-
1
-
-
20444412281
-
Molecular genetics of attention-deficit/hyperactivity disorder
-
DOI 10.1016/j.biopsych.2004.11.024, PII S0006322304012260
-
Faraone SV, Perlis RH, Doyle AE, Smoller JW, Goralnick JJ, Holmgren MA, Sklar P: Molecular genetics of attention-deficit/hyperactivity disorder. Biol Psychiatry 2005; 57:1313-1323 (Pubitemid 40798551)
-
(2005)
Biological Psychiatry
, vol.57
, Issue.11
, pp. 1313-1323
-
-
Faraone, S.V.1
Perlis, R.H.2
Doyle, A.E.3
Smoller, J.W.4
Goralnick, J.J.5
Holmgren, M.A.6
Sklar, P.7
-
2
-
-
80053924932
-
Fitting the pieces together: Current research on the genetic basis of attention-deficit/hyperactivity disorder (ADHD)
-
Stergiakouli E, Thapar A: Fitting the pieces together: current research on the genetic basis of attention-deficit/hyperactivity disorder (ADHD). Neuropsychiatr Dis Treat 2010; 6:551-560
-
(2010)
Neuropsychiatr Dis Treat
, vol.6
, pp. 551-560
-
-
Stergiakouli, E.1
Thapar, A.2
-
3
-
-
77952887857
-
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
-
Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT, D'Arcy M, Deberardinis R, Frackelton E, Kim C, Lantieri F, Muganga BM, Wang L, Takeda T, Rappaport EF, Grant SF, Berrettini W, Devoto M, Shaikh TH, Hakonarson H, White PS: Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Mol Psychiatry 2010; 15:637-646
-
(2010)
Mol Psychiatry
, vol.15
, pp. 637-646
-
-
Elia, J.1
Gai, X.2
Xie, H.M.3
Perin, J.C.4
Geiger, E.5
Glessner, J.T.6
D'Arcy, M.7
Deberardinis, R.8
Frackelton, E.9
Kim, C.10
Lantieri, F.11
Muganga, B.M.12
Wang, L.13
Takeda, T.14
Rappaport, E.F.15
Grant, S.F.16
Berrettini, W.17
Devoto, M.18
Shaikh, T.H.19
Hakonarson, H.20
White, P.S.21
more..
-
4
-
-
79955470881
-
Genome-wide copy number variation analysis in attention-deficit/ hyperactivity disorder: Association with neuropeptide Y gene dosage in an extended pedigree
-
Lesch KP, Selch S, Renner TJ, Jacob C, Nguyen TT, Hahn T, Romanos M, Walitza S, Shoichet S, Dempfle A, Heine M, Boreatti- Hummer A, Romanos J, Gross-Lesch S, Zerlaut H, Wultsch T, Heinzel S, Fassnacht M, Fallgatter A, Allolio B, Schafer H, Warnke A, Reif A, Ropers HH, Ullmann R: Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree. Mol Psychiatry 2011; 16:491-503
-
(2011)
Mol Psychiatry
, vol.16
, pp. 491-503
-
-
Lesch, K.P.1
Selch, S.2
Renner, T.J.3
Jacob, C.4
Nguyen, T.T.5
Hahn, T.6
Romanos, M.7
Walitza, S.8
Shoichet, S.9
Dempfle, A.10
Heine, M.11
Boreatti- Hummer, A.12
Romanos, J.13
Gross-Lesch, S.14
Zerlaut, H.15
Wultsch, T.16
Heinzel, S.17
Fassnacht, M.18
Fallgatter, A.19
Allolio, B.20
Schafer, H.21
Warnke, A.22
Reif, A.23
Ropers, H.H.24
Ullmann, R.25
more..
-
5
-
-
78049303903
-
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: A genome-wide analysis
-
Williams NM, Zaharieva I, Martin A, Langley K, Mantripragada K, Fossdal R, Stefansson H, Stefansson K, Magnusson P, Gudmundsson OO, Gustafsson O, Holmans P, Owen MJ, O'Donovan M, Thapar A: Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. Lancet 2010; 376:1401-1408
-
(2010)
Lancet
, vol.376
, pp. 1401-1408
-
-
Williams, N.M.1
Zaharieva, I.2
Martin, A.3
Langley, K.4
Mantripragada, K.5
Fossdal, R.6
Stefansson, H.7
Stefansson, K.8
Magnusson, P.9
Gudmundsson, O.O.10
Gustafsson, O.11
Holmans, P.12
Owen, M.J.13
O'Donovan, M.14
Thapar, A.15
-
6
-
-
55349128167
-
Molecular genetics of adult ADHD: Converging evidence from genome-wide association and extended pedigree linkage studies
-
Lesch KP, Timmesfeld N, Renner TJ, Halperin R, Roser C, Nguyen TT, Craig DW, Romanos J, Heine M, Meyer J, Freitag C, Warnke A, Romanos M, Schafer H, Walitza S, Reif A, Stephan DA, Jacob C: Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. J Neural Transm 2008; 115:1573-1585
-
(2008)
J Neural Transm
, vol.115
, pp. 1573-1585
-
-
Lesch, K.P.1
Timmesfeld, N.2
Renner, T.J.3
Halperin, R.4
Roser, C.5
Nguyen, T.T.6
Craig, D.W.7
Romanos, J.8
Heine, M.9
Meyer, J.10
Freitag, C.11
Warnke, A.12
Romanos, M.13
Schafer, H.14
Walitza, S.15
Reif, A.16
Stephan, D.A.17
Jacob, C.18
-
7
-
-
77955668718
-
Family-based genome-wide association scan of attentiondeficit/ hyperactivity disorder
-
Mick E, Todorov A, Smalley S, Hu X, Loo S, Todd RD, Biederman J, Byrne D, Dechairo B, Guiney A, McCracken J, McGough J, Nelson SF, Reiersen AM, Wilens TE, Wozniak J, Neale BM, Faraone SV: Family-based genome-wide association scan of attentiondeficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010; 49:898-905
-
(2010)
J Am Acad Child Adolesc Psychiatry
, vol.49
, pp. 898-905
-
-
Mick, E.1
Todorov, A.2
Smalley, S.3
Hu, X.4
Loo, S.5
Todd, R.D.6
Biederman, J.7
Byrne, D.8
Dechairo, B.9
Guiney, A.10
McCracken, J.11
McGough, J.12
Nelson, S.F.13
Reiersen, A.M.14
Wilens, T.E.15
Wozniak, J.16
Neale, B.M.17
Faraone, S.V.18
-
8
-
-
57349166006
-
Genome-wide association scan of attention deficit hyperactivity disorder
-
Neale BM, Lasky-Su J, Anney R, Franke B, Zhou K, Maller JB, Vasquez AA, Asherson P, Chen W, Banaschewski T, Buitelaar J, Ebstein R, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Sonuga-Barke E, Mulas F, Taylor E, Laird N, Lange C, Daly M, Faraone SV: Genome-wide association scan of attention deficit hyperactivity disorder. Am J Med Genet B Neuropsychiatr Genet 2008; 147B:1337-1344
-
(2008)
Am J Med Genet B Neuropsychiatr Genet
, vol.147 B
, pp. 1337-1344
-
-
Neale, B.M.1
Lasky-Su, J.2
Anney, R.3
Franke, B.4
Zhou, K.5
Maller, J.B.6
Vasquez, A.A.7
Asherson, P.8
Chen, W.9
Banaschewski, T.10
Buitelaar, J.11
Ebstein, R.12
Gill, M.13
Miranda, A.14
Oades, R.D.15
Roeyers, H.16
Rothenberger, A.17
Sergeant, J.18
Steinhausen, H.C.19
Sonuga-Barke, E.20
Mulas, F.21
Taylor, E.22
Laird, N.23
Lange, C.24
Daly, M.25
Faraone, S.V.26
more..
-
9
-
-
77956180603
-
Case-control genome-wide association study of attention-deficit/ hyperactivity disorder
-
Neale BM, Medland S, Ripke S, Anney RJ, Asherson P, Buitelaar J, Franke B, Gill M, Kent L, Holmans P, Middleton F, Thapar A, Lesch KP, Faraone SV, Daly M, Nguyen TT, Schafer H, Steinhausen HC, Reif A, Renner TJ, Romanos M, Romanos J, Warnke A, Walitza S, Freitag C, Meyer J, Palmason H, Rothenberger A, Hawi Z, Sergeant J, Roeyers H, Mick E, Biederman J: Case-control genome-wide association study of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010; 49:906-920
-
(2010)
J Am Acad Child Adolesc Psychiatry
, vol.49
, pp. 906-920
-
-
Neale, B.M.1
Medland, S.2
Ripke, S.3
Anney, R.J.4
Asherson, P.5
Buitelaar, J.6
Franke, B.7
Gill, M.8
Kent, L.9
Holmans, P.10
Middleton, F.11
Thapar, A.12
Lesch, K.P.13
Faraone, S.V.14
Daly, M.15
Nguyen, T.T.16
Schafer, H.17
Steinhausen, H.C.18
Reif, A.19
Renner, T.J.20
Romanos, M.21
Romanos, J.22
Warnke, A.23
Walitza, S.24
Freitag, C.25
Meyer, J.26
Palmason, H.27
Rothenberger, A.28
Hawi, Z.29
Sergeant, J.30
Roeyers, H.31
Mick, E.32
Biederman, J.33
more..
-
10
-
-
77956178166
-
Metaanalysis of genome-wide association studies of attention-deficit/ hyperactivity disorder
-
Neale BM, Medland SE, Ripke S, Asherson P, Franke B, Lesch KP, Faraone SV, Nguyen TT, Schafer H, Holmans P, Daly M, Steinhausen HC, Freitag C, Reif A, Renner TJ, Romanos M, Romanos J, Walitza S, Warnke A, Meyer J, Palmason H, Buitelaar J, Vasquez AA, Lambregts-Rommelse N, Gill M, Anney RJ, Langely K, O'Donovan M, Williams N, Owen M, Thapar A, Kent L, Sergeant J, Roeyers H, Mick E, Biederman J, Doyle A, Smalley S, Loo S, Hakonarson H, Elia J, Todorov A, Miranda A, Mulas F, Ebstein RP, Rothenberger A, Banaschewski T, Oades RD, Sonuga-Barke E, McGough J, Nisenbaum L, Middleton F, Hu X, Nelson S: Metaanalysis of genome-wide association studies of attention-deficit/ hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2010; 49:884-897
-
(2010)
J Am Acad Child Adolesc Psychiatry
, vol.49
, pp. 884-897
-
-
Neale, B.M.1
Medland, S.E.2
Ripke, S.3
Asherson, P.4
Franke, B.5
Lesch, K.P.6
Faraone, S.V.7
Nguyen, T.T.8
Schafer, H.9
Holmans, P.10
Daly, M.11
Steinhausen, H.C.12
Freitag, C.13
Reif, A.14
Renner, T.J.15
Romanos, M.16
Romanos, J.17
Walitza, S.18
Warnke, A.19
Meyer, J.20
Palmason, H.21
Buitelaar, J.22
Vasquez, A.A.23
Lambregts-Rommelse, N.24
Gill, M.25
Anney, R.J.26
Langely, K.27
O'Donovan, M.28
Williams, N.29
Owen, M.30
Thapar, A.31
Kent, L.32
Sergeant, J.33
Roeyers, H.34
Mick, E.35
Biederman, J.36
Doyle, A.37
Smalley, S.38
Loo, S.39
Hakonarson, H.40
Elia, J.41
Todorov, A.42
Miranda, A.43
Mulas, F.44
Ebstein, R.P.45
Rothenberger, A.46
Banaschewski, T.47
Oades, R.D.48
Sonuga-Barke, E.49
McGough, J.50
Nisenbaum, L.51
Middleton, F.52
Hu, X.53
Nelson, S.54
more..
-
11
-
-
45549110436
-
Genome-wide association studies in psychiatry: Lessons from early studies of non-psychiatric and psychiatric phenotypes
-
DOI 10.1038/mp.2008.45, PII MP200845
-
Craddock N, O'Donovan MC, Owen MJ: Genome-wide association studies in psychiatry: lessons from early studies of nonpsychiatric and psychiatric phenotypes. Mol Psychiatry 2008; 13:649-653 (Pubitemid 351861534)
-
(2008)
Molecular Psychiatry
, vol.13
, Issue.7
, pp. 649-653
-
-
Craddock, N.1
O'Donovan, M.C.2
Owen, M.J.3
-
13
-
-
34948877698
-
Prediction of individual genetic risk to disease from genome-wide association studies
-
Wray NR, Goddard ME, Visscher PM: Prediction of individual genetic risk to disease from genome-wide association studies. Genome Res 2007; 17:1520-158
-
(2007)
Genome Res
, vol.17
, pp. 1520-2158
-
-
Wray, N.R.1
Goddard, M.E.2
Visscher, P.M.3
-
14
-
-
13144265739
-
Genome-wide association studies: Theoretical and practical concerns
-
DOI 10.1038/nrg1522
-
Wang W, Barratt B, Clayton D, Todd J: Genome-wide association studies: theoretical and practical concerns. Nat Rev Genet 2005; 6:109-118 (Pubitemid 40179533)
-
(2005)
Nature Reviews Genetics
, vol.6
, Issue.2
, pp. 109-118
-
-
Wang, W.Y.S.1
Barratt, B.J.2
Clayton, D.G.3
Todd, J.A.4
-
15
-
-
66149185456
-
Genomewide association studies: History, rationale, and prospects for psychiatric disorders
-
Psychiatric GWAS Consortium Coordinating Committee
-
Psychiatric GWAS Consortium Coordinating Committee, Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF: Genomewide association studies: history, rationale, and prospects for psychiatric disorders. Am J Psychiatry 2009; 166:540-556
-
(2009)
Am J Psychiatry
, vol.166
, pp. 540-556
-
-
Cichon, S.1
Craddock, N.2
Daly, M.3
Faraone, S.V.4
Gejman, P.V.5
Kelsoe, J.6
Lehner, T.7
Levinson, D.F.8
Moran, A.9
Sklar, P.10
Sullivan, P.F.11
-
17
-
-
0345742555
-
The Child Attention-Deficit Hyperactivity Disorder Teacher Telephone Interview (CHATTI): Reliability and validity
-
DOI 10.1192/bjp.184.1.74
-
Holmes J, Lawson D, Langley K, Fitzpatrick H, Trumper A, Pay H, Harrington R, Thapar A: The Child Attention-Deficit Hyperactivity Disorder Teacher Telephone Interview (CHATTI): reliability and validity. Br J Psychiatry 2004; 184:74-78 (Pubitemid 38085218)
-
(2004)
British Journal of Psychiatry
, vol.184
, Issue.JAN.
, pp. 74-78
-
-
Holmes, J.1
Lawson, D.2
Langley, K.3
Fitzpatrick, H.4
Trumper, A.5
Pay, H.6
Harrington, R.7
Thapar, A.8
-
20
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
The Wellcome Trust Case Control Consortium
-
The Wellcome Trust Case Control Consortium: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007; 447:661-678
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
21
-
-
24944580962
-
Design of case-controls studies with unscreened controls
-
DOI 10.1111/j.1529-8817.2005.00175.x
-
Moskvina V, Holmans P, Schmidt KM, Craddock N: Design of case-controls studies with unscreened controls. Ann Hum Genet 2005; 69(part 5):566-576 (Pubitemid 41309434)
-
(2005)
Annals of Human Genetics
, vol.69
, Issue.5
, pp. 566-576
-
-
Moskvina, V.1
Holmans, P.2
Schmidt, K.M.3
Craddock, N.4
-
22
-
-
84947649513
-
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
-
Ingason A, Rujescu D, Cichon S, Sigurdsson E, Sigmundsson T, Pietilainen OP, Buizer-Voskamp JE, Strengman E, Francks C, Muglia P, Gylfason A, Gustafsson O, Olason PI, Steinberg S, Hansen T, Jakobsen KD, Rasmussen HB, Giegling I, Moller HJ, Hartmann A, Crombie C, Fraser G, Walker N, Lonnqvist J, Suvisaari J, Tuulio-Henriksson A, Bramon E, Kiemeney LA, Franke B, Murray R, Vassos E, Toulopoulou T, Muhleisen TW, Tosato S, Ruggeri M, Djurovic S, Andreassen OA, Zhang Z, Werge T, Ophoff RA, Rietschel M, Nothen MM, Petursson H, Stefansson H, Peltonen L, Collier D, Stefansson K, Clair DM: Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Mol Psychiatry 2011; 16:17-25
-
(2011)
Mol Psychiatry
, vol.16
, pp. 17-25
-
-
Ingason, A.1
Rujescu, D.2
Cichon, S.3
Sigurdsson, E.4
Sigmundsson, T.5
Pietilainen, O.P.6
Buizer-Voskamp, J.E.7
Strengman, E.8
Francks, C.9
Muglia, P.10
Gylfason, A.11
Gustafsson, O.12
Olason, P.I.13
Steinberg, S.14
Hansen, T.15
Jakobsen, K.D.16
Rasmussen, H.B.17
Giegling, I.18
Moller, H.J.19
Hartmann, A.20
Crombie, C.21
Fraser, G.22
Walker, N.23
Lonnqvist, J.24
Suvisaari, J.25
Tuulio-Henriksson, A.26
Bramon, E.27
Kiemeney, L.A.28
Franke, B.29
Murray, R.30
Vassos, E.31
Toulopoulou, T.32
Muhleisen, T.W.33
Tosato, S.34
Ruggeri, M.35
Djurovic, S.36
Andreassen, O.A.37
Zhang, Z.38
Werge, T.39
Ophoff, R.A.40
Rietschel, M.41
Nothen, M.M.42
Petursson, H.43
Stefansson, H.44
Peltonen, L.45
Collier, D.46
Stefansson, K.47
Clair, D.M.48
more..
-
23
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
DOI 10.1086/519795
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81:559-575 (Pubitemid 47330214)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.3
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.W.9
Daly, M.J.10
Sham, P.C.11
-
24
-
-
35948984173
-
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
-
DOI 10.1101/gr.6861907
-
Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, Hakonarson H, Bucan M: PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 2007; 17:1665-1674 (Pubitemid 350074862)
-
(2007)
Genome Research
, vol.17
, Issue.11
, pp. 1665-1674
-
-
Wang, K.1
Li, M.2
Hadley, D.3
Liu, R.4
Glessner, J.5
Grant, S.F.A.6
Hakonarson, H.7
Bucan, M.8
-
25
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
DOI 10.1038/ng1847, PII NG1847
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D: Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006; 38:904-909 (Pubitemid 44141658)
-
(2006)
Nature Genetics
, vol.38
, Issue.8
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
26
-
-
43249125992
-
Estimation of the multiple testing burden for genomewide association studies of nearly all common variants
-
DOI 10.1002/gepi.20303
-
Pe'er I, Yelensky R, Altshuler D, Daly MJ: Estimation of the multiple testing burden for genomewide association studies of nearly all common variants. Genet Epidemiol 2008; 32:381-385 (Pubitemid 351656309)
-
(2008)
Genetic Epidemiology
, vol.32
, Issue.4
, pp. 381-385
-
-
Pe'er, I.1
Yelensky, R.2
Altshuler, D.3
Daly, M.J.4
-
27
-
-
67649345185
-
An improved Bonferroni procedure for multiple tests of significance
-
Simes RJ: An improved Bonferroni procedure for multiple tests of significance. Biometrika 1986; 73:751-754
-
(1986)
Biometrika
, vol.73
, pp. 751-754
-
-
Simes, R.J.1
-
28
-
-
67649584052
-
Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder
-
Holmans P, Green EK, Pahwa JS, Ferreira MA, Purcell SM, Sklar P, Owen MJ, O'Donovan MC, Craddock N: Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. Am J Hum Genet 2009; 85:13-24
-
(2009)
Am J Hum Genet
, vol.85
, pp. 13-24
-
-
Holmans, P.1
Green, E.K.2
Pahwa, J.S.3
Ferreira, M.A.4
Purcell, S.M.5
Sklar, P.6
Owen, M.J.7
O'Donovan, M.C.8
Craddock, N.9
-
29
-
-
0034069495
-
Gene ontology: Tool for the unification of biology
-
DOI 10.1038/75556
-
Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS, Eppig JT, Harris MA, Hill DP, Issel-Tarver L, Kasarskis A, Lewis S, Matese JC, Richardson JE, Ringwald M, Rubin GM, Sherlock G: Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet 2000; 25:25-29 (Pubitemid 30257031)
-
(2000)
Nature Genetics
, vol.25
, Issue.1
, pp. 25-29
-
-
Ashburner, M.1
Ball, C.A.2
Blake, J.A.3
Botstein, D.4
Butler, H.5
Cherry, J.M.6
Davis, A.P.7
Dolinski, K.8
Dwight, S.S.9
Eppig, J.T.10
Harris, M.A.11
Hill, D.P.12
Issel-Tarver, L.13
Kasarskis, A.14
Lewis, S.15
Matese, J.C.16
Richardson, J.E.17
Ringwald, M.18
Rubin, G.M.19
Sherlock, G.20
more..
-
30
-
-
38549174065
-
The Mouse Genome Database (MGD): Mouse biology and model systems
-
DOI 10.1093/nar/gkm961
-
Bult CJ, Eppig JT, Kadin JA, Richardson JE, Blake JA: The Mouse Genome Database (MGD): mouse biology and model systems. Nucleic Acids Res 2008; 36:D724-D728 (Pubitemid 351149814)
-
(2008)
Nucleic Acids Research
, vol.36
, Issue.SUPPL. 1
-
-
Bult, C.J.1
Eppig, J.T.2
Kadin, J.A.3
Richardson, J.E.4
Blake, J.A.5
Airey, M.T.6
Anagnostopoulos, A.7
Babiuk, R.8
Baldarelli, R.M.9
Baya, M.10
Beal, J.S.11
Bello, S.M.12
Bradt, D.W.13
Burkart, D.L.14
Butler, N.E.15
Campbell, J.16
Corbani, L.E.17
Cousins, S.L.18
Dahmen, D.J.19
Dene, H.20
Dolan, M.E.21
Forthofer, K.L.22
Frazer, K.S.23
Frost, P.24
Hall, M.25
Knowlton, M.26
Lewis, J.R.27
Lu, I.28
Maltais, L.J.29
McAndrews-Hill, M.30
McClatchy, S.31
McCrossin, M.J.32
Mason, J.33
Miers, D.B.34
Miller, L.A.35
Ni, L.36
Onda, H.37
Ormsby, J.E.38
Reddy, T.B.K.39
Reed, D.J.40
Richards-Smith, B.41
Shaw, D.R.42
Sinclair, R.43
Sitnikov, D.44
Smith, C.L.45
Szauter, P.46
Tomczuk, M.47
Updegraff, M.A.48
Washburn, L.L.49
Witham, I.T.50
Zhu, Y.51
more..
-
31
-
-
75549084894
-
PANTHER version 7: Improved phylogenetic trees, orthologs and collaboration with the Gene Ontology Consortium
-
Mi H, Dong Q, Muruganujan A, Gaudet P, Lewis S, Thomas PD: PANTHER version 7: improved phylogenetic trees, orthologs and collaboration with the Gene Ontology Consortium. Nucleic Acids Res 2010; 38:D204-D210
-
(2010)
Nucleic Acids Res
, vol.38
-
-
Mi, H.1
Dong, Q.2
Muruganujan, A.3
Gaudet, P.4
Lewis, S.5
Thomas, P.D.6
-
32
-
-
78649573450
-
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease
-
Jones L, Holmans PA, Hamshere ML, Harold D, Moskvina V, Ivanov D, Pocklington A, Abraham R, Hollingworth P, Sims R, Gerrish A, Pahwa JS, Jones N, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schurmann B, van den Bussche H, Heuser I, Peters O, Kornhuber J, Wiltfang J, Dichgans M, Frolich L, Hampel H, Hull M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Singleton AB, Guerreiro R, Muhleisen TW, Nothen MM, Moebus S, Jockel KH, Klopp N, Wichmann HE, Ruther E, Carrasquillo MM, Pankratz VS, Younkin SG, Hardy J, O'Donovan MC, Owen MJ, Williams J: Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. PLoS One 2010; 5:e13950
-
(2010)
PLoS One
, vol.5
-
-
Jones, L.1
Holmans, P.A.2
Hamshere, M.L.3
Harold, D.4
Moskvina, V.5
Ivanov, D.6
Pocklington, A.7
Abraham, R.8
Hollingworth, P.9
Sims, R.10
Gerrish, A.11
Pahwa, J.S.12
Jones, N.13
Stretton, A.14
Morgan, A.R.15
Lovestone, S.16
Powell, J.17
Proitsi, P.18
Lupton, M.K.19
Brayne, C.20
Rubinsztein, D.C.21
Gill, M.22
Lawlor, B.23
Lynch, A.24
Morgan, K.25
Brown, K.S.26
Passmore, P.A.27
Craig, D.28
McGuinness, B.29
Todd, S.30
Holmes, C.31
Mann, D.32
Smith, A.D.33
Love, S.34
Kehoe, P.G.35
Mead, S.36
Fox, N.37
Rossor, M.38
Collinge, J.39
Maier, W.40
Jessen, F.41
Schurmann, B.42
Van Den Bussche, H.43
Heuser, I.44
Peters, O.45
Kornhuber, J.46
Wiltfang, J.47
Dichgans, M.48
Frolich, L.49
Hampel, H.50
Hull, M.51
Rujescu, D.52
Goate, A.M.53
Kauwe, J.S.54
Cruchaga, C.55
Nowotny, P.56
Morris, J.C.57
Mayo, K.58
Livingston, G.59
Bass, N.J.60
Gurling, H.61
McQuillin, A.62
Gwilliam, R.63
Deloukas, P.64
Al-Chalabi, A.65
Shaw, C.E.66
Singleton, A.B.67
Guerreiro, R.68
Muhleisen, T.W.69
Nothen, M.M.70
Moebus, S.71
Jockel, K.H.72
Klopp, N.73
Wichmann, H.E.74
Ruther, E.75
Carrasquillo, M.M.76
Pankratz, V.S.77
Younkin, S.G.78
Hardy, J.79
O'Donovan, M.C.80
Owen, M.J.81
Williams, J.82
more..
-
33
-
-
78049450213
-
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function
-
Raychaudhuri S, Korn JM, McCarroll SA, Altshuler D, Sklar P, Purcell S, Daly MJ: Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genet 2010; 6:e1001097
-
(2010)
PLoS Genet
, vol.6
-
-
Raychaudhuri, S.1
Korn, J.M.2
McCarroll, S.A.3
Altshuler, D.4
Sklar, P.5
Purcell, S.6
Daly, M.J.7
-
34
-
-
77955397870
-
Single particle tracking of alpha7 nicotinic AChR in hippocampal neurons reveals regulated confinement at glutamatergic and GABAergic perisynaptic sites
-
Burli T, Baer K, Ewers H, Sidler C, Fuhrer C, Fritschy JM: Single particle tracking of alpha7 nicotinic AChR in hippocampal neurons reveals regulated confinement at glutamatergic and GABAergic perisynaptic sites. PLoS One 2010; 5:e11507
-
(2010)
PLoS One
, vol.5
-
-
Burli, T.1
Baer, K.2
Ewers, H.3
Sidler, C.4
Fuhrer, C.5
Fritschy, J.M.6
-
35
-
-
29244456419
-
P50 sensory gating deficit in children with centrotemporal spikes and sharp waves in the EEG
-
DOI 10.1016/j.neulet.2005.09.071, PII S0304394005011316
-
Fiedler BJ, Debus OM, Neubauer BA, Kienle M, Kurlemann G: P50 sensory gating deficit in children with centrotemporal spikes and sharp waves in the EEG. Neurosci Lett 2006; 393:206-210 (Pubitemid 41821109)
-
(2006)
Neuroscience Letters
, vol.393
, Issue.2-3
, pp. 206-210
-
-
Fiedler, B.J.1
Debus, O.M.2
Neubauer, B.A.3
Kienle, M.4
Kurlemann, G.5
-
36
-
-
0036897309
-
Association of promoter variants in the alpha7 nicotinic acetylcholine receptor subunit gene with an inhibitory deficit found in schizophrenia
-
DOI 10.1001/archpsyc.59.12.1085
-
Leonard S, Gault J, Hopkins J, Logel J, Vianzon R, Short M, Drebing C, Berger R, Venn D, Sirota P, Zerbe G, Olincy A, Ross RG, Adler LE, Freedman R: Association of promoter variants in the alpha7 nicotinic acetylcholine receptor subunit gene with an inhibitory deficit found in schizophrenia. Arch Gen Psychiatry 2002; 59:1085-1096 (Pubitemid 35424018)
-
(2002)
Archives of General Psychiatry
, vol.59
, Issue.12
, pp. 1085-1096
-
-
Leonard, S.1
Gault, J.2
Hopkins, J.3
Logel, J.4
Vianzon, R.5
Short, M.6
Drebing, C.7
Berger, R.8
Venn, D.9
Sirota, P.10
Zerbe, G.11
Olincy, A.12
Ross, R.G.13
Adler, L.E.14
Freedman, R.15
-
37
-
-
0035829966
-
No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder
-
DOI 10.1002/ajmg.1553
-
Kent L, Green E, Holmes J, Thapar A, Gill M, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mills J, Payton A, Craddock N: No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder. Am J Med Genet 2001; 105:686-689 (Pubitemid 33101467)
-
(2001)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.105
, Issue.8
, pp. 686-689
-
-
Kent, L.1
Green, E.2
Holmes, J.3
Thapar, A.4
Gill, M.5
Hawi, Z.6
Fitzgerald, M.7
Asherson, P.8
Curran, S.9
Mills, J.10
Payton, A.11
Craddock, N.12
-
38
-
-
70649089208
-
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes
-
Shinawi M, Schaaf CP, Bhatt SS, Xia Z, Patel A, Cheung SW, Lanpher B, Nagl S, Herding HS, Nevinny-Stickel C, Immken LL, Patel GS, German JR, Beaudet AL, Stankiewicz P: A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nat Genet 2009; 41:1269-1271
-
(2009)
Nat Genet
, vol.41
, pp. 1269-1271
-
-
Shinawi, M.1
Schaaf, C.P.2
Bhatt, S.S.3
Xia, Z.4
Patel, A.5
Cheung, S.W.6
Lanpher, B.7
Nagl, S.8
Herding, H.S.9
Nevinny-Stickel, C.10
Immken, L.L.11
Patel, G.S.12
German, J.R.13
Beaudet, A.L.14
Stankiewicz, P.15
-
39
-
-
65949085347
-
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
-
Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ, Hegde V, Hundley R, Khwaja O, Kothare S, Luedke C, Nasir R, Poduri A, Prasad K, Raffalli P, Reinhard A, Smith SE, Sobeih MM, Soul JS, Stoler J, Takeoka M, Tan WH, Thakuria J, Wolff R, Yusupov R, Gusella JF, Daly MJ, Wu BL: Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. J Med Genet 2009; 46:242-248
-
(2009)
J Med Genet
, vol.46
, pp. 242-248
-
-
Miller, D.T.1
Shen, Y.2
Weiss, L.A.3
Korn, J.4
Anselm, I.5
Bridgemohan, C.6
Cox, G.F.7
Dickinson, H.8
Gentile, J.9
Harris, D.J.10
Hegde, V.11
Hundley, R.12
Khwaja, O.13
Kothare, S.14
Luedke, C.15
Nasir, R.16
Poduri, A.17
Prasad, K.18
Raffalli, P.19
Reinhard, A.20
Smith, S.E.21
Sobeih, M.M.22
Soul, J.S.23
Stoler, J.24
Takeoka, M.25
Tan, W.H.26
Thakuria, J.27
Wolff, R.28
Yusupov, R.29
Gusella, J.F.30
Daly, M.J.31
Wu, B.L.32
more..
-
40
-
-
77954093814
-
Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: Benign or pathological?
-
Szafranski P, Schaaf CP, Person RE, Gibson IB, Xia Z, Mahadevan S, Wiszniewska J, Bacino CA, Lalani S, Potocki L, Kang SH, Patel A, Cheung SW, Probst FJ, Graham BH, Shinawi M, Beaudet AL, Stankiewicz P: Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological? Hum Mutat 2010; 31:840-850
-
(2010)
Hum Mutat
, vol.31
, pp. 840-850
-
-
Szafranski, P.1
Schaaf, C.P.2
Person, R.E.3
Gibson, I.B.4
Xia, Z.5
Mahadevan, S.6
Wiszniewska, J.7
Bacino, C.A.8
Lalani, S.9
Potocki, L.10
Kang, S.H.11
Patel, A.12
Cheung, S.W.13
Probst, F.J.14
Graham, B.H.15
Shinawi, M.16
Beaudet, A.L.17
Stankiewicz, P.18
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