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A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
Published in:
Diabetologia, 2007, v. 50, n. 7, p. 1418, doi. 10.1007/s00125-007-0658-4
By:
- Hoffmann, K.;
- Mattheisen, M.;
- Dahm, S.;
- Nürnberg, P.;
- Roe, C.;
- Johnson, J.;
- Cox, N.;
- Wichmann, H.;
- Wienker, T.;
- Schulze, J.;
- Schwarz, P.;
- Lindner, T.
Publication type:
Article
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS.
Published in:
Molecular Psychiatry, 2015, v. 20, n. 3, p. 337, doi. 10.1038/mp.2014.43
By:
- Mattheisen, M.;
- Samuels, J. F.;
- Wang, Y.;
- Greenberg, B. D.;
- Fyer, A. J.;
- McCracken, J. T.;
- Geller, D. A.;
- Murphy, D. L.;
- Knowles, J. A.;
- Grados, M. A.;
- Riddle, M. A.;
- Rasmussen, S. A.;
- McLaughlin, N. C.;
- Nurmi, E. L.;
- Askland, K. D.;
- Qin, H. -.D;
- Cullen, B. A.;
- Piacentini, J.;
- Pauls, D. L.;
- Bienvenu, O. J.
Publication type:
Article
Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 7, p. 774, doi. 10.1038/mp.2013.103
By:
- Luo, X-j;
- Li, M;
- Huang, L;
- Steinberg, S;
- Mattheisen, M;
- Liang, G;
- Donohoe, G;
- Shi, Y;
- Chen, C;
- Yue, W;
- Alkelai, A;
- Lerer, B;
- Li, Z;
- Yi, Q;
- Rietschel, M;
- Cichon, S;
- Collier, D A;
- Tosato, S;
- Suvisaari, J;
- Rujescu, Dan
Publication type:
Article
Rare autosomal copy number variations in early-onset familial Alzheimer's disease.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 6, p. 676, doi. 10.1038/mp.2013.77
By:
- Hooli, B V;
- Kovacs-Vajna, Z M;
- Mullin, K;
- Blumenthal, M A;
- Mattheisen, M;
- Zhang, C;
- Lange, C;
- Mohapatra, G;
- Bertram, L;
- Tanzi, R E
Publication type:
Article
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 4, p. 527, doi. 10.1038/mp.2013.73
By:
- Li, M;
- Luo, X-j;
- Rietschel, M;
- Lewis, C M;
- Mattheisen, M;
- Müller-Myhsok, B;
- Jamain, S;
- Leboyer, M;
- Landén, M;
- Thompson, P M;
- Cichon, S;
- Nöthen, M M;
- Schulze, T G;
- Sullivan, P F;
- Bergen, S E;
- Donohoe, G;
- Morris, D W;
- Hargreaves, A;
- Gill, M;
- Corvin, A
Publication type:
Article
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 4, p. 452, doi. 10.1038/mp.2013.37
By:
- Li, M;
- Luo, X-j;
- Rietschel, M;
- Lewis, C M;
- Mattheisen, M;
- Müller-Myhsok, B;
- Jamain, S;
- Leboyer, M;
- Landén, M;
- Thompson, P M;
- Cichon, S;
- Nöthen, M M;
- Schulze, T G;
- Sullivan, P F;
- Bergen, S E;
- Donohoe, G;
- Morris, D W;
- Hargreaves, A;
- Gill, M;
- Corvin, A
Publication type:
Article
Common variant at 16p11.2 conferring risk of psychosis.
Published in:
Molecular Psychiatry, 2014, v. 19, n. 1, p. 108, doi. 10.1038/mp.2012.157
By:
- Steinberg, S;
- de Jong, S;
- Mattheisen, M;
- Costas, J;
- Demontis, D;
- Jamain, S;
- Pietiläinen, O P H;
- Lin, K;
- Papiol, S;
- Huttenlocher, J;
- Sigurdsson, E;
- Vassos, E;
- Giegling, I;
- Breuer, R;
- Fraser, G;
- Walker, N;
- Melle, I;
- Djurovic, S;
- Agartz, I;
- Tuulio-Henriksson, A
Publication type:
Article
Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.
Published in:
Molecular Psychiatry, 2012, v. 17, n. 9, p. 906, doi. 10.1038/mp.2011.80
By:
- Rietschel, M;
- Mattheisen, M;
- Degenhardt, F;
- Kahn, René S;
- Linszen, Don H;
- Os, Jim van;
- Wiersma, Durk;
- Bruggeman, Richard;
- Cahn, Wiepke;
- de Haan, Lieuwe;
- Krabbendam, Lydia;
- Myin-Germeys, Inez;
- Mühleisen, T W;
- Kirsch, P;
- Esslinger, C;
- Herms, S;
- Demontis, D;
- Steffens, M;
- Strohmaier, J;
- Haenisch, B
Publication type:
Article
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.
Published in:
Molecular Psychiatry, 2012, v. 17, n. 4, p. 421, doi. 10.1038/mp.2011.8
By:
- Priebe, L;
- Degenhardt, F A;
- Herms, S;
- Haenisch, B;
- Mattheisen, M;
- Nieratschker, V;
- Weingarten, M;
- Witt, S;
- Breuer, R;
- Paul, T;
- Alblas, M;
- Moebus, S;
- Lathrop, M;
- Leboyer, M;
- Schreiber, S;
- Grigoroiu-Serbanescu, M;
- Maier, W;
- Propping, P;
- Rietschel, M;
- Nöthen, M M
Publication type:
Article
Independent evidence for the selective influence of GABA<sub>A</sub> 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
Polymorphisms in SREBF1 and SREBF2, two antipsychotic-activated transcription factors controlling cellular lipogenesis, are associated with schizophrenia in German and Scandinavian samples.
Published in:
Molecular Psychiatry, 2010, v. 15, n. 5, p. 463, doi. 10.1038/mp.2008.110
By:
- Le Hellard, S.;
- Mühleisen, T. W.;
- Djurovic, S.;
- Fernø, J.;
- Ouriaghi, Z.;
- Mattheisen, M.;
- Vasilescu, C.;
- Raeder, M. B.;
- Hansen, T.;
- Strohmaier, J.;
- Georgi, A.;
- Brockschmidt, F. F.;
- Melle, I.;
- Nenadic, I.;
- Sauer, H.;
- Rietschel, M.;
- Nöthen, M. M.;
- Werge, T.;
- Andreassen, O. A.;
- Cichon, S.
Publication type:
Article
Supporting evidence for LRRTM1 imprinting effects in schizophrenia.
Published in:
2009
By:
- Ludwig, K. U.;
- Mattheisen, M.;
- Mühleisen, T. W.;
- Roeske, D.;
- Schmäl, C.;
- Breuer, R.;
- Schulte-Körne, G.;
- Müller-Myhsok, B.;
- Nöthen, M. M.;
- Hoffmann, P.;
- Rietschel, M.;
- Cichon, S.
Publication type:
Letter
GWAS-based pathway analysis differentiates between fluid and crystallized intelligence.
Published in:
Genes, Brain & Behavior, 2014, v. 13, n. 7, p. 663, doi. 10.1111/gbb.12152
By:
- Christoforou, A.;
- Espeseth, T.;
- Davies, G.;
- Fernandes, C. P. D.;
- Giddaluru, S.;
- Mattheisen, M.;
- Tenesa, A.;
- Harris, S. E.;
- Liewald, D. C.;
- Payton, A.;
- Ollier, W.;
- Horan, M.;
- Pendleton, N.;
- Haggarty, P.;
- Djurovic, S.;
- Herms, S.;
- Hoffman, P.;
- Cichon, S.;
- Starr, J. M.;
- Lundervold, A.
Publication type:
Article
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder.
Published in:
Translational Psychiatry, 2017, v. 7, n. 2, p. e1034, doi. 10.1038/tp.2017.3
By:
- Lescai, F;
- Als, T D;
- Li, Q;
- Nyegaard, M;
- Andorsdottir, G;
- Biskopstø, M;
- Hedemand, A;
- Fiorentino, A;
- O'Brien, N;
- Jarram, A;
- Liang, J;
- Grove, J;
- Pallesen, J;
- Eickhardt, E;
- Mattheisen, M;
- Bolund, L;
- Demontis, D;
- Wang, A G;
- McQuillin, A;
- Mors, O
Publication type:
Article
Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.
Published in:
Translational Psychiatry, 2017, v. 7, n. 1, p. e997, doi. 10.1038/tp.2016.272
By:
- Erk, S;
- Mohnke, S;
- Ripke, S;
- Lett, T A;
- Veer, I M;
- Wackerhagen, C;
- Grimm, O;
- Romanczuk-Seiferth, N;
- Degenhardt, F;
- Tost, H;
- Mattheisen, M;
- Mühleisen, T W;
- Charlet, K;
- Skarabis, N;
- Kiefer, F;
- Cichon, S;
- Witt, S H;
- Nöthen, M M;
- Rietschel, M;
- Heinz, A
Publication type:
Article
Functional impact of a recently identified quantitative trait locus for hippocampal volume with genome-wide support.
Published in:
Translational Psychiatry, 2013, v. 3, n. 7, p. 1, doi. 10.1038/tp.2013.57
By:
- Erk, S.;
- Meyer-Lindenberg, A.;
- Schmierer, P.;
- Grimm, O.;
- Tost, H.;
- Mühleisen, T.;
- Mattheisen, M.;
- Seiferth, N.;
- Cichon, S.;
- Rietschel, M.;
- Nöthen, M. M.;
- Heinz, A.;
- Walter, H.
Publication type:
Article
FZD6 encoding the Wnt receptor frizzled 6 is mutated in autosomal-recessive nail dysplasia.
Published in:
British Journal of Dermatology, 2012, v. 166, n. 5, p. 1088, doi. 10.1111/j.1365-2133.2011.10800.x
By:
- Naz, G.;
- Pasternack, S.M.;
- Perrin, C.;
- Mattheisen, M.;
- Refke, M.;
- Khan, S.;
- Gul, A.;
- Simons, M.;
- Ahmad, W.;
- Betz, R.C.
Publication type:
Article
Genetic code expansion to enable site‐specific bioorthogonal labeling of functional G protein‐coupled receptors in live cells.
Published in:
Protein Science: A Publication of the Protein Society, 2023, v. 32, n. 2, p. 1, doi. 10.1002/pro.4550
By:
- Mattheisen, Jordan M.;
- Wollowitz, Jaina S.;
- Huber, Thomas;
- Sakmar, Thomas P.
Publication type:
Article

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