-
1
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei, I. A., Schmidt, S., Peshkin, L., Ramensky, V. E., Gerasimova, A., Bork, P., ... Sunyaev, S. R. (2010). A method and server for predicting damaging missense mutations. Nature Methods, 7, 248-249. doi: 10.1038/nmeth0410-248
-
(2010)
Nature Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
Sunyaev, S.R.7
-
2
-
-
77958088279
-
Rare variant association analysis methods for complex traits
-
Asimit, J., & Zeggini, E. (2010). Rare variant association analysis methods for complex traits. Annual Review of Genetics, 44, 293-308. doi: 10.1146/annurev-genet-102209-163421
-
(2010)
Annual Review of Genetics
, vol.44
, pp. 293-308
-
-
Asimit, J.1
Zeggini, E.2
-
3
-
-
0037305105
-
A review of electrophysiology in attention-deficit/hyperactivity disorder: I. Qualitative and quantitative electroencephalography
-
Barry, R. J., Clarke, A. R., & Johnstone, S. J. (2003). A review of electrophysiology in attention-deficit/hyperactivity disorder: I. Qualitative and quantitative electroencephalography. Clinical Neurophysiology, 114, 171-183.
-
(2003)
Clinical Neurophysiology
, vol.114
, pp. 171-183
-
-
Barry, R.J.1
Clarke, A.R.2
Johnstone, S.J.3
-
4
-
-
82155197222
-
Quantitative electroencephalography in schizophrenia and depression
-
Begic, D., Popovic-Knapic, V., Grubisin, J., Kosanovic-Rajacic, B., Filipcic, I., Telarovic, I., & Jakovljevic, M. (2011). Quantitative electroencephalography in schizophrenia and depression. Psychiatria Danubina, 23, 355-362.
-
(2011)
Psychiatria Danubina
, vol.23
, pp. 355-362
-
-
Begic, D.1
Popovic-Knapic, V.2
Grubisin, J.3
Kosanovic-Rajacic, B.4
Filipcic, I.5
Telarovic, I.6
Jakovljevic, M.7
-
5
-
-
0028031363
-
Resting EEG in first-episode schizophrenia patients, bipolar psychosis patients, and their first-degree relatives
-
Clementz, B. A., Sponheim, S. R., Iacono, W. G., & Beiser, M. (1994). Resting EEG in first-episode schizophrenia patients, bipolar psychosis patients, and their first-degree relatives. Psychophysiology, 31, 486-494.
-
(1994)
Psychophysiology
, vol.31
, pp. 486-494
-
-
Clementz, B.A.1
Sponheim, S.R.2
Iacono, W.G.3
Beiser, M.4
-
6
-
-
73549114881
-
EEG spectral phenotypes: Heritability and association with marijuana and alcohol dependence in an American Indian community study
-
Ehlers, C. L., Phillips, E., Gizer, I. R., Gilder, D. A., & Wilhelmsen, K. C. (2010). EEG spectral phenotypes: Heritability and association with marijuana and alcohol dependence in an American Indian community study. Drug and Alcohol Dependence, 106, 101-110. doi: 10.1016/j.drugalcdep.2009.07.024
-
(2010)
Drug and Alcohol Dependence
, vol.106
, pp. 101-110
-
-
Ehlers, C.L.1
Phillips, E.2
Gizer, I.R.3
Gilder, D.A.4
Wilhelmsen, K.C.5
-
7
-
-
0038823525
-
The endophenotype concept in psychiatry: Etymology and strategic intentions
-
Gottesman, I. I., & Gould, T. D. (2003). The endophenotype concept in psychiatry: Etymology and strategic intentions. American Journal of Psychiatry, 160, 636-645.
-
(2003)
American Journal of Psychiatry
, vol.160
, pp. 636-645
-
-
Gottesman, I.I.1
Gould, T.D.2
-
8
-
-
33244481978
-
Dynamic spectral analysis findings in first episode and chronic schizophrenia
-
Harris, A., Melkonian, D., Williams, L., & Gordon, E. (2006). Dynamic spectral analysis findings in first episode and chronic schizophrenia. International Journal of Neuroscience, 116, 223-246. doi: 10.1080/00207450500402977
-
(2006)
International Journal of Neuroscience
, vol.116
, pp. 223-246
-
-
Harris, A.1
Melkonian, D.2
Williams, L.3
Gordon, E.4
-
9
-
-
84865760395
-
GENCODE: The reference human genome annotation for The ENCODE Project
-
Harrow, J., Frankish, A., Gonzalez, J. M., Tapanari, E., Diekhans, M., Kokocinski, F., ... Hubbard, T. J. (2012). GENCODE: The reference human genome annotation for The ENCODE Project. Genome Research, 22, 1760-1774. doi: 10.1101/gr.135350.111
-
(2012)
Genome Research
, vol.22
, pp. 1760-1774
-
-
Harrow, J.1
Frankish, A.2
Gonzalez, J.M.3
Tapanari, E.4
Diekhans, M.5
Kokocinski, F.6
Hubbard, T.J.7
-
10
-
-
84930351179
-
Genome-wide scans of genetic variants for psychophysiological endophenotypes: A methodological overview
-
Iacono, W. G., Malone, S. M., Vaidyanathan, U., & Vrieze, S. I. (2014). Genome-wide scans of genetic variants for psychophysiological endophenotypes: A methodological overview. Psychophysiology, 51, 1207-1224.
-
(2014)
Psychophysiology
, vol.51
, pp. 1207-1224
-
-
Iacono, W.G.1
Malone, S.M.2
Vaidyanathan, U.3
Vrieze, S.I.4
-
12
-
-
33846195362
-
Minnesota Center for Twin and Family Research
-
Iacono, W. G., McGue, M., & Krueger, R. F. (2006). Minnesota Center for Twin and Family Research. Twin Research and Human Genetics, 9, 978-984. doi: 10.1375/183242706779462642
-
(2006)
Twin Research and Human Genetics
, vol.9
, pp. 978-984
-
-
Iacono, W.G.1
McGue, M.2
Krueger, R.F.3
-
13
-
-
84930349693
-
-
Efficient and Parallelizable Association Container Toolbox (EPACTS). Retrieved from
-
Kang, H. M. (2014). Efficient and Parallelizable Association Container Toolbox (EPACTS). Retrieved from http://genome.sph.umich.edu/wiki/EPACTS
-
(2014)
-
-
Kang, H.M.1
-
14
-
-
77950301214
-
Variance component model to account for sample structure in genome-wide association studies
-
Kang, H. M., Sul, J. H., Service, S. K., Zaitlen, N. A., Kong, S. Y., Freimer, N. B., ... Eskin, E. (2010). Variance component model to account for sample structure in genome-wide association studies. Nature Genetics, 42, 348-354. doi: 10.1038/Ng.548
-
(2010)
Nature Genetics
, vol.42
, pp. 348-354
-
-
Kang, H.M.1
Sul, J.H.2
Service, S.K.3
Zaitlen, N.A.4
Kong, S.Y.5
Freimer, N.B.6
Eskin, E.7
-
15
-
-
74949101658
-
The enrichment study of the Minnesota Twin Family Study: Increasing the yield of twin families at high risk for externalizing psychopathology
-
Keyes, M. A., Malone, S. M., Elkins, I. J., Legrand, L. N., McGue, M., & Iacono, W. G. (2009). The enrichment study of the Minnesota Twin Family Study: Increasing the yield of twin families at high risk for externalizing psychopathology. Twin Research and Human Genetics, 12, 489-501. doi: 10.1375/twin.12.5.489
-
(2009)
Twin Research and Human Genetics
, vol.12
, pp. 489-501
-
-
Keyes, M.A.1
Malone, S.M.2
Elkins, I.J.3
Legrand, L.N.4
McGue, M.5
Iacono, W.G.6
-
16
-
-
84863339254
-
Association study between polymorphisms of the PARD3 gene and schizophrenia
-
Kim, S. K., Lee, J. Y., Park, H. J., Kim, J. W., & Chung, J.-H. (2012). Association study between polymorphisms of the PARD3 gene and schizophrenia. Experimental and Therapeutic Medicine, 3, 881-885.
-
(2012)
Experimental and Therapeutic Medicine
, vol.3
, pp. 881-885
-
-
Kim, S.K.1
Lee, J.Y.2
Park, H.J.3
Kim, J.W.4
Chung, J.-H.5
-
17
-
-
84895858942
-
A general framework for estimating the relative pathogenicity of human genetic variants
-
Kircher, M., Witten, D. M., Jain, P., O'Roak, B. J., Cooper, G. M., & Shendure, J. (2014). A general framework for estimating the relative pathogenicity of human genetic variants. Nature Genetics, 46, 310-315. doi: 10.1038/ng.2892
-
(2014)
Nature Genetics
, vol.46
, pp. 310-315
-
-
Kircher, M.1
Witten, D.M.2
Jain, P.3
O'Roak, B.J.4
Cooper, G.M.5
Shendure, J.6
-
18
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
Kumar, P., Henikoff, S., & Ng, P. C. (2009). Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nature Protocols, 4, 1073-1081. doi: 10.1038/nprot.2009.86
-
(2009)
Nature Protocols
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
19
-
-
0004311807
-
-
Gainesville, FL: The Center for Research in Psychophysiology, University of Florida.
-
Lang, P. J., Bradley, M. M., & Cuthbert, B. N. (1999). International affective picture system (IAPS): Technical manual and affective ratings. Gainesville, FL: The Center for Research in Psychophysiology, University of Florida.
-
(1999)
International affective picture system (IAPS): Technical manual and affective ratings
-
-
Lang, P.J.1
Bradley, M.M.2
Cuthbert, B.N.3
-
20
-
-
84904006087
-
Rare-variant association analysis: Study designs and statistical tests
-
Lee, S., Abecasis, G. R., Boehnke, M., & Lin, X. (2014). Rare-variant association analysis: Study designs and statistical tests. American Journal of Human Genetics, 95, 5-23. doi: 10.1016/j.ajhg.2014.06.009
-
(2014)
American Journal of Human Genetics
, vol.95
, pp. 5-23
-
-
Lee, S.1
Abecasis, G.R.2
Boehnke, M.3
Lin, X.4
-
21
-
-
50949095168
-
Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data
-
Li, B. S., & Leal, S. M. (2008). Methods for detecting associations with rare variants for common diseases: Application to analysis of sequence data. American Journal of Human Genetics, 83, 311-321. doi: 10.1016/j.ajhg.2008.06.024
-
(2008)
American Journal of Human Genetics
, vol.83
, pp. 311-321
-
-
Li, B.S.1
Leal, S.M.2
-
22
-
-
84861988364
-
Improved linear mixed models for genome-wide association studies
-
Listgarten, J., Lippert, C., Kadie, C. M., Davidson, R. I., Eskin, E., & Heckerman, D. (2012). Improved linear mixed models for genome-wide association studies. Nature Methods, 9, 525-526. doi: 10.1038/nmeth.2037
-
(2012)
Nature Methods
, vol.9
, pp. 525-526
-
-
Listgarten, J.1
Lippert, C.2
Kadie, C.M.3
Davidson, R.I.4
Eskin, E.5
Heckerman, D.6
-
23
-
-
84925938278
-
Heritability and molecular genetic basis of resting EEG activity: A genome-wide association study
-
Malone, S. M., Burwell, S. J., Vaidyanathan, U., Miller, M. B., McGue, M., & Iacono, W. G. (2014). Heritability and molecular genetic basis of resting EEG activity: A genome-wide association study. Psychophysiology, 51, 1225-1245.
-
(2014)
Psychophysiology
, vol.51
, pp. 1225-1245
-
-
Malone, S.M.1
Burwell, S.J.2
Vaidyanathan, U.3
Miller, M.B.4
McGue, M.5
Iacono, W.G.6
-
24
-
-
84930328671
-
Heritability and molecular genetic basis of P3 event-related brain potential amplitude: A genome-wide association study
-
Malone, S. M., Vaidyanathan, U., Basu, S., Miller, M. B., McGue, M., & Iacono, W. G. (2014). Heritability and molecular genetic basis of P3 event-related brain potential amplitude: A genome-wide association study. Psychophysiology, 51, 1246-1258.
-
(2014)
Psychophysiology
, vol.51
, pp. 1246-1258
-
-
Malone, S.M.1
Vaidyanathan, U.2
Basu, S.3
Miller, M.B.4
McGue, M.5
Iacono, W.G.6
-
25
-
-
77955405475
-
Deriving the consequences of genomic variants with the ensembl API and SNP effect predictor
-
McLaren, W., Pritchard, B., Rios, D., Chen, Y. A., Flicek, P., & Cunningham, F. (2010). Deriving the consequences of genomic variants with the ensembl API and SNP effect predictor. Bioinformatics, 26, 2069-2070. doi: 10.1093/bioinformatics/btq330
-
(2010)
Bioinformatics
, vol.26
, pp. 2069-2070
-
-
McLaren, W.1
Pritchard, B.2
Rios, D.3
Chen, Y.A.4
Flicek, P.5
Cunningham, F.6
-
26
-
-
84873870794
-
The Minnesota Center for Twin and Family Research genome-wide association study
-
Miller, M. B., Basu, S., Cunningham, J., Eskin, E., Malone, S. M., Oetting, W. S., ... McGue, M. (2012). The Minnesota Center for Twin and Family Research genome-wide association study. Twin Research and Human Genetics, 15, 767-774.
-
(2012)
Twin Research and Human Genetics
, vol.15
, pp. 767-774
-
-
Miller, M.B.1
Basu, S.2
Cunningham, J.3
Eskin, E.4
Malone, S.M.5
Oetting, W.S.6
McGue, M.7
-
27
-
-
84930355916
-
-
Genetic visualization with GENVISIS. Manuscript in preparation.
-
Pankratz, N. (2014). Genetic visualization with GENVISIS. Manuscript in preparation.
-
(2014)
-
-
Pankratz, N.1
-
28
-
-
77953121877
-
Pooled association tests for rare variants in exon-resequencing studies
-
Price, A. L., Kryukov, G. V., de Bakker, P. I., Purcell, S. M., Staples, J., Wei, L. J., & Sunyaev, S. R. (2010). Pooled association tests for rare variants in exon-resequencing studies. American Journal of Human Genetics, 86, 832-838. doi: 10.1016/j.ajhg.2010.04.005
-
(2010)
American Journal of Human Genetics
, vol.86
, pp. 832-838
-
-
Price, A.L.1
Kryukov, G.V.2
de Bakker, P.I.3
Purcell, S.M.4
Staples, J.5
Wei, L.J.6
Sunyaev, S.R.7
-
29
-
-
0037392258
-
Theta power in the EEG of alcoholics
-
Rangaswamy, M., Porjesz, B., Chorlian, D. B., Choi, K., Jones, K. A., Wang, K., ... Begleiter, H. (2003). Theta power in the EEG of alcoholics. Alcoholism, Clinical and Experimental Research, 27, 607-615. doi: 10.1097/01.ALC.0000060523.95470.8F
-
(2003)
Alcoholism, Clinical and Experimental Research
, vol.27
, pp. 607-615
-
-
Rangaswamy, M.1
Porjesz, B.2
Chorlian, D.B.3
Choi, K.4
Jones, K.A.5
Wang, K.6
Begleiter, H.7
-
30
-
-
84875814010
-
Neuropathy target esterase (NTE): Overview and future
-
Richardson, R. J., Hein, N. D., Wijeyesakere, S. J., Fink, J. K., & Makhaeva, G. F. (2013). Neuropathy target esterase (NTE): Overview and future. Chemico-Biological Interactions, 203, 238-244. doi: 10.1016/j.cbi.2012.10.024
-
(2013)
Chemico-Biological Interactions
, vol.203
, pp. 238-244
-
-
Richardson, R.J.1
Hein, N.D.2
Wijeyesakere, S.J.3
Fink, J.K.4
Makhaeva, G.F.5
-
31
-
-
0028084465
-
Resting EEG in first-episode and chronic schizophrenia
-
Sponheim, S. R., Clementz, B. A., Iacono, W. G., & Beiser, M. (1994). Resting EEG in first-episode and chronic schizophrenia. Psychophysiology, 31, 37-43.
-
(1994)
Psychophysiology
, vol.31
, pp. 37-43
-
-
Sponheim, S.R.1
Clementz, B.A.2
Iacono, W.G.3
Beiser, M.4
-
32
-
-
0034559403
-
Clinical and biological concomitants of resting state EEG power abnormalities in schizophrenia
-
Sponheim, S. R., Clementz, B. A., Iacono, W. G., & Beiser, M. (2000). Clinical and biological concomitants of resting state EEG power abnormalities in schizophrenia. Biological Psychiatry, 48, 1088-1097.
-
(2000)
Biological Psychiatry
, vol.48
, pp. 1088-1097
-
-
Sponheim, S.R.1
Clementz, B.A.2
Iacono, W.G.3
Beiser, M.4
-
33
-
-
0042206876
-
Sensitivity and specificity of select biological indices in characterizing psychotic patients and their relatives
-
Sponheim, S. R., Iacono, W. G., Thuras, P. D., Nugent, S. M., & Beiser, M. (2003). Sensitivity and specificity of select biological indices in characterizing psychotic patients and their relatives. Schizophrenia Research, 63, 27-38.
-
(2003)
Schizophrenia Research
, vol.63
, pp. 27-38
-
-
Sponheim, S.R.1
Iacono, W.G.2
Thuras, P.D.3
Nugent, S.M.4
Beiser, M.5
-
34
-
-
84860351742
-
Identification of common variants associated with human hippocampal and intracranial volumes
-
Stein, J. L., Medland, S. E., Vasquez, A. A., Hibar, D. P., Senstad, R. E., Winkler, A. M., ... Thompson, P. M. (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics, 44, 552-561.
-
(2012)
Nature Genetics
, vol.44
, pp. 552-561
-
-
Stein, J.L.1
Medland, S.E.2
Vasquez, A.A.3
Hibar, D.P.4
Senstad, R.E.5
Winkler, A.M.6
Thompson, P.M.7
-
35
-
-
0032779036
-
Topographic quantitative EEG sequelae of chronic marihuana use: A replication using medically and psychiatrically screened normal subjects
-
Struve, F. A., Straumanis, J. J., Patrick, G., Leavitt, J., Manno, J. E., & Manno, B. R. (1999). Topographic quantitative EEG sequelae of chronic marihuana use: A replication using medically and psychiatrically screened normal subjects. Drug and Alcohol Dependence, 56, 167-179.
-
(1999)
Drug and Alcohol Dependence
, vol.56
, pp. 167-179
-
-
Struve, F.A.1
Straumanis, J.J.2
Patrick, G.3
Leavitt, J.4
Manno, J.E.5
Manno, B.R.6
-
36
-
-
84863556835
-
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
-
NHLBI Exome Sequencing Project.
-
Tennessen, J. A., Bigham, A. W., O'Connor, T. D., Fu, W., Kenny, E. E., Gravel, S., ... NHLBI Exome Sequencing Project. (2012). Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science, 337, 64-69. doi: 10.1126/science.1219240
-
(2012)
Science
, vol.337
, pp. 64-69
-
-
Tennessen, J.A.1
Bigham, A.W.2
O'Connor, T.D.3
Fu, W.4
Kenny, E.E.5
Gravel, S.6
-
37
-
-
84899930958
-
The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data
-
Thompson, P. M., Stein, J. L., Medland, S. E., Hibar, D. P., Vasquez, A. A., Renteria, M. E., ... Drevets, W. (2014). The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 1-30. doi: 10.1007/s11682-013-9269-5
-
(2014)
Brain Imaging and Behavior
, pp. 1-30
-
-
Thompson, P.M.1
Stein, J.L.2
Medland, S.E.3
Hibar, D.P.4
Vasquez, A.A.5
Renteria, M.E.6
Drevets, W.7
-
38
-
-
84930332490
-
Heritability and molecular genetic basis of electrodermal activity: A genome-wide association study
-
Vaidyanathan, U., Isen, J. D., Malone, S. M., Miller, M. B., McGue, M., & Iacono, W. G. (2014). Heritability and molecular genetic basis of electrodermal activity: A genome-wide association study. Psychophysiology, 51, 1259-1271.
-
(2014)
Psychophysiology
, vol.51
, pp. 1259-1271
-
-
Vaidyanathan, U.1
Isen, J.D.2
Malone, S.M.3
Miller, M.B.4
McGue, M.5
Iacono, W.G.6
-
39
-
-
84925958019
-
Heritability and molecular genetic basis of antisaccade eye tracking error rate: A genome-wide association study
-
Vaidyanathan, U., Malone, S. M., Donnelly, J. M., Hammer, M. A., Miller, M. B., McGue, M., & Iacono, W. G. (2014). Heritability and molecular genetic basis of antisaccade eye tracking error rate: A genome-wide association study. Psychophysiology, 51, 1272-1284.
-
(2014)
Psychophysiology
, vol.51
, pp. 1272-1284
-
-
Vaidyanathan, U.1
Malone, S.M.2
Donnelly, J.M.3
Hammer, M.A.4
Miller, M.B.5
McGue, M.6
Iacono, W.G.7
-
40
-
-
84925936512
-
Heritability and molecular genetic basis of acoustic startle eye blink and affectively modulated startle response: A genome-wide association study
-
Vaidyanathan, U., Malone, S. M., Miller, M. B., McGue, M., & Iacono, W. G. (2014). Heritability and molecular genetic basis of acoustic startle eye blink and affectively modulated startle response: A genome-wide association study. Psychophysiology, 51, 1285-1299.
-
(2014)
Psychophysiology
, vol.51
, pp. 1285-1299
-
-
Vaidyanathan, U.1
Malone, S.M.2
Miller, M.B.3
McGue, M.4
Iacono, W.G.5
-
41
-
-
84924888531
-
In search of rare variants: Preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes
-
Vrieze, S. I., Malone, S. M., Vaidyanathan, U., Kwong, A., Kang, H. M., Zhan, X., ... Iacono, W. G. (2014). In search of rare variants: Preliminary results from whole genome sequencing of 1, 325 individuals with psychophysiological endophenotypes. Psychophysiology, 51, 1309-1320.
-
(2014)
Psychophysiology
, vol.51
, pp. 1309-1320
-
-
Vrieze, S.I.1
Malone, S.M.2
Vaidyanathan, U.3
Kwong, A.4
Kang, H.M.5
Zhan, X.6
Iacono, W.G.7
-
42
-
-
33748745960
-
Characterization of the human patatin-like phospholipase family
-
Wilson, P. A., Gardner, S. D., Lambie, N. M., Commans, S. A., & Crowther, D. J. (2006). Characterization of the human patatin-like phospholipase family. Journal of Lipid Research, 47, 1940-1949. doi: 10.1194/jlr.M600185-JLR200
-
(2006)
Journal of Lipid Research
, vol.47
, pp. 1940-1949
-
-
Wilson, P.A.1
Gardner, S.D.2
Lambie, N.M.3
Commans, S.A.4
Crowther, D.J.5
-
43
-
-
80051499915
-
Rare-variant association testing for sequencing data with the sequence kernel association test
-
Wu, M. C., Lee, S., Cai, T. X., Li, Y., Boehnke, M., & Lin, X. H. (2011). Rare-variant association testing for sequencing data with the sequence kernel association test. American Journal of Human Genetics, 89, 82-93. doi: 10.1016/j.ajhg.2011.05.029
-
(2011)
American Journal of Human Genetics
, vol.89
, pp. 82-93
-
-
Wu, M.C.1
Lee, S.2
Cai, T.X.3
Li, Y.4
Boehnke, M.5
Lin, X.H.6
|