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Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families.
Schwab SG, Knapp M, Mondabon S, Hallmayer J, Borrmann-Hassenbach M, Albus M, Lerer B, Rietschel M, Trixler M, Maier W, Wildenauer DB. Schwab SG, et al. Among authors: rietschel m. Am J Hum Genet. 2003 Jan;72(1):185-90. doi: 10.1086/345463. Epub 2002 Dec 9. Am J Hum Genet. 2003. PMID: 12474144 Free PMC article.
MASA syndrome: clinical variability and linkage analysis.
Rietschel M, Friedl W, Uhlhaas S, Neugebauer M, Heimann D, Zerres K. Rietschel M, et al. Am J Med Genet. 1991 Oct 1;41(1):10-4. doi: 10.1002/ajmg.1320410104. Am J Med Genet. 1991. PMID: 1951449
Tyrosine hydroxylase gene and manic-depressive illness.
Rietschel M, Nöthen MM, Maier W, Albus M, Franzek E, Propping P. Rietschel M, et al. Lancet. 1995 May 27;345(8961):1368. doi: 10.1016/s0140-6736(95)92566-x. Lancet. 1995. PMID: 7752774 No abstract available.
Dopamine D2 receptor molecular variant and schizophrenia.
Nöthen MM, Wildenauer D, Cichon S, Albus M, Maier W, Minges J, Lichtermann D, Bondy B, Rietschel M, Körner J, et al. Nöthen MM, et al. Among authors: rietschel m. Lancet. 1994 May 21;343(8908):1301-2. doi: 10.1016/s0140-6736(94)92194-6. Lancet. 1994. PMID: 7910313 No abstract available.
Mutation in the beta amyloid precursor protein gene and schizophrenia.
Nöthen MM, Erdmann J, Propping P, Lanczik M, Rietschel M, Körner J, Maier W, Albus M, Ertl MA, Wildenauer DB. Nöthen MM, et al. Among authors: rietschel m. Biol Psychiatry. 1993 Oct 1;34(7):502. doi: 10.1016/0006-3223(93)90244-8. Biol Psychiatry. 1993. PMID: 8268336 No abstract available.
937 results