Dinucleotide repeat polymorphism at the human CD59 locusNÖTHEN, M. M; DEWALD, G.Clinical genetics. 1995, Vol 47, Num 3, pp 165-166, issn 0009-9163Article

Linkage disequilibrium mapping at DAT1, DRD5 and DBH narrows the search for ADHD susceptibility alleles at these lociHAWI, Z; LOWER, N; KIRLEY, A et al.Molecular psychiatry. 2003, Vol 8, Num 3, pp 299-308, issn 1359-4184, 10 p.Article

Dinucleotide repeat polymorphism at the D18S99 locusERDMANN, J; NÖTHEN, M.Human molecular genetics (Print). 1993, Vol 2, Num 1, issn 0964-6906, p. 91Article

An association study of a neurotrophin-3 (NT-3) gene polymorphism with schizophreniaDAWSON, E; POWELL, J. F; MURRAY, R. M et al.Acta psychiatrica Scandinavica. 1995, Vol 92, Num 6, pp 425-428, issn 0001-690XArticle

A genome-wide association study of attempted suicideWILLOUR, V. L; SEIFUDDIN, F; PERLIS, R. H et al.Molecular psychiatry. 2012, Vol 17, Num 4, pp 433-444, issn 1359-4184, 12 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

A common amino acid polymorphism in complement component C1RNÖTHEN, M. M; DEWALD, G.Human molecular genetics (Print). 1994, Vol 3, Num 1, issn 0964-6906, p. 217Article

Meta-analysis of association between the 5-HT_2a receptor T102C polymorphism and schizophreniaWILLIAMS, J; MCGUFFIN, P; NÖTHEN, M et al.Lancet (British edition). 1997, Vol 349, Num 9060, issn 0140-6736, p. 1221Article

Localization of the human glucosidase I gene to chromosome 2p12-p13 by fluorescence in situ hybridization and PCR analysis of somatic cell hybridsKALZ-FÜLLER, B; HEIDRICH-KAUL, C; NÖTHEN, M et al.Genomics (San Diego, Calif.). 1996, Vol 34, Num 3, pp 442-444, issn 0888-7543, 2 p.Article

Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1DAWSON, E; PARFITT, E; REUNER, U et al.American journal of medical genetics. 1995, Vol 60, Num 2, pp 94-102, issn 0148-7299Article

Polymorphism of human complement component C6 : an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 BDEWALD, G; NÖTHEN, M. M; CICHON, S et al.Biochemical and biophysical research communications (Print). 1993, Vol 194, Num 1, pp 458-464, issn 0006-291XArticle

Delineation of marker chromosomes by reverse chromosome painting using only a small number of DOP-PCR amplified microdissected chromosomesVIERSBACH, R; SCHWANITZ, G; NÖTHEN, M. M et al.Human genetics. 1994, Vol 93, Num 6, pp 663-667, issn 0340-6717Article

Association versus linkage studies in psychosis geneticsNÖTHEN, M. M; PROPPING, P; FIMMERS, R et al.Journal of medical genetics. 1993, Vol 30, Num 8, pp 634-637, issn 0022-2593Article

Molecular diagnosis of trisomy 18 using DNA recovered from paraffin embedded tissues and possible implications for genetic counselling = Diagnostic moléculaire de trisomie 18. DNA obtenu à partir de tissus inclus dans la paraffine. Implications possibles pour le conseil génétiqueEGGERMANN, T; NOTHEN, M. M; PROPPINP et al.Annales de génétique (Paris). 1993, Vol 36, Num 4, pp 214-216, issn 0003-3995Article

Dinucleotide repeat polymorphism at the D18S365 locusABELS, S; ERDMANN, J; NÖTHEN, M. M et al.Human molecular genetics (Print). 1993, Vol 2, Num 10, issn 0964-6906, p. 1747Article

Human complement component C8 : molecular basis of the β-chain polymorphismDEWALD, G; HEMMER, S; NÖTHEN, M. M et al.FEBS letters. 1994, Vol 340, Num 3, pp 211-215, issn 0014-5793Article

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

Lack of genetically determined structural variants of the human serotonin-1E (5-HT_1E) receptor protein points to its evolutionary conservationSHIMRON-ABARBANELL, D; NÖTHEN, M. M; ERDMANN, J et al.Molecular brain research. 1995, Vol 29, Num 2, pp 387-390, issn 0169-328XArticle

Detection of four polymorphic sites in the human dopamine D1 receptor gene (DRD1)CICHON, S; NÖTHEN, M. M; ERDMANN, J et al.Human molecular genetics (Print). 1994, Vol 3, Num 1, issn 0964-6906, p. 209Article

Steinfeld syndrome : report of a second family and further delineation of a rare autosomal dominant disorderNÖTHEN, M. M; KNÖPFLE, G; FÖDISCH, H.-J et al.American journal of medical genetics. 1993, Vol 46, Num 4, pp 467-470, issn 0148-7299Article

Efficacy and side-effects of clozapine not associated with variation in the 5-HT_2C receptorRIETSCHEL, M; NABER, D; FIMMERS, R et al.Neuroreport (Oxford). 1997, Vol 8, Num 8, pp 1999-2003, issn 0959-4965Article

Distribution of a novel mutation in the first exon of the human dopamine D₄ receptor gene in psychotic patientsCATALANO, M; NOBILE, M; NOVELLI, E et al.Biological psychiatry (1969). 1993, Vol 34, Num 7, pp 459-464, issn 0006-3223Article

A novel missense mutation in the DNA mismatch repair gene hMLH1 present among east Asians but not among EuropeansYAPING WANG; FRIEDL, W; LAMBERTI, C et al.Human heredity. 1998, Vol 48, Num 2, pp 87-91, issn 0001-5652Article

Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors : Replication testsKÜHN, K.-U; MEYER, K; NÖTHEN, M. M et al.American journal of medical genetics. 1999, Vol 88, Num 2, pp 168-172, issn 0148-7299Article

Modified ligand binding to the naturally occurring Cys-124 variant of the human serotonin 5-HT_1B receptorBRÜSS, M; BÖNISCH, H; BÜHLEN, M et al.Pharmacogenetics (London). 1999, Vol 9, Num 1, pp 95-102, issn 0960-314XArticle