-
1
-
-
0033909546
-
A general test of association for quantitative traits in nuclear families
-
Abecasis, G.R., Cardon, L.R., & Cookson, W.O.C. (2000). A general test of association for quantitative traits in nuclear families. American Journal of Human Genetics, 66, 279-292.
-
(2000)
American Journal of Human Genetics
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.C.3
-
2
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis, G.R., Cherny, S.S., Cookson, W.O., & Cardon, L.R. (2002), Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nature Genetics, 30, 97-101.
-
(2002)
Nature Genetics
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
3
-
-
0034017850
-
GOLD-graphical overview of linkage disequilibrium
-
Abecasis, G.R., & Cookson, W.O. (2000). GOLD-graphical overview of linkage disequilibrium. Bioinformatics, 16, 182-183.
-
(2000)
Bioinformatics
, vol.16
, pp. 182-183
-
-
Abecasis, G.R.1
Cookson, W.O.2
-
4
-
-
0033362231
-
Direct powear comparisons between simple lod scores and NPL scores for linkage analysis in complex disease
-
Abreu, P.C., Greenberg, D.A., & Hodge, S.E. (1999). Direct powear comparisons between simple lod scores and NPL scores for linkage analysis in complex disease. American Journal of Human Genetics, 65, 847-857.
-
(1999)
American Journal of Human Genetics
, vol.65
, pp. 847-857
-
-
Abreu, P.C.1
Greenberg, D.A.2
Hodge, S.E.3
-
5
-
-
0029886586
-
The use of discordant sibling pairs for finding genetic loci linked to obesity: Practical considerations
-
Allison, D.B. (1996). The use of discordant sibling pairs for finding genetic loci linked to obesity: Practical considerations. International Journal on Obesity, 20, 553-560.
-
(1996)
International Journal on Obesity
, vol.20
, pp. 553-560
-
-
Allison, D.B.1
-
6
-
-
0031028361
-
Transmission-disequilibrium tests for quantitative traits
-
Allison, D.B. (1997). Transmission-disequilibrium tests for quantitative traits. American Journal of Human Genetics, 60, 676-690.
-
(1997)
American Journal of Human Genetics
, vol.60
, pp. 676-690
-
-
Allison, D.B.1
-
7
-
-
0033358532
-
Sibling-based tests of linkage and association for quantitative traits
-
Allison, D.B., Heo, M., Kaplan, N., & Martin, E.R. (1999). Sibling-based tests of linkage and association for quantitative traits. American Journal of Human Genetics, 64, 1754-1764.
-
(1999)
American Journal of Human Genetics
, vol.64
, pp. 1754-1764
-
-
Allison, D.B.1
Heo, M.2
Kaplan, N.3
Martin, E.R.4
-
8
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
Almasy, L., & Blangero, J. (1998). Multipoint quantitative-trait linkage analysis in general pedigrees. American Journal of Human Genetics, 62, 1198-1211.
-
(1998)
American Journal of Human Genetics
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
9
-
-
0028058128
-
Robust variance-components approach for assessing genetic linkage in pedigrees
-
Amos, C.I. (1994). Robust variance-components approach for assessing genetic linkage in pedigrees. American Journal of Human Genetics, 54, 535-543.
-
(1994)
American Journal of Human Genetics
, vol.54
, pp. 535-543
-
-
Amos, C.I.1
-
10
-
-
0036302206
-
A major susceptibility locus for specific language impairment is located on 13q21
-
Bartlett, C.W., Flax, J.F., Logue, M.W., Vieland, V.J., Bassett, A.S., Tallal, P., & Brzustowicz, L.M. (2002). A major susceptibility locus for specific language impairment is located on 13q21. American Journal of Human Genetics, 71, 45-55.
-
(2002)
American Journal of Human Genetics
, vol.71
, pp. 45-55
-
-
Bartlett, C.W.1
Flax, J.F.2
Logue, M.W.3
Vieland, V.J.4
Bassett, A.S.5
Tallal, P.6
Brzustowicz, L.M.7
-
11
-
-
0141487850
-
Current concepts on the neurobiology of AttentionDeficit/Hyperactivity Disorder
-
Biederman, J., & Faraone, S.V. (2002). Current concepts on the neurobiology of AttentionDeficit/Hyperactivity Disorder. Journal of Attention Disorders, 6 (Suppl.) 1, S7-S16.
-
(2002)
Journal of Attention Disorders
, vol.6
, Issue.1
, pp. S7-S16
-
-
Biederman, J.1
Faraone, S.V.2
-
12
-
-
0028872434
-
Genetic basis of specific language impairment: Evidence from a twin study
-
Bishop, D.V., North, T., & Donlan, C. (1995). Genetic basis of specific language impairment: Evidence from a twin study. Developmental Medicine and Child Neurology, 37, 56-71.
-
(1995)
Developmental Medicine and Child Neurology
, vol.37
, pp. 56-71
-
-
Bishop, D.V.1
North, T.2
Donlan, C.3
-
13
-
-
0037373275
-
Discovering genotypes underlying human phenotypes:Past successes for mendelian disease, future approaches for complex disease
-
Botstein, D., & Risch, N. (2003). Discovering genotypes underlying human phenotypes:Past successes for mendelian disease, future approaches for complex disease. Nature Genetics, Supplement 33, 228-237.
-
(2003)
Nature Genetics, Supplement
, vol.33
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
14
-
-
0029611015
-
Linkage analysis of a common oligogenic disease using selected sib pairs
-
Cardon, L.R., Fulker, D.W., & Cherny, S.S. (1995). Linkage analysis of a common oligogenic disease using selected sib pairs. Genetics of Epidemiology, 12(6), 741-746.
-
(1995)
Genetics of Epidemiology
, vol.12
, Issue.6
, pp. 741-746
-
-
Cardon, L.R.1
Fulker, D.W.2
Cherny, S.S.3
-
15
-
-
0029003528
-
Quantitative trait locus for reading disability: A correction
-
Cardon, L.R., Smith, S.D., Fulker, D.W., Kimberling, W.J., Pennington, B.F., & DeFries, J.C. (1995). Quantitative trait locus for reading disability: A correction. Science, 268, 1553.
-
(1995)
Science
, vol.268
, pp. 1553
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Kimberling, W.J.4
Pennington, B.F.5
DeFries, J.C.6
-
16
-
-
0028030006
-
Quantitative trait locus on chromosome 6 predisposing to reading disability
-
Cardon, L.R., Smith, S.D., Fulker, D.W., Pennington, B.F., Kimberling, W.J., & DeFries, J.C. (1994). Quantitative trait locus on chromosome 6 predisposing to reading disability. Science, 266, 276-279.
-
(1994)
Science
, vol.266
, pp. 276-279
-
-
Cardon, L.R.1
Smith, S.D.2
Fulker, D.W.3
Pennington, B.F.4
Kimberling, W.J.5
DeFries, J.C.6
-
17
-
-
0027366195
-
Faster sequential genetic linkage computations
-
Cottingham, R.W., Jr., Idury, R.M., & Schäffer, A.A. (1993). Faster sequential genetic linkage computations, American Journal of Human Genetics, 53, 252-263.
-
(1993)
American Journal of Human Genetics
, vol.53
, pp. 252-263
-
-
Cottingham, R.W.1
Idury, R.M.2
Schäffer, A.A.3
-
18
-
-
0037835766
-
Mice lacking Tropomodulin-2 show enhanced long-term potentiation, hyperactivity, and deficits in learning and memory
-
Cox, P.R., Fowler, V., Xu, B., Sweatt, J.D., Paylor, R., & Zoghbi, H.Y. (2003). Mice lacking Tropomodulin-2 show enhanced long-term potentiation, hyperactivity, and deficits in learning and memory. Molecular and Cellular Neuroscience, 23, 1-12.
-
(2003)
Molecular and Cellular Neuroscience
, vol.23
, pp. 1-12
-
-
Cox, P.R.1
Fowler, V.2
Xu, B.3
Sweatt, J.D.4
Paylor, R.5
Zoghbi, H.Y.6
-
20
-
-
0022396848
-
Multiple regression analysis of twin data
-
DeFries, J.C., & Fulker, D.W. (1985). Multiple regression analysis of twin data. Behavior Genetics, 25, 467-473.
-
(1985)
Behavior Genetics
, vol.25
, pp. 467-473
-
-
DeFries, J.C.1
Fulker, D.W.2
-
21
-
-
0033949377
-
Haseman and Elston revisited
-
Elston, R.C., Buxbaum, S., Jacobs, K.B., & Olson, J.M. (2000). Haseman and Elston revisited. Genetics of Epidemiology, 19, 1-17.
-
(2000)
Genetics of Epidemiology
, vol.19
, pp. 1-17
-
-
Elston, R.C.1
Buxbaum, S.2
Jacobs, K.B.3
Olson, J.M.4
-
22
-
-
0023235253
-
Haplotype relative risks: An easy reliable way to construct a proper control sample for risk calculations
-
Falk, C.T., & Rubinstein, P. (1987). Haplotype relative risks: An easy reliable way to construct a proper control sample for risk calculations. Annals of Human Genetics, 51, 227-233.
-
(1987)
Annals of Human Genetics
, vol.51
, pp. 227-233
-
-
Falk, C.T.1
Rubinstein, P.2
-
23
-
-
0032533256
-
Neurobiology of attention-deficit hyperactivity disorder
-
Faraone, S.V., & Biederman, J. (1998). Neurobiology of attention-deficit hyperactivity disorder. Biological Psychiatry, 44, 951-958.
-
(1998)
Biological Psychiatry
, vol.44
, pp. 951-958
-
-
Faraone, S.V.1
Biederman, J.2
-
24
-
-
0035528922
-
Methods of linkage analysis of quantitative trait loci in humans
-
Feingold, E. (2001). Methods of linkage analysis of quantitative trait loci in humans. Theoretical Population Biology, 60, 167-180.
-
(2001)
Theoretical Population Biology
, vol.60
, pp. 167-180
-
-
Feingold, E.1
-
25
-
-
0036076138
-
Invited editorial: Regression-based quantitative-trait-locus mapping in the 21st century
-
Feingold, E. (2002), Invited editorial: Regression-based quantitative-trait-locus mapping in the 21st century. American Journal of Human Genetics, 71, 217-222.
-
(2002)
American Journal of Human Genetics
, vol.71
, pp. 217-222
-
-
Feingold, E.1
-
26
-
-
0036779497
-
Developmental dyslexia: Genetic dissection of a complex cognitive trait
-
Fisher, S.E., & DeFries, J.C. (2002). Developmental dyslexia: Genetic dissection of a complex cognitive trait. Nature Reviews: Neuroscience, 3, 767-780.
-
(2002)
Nature Reviews: Neuroscience
, vol.3
, pp. 767-780
-
-
Fisher, S.E.1
DeFries, J.C.2
-
27
-
-
0033366739
-
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
-
Fisher, S.E., Marlow, A.J., Lamb, J., Maestrini, E., Williams, D.F., Richardson, A.J., Weeks, D.E., Stein, J.F., & Monaco, A.P. (1999). A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. American Journal of Human Genetics, 64, 146-156.
-
(1999)
American Journal of Human Genetics
, vol.64
, pp. 146-156
-
-
Fisher, S.E.1
Marlow, A.J.2
Lamb, J.3
Maestrini, E.4
Williams, D.F.5
Richardson, A.J.6
Weeks, D.E.7
Stein, J.F.8
Monaco, A.P.9
-
28
-
-
0025778539
-
Etiology of autism: Genetic influences
-
Folstein, S.E., & Piven, J. (1991). Etiology of autism: Genetic influences. Pediatrics, 87, 767-773.
-
(1991)
Pediatrics
, vol.87
, pp. 767-773
-
-
Folstein, S.E.1
Piven, J.2
-
29
-
-
0033925884
-
Composite statistics for QTL mapping with moderately discordant sibling pairs
-
Forrest, W.F., & Feingold, E. (2000). Composite statistics for QTL mapping with moderately discordant sibling pairs. American Journal of Human Genetics, 66(5), 1642-1660.
-
(2000)
American Journal of Human Genetics
, vol.66
, Issue.5
, pp. 1642-1660
-
-
Forrest, W.F.1
Feingold, E.2
-
30
-
-
0000138745
-
Multiple regression analysis of sib pair data on reading to detect quantitative trait loci
-
Fulker, D.W., Cardon, L.R., DeFries, J.C., Kimberling, W.J., Pennington, B.F., & Smith, S.D. (1991). Multiple regression analysis of sib pair data on reading to detect quantitative trait loci. Reading and Writing: An Interdisciplinary Journal, 3, 299-313.
-
(1991)
Reading and Writing: An Interdisciplinary Journal
, vol.3
, pp. 299-313
-
-
Fulker, D.W.1
Cardon, L.R.2
DeFries, J.C.3
Kimberling, W.J.4
Pennington, B.F.5
Smith, S.D.6
-
31
-
-
0035571529
-
Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities
-
Gayán, J., & Olson, R.K. (2001). Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities. Developmental Neuropsychology, 20, 483-507.
-
(2001)
Developmental Neuropsychology
, vol.20
, pp. 483-507
-
-
Gayán, J.1
Olson, R.K.2
-
32
-
-
0033364213
-
Quantitative trait locus for specific language and reading disability on chromosome 6p
-
Gayán, J., Smith, S.D., Cherny, S.S., Cardon, L., Fulker, D.W., Brower, A.M., Olson, R.K., Pennington, B.F., & DeFries, J.C. (1999). Quantitative trait locus for specific language and reading disability on chromosome 6p. American Journal of Human Genetics, 64, 157-164.
-
(1999)
American Journal of Human Genetics
, vol.64
, pp. 157-164
-
-
Gayán, J.1
Smith, S.D.2
Cherny, S.S.3
Cardon, L.4
Fulker, D.W.5
Brower, A.M.6
Olson, R.K.7
Pennington, B.F.8
DeFries, J.C.9
-
33
-
-
0036867682
-
Linkage mapping of quantitative trait loci in humans: An overview
-
Ghosh, S., Reich, T., & Majumder, P.P. (2002). Linkage mapping of quantitative trait loci in humans: An overview. Annals of Human Genetics, 66, 431-438.
-
(2002)
Annals of Human Genetics
, vol.66
, pp. 431-438
-
-
Ghosh, S.1
Reich, T.2
Majumder, P.P.3
-
34
-
-
0035186189
-
Determining trait locus position from multipoint analysis: Accuracy and power of three different statistics
-
Greenberg, D.A., & Abreu, P. (2001). Determining trait locus position from multipoint analysis: Accuracy and power of three different statistics. Genetics of Epidemiology, 21, 299-314.
-
(2001)
Genetics of Epidemiology
, vol.21
, pp. 299-314
-
-
Greenberg, D.A.1
Abreu, P.2
-
35
-
-
0031027824
-
Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
-
Grigorenko, E.L., Wood, F.B., Meyer, M.S., Hart, L.A., Speed, W.C., Shuster, A., & Pauls, D.L. (1997), Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. American Journal of Human Genetics, 60, 27-39.
-
(1997)
American Journal of Human Genetics
, vol.60
, pp. 27-39
-
-
Grigorenko, E.L.1
Wood, F.B.2
Meyer, M.S.3
Hart, L.A.4
Speed, W.C.5
Shuster, A.6
Pauls, D.L.7
-
36
-
-
0033928210
-
Chromosome 6p influences on different dyslexia-related cognitive processes: Further confirmation
-
Grigorenko, E.L., Wood, F.B., Meyer, M.S., & Pauls, D.L. (2000). Chromosome 6p influences on different dyslexia-related cognitive processes: Further confirmation. American Journal of Human Genetics, 66, 715-723.
-
(2000)
American Journal of Human Genetics
, vol.66
, pp. 715-723
-
-
Grigorenko, E.L.1
Wood, F.B.2
Meyer, M.S.3
Pauls, D.L.4
-
37
-
-
0015309467
-
The investigation of linkage between a quantitative trait and a marker locus
-
Haseman, J.K., & Elston, R.C. (1972). The investigation of linkage between a quantitative trait and a marker locus. Behavior Genetics, 2, 3-19.
-
(1972)
Behavior Genetics
, vol.2
, pp. 3-19
-
-
Haseman, J.K.1
Elston, R.C.2
-
38
-
-
0036152559
-
HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity
-
Hodge, S.E., Vieland, V.J., & Greenberg, D.A. (2002). HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity. American Journal of Human Genetics, 70, 556-557.
-
(2002)
American Journal of Human Genetics
, vol.70
, pp. 556-557
-
-
Hodge, S.E.1
Vieland, V.J.2
Greenberg, D.A.3
-
39
-
-
0037648359
-
Control of confounding of genetic associations in stratified populations
-
Hoggart, C.J., Esteban, J., Parra, E.J., Shriver, M.D., Bonilla, C., Kittles, R.A., Clayton, D.G., & McKeigue, P.M. (2003). Control of confounding of genetic associations in stratified populations. American Journal of Human Genetics, 72, 1492-1504.
-
(2003)
American Journal of Human Genetics
, vol.72
, pp. 1492-1504
-
-
Hoggart, C.J.1
Esteban, J.2
Parra, E.J.3
Shriver, M.D.4
Bonilla, C.5
Kittles, R.A.6
Clayton, D.G.7
McKeigue, P.M.8
-
40
-
-
0035055544
-
The family based association test method:Strategies for studying general genotype-phenotype associations
-
Horvath, S., Xu, X., & Laird, N. (2001). The family based association test method:Strategies for studying general genotype-phenotype associations. European Journal of Human Genetics, 9, 301-306.
-
(2001)
European Journal of Human Genetics
, vol.9
, pp. 301-306
-
-
Horvath, S.1
Xu, X.2
Laird, N.3
-
41
-
-
0037042057
-
Familial aggregation of dyslexia phenotypes: II. Paired correlated measures
-
Hsu, L., Wijsman, E.M., Berninger, V.W., Thomson, J.B., & Raskind, W.H. (2002). Familial aggregation of dyslexia phenotypes: II. Paired correlated measures. American Journal of Medical Genetics (Neuropsychiatric Genetics), 114, 471-478.
-
(2002)
American Journal of Medical Genetics (Neuropsychiatric Genetics)
, vol.114
, pp. 471-478
-
-
Hsu, L.1
Wijsman, E.M.2
Berninger, V.W.3
Thomson, J.B.4
Raskind, W.H.5
-
42
-
-
0035162422
-
The null distribution of the heterogeneity lod score does depend on the assumed genetic model for the trait
-
Huang, J., & Vieland, V.J. (2001). The null distribution of the heterogeneity lod score does depend on the assumed genetic model for the trait. Human Heredity, 52, 217-222.
-
(2001)
Human Heredity
, vol.52
, pp. 217-222
-
-
Huang, J.1
Vieland, V.J.2
-
43
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium. (1998). A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Human Molecular Genetics, 7, 71-578.
-
(1998)
Human Molecular Genetics
, vol.7
, pp. 71-578
-
-
-
44
-
-
0035179971
-
Replication validity of genetic association studies
-
loannidis, J.P. A., Ntzani, E.E., Trikalinos, T.A., & Contopoulos-Ionnidis, D.G. (2001). Replication validity of genetic association studies. Nature Genetics, 29, 306-309.
-
(2001)
Nature Genetics
, vol.29
, pp. 306-309
-
-
Loannidis, J.P.A.1
Ntzani, E.E.2
Trikalinos, T.A.3
Contopoulos-Ionnidis, D.G.4
-
45
-
-
0036265069
-
How many SNPs does a genome-wide haplotype map require?
-
Judson, R., Salisbury, B., Schneider, J., Windemuth, A., & Stephens, J.C. (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
Windemuth, A.4
Stephens, J.C.5
-
46
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak, L., Daly, M.J., Reeve-Daly, M.P., & Lander, E.S. (1996). Parametric and nonparametric linkage analysis: A unified multipoint approach. American Journal of Human Genetics, 58(6), 1347-1363.
-
(1996)
American Journal of Human Genetics
, vol.58
, Issue.6
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
47
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander, E.S., & Kruglyak, L. (1995). Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results. Nature Genetics, 11, 241-247.
-
(1995)
Nature Genetics
, vol.11
, pp. 241-247
-
-
Lander, E.S.1
Kruglyak, L.2
-
48
-
-
0342499587
-
Strategies for multilocus linkage analysis in humans
-
Lathrop, G.M., Lalouel, J.M., Julier, C., & Ott, J. (1984). Strategies for multilocus linkage analysis in humans. Proceedings of the National Academy of Science USA, 81, 3443-3446.
-
(1984)
Proceedings of the National Academy of Science USA
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
49
-
-
0035011450
-
DeFries-Fulker Multiple Regression of Sibship QTL Data: A SAS Macro
-
Lessem, J.M., & Cherny, S.S. (2001). DeFries-Fulker Multiple Regression of Sibship QTL Data: A SAS Macro. Bioinformatics, 17, 371-372.
-
(2001)
Bioinformatics
, vol.17
, pp. 371-372
-
-
Lessem, J.M.1
Cherny, S.S.2
-
50
-
-
0034920299
-
A genomewide screen for autism susceptibility loci
-
Liu, J., Nyholt, D.R., Magnussen, P., Parano, E., Pavone, P., Geschwind, D., Lord, C., Iversen, P., Hoh, J., Ott, J., & Gilliam, T.C. (2001). A genomewide screen for autism susceptibility loci. American Journal of Human Genetics, 69, 327-340.
-
(2001)
American Journal of Human Genetics
, vol.69
, pp. 327-340
-
-
Liu, J.1
Nyholt, D.R.2
Magnussen, P.3
Parano, E.4
Pavone, P.5
Geschwind, D.6
Lord, C.7
Iversen, P.8
Hoh, J.9
Ott, J.10
Gilliam, T.C.11
-
51
-
-
0043048571
-
Sequential tests for the detection of linkage
-
Morton, N.E. (1955). Sequential tests for the detection of linkage. American Journal of Human Genetics, 7, 277-328.
-
(1955)
American Journal of Human Genetics
, vol.7
, pp. 277-328
-
-
Morton, N.E.1
-
52
-
-
0031588662
-
Letter in response to Risch and Merikangas, 1996
-
Muller-Myhsok, B., & Abel, L. (1997). Letter in response to Risch and Merikangas, 1996. Science, 275, 1328-1329.
-
(1997)
Science
, vol.275
, pp. 1328-1329
-
-
Muller-Myhsok, B.1
Abel, L.2
-
53
-
-
18344368187
-
FOXP2 is not a major susceptibility gene for autism or specific language impairment
-
Newbury, D.F., Bonora, E., Lamb, J.A., Fisher, S.E., Lai, C.S., Baird, G., Jannoun, L., Slonims, V., Stott, M., Merricks, M.J., Bolton, P.F., Bailey, A.J., & Monaco, A.P. International Molecular Genetic Study of Autism Consortium (2002). FOXP2 is not a major susceptibility gene for autism or specific language impairment. American Journal of Human Genetics, 70(5), 1318-1327.
-
(2002)
American Journal of Human Genetics
, vol.70
, Issue.5
, pp. 1318-1327
-
-
Newbury, D.F.1
Bonora, E.2
Lamb, J.A.3
Fisher, S.E.4
Lai, C.S.5
Baird, G.6
Jannoun, L.7
Slonims, V.8
Stott, M.9
Merricks, M.J.10
Bolton, P.F.11
Bailey, A.J.12
Monaco, A.P.13
-
54
-
-
0033792625
-
Two translocations of chromosome 15q associated with dyslexia
-
Nopola-Hemmi, J., Taipale, M., Haltia, T., Lehesjoki, A.E., Voutilainen, A., & Kere, J. (2000). Two translocations of chromosome 15q associated with dyslexia. Journal of Medical Genetics, 37, 771-775.
-
(2000)
Journal of Medical Genetics
, vol.37
, pp. 771-775
-
-
Nopola-Hemmi, J.1
Taipale, M.2
Haltia, T.3
Lehesjoki, A.E.4
Voutilainen, A.5
Kere, J.6
-
55
-
-
0038692088
-
Association of specific language impairment (SLI) to the region of 7q31
-
O'Brien, E.K., Zhang, X., Nishimura, C., Tomblin, J.B., & Murray, J.C. (2003). Association of specific language impairment (SLI) to the region of 7q31. American Journal of Human Genetics, 72, 1536-1543.
-
(2003)
American Journal of Human Genetics
, vol.72
, pp. 1536-1543
-
-
O'Brien, E.K.1
Zhang, X.2
Nishimura, C.3
Tomblin, J.B.4
Murray, J.C.5
-
56
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
O'Connell, J.R., & Weeks, D.E. (1995). The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nature Genetics, 11, 402-408.
-
(1995)
Nature Genetics
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
57
-
-
0038752692
-
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: Suggestive linkage on 17p11
-
Ogdie, M.N., Macphie, I.L., Minassian, S.L., Yang, M., Fisher, S.E., Francks, C., Cantor, R.M., McCracken, J.T., McGough, J.J., Nelson, S.F., Monaco, A.P., & Smalley, S.L. (2003). A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: Suggestive linkage on 17p11. American Journal of Human Genetics, 72, 1268-1279.
-
(2003)
American Journal of Human Genetics
, vol.72
, pp. 1268-1279
-
-
Ogdie, M.N.1
Macphie, I.L.2
Minassian, S.L.3
Yang, M.4
Fisher, S.E.5
Francks, C.6
Cantor, R.M.7
McCracken, J.T.8
McGough, J.J.9
Nelson, S.F.10
Monaco, A.P.11
Smalley, S.L.12
-
58
-
-
0024689078
-
Specific deficits in component reading and language skills: Genetic and environmental influences
-
Olson, R., Wise, B., Conners, F., Rack, J., & Fulker, D. (1989). Specific deficits in component reading and language skills: Genetic and environmental influences. Journal of Learning Disabilities, 22, 339-348.
-
(1989)
Journal of Learning Disabilities
, vol.22
, pp. 339-348
-
-
Olson, R.1
Wise, B.2
Conners, F.3
Rack, J.4
Fulker, D.5
-
59
-
-
0022919732
-
Linkage probability and its approximate confidence interval under possible heterogeneity
-
Ott, J. (1986). Linkage probability and its approximate confidence interval under possible heterogeneity. Genetics of Epidemiology, Supplement 1, 251-257.
-
(1986)
Genetics of Epidemiology
, pp. 251-257
-
-
Ott, J.1
-
60
-
-
0035234944
-
Major strengths and weaknesses of the lod score method
-
Ott, J. (2001). Major strengths and weaknesses of the lod score method. Advances in Genetics, 42, 125-132.
-
(2001)
Advances in Genetics
, vol.42
, pp. 125-132
-
-
Ott, J.1
-
61
-
-
0033697005
-
Haseman and Elston revisited: The effects of ascertainment and residual familial correlations on power to detect linkage
-
Palmer, L.J., Jacobs, K.B., & Elston, R.C. (2000). Haseman and Elston revisited: The effects of ascertainment and residual familial correlations on power to detect linkage. Genetics of Epidemiology, 19, 456-460.
-
(2000)
Genetics of Epidemiology
, vol.19
, pp. 456-460
-
-
Palmer, L.J.1
Jacobs, K.B.2
Elston, R.C.3
-
62
-
-
0035941029
-
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
-
Patil, N., Berno, A.J., Hinds, D.A., Barrett, W.A., Doshi, J.M., Hacker, C.R., Kautzer, C.R., Lee, D.H., Marjoribanks, C., McDonough, D.P., Nguyen, B.T., Norris, M.C., Sheehan, J.B., Shen, N., Stern, D., Stokowski, R.P., Thomas, D.J., Trulson, M.O., Vyas, K.R., Frazer, K.A., Fodor, S.P., & Cox, D, R. (2001). Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science, 294, 1719-1723.
-
(2001)
Science
, vol.294
, pp. 1719-1723
-
-
Patil, N.1
Berno, A.J.2
Hinds, D.A.3
Barrett, W.A.4
Doshi, J.M.5
Hacker, C.R.6
Kautzer, C.R.7
Lee, D.H.8
Marjoribanks, C.9
McDonough, D.P.10
Nguyen, B.T.11
Norris, M.C.12
Sheehan, J.B.13
Shen, N.14
Stern, D.15
Stokowski, R.P.16
Thomas, D.J.17
Trulson, M.O.18
Vyas, K.R.19
Frazer, K.A.20
Fodor, S.P.21
Cox, D.R.22
more..
-
64
-
-
0025992157
-
Evidence for Dominant Transmission of Developmental Dyslexia
-
Pennington, B.F., Gilger, J., Pauls, D., Smith, S.A., Smith, S.D., & DeFries, J.C. (1991). Evidence for Dominant Transmission of Developmental Dyslexia. The Journal of the American Medical Association, 266, 1527-1534.
-
(1991)
The Journal of the American Medical Association
, vol.266
, pp. 1527-1534
-
-
Pennington, B.F.1
Gilger, J.2
Pauls, D.3
Smith, S.A.4
Smith, S.D.5
DeFries, J.C.6
-
65
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
-
Philippe, A., Martinez, M., Guilloud-Bataille, M., Gillberg, C., Rastam, M., Sponheim, E., Coleman, M., Zappella, M., Aschauer, H., Van Maldergem, L., Penet, C., Feingold, J., Brice, A., & Leboyer, M. (1999). Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Human Molecular Genetics, 8, 805-812.
-
(1999)
Human Molecular Genetics
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
Coleman, M.7
Zappella, M.8
Aschauer, H.9
Van Maldergem, L.10
Penet, C.11
Feingold, J.12
Brice, A.13
Leboyer, M.14
-
66
-
-
0030827556
-
A transmission disequilibrium test for quantitative trait loci
-
Rabinowitz, D. (1997). A transmission disequilibrium test for quantitative trait loci. Human Heredity, 47, 342-350.
-
(1997)
Human Heredity
, vol.47
, pp. 342-350
-
-
Rabinowitz, D.1
-
67
-
-
0034472038
-
Familial aggregation of dyslexia phenotypes
-
Raskind, W.H., Hsu, L., Berninger, V.W., Thomson, J.B., & Wijsman, E.M. (2000). Familial aggregation of dyslexia phenotypes. Behavioral Genetics, 30, 385-396.
-
(2000)
Behavioral Genetics
, vol.30
, pp. 385-396
-
-
Raskind, W.H.1
Hsu, L.2
Berninger, V.W.3
Thomson, J.B.4
Wijsman, E.M.5
-
68
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N., & Merikangas, K. (1996). The future of genetic studies of complex human diseases. Science, 273(5281), 1516-1517.
-
(1996)
Science
, vol.273
, Issue.5281
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
69
-
-
0029979336
-
Mapping quantitative trait loci with extreme discordant sib pairs: Sampling considerations
-
Risch, N.J., & Zhang, H. (1996). Mapping quantitative trait loci with extreme discordant sib pairs: Sampling considerations. American Journal of Human Genetics, 58, 836-843.
-
(1996)
American Journal of Human Genetics
, vol.58
, pp. 836-843
-
-
Risch, N.J.1
Zhang, H.2
-
70
-
-
84917326015
-
-
Computer program package available from the Department of Epidemiology and Biostatistics, Rammelkamp Center for Education and Research, MetroHealth Campus, Case Western Reserve University, Cleveland
-
S.A.G.E. (2001). Statistical Package for Genetic Epidemiology, S.A.G.E. 4.2. Computer program package available from the Department of Epidemiology and Biostatistics, Rammelkamp Center for Education and Research, MetroHealth Campus, Case Western Reserve University, Cleveland.
-
(2001)
Statistical Package for Genetic Epidemiology, S.A.G.E. 4.2
-
-
-
71
-
-
0033927466
-
Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data
-
Sham, P.C., Cherny, S.S., Purcell, S., & Hewitt, J.K. (2000). Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data. American Journal of Human Genetics, 66, 1616-1630.
-
(2000)
American Journal of Human Genetics
, vol.66
, pp. 1616-1630
-
-
Sham, P.C.1
Cherny, S.S.2
Purcell, S.3
Hewitt, J.K.4
-
72
-
-
0028909113
-
Monte Carlo tests for associations between disease and alleles at highly polymorphic loci
-
Sham, P.C., & Curtis, D. (1995). Monte Carlo tests for associations between disease and alleles at highly polymorphic loci. Annals of Human Genetics, 59, 97-105.
-
(1995)
Annals of Human Genetics
, vol.59
, pp. 97-105
-
-
Sham, P.C.1
Curtis, D.2
-
73
-
-
0036077215
-
Powerful regressionbased quantitative-trait linkage analysis of general pedigrees
-
Sham, P.C., Purcell, S., Cherny, S.S., & Abecasis, G.R. (2002). Powerful regressionbased quantitative-trait linkage analysis of general pedigrees. American Journal of Human Genetics, 72, 238-253.
-
(2002)
American Journal of Human Genetics
, vol.72
, pp. 238-253
-
-
Sham, P.C.1
Purcell, S.2
Cherny, S.S.3
Abecasis, G.R.4
-
74
-
-
0037371673
-
Fine mapping of autistic disorder to chromosome 15q11-ql3 by use of phenotypic subtypes
-
Shao, Y., Cuccaro, M.L., Hauser, E.R., Raiford, K.L., Menold, M.M., Wolpert, C.M., Ravan, S.A., Elston, L., Decena, K., Donnelly, S.L., Abramson, R.K., Wright, H.H., DeLong, G.R., Gilbert, J.R., & Pericak-Vance, M.A. (2003). Fine mapping of autistic disorder to chromosome 15q11-ql3 by use of phenotypic subtypes. American Journal of Human Genetics, 72, 539-548.
-
(2003)
American Journal of Human Genetics
, vol.72
, pp. 539-548
-
-
Shao, Y.1
Cuccaro, M.L.2
Hauser, E.R.3
Raiford, K.L.4
Menold, M.M.5
Wolpert, C.M.6
Ravan, S.A.7
Elston, L.8
Decena, K.9
Donnelly, S.L.10
Abramson, R.K.11
Wright, H.H.12
DeLong, G.R.13
Gilbert, J.R.14
Pericak-Vance, M.A.15
-
75
-
-
18244408330
-
A genomewide scan identifies two novel loci involved in specific language impairment
-
SLI-Consortium. (2002). A genomewide scan identifies two novel loci involved in specific language impairment. American Journal of Human Genetics, 70, 384-398.
-
(2002)
American Journal of Human Genetics
, vol.70
, pp. 384-398
-
-
-
76
-
-
0023722983
-
Autism and genetics: A decade of research
-
Smalley, S.L., Asarnow, R.F., & Spence, M.A. (1988). Autism and genetics: A decade of research. Archives of General Psychiatry, 45, 953-961.
-
(1988)
Archives of General Psychiatry
, vol.45
, pp. 953-961
-
-
Smalley, S.L.1
Asarnow, R.F.2
Spence, M.A.3
-
77
-
-
19044394761
-
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16pl3, in a region implicated in autism
-
Smalley, S.L., Kustanovich, V., Minassian, S.L., Stone, J.L., Ogdie, M.N., McGough, J.J., McCracken, J.T., MacPhie, I.L., Francks, C., Fisher, S.E., Cantor, R.M., Monaco, A.P., & Nelson, S.F. (2002). Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16pl3, in a region implicated in autism. American Journal of Human Genetics, 71, 959-963.
-
(2002)
American Journal of Human Genetics
, vol.71
, pp. 959-963
-
-
Smalley, S.L.1
Kustanovich, V.2
Minassian, S.L.3
Stone, J.L.4
Ogdie, M.N.5
McGough, J.J.6
McCracken, J.T.7
MacPhie, I.L.8
Francks, C.9
Fisher, S.E.10
Cantor, R.M.11
Monaco, A.P.12
Nelson, S.F.13
-
78
-
-
0006370411
-
Dyslexia and other language/learning disorders
-
D.L. Rimoin, J.M. Conner, & R. Pyeritz (Eds.), 4th ed, New York: Churchill Livingstone
-
Smith, S.D., Gilger, J.W., & Pennington, B.F. (2002). Dyslexia and other language/learning disorders. In D.L. Rimoin, J.M. Conner, & R. Pyeritz (Eds.), Emery and Rimoin's Principles and Practice of Medical Genetics (4th ed., pp. 2827-2865). New York: Churchill Livingstone.
-
(2002)
Emery and Rimoin's Principles and Practice of Medical Genetics
, pp. 2827-2865
-
-
Smith, S.D.1
Gilger, J.W.2
Pennington, B.F.3
-
79
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman, R.S., McGinnis, R.E., & Ewens, W.J. (1993). Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM). American Journal of Human Genetics, 52, 506-516.
-
(1993)
American Journal of Human Genetics
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
80
-
-
0036255811
-
Candidate-gene approaches for studying complex genetic traits: Practical considerations
-
Tabor, H.K., Risch, N.J., & Myers, R.M. (2002). Candidate-gene approaches for studying complex genetic traits: Practical considerations. Nature Reviews Genetics, 3, 1-7.
-
(2002)
Nature Reviews Genetics
, vol.3
, pp. 1-7
-
-
Tabor, H.K.1
Risch, N.J.2
Myers, R.M.3
-
81
-
-
0026494911
-
A haplotype-based "haplotype relative risk" approach to detecting allelic associations
-
Terwilliger, J.D., & Ott, J. (1992). A haplotype-based "haplotype relative risk" approach to detecting allelic associations. Human Heredity, 42, 337-346.
-
(1992)
Human Heredity
, vol.42
, pp. 337-346
-
-
Terwilliger, J.D.1
Ott, J.2
-
82
-
-
0028067197
-
Identifying complex disease genes: Progress and paradigms
-
Thomson, G. (1994). Identifying complex disease genes: Progress and paradigms. Nature Genetics, 8, 108-110.
-
(1994)
Nature Genetics
, vol.8
, pp. 108-110
-
-
Thomson, G.1
-
83
-
-
0024507073
-
Familial concentration of developmental language impairment
-
Tomblin, J.B. (1989). Familial concentration of developmental language impairment. Journal of Speech and Hearing Disorders, 54, 287-295.
-
(1989)
Journal of Speech and Hearing Disorders
, vol.54
, pp. 287-295
-
-
Tomblin, J.B.1
-
84
-
-
0035185279
-
The replication requirement
-
Vieland, V.J. (2001). The replication requirement. Nature Genetics, 29, 244-245.
-
(2001)
Nature Genetics
, vol.29
, pp. 244-245
-
-
Vieland, V.J.1
-
85
-
-
0036128126
-
HLODs, trait models, and ascertainment:Implications of admixture for parameter estimation and linkage detection
-
Vieland, V.J., & Logue, M. (2002). HLODs, trait models, and ascertainment:Implications of admixture for parameter estimation and linkage detection. Human Heredity, 53, 23-35.
-
(2002)
Human Heredity
, vol.53
, pp. 23-35
-
-
Vieland, V.J.1
Logue, M.2
-
86
-
-
0035827826
-
Evidence supporting WNT2 as an autism susceptibility gene
-
Wassink, T.H., Piven, J., Vieland, V.J., Huang, J., Swiderski, R.E., Pietila, J., Braun, T., Beck, G., Folstein, S.E., Haines, J.L., & Sheffield, V.C. (2001). Evidence supporting WNT2 as an autism susceptibility gene, American Journal of Medical Genetics, 105, 406-413.
-
(2001)
American Journal of Medical Genetics
, vol.105
, pp. 406-413
-
-
Wassink, T.H.1
Piven, J.2
Vieland, V.J.3
Huang, J.4
Swiderski, R.E.5
Pietila, J.6
Braun, T.7
Beck, G.8
Folstein, S.E.9
Haines, J.L.10
Sheffield, V.C.11
-
87
-
-
0037041301
-
Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for ADHD
-
Willcutt, E.G., Pennington, B.F., Smith, S.D., Cardon, L.R., Gayán, J., Knopik, V.S., Olson, R.K., & DeFries, J.C. (2002). Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for ADHD. American Journal of Medical Genetics, 114, 260-268.
-
(2002)
American Journal of Medical Genetics
, vol.114
, pp. 260-268
-
-
Willcutt, E.G.1
Pennington, B.F.2
Smith, S.D.3
Cardon, L.R.4
Gayán, J.5
Knopik, V.S.6
Olson, R.K.7
DeFries, J.C.8
-
88
-
-
0025048029
-
On the asymptotic behavior of the estimate of the recombination fraction under the null hypothesis of no linkage with the model is misspecified
-
Williamson, J.A., & Amos, C.I. (1990). On the asymptotic behavior of the estimate of the recombination fraction under the null hypothesis of no linkage with the model is misspecified. Genetics of Epidemiology, 7, 309-318.
-
(1990)
Genetics of Epidemiology
, vol.7
, pp. 309-318
-
-
Williamson, J.A.1
Amos, C.I.2
-
89
-
-
0036553050
-
The social deficits of the oxytocin knockout mouse
-
Winslow, J.T., & Insel, T.R. (2002). The social deficits of the oxytocin knockout mouse. Neuropeptides, 36, 221-229.
-
(2002)
Neuropeptides
, vol.36
, pp. 221-229
-
-
Winslow, J.T.1
Insel, T.R.2
-
90
-
-
0031018305
-
The phenotypic difference discards sib-pair QTL linkage information
-
Wright, F.A. (1997). The phenotypic difference discards sib-pair QTL linkage information. American Journal of Human Genetics, 60, 740-742.
-
(1997)
American Journal of Human Genetics
, vol.60
, pp. 740-742
-
-
Wright, F.A.1
-
92
-
-
0037188541
-
A dynamic programming algorithm for haplotype block partitioning
-
Zhang, K., Deng, M., Chen, T., Waterman, M.S., & Sun, F. (2002). A dynamic programming algorithm for haplotype block partitioning. Proceedings of the National Academy of Science USA, 99, 7335-7339.
-
(2002)
Proceedings of the National Academy of Science USA
, vol.99
, pp. 7335-7339
-
-
Zhang, K.1
Deng, M.2
Chen, T.3
Waterman, M.S.4
Sun, F.5
|