-
1
-
-
0033624575
-
The common PPARGPro12Ala polymorphism is associated with decreased risk of type 2 diabetes
-
Altshuler,D.,Hirschhorn, J. N., Klannemark, M. et al. (2000). The common PPARGPro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet 26, 76-80.
-
(2000)
Nat Genet
, vol.26
, pp. 76-80
-
-
Altshuler, D.1
Hirschhorn, J.N.2
Klannemark, M.3
-
2
-
-
33745237158
-
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
-
Arking, D. E., Pfeufer, A., Post, W. et al. (2006). A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat Genet 38(6), 644-651.
-
(2006)
Nat Genet
, vol.38
, Issue.6
, pp. 644-651
-
-
Arking, D.E.1
Pfeufer, A.2
Post, W.3
-
3
-
-
0034069495
-
Gene ontology: tool for the unification of biology
-
The Gene Ontology Consortium
-
Ashburner, M., Ball, C. A., Blake, J. A. et al. (2000). Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet 25(1), 25-29.
-
(2000)
Nat Genet
, vol.25
, Issue.1
, pp. 25-29
-
-
Ashburner, M.1
Ball, C.A.2
Blake, J.A.3
-
4
-
-
84889395646
-
Handbook of Statistical Genetics, 2nd edn
-
Chichester:Wiley
-
Balding, D. J., Bishop, M. and Cannings, C. (Eds) (2003). Handbook of Statistical Genetics, 2nd edn. Chichester:Wiley.
-
(2003)
-
-
Balding, D.J.1
Bishop, M.2
Cannings, C.3
-
5
-
-
0001677717
-
Controlling the false discovery rate: a practical and powerful approach to multiple testing
-
Benjamini, Y. and Hochberg, Y. (1995). Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc [Ser B] 57, 289-300.
-
(1995)
J R Stat Soc [Ser B]
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
6
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease
-
Botstein, D. and Risch, N. (2003). Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat Genet 33 (Suppl.) 228-237.
-
(2003)
Nat Genet
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
7
-
-
0036325415
-
Serotonin-transporter polymorphism pharmacogenetics in diarrhea-predominant irritable bowel syndrome
-
Camilleri, M., Atanasova, E., Carlson, P. J. et al. (2002). Serotonin-transporter polymorphism pharmacogenetics in diarrhea-predominant irritable bowel syndrome. Gastroenterology 123(2), 425-432.
-
(2002)
Gastroenterology
, vol.123
, Issue.2
, pp. 425-432
-
-
Camilleri, M.1
Atanasova, E.2
Carlson, P.J.3
-
8
-
-
0037442092
-
Population stratification and spurious allelic association
-
Cardon, L. R. and Palmer, L. J. (2003). Population stratification and spurious allelic association. Lancet 361, 598-604.
-
(2003)
Lancet
, vol.361
, pp. 598-604
-
-
Cardon, L.R.1
Palmer, L.J.2
-
9
-
-
0028151261
-
Empirical threshold values for quantitative trait mapping
-
Churchill, G. A. and Doerge, R. W. (1994). Empirical threshold values for quantitative trait mapping. Genetics 138, 963-971.
-
(1994)
Genetics
, vol.138
, pp. 963-971
-
-
Churchill, G.A.1
Doerge, R.W.2
-
10
-
-
27544474337
-
Ascertainment bias in studies of human genome-wide polymorphism
-
Clark, A. G., Hubisz, M. J., Bustamante, C. D. et al. (2005). Ascertainment bias in studies of human genome-wide polymorphism. Genome Res 15, 1496-1502.
-
(2005)
Genome Res
, vol.15
, pp. 1496-1502
-
-
Clark, A.G.1
Hubisz, M.J.2
Bustamante, C.D.3
-
11
-
-
33646870783
-
Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease
-
Clarimon, J., Scholz, S., Fung, H.-C. et al. (2006). Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. Am J Hum Genet 78, 1082-1084.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 1082-1084
-
-
Clarimon, J.1
Scholz, S.2
Fung, H.-C.3
-
12
-
-
32444441330
-
Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels
-
Cohen, J. C., Pertsemlidis, A., Fahmi, S. et al. (2006). Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels. Proc Natl Acad Sci U S A 103(6), 1810-1815.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, Issue.6
, pp. 1810-1815
-
-
Cohen, J.C.1
Pertsemlidis, A.2
Fahmi, S.3
-
13
-
-
0036797562
-
Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans
-
Cordell, H. J. (2002). Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans. Hum Mol Genet 11, 2463-2468.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2463-2468
-
-
Cordell, H.J.1
-
14
-
-
27644439141
-
Efficiency andpower in genetic association studies
-
de Bakker,P. I.,Yelensky, R.,Pe'er, I. et al. (2005). Efficiency andpower in genetic association studies. Nat Genet 37(11), 1217-1223.
-
(2005)
Nat Genet
, vol.37
, Issue.11
, pp. 1217-1223
-
-
De Bakker, P.I.1
Yelensky, R.2
Pe'er, I.3
-
15
-
-
0038005018
-
DAVID: Database for Annotation, Visualization, and Integrated Discovery
-
Dennis, G., Jr., Sherman, B. T., Hosack, D. A. et al. (2003). DAVID: Database for Annotation, Visualization, and Integrated Discovery. Genome Biol 4(5), P3.
-
(2003)
Genome Biol
, vol.4
, Issue.5
-
-
Dennis Jr, G.1
Sherman, B.T.2
Hosack, D.A.3
-
16
-
-
33646887765
-
A note on permutation tests inmultistage association scans
-
Dudbridge, F. (2006). A note on permutation tests inmultistage association scans.AmJHum Genet 78(6), 1094-1095.
-
(2006)
AmJHum Genet
, vol.78
, Issue.6
, pp. 1094-1095
-
-
Dudbridge, F.1
-
17
-
-
33645228354
-
Detecting multiple associations in genome-wide studies
-
Dudbridge, F., Gusnanto, A., Koeleman, B. P. (2006). Detecting multiple associations in genome-wide studies. Hum Genomics 2(5), 310-317.
-
(2006)
Hum Genomics
, vol.2
, Issue.5
, pp. 310-317
-
-
Dudbridge, F.1
Gusnanto, A.2
Koeleman, B.P.3
-
18
-
-
7444260846
-
The ENCODE (ENCyclopedia Of DNA Elements) Project
-
ENCODE Project Consortium
-
ENCODE Project Consortium (2004). The ENCODE (ENCyclopedia Of DNA Elements) Project. Science 306(5696), 636-640.
-
(2004)
Science
, vol.306
, Issue.5696
, pp. 636-640
-
-
-
19
-
-
33646894113
-
Genomewide association, Parkinson disease, and PARK10
-
Farrer, M. J., Haugarvoll, K., Ross, O. A. et al. (2006). Genomewide association, Parkinson disease, and PARK10. Am J Hum Genet 78, 1084-1088.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 1084-1088
-
-
Farrer, M.J.1
Haugarvoll, K.2
Ross, O.A.3
-
20
-
-
33645116252
-
Genetics of Parkinson disease: paradigmshifts and future prospects
-
Farrer, M. J. (2006). Genetics of Parkinson disease: paradigmshifts and future prospects. Nat Rev Genet 7(4), 306-318.
-
(2006)
Nat Rev Genet
, vol.7
, Issue.4
, pp. 306-318
-
-
Farrer, M.J.1
-
21
-
-
33646891505
-
No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening
-
Goris, A., Williams-Gray, C. H., Foltynie, T. et al. (2006). No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening. Am J Hum Genet 78, 1088-1090.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 1088-1090
-
-
Goris, A.1
Williams-Gray, C.H.2
Foltynie, T.3
-
22
-
-
13844313862
-
Whole-genome patterns of common DNA variation in three human populations
-
Hinds, D. A., Stuve, L. L., Nilsen, G. B. et al. (2005). Whole-genome patterns of common DNA variation in three human populations. Science 307, 1072-1079.
-
(2005)
Science
, vol.307
, pp. 1072-1079
-
-
Hinds, D.A.1
Stuve, L.L.2
Nilsen, G.B.3
-
23
-
-
0141995596
-
Theautosomal recessive juvenileParkinson disease gene product, parkin, interactswith and ubiquitinates synaptotagmin XI
-
Huynh,D.P., Scoles,D. R.,Nguyen,D. et al. (2003). Theautosomal recessive juvenileParkinson disease gene product, parkin, interactswith and ubiquitinates synaptotagmin XI HumMol Genet 12(20), 2587-2597.
-
(2003)
HumMol Genet
, vol.12
, Issue.20
, pp. 2587-2597
-
-
Huynh, D.P.1
Scoles, D.R.2
Nguyen, D.3
-
24
-
-
33644537955
-
Large-scale characterization of public database SNPs causing non-synonymous changes in three ethnic groups
-
Ireland, J., Carlton, V. E., Falkowski, M. et al. (2006). Large-scale characterization of public database SNPs causing non-synonymous changes in three ethnic groups Hum Genet 119(1-2), 75-83.
-
(2006)
Hum Genet
, vol.119
, Issue.1-2
, pp. 75-83
-
-
Ireland, J.1
Carlton, V.E.2
Falkowski, M.3
-
25
-
-
0036265069
-
How many SNPs does a genome-wide haplotype map require?
-
Judson, R., Salisbury, B., Schneider, J. et al. (2002). How many SNPs does a genome-wide haplotype map require? Pharmacogenomics 3, 379-391.
-
(2002)
Pharmacogenomics
, vol.3
, pp. 379-391
-
-
Judson, R.1
Salisbury, B.2
Schneider, J.3
-
26
-
-
0345863935
-
The KEGG resource for deciphering the genome
-
Database Issue
-
Kanehisa, M., Goto, S., Kawashima, S. et al. (2004). The KEGG resource for deciphering the genome Nucleic Acids Res 32(Database Issue), D277-280.
-
(2004)
Nucleic Acids Res
, vol.32
-
-
Kanehisa, M.1
Goto, S.2
Kawashima, S.3
-
27
-
-
12144290432
-
The impact of SNP density on fine-scale patterns of linkage disequilibrium
-
Ke, X., Hunt, S., Tapper,W. et al. (2004). The impact of SNP density on fine-scale patterns of linkage disequilibrium. Hum Mol Genet 13(6), 577-588.
-
(2004)
Hum Mol Genet
, vol.13
, Issue.6
, pp. 577-588
-
-
Ke, X.1
Hunt, S.2
Tapper, W.3
-
28
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
Klein, R. J., Zeiss, C., Chew, E. Y. et al. (2005). Complement factor H polymorphism in age-related macular degeneration. Science 308(5720), 385-389.
-
(2005)
Science
, vol.308
, Issue.5720
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
-
29
-
-
0033039497
-
Prospects for whole-genome linkage disequilibriummapping of common disease genes
-
Kruglyak, L. (1999). Prospects for whole-genome linkage disequilibriummapping of common disease genes. Nat Genet 22, 139-144.
-
(1999)
Nat Genet
, vol.22
, pp. 139-144
-
-
Kruglyak, L.1
-
30
-
-
28444499033
-
Power tools for human genetics
-
Kruglyak, L. (2005). Power tools for human genetics. Nat Genet 37, 1299-1300.
-
(2005)
Nat Genet
, vol.37
, pp. 1299-1300
-
-
Kruglyak, L.1
-
31
-
-
77949955794
-
First human ventral mesencephalon and striatum cografting in a Parkinson patient
-
Lee, C. C., Lin, S. Z.,Wang, Y. et al. (2003). First human ventral mesencephalon and striatum cografting in a Parkinson patient. Acta Neurochir Suppl 87, 159-162.
-
(2003)
Acta Neurochir Suppl
, vol.87
, pp. 159-162
-
-
Lee, C.C.1
Lin, S.Z.2
Wang, Y.3
-
32
-
-
33646871346
-
A case-control association study of the 12 singlenucleotide polymorphisms implicated in Parkinson disease by a recent genome scan
-
Li, Y., Rowland, C., Schrodi, S. et al. (2006). A case-control association study of the 12 singlenucleotide polymorphisms implicated in Parkinson disease by a recent genome scan. Am J Hum Genet 78, 1090-1092.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 1090-1092
-
-
Li, Y.1
Rowland, C.2
Schrodi, S.3
-
33
-
-
0037131567
-
The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility
-
Liu, Y., Fallon, L., Lashuel, H. A. et al. (2002). The UCH-L1 gene encodes two opposing enzymatic activities that affect alpha-synuclein degradation and Parkinson's disease susceptibility. Cell 111(2), 209-218.
-
(2002)
Cell
, vol.111
, Issue.2
, pp. 209-218
-
-
Liu, Y.1
Fallon, L.2
Lashuel, H.A.3
-
34
-
-
27744495232
-
Get ready to GO! A biologist's guide to the Gene Ontology
-
Lomax, J. (2005). Get ready to GO! A biologist's guide to the Gene Ontology. Brief Bioinform 6(3), 298-304.
-
(2005)
Brief Bioinform
, vol.6
, Issue.3
, pp. 298-304
-
-
Lomax, J.1
-
35
-
-
3242768295
-
Cost-effective analysis of candidate genes using htSNPs: a staged approach
-
Lowe, C. E., Cooper, J. D., Chapman, J. M. et al. (2004). Cost-effective analysis of candidate genes using htSNPs: a staged approach. Genes Immun 5, 301-305.
-
(2004)
Genes Immun
, vol.5
, pp. 301-305
-
-
Lowe, C.E.1
Cooper, J.D.2
Chapman, J.M.3
-
36
-
-
12144289221
-
UCHL1 is a Parkinson's disease susceptibility gene
-
and UCHL1 Global Genetics Consortium
-
Maraganore, D. M., Lesnick, T. G., Elbaz, A. et al. and UCHL1 Global Genetics Consortium (2004). UCHL1 is a Parkinson's disease susceptibility gene. Ann Neurol 55, 512-521.
-
(2004)
Ann Neurol
, vol.55
, pp. 512-521
-
-
Maraganore, D.M.1
Lesnick, T.G.2
Elbaz, A.3
-
37
-
-
27244451809
-
High-resolution wholegenome association study of Parkinson disease
-
Maraganore, D. M., de Andrade, M., Lesnick, T. G. et al. (2005). High-resolution wholegenome association study of Parkinson disease. Am J Hum Genet 77, 685-693.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 685-693
-
-
Maraganore, D.M.1
de Andrade, M.2
Lesnick, T.G.3
-
38
-
-
33646888629
-
Response from Maraganore et al.
-
Maraganore, D. M., de Andrade, M., Lesnick, T. G. et al. (2006). Response from Maraganore et al. Am J Hum Genet 78, 1092-1094.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 1092-1094
-
-
Maraganore, D.M.1
de Andrade, M.2
Lesnick, T.G.3
-
39
-
-
16844366786
-
Genome-wide strategies for detecting multiple loci that influence complex diseases
-
Marchini, J., Donnelly, P. and Cardon, L. R. (2005). Genome-wide strategies for detecting multiple loci that influence complex diseases. Nat Genet 37(4), 413-417.
-
(2005)
Nat Genet
, vol.37
, Issue.4
, pp. 413-417
-
-
Marchini, J.1
Donnelly, P.2
Cardon, L.R.3
-
40
-
-
0031587977
-
Expression of a kinase-defectiveEph-like receptor in the normal human brain
-
Matsuoka, H., Iwata, N., Ito,M.et al. (1997). Expression of a kinase-defectiveEph-like receptor in the normal human brain. Biochem Biophys Res Commun 235(3), 487-492.
-
(1997)
Biochem Biophys Res Commun
, vol.235
, Issue.3
, pp. 487-492
-
-
Matsuoka, H.1
Iwata, N.2
Ito, M.3
-
41
-
-
20844455582
-
Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays
-
Matsuzaki, H., Dong, S., Loi, H. et al. (2004). Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays. Nat Methods 1, 109-111.
-
(2004)
Nat Methods
, vol.1
, pp. 109-111
-
-
Matsuzaki, H.1
Dong, S.2
Loi, H.3
-
42
-
-
0037371453
-
Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test
-
Mitchell, A. A., Cutler, D. J. and Chakravarti, A. (2003). Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test. Am J Hum Genet 72, 598-610.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 598-610
-
-
Mitchell, A.A.1
Cutler, D.J.2
Chakravarti, A.3
-
43
-
-
0037458031
-
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics
-
Mootha, V. K., Lepage, P., Miller, K. et al. (2003). Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proc Natl Acad Sci U S A 100(2), 605-610.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, Issue.2
, pp. 605-610
-
-
Mootha, V.K.1
Lepage, P.2
Miller, K.3
-
44
-
-
23944481324
-
Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes
-
Morris, A. P. (2005). Direct analysis of unphased SNP genotype data in population-based association studies via Bayesian partition modelling of haplotypes. Genet Epidemiol 29(2), 91-107.
-
(2005)
Genet Epidemiol
, vol.29
, Issue.2
, pp. 91-107
-
-
Morris, A.P.1
-
45
-
-
33645118069
-
High-throughput genotyping of intermediate-size structural variation
-
Newman, T. L., Rieder, M. J., Morrison, V. A. et al. (2006). High-throughput genotyping of intermediate-size structural variation. Hum Mol Genet 15(7), 1159-1167.
-
(2006)
Hum Mol Genet
, vol.15
, Issue.7
, pp. 1159-1167
-
-
Newman, T.L.1
Rieder, M.J.2
Morrison, V.A.3
-
46
-
-
33646898463
-
Coverage and characteristics of theAffymetrix GeneChip Human Mapping 100K SNP Set
-
Nicolae,D. L.,Wen, X.,Voight,B.F. et al. (2006). Coverage and characteristics of theAffymetrix GeneChip Human Mapping 100K SNP Set PLoS Genet 2(5), e67.
-
(2006)
PLoS Genet
, vol.2
, Issue.5
-
-
Nicolae, D.L.1
Wen, X.2
Voight, B.F.3
-
47
-
-
33645474288
-
Biases and reconciliation in estimates of linkage disequilibrium in the human genome
-
Pe'er, I., Chretien, Y. R., de Bakker, P. I. et al. (2006a). Biases and reconciliation in estimates of linkage disequilibrium in the human genome. Am J Hum Genet 78, 588-603.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 588-603
-
-
Pe'er, I.1
Chretien, Y.R.2
de Bakker, P.I.3
-
48
-
-
33745279392
-
Evaluating and improving power in wholegenome association studies using fixed marker sets
-
Pe'er, I., de Bakker, P. I., Maller, J. et al. (2006b). Evaluating and improving power in wholegenome association studies using fixed marker sets. Nat Genet 38(6), 663-667.
-
(2006)
Nat Genet
, vol.38
, Issue.6
, pp. 663-667
-
-
Pe'er, I.1
de Bakker, P.I.2
Maller, J.3
-
49
-
-
20344383535
-
Striatal synaptic plasticity: implications for motor learning and Parkinson's disease
-
Pisani, A., Centonze, D., Bernardi, G. et al. (2005). Striatal synaptic plasticity: implications for motor learning and Parkinson's disease. Mov Disord 20(4), 395-402.
-
(2005)
Mov Disord
, vol.20
, Issue.4
, pp. 395-402
-
-
Pisani, A.1
Centonze, D.2
Bernardi, G.3
-
50
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
Pritchard, J. K. (2001). Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 69, 124-137.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 124-137
-
-
Pritchard, J.K.1
-
51
-
-
0034977045
-
Linkage disequilibrium in humans: models and data
-
Pritchard, J. K. and Przeworski, M. (2001). Linkage disequilibrium in humans: models and data. Am J Hum Genet 69(1), 1-14.
-
(2001)
Am J Hum Genet
, vol.69
, Issue.1
, pp. 1-14
-
-
Pritchard, J.K.1
Przeworski, M.2
-
52
-
-
12244264435
-
Genetic power calculator: design of linkage and association genetic mapping studies of complex traits
-
Purcell, S., Cherny, S. S. and Sham, P. C. (2003). Genetic power calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics 19(1), 149-150.
-
(2003)
Bioinformatics
, vol.19
, Issue.1
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
53
-
-
0035375137
-
Computational analysis of microarray data
-
Quackenbush, J. (2001). Computational analysis of microarray data. Nat Rev Genet 2(6), 418-427.
-
(2001)
Nat Rev Genet
, vol.2
, Issue.6
, pp. 418-427
-
-
Quackenbush, J.1
-
54
-
-
0035451780
-
On the allelic spectrum of human disease
-
Reich, D. E. and Lander, E. S. (2001). On the allelic spectrum of human disease. Trends Genet 17, 502-510.
-
(2001)
Trends Genet
, vol.17
, pp. 502-510
-
-
Reich, D.E.1
Lander, E.S.2
-
55
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N. and Merikangas, K. (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
-
56
-
-
22144467302
-
Issues in the analysis of oligonucleotide tiling microarrays for transcript mapping
-
Royce, T. E., Rozowsky, J. S., Bertone, P. et al. (2005). Issues in the analysis of oligonucleotide tiling microarrays for transcript mapping. Trends Genet 21(8), 466-475.
-
(2005)
Trends Genet
, vol.21
, Issue.8
, pp. 466-475
-
-
Royce, T.E.1
Rozowsky, J.S.2
Bertone, P.3
-
57
-
-
0032231911
-
Use of parents, sibs, and unrelated controls for detection of associations between genetic markers and disease
-
Schaid,D. J. and Rowland, C. (1998). Use of parents, sibs, and unrelated controls for detection of associations between genetic markers and disease. Am J Hum Genet 63, 1492-1506.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1492-1506
-
-
Schaid, D.J.1
Rowland, C.2
-
58
-
-
33645072440
-
Gene sequencing
-
The race for the $1000 genome
-
Service, R. F. (2006). Gene sequencing. The race for the $1000 genome. Science 311(5767), 1544-1546.
-
(2006)
Science
, vol.311
, Issue.5767
, pp. 1544-1546
-
-
Service, R.F.1
-
59
-
-
28744453588
-
Comprehensive evaluation of common genetic variationwithin LRRK2 reveals evidence for associationwith sporadic Parkinson's disease
-
Skipper, L., Li, Y., Bonnard, C. et al. (2005). Comprehensive evaluation of common genetic variationwithin LRRK2 reveals evidence for associationwith sporadic Parkinson's disease. Hum Mol Genet 14(23), 3549-3556.
-
(2005)
Hum Mol Genet
, vol.14
, Issue.23
, pp. 3549-3556
-
-
Skipper, L.1
Li, Y.2
Bonnard, C.3
-
60
-
-
27244449351
-
High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs
-
Slater, H. R., Bailey,D. K.,Ren, H. et al. (2005). High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs Am J Hum Genet 77(5), 709-726.
-
(2005)
Am J Hum Genet
, vol.77
, Issue.5
, pp. 709-726
-
-
Slater, H.R.1
Bailey, D.K.2
Ren, H.3
-
61
-
-
0035865322
-
A map of human genome sequence variation containing 1.4 million SNPs
-
SNP Consortium
-
SNP Consortium (2001). A map of human genome sequence variation containing 1.4 million SNPs. Nature 409, 928-933.
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
-
62
-
-
33646337898
-
When is a replication not a replication? Or how to spot a good genetic association study
-
Spector, T.D., Ahmadi, K. R. andValdes, A. M. (2006). When is a replication not a replication? Or how to spot a good genetic association study Arthritis Rheum 54(4), 1051-1054.
-
(2006)
Arthritis Rheum
, vol.54
, Issue.4
, pp. 1051-1054
-
-
Spector, T.D.1
Ahmadi, K.R.2
Valdes, A.M.3
-
63
-
-
31344476038
-
Whole-genome genotypingwith the single-base extension assay
-
Steemers, F. J., Chang,W., Lee, G. et al. (2006). Whole-genome genotypingwith the single-base extension assay Nat Methods 3(1), 31-33.
-
(2006)
Nat Methods
, vol.3
, Issue.1
, pp. 31-33
-
-
Steemers, F.J.1
Chang, W.2
Lee, G.3
-
64
-
-
30744474461
-
Impaired transcriptional upregulation of parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association
-
Tan, E. K., Puong, K. Y., Chan, D. K. et al. (2005). Impaired transcriptional upregulation of parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association Hum Genet 118(3-4), 484-488.
-
(2005)
Hum Genet
, vol.118
, Issue.3-4
, pp. 484-488
-
-
Tan, E.K.1
Puong, K.Y.2
Chan, D.K.3
-
65
-
-
33645775067
-
An utter refutation of the 'fundamental theorem of the HapMap'
-
Terwilliger, J. D. and Hiekkalinna, T. (2006). An utter refutation of the 'fundamental theorem of the HapMap'. Eur J HumGenet 14, 426-437.
-
(2006)
Eur J HumGenet
, vol.14
, pp. 426-437
-
-
Terwilliger, J.D.1
Hiekkalinna, T.2
-
66
-
-
23944469845
-
Recent developments in genomewide association scans: a workshop summary and review
-
Thomas, D. C., Haile, R. W. and Duggan, D. (2005). Recent developments in genomewide association scans: a workshop summary and review. Am J Hum Genet 77, 337-345.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 337-345
-
-
Thomas, D.C.1
Haile, R.W.2
Duggan, D.3
-
67
-
-
33646761944
-
Microarray analysis of gene expression: considerations in data mining and statistical treatment
-
Verducci, J. S., Melfi, V. F., Lin, S. et al. (2006). Microarray analysis of gene expression: considerations in data mining and statistical treatment. Physiol Genomics 25(3), 355-363.
-
(2006)
Physiol Genomics
, vol.25
, Issue.3
, pp. 355-363
-
-
Verducci, J.S.1
Melfi, V.F.2
Lin, S.3
-
68
-
-
18444381172
-
CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure
-
Vermeire, S.,Wild, G., Kocher, K. et al. (2002). CARD15 genetic variation in a Quebec population: prevalence, genotype-phenotype relationship, and haplotype structure. Am J Hum Genet 71(1), 74-83.
-
(2002)
Am J Hum Genet
, vol.71
, Issue.1
, pp. 74-83
-
-
Vermeire, S.1
Wild, G.2
Kocher, K.3
-
69
-
-
13144265739
-
Genome-wide association studies: theoretical and practical concerns
-
Wang, W. Y., Barratt, B. J., Clayton, D. G. et al. (2005). Genome-wide association studies: theoretical and practical concerns. Nat Rev Genet 6(2), 109-118.
-
(2005)
Nat Rev Genet
, vol.6
, Issue.2
, pp. 109-118
-
-
Wang, W.Y.1
Barratt, B.J.2
Clayton, D.G.3
-
70
-
-
33646250184
-
Optimal two-stage genotyping designs for genome-wide association scans
-
Wang, H., Thomas, D. C., Pe'er, I. et al. (2006). Optimal two-stage genotyping designs for genome-wide association scans. Genet Epidemiol 30(4), 356-368.
-
(2006)
Genet Epidemiol
, vol.30
, Issue.4
, pp. 356-368
-
-
Wang, H.1
Thomas, D.C.2
Pe'er, I.3
-
71
-
-
0033780104
-
How many diseases does it take to map a gene with SNPs?
-
Weiss, K. M. and Terwilliger, J. D. (2000). How many diseases does it take to map a gene with SNPs? Nat Genet 26, 151-157.
-
(2000)
Nat Genet
, vol.26
, pp. 151-157
-
-
Weiss, K.M.1
Terwilliger, J.D.2
-
72
-
-
0037108727
-
Functional association of the parkin gene promoter with idiopathic Parkinson's disease
-
West, A. B.,Maraganore, D., Crook, J. et al. (2002). Functional association of the parkin gene promoter with idiopathic Parkinson's disease. Hum Mol Genet 11(22), 2787-2792.
-
(2002)
Hum Mol Genet
, vol.11
, Issue.22
, pp. 2787-2792
-
-
West, A.B.1
Maraganore, D.2
Crook, J.3
-
73
-
-
0034892062
-
Complex genetic diseases: controversy over theCroesus code
-
Wright, A. F. and Hastie, N.D. (2001). Complex genetic diseases: controversy over theCroesus code. Genome Biol 2, 2007.
-
(2001)
Genome Biol
, vol.2
, pp. 2007
-
-
Wright, A.F.1
Hastie, N.D.2
|