-
1
-
-
0343059882
-
Inverse inbreeding coefficient problems with an application to linkage analysis of recessive diseases in inbred populations
-
in press
-
Agarwala, R., L.G. Biesecker, and A.A. Schäffer. 2000. Inverse inbreeding coefficient problems with an application to linkage analysis of recessive diseases in inbred populations. Discrete Appl. Math. (in press).
-
(2000)
Discrete Appl. Math.
-
-
Agarwala, R.1
Biesecker, L.G.2
Schäffer, A.A.3
-
2
-
-
0012119330
-
Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration
-
Allikmets, R., N.F. Shroyer, N. Singh et al. 1997. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science 277:1805-1807.
-
(1997)
Science
, vol.277
, pp. 1805-1807
-
-
Allikmets, R.1
Shroyer, N.F.2
Singh, N.3
-
3
-
-
0033361796
-
Human pedigree-based quantitative-trait-locus mapping: Localization of two genes influencing HDL-cholesterol metabolism
-
Almasy, L., J.E. Hixson, D.L. Rainwater et al. 1999. Human pedigree-based quantitative-trait-locus mapping: Localization of two genes influencing HDL-cholesterol metabolism. Am. J. Hum. Genet. 64:1686-1693.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1686-1693
-
-
Almasy, L.1
Hixson, J.E.2
Rainwater, D.L.3
-
5
-
-
0343931626
-
Greenland medical bibliography
-
Andersen, S. 1981. Greenland medical bibliography. Arct. Med. Res. 29:1-137.
-
(1981)
Arct. Med. Res.
, vol.29
, pp. 1-137
-
-
Andersen, S.1
-
6
-
-
0029819112
-
Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrences of the disease
-
Arolt, V., R. Lencer, A. Nolte et al. 1996. Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrences of the disease. Am. J. Med. Genet. 67:564-579.
-
(1996)
Am. J. Med. Genet.
, vol.67
, pp. 564-579
-
-
Arolt, V.1
Lencer, R.2
Nolte, A.3
-
7
-
-
0030983803
-
Complicated cataracts in various forms of retinitis pigmentosa: Type and incidence
-
Auffarth, G.U., M.R. Tetz, H. Krastel et al. 1997. Complicated cataracts in various forms of retinitis pigmentosa: Type and incidence. Der Ophthalmologe 94:642-646.
-
(1997)
Der Ophthalmologe
, vol.94
, pp. 642-646
-
-
Auffarth, G.U.1
Tetz, M.R.2
Krastel, H.3
-
9
-
-
0032231878
-
Optimal ascertainment strategies to detect linkage to common disease alleles
-
Badner, J.A., E.S. Gershon, and L.R. Goldin. 1998. Optimal ascertainment strategies to detect linkage to common disease alleles. Am. J. Hum. Genet. 63:880-888.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 880-888
-
-
Badner, J.A.1
Gershon, E.S.2
Goldin, L.R.3
-
11
-
-
0031026078
-
Variable expressivity of patched mutations in flies and humans
-
Bale, A.E. 1997. Variable expressivity of patched mutations in flies and humans. Am. J. Hum. Genet. 60:10-12.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 10-12
-
-
Bale, A.E.1
-
13
-
-
0002672462
-
The linkage between the genes for color blindness and hemophilia in man
-
Bell, J., and J.B.S. Haldane. 1937. The linkage between the genes for color blindness and hemophilia in man. Proc. R. Soc. Lond., ser. B, 123:119-150.
-
(1937)
Proc. R. Soc. Lond., Ser. B
, vol.123
, pp. 119-150
-
-
Bell, J.1
Haldane, J.B.S.2
-
15
-
-
0029035306
-
Retinal photoreceptor dystrophies
-
Bird, A.C. 1995. Retinal photoreceptor dystrophies. Am. J. Ophthalmol. 119:543-562.
-
(1995)
Am. J. Ophthalmol.
, vol.119
, pp. 543-562
-
-
Bird, A.C.1
-
17
-
-
0021957675
-
A comparison of sib-pair linkage tests for disease susceptibility loci
-
Blackwelder, W.C., and R.C. Elston. 1985. A comparison of sib-pair linkage tests for disease susceptibility loci. Genet. Epidemiol. 2:85-97.
-
(1985)
Genet. Epidemiol.
, vol.2
, pp. 85-97
-
-
Blackwelder, W.C.1
Elston, R.C.2
-
18
-
-
0026033848
-
DNA markers and biological vulnerability markers in families multiply affected with schizophrenia
-
Blackwood, D., D. St Clair, and W. Muir. 1991. DNA markers and biological vulnerability markers in families multiply affected with schizophrenia. Eur. Arch. Psychiatr. Clin. Neurosci. 240:191-196.
-
(1991)
Eur. Arch. Psychiatr. Clin. Neurosci.
, vol.240
, pp. 191-196
-
-
Blackwood, D.1
St Clair, D.2
Muir, W.3
-
19
-
-
0034143958
-
Quantitative trait locus mapping using human pedigrees
-
this issue
-
Blangero, J., J.T. Williams, and L. Almasy. 2000. Quantitative trait locus mapping using human pedigrees. Hum. Biol. 72:35-62 (this issue).
-
(2000)
Hum. Biol.
, vol.72
, pp. 35-62
-
-
Blangero, J.1
Williams, J.T.2
Almasy, L.3
-
21
-
-
0031242547
-
Metabolical changes induced by adaptation to circumpolar conditions in Spitsbergen
-
Bojko, E.R. 1997. Metabolical changes induced by adaptation to circumpolar conditions in Spitsbergen. Int. J. Circumpolar Health 56:134-141.
-
(1997)
Int. J. Circumpolar Health
, vol.56
, pp. 134-141
-
-
Bojko, E.R.1
-
22
-
-
0019302053
-
Construction of a genetic linkage map in man using restriction fragment length polymorphisms
-
Botstein, D., R.L. White, M.H. Skolnick et al. 1980. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am. J. Hum. Genet. 32:314-331.
-
(1980)
Am. J. Hum. Genet.
, vol.32
, pp. 314-331
-
-
Botstein, D.1
White, R.L.2
Skolnick, M.H.3
-
23
-
-
0002101881
-
Genetics of aerobic power and capacity
-
R.M. Malina and C. Bouchard, eds. Champaign, IL: Human Kinetics
-
Bouchard, C. 1986. Genetics of aerobic power and capacity. In Sport and Human Genetics, R.M. Malina and C. Bouchard, eds. Champaign, IL: Human Kinetics, 59-89.
-
(1986)
Sport and Human Genetics
, pp. 59-89
-
-
Bouchard, C.1
-
24
-
-
0029113623
-
Genetic markers of obesity: An update on molecular markers
-
Bouchard, C. 1995. Genetic markers of obesity: An update on molecular markers. Int. J. Obesity 19:S10-S13.
-
(1995)
Int. J. Obesity
, vol.19
-
-
Bouchard, C.1
-
26
-
-
0031812658
-
Breast cancer susceptibility genes BRCA1 and BRCA2
-
Brody, L.C., and B.B. Biesecker. 1998. Breast cancer susceptibility genes BRCA1 and BRCA2. Medicine (Baltimore) 77:208-226.
-
(1998)
Medicine (Baltimore)
, vol.77
, pp. 208-226
-
-
Brody, L.C.1
Biesecker, B.B.2
-
27
-
-
0032997217
-
The essence of SNPs
-
Brookes, A.J. 1999. The essence of SNPs. Gene 234:177-186.
-
(1999)
Gene
, vol.234
, pp. 177-186
-
-
Brookes, A.J.1
-
28
-
-
0027254790
-
Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosa
-
Bunge, S., H. Wedemann, D. David et al. 1993. Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosa. Genomics 17:230-233.
-
(1993)
Genomics
, vol.17
, pp. 230-233
-
-
Bunge, S.1
Wedemann, H.2
David, D.3
-
29
-
-
0026047218
-
Linkage analysis of quantitative traits: Increased power by using selected samples
-
Carey, G., and J. Williamson. 1991. Linkage analysis of quantitative traits: Increased power by using selected samples. Am. J. Hum. Genet. 49:786-796.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 786-796
-
-
Carey, G.1
Williamson, J.2
-
30
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
Cargill, M., D. Altshuler, J. Ireland et al. 1999. Characterization of single-nucleotide polymorphisms in coding regions of human genes. Natur. Genet. 22:231-238.
-
(1999)
Natur. Genet.
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
-
31
-
-
0010637544
-
-
Cambridge, MA: Harvard University Press
-
Castle, W.E. 1916. Genetics and Eugenics. Cambridge, MA: Harvard University Press.
-
(1916)
Genetics and Eugenics
-
-
Castle, W.E.1
-
33
-
-
0024209791
-
Admixture as a tool for finding linked genes and detecting that difference from allelic association between loci
-
Chakraborty, R., and K.M. Weiss. 1988. Admixture as a tool for finding linked genes and detecting that difference from allelic association between loci. Proc. Natl. Acad. Sci. USA 85:9119-9123.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 9119-9123
-
-
Chakraborty, R.1
Weiss, K.M.2
-
35
-
-
0032231888
-
Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase
-
Clark, A.G., K.M. Weiss, D.A. Nickerson et al. 1998. Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. Am. J. Hum. Genet. 63:595-612.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 595-612
-
-
Clark, A.G.1
Weiss, K.M.2
Nickerson, D.A.3
-
36
-
-
85196608724
-
Secrets of the mental calendar: Becoming a walking WEEKDAY function
-
Clark, M.R. 1994. Secrets of the mental calendar: Becoming a walking WEEKDAY function. Observations Second Quarter 1994:30-42.
-
(1994)
Observations Second Quarter
, vol.1994
, pp. 30-42
-
-
Clark, M.R.1
-
37
-
-
0022728801
-
Effects of misspecifying genetic parameters in lod score analysis
-
Clerget-Darpoux, F., C. Bonaiti-Pellie, and J. Hochez. 1986. Effects of misspecifying genetic parameters in lod score analysis. Biometrics 42:393-399.
-
(1986)
Biometrics
, vol.42
, pp. 393-399
-
-
Clerget-Darpoux, F.1
Bonaiti-Pellie, C.2
Hochez, J.3
-
41
-
-
0031455789
-
Comparison of nonparametric statistics for detection of linkage in nuclear families: Single-marker evaluation
-
Davis, S., and D.E. Weeks. 1997. Comparison of nonparametric statistics for detection of linkage in nuclear families: Single-marker evaluation. Am. J. Hum. Genet. 61:1431-1444.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 1431-1444
-
-
Davis, S.1
Weeks, D.E.2
-
43
-
-
0027254087
-
Genetic influences on daily intake and meal patterns of humans
-
De Castro, J.M. 1993. Genetic influences on daily intake and meal patterns of humans. Physiol. Behav. 53:777-782.
-
(1993)
Physiol. Behav.
, vol.53
, pp. 777-782
-
-
De Castro, J.M.1
-
44
-
-
0343059861
-
The human major histocompatibility complex and disease susceptibility
-
D.L. Rimoin, J.M. Connor, and E.D. Peyritz, eds. Edinburgh, Scotland: Churchill-Livingstone
-
Doherty, D.G., and G.T. Nepom. 1996. The human major histocompatibility complex and disease susceptibility. In Emory and Rimoin's Principles and Practice of Medical Genetics, 3d ed., D.L. Rimoin, J.M. Connor, and E.D. Peyritz, eds. Edinburgh, Scotland: Churchill-Livingstone, 479-504.
-
(1996)
Emory and Rimoin's Principles and Practice of Medical Genetics, 3d Ed
, pp. 479-504
-
-
Doherty, D.G.1
Nepom, G.T.2
-
46
-
-
0004128472
-
-
Cambridge, England: Cambridge University Press
-
Edwards, A.W.F. 1972. Likelihood. Cambridge, England: Cambridge University Press.
-
(1972)
Likelihood
-
-
Edwards, A.W.F.1
-
47
-
-
33744932985
-
The early history of the statistical estimation of linkage
-
Edwards, A.W.F. 1996. The early history of the statistical estimation of linkage. Ann. Hum. Genet. 60:237-249.
-
(1996)
Ann. Hum. Genet.
, vol.60
, pp. 237-249
-
-
Edwards, A.W.F.1
-
48
-
-
0017174407
-
The interpretation of lod scores in linkage analysis
-
Edwards, J.H. 1976. The interpretation of lod scores in linkage analysis. Cytogenet. Cell Genet. 16:289-293.
-
(1976)
Cytogenet. Cell Genet.
, vol.16
, pp. 289-293
-
-
Edwards, J.H.1
-
49
-
-
0030902847
-
Genetic analyses of emotionality
-
Eley, T.C., and R. Plomin. 1997. Genetic analyses of emotionality. Curr. Opin. Neurobiol. 7:279-284.
-
(1997)
Curr. Opin. Neurobiol.
, vol.7
, pp. 279-284
-
-
Eley, T.C.1
Plomin, R.2
-
50
-
-
0031066950
-
Algorithms and inferences: The challenge of multifactorial diseases
-
Elston, R.C. 1997. Algorithms and inferences: The challenge of multifactorial diseases. Am. J. Hum. Genet. 60:255-262.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 255-262
-
-
Elston, R.C.1
-
51
-
-
0031795349
-
Linkage and association
-
Elston, R.C. 1998. Linkage and association. Genet. Epidemiol. 15:565-576.
-
(1998)
Genet. Epidemiol.
, vol.15
, pp. 565-576
-
-
Elston, R.C.1
-
52
-
-
0003407869
-
Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: An initial screen for bipolar disorder loci on chromosome 18
-
Escamilla, M.A., L.A. McInnes, M. Spesny et al. 1999. Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: An initial screen for bipolar disorder loci on chromosome 18. Am. J. Hum. Genet. 64:1670-1678.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1670-1678
-
-
Escamilla, M.A.1
McInnes, L.A.2
Spesny, M.3
-
53
-
-
0029075560
-
The transmission/disequilibrium test: History, subdivision, and admixture
-
Ewens, W.J., and R.S. Spielman. 1995. The transmission/disequilibrium test: History, subdivision, and admixture. Am. J. Hum. Genet. 57:455-464.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 455-464
-
-
Ewens, W.J.1
Spielman, R.S.2
-
54
-
-
0023235253
-
Haplotype relative risks: An easy way to construct a control sample for risk calculations
-
Falk, C.T., and P. Rubinstein. 1987. Haplotype relative risks: An easy way to construct a control sample for risk calculations. Ann. Hum. Genet. 51:227-233.
-
(1987)
Ann. Hum. Genet.
, vol.51
, pp. 227-233
-
-
Falk, C.T.1
Rubinstein, P.2
-
55
-
-
0032507879
-
BRCA1 as a potential human prostate tumor suppressor: Modulation of proliferation, damage responses, and expression of cell regulatory proteins
-
Fan, S., J.A. Wang, R.Q. Yuan et al. 1998. BRCA1 as a potential human prostate tumor suppressor: Modulation of proliferation, damage responses, and expression of cell regulatory proteins. Oncogene 16:3069-3082.
-
(1998)
Oncogene
, vol.16
, pp. 3069-3082
-
-
Fan, S.1
Wang, J.A.2
Yuan, R.Q.3
-
56
-
-
85114526572
-
LOD wars: The affected sib-pair paradigm strikes back
-
Farrall, M. 1997. LOD wars: The affected sib-pair paradigm strikes back. Am. J. Hum. Genet. 60:735-738.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 735-738
-
-
Farrall, M.1
-
57
-
-
85196602284
-
-
Copenhagen, Denmark: Nordic Council of Ministers
-
Feldbæk, I, ed. 1997. Nordisk statistisk årsbok 1997. Copenhagen, Denmark: Nordic Council of Ministers.
-
(1997)
Nordisk Statistisk Årsbok 1997
-
-
Feldbæk, I.1
-
58
-
-
84971185409
-
The correlation between relatives on the supposition of Mendelian inheritance
-
Fisher, R.A. 1918. The correlation between relatives on the supposition of Mendelian inheritance. Trans. R. Soc. Edinburgh 52:399-433.
-
(1918)
Trans. R. Soc. Edinburgh
, vol.52
, pp. 399-433
-
-
Fisher, R.A.1
-
59
-
-
0001735517
-
On the mathematical foundations of theoretical statistics
-
Fisher, R.A. 1922a. On the mathematical foundations of theoretical statistics. Phil. Trans. R. Soc. Lond., ser. A, 202:309-368.
-
(1922)
Phil. Trans. R. Soc. Lond., Ser. A
, vol.202
, pp. 309-368
-
-
Fisher, R.A.1
-
60
-
-
0001007326
-
The systematic location of genes by means of crossover observations
-
Fisher, R.A. 1922b. The systematic location of genes by means of crossover observations. Am. Natur. 56:406-411.
-
(1922)
Am. Natur.
, vol.56
, pp. 406-411
-
-
Fisher, R.A.1
-
61
-
-
17744401588
-
The health of the Inuit of North America: A bibliography from the earliest times through 1990
-
Fortuine, R. 1993. The health of the Inuit of North America: A bibliography from the earliest times through 1990. Arct. Med. Res. 52(suppl. 8):1-353.
-
(1993)
Arct. Med. Res.
, vol.52
, Issue.SUPPL. 8
, pp. 1-353
-
-
Fortuine, R.1
-
62
-
-
0032527873
-
Loss of heterozygosity in the region including the BRCA1 gene on 17q in colon cancer
-
Garcia-Patino, E., B. Gomendio, M. Lleonart et al. 1998. Loss of heterozygosity in the region including the BRCA1 gene on 17q in colon cancer. Cancer Genet. Cytogenet. 104:119-123.
-
(1998)
Cancer Genet. Cytogenet.
, vol.104
, pp. 119-123
-
-
Garcia-Patino, E.1
Gomendio, B.2
Lleonart, M.3
-
63
-
-
13344260701
-
A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish
-
Ginns, E.I., J. Ott, J.A. Egeland et al. 1996. A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish. Natur. Genet. 12:431-435.
-
(1996)
Natur. Genet.
, vol.12
, pp. 431-435
-
-
Ginns, E.I.1
Ott, J.2
Egeland, J.A.3
-
65
-
-
0033942602
-
Linkage analysis in the presence of errors. I. Complex-valued recombination fractions and complex phenotypes
-
Göring, H.H.H., and J.D. Terwilliger. 2000a. Linkage analysis in the presence of errors. I. Complex-valued recombination fractions and complex phenotypes. Am. J. Hum. Genet. (in press).
-
(2000)
Am. J. Hum. Genet. (In Press)
-
-
Göring, H.H.H.1
Terwilliger, J.D.2
-
66
-
-
0033942718
-
Linkage analysis in the presence of errors. II. Marker-locus genotyping errors modeled with hypercomplex recombination fractions
-
Göring, H.H.H., and J.D. Terwilliger. 2000b. Linkage analysis in the presence of errors. II. Marker-locus genotyping errors modeled with hypercomplex recombination fractions. Am. J. Hum. Genet. (in press).
-
(2000)
Am. J. Hum. Genet. (In Press)
-
-
Göring, H.H.H.1
Terwilliger, J.D.2
-
67
-
-
0034164617
-
Linkage analysis in the presence of errors. III. Marker loci and their map as nuisance parameters
-
Göring, H.H.H., and J.D. Terwilliger. 2000c. Linkage analysis in the presence of errors. III. Marker loci and their map as nuisance parameters. Am. J. Hum. Genet. (in press).
-
(2000)
Am. J. Hum. Genet. (In Press)
-
-
Göring, H.H.H.1
Terwilliger, J.D.2
-
68
-
-
0000874908
-
Linkage analysis in the presence of errors. IV. Joint pseudomarker analysis of linkage and/or LD on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified
-
Göring, H.H.H., and J.D. Terwilliger. 2000d. Linkage analysis in the presence of errors. IV. Joint pseudomarker analysis of linkage and/or LD on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified. Am. J. Hum. Genet. (in press).
-
(2000)
Am. J. Hum. Genet. (In Press)
-
-
Göring, H.H.H.1
Terwilliger, J.D.2
-
69
-
-
0029957150
-
Partitioned association-linkage test: Distinguishing "necessary" from "susceptibility" loci
-
Greenberg, D.A., and P. Doneshka. 1996. Partitioned association-linkage test: Distinguishing "necessary" from "susceptibility" loci. Genet. Epidemiol. 13:243-252.
-
(1996)
Genet. Epidemiol.
, vol.13
, pp. 243-252
-
-
Greenberg, D.A.1
Doneshka, P.2
-
71
-
-
0029135425
-
Assignment of the dystonia-Parkinsonism syndrome locus DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1
-
Haberhausen, G., I. Schmitt, A. Kohler et al. 1995. Assignment of the dystonia-Parkinsonism syndrome locus DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1. Am. J. Hum. Genet. 57:644-650.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 644-650
-
-
Haberhausen, G.1
Schmitt, I.2
Kohler, A.3
-
72
-
-
0000178021
-
The combination of linkage values and the calculation of distance between the loci of linked factors
-
Haldane, J.B.S. 1919. The combination of linkage values and the calculation of distance between the loci of linked factors. J. Genet. 8:299-309.
-
(1919)
J. Genet.
, vol.8
, pp. 299-309
-
-
Haldane, J.B.S.1
-
73
-
-
0002439565
-
Methods for the detection of autosomal linkage in man
-
Haldane, J.B.S. 1934. Methods for the detection of autosomal linkage in man. Ann. Eugen. 6:26-35.
-
(1934)
Ann. Eugen.
, vol.6
, pp. 26-35
-
-
Haldane, J.B.S.1
-
74
-
-
0342625623
-
A provisional map of a human chromosome
-
Haldane, J.B.S. 1936. A provisional map of a human chromosome. Nature 137:398-400.
-
(1936)
Nature
, vol.137
, pp. 398-400
-
-
Haldane, J.B.S.1
-
75
-
-
0342625622
-
Blood royal: A study of hemophilia in the royal families of Europe
-
Haldane, J.B.S. 1938. Blood royal: A study of hemophilia in the royal families of Europe. Mod. Q. 1:129-139.
-
(1938)
Mod. Q.
, vol.1
, pp. 129-139
-
-
Haldane, J.B.S.1
-
76
-
-
0011530182
-
Inbreeding in Mendelian populations with a special reference to first cousin marriage
-
Haldane, J.B.S., and P. Moshinsky. 1939. Inbreeding in Mendelian populations with a special reference to first cousin marriage. Ann. Eugen. 9:321-340.
-
(1939)
Ann. Eugen.
, vol.9
, pp. 321-340
-
-
Haldane, J.B.S.1
Moshinsky, P.2
-
77
-
-
78651020237
-
A new estimate of the linkage between the genes for color-blindness and hemophilia in man
-
Haldane, J.B.S., and C.A.B. Smith. 1947. A new estimate of the linkage between the genes for color-blindness and hemophilia in man. Ann. Eugen. 14:10-31.
-
(1947)
Ann. Eugen.
, vol.14
, pp. 10-31
-
-
Haldane, J.B.S.1
Smith, C.A.B.2
-
78
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
-
Halushka, M.K., J.B. Fan, K. Bentley et al. 1999. Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis. Natur. Genet. 22:239-247.
-
(1999)
Natur. Genet.
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.B.2
Bentley, K.3
-
79
-
-
0008382355
-
-
Seoul, South Korea: Eul-Yoo Publishing Company
-
Han, W.K. 1970. The History of Korea. Seoul, South Korea: Eul-Yoo Publishing Company.
-
(1970)
The History of Korea
-
-
Han, W.K.1
-
80
-
-
37049251476
-
Mendelian proportions in a mixed population
-
Hardy, G.H. 1908. Mendelian proportions in a mixed population. Science 28:49-50.
-
(1908)
Science
, vol.28
, pp. 49-50
-
-
Hardy, G.H.1
-
81
-
-
0024145576
-
Breakup of an isolate
-
Harvald, B. 1988. Breakup of an isolate. Arct. Med. Res. 47:41-42.
-
(1988)
Arct. Med. Res.
, vol.47
, pp. 41-42
-
-
Harvald, B.1
-
82
-
-
0024747267
-
The genetic epidemiology of Greenland
-
Harvald, B. 1989. The genetic epidemiology of Greenland. Arct. Med. Res. 48:171-174.
-
(1989)
Arct. Med. Res.
, vol.48
, pp. 171-174
-
-
Harvald, B.1
-
85
-
-
19244381008
-
Multicenter genetic study of retinitis pigmentosa in Japan. I. Genetic heterogeneity in typical retinitis pigmentosa
-
Hayakawa, M., K. Fujiki, A. Kanai et al. 1997a. Multicenter genetic study of retinitis pigmentosa in Japan. I. Genetic heterogeneity in typical retinitis pigmentosa. Jpn. J. Ophthalmol. 41:1-6.
-
(1997)
Jpn. J. Ophthalmol.
, vol.41
, pp. 1-6
-
-
Hayakawa, M.1
Fujiki, K.2
Kanai, A.3
-
86
-
-
0030994632
-
Multicenter genetic study of retinitis pigmentosa in Japan. II. Prevalence of autosomal recessive retinitis pigmentosa
-
Hayakawa, M., K. Fujiki, A. Kanai. et al. 1997b. Multicenter genetic study of retinitis pigmentosa in Japan. II. Prevalence of autosomal recessive retinitis pigmentosa. Jpn. J. Ophthalmol. 41:7-11.
-
(1997)
Jpn. J. Ophthalmol.
, vol.41
, pp. 7-11
-
-
Hayakawa, M.1
Fujiki, K.2
Kanai, A.3
-
87
-
-
0346950420
-
Hereditary retinal and choroidal degenerations
-
D.L. Rimoin, J.M. Connor, and R.E. Pyeritz, eds. Edinburgh, Scotland: Churchill-Livingstone
-
Heckenlively, J.R., and S.P. Daiger. 1996. Hereditary retinal and choroidal degenerations. In Emory and Rimoin's Principles and Practice of Medical Genetics, 3d ed., D.L. Rimoin, J.M. Connor, and R.E. Pyeritz, eds. Edinburgh, Scotland: Churchill-Livingstone, 2555-2576.
-
(1996)
Emory and Rimoin's Principles and Practice of Medical Genetics, 3d Ed
, pp. 2555-2576
-
-
Heckenlively, J.R.1
Daiger, S.P.2
-
88
-
-
0027315230
-
Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLNI) locus at 1p32: Incorporation of linkage disequilibrium in multipoint analysis
-
Hellsten, E., J. Vesi, M.C. Speer et al. 1993. Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLNI) locus at 1p32: Incorporation of linkage disequilibrium in multipoint analysis. Genomics 16:720-725.
-
(1993)
Genomics
, vol.16
, pp. 720-725
-
-
Hellsten, E.1
Vesi, J.2
Speer, M.C.3
-
89
-
-
0029895717
-
Genetics of infectious disease resistance
-
Hill, A.V. 1996. Genetics of infectious disease resistance. Curr. Opin. Genet. Dev. 6:348-353.
-
(1996)
Curr. Opin. Genet. Dev.
, vol.6
, pp. 348-353
-
-
Hill, A.V.1
-
92
-
-
0033364825
-
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation suggesting multiple susceptibility loci
-
Hovatta, I., T. Varilo, J. Suvisaari et al. 1999. A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation suggesting multiple susceptibility loci. Am. J. Hum. Genet. 65:1114-1124.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1114-1124
-
-
Hovatta, I.1
Varilo, T.2
Suvisaari, J.3
-
93
-
-
0031822951
-
Molecular genetics of human retinal dystrophies
-
Inglehearn, C.F. 1998. Molecular genetics of human retinal dystrophies. Eye 12:571-579.
-
(1998)
Eye
, vol.12
, pp. 571-579
-
-
Inglehearn, C.F.1
-
95
-
-
0033593550
-
Molecular biology of aging
-
Johnson, F.B., and D.A. Sinclair. 1999. Molecular biology of aging. Cell 96:291-302.
-
(1999)
Cell
, vol.96
, pp. 291-302
-
-
Johnson, F.B.1
Sinclair, D.A.2
-
96
-
-
0033037576
-
The renin-angiotensin system in essential hypertension: Evidence for involvement of the angiotensin receptor type-I gene in Finnish patients
-
Kainulainen, K., M. Perola, J. Terwilliger et al. 1999. The renin-angiotensin system in essential hypertension: Evidence for involvement of the angiotensin receptor type-I gene in Finnish patients. Hypertension 33:844-849.
-
(1999)
Hypertension
, vol.33
, pp. 844-849
-
-
Kainulainen, K.1
Perola, M.2
Terwilliger, J.3
-
97
-
-
0342625618
-
The researches of the Korean population genetics
-
Kang, Y.S., and C.C. Lee. 1973. The researches of the Korean population genetics. J. Natl. Acad. Sci. (Korea) 12:115-137.
-
(1973)
J. Natl. Acad. Sci. (Korea)
, vol.12
, pp. 115-137
-
-
Kang, Y.S.1
Lee, C.C.2
-
99
-
-
0022167412
-
Bibliography on Arctic medical research in the USSR
-
Kaznacheev, V.P., V.J. Kulikov, E. Soli et al. 1985. Bibliography on Arctic medical research in the USSR. Arct. Med. Res. 39:1-143.
-
(1985)
Arct. Med. Res.
, vol.39
, pp. 1-143
-
-
Kaznacheev, V.P.1
Kulikov, V.J.2
Soli, E.3
-
100
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem, B., J.M. Rommens, J.A. Buchanan et al. 1989. Identification of the cystic fibrosis gene: Genetic analysis. Science 245:1073-1080.
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
Rommens, J.M.2
Buchanan, J.A.3
-
101
-
-
0030473619
-
Genotype-phenotype correlations in cystic fibrosis
-
Kerem, E., and B. Kerem. 1996. Genotype-phenotype correlations in cystic fibrosis. Pediatr. Pulmonol. 22:387-395.
-
(1996)
Pediatr. Pulmonol.
, vol.22
, pp. 387-395
-
-
Kerem, E.1
Kerem, B.2
-
102
-
-
85196611876
-
-
Almaty, Kazakhstan: Assotsiatsiia Koreitsev Kazakhstana
-
Khan, G.V. 1994. Koreans of Kazakhstan. Almaty, Kazakhstan: Assotsiatsiia Koreitsev Kazakhstana.
-
(1994)
Koreans of Kazakhstan
-
-
Khan, G.V.1
-
103
-
-
0343059844
-
-
Studia Orientalia 61. Helsinki, Finland: Finnish Oriental Society
-
Kho, S.M. 1987. Koreans in Soviet Central Asia. Studia Orientalia 61. Helsinki, Finland: Finnish Oriental Society.
-
(1987)
Koreans in Soviet Central Asia
-
-
Kho, S.M.1
-
104
-
-
0022137287
-
Marriage pattern of the Korean population in Japan
-
Kim, Y.S. 1985. Marriage pattern of the Korean population in Japan. J. Biosoc. Sci. 17:445-450.
-
(1985)
J. Biosoc. Sci.
, vol.17
, pp. 445-450
-
-
Kim, Y.S.1
-
107
-
-
0028123781
-
Linkage analysis in nuclear families: Relationship between affected sib-pair tests and lod score analysis
-
Knapp, M., S.A. Seuchter, and M.P. Baur. 1994. Linkage analysis in nuclear families: Relationship between affected sib-pair tests and lod score analysis. Hum. Hered. 44:44-51.
-
(1994)
Hum. Hered.
, vol.44
, pp. 44-51
-
-
Knapp, M.1
Seuchter, S.A.2
Baur, M.P.3
-
108
-
-
0031723115
-
Intraethnic comparison of eating attitudes in native Koreans and Korean Americans using a Korean translation of the eating attitudes test
-
Ko, C., and H. Cohen. 1998. Intraethnic comparison of eating attitudes in native Koreans and Korean Americans using a Korean translation of the eating attitudes test. J. Nerv. Ment. Dis. 186:631-636.
-
(1998)
J. Nerv. Ment. Dis.
, vol.186
, pp. 631-636
-
-
Ko, C.1
Cohen, H.2
-
109
-
-
0019293677
-
Epidemiological studies in the Upernavik District, Greenland: Incidence of some chronic diseases 1950-1974
-
Kromann, N., and A. Green. 1980. Epidemiological studies in the Upernavik District, Greenland: Incidence of some chronic diseases 1950-1974. Acta Med. Scand. 208:401-406.
-
(1980)
Acta Med. Scand.
, vol.208
, pp. 401-406
-
-
Kromann, N.1
Green, A.2
-
110
-
-
0030879571
-
Nonparametric linkage tests are model-free
-
Kruglyak, L. 1997. Nonparametric linkage tests are model-free. Am. J. Hum. Genet. 61:254-255.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 254-255
-
-
Kruglyak, L.1
-
111
-
-
0033573934
-
Genetic isolates: Separate but equal?
-
Kruglyak, L. 1999. Genetic isolates: Separate but equal? Proc. Natl. Acad. Sci. USA 96:1170-1172.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 1170-1172
-
-
Kruglyak, L.1
-
112
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak, L., M.J. Daly, M.P. Reeve-Daly et al. 1996. Parametric and nonparametric linkage analysis: A unified multipoint approach. Am. J. Hum. Genet. 58:1347-1363.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
-
113
-
-
0030017175
-
A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2
-
Kuokkanen, S., M. Sundvall, J.D. Terwilliger et al. 1996. A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2. Natur. Genet. 13:477-480.
-
(1996)
Natur. Genet.
, vol.13
, pp. 477-480
-
-
Kuokkanen, S.1
Sundvall, M.2
Terwilliger, J.D.3
-
114
-
-
0032231562
-
Mapping genes by drift-generated disequilibrium
-
Laan, M., and S. Pääbo. 1998. Mapping genes by drift-generated disequilibrium. Am. J. Hum. Genet. 63:654-656.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 654-656
-
-
Laan, M.1
Pääbo, S.2
-
115
-
-
0024190141
-
Programs for pedigree analysis: MENDEL, FISHER, and dGENE
-
Lange, K., D. Weeks, and M. Boehnke. 1988. Programs for pedigree analysis: MENDEL, FISHER, and dGENE. Genet. Epidemiol. 5:471-472.
-
(1988)
Genet. Epidemiol.
, vol.5
, pp. 471-472
-
-
Lange, K.1
Weeks, D.2
Boehnke, M.3
-
118
-
-
0031778849
-
A quantitative review of mortality and developmental disability in extremely premature newborns
-
Lorenz, J.M., D.E. Wooliever, J.R. Jetton et al. 1998. A quantitative review of mortality and developmental disability in extremely premature newborns. Arch. Pediatr. Adol. Med. 152:425-435.
-
(1998)
Arch. Pediatr. Adol. Med.
, vol.152
, pp. 425-435
-
-
Lorenz, J.M.1
Wooliever, D.E.2
Jetton, J.R.3
-
120
-
-
0031615994
-
Molecular genetics of Huntington's disease
-
MacDonald, M.E. 1998. Molecular genetics of Huntington's disease. Results Probl. Cell Differ. 21:47-75.
-
(1998)
Results Probl. Cell Differ.
, vol.21
, pp. 47-75
-
-
MacDonald, M.E.1
-
121
-
-
0030087712
-
The nature of quantitative genetic variation revisited: Lessons from Drosophila bristles
-
Mackay, T.F.C. 1996. The nature of quantitative genetic variation revisited: Lessons from Drosophila bristles. BioEssays 18:113-121.
-
(1996)
BioEssays
, vol.18
, pp. 113-121
-
-
Mackay, T.F.C.1
-
122
-
-
0032231759
-
Chinese geneticists' views of ethical issues in genetic testing and screening: Evidence for eugenics in China
-
Mao, X. 1998. Chinese geneticists' views of ethical issues in genetic testing and screening: Evidence for eugenics in China. Am. J. Hum. Genet. 63:688-695.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 688-695
-
-
Mao, X.1
-
123
-
-
85196609630
-
The biological basis of aging: Implications for medical genetics
-
D.L. Rimoin, J.M. Connor, and R.E. Pyeritz, eds. Edinburgh, Scotland: Churchill-Livingstone
-
Martin, G.M., and G.R. Martin. 1996. The biological basis of aging: Implications for medical genetics. In Emory and Rimoin's Principles and Practice of Medical Genetics, 3d ed., D.L. Rimoin, J.M. Connor, and R.E. Pyeritz, eds. Edinburgh, Scotland: Churchill-Livingstone, 439-454.
-
(1996)
Emory and Rimoin's Principles and Practice of Medical Genetics, 3d Ed
, pp. 439-454
-
-
Martin, G.M.1
Martin, G.R.2
-
124
-
-
0031770027
-
Alzheimer's disease genetics: Home runs and strikeouts
-
Mayeux, R., and R. Ottman. 1998. Alzheimer's disease genetics: Home runs and strikeouts. Ann. Neurol. 44(5):716-719.
-
(1998)
Ann. Neurol.
, vol.44
, Issue.5
, pp. 716-719
-
-
Mayeux, R.1
Ottman, R.2
-
125
-
-
0032231748
-
Mapping genes that underlie ethnic differences in disease risk: Methods for detecting linkage in admixed populations by conditioning on parental admixture
-
McKeigue, P.M. 1998. Mapping genes that underlie ethnic differences in disease risk: Methods for detecting linkage in admixed populations by conditioning on parental admixture. Am. J. Hum. Genet. 63:241-251.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 241-251
-
-
McKeigue, P.M.1
-
127
-
-
0000596361
-
Note on the sampling error of the difference between correlated proportions or percentages
-
McNemar, Q. 1947. Note on the sampling error of the difference between correlated proportions or percentages. Psychometrika 12:153-157.
-
(1947)
Psychometrika
, vol.12
, pp. 153-157
-
-
McNemar, Q.1
-
130
-
-
0001378215
-
Sex limited inheritance in Drosophila
-
Morgan, T.H. 1910. Sex limited inheritance in Drosophila. Science 32:120-122.
-
(1910)
Science
, vol.32
, pp. 120-122
-
-
Morgan, T.H.1
-
131
-
-
0043048571
-
Sequential tests for the detection of linkage
-
Morton, N.E. 1955. Sequential tests for the detection of linkage. Am. J. Hum. Genet. 7:277-318.
-
(1955)
Am. J. Hum. Genet.
, vol.7
, pp. 277-318
-
-
Morton, N.E.1
-
132
-
-
0023734677
-
Multipoint mapping and the emperor's clothes
-
Morton, N.E. 1988. Multipoint mapping and the emperor's clothes. Ann. Hum. Genet. 52:309-318.
-
(1988)
Ann. Hum. Genet.
, vol.52
, pp. 309-318
-
-
Morton, N.E.1
-
133
-
-
85196585229
-
-
Moscow, Russia: Institut Vostokovedeniya, Rossiskaya Akademia Nauk
-
Nam, S.G. 1998. Russian Koreans: History and Culture. Moscow, Russia: Institut Vostokovedeniya, Rossiskaya Akademia Nauk.
-
(1998)
Russian Koreans: History and Culture
-
-
Nam, S.G.1
-
135
-
-
0032453237
-
Type II diabetes, essential hypertension, and obesity as "syndromes of impaired genetic homeostasis": The "thrifty genotype" hypothesis enters the 21st century
-
Neel, J.V., A.B. Weder, and S. Julius. 1998. Type II diabetes, essential hypertension, and obesity as "syndromes of impaired genetic homeostasis": The "thrifty genotype" hypothesis enters the 21st century. Perspect. Biol. Med. 42:44-74.
-
(1998)
Perspect. Biol. Med.
, vol.42
, pp. 44-74
-
-
Neel, J.V.1
Weder, A.B.2
Julius, S.3
-
136
-
-
17344364213
-
DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene
-
Nickerson, D.A., S.L. Taylor, K.M. Weiss et al. 1998. DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene. Natur. Genet. 19:233-240.
-
(1998)
Natur. Genet.
, vol.19
, pp. 233-240
-
-
Nickerson, D.A.1
Taylor, S.L.2
Weiss, K.M.3
-
137
-
-
0022832977
-
Cancer incidence in Greenland
-
Nielsen, N.H. 1986. Cancer incidence in Greenland. Arct. Med. Res. 43:1-168.
-
(1986)
Arct. Med. Res.
, vol.43
, pp. 1-168
-
-
Nielsen, N.H.1
-
138
-
-
0028949919
-
Random search for shared chromosomal regions in four affected individuals: The assignment of a new hereditary ataxia locus
-
Nikali, K., A. Suomalainen, J. Terwilliger et al. 1995. Random search for shared chromosomal regions in four affected individuals: The assignment of a new hereditary ataxia locus. Am. J. Hum. Genet. 56:1088-1095.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1088-1095
-
-
Nikali, K.1
Suomalainen, A.2
Terwilliger, J.3
-
141
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
O'Connell, J.R., and D.E. Weeks. 1995. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Natur. Genet. 11:34-35.
-
(1995)
Natur. Genet.
, vol.11
, pp. 34-35
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
142
-
-
0016302483
-
Estimation of the recombination fraction in human pedigrees: Efficient computation of the likelihood for human linkage studies
-
Ott, J. 1974. Estimation of the recombination fraction in human pedigrees: Efficient computation of the likelihood for human linkage studies. Am. J. Hum. Genet. 26:588-597.
-
(1974)
Am. J. Hum. Genet.
, vol.26
, pp. 588-597
-
-
Ott, J.1
-
144
-
-
0025190712
-
Localizing multiple X-chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests
-
Ott, J., S. Bhattacharya, J.D. Chen et al. 1990. Localizing multiple X-chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests. Proc. Natl. Acad. Sci. USA 87:701-704.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 701-704
-
-
Ott, J.1
Bhattacharya, S.2
Chen, J.D.3
-
145
-
-
0031918837
-
Linkage of familial combined hyperlipidemia to chromosome 1q21-q23
-
Pajukanta, P., I. Nuotio, J.D. Terwilliger et al. 1998. Linkage of familial combined hyperlipidemia to chromosome 1q21-q23. Natur. Genet. 18:369-373.
-
(1998)
Natur. Genet.
, vol.18
, pp. 369-373
-
-
Pajukanta, P.1
Nuotio, I.2
Terwilliger, J.D.3
-
146
-
-
0033362160
-
Genome-wide scan for familial combined hyperlipidemia genes in Finnish families suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
-
Pajukanta, P., J.D. Terwilliger, M. Perola et al. 1999. Genome-wide scan for familial combined hyperlipidemia genes in Finnish families suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels. Am. J. Hum. Genet. 64:1453-1463.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1453-1463
-
-
Pajukanta, P.1
Terwilliger, J.D.2
Perola, M.3
-
147
-
-
85196591541
-
-
Irkutsk, Russia: Irkutsk State Pedagogical Institute
-
Pak, B.D. 1994. Koreans in the Russian Empire. Irkutsk, Russia: Irkutsk State Pedagogical Institute.
-
(1994)
Koreans in the Russian Empire
-
-
Pak, B.D.1
-
152
-
-
85196585498
-
On the ancestral genetic correlations of a Mendelian population mating at random
-
Pearson, K. 1909. On the ancestral genetic correlations of a Mendelian population mating at random. Proc. R. Soc. 81:219-225.
-
(1909)
Proc. R. Soc.
, vol.81
, pp. 219-225
-
-
Pearson, K.1
-
153
-
-
0032403494
-
Fine scale mapping of a novel dementia gene, PLO-SL, by linkage disequilibrium
-
Pekkarinen, P., M. Kestila, J. Paloneva et al. 1998. Fine scale mapping of a novel dementia gene, PLO-SL, by linkage disequilibrium. Genomics 54:307-315.
-
(1998)
Genomics
, vol.54
, pp. 307-315
-
-
Pekkarinen, P.1
Kestila, M.2
Paloneva, J.3
-
154
-
-
0032544280
-
A closer look at SNPs suggests difficulties
-
Pennisi, E. 1998. A closer look at SNPs suggests difficulties. Science 281:1787-1789.
-
(1998)
Science
, vol.281
, pp. 1787-1789
-
-
Pennisi, E.1
-
155
-
-
0000877874
-
The detection of autosomal linkage in data which consists of pairs of brothers and sisters
-
Penrose, L.S. 1935. The detection of autosomal linkage in data which consists of pairs of brothers and sisters. Ann. Eugen. 6:133-138.
-
(1935)
Ann. Eugen.
, vol.6
, pp. 133-138
-
-
Penrose, L.S.1
-
157
-
-
0021716964
-
Sensitivity of maximal aerobic power to training is genotype dependent
-
Prud'homme, D., C. Bouchard, C. Leblanc et al. 1984. Sensitivity of maximal aerobic power to training is genotype dependent. Med. Sci. Sports Exerc. 16:489-493.
-
(1984)
Med. Sci. Sports Exerc.
, vol.16
, pp. 489-493
-
-
Prud'homme, D.1
Bouchard, C.2
Leblanc, C.3
-
158
-
-
0028805511
-
New polymorphic microsatellite markers place the hemochromatosis gene telomeric to D6S105
-
Raha-Choudhury, R., D.J. Bowen, C. Stone et al. 1995. New polymorphic microsatellite markers place the hemochromatosis gene telomeric to D6S105. Hum. Molec. Genet. 4:1869-1874.
-
(1995)
Hum. Molec. Genet.
, vol.4
, pp. 1869-1874
-
-
Raha-Choudhury, R.1
Bowen, D.J.2
Stone, C.3
-
159
-
-
25944453426
-
A computer program for the processing of linkage data from large pedigrees
-
Renwick, J.H., and J. Schulze. 1961. A computer program for the processing of linkage data from large pedigrees. Excerpta Med. Int. Congr. Ser. 32:E145.
-
(1961)
Excerpta Med. Int. Congr. Ser.
, vol.32
-
-
Renwick, J.H.1
Schulze, J.2
-
160
-
-
85196612579
-
-
Seoul, South Korea: Myong Ji University Press
-
Rhee, T.C. 1998. A History of Eurasia Korean. Seoul, South Korea: Myong Ji University Press.
-
(1998)
A History of Eurasia Korean
-
-
Rhee, T.C.1
-
161
-
-
0031581778
-
The role of meta-analysis in linkage studies of complex traits
-
Rice, J.P. 1997. The role of meta-analysis in linkage studies of complex traits. Am. J. Med. Genet. 74:112-114.
-
(1997)
Am. J. Med. Genet.
, vol.74
, pp. 112-114
-
-
Rice, J.P.1
-
162
-
-
0025008677
-
Linkage strategies for genetically complex traits. II. The power of affected relative pairs
-
Risch, N. 1990. Linkage strategies for genetically complex traits. II. The power of affected relative pairs. Am. J. Hum. Genet. 46:229-241.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
163
-
-
0026529005
-
Model misspecification and multipoint linkage analysis
-
Risch, N., and L. Giuffra. 1992. Model misspecification and multipoint linkage analysis. Hum. Hered. 42:77-92.
-
(1992)
Hum. Hered.
, vol.42
, pp. 77-92
-
-
Risch, N.1
Giuffra, L.2
-
164
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N., and K. Merikangas. 1996. The future of genetic studies of complex human diseases. Science 273:1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
167
-
-
0000575788
-
Genetics of HLA disease associations: The use of the haplotype relative risk (HRR) and the haplo-delta (Dh) estimates in juvenile diabetes from three racial groups
-
Rubinstein, P., M. Walker, C. Carpenter et al. 1981. Genetics of HLA disease associations: The use of the haplotype relative risk (HRR) and the haplo-delta (Dh) estimates in juvenile diabetes from three racial groups. Hum. Immunol. 3:384.
-
(1981)
Hum. Immunol.
, vol.3
, pp. 384
-
-
Rubinstein, P.1
Walker, M.2
Carpenter, C.3
-
169
-
-
0026608422
-
Origin of the Koreans: A population genetic study
-
Saha, N., and J.S.H. Tay. 1992. Origin of the Koreans: A population genetic study. Am. J. Phys. Anthropol. 88:27-36.
-
(1992)
Am. J. Phys. Anthropol.
, vol.88
, pp. 27-36
-
-
Saha, N.1
Tay, J.S.H.2
-
170
-
-
0029112804
-
Clinical expression correlates with the location of rhodopsin mutation in dominant retinitis pigmentosa
-
Sandberg, M.A., C. Weigel-DiFranco, T.P. Dryja et al. 1995. Clinical expression correlates with the location of rhodopsin mutation in dominant retinitis pigmentosa. Invest. Ophthalmol. Vis. Sci. 36:1934-1942.
-
(1995)
Invest. Ophthalmol. Vis. Sci.
, vol.36
, pp. 1934-1942
-
-
Sandberg, M.A.1
Weigel-DiFranco, C.2
Dryja, T.P.3
-
171
-
-
85196611818
-
Yoojunjanun dangshinui jilbyungul algo issda [genes are knowing your diseases]
-
in Korean
-
Sang, J.J. 1999. Yoojunjanun dangshinui jilbyungul algo issda [Genes are knowing your diseases]. Newsmaker 243:48-51 (in Korean).
-
(1999)
Newsmaker
, vol.243
, pp. 48-51
-
-
Sang, J.J.1
-
172
-
-
0003792728
-
-
Cambridge, England: Cambridge University Press
-
Sarkar, S. 1998. Genetics and Reductionism. Cambridge, England: Cambridge University Press.
-
(1998)
Genetics and Reductionism
-
-
Sarkar, S.1
-
173
-
-
16044373177
-
Two-stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7, and 12
-
Satsangi, J., M. Parkes, E. Louis et al. 1996. Two-stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7, and 12. Natur. Genet. 14:199-202.
-
(1996)
Natur. Genet.
, vol.14
, pp. 199-202
-
-
Satsangi, J.1
Parkes, M.2
Louis, E.3
-
175
-
-
0032126964
-
The future of genetic epidemiology
-
Schork, N.J., L.R. Cardon, and X. Xu. 1998. The future of genetic epidemiology. Tr. Genet. 14:266-272.
-
(1998)
Tr. Genet.
, vol.14
, pp. 266-272
-
-
Schork, N.J.1
Cardon, L.R.2
Xu, X.3
-
181
-
-
0342625598
-
The estimation of linkage on an electronic computer
-
Simpson, H.R. 1958. The estimation of linkage on an electronic computer. Am. J. Hum. Genet. 22:356-361.
-
(1958)
Am. J. Hum. Genet.
, vol.22
, pp. 356-361
-
-
Simpson, H.R.1
-
182
-
-
0000655012
-
The detection of linkage in human genetics
-
Smith, C.A.B. 1953. The detection of linkage in human genetics. J. R. Stat. Soc., ser. B, 15:153-192.
-
(1953)
J. R. Stat. Soc., Ser. B
, vol.15
, pp. 153-192
-
-
Smith, C.A.B.1
-
183
-
-
13344290899
-
Counting methods in genetical statistics
-
Smith, C.A.B. 1957. Counting methods in genetical statistics. Ann. Hum. Genet. 21:254-276.
-
(1957)
Ann. Hum. Genet.
, vol.21
, pp. 254-276
-
-
Smith, C.A.B.1
-
184
-
-
0002422396
-
Test of significance for Mendelian ratios when classification is uncertain
-
Smith, H.F. 1937. Test of significance for Mendelian ratios when classification is uncertain. Ann. Eugen. 8:94-95.
-
(1937)
Ann. Eugen.
, vol.8
, pp. 94-95
-
-
Smith, H.F.1
-
185
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman, R.S., R.E. McGinnis, and W.J. Ewens. 1993. Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am. J. Hum. Genet. 52:506-516.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
186
-
-
0006527930
-
Cancer of the breast and female reproductive tract
-
D.L. Rimoin, J.M. Connor, and R.E. Pyeritz, eds. Edinburgh, Scotland: Churchill-Livingstone
-
Steel, C.M. 1996. Cancer of the breast and female reproductive tract. In Emory and Rimoin's Principles and Practice of Medical Genetics, 3d ed., D.L. Rimoin, J.M. Connor, and R.E. Pyeritz, eds. Edinburgh, Scotland: Churchill-Livingstone, 1501-1524.
-
(1996)
Emory and Rimoin's Principles and Practice of Medical Genetics, 3d Ed
, pp. 1501-1524
-
-
Steel, C.M.1
-
188
-
-
0014944130
-
Temperature-sensitive mutations in Drosophila melanogaster
-
Suzuki, D. 1970. Temperature-sensitive mutations in Drosophila melanogaster. Science 170:695-706.
-
(1970)
Science
, vol.170
, pp. 695-706
-
-
Suzuki, D.1
-
190
-
-
0031803013
-
The Australian mortality decline: All-cause mortality 1788-1990
-
Taylor, R., M. Lewis, and J. Powles. 1998a. The Australian mortality decline: All-cause mortality 1788-1990. Aust. N.Z. J. Public Health 22:27-36.
-
(1998)
Aust. N.Z. J. Public Health
, vol.22
, pp. 27-36
-
-
Taylor, R.1
Lewis, M.2
Powles, J.3
-
191
-
-
0031803297
-
The Australian mortality decline: Cause-specific mortality 1907-1990
-
Taylor, R., M. Lewis, and J. Powles. 1998b. The Australian mortality decline: Cause-specific mortality 1907-1990. Aust. N.Z. J. Public Health 22:37-44.
-
(1998)
Aust. N.Z. J. Public Health
, vol.22
, pp. 37-44
-
-
Taylor, R.1
Lewis, M.2
Powles, J.3
-
192
-
-
0003195092
-
The available possibilities to analyze data of polygenic disease statistically
-
Helsinki, Finland
-
Terwilliger, J.D. 1994. The available possibilities to analyze data of polygenic disease statistically. In Fourth Workshop of the Nordic Genome Initiative. Helsinki, Finland.
-
(1994)
Fourth Workshop of the Nordic Genome Initiative
-
-
Terwilliger, J.D.1
-
193
-
-
0028968329
-
A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci
-
Terwilliger, J.D. 1995. A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci. Am. J. Hum. Genet. 56:777-787.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 777-787
-
-
Terwilliger, J.D.1
-
194
-
-
0001355755
-
Linkage analysis: Model based
-
New York: Wiley
-
Terwilliger, J.D. 1998. Linkage analysis: Model based. In Encyclopedia of Biostatistics. New York: Wiley, 2279-2291.
-
(1998)
Encyclopedia of Biostatistics
, pp. 2279-2291
-
-
Terwilliger, J.D.1
-
195
-
-
0343931588
-
On the resolution and feasibility of genome scanning approaches to unraveling the genetic components of multifactorial phenotypes
-
D.C. Rao, ed. San Diego, CA: Academic Press (in press)
-
Terwilliger, J.D. 2000. On the resolution and feasibility of genome scanning approaches to unraveling the genetic components of multifactorial phenotypes. In Genetic Dissection of Complex Traits, D.C. Rao, ed. San Diego, CA: Academic Press (in press).
-
(2000)
Genetic Dissection of Complex Traits
-
-
Terwilliger, J.D.1
-
196
-
-
0026494911
-
A haplotype-based haplotype relative risk approach to detecting allelic associations
-
Terwilliger, J.D., and J. Ott. 1992. A haplotype-based haplotype relative risk approach to detecting allelic associations. Hum. Hered. 42:337-346.
-
(1992)
Hum. Hered.
, vol.42
, pp. 337-346
-
-
Terwilliger, J.D.1
Ott, J.2
-
198
-
-
0032403973
-
Linkage disequilibrium mapping of complex disease: Fantasy or reality?
-
Terwilliger, J.D., and K.M. Weiss. 1998. Linkage disequilibrium mapping of complex disease: Fantasy or reality? Curr. Opin. Biotechnol. 9:578-594.
-
(1998)
Curr. Opin. Biotechnol.
, vol.9
, pp. 578-594
-
-
Terwilliger, J.D.1
Weiss, K.M.2
-
199
-
-
0030851777
-
True and false positive peaks in genome-wide scans: Applications of length-biased sampling to linkage mapping
-
Terwilliger, J.D., W.D. Shannon, G.M. Lathrop et al. 1997. True and false positive peaks in genome-wide scans: Applications of length-biased sampling to linkage mapping. Am. J. Hum. Genet. 61:430-438.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 430-438
-
-
Terwilliger, J.D.1
Shannon, W.D.2
Lathrop, G.M.3
-
200
-
-
0031946381
-
Mapping genes through the use of linkage disequilibrium generated by genetic drift: Drift mapping in small populations with no demographic expansion
-
Terwilliger, J.D., S. Zöllner, M. Laan et al. 1998. Mapping genes through the use of linkage disequilibrium generated by genetic drift: Drift mapping in small populations with no demographic expansion. Hum. Hered. 48:138-154.
-
(1998)
Hum. Hered.
, vol.48
, pp. 138-154
-
-
Terwilliger, J.D.1
Zöllner, S.2
Laan, M.3
-
202
-
-
0030490120
-
Likelihood and linkage: From Fisher to the future
-
Thompson, E.A. 1996. Likelihood and linkage: From Fisher to the future. Ann. Stat. 24:449-465.
-
(1996)
Ann. Stat.
, vol.24
, pp. 449-465
-
-
Thompson, E.A.1
-
203
-
-
0025872948
-
Transferrin types in different ethnic groups of the USSR and Mongolia
-
Titenko, N.V., V.A. Spitsyn, and T.I. Alekseeva. 1991. Transferrin types in different ethnic groups of the USSR and Mongolia. Hum. Hered. 41:201-205.
-
(1991)
Hum. Hered.
, vol.41
, pp. 201-205
-
-
Titenko, N.V.1
Spitsyn, V.A.2
Alekseeva, T.I.3
-
204
-
-
8244228677
-
Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two-stage genome-wide search in psoriasis
-
Trembath, R.C., R.L. Clough, J.L. Rosbotham et al. 1997. Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two-stage genome-wide search in psoriasis. Hum. Molec. Genet. 6:813-820.
-
(1997)
Hum. Molec. Genet.
, vol.6
, pp. 813-820
-
-
Trembath, R.C.1
Clough, R.L.2
Rosbotham, J.L.3
-
205
-
-
0030946546
-
Nonsyndromic hearing impairment: Unparalleled heterogeneity
-
van Camp, G., P.J. Willems, and R.J. Smith. 1997. Nonsyndromic hearing impairment: Unparalleled heterogeneity. Am. J. Hum. Genet. 60:758-764.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 758-764
-
-
Van Camp, G.1
Willems, P.J.2
Smith, R.J.3
-
207
-
-
0028907342
-
A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q
-
Vaxillaire, M., V. Boccio, A. Philippi et al. 1995. A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q. Natur. Genet. 9:418-423.
-
(1995)
Natur. Genet.
, vol.9
, pp. 418-423
-
-
Vaxillaire, M.1
Boccio, V.2
Philippi, A.3
-
209
-
-
0030940669
-
Genetics and behavioral medicine: Risk factors for cardiovascular disease
-
Vogler, G.P., G.E. McClearn, H. Snieder et al. 1997. Genetics and behavioral medicine: Risk factors for cardiovascular disease. Behav. Med. 22:141-149.
-
(1997)
Behav. Med.
, vol.22
, pp. 141-149
-
-
Vogler, G.P.1
McClearn, G.E.2
Snieder, H.3
-
211
-
-
0028141921
-
Linkage disequilibrium patterns vary with chromosomal location: A case study from the Von Willebrand factor region
-
Watkins, W.S., R. Zenger, E. O'Brien et al. 1994. Linkage disequilibrium patterns vary with chromosomal location: A case study from the von Willebrand factor region. Am. J. Hum. Genet. 55:348-355.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, pp. 348-355
-
-
Watkins, W.S.1
Zenger, R.2
O'Brien, E.3
-
214
-
-
0030078281
-
Is there a paradigm shift in human genetics? Lessons from the study of human diseases
-
Weiss, K.M. 1996. Is there a paradigm shift in human genetics? Lessons from the study of human diseases. Molec. Phylogenet. Evol. 5:259-265.
-
(1996)
Molec. Phylogenet. Evol.
, vol.5
, pp. 259-265
-
-
Weiss, K.M.1
-
215
-
-
0031687751
-
Perspective: In search of human variation
-
Weiss, K.M. 1998. Perspective: In search of human variation. Genome Res. 8:691-697.
-
(1998)
Genome Res.
, vol.8
, pp. 691-697
-
-
Weiss, K.M.1
-
216
-
-
85196594593
-
Review of mendelian inheritance in man
-
in press
-
Weiss, K.M. 2000. Review of Mendelian Inheritance in Man. Genet. Epidemiol. (in press).
-
(2000)
Genet. Epidemiol.
-
-
Weiss, K.M.1
-
218
-
-
0025048029
-
On the asymptotic behavior of the estimate of the recombination fraction under the null hypothesis of no linkage when the model is misspecified
-
Williamson, J.A., and C.I. Amos. 1990. On the asymptotic behavior of the estimate of the recombination fraction under the null hypothesis of no linkage when the model is misspecified. Genet. Epidemiol. 7:309-318.
-
(1990)
Genet. Epidemiol.
, vol.7
, pp. 309-318
-
-
Williamson, J.A.1
Amos, C.I.2
-
219
-
-
0030628753
-
Genetics, response to exercise, and risk factors: The HERITAGE family study
-
Wilmore, J.H., A.S. Leon, D.C. Rao et al. 1997. Genetics, response to exercise, and risk factors: The HERITAGE family study. World Rev. Nutr. Diet. 81:72-83.
-
(1997)
World Rev. Nutr. Diet.
, vol.81
, pp. 72-83
-
-
Wilmore, J.H.1
Leon, A.S.2
Rao, D.C.3
-
220
-
-
0001752079
-
The relative importance of heredity and environment in determining the piebald pattern of guinea pigs
-
Wright, S. 1920. The relative importance of heredity and environment in determining the piebald pattern of guinea pigs. Proc. Natl. Acad. Sci. USA 6:320-332.
-
(1920)
Proc. Natl. Acad. Sci. USA
, vol.6
, pp. 320-332
-
-
Wright, S.1
-
221
-
-
0000929750
-
Systems of mating
-
Wright, S. 1921. Systems of mating. Genetics 6:111-1278.
-
(1921)
Genetics
, vol.6
, pp. 111-1278
-
-
Wright, S.1
-
222
-
-
0003470431
-
Evolution and the Genetics of Populations, v. 1
-
Chicago, IL: University of Chicago Press
-
Wright, S. 1968. Evolution and the Genetics of Populations, v. 1, Genetics and Biometric Foundations. Chicago, IL: University of Chicago Press.
-
(1968)
Genetics and Biometric Foundations
, vol.1
-
-
Wright, S.1
-
223
-
-
2642631618
-
Evolution and the Genetics of Populations, v. 2
-
Chicago, IL: University of Chicago Press
-
Wright, S. 1969. Evolution and the Genetics of Populations, v. 2, The Theory of Gene Frequencies. Chicago, IL: University of Chicago Press.
-
(1969)
The Theory of Gene Frequencies
, vol.2
-
-
Wright, S.1
-
224
-
-
0003470431
-
Evolution and the Genetics of Populations, v. 3
-
Chicago, IL: University of Chicago Press.
-
Wright, S. 1977. Evolution and the Genetics of Populations, v. 3, Experimental Results and Evolutionary Deductions. Chicago, IL: University of Chicago Press.
-
(1977)
Experimental Results and Evolutionary Deductions
, vol.3
-
-
Wright, S.1
-
225
-
-
0003470431
-
Evolution and the Genetics of Populations, v. 4
-
Chicago, IL: University of Chicago Press
-
Wright, S. 1978. Evolution and the Genetics of Populations, v. 4, Variability Within and Among Natural Populations. Chicago, IL: University of Chicago Press.
-
(1978)
Variability Within and Among Natural Populations
, vol.4
-
-
Wright, S.1
-
226
-
-
0030696738
-
Evolving methods in genetic epidemiology. III. Gene-environment interaction in epidemiologic research
-
Yang, Q., and M.J. Khoury. 1997. Evolving methods in genetic epidemiology. III. Gene-environment interaction in epidemiologic research. Epidemiol. Rev. 19:33-43.
-
(1997)
Epidemiol. Rev.
, vol.19
, pp. 33-43
-
-
Yang, Q.1
Khoury, M.J.2
-
228
-
-
84942102034
-
Mendel's laws and their probable relation to intra-racial heredity
-
Yule, G.U. 1902. Mendel's laws and their probable relation to intra-racial heredity. New Phytol. 1:193-238.
-
(1902)
New Phytol.
, vol.1
, pp. 193-238
-
-
Yule, G.U.1
|