-
1
-
-
77957735529
-
A genome-wide scan for common alleles affecting risk for autism
-
Anney, R., Klei, L., Pinto, D., Regan, R., Conroy, J., Magalhaes, T. R., Cook, E. H. (2010). A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics, 19, 4072-4082.
-
(2010)
Human Molecular Genetics
, vol.19
, pp. 4072-4082
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Regan, R.4
Conroy, J.5
Magalhaes, T.R.6
Cook, E.H.7
-
2
-
-
79957658264
-
Genetic analysis of complex traits in the emerging Collaborative Cross
-
Aylor, D. L., Valdar, W., Foulds-Mathes, W., Buus, R. J., Verdugo, R. A., Baric, R. S., Churchill, G. A. (2011). Genetic analysis of complex traits in the emerging Collaborative Cross. Genome Research, 21, 1213-1222.
-
(2011)
Genome Research
, vol.21
, pp. 1213-1222
-
-
Aylor, D.L.1
Valdar, W.2
Foulds-Mathes, W.3
Buus, R.J.4
Verdugo, R.A.5
Baric, R.S.6
Churchill, G.A.7
-
3
-
-
0035167107
-
The replicability of QTLs for murine alcohol preference drinking behavior across eight independent studies
-
Belknap, J. K., & Atkins, A. L. (2001). The replicability of QTLs for murine alcohol preference drinking behavior across eight independent studies. Mammalian Genome, 12, 893-899.
-
(2001)
Mammalian Genome
, vol.12
, pp. 893-899
-
-
Belknap, J.K.1
Atkins, A.L.2
-
4
-
-
77957940722
-
The NIH Roadmap Epigenomics Mapping Consortium
-
Bernstein, B. E., Stamatoyannopoulos, J. A., Costello, J. F., Ren, B., Milosavljevic, A., Meissner, A., Thomson, J. A. (2010). The NIH Roadmap Epigenomics Mapping Consortium. Nature Biotechnology, 28, 1045-1048.
-
(2010)
Nature Biotechnology
, vol.28
, pp. 1045-1048
-
-
Bernstein, B.E.1
Stamatoyannopoulos, J.A.2
Costello, J.F.3
Ren, B.4
Milosavljevic, A.5
Meissner, A.6
Thomson, J.A.7
-
5
-
-
84861921431
-
The evolution of intelligence
-
Bitterman, M. E. (1965a). The evolution of intelligence. Scientific American, 229, 24-37.
-
(1965)
Scientific American
, vol.229
, pp. 24-37
-
-
Bitterman, M.E.1
-
6
-
-
0000290919
-
Phyletic differences in learning
-
Bitterman, M. E. (1965b). Phyletic differences in learning. American Psychologist, 20, 396-410.
-
(1965)
American Psychologist
, vol.20
, pp. 396-410
-
-
Bitterman, M.E.1
-
7
-
-
0034068758
-
List of transgenic and knockout mice: Behavioral profiles
-
Bolivar, V., Cook, M., & Flaherty, L. (2000). List of transgenic and knockout mice: Behavioral profiles. Mammalian Genome, 11, 260-274.
-
(2000)
Mammalian Genome
, vol.11
, pp. 260-274
-
-
Bolivar, V.1
Cook, M.2
Flaherty, L.3
-
8
-
-
0028359950
-
A case-control family history study of autism
-
Bolton, P., Macdonald, H., Pickles, A., Rios, P., Goode, S., Crowson, M., Rutter, M. (1994). A case-control family history study of autism. Journal of Child Psychololgy and Psychiatry, 35, 877-900.
-
(1994)
Journal of Child Psychololgy and Psychiatry
, vol.35
, pp. 877-900
-
-
Bolton, P.1
Macdonald, H.2
Pickles, A.3
Rios, P.4
Goode, S.5
Crowson, M.6
Rutter, M.7
-
9
-
-
33645754065
-
Cognitive traits link to human chromosomal regions
-
Buyske, S., Bates, M. E., Gharani, N., Matise, T. C., Tischfield, J. A., & Manowitz, P. (2006). Cognitive traits link to human chromosomal regions. Behavior Genetics, 36, 65-76.
-
(2006)
Behavior Genetics
, vol.36
, pp. 65-76
-
-
Buyske, S.1
Bates, M.E.2
Gharani, N.3
Matise, T.C.4
Tischfield, J.A.5
Manowitz, P.6
-
10
-
-
84871911113
-
New autism rule will trim many, a study suggests
-
Carey, B. (2012). New autism rule will trim many, a study suggests. New York Times, CLXI, A1-A3.
-
(2012)
New York Times
, vol.161
-
-
Carey, B.1
-
11
-
-
84861451528
-
Most reported genetics associations with general intelligence are probably false positives
-
press
-
Chabris, C. F., Hebert, B. M., Benjamin, D. J., Beauchamp, J. P., Cesarini, D., van der Loos, M. J. H. M., Laibson, D. (2012). Most reported genetics associations with general intelligence are probably false positives. Psychological Science, in press.
-
(2012)
Psychological Science
-
-
Chabris, C.F.1
Hebert, B.M.2
Benjamin, D.J.3
Beauchamp, J.P.4
Cesarini, D.5
van der Loos, M.J.H.M.6
Laibson, D.7
-
13
-
-
0039172262
-
A qunatitative trait locus associated with cognitive ability in children
-
Chorney, M. J., Chorney, K., Seese, N., Owen, M. J., Daniels, J., McGuffin, P., Plomin, R. (1998). A qunatitative trait locus associated with cognitive ability in children. Psychological Science, 9, 159-166.
-
(1998)
Psychological Science
, vol.9
, pp. 159-166
-
-
Chorney, M.J.1
Chorney, K.2
Seese, N.3
Owen, M.J.4
Daniels, J.5
McGuffin, P.6
Plomin, R.7
-
15
-
-
80053132878
-
Genome-wide association studies establish that human intelligence is highly heritable and polygenic
-
Davies, G., Tenesa, A., Payton, A., Yang, J., Harris, S. E., Liewald, D., Deary, I. J. (2011). Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Molecular Psychiatry, 16, 996-1005.
-
(2011)
Molecular Psychiatry
, vol.16
, pp. 996-1005
-
-
Davies, G.1
Tenesa, A.2
Payton, A.3
Yang, J.4
Harris, S.E.5
Liewald, D.6
Deary, I.J.7
-
16
-
-
84857356586
-
Meta-analysis of genome-wide association studies for personality
-
de Moor, M. H., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J., Toshiko, T., Boomsma, D. I. (2012). Meta-analysis of genome-wide association studies for personality. Molecular Psychiatry, 17, 337-349.
-
(2012)
Molecular Psychiatry
, vol.17
, pp. 337-349
-
-
de Moor, M.H.1
Costa, P.T.2
Terracciano, A.3
Krueger, R.F.4
de Geus, E.J.5
Toshiko, T.6
Boomsma, D.I.7
-
17
-
-
0030855087
-
The heritability of IQ
-
Devlin, B., Daniels, M., & Roeder, K. (1997). The heritability of IQ. Nature, 388, 468-471.
-
(1997)
Nature
, vol.388
, pp. 468-471
-
-
Devlin, B.1
Daniels, M.2
Roeder, K.3
-
18
-
-
33645785889
-
Linkage analyses of IQ in the collaborative study on the genetics of alcoholism (COGA) sample
-
Dick, D. M., Aliev, F., Bierut, L., Goate, A., Rice, J., Hinrichs, A., Hesselbrock, V. (2006). Linkage analyses of IQ in the collaborative study on the genetics of alcoholism (COGA) sample. Behavior Genetics, 36, 77-86.
-
(2006)
Behavior Genetics
, vol.36
, pp. 77-86
-
-
Dick, D.M.1
Aliev, F.2
Bierut, L.3
Goate, A.4
Rice, J.5
Hinrichs, A.6
Hesselbrock, V.7
-
19
-
-
33744469026
-
Genetics of intelligence
-
Dreary, I. J., Spinath, F. M., & Bates, T. C. (2006). Genetics of intelligence. European Journal of Human Genetics, 14, 690-700.
-
(2006)
European Journal of Human Genetics
, vol.14
, pp. 690-700
-
-
Dreary, I.J.1
Spinath, F.M.2
Bates, T.C.3
-
20
-
-
76749141396
-
A comparison of selected quantitative trait loci associated with alcohol use phenotypes in humans and mouse models
-
Ehlers, C. L., Walter, N. A., Dick, D. M., Buck, K. J., & Crabbe, J. C. (2010). A comparison of selected quantitative trait loci associated with alcohol use phenotypes in humans and mouse models. Addiction Biology, 15, 185-199.
-
(2010)
Addiction Biology
, vol.15
, pp. 185-199
-
-
Ehlers, C.L.1
Walter, N.A.2
Dick, D.M.3
Buck, K.J.4
Crabbe, J.C.5
-
21
-
-
79951562124
-
Behavioral profiles of mouse models for autism spectrum disorders
-
Ey, E., Leblond, C. S., & Bourgeron, T. (2011). Behavioral profiles of mouse models for autism spectrum disorders. Autism Research, 4, 5-16.
-
(2011)
Autism Research
, vol.4
, pp. 5-16
-
-
Ey, E.1
Leblond, C.S.2
Bourgeron, T.3
-
23
-
-
0017337957
-
Genetic influences and infantile autism
-
Folstein, S. & Rutter, M. (1977). Genetic influences and infantile autism. Nature, 265, 726-728.
-
(1977)
Nature
, vol.265
, pp. 726-728
-
-
Folstein, S.1
Rutter, M.2
-
24
-
-
79959501145
-
Soluble tau species, not neurofibrillary aggregates, disrupt neural system integration in a tau transgenic model
-
Fox, L. M., William, C. M., Adamowicz, D. H., Pitstick, R., Carlson, G. A., Spires-Jones, T. L., & Hyman, B. T. (2011). Soluble tau species, not neurofibrillary aggregates, disrupt neural system integration in a tau transgenic model. Journal of Neuropathology and Experimental Neurology, 70, 588-595.
-
(2011)
Journal of Neuropathology and Experimental Neurology
, vol.70
, pp. 588-595
-
-
Fox, L.M.1
William, C.M.2
Adamowicz, D.H.3
Pitstick, R.4
Carlson, G.A.5
Spires-Jones, T.L.6
Hyman, B.T.7
-
26
-
-
77049105158
-
Beyond genome-wide association studies: Genetic heterogeneity and individual predisposition to cancer
-
Galvan, A., Ioannidis, J. P., & Dragani, T. A. (2010). Beyond genome-wide association studies: Genetic heterogeneity and individual predisposition to cancer. Trends in Genetics, 26, 132-141.
-
(2010)
Trends in Genetics
, vol.26
, pp. 132-141
-
-
Galvan, A.1
Ioannidis, J.P.2
Dragani, T.A.3
-
27
-
-
80051920294
-
Genetics of autism spectrum disorders
-
Geschwind, D. H. (2011). Genetics of autism spectrum disorders. Trends in Cognitive Science, 15, 409-416.
-
(2011)
Trends in Cognitive Science
, vol.15
, pp. 409-416
-
-
Geschwind, D.H.1
-
28
-
-
79958035893
-
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
-
Gilman, S. R., Iossifov, I., Levy, D., Ronemus, M., Wigler, M., & Vitkup, D. (2011). Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron, 70, 898-907.
-
(2011)
Neuron
, vol.70
, pp. 898-907
-
-
Gilman, S.R.1
Iossifov, I.2
Levy, D.3
Ronemus, M.4
Wigler, M.5
Vitkup, D.6
-
29
-
-
0000073196
-
Some effects of conditioning on social dominance and subordination in inbred strains of mice
-
Ginsburg, B., & Allee, W. C. (1942). Some effects of conditioning on social dominance and subordination in inbred strains of mice. Physiological Zoology, 15, 485-506.
-
(1942)
Physiological Zoology
, vol.15
, pp. 485-506
-
-
Ginsburg, B.1
Allee, W.C.2
-
32
-
-
2642549080
-
Neurobiology of intelligence: Science and ethics
-
Gray, J. R., & Thompson, P. M. (2004). Neurobiology of intelligence: Science and ethics. Nature Reviews in Neuroscience, 5, 471-482.
-
(2004)
Nature Reviews in Neuroscience
, vol.5
, pp. 471-482
-
-
Gray, J.R.1
Thompson, P.M.2
-
33
-
-
77249138258
-
A review of current large-scale mouse knockout efforts
-
Guan, C., Ye, C., Yang, X., & Gao, J. (2010). A review of current large-scale mouse knockout efforts. Genesis, 48, 73-85.
-
(2010)
Genesis
, vol.48
, pp. 73-85
-
-
Guan, C.1
Ye, C.2
Yang, X.3
Gao, J.4
-
34
-
-
65949104586
-
Genomewide association studies and human disease
-
Hardy, J., & Singleton, A. (2009). Genomewide association studies and human disease. New England Journal of Medicine, 360, 1759-1768.
-
(2009)
New England Journal of Medicine
, vol.360
, pp. 1759-1768
-
-
Hardy, J.1
Singleton, A.2
-
36
-
-
0036835069
-
A quantitative trait locus not associated with cognitive ability in children: A failure to replicate
-
Hill, L., Chorney, M. J., Lubinski, D., Thompson, L. A., & Plomin, R. (2002). A quantitative trait locus not associated with cognitive ability in children: A failure to replicate. Psychological Science, 13, 561-562.
-
(2002)
Psychological Science
, vol.13
, pp. 561-562
-
-
Hill, L.1
Chorney, M.J.2
Lubinski, D.3
Thompson, L.A.4
Plomin, R.5
-
38
-
-
79952504917
-
The meaning of the Human Genome Project for neuropsychiatric disorders
-
Hyman, S. E. (2011). The meaning of the Human Genome Project for neuropsychiatric disorders. Science, 331, 1026.
-
(2011)
Science
, vol.331
, pp. 1026
-
-
Hyman, S.E.1
-
39
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium.
-
International Schizophrenia Consortium. (2008). Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature, 455, 237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
40
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
International Schizophrenia Consortium.
-
International Schizophrenia Consortium. (2009). Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature, 460, 748-752.
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
-
41
-
-
33846563409
-
Why most published research findings are false
-
Ioannidis, J. P. (2005). Why most published research findings are false. PLoS Medicine, 2, e124.
-
(2005)
PLoS Medicine
, vol.2
-
-
Ioannidis, J.P.1
-
42
-
-
0042181578
-
How much can be boost IQ and scholastic achievement
-
Reprint series no. 2)
-
Jensen, A. (1969). How much can be boost IQ and scholastic achievement? Harvard Educational Review, 39, 1-123 (Reprint series no. 2).
-
(1969)
Harvard Educational Review
, vol.39
, pp. 1-123
-
-
Jensen, A.1
-
44
-
-
84971720993
-
How does one apply statistical analysis to our understanding of the development of human relationships
-
Kempthorne, O. (1990). How does one apply statistical analysis to our understanding of the development of human relationships? Behavioral and Brain Sciences, 13, 138-139.
-
(1990)
Behavioral and Brain Sciences
, vol.13
, pp. 138-139
-
-
Kempthorne, O.1
-
45
-
-
84855631913
-
The single nucleotide polymorphism database (dbSNP) of nucelotide sequence variation.
-
J. McEntyre & J. Ostell (Eds.), 2009 ed. Bethesda, MD: National Center for Biotechnology Information (US)
-
Kitts, A., & Sherry, S. (2002). The single nucleotide polymorphism database (dbSNP) of nucelotide sequence variation. In J. McEntyre & J. Ostell (Eds.), The NCBI Handbook (Internet) (2009 ed., pp. 1-17). Bethesda, MD: National Center for Biotechnology Information (US).
-
(2002)
The NCBI Handbook (Internet)
, pp. 1-17
-
-
Kitts, A.1
Sherry, S.2
-
46
-
-
84871796966
-
Path is found for the spread of Alzheimer's
-
Kolata, G. (2012). Path is found for the spread of Alzheimer's. New York Times, A1-A13.
-
(2012)
New York Times
-
-
Kolata, G.1
-
47
-
-
79951481957
-
Initial impact of the sequencing of the human genome
-
Lander, E. S. (2011). Initial impact of the sequencing of the human genome. Nature, 470, 187-197.
-
(2011)
Nature
, vol.470
, pp. 187-197
-
-
Lander, E.S.1
-
48
-
-
79958032110
-
Rare de novo and transmitted copy-number variation in autistic spectrum disorders
-
Levy, D., Ronemus, M., Yamrom, B., Lee, Y. H., Leotta, A., Kendall, J., Wigler, M. (2011). Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron, 70, 886-897.
-
(2011)
Neuron
, vol.70
, pp. 886-897
-
-
Levy, D.1
Ronemus, M.2
Yamrom, B.3
Lee, Y.H.4
Leotta, A.5
Kendall, J.6
Wigler, M.7
-
49
-
-
33645768819
-
Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q
-
Luciano, M., Wright, M. J., Duffy, D. L., Wainwright, M. A., Zhu, G., Evans, D. M., Martin, N. G. (2006). Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q. Behavior Genetics, 36, 45-55.
-
(2006)
Behavior Genetics
, vol.36
, pp. 45-55
-
-
Luciano, M.1
Wright, M.J.2
Duffy, D.L.3
Wainwright, M.A.4
Zhu, G.5
Evans, D.M.6
Martin, N.G.7
-
50
-
-
84155191408
-
High frequencies of de novo CNVs in bipolar disorder and schizophrenia
-
Malhotra, D., McCarthy, S., Michaelson, J. J., Vacic, V., Burdick, K. E., Yoon, S., Sebat, J. (2011). High frequencies of de novo CNVs in bipolar disorder and schizophrenia. Neuron, 72, 951-963.
-
(2011)
Neuron
, vol.72
, pp. 951-963
-
-
Malhotra, D.1
McCarthy, S.2
Michaelson, J.J.3
Vacic, V.4
Burdick, K.E.5
Yoon, S.6
Sebat, J.7
-
51
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
-
Mangiarini, L., Sathasivam, K., Seller, M., Cozens, B., Harper, A., Hetherington, C., Bates, G. P. (1996). Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell, 87, 493-506.
-
(1996)
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
Sathasivam, K.2
Seller, M.3
Cozens, B.4
Harper, A.5
Hetherington, C.6
Bates, G.P.7
-
52
-
-
77951702343
-
Genetic heterogeneity in human disease
-
McClellan, J., & King, M. C. (2010). Genetic heterogeneity in human disease. Cell, 141, 210-217.
-
(2010)
Cell
, vol.141
, pp. 210-217
-
-
McClellan, J.1
King, M.C.2
-
53
-
-
83755202241
-
Autism candidate genes via mouse phenomics
-
Meehan, T. F., Carr, C. J., Jay, J. J., Bult, C. J., Chesler, E. J., & Blake, J. A. (2011). Autism candidate genes via mouse phenomics. Journal of Biomedical Informatics, 44(Suppl. 1), S5-S11.
-
(2011)
Journal of Biomedical Informatics
, vol.44
, Issue.SUPPL. 1
-
-
Meehan, T.F.1
Carr, C.J.2
Jay, J.J.3
Bult, C.J.4
Chesler, E.J.5
Blake, J.A.6
-
54
-
-
68249155312
-
Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models
-
Menalled, L., El-Khodor, B. F., Patry, M., Suárez-Fariñas, M., Orenstein, S. J., Zahasky, B., Brunner, D. (2009). Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models. Neurobiology of Disease, 35, 319-336.
-
(2009)
Neurobiology of Disease
, vol.35
, pp. 319-336
-
-
Menalled, L.1
El-Khodor, B.F.2
Patry, M.3
Suárez-Fariñas, M.4
Orenstein, S.J.5
Zahasky, B.6
Brunner, D.7
-
55
-
-
77955114844
-
Is pharma running out of brainy ideas
-
Miller, G. (2010). Is pharma running out of brainy ideas? Science, 329, 502-504.
-
(2010)
Science
, vol.329
, pp. 502-504
-
-
Miller, G.1
-
56
-
-
77956143953
-
Identifying quantitative trait loci (QTLs) and genes (QTGs) for alcohol-related phenotypes in mice
-
Milner, L. C., & Buck, K. J. (2010). Identifying quantitative trait loci (QTLs) and genes (QTGs) for alcohol-related phenotypes in mice. International Review of Neurobiology, 91, 173-204.
-
(2010)
International Review of Neurobiology
, vol.91
, pp. 173-204
-
-
Milner, L.C.1
Buck, K.J.2
-
57
-
-
33845284824
-
Mouse behavioral tasks relevant to autism: Phenotypes of 10 inbred strains
-
Moy, S. S., Nadler, J. J., Young, N. B., Perez, A., Holloway, L. P., Barbaro, R. P., Crawley, J. N. (2007). Mouse behavioral tasks relevant to autism: Phenotypes of 10 inbred strains. Behavioural Brain Research, 176, 4-20.
-
(2007)
Behavioural Brain Research
, vol.176
, pp. 4-20
-
-
Moy, S.S.1
Nadler, J.J.2
Young, N.B.3
Perez, A.4
Holloway, L.P.5
Barbaro, R.P.6
Crawley, J.N.7
-
58
-
-
57149090077
-
Dissection of a QTL hotspot on mouse distal chromosome 1 that modulates neurobehavioral phenotypes and gene expression
-
Mozhui, K., Ciobanu, D. C., Schikorski, T., Wang, X., Lu, L., & Williams, R. W. (2008). Dissection of a QTL hotspot on mouse distal chromosome 1 that modulates neurobehavioral phenotypes and gene expression. PLoS Genetics, 4, e1000260.
-
(2008)
PLoS Genetics
, vol.4
-
-
Mozhui, K.1
Ciobanu, D.C.2
Schikorski, T.3
Wang, X.4
Lu, L.5
Williams, R.W.6
-
59
-
-
79954946162
-
Complex traits: Mice line up for success
-
Muers, M. (2011). Complex traits: Mice line up for success. Nature Reviews in Genetics, 12, 298.
-
(2011)
Nature Reviews in Genetics
, vol.12
, pp. 298
-
-
Muers, M.1
-
60
-
-
77958566761
-
Phenothiazine-mediated rescue of cognition in tau transgenic mice requires neuroprotection and reduced soluble tau burden
-
O'Leary, J. C., 3rd, Li, Q., Marinec, P., Blair, L. J., Congdon, E. E., Johnson, A. G., Dickey, C. A. (2010). Phenothiazine-mediated rescue of cognition in tau transgenic mice requires neuroprotection and reduced soluble tau burden. Molecular Neurodegeneration, 5, 45.
-
(2010)
Molecular Neurodegeneration
, vol.5
, pp. 45
-
-
O'Leary 3rd, J.C.1
Li, Q.2
Marinec, P.3
Blair, L.J.4
Congdon, E.E.5
Johnson, A.G.6
Dickey, C.A.7
-
61
-
-
33646203242
-
Investigating cognitive genetics and its implications for the treatment of cognitive deficit
-
Payton, A. (2006). Investigating cognitive genetics and its implications for the treatment of cognitive deficit. Genes, Brain and Behavior, 5(Suppl. 1), 44-53.
-
(2006)
Genes, Brain and Behavior
, vol.5
, Issue.SUPPL. 1
, pp. 44-53
-
-
Payton, A.1
-
62
-
-
72049114431
-
The impact of genetic research on our understanding of normal cognitive ageing: 1995 to 2009
-
Payton, A. (2009). The impact of genetic research on our understanding of normal cognitive ageing: 1995 to 2009. Neuropsychological Review, 19, 451-477.
-
(2009)
Neuropsychological Review
, vol.19
, pp. 451-477
-
-
Payton, A.1
-
63
-
-
12244267952
-
Cathepsin D exon 2 polymorphism associated with general intelligence in a healthy older population
-
Payton, A., Holland, F., Diggle, P., Rabbitt, P., Horan, M., Davidson, Y., Pendleton, N. (2003). Cathepsin D exon 2 polymorphism associated with general intelligence in a healthy older population. Molecular Psychiatry, 8, 14-18.
-
(2003)
Molecular Psychiatry
, vol.8
, pp. 14-18
-
-
Payton, A.1
Holland, F.2
Diggle, P.3
Rabbitt, P.4
Horan, M.5
Davidson, Y.6
Pendleton, N.7
-
64
-
-
77949268283
-
A method for mapping intralocus interactions influencing excessive alcohol drinking
-
Phillips, T. J., Reed, C., Burkhart-Kasch, S., Li, N., Hitzemann, R., Yu, C. H., Belknap, J. K. (2010). A method for mapping intralocus interactions influencing excessive alcohol drinking. Mammalian Genome, 21, 39-51.
-
(2010)
Mammalian Genome
, vol.21
, pp. 39-51
-
-
Phillips, T.J.1
Reed, C.2
Burkhart-Kasch, S.3
Li, N.4
Hitzemann, R.5
Yu, C.H.6
Belknap, J.K.7
-
65
-
-
0031722020
-
Using knockout and transgenic mice to study neurophysiology and behavior
-
Picciotto, M. R., & Wickman, K. (1998). Using knockout and transgenic mice to study neurophysiology and behavior. Physiological Review, 78, 1131-1163.
-
(1998)
Physiological Review
, vol.78
, pp. 1131-1163
-
-
Picciotto, M.R.1
Wickman, K.2
-
66
-
-
33750403168
-
The quest for quantitative trait loci associated with intelligence
-
Plomin, R., Kennedy, J. K. J., & Craig, I. W. (2006). The quest for quantitative trait loci associated with intelligence. Intelligence, 34, 513-526.
-
(2006)
Intelligence
, vol.34
, pp. 513-526
-
-
Plomin, R.1
Kennedy, J.K.J.2
Craig, I.W.3
-
68
-
-
22544482638
-
A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p
-
Posthuma, D., Luciano, M., Geus, E. J., Wright, M. J., Slagboom, P. E., Montgomery, G. W., Martin, N. G. (2005). A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p. American Journal of Human Genetics, 77, 318-326.
-
(2005)
American Journal of Human Genetics
, vol.77
, pp. 318-326
-
-
Posthuma, D.1
Luciano, M.2
Geus, E.J.3
Wright, M.J.4
Slagboom, P.E.5
Montgomery, G.W.6
Martin, N.G.7
-
69
-
-
0028838676
-
Contribution of the FMR1 gene mutation to human intellectual dysfunction
-
Reiss, A. L., Freund, L. S., Baumgardner, T. L., Abrams, M. T., & Denckla, M. B. (1995). Contribution of the FMR1 gene mutation to human intellectual dysfunction. Nature Genetics, 11, 331-334.
-
(1995)
Nature Genetics
, vol.11
, pp. 331-334
-
-
Reiss, A.L.1
Freund, L.S.2
Baumgardner, T.L.3
Abrams, M.T.4
Denckla, M.B.5
-
70
-
-
79551711846
-
The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 subjects
-
Rizzi, T. S., Arias-Vasquez, A., Rommelse, N., Kuntsi, J., Anney, R., Asherson, P., Posthuma, D. (2011). The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4, 963 subjects. American Journal of Medical Genetics. B Neuropsychiatric Genetics, 156, 145-157.
-
(2011)
American Journal of Medical Genetics. B Neuropsychiatric Genetics
, vol.156
, pp. 145-157
-
-
Rizzi, T.S.1
Arias-Vasquez, A.2
Rommelse, N.3
Kuntsi, J.4
Anney, R.5
Asherson, P.6
Posthuma, D.7
-
71
-
-
79954603776
-
A systems genetic analysis of alcohol drinking by mice, rats and men: Influence of brain GABAergic transmission
-
Saba, L. M., Bennett, B., Hoffman, P. L., Barcomb, K., Ishii, T., Kechris, K., & Tabakoff, B. (2011). A systems genetic analysis of alcohol drinking by mice, rats and men: Influence of brain GABAergic transmission. Neuropharmacology, 60, 1269-1280.
-
(2011)
Neuropharmacology
, vol.60
, pp. 1269-1280
-
-
Saba, L.M.1
Bennett, B.2
Hoffman, P.L.3
Barcomb, K.4
Ishii, T.5
Kechris, K.6
Tabakoff, B.7
-
72
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
-
Sanders, S. J., Ercan-Sencicek, A. G., Hus, V., Luo, R., Murtha, M. T., Moreno-De-Luca, D., State, M. W. (2011). Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron, 70, 863-885.
-
(2011)
Neuron
, vol.70
, pp. 863-885
-
-
Sanders, S.J.1
Ercan-Sencicek, A.G.2
Hus, V.3
Luo, R.4
Murtha, M.T.5
Moreno-De-Luca, D.6
State, M.W.7
-
73
-
-
0002157342
-
The concept of development in comparative psychology.
-
D. B. Harris (Ed.), Minneapolis: University of Minnesota Press
-
Schneirla, T. C. (1957). The concept of development in comparative psychology. In D. B. Harris (Ed.), The concept of development. Minneapolis: University of Minnesota Press.
-
(1957)
The concept of development
-
-
Schneirla, T.C.1
-
74
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Wigler, M. (2007). Strong association of de novo copy number mutations with autism. Science, 316, 445-449.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
Wigler, M.7
-
75
-
-
70449732249
-
Rare structural variants in schizophrenia: One disorder, multiple mutations; one mutation, multiple disorders
-
Sebat, J., Levy, D. L., & McCarthy, S. E. (2009). Rare structural variants in schizophrenia: One disorder, multiple mutations; one mutation, multiple disorders. Trends in Genetics, 25, 528-535.
-
(2009)
Trends in Genetics
, vol.25
, pp. 528-535
-
-
Sebat, J.1
Levy, D.L.2
McCarthy, S.E.3
-
76
-
-
68449096727
-
Common variants on chromosome 6p22.1 are associated with schizophrenia
-
Shi, J., Levinson, D. F., Duan, J., Sanders, A. R., Zheng, Y., Pe'er, I., Gejman, P. V. (2009). Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature, 460, 753-757.
-
(2009)
Nature
, vol.460
, pp. 753-757
-
-
Shi, J.1
Levinson, D.F.2
Duan, J.3
Sanders, A.R.4
Zheng, Y.5
Pe'er, I.6
Gejman, P.V.7
-
77
-
-
77953800799
-
Behavioural phenotyping assays for mouse models of autism
-
Silverman, J. L., Yang, M., Lord, C., & Crawley, J. N. (2010). Behavioural phenotyping assays for mouse models of autism. Nature Reviews in Neuroscience, 11, 490-502.
-
(2010)
Nature Reviews in Neuroscience
, vol.11
, pp. 490-502
-
-
Silverman, J.L.1
Yang, M.2
Lord, C.3
Crawley, J.N.4
-
78
-
-
11144355685
-
Genetic dissection of complex traits with chromosome substitution strains of mice
-
Singer, J. B., Hill, A. E., Burrage, L. C., Olszens, K. R., Song, J., Justice, M., Nadeau, J. H. (2004). Genetic dissection of complex traits with chromosome substitution strains of mice. Science, 304, 445-448.
-
(2004)
Science
, vol.304
, pp. 445-448
-
-
Singer, J.B.1
Hill, A.E.2
Burrage, L.C.3
Olszens, K.R.4
Song, J.5
Justice, M.6
Nadeau, J.H.7
-
79
-
-
57749170986
-
Copy number variation and schizophrenia
-
St. Clair, D. (2009). Copy number variation and schizophrenia. Schizophrenia Bulletin, 35, 9-12.
-
(2009)
Schizophrenia Bulletin
, vol.35
, pp. 9-12
-
-
St Clair, D.1
-
80
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson, H., Ophoff, R. A., Steinberg, S., Andreassen, O. A., Cichon, S., Rujescu, D., Collier, D. A. (2009). Common variants conferring risk of schizophrenia. Nature, 460, 744-747.
-
(2009)
Nature
, vol.460
, pp. 744-747
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
Andreassen, O.A.4
Cichon, S.5
Rujescu, D.6
Collier, D.A.7
-
81
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson, H., Rujescu, D., Cichon, S., Pietilainen, O. P., Ingason, A., Steinberg, S., Stefansson, K. (2008). Large recurrent microdeletions associated with schizophrenia. Nature, 455, 232-236.
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietilainen, O.P.4
Ingason, A.5
Steinberg, S.6
Stefansson, K.7
-
82
-
-
0028245444
-
Forward and reverse genetic approaches to behavior in the mouse
-
Takahashi, J. S., Pinto, L. H., & Vitaterna, M. H. (1994). Forward and reverse genetic approaches to behavior in the mouse. Science, 264, 1724-1733.
-
(1994)
Science
, vol.264
, pp. 1724-1733
-
-
Takahashi, J.S.1
Pinto, L.H.2
Vitaterna, M.H.3
-
83
-
-
0000148657
-
The inheritance of behavior: Behavioral differences in fifteen mouse strains
-
Thompson, W. R. (1953). The inheritance of behavior: Behavioral differences in fifteen mouse strains. Canadian Journal of Psychology, 7, 145-155.
-
(1953)
Canadian Journal of Psychology
, vol.7
, pp. 145-155
-
-
Thompson, W.R.1
-
84
-
-
84860151961
-
Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses
-
Visscher, P. M., Goddard, M. E., Derks, E. M., & Wray, N. R. (2012). Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses. Molecular Psychiatry, 17, 474-485.
-
(2012)
Molecular Psychiatry
, vol.17
, pp. 474-485
-
-
Visscher, P.M.1
Goddard, M.E.2
Derks, E.M.3
Wray, N.R.4
-
85
-
-
0002554596
-
Sample size to detect a planned contrast and a one degree-of-freedom interaction effect
-
Wahlsten, D. (1991). Sample size to detect a planned contrast and a one degree-of-freedom interaction effect. Psychological Bulletin, 110, 587-595.
-
(1991)
Psychological Bulletin
, vol.110
, pp. 587-595
-
-
Wahlsten, D.1
-
86
-
-
84929717816
-
The intelligence of heritability
-
Wahlsten, D. (1994). The intelligence of heritability. Canadian Psychology, 35, 244-258.
-
(1994)
Canadian Psychology
, vol.35
, pp. 244-258
-
-
Wahlsten, D.1
-
88
-
-
84861952026
-
Special challenges of complex behavioural traits: Discovery and applications.
-
L. Maheu & R. A. Macdonald (Eds.). Montreal: McGill-Queen's University Press
-
Wahlsten, D. (2011b). Special challenges of complex behavioural traits: Discovery and applications. In L. Maheu & R. A. Macdonald (Eds.), Challenging genetic determinism. New perspectives on the gene in its multiple environments (pp. 51-77). Montreal: McGill-Queen's University Press.
-
(2011)
Challenging genetic determinism. New perspectives on the gene in its multiple environments
, pp. 51-77
-
-
Wahlsten, D.1
-
89
-
-
33750829156
-
Stability of inbred mouse strain differences in behavior and brain size between laboratories and across decades
-
Wahlsten, D., Bachmanov, A. A., Finn, D. A., & Crabbe, J. C. (2006). Stability of inbred mouse strain differences in behavior and brain size between laboratories and across decades. Proceedings of the National Academy of Sciences United States of America, 103, 16364-16369.
-
(2006)
Proceedings of the National Academy of Sciences United States of America
, vol.103
, pp. 16364-16369
-
-
Wahlsten, D.1
Bachmanov, A.A.2
Finn, D.A.3
Crabbe, J.C.4
-
90
-
-
33645752337
-
A linkage study of academic skills defined by the Queensland core skills test
-
Wainwright, M. A., Wright, M. J., Luciano, M., Montgomery, G. W., Geffen, G. M., & Martin, N. G. (2006). A linkage study of academic skills defined by the Queensland core skills test. Behavior Genetics, 36, 56-64.
-
(2006)
Behavior Genetics
, vol.36
, pp. 56-64
-
-
Wainwright, M.A.1
Wright, M.J.2
Luciano, M.3
Montgomery, G.W.4
Geffen, G.M.5
Martin, N.G.6
-
92
-
-
84862832916
-
New mouse models of autism highlight need for standardized tests
-
Williams, S. C. (2011). New mouse models of autism highlight need for standardized tests. Nature Medicine, 17, 1324.
-
(2011)
Nature Medicine
, vol.17
, pp. 1324
-
-
Williams, S.C.1
-
93
-
-
84856405512
-
The mystery of missing heritability: Genetic interactions create phantom heritability
-
Zuk, O., Hechter, E., Sunyaev, S. R., & Lander, E. S., (2012). The mystery of missing heritability: Genetic interactions create phantom heritability. Proceedings of the National Academy of Sciences United States of America, 109, 1193-1198.
-
(2012)
Proceedings of the National Academy of Sciences United States of America
, vol.109
, pp. 1193-1198
-
-
Zuk, O.1
Hechter, E.2
Sunyaev, S.R.3
Lander, E.S.4
|