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Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 12, p. 1302, doi. 10.1038/mp.2012.142
By:
- Green, E K;
- Hamshere, M;
- Forty, L;
- Gordon-Smith, K;
- Fraser, C;
- Russell, E;
- Grozeva, D;
- Kirov, G;
- Holmans, P;
- Moran, J L;
- Purcell, S;
- Sklar, P;
- Owen, M J;
- O'Donovan, M C;
- Jones, L;
- Jones, I R;
- Craddock, N
Publication type:
Article
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 6, p. 708, doi. 10.1038/mp.2012.67
By:
- Hamshere, M L;
- Walters, J T R;
- Smith, R;
- Richards, A L;
- Green, E;
- Grozeva, D;
- Jones, I;
- Forty, L;
- Jones, L;
- Gordon-Smith, K;
- Riley, B;
- O'Neill, T;
- Kendler, K S;
- Sklar, P;
- Purcell, S;
- Kranz, J;
- Morris, D;
- Gill, M;
- Holmans, P;
- Craddock, N
Publication type:
Article
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 6, p. 738, doi. 10.1038/mp.2012.89
By:
- Hamshere, M L;
- Walters, J T R;
- Smith, R;
- Richards, A L;
- Green, E;
- Grozeva, D;
- Jones, I;
- Forty, L;
- Jones, L;
- Gordon-Smith, K;
- Riley, B;
- O'Neill, T;
- Kendler, K S;
- Sklar, P;
- Purcell, S;
- Kranz, J;
- Morris, D;
- Gill, M;
- Holmans, P;
- Craddock, N
Publication type:
Article
Association at SYNE1 in both bipolar disorder and recurrent major depression.
Published in:
Molecular Psychiatry, 2013, v. 18, n. 5, p. 614, doi. 10.1038/mp.2012.48
By:
- Green, E K;
- Grozeva, D;
- Forty, L;
- Gordon-Smith, K;
- Russell, E;
- Farmer, A;
- Hamshere, M;
- Jones, I R;
- Jones, L;
- McGuffin, P;
- Moran, J L;
- Purcell, S;
- Sklar, P;
- Owen, M J;
- O'Donovan, M C;
- Craddock, N
Publication type:
Article
Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.
Published in:
Molecular Psychiatry, 2012, v. 17, n. 8, p. 818, doi. 10.1038/mp.2011.89
By:
- Badner, J A;
- Koller, D;
- Foroud, T;
- Edenberg, H;
- Nurnberger, J I;
- Zandi, P P;
- Willour, V L;
- McMahon, F J;
- Potash, J B;
- Hamshere, M;
- Grozeva, D;
- Green, E;
- Kirov, G;
- Jones, I;
- Jones, L;
- Craddock, N;
- Morris, D;
- Segurado, R;
- Gill, M;
- Sadovnick, D
Publication type:
Article
Independent evidence for the selective influence of GABAA receptors on one component of the bipolar disorder phenotype.
Published in:
2011
By:
- Breuer, R.;
- Hamshere, M. L.;
- Strohmaier, J.;
- Mattheisen, M.;
- Degenhardt, F.;
- Meier, S.;
- Paul, T.;
- O'Donovan, M. C.;
- Mühleisen, T. W.;
- Schulze, T. G.;
- Nöthen, M. M.;
- Cichon, S.;
- Craddock, N.;
- Rietschel, M.
Publication type:
Letter
Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.
Published in:
Molecular Psychiatry, 2011, v. 16, n. 1, p. 2, doi. 10.1038/mp.2009.107
By:
- Y. Liu;
- Blackwood, D. H.;
- Caesar, S.;
- de Geus, E. J. C.;
- Farmer, A.;
- Ferreira, M. A. R.;
- Ferrier, I. N.;
- Fraser, C.;
- Gordon-Smith, K.;
- Green, E. K.;
- Grozeva, D.;
- Gurling, H. M.;
- Hamshere, M. L.;
- Heutink, P.;
- Holmans, P A;
- Hoogendijk, W. J.;
- Hottenga, J. J.;
- Jones, L.;
- Jones, I. R.;
- Kirov, G.
Publication type:
Article
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype.
Published in:
2010
By:
- Craddock, N;
- Jones, L;
- Jones, I R;
- Kirov, G;
- Green, E K;
- Grozeva, D;
- Moskvina, V;
- Nikolov, I;
- Hamshere, M L;
- Vukcevic, D;
- Caesar, S;
- Gordon-Smith, K;
- Fraser, C;
- Russell, E;
- Norton, N;
- Breen, G;
- St Clair, D;
- Collier, D A;
- Young, A H;
- Ferrier, I N
Publication type:
Correction Notice
The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia.
Published in:
Molecular Psychiatry, 2010, v. 15, n. 10, p. 1016, doi. 10.1038/mp.2009.49
By:
- Green, E. K.;
- Grozeva, D.;
- Jones, I.;
- Jones, L.;
- Kirov, G.;
- Caesar, S.;
- Gordon-Smith, K.;
- Fraser, C.;
- Forty, L.;
- Russell, E.;
- Hamshere, M. L.;
- Moskvina, V.;
- Nikolov, I.;
- Farmer, A.;
- McGuffin, P.;
- Holmans, P. A.;
- Owen, M. J.;
- O'Donovan, M. C.;
- Craddock, N.
Publication type:
Article
Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype.
Published in:
Molecular Psychiatry, 2010, v. 15, n. 2, p. 146, doi. 10.1038/mp.2008.66
By:
- Craddock, N.;
- Jones, L.;
- Jones, I. R.;
- Kirov, G.;
- Green, E. K.;
- Grozeva, D.;
- Moskvina, V.;
- Nikolov, I.;
- Hamshere, M. L.;
- Vukcevic, D.;
- Caesar, S.;
- Gordon-Smith, K.;
- Fraser, C.;
- Russell, E.;
- Norton, N.;
- Breen, G.;
- St Clair, D.;
- Collier, D. A.;
- Young, A. H.;
- Ferrier, I. N.
Publication type:
Article
Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.
Published in:
Molecular Psychiatry, 2009, v. 14, n. 1, p. 30, doi. 10.1038/mp.2008.108
By:
- O'Donovan, M. C.;
- Norton, N.;
- Williams, H.;
- Peirce, T.;
- Moskvina, V.;
- Nikolov, I.;
- Hamshere, M.;
- Carroll, L.;
- Georgieva, L.;
- Dwyer, S.;
- Holmans, P.;
- Marchini, J. L.;
- Spencer, C. C. A.;
- Howie, B.;
- Leung, H.-T.;
- Giegling, I.;
- Hartmann, A. M.;
- Möller, H.-J.;
- Morris, D. W.;
- Shi, Y.
Publication type:
Article
Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement.
Published in:
2008
By:
- Baum, A. E.;
- Hamshere, M.;
- Green, E.;
- Cichon, S.;
- Rietschel, M.;
- Noethen, M. M.;
- Craddock, N.;
- McMahon, F. J.
Publication type:
Letter
Identification of a Novel Valosin-Containing Protein Polymorphism in Late-Onset Alzheimer’s Disease.
Published in:
Neurodegenerative Diseases, 2007, v. 4, n. 5, p. 376, doi. 10.1159/000105158
By:
- Kaleem, M.;
- Zhao, A.;
- Hamshere, M.;
- Myers, A. J.
Publication type:
Article
Doppler echocardiography underestimates the prevalence and magnitude of mid‐cavity obstruction in patients with symptomatic hypertrophic cardiomyopathy.
Published in:
Catheterization & Cardiovascular Interventions, 2018, v. 91, n. 4, p. 783, doi. 10.1002/ccd.27143
By:
- Malcolmson, James W.;
- Hamshere, Stephen M.;
- Joshi, Abhishek;
- O'Mahony, Constantinos;
- Dhinoja, Mehul;
- Petersen, Steffen E.;
- Sekhri, Neha;
- Mohiddin, Saidi A.
Publication type:
Article
Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22.
Published in:
2006
By:
- Lambert, D;
- Middle, F;
- Hamshere, M L;
- Segurado, R;
- Raybould, R;
- Corvin, A;
- Green, E;
- O'Mahony, E;
- Nikolov, I;
- Mulcahy, T;
- Haque, S;
- Bort, S;
- Bennett, P;
- Norton, N;
- Owen, M J;
- Kirov, G;
- Lendon, C;
- Jones, L;
- Jones, I;
- Holmans, P
Publication type:
Correction Notice
Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22.
Published in:
Molecular Psychiatry, 2005, v. 10, n. 9, p. 831, doi. 10.1038/sj.mp.4001684
By:
- Lambert, D.;
- Middle, F.;
- Hamshere, M. L.;
- Segurado, R.;
- Raybould, R.;
- Corvin, A.;
- Green, E.;
- O'Mahony, E.;
- Nikolov, I;
- Mulcahy, T.;
- Haque, S.;
- Bort, S.;
- Bennett, P.;
- Norton, N.;
- Owen, M. J.;
- Kirov, G.;
- Lendon, C.;
- Jones, L.;
- Jones, I.;
- Holmans, P.
Publication type:
Article
Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.
Published in:
Molecular Psychiatry, 2003, v. 8, n. 2, p. 176, doi. 10.1038/sj.mp.4001216
By:
- Turic, D.;
- Robinson, L.;
- Duke, M.;
- Morris, D. W.;
- Webb, V.;
- Hamshere, M.;
- Milham, C.;
- Hopkin, E.;
- Pound, K.;
- Fernando, S.;
- Grierson, A.;
- Easton, M.;
- Williams, N.;
- Van Den Bree, M.;
- Chowdhury, R.;
- Gruen, J.;
- Stevenson, J.;
- Krawczak, M.;
- Owen, M. J.;
- O'Donovan, M. C.
Publication type:
Article

Found: 17

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample.

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

Association at SYNE1 in both bipolar disorder and recurrent major depression.

Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.

Independent evidence for the selective influence of GABA<sub>A</sub> receptors on one component of the bipolar disorder phenotype.

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.

Strong genetic evidence for a selective influence of GABA<sub>A</sub> receptors on a component of the bipolar disorder phenotype.

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia.

Strong genetic evidence for a selective influence of GABA<sub>A</sub> receptors on a component of the bipolar disorder phenotype.

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

Meta-analysis of two genome-wide association studies of bipolar disorder reveals important points of agreement.

Identification of a Novel Valosin-Containing Protein Polymorphism in Late-Onset Alzheimer’s Disease.

Doppler echocardiography underestimates the prevalence and magnitude of mid‐cavity obstruction in patients with symptomatic hypertrophic cardiomyopathy.

Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22.

Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22.

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.