function variants in the genomes of healthy humans. Hum. Mol. Genet. 2010, 19:R125-R130.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. R125-R130
-
-
MacArthur, D.G.1
Tyler-Smith, C.2
-
2
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000 Genomes Project Consortium, et al. A map of human genome variation from population-scale sequencing. Nature 2010, 467:1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
3
-
-
84900476010
-
Analytical validation of whole exome and whole genome sequencing for clinical applications
-
Linderman M.D., et al. Analytical validation of whole exome and whole genome sequencing for clinical applications. BMC Med. Genomics 2014, 7:20.
-
(2014)
BMC Med. Genomics
, vol.7
, pp. 20
-
-
Linderman, M.D.1
-
4
-
-
84907395628
-
Diagnostic clinical genome and exome sequencing
-
Biesecker L.G., et al. Diagnostic clinical genome and exome sequencing. N. Engl. J. Med. 2014, 371:1169-1170.
-
(2014)
N. Engl. J. Med.
, vol.371
, pp. 1169-1170
-
-
Biesecker, L.G.1
-
5
-
-
84901410645
-
Choice of transcripts and software has a large effect on variant annotation
-
McCarthy D.J., et al. Choice of transcripts and software has a large effect on variant annotation. Genome Med. 2014, 6:26.
-
(2014)
Genome Med.
, vol.6
, pp. 26
-
-
McCarthy, D.J.1
-
6
-
-
13444306641
-
NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins
-
Pruitt K.D., et al. NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins. Nucleic Acids Res. 2005, 33:D501-D504.
-
(2005)
Nucleic Acids Res.
, vol.33
, pp. D501-D504
-
-
Pruitt, K.D.1
-
7
-
-
84865760395
-
GENCODE: the reference human genome annotation for The ENCODE Project
-
Harrow J., et al. GENCODE: the reference human genome annotation for The ENCODE Project. Genome Res. 2012, 22:1760-1774.
-
(2012)
Genome Res.
, vol.22
, pp. 1760-1774
-
-
Harrow, J.1
-
8
-
-
84942518519
-
Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR
-
Yang H., Wang K. Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR. Nat. Protoc. 2015, 10:1556-1566.
-
(2015)
Nat. Protoc.
, vol.10
, pp. 1556-1566
-
-
Yang, H.1
Wang, K.2
-
9
-
-
77955405475
-
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
-
McLaren W., et al. Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor. Bioinformatics 2010, 26:2069-2070.
-
(2010)
Bioinformatics
, vol.26
, pp. 2069-2070
-
-
McLaren, W.1
-
10
-
-
78650901894
-
Gene inactivation and its implications for annotation in the era of personal genomics
-
Balasubramanian S., et al. Gene inactivation and its implications for annotation in the era of personal genomics. Genes Dev. 2011, 25:1-10.
-
(2011)
Genes Dev.
, vol.25
, pp. 1-10
-
-
Balasubramanian, S.1
-
11
-
-
84922469439
-
Impact of regulatory variation from RNA to protein
-
Battle A., et al. Impact of regulatory variation from RNA to protein. Science 2015, 347:664-667.
-
(2015)
Science
, vol.347
, pp. 664-667
-
-
Battle, A.1
-
12
-
-
33646558843
-
Loss of desmoplakin isoform I causes early onset cardiomyopathy and heart failure in a Naxos-like syndrome
-
Uzumcu A., et al. Loss of desmoplakin isoform I causes early onset cardiomyopathy and heart failure in a Naxos-like syndrome. J. Med. Genet. 2006, 43:e5.
-
(2006)
J. Med. Genet.
, vol.43
, pp. e5
-
-
Uzumcu, A.1
-
13
-
-
0037452879
-
Human specific loss of olfactory receptor genes
-
Gilad Y., et al. Human specific loss of olfactory receptor genes. Proc. Natl. Acad. Sci. U.S.A. 2003, 100:3324-3327.
-
(2003)
Proc. Natl. Acad. Sci. U.S.A.
, vol.100
, pp. 3324-3327
-
-
Gilad, Y.1
-
14
-
-
80053906761
-
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
-
Najmabadi H., et al. Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature 2011, 478:57-63.
-
(2011)
Nature
, vol.478
, pp. 57-63
-
-
Najmabadi, H.1
-
15
-
-
84926522440
-
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
-
Wright C.F., et al. Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data. Lancet 2015, 385:1305-1314.
-
(2015)
Lancet
, vol.385
, pp. 1305-1314
-
-
Wright, C.F.1
-
16
-
-
84924666082
-
Large-scale discovery of novel genetic causes of developmental disorders
-
Deciphering Developmental Disorders Study Large-scale discovery of novel genetic causes of developmental disorders. Nature 2015, 519:223-228.
-
(2015)
Nature
, vol.519
, pp. 223-228
-
-
-
17
-
-
84928377935
-
Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency
-
Ciancanelli M.J., et al. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency. Science 2015, 348:448-453.
-
(2015)
Science
, vol.348
, pp. 448-453
-
-
Ciancanelli, M.J.1
-
18
-
-
84875939542
-
Lifting the lid on unborn lethal Mendelian phenotypes through exome sequencing
-
Shamseldin H.E., et al. Lifting the lid on unborn lethal Mendelian phenotypes through exome sequencing. Genet. Med. 2013, 15:307-309.
-
(2013)
Genet. Med.
, vol.15
, pp. 307-309
-
-
Shamseldin, H.E.1
-
19
-
-
84938910188
-
Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families
-
Shamseldin H.E., et al. Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families. Genome Biol. 2015, 16:116.
-
(2015)
Genome Biol.
, vol.16
, pp. 116
-
-
Shamseldin, H.E.1
-
20
-
-
84957823399
-
Analysis of protein-coding genetic variation in 60,706 humans
-
Published online October 30, 2015
-
Exome Aggregation Consortium, et al. Analysis of protein-coding genetic variation in 60,706 humans. bioRxiv 2015, Published online October 30, 2015. 10.1101/030338.
-
(2015)
bioRxiv
-
-
-
21
-
-
84940056351
-
Multiple loss-of-function variants of taste receptors in modern humans
-
Fujikura K. Multiple loss-of-function variants of taste receptors in modern humans. Sci. Rep. 2015, 5:12349.
-
(2015)
Sci. Rep.
, vol.5
, pp. 12349
-
-
Fujikura, K.1
-
22
-
-
84922394049
-
A framework for the interpretation of de novo mutation in human disease
-
Samocha K.E., et al. A framework for the interpretation of de novo mutation in human disease. Nat. Genet. 2014, 46:944-950.
-
(2014)
Nat. Genet.
, vol.46
, pp. 944-950
-
-
Samocha, K.E.1
-
23
-
-
84945319215
-
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
-
Akawi N., et al. Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families. Nat. Genet. 2015, 47:1363-1369.
-
(2015)
Nat. Genet.
, vol.47
, pp. 1363-1369
-
-
Akawi, N.1
-
24
-
-
84872143942
-
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
-
Fu W., et al. Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants. Nature 2013, 493:216-220.
-
(2013)
Nature
, vol.493
, pp. 216-220
-
-
Fu, W.1
-
25
-
-
84929133372
-
Identification of a large set of rare complete human knockouts
-
Sulem P., et al. Identification of a large set of rare complete human knockouts. Nat. Genet. 2015, 47:448-452.
-
(2015)
Nat. Genet.
, vol.47
, pp. 448-452
-
-
Sulem, P.1
-
26
-
-
84905460411
-
Distribution and medical impact of loss-of-function variants in the Finnish founder population
-
Lim E.T., et al. Distribution and medical impact of loss-of-function variants in the Finnish founder population. PLoS Genet. 2014, 10:e1004494.
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004494
-
-
Lim, E.T.1
-
27
-
-
84906226932
-
A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes
-
Moltke I., et al. A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes. Nature 2014, 512:190-193.
-
(2014)
Nature
, vol.512
, pp. 190-193
-
-
Moltke, I.1
-
29
-
-
84961734148
-
Human knockouts in a cohort with a high rate of consanguinity
-
Saleheen D., et al. Human knockouts in a cohort with a high rate of consanguinity. bioRxiv 2015, 031518.
-
(2015)
bioRxiv
, pp. 031518
-
-
Saleheen, D.1
-
30
-
-
84960087088
-
Health and population effects of rare gene knockouts in adult humans with related parents
-
Science Published online March 3, 2016
-
Narasimhan V.M., et al. Health and population effects of rare gene knockouts in adult humans with related parents. bioRxiv 2016, Science Published online March 3, 2016. 10.1126/science.aac8624.
-
(2016)
bioRxiv
-
-
Narasimhan, V.M.1
-
31
-
-
84947471999
-
Identification and characterization of essential genes in the human genome
-
Wang T., et al. Identification and characterization of essential genes in the human genome. Science 2015, 350:1096-1101.
-
(2015)
Science
, vol.350
, pp. 1096-1101
-
-
Wang, T.1
-
32
-
-
84947471998
-
Gene essentiality and synthetic lethality in haploid human cells
-
Blomen V.A., et al. Gene essentiality and synthetic lethality in haploid human cells. Science 2015, 350:1092-1096.
-
(2015)
Science
, vol.350
, pp. 1092-1096
-
-
Blomen, V.A.1
-
33
-
-
10744230485
-
Global mapping of the yeast genetic interaction network
-
Tong A.H.Y. Global mapping of the yeast genetic interaction network. Science 2004, 303:808-813.
-
(2004)
Science
, vol.303
, pp. 808-813
-
-
Tong, A.H.Y.1
-
34
-
-
84884905922
-
Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease
-
Cooper D.N., et al. Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease. Hum. Genet. 2013, 132:1077-1130.
-
(2013)
Hum. Genet.
, vol.132
, pp. 1077-1130
-
-
Cooper, D.N.1
-
35
-
-
0037903275
-
Human Gene Mutation Database (HGMD): 2003 update
-
Stenson P.D., et al. Human Gene Mutation Database (HGMD): 2003 update. Hum. Mutat. 2003, 21:577-581.
-
(2003)
Hum. Mutat.
, vol.21
, pp. 577-581
-
-
Stenson, P.D.1
-
36
-
-
84891809093
-
ClinVar: public archive of relationships among sequence variation and human phenotype
-
Landrum M.J., et al. ClinVar: public archive of relationships among sequence variation and human phenotype. Nucleic Acids Res. 2014, 42:D980-D985.
-
(2014)
Nucleic Acids Res.
, vol.42
, pp. D980-D985
-
-
Landrum, M.J.1
-
37
-
-
84960462299
-
Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders
-
Singh T., et al. Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders. bioRxiv 2016, 036384.
-
(2016)
bioRxiv
, pp. 036384
-
-
Singh, T.1
-
38
-
-
55549101314
-
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results
-
Plon S.E., et al. Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results. Hum. Mutat. 2008, 29:1282-1291.
-
(2008)
Hum. Mutat.
, vol.29
, pp. 1282-1291
-
-
Plon, S.E.1
-
39
-
-
84895789502
-
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
-
Thompson B.A., et al. Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database. Nat. Genet. 2014, 46:107-115.
-
(2014)
Nat. Genet.
, vol.46
, pp. 107-115
-
-
Thompson, B.A.1
-
40
-
-
84899476119
-
Guidelines for investigating causality of sequence variants in human disease
-
MacArthur D.G., et al. Guidelines for investigating causality of sequence variants in human disease. Nature 2014, 508:469-476.
-
(2014)
Nature
, vol.508
, pp. 469-476
-
-
MacArthur, D.G.1
-
41
-
-
84951573995
-
Medical genomics: the intricate path from genetic variant identification to clinical interpretation
-
Quintáns B., et al. Medical genomics: the intricate path from genetic variant identification to clinical interpretation. Appl. Transl. Genomics 2014, 3:60-67.
-
(2014)
Appl. Transl. Genomics
, vol.3
, pp. 60-67
-
-
Quintáns, B.1
-
42
-
-
55549137442
-
Genetic evidence and integration of various data sources for classifying uncertain variants into a single model
-
Goldgar D.E., et al. Genetic evidence and integration of various data sources for classifying uncertain variants into a single model. Hum. Mutat. 2008, 29:1265-1272.
-
(2008)
Hum. Mutat.
, vol.29
, pp. 1265-1272
-
-
Goldgar, D.E.1
-
43
-
-
84863116742
-
A systematic survey of loss-of-function variants in human protein-coding genes
-
MacArthur D.G., et al. A systematic survey of loss-of-function variants in human protein-coding genes. Science 2012, 335:823-828.
-
(2012)
Science
, vol.335
, pp. 823-828
-
-
MacArthur, D.G.1
-
44
-
-
84892688767
-
Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation
-
Alsalem A.B., et al. Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation. PLoS Genet. 2013, 9:e1004030.
-
(2013)
PLoS Genet.
, vol.9
, pp. e1004030
-
-
Alsalem, A.B.1
-
45
-
-
45449101500
-
Natural selection on genes that underlie human disease susceptibility
-
Blekhman R., et al. Natural selection on genes that underlie human disease susceptibility. Curr. Biol. 2008, 18:883-889.
-
(2008)
Curr. Biol.
, vol.18
, pp. 883-889
-
-
Blekhman, R.1
-
46
-
-
84926500255
-
An estimate of the average number of recessive lethal mutations carried by humans
-
Gao Z., et al. An estimate of the average number of recessive lethal mutations carried by humans. Genetics 2015, 199:1243-1254.
-
(2015)
Genetics
, vol.199
, pp. 1243-1254
-
-
Gao, Z.1
-
47
-
-
60549090253
-
Long-term control of HIV by CCR5 delta32/delta32 stem-cell transplantation
-
Hütter G., et al. Long-term control of HIV by CCR5 delta32/delta32 stem-cell transplantation. N. Engl. J. Med. 2009, 360:692-698.
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 692-698
-
-
Hütter, G.1
-
48
-
-
0041385595
-
ACTN3 genotype is associated with human elite athletic performance
-
Yang N., et al. ACTN3 genotype is associated with human elite athletic performance. Am. J. Hum. Genet. 2003, 73:627.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 627
-
-
Yang, N.1
-
49
-
-
33645462359
-
Spread of an inactive form of caspase-12 in humans is due to recent positive selection
-
Xue Y., et al. Spread of an inactive form of caspase-12 in humans is due to recent positive selection. Am. J. Hum. Genet. 2006, 78:659-670.
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 659-670
-
-
Xue, Y.1
-
50
-
-
84923186799
-
The African Genome Variation Project shapes medical genetics in Africa
-
Gurdasani D., et al. The African Genome Variation Project shapes medical genetics in Africa. Nature 2015, 517:327-332.
-
(2015)
Nature
, vol.517
, pp. 327-332
-
-
Gurdasani, D.1
-
51
-
-
84881315517
-
Validating therapeutic targets through human genetics
-
Plenge R.M., et al. Validating therapeutic targets through human genetics. Nat. Rev. Drug Discov. 2013, 12:581-594.
-
(2013)
Nat. Rev. Drug Discov.
, vol.12
, pp. 581-594
-
-
Plenge, R.M.1
-
52
-
-
58149262866
-
A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection
-
Pollin T.I., et al. A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. Science 2008, 322:1702-1705.
-
(2008)
Science
, vol.322
, pp. 1702-1705
-
-
Pollin, T.I.1
-
53
-
-
84876260798
-
Genetics: a gene of rare effect
-
Hall S.S. Genetics: a gene of rare effect. Nature 2013, 496:152-155.
-
(2013)
Nature
, vol.496
, pp. 152-155
-
-
Hall, S.S.1
-
54
-
-
84882986868
-
Targeting the unstable plaque in acute coronary syndromes
-
Thompson P.L., et al. Targeting the unstable plaque in acute coronary syndromes. Clin. Ther. 2013, 35:1099-1107.
-
(2013)
Clin. Ther.
, vol.35
, pp. 1099-1107
-
-
Thompson, P.L.1
-
55
-
-
84877135776
-
The search for genetic modifiers of disease severity in the β-hemoglobinopathies
-
Lettre G. The search for genetic modifiers of disease severity in the β-hemoglobinopathies. Cold Spring Harb. Perspect. Med. 2012, 2:a015032.
-
(2012)
Cold Spring Harb. Perspect. Med.
, vol.2
, pp. a015032
-
-
Lettre, G.1
-
56
-
-
78649469071
-
Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation
-
Galarneau G., et al. Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation. Nat. Genet. 2010, 42:1049-1051.
-
(2010)
Nat. Genet.
, vol.42
, pp. 1049-1051
-
-
Galarneau, G.1
-
57
-
-
84901610068
-
Clues from the resilient
-
Friend S.H., Schadt E.E. Clues from the resilient. Science 2014, 344:970-972.
-
(2014)
Science
, vol.344
, pp. 970-972
-
-
Friend, S.H.1
Schadt, E.E.2
-
59
-
-
84929015299
-
Effect of predicted protein-truncating genetic variants on the human transcriptome
-
Rivas M.A., et al. Effect of predicted protein-truncating genetic variants on the human transcriptome. Science 2015, 348:666-669.
-
(2015)
Science
, vol.348
, pp. 666-669
-
-
Rivas, M.A.1
-
60
-
-
84958580914
-
Polypyrimidine tract binding protein 1 protects mRNAs from recognition by the nonsense-mediated mRNA decay pathway
-
Ge Z., et al. Polypyrimidine tract binding protein 1 protects mRNAs from recognition by the nonsense-mediated mRNA decay pathway. Elife 2016, 5:e11155.
-
(2016)
Elife
, vol.5
, pp. e11155
-
-
Ge, Z.1
-
61
-
-
84895858942
-
A general framework for estimating the relative pathogenicity of human genetic variants
-
Kircher M., et al. A general framework for estimating the relative pathogenicity of human genetic variants. Nat. Genet. 2014, 46:310-315.
-
(2014)
Nat. Genet.
, vol.46
, pp. 310-315
-
-
Kircher, M.1
-
62
-
-
84895510920
-
Functional annotation of noncoding sequence variants
-
Ritchie G.R.S., et al. Functional annotation of noncoding sequence variants. Nat. Methods 2014, 11:294-296.
-
(2014)
Nat. Methods
, vol.11
, pp. 294-296
-
-
Ritchie, G.R.S.1
-
63
-
-
84941656377
-
Comparison of predicted and actual consequences of missense mutations
-
Miosge L.A., et al. Comparison of predicted and actual consequences of missense mutations. Proc. Natl. Acad. Sci. U.S.A. 2015, 112:E5189-E5198.
-
(2015)
Proc. Natl. Acad. Sci. U.S.A.
, vol.112
, pp. E5189-E5198
-
-
Miosge, L.A.1
-
64
-
-
84884592445
-
Genic intolerance to functional variation and the interpretation of personal genomes
-
Petrovski S., et al. Genic intolerance to functional variation and the interpretation of personal genomes. PLoS Genet. 2013, 9:e1003709.
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003709
-
-
Petrovski, S.1
-
65
-
-
84946595515
-
The human gene damage index as a gene-level approach to prioritizing exome variants
-
Itan Y., et al. The human gene damage index as a gene-level approach to prioritizing exome variants. Proc. Natl. Acad. Sci. U.S.A. 2015, 112:13615-13620.
-
(2015)
Proc. Natl. Acad. Sci. U.S.A.
, vol.112
, pp. 13615-13620
-
-
Itan, Y.1
-
66
-
-
84961309083
-
The mutation significance cutoff: gene-level thresholds for variant predictions
-
Itan Y., et al. The mutation significance cutoff: gene-level thresholds for variant predictions. Nat. Methods 2016, 13:109-110.
-
(2016)
Nat. Methods
, vol.13
, pp. 109-110
-
-
Itan, Y.1
-
67
-
-
84875826166
-
The human gene connectome as a map of short cuts for morbid allele discovery
-
Itan Y., et al. The human gene connectome as a map of short cuts for morbid allele discovery. Proc. Natl. Acad. Sci. U.S.A. 2013, 110:5558-5563.
-
(2013)
Proc. Natl. Acad. Sci. U.S.A.
, vol.110
, pp. 5558-5563
-
-
Itan, Y.1
-
68
-
-
84895867277
-
The deleterious mutation load is insensitive to recent population history
-
Simons Y.B., et al. The deleterious mutation load is insensitive to recent population history. Nat. Genet. 2014, 46:220-224.
-
(2014)
Nat. Genet.
, vol.46
, pp. 220-224
-
-
Simons, Y.B.1
-
69
-
-
84926169268
-
No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans
-
Do R., et al. No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans. Nat. Genet. 2015, 47:126-131.
-
(2015)
Nat. Genet.
, vol.47
, pp. 126-131
-
-
Do, R.1
-
70
-
-
84921818763
-
Characteristics of neutral and deleterious protein-coding variation among individuals and populations
-
Fu W., et al. Characteristics of neutral and deleterious protein-coding variation among individuals and populations. Am. J. Hum. Genet. 2014, 95:421-436.
-
(2014)
Am. J. Hum. Genet.
, vol.95
, pp. 421-436
-
-
Fu, W.1
-
71
-
-
84955508579
-
Distance from sub-Saharan Africa predicts mutational load in diverse human genomes
-
Henn B.M., et al. Distance from sub-Saharan Africa predicts mutational load in diverse human genomes. Proc. Natl. Acad. Sci. U.S.A. 2016, 113:E440-E449.
-
(2016)
Proc. Natl. Acad. Sci. U.S.A.
, vol.113
, pp. E440-E449
-
-
Henn, B.M.1
-
72
-
-
84927589000
-
Mountain gorilla genomes reveal the impact of long-term population decline and inbreeding
-
Xue Y., et al. Mountain gorilla genomes reveal the impact of long-term population decline and inbreeding. Science 2015, 348:242-245.
-
(2015)
Science
, vol.348
, pp. 242-245
-
-
Xue, Y.1
|