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Randomized clinical trial of visualization versus neuromonitoring of recurrent laryngeal nerves during thyroidectomyBARCZYNSKI, M; KONTUREK, A; CICHON, S et al.British journal of surgery. 2009, Vol 96, Num 3, pp 240-246, issn 0007-1323, 7 p.Conference Paper

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2O'DONOVAN, M. C; NORTON, N; HOLMANS, P et al.Molecular psychiatry. 2009, Vol 14, Num 1, pp 30-36, issn 1359-4184, 7 p.Article

Lack of imprinting of the human dopamine D4 receptor (DRD4) geneCICHON, S; NÖTHEN, M. M; WOLF, H. K et al.American journal of medical genetics. 1996, Vol 67, Num 2, pp 229-231, issn 0148-7299Article

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibilityLI, M; LUO, X-J; CICHON, S et al.Molecular psychiatry. 2014, Vol 19, Num 4, pp 452-461, issn 1359-4184, 10 p.Article

Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband : supportive evidence for linkage at 3p14ETAIN, B; MATHIEU, F; BELLIVIER, F et al.Molecular psychiatry. 2006, Vol 11, Num 7, pp 685-694, issn 1359-4184, 10 p.Article

The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approachHILLMER, A. M; KRUSE, R; MACCIARDI, F et al.British journal of dermatology (1951). 2002, Vol 146, Num 4, pp 601-608, issn 0007-0963Article

A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26CICHON, S; SCHMIDT-WOLF, G; FRITZE, J et al.Molecular psychiatry. 2001, Vol 6, Num 3, pp 342-349, issn 1359-4184Article

Genetic linkage analysis with dyslexia : Evidence for linkage of spelling disability to chromosome 15NÖTHEN, M. M; SCHULTE-KÖRNE, G; GRIMM, T et al.European child & adolescent psychiatry. 1999, Vol 8, pp 56-59, issn 1018-8827, SUP3Article

A gene for universal congenital alopecia maps to chromosome 8p21-22NÖTHEN, M. M; CICHON, S; AHMAD, M et al.American journal of human genetics. 1998, Vol 62, Num 2, pp 386-390, issn 0002-9297Article

A serine to glycine substitution at position 9 in the extracellular N-terminal part of the dopamine D₃ receptor protein : no role in the genetic predisposition to bipolar affective disorderRIETSCHEL, M; NÖTHEN, M. M; MÖLLER, H.-J et al.Psychiatry research. 1993, Vol 46, Num 3, pp 253-259, issn 0165-1781Article

Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility geneLUO, X-J; LI, M; ALKELAI, A et al.Molecular psychiatry. 2014, Vol 19, Num 7, pp 774-783, issn 1359-4184, 10 p.Article

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia lociBØRGLUM, A. D; DEMONTIS, D; ØRNTOFT, T et al.Molecular psychiatry. 2014, Vol 19, Num 3, pp 325-333, issn 1359-4184, 9 p.Article

Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorderCHEN, D. T; JIANG, X; CHENG, A et al.Molecular psychiatry. 2013, Vol 18, Num 2, pp 195-205, issn 1359-4184, 11 p.Article

Effects of a genome-wide supported psychosis risk variant on neural activation during a theory-of-mind taskWALTER, H; SCHNELL, K; NÖTHEN, M. M et al.Molecular psychiatry. 2011, Vol 16, Num 4, pp 462-470, issn 1359-4184, 9 p.Article

Expanding the range of ZNF804A variants conferring risk of psychosisSTEINBERG, S; MORS, O; OLASON, P et al.Molecular psychiatry. 2011, Vol 16, Num 1, pp 59-66, issn 1359-4184, 8 p.Article

Tourette syndrome and the norepinephrine transporter gene : Results of a systematic mutation screeningSTÖBER, G; HEBEBRAND, J; NÖTHEN, M. M et al.American journal of medical genetics. 1999, Vol 88, Num 2, pp 158-163, issn 0148-7299Article

The human complement C8G gene, a member of the lipocalin gene family : polymorphisms and mapping to chromosome 9q34.3DEWALD, G; CICHON, S; BRYANT, S. P et al.Annals of human genetics. 1996, Vol 60, pp 281-291, issn 0003-4800, 4Article

Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophreniaSCHULTZ, C. C; MÜHLEISEN, T. W; KIEHNTOPF, M et al.Psychological medicine (Print). 2014, Vol 44, Num 4, pp 811-820, issn 0033-2917, 10 p.Article

The KMO allele encoding Arg⁴⁵² is associated with psychotic features in bipolar disorder type 1, and with increased CSF KYNA level and reduced KMO expressionLAVEBRATT, C; OLSSON, S; ÖSBY, U et al.Molecular psychiatry. 2014, Vol 19, Num 3, pp 334-341, issn 1359-4184, 8 p.Article

TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studiesERHARDT, A; CZIBERE, L; HECK, A et al.Molecular psychiatry. 2011, Vol 16, Num 6, pp 647-663, issn 1359-4184, 17 p.Article

Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorderABOU JAMRA, R; BECKER, T; NÖTHEN, M. M et al.Molecular psychiatry. 2008, Vol 13, Num 3, pp 277-284, issn 1359-4184, 8 p.Article

Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approachWANG, T; FRANKE, P; NEIDT, H et al.Molecular psychiatry. 2001, Vol 6, Num 1, pp 109-111, issn 1359-4184Article

A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German familyCICHON, S; KRUSE, R; HILLMER, A. M et al.British journal of dermatology (1951). 2000, Vol 143, Num 4, pp 811-814, issn 0007-0963Article

Localization of a gene for syndactyly type 1 to chromosome 2q34-q36BOSSE, K; BETZ, R. C; LEE, Y.-A et al.American journal of human genetics. 2000, Vol 67, Num 2, pp 492-497, issn 0002-9297Article