-
1
-
-
0040920369
-
-
McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD), 2001, World Wide Web
-
Online Mendelian Inheritance in Man, OMIM™. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Center for Biotechnology Information, National Library of Medicine (Bethesda, MD), 2001, World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/.
-
Online Mendelian Inheritance in Man, OMIM™
-
-
-
3
-
-
0003995062
-
-
Longman, Burnt Mill, Harlow, Essex, England
-
Falconer, D. S. and Mackay, T. F. C., Introduction to Quantitative Genetics Longman, Burnt Mill, Harlow, Essex, England, 1996.
-
(1996)
Introduction to Quantitative Genetics
-
-
Falconer, D.S.1
Mackay, T.F.C.2
-
4
-
-
0033168459
-
Shattuck Lecture - medical and societal consequences of the Human Genome Project
-
Collins, F. S., Shattuck Lecture - medical and societal consequences of the Human Genome Project, N. Engl. J. Med., 341, 28-37, 1999.
-
(1999)
N. Engl. J. Med.
, vol.341
, pp. 28-37
-
-
Collins, F.S.1
-
5
-
-
0034640703
-
Genetics of attention deficit/hyperactivity disorder: Are we ready for molecular genetic studies?
-
Todd, R. D., Genetics of attention deficit/hyperactivity disorder: Are we ready for molecular genetic studies?, Am. J. Med. Genet., 96, 241-243, 2000.
-
(2000)
Am. J. Med. Genet.
, vol.96
, pp. 241-243
-
-
Todd, R.D.1
-
6
-
-
0034640718
-
Update on chromosomal locations for psychiatric disorders: Report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, CA, Oct. 14-18, 1999
-
DeLisi, L. E., Craddock, N. J., Detera-Wadleigh, S., et al., Update on chromosomal locations for psychiatric disorders: Report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, CA, Oct. 14-18, 1999, Am. J. Med. Genet., 96, 434-449, 2000.
-
(2000)
Am. J. Med. Genet.
, vol.96
, pp. 434-449
-
-
DeLisi, L.E.1
Craddock, N.J.2
Detera-Wadleigh, S.3
-
7
-
-
0035121790
-
Genetics of schizophrenia and the new millennium: Progress and pitfalls
-
Baron, M., Genetics of schizophrenia and the new millennium: Progress and pitfalls, Am. J. Hum. Genet., 68, 299-312, 2001.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 299-312
-
-
Baron, M.1
-
8
-
-
17344364477
-
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
-
Blouin, J. L., Dombroski, B. A., Nath, S. K. et al., Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21, Nat. Genet., 20, 70-73, 1998.
-
(1998)
Nat. Genet.
, vol.20
, pp. 70-73
-
-
Blouin, J.L.1
Dombroski, B.A.2
Nath, S.K.3
-
9
-
-
18744432779
-
Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder
-
DeLisi, L. E., Shaw, S., Sherrington, R. et al., Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder, Am. J. Med. Genet., 96, 335-341, 2000.
-
(2000)
Am. J. Med. Genet.
, vol.96
, pp. 335-341
-
-
DeLisi, L.E.1
Shaw, S.2
Sherrington, R.3
-
10
-
-
18144434579
-
Genome-wide scan for schizophrenia in the Finnish population: Evidence for a locus on chromosome 7q22
-
Ekelund, J., Lichtermann, D., Hovatta, I. et al., Genome-wide scan for schizophrenia in the Finnish population: Evidence for a locus on chromosome 7q22, Hum. Mol. Genet., 9, 1049-1057, 2000.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1049-1057
-
-
Ekelund, J.1
Lichtermann, D.2
Hovatta, I.3
-
11
-
-
0034724924
-
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22
-
Brzustowicz, L. M., Hodgkinson, K. A., Chow, E. W. et al., Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22, Science, 288, 678-682, 2000.
-
(2000)
Science
, vol.288
, pp. 678-682
-
-
Brzustowicz, L.M.1
Hodgkinson, K.A.2
Chow, E.W.3
-
12
-
-
0033842462
-
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III
-
Levinson, D. F., Holmans, P., Straub, R. E. et al., Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III, Am. J. Hum. Genet., 67, 652-663, 2000.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 652-663
-
-
Levinson, D.F.1
Holmans, P.2
Straub, R.E.3
-
13
-
-
0033647377
-
A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: Support for loci on chromosome 10p and 6
-
Schwab, S. G., Hallmayer, J., Albus, M. et al., A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: Support for loci on chromosome 10p and 6, Mol. Psychiatry, 5, 638-649, 2000.
-
(2000)
Mol. Psychiatry
, vol.5
, pp. 638-649
-
-
Schwab, S.G.1
Hallmayer, J.2
Albus, M.3
-
14
-
-
0032742796
-
Detecting QTL for uni- and bipolar disorder using a variance component method
-
Visscher, P. M., Haley, C. S., Heath, S. C. et al., Detecting QTL for uni- and bipolar disorder using a variance component method, Psychiatr. Genet., 9, 75-84, 1999.
-
(1999)
Psychiatr. Genet.
, vol.9
, pp. 75-84
-
-
Visscher, P.M.1
Haley, C.S.2
Heath, S.C.3
-
15
-
-
0034606204
-
Search for bipolar disorder susceptibility loci: The application of a modified genome scan concentrating on generich regions
-
Murphy, V. E., Mynett-Johnson, L. A., Claffey, E. et al., Search for bipolar disorder susceptibility loci: The application of a modified genome scan concentrating on generich regions, Am. J. Med. Genet., 96, 728-732, 2000.
-
(2000)
Am. J. Med. Genet.
, vol.96
, pp. 728-732
-
-
Murphy, V.E.1
Mynett-Johnson, L.A.2
Claffey, E.3
-
16
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
International Human Genome Study Consortium, Initial sequencing and analysis of the human genome, Nature, 409, 860-921, 2001.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
-
17
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
-
The International SNP Map 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
-
-
-
18
-
-
0035895505
-
The sequence of the human genome
-
Venter, J. C., Adams, M. D., Myers, E. W. et al., The sequence of the human genome, Science, 291, 1304-1351, 2001.
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
-
19
-
-
0030688004
-
Variations on a theme: Cataloging human DNA sequence variation
-
Collins, F. S., Guyer, M. S., and Chakravarti, A., Variations on a theme: Cataloging human DNA sequence variation, Science, 278, 1580-1581, 1997.
-
(1997)
Science
, vol.278
, pp. 1580-1581
-
-
Collins, F.S.1
Guyer, M.S.2
Chakravarti, A.3
-
20
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
-
Halushka, M. K., Fan, J. B., Bentley, K. et al., Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis, Nat. Genet., 22, 239-247, 1999.
-
(1999)
Nat. Genet.
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.B.2
Bentley, K.3
-
21
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
Cargill, M., Altshuler, D., Ireland, J. et al., Characterization of single-nucleotide polymorphisms in coding regions of human genes, Nat. Genet., 22, 231-238, 1999.
-
(1999)
Nat. Genet.
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
-
22
-
-
0030034357
-
Intraspecific nuclear DNA variation in Drosophila
-
Moriyama, E. N. and Powell, J. R., Intraspecific nuclear DNA variation in Drosophila, Mol. Biol. Evol., 13, 261-277, 1996.
-
(1996)
Mol. Biol. Evol.
, vol.13
, pp. 261-277
-
-
Moriyama, E.N.1
Powell, J.R.2
-
23
-
-
0034570964
-
Patterns of genetic variation in Mendelian and complex traits
-
Zwick, M. E., Cutler, D. J., and Chakravarti, A., Patterns of genetic variation in Mendelian and complex traits, in Annu. Rev. Genomics Hum. Genet., 1, 387-407, 2000.
-
(2000)
Annu. Rev. Genomics Hum. Genet.
, vol.1
, pp. 387-407
-
-
Zwick, M.E.1
Cutler, D.J.2
Chakravarti, A.3
-
24
-
-
0033967692
-
Introducing RefSeq and LocusLink:Curated human genome resources at the NCBI
-
Pruitt, K. D., Katz, K. S., Sicotte, H. et al., Introducing RefSeq and LocusLink:Curated human genome resources at the NCBI, Trends Genet., 16, 44-47, 2000.
-
(2000)
Trends Genet.
, vol.16
, pp. 44-47
-
-
Pruitt, K.D.1
Katz, K.S.2
Sicotte, H.3
-
25
-
-
0035230102
-
Quantitative trait loci in Drosophila
-
Mackay, T. F. C., Quantitative trait loci in Drosophila, Nat. Reviews, 2, 11-20, 2001.
-
(2001)
Nat. Reviews
, vol.2
, pp. 11-20
-
-
Mackay, T.F.C.1
-
26
-
-
84984933234
-
High density synthetic oligonucleotide arrays
-
Lipshutz, R. J., Fodor, S. P., Gingeras, T. R. et al., High density synthetic oligonucleotide arrays, Nat. Genet., 21, 20-24, 1999.
-
(1999)
Nat. Genet.
, vol.21
, pp. 20-24
-
-
Lipshutz, R.J.1
Fodor, S.P.2
Gingeras, T.R.3
-
27
-
-
84984932946
-
Population genetics - making sense out of sequence
-
Chakravarti, A., Population genetics - making sense out of sequence, Nat. Genet., 21, 56-60, 1999.
-
(1999)
Nat. Genet.
, vol.21
, pp. 56-60
-
-
Chakravarti, A.1
-
28
-
-
0015862142
-
The age of a neutral mutant persisting in a finite population
-
Kimura, M. and Ohta, T., The age of a neutral mutant persisting in a finite population, Genetics, 75, 199-212, 1973.
-
(1973)
Genetics
, vol.75
, pp. 199-212
-
-
Kimura, M.1
Ohta, T.2
-
30
-
-
0031669184
-
Overlapping genomic sequences: A treasure trove of single-nucleotide polymorphisms
-
Taillon-Miller, P., Gu, Z., Li, Q. et al., Overlapping genomic sequences: A treasure trove of single-nucleotide polymorphisms, Genome Res., 8, 748-754, 1998.
-
(1998)
Genome Res.
, vol.8
, pp. 748-754
-
-
Taillon-Miller, P.1
Gu, Z.2
Li, Q.3
-
31
-
-
0034727107
-
An SNP map of the human genome generated by reduced representation shotgun sequencing
-
Altshuler, D., Pollara, V. J., Cowles, C. R. et al., An SNP map of the human genome generated by reduced representation shotgun sequencing, Nature, 407, 513-516, 2000.
-
(2000)
Nature
, vol.407
, pp. 513-516
-
-
Altshuler, D.1
Pollara, V.J.2
Cowles, C.R.3
-
32
-
-
17344380534
-
An SNP map of human chromosome 22
-
Mullikin, J. C., Hunt, S. E., Cole, C. G. et al., An SNP map of human chromosome 22, Nature, 407, 516-520, 2000.
-
(2000)
Nature
, vol.407
, pp. 516-520
-
-
Mullikin, J.C.1
Hunt, S.E.2
Cole, C.G.3
-
33
-
-
0003834965
-
-
Burgess Publishing Company, Minneapolis
-
Crow, J. F. and Kimura, M., An Introduction to Population Genetics Theory, Burgess Publishing Company, Minneapolis, 1970, 48.
-
(1970)
An Introduction to Population Genetics Theory
, pp. 48
-
-
Crow, J.F.1
Kimura, M.2
-
34
-
-
0003752712
-
-
Sinauer Associates, Sunderland, MA
-
Weir, B. S., Genetic Data Analysis II, Sinauer Associates, Sunderland, MA, 1996, 231.
-
(1996)
Genetic Data Analysis II
, pp. 231
-
-
Weir, B.S.1
-
35
-
-
0026460082
-
Population genetics of polymorphism and divergence
-
Sawyer, S. A. and Hartl, D. L., Population genetics of polymorphism and divergence, Genetics, 132, 1161-1176, 1992.
-
(1992)
Genetics
, vol.132
, pp. 1161-1176
-
-
Sawyer, S.A.1
Hartl, D.L.2
-
36
-
-
0016121072
-
A note on the sampling theory for infinite alleles and infinite sites models
-
Ewens, W. J., A note on the sampling theory for infinite alleles and infinite sites models, Theor. Pop. Biol., 6, 143-148, 1974.
-
(1974)
Theor. Pop. Biol.
, vol.6
, pp. 143-148
-
-
Ewens, W.J.1
|