-
1
-
-
0003979578
-
-
eds Motulsky, A. G., Harper, P. S., Scriver, C. & Bobrow, M. Oxford Univ. Press, Oxford
-
King, R. A., Rotter, J. I. & Motulsky, A. G. The Genetic Basis of Common Diseases Vol. 20 (eds Motulsky, A. G., Harper, P. S., Scriver, C. & Bobrow, M.) (Oxford Univ. Press, Oxford, 1992).
-
(1992)
The Genetic Basis of Common Diseases
, vol.20
-
-
King, R.A.1
Rotter, J.I.2
Motulsky, A.G.3
-
2
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch, N. J. Searching for genetic determinants in the new millennium. Nature 405, 847-856 (2000).
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
3
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
-
Botstein, D. & Risch, N. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nature Genet. 33 (Suppl.), 228-237 (2003).
-
(2003)
Nature Genet.
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
4
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N. & Merikangas, K. The future of genetic studies of complex human diseases. Science 273, 1516-1517 (1996).
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
5
-
-
0025152043
-
Worldwide differences in the incidence of type 1 diabetes are associated with amino acid variation at position 57 of the HLA-DQ β chain
-
Dorman, J. S., LaPorte, R. E., Stone, R. A. & Trucco, M. Worldwide differences in the incidence of type 1 diabetes are associated with amino acid variation at position 57 of the HLA-DQ β chain. Proc. Natl Acad. Sci. USA 87, 7370-7374 (1990).
-
(1990)
Proc. Natl Acad. Sci. USA
, vol.87
, pp. 7370-7374
-
-
Dorman, J.S.1
LaPorte, R.E.2
Stone, R.A.3
Trucco, M.4
-
6
-
-
0021343570
-
A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus
-
Bell, G. I., Horita, S. & Karam, J. H. A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus. Diabetes 33, 176-183 (1984).
-
(1984)
Diabetes
, vol.33
, pp. 176-183
-
-
Bell, G.I.1
Horita, S.2
Karam, J.H.3
-
7
-
-
8944259914
-
The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes
-
Nisticò, L. et al. The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Hum. Mol. Genet. 5, 1075-1080 (1996).
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1075-1080
-
-
Nisticò, L.1
-
9
-
-
1842290346
-
506 Q mutation is a common risk factor for venous thrombosis
-
506 Q mutation is a common risk factor for venous thrombosis. Thromb. Haemost. 78, 483-488 (1997).
-
(1997)
Thromb. Haemost.
, vol.78
, pp. 483-488
-
-
Dahlbäck, B.1
-
10
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot, J. P et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 411, 599-603 (2001).
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
-
11
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura, Y. et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 411, 603-606 (2001).
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
-
12
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
Rioux, J. D. et al. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nature Genet. 29, 223-228 (2001).
-
(2001)
Nature Genet.
, vol.29
, pp. 223-228
-
-
Rioux, J.D.1
-
13
-
-
0035812707
-
An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing
-
Pennacchio, L. A. et al. An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing. Science 294, 169-173 (2001).
-
(2001)
Science
, vol.294
, pp. 169-173
-
-
Pennacchio, L.A.1
-
14
-
-
0031595923
-
A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity
-
Deeb, S. S. et al. A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity. Nature Genet. 20, 284-287 (1998).
-
(1998)
Nature Genet.
, vol.20
, pp. 284-287
-
-
Deeb, S.S.1
-
15
-
-
0033624575
-
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
-
Altshuler, D. et al. The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nature Genet. 26, 76-80 (2000).
-
(2000)
Nature Genet.
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
-
16
-
-
0013375948
-
Neuregulin 1 and susceptibility to schizophrenia
-
Stefansson, H. et al. Neuregulin 1 and susceptibility to schizophrenia. Am. J. Hum. Genet. 71, 877-892 (2002).
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 877-892
-
-
Stefansson, H.1
-
17
-
-
0037173639
-
Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness
-
Van Eerdewegh, P et al. Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness. Nature 418, 426-430 (2002).
-
(2002)
Nature
, vol.418
, pp. 426-430
-
-
Van Eerdewegh, P.1
-
18
-
-
0141819194
-
The gene encoding phosphodiesterase 4D confers risk of ischemic stroke
-
Gretarsdottir, S. et al. The gene encoding phosphodiesterase 4D confers risk of ischemic stroke. Nature Genet. 35, 131-138 (2003).
-
(2003)
Nature Genet.
, vol.35
, pp. 131-138
-
-
Gretarsdottir, S.1
-
19
-
-
18744407845
-
Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction
-
Ozaki, K. et al. Functional SNPs in the lymphotoxin-α gene that are associated with susceptibility to myocardial infarction. Nature. Genet. 32, 650-654 (2002).
-
(2002)
Nature. Genet.
, vol.32
, pp. 650-654
-
-
Ozaki, K.1
-
20
-
-
0030688004
-
Variations on a theme: Cataloging human DNA sequence variation
-
Gollins, E S., Guyer, M. S. & Ghakravarti, A. Variations on a theme: cataloging human DNA sequence variation. Science 278, 1580-1581 (1997).
-
(1997)
Science
, vol.278
, pp. 1580-1581
-
-
Gollins, E.S.1
Guyer, M.S.2
Ghakravarti, A.3
-
21
-
-
0035094764
-
Variation is the spice of life
-
Kruglyak, L. & Nickerson, D. A. Variation is the spice of life. Nature Genet. 27, 234-236 (2001).
-
(2001)
Nature Genet.
, vol.27
, pp. 234-236
-
-
Kruglyak, L.1
Nickerson, D.A.2
-
22
-
-
0024423668
-
Identification of the cystic fibrosis gene: Genetic analysis
-
Kerem, B. et al. Identification of the cystic fibrosis gene: genetic analysis. Science 245, 1073-1080 (1989).
-
(1989)
Science
, vol.245
, pp. 1073-1080
-
-
Kerem, B.1
-
23
-
-
0026949420
-
Linkage disequilibrium mapping in isolated founder populations: Diastrophic dysplasia in Finland
-
Hästbacka, J. et al. Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland. Nature Genet. 2, 204-211 (1992).
-
(1992)
Nature Genet.
, vol.2
, pp. 204-211
-
-
Hästbacka, J.1
-
24
-
-
0026053092
-
Low nucleotide diversity in man
-
Li, W. H. & Sadler, L. A. Low nucleotide diversity in man. Genetics 129, 513-523 (1991).
-
(1991)
Genetics
, vol.129
, pp. 513-523
-
-
Li, W.H.1
Sadler, L.A.2
-
25
-
-
0032524383
-
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
-
Wang, D. G. et al. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science 280, 1077-1082 (1998).
-
(1998)
Science
, vol.280
, pp. 1077-1082
-
-
Wang, D.G.1
-
26
-
-
0032991552
-
Gharacterization of single-nucleotide polymorphisms in coding regions of human genes
-
Gargill, M. et al. Gharacterization of single-nucleotide polymorphisms in coding regions of human genes. Nature Genet. 22, 231-238 (1999).
-
(1999)
Nature Genet.
, vol.22
, pp. 231-238
-
-
Gargill, M.1
-
27
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for bloodpressure homeostasis
-
Halushka, M. K. et al. Patterns of single-nucleotide polymorphisms in candidate genes for bloodpressure homeostasis. Nature Genet. 22, 239-247 (1999).
-
(1999)
Nature Genet.
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
-
28
-
-
0037381234
-
Quality and completeness of SNP databases
-
Reich, D. E., Gabriel, S. B. & Altshuler, D. Quality and completeness of SNP databases. Nature Genet. 33, 457-458 (2003).
-
(2003)
Nature Genet.
, vol.33
, pp. 457-458
-
-
Reich, D.E.1
Gabriel, S.B.2
Altshuler, D.3
-
29
-
-
0037461782
-
The mosaic that is our genome
-
Pääbo, S. The mosaic that is our genome. Nature 421, 409-412 (2003).
-
(2003)
Nature
, vol.421
, pp. 409-412
-
-
Pääbo, S.1
-
30
-
-
0034795550
-
Intensely punctate meiotic recombination in the class 11 region of the major histocompatibility complex
-
Jeffreys, A. J., Kauppi, L. & Neumann, R. Intensely punctate meiotic recombination in the class 11 region of the major histocompatibility complex. Nature. Genet. 29, 217-222 (2001).
-
(2001)
Nature. Genet.
, vol.29
, pp. 217-222
-
-
Jeffreys, A.J.1
Kauppi, L.2
Neumann, R.3
-
31
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel, S. B. et al. The structure of haplotype blocks in the human genome. Science 296, 2225-2229 (2002).
-
(2002)
Science
, vol.296
, pp. 2225-2229
-
-
Gabriel, S.B.1
-
32
-
-
0035837267
-
Linkage disequilibrium in the human genome
-
Reich, D. E. et al. Linkage disequilibrium in the human genome. Nature. 411, 199-204 (2001).
-
(2001)
Nature.
, vol.411
, pp. 199-204
-
-
Reich, D.E.1
-
33
-
-
0035163547
-
Extent and distribution of linkage disequilibrium in three genomic regions
-
Abecasis, G. R. et al. Extent and distribution of linkage disequilibrium in three genomic regions. Am. J. Hum. Genet. 68, 191-197 (2001).
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 191-197
-
-
Abecasis, G.R.1
-
34
-
-
18444396271
-
A first-generation linkage disequilibrium map of human chromosome 22
-
Dawson, E. et al. A first-generation linkage disequilibrium map of human chromosome 22. Nature. 418, 544-548 (2002).
-
(2002)
Nature.
, vol.418
, pp. 544-548
-
-
Dawson, E.1
-
35
-
-
0034791035
-
High-resolution haplotype structure in the human genome
-
Daly, M. J., Rioux, J. D., Schaffner, S. E, Hudson, T J. & Lander, E. S. High-resolution haplotype structure in the human genome. Nature. Genet. 29, 229-232 (2001).
-
(2001)
Nature. Genet.
, vol.29
, pp. 229-232
-
-
Daly, M.J.1
Rioux, J.D.2
Schaffner, S.E.3
Hudson, T.J.4
Lander, E.S.5
-
36
-
-
0035941029
-
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
-
Patil, N. et al. Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science 294, 1719-1723 (2001).
-
(2001)
Science
, vol.294
, pp. 1719-1723
-
-
Patil, N.1
-
37
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
Johnson, G. C. L. et al. Haplotype tagging for the identification of common disease genes. Nature Genet. 29, 233-237 (2001).
-
(2001)
Nature Genet.
, vol.29
, pp. 233-237
-
-
Johnson, G.C.L.1
-
38
-
-
0344091561
-
Additional SNPs and linkage-disequilibrium analyses are necessary for wholegenome association studies in humans
-
Garlson, G. S. et al. Additional SNPs and linkage-disequilibrium analyses are necessary for wholegenome association studies in humans. Nature. Genet. 33, 518-521 (2003).
-
(2003)
Nature. Genet.
, vol.33
, pp. 518-521
-
-
Garlson, G.S.1
-
39
-
-
0242380286
-
Genome scans and candidate gene approaches in the study of common diseases and variable drug responses
-
Goldstein, D. B., Ahmadi, K. R., Weale, M. E. & Wood, N. W. Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. Trends Genet. 19, 615-622 (2003).
-
(2003)
Trends Genet.
, vol.19
, pp. 615-622
-
-
Goldstein, D.B.1
Ahmadi, K.R.2
Weale, M.E.3
Wood, N.W.4
-
40
-
-
0033930144
-
Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28
-
Taillon-Miller, P et al. Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28. Nature Genet. 25, 324-328 (2000).
-
(2000)
Nature Genet.
, vol.25
, pp. 324-328
-
-
Taillon-Miller, P.1
-
41
-
-
84984932946
-
Population genetics - Making sense out of sequence
-
Chakravarti, A. Population genetics - making sense out of sequence. Nature Genet. 21, 56-60 (1999).
-
(1999)
Nature Genet.
, vol.21
, pp. 56-60
-
-
Chakravarti, A.1
-
42
-
-
0021679717
-
Nonuniform recombination within the human β-globin gene cluster
-
Chakravarti, A. et al. Nonuniform recombination within the human β-globin gene cluster. Am. J. Hum. Genet. 36, 1239-1258 (1984).
-
(1984)
Am. J. Hum. Genet.
, vol.36
, pp. 1239-1258
-
-
Chakravarti, A.1
-
43
-
-
0029667388
-
Global patterns of linkage disequilibrium at the CD4 locus and modern human origins
-
Tishkoff, S. A. et al. Global patterns of linkage disequilibrium at the CD4 locus and modern human origins. Science 271, 1380-1387 (1996).
-
(1996)
Science
, vol.271
, pp. 1380-1387
-
-
Tishkoff, S.A.1
-
44
-
-
0003675970
-
-
Princeton Univ. Press, Princeton
-
Cavalli-Sforza, L. L., Menozzi, P. & Piazza, A. The History and Geography of Human Genes (Princeton Univ. Press, Princeton, 1994).
-
(1994)
The History and Geography of Human Genes
-
-
Cavalli-Sforza, L.L.1
Menozzi, P.2
Piazza, A.3
-
45
-
-
0036075767
-
Race, ethnicity, and genomics: Social classifications as proxies of biological heterogeneity
-
Foster, M. W. & Sharp, R. R. Race, ethnicity, and genomics: social classifications as proxies of biological heterogeneity. Genome Res. 12, 844-850 (2002).
-
(2002)
Genome Res.
, vol.12
, pp. 844-850
-
-
Foster, M.W.1
Sharp, R.R.2
-
46
-
-
0030955071
-
An apportionment of human DNA diversity
-
Barbujani, G., Magagni, A., Minch, E. & Cavalli-Sforza, L. L. An apportionment of human DNA diversity. Proc. Natl Acad. Sci. USA 94, 4516-4519 (1997).
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 4516-4519
-
-
Barbujani, G.1
Magagni, A.2
Minch, E.3
Cavalli-Sforza, L.L.4
-
47
-
-
0037147189
-
Genetic structure of human populations
-
Rosenberg, N. A. et al. Genetic structure of human populations. Science 298, 2381-2385 (2002).
-
(2002)
Science
, vol.298
, pp. 2381-2385
-
-
Rosenberg, N.A.1
-
48
-
-
0030947277
-
Microsatellite diversity and the demographic history of modern humans
-
Jorde, L. B. et al. Microsatellite diversity and the demographic history of modern humans. Proc. Natl Acad. Sci. USA 94, 3100-3103 (1997).
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 3100-3103
-
-
Jorde, L.B.1
-
49
-
-
0025280026
-
Centre d'Etude du Polymorphisme Humain (CEPH): Collaborative genetic mapping of the human genome
-
Dausset, J. et al. Centre d'Etude du Polymorphisme Humain (CEPH): collaborative genetic mapping of the human genome. Genomics 6, 575-577 (1990).
-
(1990)
Genomics
, vol.6
, pp. 575-577
-
-
Dausset, J.1
-
50
-
-
0035173378
-
DbSNP: The NCBI database of genetic variation
-
Sherry, S. T et al. dbSNP: the NCBI database of genetic variation. Nucleic Acids Res. 29, 308-311 (2001).
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. 308-311
-
-
Sherry, S.T.1
-
51
-
-
0034764307
-
SSAHA: A fast search method for large DNA databases
-
Ning, Z., Gox, A. J. & Mullikin, J. C. SSAHA: a fast search method for large DNA databases. Genome Res. 11, 1725-1729 (2001).
-
(2001)
Genome Res.
, vol.11
, pp. 1725-1729
-
-
Ning, Z.1
Gox, A.J.2
Mullikin, J.C.3
-
52
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
-
The International SNP Working Group
-
The International SNP Working Group. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature. 409, 928-933 (2001).
-
(2001)
Nature.
, vol.409
, pp. 928-933
-
-
-
53
-
-
0035895505
-
The sequence of the human genome
-
Venter, J. C. et al. The sequence of the human genome. Science 291, 1304-1351 (2001).
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
-
54
-
-
0002907949
-
The interaction of selection and linkage. 1. General considerations: Heterotic models
-
Lewontin, R. C. The interaction of selection and linkage. 1. General considerations: heterotic models. Genetics 49, 49-67 (1964).
-
(1964)
Genetics
, vol.49
, pp. 49-67
-
-
Lewontin, R.C.1
-
55
-
-
33646226097
-
Linkage disequilibrium in finite populations
-
Hill, W. G. & Robertson, A. Linkage disequilibrium in finite populations. Theor. Appl. Genet. 38, 226-231 (1968).
-
(1968)
Theor. Appl. Genet.
, vol.38
, pp. 226-231
-
-
Hill, W.G.1
Robertson, A.2
-
56
-
-
33645650359
-
Linkage disequilibrium due to random genetic drift
-
Ohta, T. & Kimura, M. Linkage disequilibrium due to random genetic drift. Genet. Res. 13, 47-55 (1969).
-
(1969)
Genet. Res.
, vol.13
, pp. 47-55
-
-
Ohta, T.1
Kimura, M.2
-
57
-
-
0033857962
-
The decay of linkage disequilibrium under random union of gametes: How to calculate Bennett's principal components
-
Dawson, K. J. The decay of linkage disequilibrium under random union of gametes: how to calculate Bennett's principal components. Theor. Popul. Biol. 58, 1-20 (2000).
-
(2000)
Theor. Popul. Biol.
, vol.58
, pp. 1-20
-
-
Dawson, K.J.1
-
58
-
-
0016149819
-
The direction of linkage disequilibrium
-
Langley, C. H. & Crow, J. F. The direction of linkage disequilibrium. Gmetics 78, 937-941 (1974).
-
(1974)
Gmetics
, vol.78
, pp. 937-941
-
-
Langley, C.H.1
Crow, J.F.2
-
59
-
-
0037133218
-
The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis
-
Maniatis, N. et al. The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis. Proc. Natl Acad. Sci. USA 99, 2228-2233 (2002).
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 2228-2233
-
-
Maniatis, N.1
-
60
-
-
0023612034
-
Estimating the recombination parameter of a finite population model without selection
-
Hudson, R. R. Estimating the recombination parameter of a finite population model without selection. Genet. Res. 50, 245-250 (1987).
-
(1987)
Genet. Res.
, vol.50
, pp. 245-250
-
-
Hudson, R.R.1
-
61
-
-
0035675042
-
Estimating recombination rates from population genetic data
-
Fearnhead, P & Donnelly, P Estimating recombination rates from population genetic data. Genetics 159, 1299-1318 (2001).
-
(2001)
Genetics
, vol.159
, pp. 1299-1318
-
-
Fearnhead, P.1
Donnelly, P.2
-
62
-
-
0036199914
-
A coalescent-based method for detecting and estimating recombination from gene sequences
-
McVean, G., Awadalla, P & Fearnhead, P A coalescent-based method for detecting and estimating recombination from gene sequences. Genetics 160, 1231-1241 (2002).
-
(2002)
Genetics
, vol.160
, pp. 1231-1241
-
-
McVean, G.1
Awadalla, P.2
Fearnhead, P.3
-
63
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
International Human Genome Sequencing Consortium
-
International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome. Nature. 409, 860-921 (2001).
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
-
64
-
-
0036598951
-
The complex relationship of genetics, groups, and health: What it means for public health
-
Clayton, E. W. The complex relationship of genetics, groups, and health: what it means for public health. J. Law Med. Ethics 30, 290-297 (2002).
-
(2002)
J. Law Med. Ethics
, vol.30
, pp. 290-297
-
-
Clayton, E.W.1
-
65
-
-
0034142084
-
Genetic research and culturally specific risks: One size does not fit all
-
Foster, M. W. & Sharp, R. R. Genetic research and culturally specific risks: one size does not fit all. Trends Genet. 16, 93-95 (2000).
-
(2000)
Trends Genet.
, vol.16
, pp. 93-95
-
-
Foster, M.W.1
Sharp, R.R.2
-
66
-
-
0034153572
-
Involving study populations in the review of genetic research
-
Sharp, R. R. & Foster, M. W. Involving study populations in the review of genetic research. J. Law Med. Ethics 28, 41-51 (2000).
-
(2000)
J. Law Med. Ethics
, vol.28
, pp. 41-51
-
-
Sharp, R.R.1
Foster, M.W.2
-
67
-
-
0035167444
-
Ethical challenges in community-based research
-
Marshall, P. A. & Rotimi, C. Ethical challenges in community-based research. Am. J. Med. Sci. 322, 241-245 (2001).
-
(2001)
Am. J. Med. Sci.
, vol.322
, pp. 241-245
-
-
Marshall, P.A.1
Rotimi, C.2
-
68
-
-
0034149801
-
Commentary: What "community review" can and cannot do
-
Juengst, E. T. Commentary: what "community review" can and cannot do. J. Law Med. Ethics 28, 52-54 (2000).
-
(2000)
J. Law Med. Ethics
, vol.28
, pp. 52-54
-
-
Juengst, E.T.1
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