-
1
-
-
27244437783
-
Handling marker-marker linkage disequilibrium: Pedigree analysis with clustered markers
-
Abecasis GR, Wigginton JE. 2005. Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers. Am. J. Hum. Genet. 77:754-67
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 754-767
-
-
Abecasis, G.R.1
Wigginton, J.E.2
-
2
-
-
82455194217
-
Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives
-
Akula N, Detera-Wadleigh S, Shugart Y, Nalls M, Steele J, McMahon FJ. 2011. Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives. BMC Proc. 5(Suppl. 9):S76
-
(2011)
BMC Proc.
, vol.5
, Issue.SUPPL. 9
-
-
Akula, N.1
Detera-Wadleigh, S.2
Shugart, Y.3
Nalls, M.4
Steele, J.5
McMahon, F.J.6
-
3
-
-
79960895154
-
Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome
-
Albers CA, Cvejic A, Favier R, Bouwmans EE, Alessi MC, et al. 2011. Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome. Nat. Genet. 43:735-37
-
(2011)
Nat. Genet.
, vol.43
, pp. 735-737
-
-
Albers, C.A.1
Cvejic, A.2
Favier, R.3
Bouwmans, E.E.4
Alessi, M.C.5
-
4
-
-
41149128766
-
Multipoint approximations of identityby- descent probabilities for accurate linkage analysis of distantly related individuals
-
Albers CA, Stankovich J, Thomson R, Bahlo M, Kappen HJ. 2008. Multipoint approximations of identityby- descent probabilities for accurate linkage analysis of distantly related individuals. Am. J. Hum. Genet. 82:607-22
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 607-622
-
-
Albers, C.A.1
Stankovich, J.2
Thomson, R.3
Bahlo, M.4
Kappen, H.J.5
-
5
-
-
66249112837
-
Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium
-
Albrechtsen A, Korneliussen TS, Moltle I, Hansen TV, Nielsen FC, Nielsen R. 2009. Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium. Genet. Epidemiol. 33:266-74
-
(2009)
Genet. Epidemiol.
, vol.33
, pp. 266-274
-
-
Albrechtsen, A.1
Korneliussen, T.S.2
Moltle, I.3
Hansen, T.V.4
Nielsen, F.C.5
Nielsen, R.6
-
6
-
-
78751676360
-
Natural selection and the distribution of identity-by-descent in the human genome
-
Albrechtsen A, Moltke I, Nielsen R. 2010. Natural selection and the distribution of identity-by-descent in the human genome. Genetics 186:295-308
-
(2010)
Genetics
, vol.186
, pp. 295-308
-
-
Albrechtsen, A.1
Moltke, I.2
Nielsen, R.3
-
7
-
-
84859621557
-
Inferring coancestry in population samples in the presence of linkage disequilibrium
-
Brown MD, Glazner CG, Zheng C, Thompson EA. 2012. Inferring coancestry in population samples in the presence of linkage disequilibrium. Genetics 190:1447-60
-
(2012)
Genetics
, vol.190
, pp. 1447-1460
-
-
Brown, M.D.1
Glazner, C.G.2
Zheng, C.3
Thompson, E.A.4
-
8
-
-
10844249215
-
Linkage analysis using single nucleotide polymorphisms
-
Browning BL, Brashear DL, Butler AA, Cyr DD, Harris EC, et al. 2004. Linkage analysis using single nucleotide polymorphisms. Hum. Hered. 57:220-27
-
(2004)
Hum. Hered.
, vol.57
, pp. 220-227
-
-
Browning, B.L.1
Brashear, D.L.2
Butler, A.A.3
Cyr, D.D.4
Harris, E.C.5
-
9
-
-
62649155943
-
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals
-
Browning BL, Browning SR. 2009. A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. Am. J. Hum. Genet. 84:210-23
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 210-223
-
-
Browning, B.L.1
Browning, S.R.2
-
10
-
-
79851497145
-
A fast, powerful method for detecting identity by descent
-
Browning BL, Browning SR. 2011. A fast, powerful method for detecting identity by descent. Am. J. Hum. Genet. 88:173-82
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 173-182
-
-
Browning, B.L.1
Browning, S.R.2
-
11
-
-
71149112981
-
Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies
-
Browning BL, Yu Z. 2009. Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies. Am. J. Hum. Genet. 85:847-61
-
(2009)
Am. J. Hum. Genet.
, vol.85
, pp. 847-861
-
-
Browning, B.L.1
Yu, Z.2
-
12
-
-
33646869900
-
Multilocus association mapping using variable-length Markov chains
-
Browning SR. 2006. Multilocus association mapping using variable-length Markov chains. Am. J. Hum. Genet. 78:903-13
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 903-913
-
-
Browning, S.R.1
-
13
-
-
45849112925
-
Estimation of pairwise identity by descent from dense genetic marker data in a population sample of haplotypes
-
Browning SR. 2008. Estimation of pairwise identity by descent from dense genetic marker data in a population sample of haplotypes. Genetics 178:2123-32
-
(2008)
Genetics
, vol.178
, pp. 2123-2132
-
-
Browning, S.R.1
-
14
-
-
35348817330
-
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering
-
Browning SR, Browning BL. 2007. Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering.Am. J. Hum. Genet. 81:1084-97
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 1084-1097
-
-
Browning, S.R.1
Browning, B.L.2
-
15
-
-
77950332127
-
High-resolution detection of identity by descent in unrelated individuals
-
Browning SR, Browning BL. 2010. High-resolution detection of identity by descent in unrelated individuals. Am. J. Hum. Genet. 86:526-39
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 526-539
-
-
Browning, S.R.1
Browning, B.L.2
-
16
-
-
80053019891
-
Haplotype phasing: Existing methods and new developments
-
Browning SR, Browning BL. 2011. Haplotype phasing: existing methods and new developments. Nat. Rev. Genet. 12:703-14
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 703-714
-
-
Browning, S.R.1
Browning, B.L.2
-
17
-
-
80051538026
-
Population structure can inflate SNP-based heritability estimates
-
author reply 193-95
-
Browning SR, Browning BL. 2011. Population structure can inflate SNP-based heritability estimates. Am. J. Hum. Genet. 89:191-93; author reply 193-95
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 191-193
-
-
Browning, S.R.1
Browning, B.L.2
-
18
-
-
84859588748
-
Detecting rare variant associations by identity-by-descent mapping in case-control studies
-
Browning SR, Thompson EA. 2012. Detecting rare variant associations by identity-by-descent mapping in case-control studies. Genetics 190:1521-31
-
(2012)
Genetics
, vol.190
, pp. 1521-1531
-
-
Browning, S.R.1
Thompson, E.A.2
-
19
-
-
79956319716
-
Identification of regions of positive selection using Shared Genomic Segment analysis
-
Cai Z, Camp NJ, Cannon-Albright L, Thomas A. 2011. Identification of regions of positive selection using Shared Genomic Segment analysis. Eur. J. Hum. Genet. 19:667-71
-
(2011)
Eur. J. Hum. Genet.
, vol.19
, pp. 667-671
-
-
Cai, Z.1
Camp, N.J.2
Cannon-Albright, L.3
Thomas, A.4
-
20
-
-
78650037203
-
Deep resequencing reveals excess rare recent variants consistent with explosive population growth
-
Coventry A, Bull-Otterson LM, Liu X, Clark AG, Maxwell TJ, et al. 2010. Deep resequencing reveals excess rare recent variants consistent with explosive population growth. Nat. Commun. 1:131
-
(2010)
Nat. Commun.
, vol.1
, pp. 131
-
-
Coventry, A.1
Bull-Otterson, L.M.2
Liu, X.3
Clark, A.G.4
Maxwell, T.J.5
-
21
-
-
79958129487
-
Linkage analysis without defined pedigrees
-
Day-Williams AG, Blangero J, Dyer TD, Lange K, Sobel EM. 2011. Linkage analysis without defined pedigrees. Genet. Epidemiol. 35:360-70
-
(2011)
Genet. Epidemiol.
, vol.35
, pp. 360-370
-
-
Day-Williams, A.G.1
Blangero, J.2
Dyer, T.D.3
Lange, K.4
Sobel, E.M.5
-
22
-
-
55349099514
-
An unusual haplotype structure on human chromosome 8p23 derived from the inversion polymorphism
-
Deng L, Zhang Y, Kang J, Liu T, Zhao H, et al. 2008. An unusual haplotype structure on human chromosome 8p23 derived from the inversion polymorphism. Hum. Mutat. 29:1209-16
-
(2008)
Hum. Mutat.
, vol.29
, pp. 1209-1216
-
-
Deng, L.1
Zhang, Y.2
Kang, J.3
Liu, T.4
Zhao, H.5
-
23
-
-
79953088839
-
Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly
-
Fabbro S, Kahr WH, Hinckley J, Wang K, Moseley J, et al. 2011. Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly. Blood 117:3430-34
-
(2011)
Blood
, vol.117
, pp. 3430-3434
-
-
Fabbro, S.1
Kahr, W.H.2
Hinckley, J.3
Wang, K.4
Moseley, J.5
-
25
-
-
77649122250
-
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
-
Girirajan S, Rosenfeld JA, Cooper GM, Antonacci F, Siswara P, et al. 2010. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nat. Genet. 42:203-9
-
(2010)
Nat. Genet.
, vol.42
, pp. 203-209
-
-
Girirajan, S.1
Rosenfeld, J.A.2
Cooper, G.M.3
Antonacci, F.4
Siswara, P.5
-
26
-
-
84857717965
-
Improving pedigree-based linkage analysis by estimating coancestry among families
-
Article 11
-
Glazner C, Thompson EA. 2012. Improving pedigree-based linkage analysis by estimating coancestry among families. Stat. Appl. Genet. Mol. Biol. 11(Issue 2):Article 11
-
(2012)
Stat. Appl. Genet. Mol. Biol.
, vol.11
, Issue.2
-
-
Glazner, C.1
Thompson, E.A.2
-
27
-
-
80051497514
-
Response to browning and browning
-
Goddard ME, Lee SH, Yang J, Wray NR, Visscher PM. 2011. Response to Browning and Browning. Am. J. Hum. Genet. 89:193-95
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 193-195
-
-
Goddard, M.E.1
Lee, S.H.2
Yang, J.3
Wray, N.R.4
Visscher, P.M.5
-
28
-
-
79960921968
-
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet alpha-granules
-
Gunay-Aygun M, Falik-Zaccai TC, Vilboux T, Zivony-Elboum Y, Gumruk F, et al. 2011. NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet alpha-granules. Nat. Genet. 43:732-34
-
(2011)
Nat. Genet.
, vol.43
, pp. 732-734
-
-
Gunay-Aygun, M.1
Falik-Zaccai, T.C.2
Vilboux, T.3
Zivony-Elboum, Y.4
Gumruk, F.5
-
29
-
-
78649744166
-
Gray platelet syndrome: Natural history of a large patient cohort and locus assignment to chromosome 3p
-
Gunay-Aygun M, Zivony-Elboum Y, Gumruk F, Geiger D, CetinM, et al. 2010. Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p. Blood 116:4990-5001
-
(2010)
Blood
, vol.116
, pp. 4990-5001
-
-
Gunay-Aygun, M.1
Zivony-Elboum, Y.2
Gumruk, F.3
Geiger, D.4
Cetin, M.5
-
30
-
-
79958863532
-
DASH: A method for identical-by-descent haplotype mapping uncovers association with recent variation
-
Gusev A, Kenny EE, Lowe JK, Salit J, Saxena R, et al. 2011. DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. Am. J. Hum. Genet. 88:706-17
-
(2011)
Am. J. Hum. Genet.
, vol.88
, pp. 706-717
-
-
Gusev, A.1
Kenny, E.E.2
Lowe, J.K.3
Salit, J.4
Saxena, R.5
-
31
-
-
59949088494
-
Whole population, genome-wide mapping of hidden relatedness
-
Gusev A, Lowe JK, StoffelM, Daly MJ, Altshuler D, et al. 2009. Whole population, genome-wide mapping of hidden relatedness. Genome Res. 19:318-26
-
(2009)
Genome Res.
, vol.19
, pp. 318-326
-
-
Gusev, A.1
Lowe, J.K.2
Stoffel, M.3
Daly, M.J.4
Altshuler, D.5
-
32
-
-
80051816176
-
Identity by descent estimation with dense genome-wide genotype data
-
Han L, Abney M. 2011. Identity by descent estimation with dense genome-wide genotype data. Genet. Epidemiol. 35:557-67
-
(2011)
Genet. Epidemiol.
, vol.35
, pp. 557-567
-
-
Han, L.1
Abney, M.2
-
33
-
-
67349247510
-
A common Greenlandic Inuit BRCA1 RING domain founder mutation
-
Hansen TV, Ejlertsen B, Albrechtsen A, Bergsten E, Bjerregaard P, et al. 2009. A common Greenlandic Inuit BRCA1 RING domain founder mutation. Breast Cancer Res. Treat. 115:69-76
-
(2009)
Breast Cancer Res. Treat.
, vol.115
, pp. 69-76
-
-
Hansen, T.V.1
Ejlertsen, B.2
Albrechtsen, A.3
Bergsten, E.4
Bjerregaard, P.5
-
34
-
-
77957712880
-
Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a nucleotide 249T
-
Hansen TV, Jonson L, Albrechtsen A, Steffensen AY, Bergsten E, et al. 2010. Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a nucleotide 249T
-
(2010)
Breast Cancer Res. Treat.
, vol.124
, pp. 259-264
-
-
Hansen, T.V.1
Jonson, L.2
Albrechtsen, A.3
Steffensen, A.Y.4
Bergsten, E.5
-
35
-
-
0027942323
-
Genome screening by searching for shared segments: Mapping a gene for benign recurrent intrahepatic cholestasis
-
Houwen RH, Baharloo S, Blankenship K, Raeymaekers P, Juyn J, et al. 1994. Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis. Nat. Genet. 8:380-86
-
(1994)
Nat. Genet.
, vol.8
, pp. 380-386
-
-
Houwen, R.H.1
Baharloo, S.2
Blankenship, K.3
Raeymaekers, P.4
Juyn, J.5
-
36
-
-
79955570035
-
Maximum-likelihood estimation of recent shared ancestry (ERSA)
-
Huff CD, Witherspoon DJ, Simonson TS, Xing J, Watkins WS, et al. 2011. Maximum-likelihood estimation of recent shared ancestry (ERSA). Genome Res. 21:768-74
-
(2011)
Genome Res.
, vol.21
, pp. 768-774
-
-
Huff, C.D.1
Witherspoon, D.J.2
Simonson, T.S.3
Xing, J.4
Watkins, W.S.5
-
37
-
-
0032426345
-
Natural selection at major histocompatibility complex loci of vertebrates
-
Hughes AL, Yeager M. 1998. Natural selection at major histocompatibility complex loci of vertebrates. Annu. Rev. Genet. 32:415-35
-
(1998)
Annu. Rev. Genet.
, vol.32
, pp. 415-435
-
-
Hughes, A.L.1
Yeager, M.2
-
38
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
Int. HapMap 3 Consort
-
Int. HapMap 3 Consort. 2010. Integrating common and rare genetic variation in diverse human populations. Nature 467:52-58
-
(2010)
Nature
, vol.467
, pp. 52-58
-
-
-
40
-
-
79960903114
-
Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome
-
Kahr WH, Hinckley J, Li L, Schwertz H, Christensen H, et al. 2011. Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome. Nat. Genet. 43:738-40
-
(2011)
Nat. Genet.
, vol.43
, pp. 738-740
-
-
Kahr, W.H.1
Hinckley, J.2
Li, L.3
Schwertz, H.4
Christensen, H.5
-
41
-
-
69549110424
-
Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae
-
Kenny EE, Gusev A, Riegel K, Lutjohann D, Lowe JK, et al. 2009. Systematic haplotype analysis resolves a complex plasma plant sterol locus on the Micronesian Island of Kosrae. Proc. Natl. Acad. Sci. USA 106:13886-91
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 13886-13891
-
-
Kenny, E.E.1
Gusev, A.2
Riegel, K.3
Lutjohann, D.4
Lowe, J.K.5
-
42
-
-
50449089222
-
Detection of sharing by descent, long-range phasing and haplotype imputation
-
Kong A, MassonG, Frigge ML, Gylfason A, Zusmanovich P, et al. 2008. Detection of sharing by descent, long-range phasing and haplotype imputation. Nat. Genet. 40:1068-75
-
(2008)
Nat. Genet.
, vol.40
, pp. 1068-1075
-
-
Kong, A.1
Masson, G.2
Frigge, M.L.3
Gylfason, A.4
Zusmanovich, P.5
-
43
-
-
77957555078
-
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome
-
Krawitz PM, Schweiger MR, Rodelsperger C, Marcelis C, Kolsch U, et al. 2010. Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nat. Genet. 42:827-29
-
(2010)
Nat. Genet.
, vol.42
, pp. 827-829
-
-
Krawitz, P.M.1
Schweiger, M.R.2
Rodelsperger, C.3
Marcelis, C.4
Kolsch, U.5
-
44
-
-
44649093326
-
A SNP streak model for the identification of genetic regions identical-by-descent
-
Article 16
-
Leibon G, Rockmore DN, Pollak MR. 2008. A SNP streak model for the identification of genetic regions identical-by-descent. Stat. Appl. Genet. Mol. Biol. 7(Issue 1):Article 16
-
(2008)
Stat. Appl. Genet. Mol. Biol.
, vol.7
, Issue.1
-
-
Leibon, G.1
Rockmore, D.N.2
Pollak, M.R.3
-
45
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, CoxNJ, GoldsteinDB, Hindorff LA, et al. 2009. Finding the missing heritability of complex diseases. Nature 461:747-53
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
-
46
-
-
33344458848
-
A comparison of phasing algorithms for trios and unrelated individuals
-
Marchini J, Cutler D, Patterson N, Stephens M, Eskin E, et al. 2006. A comparison of phasing algorithms for trios and unrelated individuals. Am. J. Hum. Genet. 78:437-50
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 437-450
-
-
Marchini, J.1
Cutler, D.2
Patterson, N.3
Stephens, M.4
Eskin, E.5
-
47
-
-
34250861479
-
Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patients
-
Miyazawa H, Kato M, Awata T, Kohda M, Iwasa H, et al. 2007. Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patients. Am. J. Hum. Genet. 80:1090-102
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 1090-1102
-
-
Miyazawa, H.1
Kato, M.2
Awata, T.3
Kohda, M.4
Iwasa, H.5
-
48
-
-
79959893242
-
A method for detecting IBD regions simultaneously in multiple individuals-with applications to disease genetics
-
Moltke I, Albrechtsen A, Hansen TV, Nielsen FC, Nielsen R. 2011. A method for detecting IBD regions simultaneously in multiple individuals-with applications to disease genetics. Genome Res. 21:1168-80
-
(2011)
Genome Res.
, vol.21
, pp. 1168-1180
-
-
Moltke, I.1
Albrechtsen, A.2
Hansen, T.V.3
Nielsen, F.C.4
Nielsen, R.5
-
49
-
-
84871201882
-
Applications of pedigree-free identityby- descent mapping to localizing disease genes
-
Oct. 11, New Orleans, LA.
-
Nelson S, Merriman B, Chen Z, Ogdie M, Stone J, Strom S. 2006. Applications of pedigree-free identityby- descent mapping to localizing disease genes. Abstr. 1530. Presented at Annu. Meet. The Am. Soc. Hum. Genet., Oct. 11, New Orleans, LA. http://www.ashg.org/genetics/ashg06s/f20776.htm
-
(2006)
Abstr. 1530. Presented at Annu. Meet. The Am. Soc. Hum. Genet.
-
-
Nelson, S.1
Merriman, B.2
Chen, Z.3
Ogdie, M.4
Stone, J.5
Strom, S.6
-
51
-
-
79952263851
-
Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individuals
-
Price AL, Helgason A, Thorleifsson G, McCarroll SA, Kong A, Stefansson K. 2011. Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individuals. PLoS Genet. 7:e1001317
-
(2011)
PLoS Genet.
, vol.7
-
-
Price, A.L.1
Helgason, A.2
Thorleifsson, G.3
McCarroll, S.A.4
Kong, A.5
Stefansson, K.6
-
52
-
-
34548292504
-
PLINK: A tool set for wholegenome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, et al. 2007. PLINK: a tool set for wholegenome association and population-based linkage analyses. Am. J. Hum. Genet. 81:559-75
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
-
53
-
-
84871191980
-
From linkage to sequencing: Using cross-family IBD sharing to refine susceptibility loci in Tourette Syndrome multi-generational families
-
Oct. 13, Montreal, Can.
-
Ramensky V, Yu D, Service S, Matthews C, Heutink P, et al. 2011. From linkage to sequencing: Using cross-family IBD sharing to refine susceptibility loci in Tourette Syndrome multi-generational families. Presented at 12th Int. Congr. Hum. Genet. /61st Annu.Meet. The Am. Soc. Hum. Genet., Oct. 13, Montreal, Can.
-
(2011)
Presented at 12th Int. Congr. Hum. Genet. /61st Annu.Meet. The Am. Soc. Hum. Genet.
-
-
Ramensky, V.1
Yu, D.2
Service, S.3
Matthews, C.4
Heutink, P.5
-
54
-
-
77951799158
-
Analysis of genetic inheritance in a family quartet by whole-genome sequencing
-
Roach JC, Glusman G, Smit AF, Huff CD, Hubley R, et al. 2010. Analysis of genetic inheritance in a family quartet by whole-genome sequencing. Science 328:636-39
-
(2010)
Science
, vol.328
, pp. 636-639
-
-
Roach, J.C.1
Glusman, G.2
Smit, A.F.3
Huff, C.D.4
Hubley, R.5
-
55
-
-
79952598349
-
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders
-
Rodelsperger C, Krawitz P, Bauer S, Hecht J, Bigham AW, et al. 2011. Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics 27:829-36
-
(2011)
Bioinformatics
, vol.27
, pp. 829-836
-
-
Rodelsperger, C.1
Krawitz, P.2
Bauer, S.3
Hecht, J.4
Bigham, A.W.5
-
56
-
-
79952387188
-
HLA type inference via haplotypes identical by descent
-
Setty MN, Gusev A, Pe'er I. 2011. HLA type inference via haplotypes identical by descent. J. Comput. Biol. 18:483-93
-
(2011)
J. Comput. Biol.
, vol.18
, pp. 483-493
-
-
Setty, M.N.1
Gusev, A.2
Pe'Er, I.3
-
57
-
-
80052833627
-
Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes
-
Smith KR, Bromhead CJ, Hildebrand MS, Shearer AE, Lockhart PJ, et al. 2011. Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes. Genome Biol. 12:R85
-
(2011)
Genome Biol.
, vol.12
-
-
Smith, K.R.1
Bromhead, C.J.2
Hildebrand, M.S.3
Shearer, A.E.4
Lockhart, P.J.5
-
58
-
-
84871240357
-
Demographic histories of African huntinggathering populations inferred from genome-wide SNP variation
-
Oct. 13, Montreal, Can.
-
Soi S, Scheinfeldt L, Lambert C, Hirbo J, Ranciaro A, et al. 2011. Demographic histories of African huntinggathering populations inferred from genome-wide SNP variation. Presented at 12th Int. Congr. Hum. Genet. /61st Annu. Meet. The Am. Soc. Hum. Genet., Oct. 13, Montreal, Can.
-
(2011)
Presented at 12th Int. Congr. Hum. Genet. /61st Annu. Meet. The Am. Soc. Hum. Genet.
-
-
Soi, S.1
Scheinfeldt, L.2
Lambert, C.3
Hirbo, J.4
Ranciaro, A.5
-
59
-
-
76649106401
-
Assessment of SNP streak statistics using gene drop simulation with linkage disequilibrium
-
Thomas A. 2010. Assessment of SNP streak statistics using gene drop simulation with linkage disequilibrium. Genet. Epidemiol. 34:119-24
-
(2010)
Genet. Epidemiol.
, vol.34
, pp. 119-124
-
-
Thomas, A.1
-
60
-
-
38949189981
-
Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays
-
Thomas A, Camp NJ, Farnham JM, Allen-BradyK, Cannon-Albright LA. 2008. Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays. Ann. Hum. Genet. 72:279-87
-
(2008)
Ann. Hum. Genet.
, vol.72
, pp. 279-287
-
-
Thomas, A.1
Camp, N.J.2
Farnham, J.M.3
Allen-Brady, K.4
Cannon-Albright, L.A.5
-
63
-
-
41149127075
-
The IBD process along four chromosomes
-
Thompson EA. 2008. The IBD process along four chromosomes. Theor. Popul. Biol. 73:369-73
-
(2008)
Theor. Popul. Biol.
, vol.73
, pp. 369-373
-
-
Thompson, E.A.1
-
64
-
-
84969213492
-
Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls
-
Wellcome Trust Case Control Consort
-
Wellcome Trust Case Control Consort. 2007. Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls. Nature 447:661-78
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
65
-
-
33751103455
-
Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees
-
Wijsman EM, Rothstein JH, Thompson EA. 2006. Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees. Am. J. Hum. Genet. 79:846-58
-
(2006)
Am. J. Hum. Genet.
, vol.79
, pp. 846-858
-
-
Wijsman, E.M.1
Rothstein, J.H.2
Thompson, E.A.3
-
66
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, et al. 2010. Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42:565-69
-
(2010)
Nat. Genet.
, vol.42
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
Gordon, S.4
Henders, A.K.5
-
67
-
-
84856405512
-
Themystery of missing heritability: Genetic interactions create phantom heritability
-
Zuk O, Hechter E, Sunyaev SR, Lander ES. 2012. Themystery of missing heritability: genetic interactions create phantom heritability. Proc. Natl. Acad. Sci. USA 109:1193-98
-
(2012)
Proc. Natl. Acad. Sci. USA
, vol.109
, pp. 1193-1198
-
-
Zuk, O.1
Hechter, E.2
Sunyaev, S.R.3
Lander, E.S.4
|