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Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia.
Shimron-Abarbanell D, Harms H, Erdmann J, Albus M, Maier W, Rietschel M, Körner J, Weigelt B, Franzek E, Sander T, Knapp M, Propping P, Nöthen MM. Shimron-Abarbanell D, et al. Among authors: knapp m. Am J Med Genet. 1996 Apr 9;67(2):225-8. doi: 10.1002/(SICI)1096-8628(19960409)67:2<225::AID-AJMG16>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723053
A gene for universal congenital alopecia maps to chromosome 8p21-22.
Nöthen MM, Cichon S, Vogt IR, Hemmer S, Kruse R, Knapp M, Höller T, Faiyaz ul Haque M, Haque S, Propping P, Ahmad M, Rietschel M. Nöthen MM, et al. Among authors: knapp m. Am J Hum Genet. 1998 Feb;62(2):386-90. doi: 10.1086/301717. Am J Hum Genet. 1998. PMID: 9463324 Free PMC article.
Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders.
Stöber G, Nöthen MM, Pörzgen P, Brüss M, Bönisch H, Knapp M, Beckmann H, Propping P. Stöber G, et al. Among authors: knapp m. Am J Med Genet. 1996 Nov 22;67(6):523-32. doi: 10.1002/(SICI)1096-8628(19961122)67:6<523::AID-AJMG3>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8950409
Human delta-opioid receptor gene and susceptibility to heroin and alcohol dependence.
Franke P, Nöthen MM, Wang T, Neidt H, Knapp M, Lichtermann D, Weiffenbach O, Mayer P, Höllt V, Propping P, Maier W. Franke P, et al. Among authors: knapp m. Am J Med Genet. 1999 Oct 15;88(5):462-4. doi: 10.1002/(sici)1096-8628(19991015)88:5<462::aid-ajmg4>3.0.co;2-s. Am J Med Genet. 1999. PMID: 10490698
1,561 results