Remschmidt H - Search Results

1

Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening.

Stöber G, Hebebrand J, Cichon S, Brüss M, Bönisch H, Lehmkuhl G, Poustka F, Schmidt M, Remschmidt H, Propping P, Nöthen MM. Stöber G, et al. Among authors: remschmidt h. Am J Med Genet. 1999 Apr 16;88(2):158-63. doi: 10.1002/(sici)1096-8628(19990416)88:2<158::aid-ajmg12>3.0.co;2-w. Am J Med Genet. 1999. PMID: 10206236

2

Human dopamine D4 receptor gene: frequent occurrence of a null allele and observation of homozygosity.

Nöthen MM, Cichon S, Hemmer S, Hebebrand J, Remschmidt H, Lehmkuhl G, Poustka F, Schmidt M, Catalano M, Fimmers R, et al. Nöthen MM, et al. Among authors: remschmidt h. Hum Mol Genet. 1994 Dec;3(12):2207-12. doi: 10.1093/hmg/3.12.2207. Hum Mol Genet. 1994. PMID: 7881421

3

Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome.

Seuchter SA, Hebebrand J, Klug B, Knapp M, Lehmkuhl G, Poustka F, Schmidt M, Remschmidt H, Baur MP. Seuchter SA, et al. Among authors: remschmidt h. Genet Epidemiol. 2000 Jan;18(1):33-47. doi: 10.1002/(SICI)1098-2272(200001)18:1<33::AID-GEPI3>3.0.CO;2-2. Genet Epidemiol. 2000. PMID: 10603457

4

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hülsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Körne G, Nöthen MM, Kere J. Schumacher J, et al. Among authors: remschmidt h. Am J Hum Genet. 2006 Jan;78(1):52-62. doi: 10.1086/498992. Epub 2005 Nov 17. Am J Hum Genet. 2006. PMID: 16385449 Free PMC article.

5

Partial trisomy 16p in an adolescent with autistic disorder and Tourette's syndrome.

Hebebrand J, Martin M, Körner J, Roitzheim B, de Braganca K, Werner W, Remschmidt H. Hebebrand J, et al. Among authors: remschmidt h. Am J Med Genet. 1994 Sep 15;54(3):268-70. doi: 10.1002/ajmg.1320540316. Am J Med Genet. 1994. PMID: 7810587

6

Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome.

Hebebrand J, Nöthen MM, Ziegler A, Klug B, Neidt H, Eggermann K, Lehmkuhl G, Poustka F, Schmidt MH, Propping P, Remschmidt H. Hebebrand J, et al. Among authors: remschmidt h. Am J Hum Genet. 1997 Jul;61(1):238-9. doi: 10.1016/S0002-9297(07)64298-0. Am J Hum Genet. 1997. PMID: 9246007 Free PMC article. No abstract available.

7

Serotonin transporter gene-linked polymorphic region: allele distributions in relationship to body weight and in anorexia nervosa.

Hinney A, Barth N, Ziegler A, von Prittwitz S, Hamann A, Hennighausen K, Pirke KM, Heils A, Rosenkranz K, Roth H, Coners H, Mayer H, Herzog W, Siegfried A, Lehmkuhl G, Poustka F, Schmidt MH, Schäfer H, Grzeschik KH, Lesch KP, Lentes KU, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: remschmidt h. Life Sci. 1997;61(21):PL 295-303. doi: 10.1016/s0024-3205(97)00888-6. Life Sci. 1997. PMID: 9395256

8

Screening for mutations in the neuropeptide Y Y5 receptor gene in cohorts belonging to different weight extremes.

Rosenkranz K, Hinney A, Ziegler A, von Prittwitz S, Barth N, Roth H, Mayer H, Siegfried W, Lehmkuhl G, Poustka F, Schmidt M, Schäfer H, Remschmidt H, Hebebrand J. Rosenkranz K, et al. Among authors: remschmidt h. Int J Obes Relat Metab Disord. 1998 Feb;22(2):157-63. doi: 10.1038/sj.ijo.0800550. Int J Obes Relat Metab Disord. 1998. PMID: 9504324

9

No evidence for involvement of polymorphisms of the dopamine D4 receptor gene in anorexia nervosa, underweight, and obesity.

Hinney A, Schneider J, Ziegler A, Lehmkuhl G, Poustka F, Schmidt MH, Mayer H, Siegfried W, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: remschmidt h. Am J Med Genet. 1999 Dec 15;88(6):594-7. Am J Med Genet. 1999. PMID: 10581473

10

Anorexia nervosa viewed as an extreme weight condition: genetic implications.

Hebebrand J, Remschmidt H. Hebebrand J, et al. Among authors: remschmidt h. Hum Genet. 1995 Jan;95(1):1-11. doi: 10.1007/BF00225065. Hum Genet. 1995. PMID: 7814009

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