Linking single nucleotide polymorphismsNÖTHEN, Markus M; CICHON, Sven.Pharmacogenetics (London). 2002, Vol 12, Num 2, pp 89-90, issn 0960-314XArticle

New findings in the genetics of major psychosesNÖTHEN, Markus M; NIERATSCHKER, Vanessa; CICHON, Sven et al.Dialogues in clinical neuroscience. 2010, Vol 12, Num 1, pp 85-93, issn 1294-8322, 9 p.Article

Prenatal diagnosis of Pfeiffer syndrome type IIBLAUMEISER, Bettina; LOQUET, Philip; WUYTS, Wim et al.Prenatal diagnosis. 2004, Vol 24, Num 8, pp 644-646, issn 0197-3851, 3 p.Article

The G721G30 gene locus in psychiatric disorders: A challenge to diagnostic boundaries?RAMI ABOU JAMRA; SCHMAEL, Christine; CICHON, Sven et al.Schizophrenia bulletin. 2006, Vol 32, Num 4, pp 599-608, issn 0586-7614, 10 p.Article

Achalasia: will genetic studies provide insights?GOCKEL, Henning R; SCHUMACHER, Johannes; GOCKEL, Ines et al.Human genetics. 2010, Vol 128, Num 4, pp 353-364, issn 0340-6717, 12 p.Article

Is there a phenotypic difference between probands in case-control versus family-based association studies?SCHULZE, Thomas G; CICHON, Sven; NÖTHEN, Markus M et al.American journal of medical genetics. 2003, Vol 118B, Num 1, pp 25-26, issn 0148-7299, 2 p.Article

A systematic eQTL study of cis-trans epistasis in 210 HapMap individualsBECKER, Jessica; WENDLAND, Jens R; HAENISCH, Britta et al.European journal of human genetics. 2012, Vol 20, Num 1, pp 97-101, issn 1018-4813, 5 p.Article

Genetics of dyslexia : the evolving landscapeSCHUMACHER, Johannes; HOFFMANN, Per; SCHMÄL, Christine et al.Journal of medical genetics. 2007, Vol 44, Num 5, pp 289-297, issn 0022-2593, 9 p.Article

Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effectsERK, Susanne; MEYER-LINDENBERG, Andreas; HADDAD, Leila et al.NeuroImage (Orlando, Fla.). 2014, Vol 94, pp 147-154, issn 1053-8119, 8 p.Article

The Effect of Neurogranin on Neural Correlates of Episodic Memory Encoding and RetrievalKRUG, Axel; KRACH, Sören; JANSEN, Andreas et al.Schizophrenia bulletin. 2013, Vol 39, Num 1, pp 141-150, issn 0586-7614, 10 p.Article

Population-Specific Association between a Polymorphic Variant in ST18, Encoding a Pro-Apoptotic Molecule, and Pemphigus VulgarisSARIG, Ofer; BERCOVICI, Sivan; BAUM, Sharon et al.Journal of investigative dermatology. 2012, Vol 132, Num 7, pp 1798-1805, issn 0022-202X, 8 p.Article

Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literatureSCHRAMM, Charlotte; DRAAKEN, Markus; KREISS-NACHTSHEIM, Martina et al.European journal of pediatrics. 2011, Vol 170, Num 6, pp 741-746, issn 0340-6199, 6 p.Article

Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patientsMÜHLEISEN, Thomas W; BUKET BASMANAV, F; MÖSSNER, Rainald et al.Schizophrenia research. 2011, Vol 127, Num 1-3, pp 35-40, issn 0920-9964, 6 p.Article

Brain Function in Carriers of a Genome-wide Supported Bipolar Disorder VariantERK, Susanne; MEYER-LINDENBERG, Andreas; CICHON, Sven et al.Archives of general psychiatry. 2010, Vol 67, Num 8, pp 803-811, issn 0003-990X, 9 p.Article

Recent positive selection of a human androgen receptor/ ectodysplasin A2 receptor haplotype and its relationship to male pattern baldnessHILLMER, Axel M; FREUDENBERG, Jan; MYLES, Sean et al.Human genetics. 2009, Vol 126, Num 2, pp 255-264, issn 0340-6717, 10 p.Article

Common variants conferring risk of schizophreniaSTEFANSSON, Hreinn; OPHOFF, Roel A; SIGURDSSON, Engilbert et al.Nature (London). 2009, Vol 460, Num 7256, pp 744-747, issn 0028-0836, 4 p.Article

Disruption of the neurexin 1 gene is associated with schizophreniaRUJESCU, Dan; INGASON, Andres; MURRAY, Robin et al.Human molecular genetics (Print). 2009, Vol 18, Num 5, pp 988-996, issn 0964-6906, 9 p.Article

Genetic Variation in the Schizophrenia-Risk Gene Neuregulin I Correlates with Brain Activation and Impaired Speech Production in a Verbal Fluency Task in Healthy IndividualsKIRCHER, Tilo; KRUG, Axel; NÖTHEN, Markus M et al.Human brain mapping. 2009, Vol 30, Num 10, pp 3406-3416, issn 1065-9471, 11 p.Article

Hypoparathyroidism-retardation-dysmorphism syndrome in a girl : A new variant not caused by a TBCE mutation-clinical report and reviewCOURTENS, Winnie; WUYTS, Wim; FOOT, Martin et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 6, pp 611-617, issn 1552-4825, 7 p.Article

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopeciaHILLMER, Axel M; HANNEKEN, Sandra; HEYN, Uwe et al.American journal of human genetics. 2005, Vol 77, Num 1, pp 140-148, issn 0002-9297, 9 p.Article

No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samplesGLASER, Beate; SCHUMACHER, Johannes; JÖNSSON, Erick G et al.Biological psychiatry (1969). 2005, Vol 58, Num 1, pp 78-80, issn 0006-3223, 3 p.Article

Family-based association studies of α-adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorderRAMI ABOU JAMRA; SCHUMACHER, Johannes; PROPPING, Peter et al.American journal of medical genetics. 2004, Vol 126B, Num 1, pp 79-81, issn 0148-7299, 3 p.Article

Association study between two variants in the DOPA decarboxylase gene in bipolar and unipolar affective disorderJAHNES, Esther; MÜLLER, Daniel J; NÖTHEN, Markus M et al.American journal of medical genetics. 2002, Vol 114, Num 5, pp 519-522, issn 0148-7299Article

Isolated Bladder Exstrophy Associated with a De Novo 0.9 Mb Microduplication on Chromosome 19p1312DRAAKEN, Markus; MUGHAL, Sadaf S; BOEMERS, Thomas M et al.Birth defects research. Clinical and molecular teratology. 2013, Vol 97, Num 3, pp 133-139, issn 1542-0752, 7 p.Article

Genetic determination of human facial morphology: links between cleft-lips and normal variationBOEHRINGER, Stefan; VAN DER LIJN, Fedde; UITTERLINDEN, Andre G et al.European journal of human genetics. 2011, Vol 19, Num 11, pp 1192-1197, issn 1018-4813, 6 p.Article