Helmut Remschmidt

发表

Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?

J. Hebebrand, A. Hinney, V. Steen, 2009, Molecular Psychiatry.

A prospective study of serum ghrelin levels in patients treated with clozapine

M. Tschöp, J. Hebebrand, H. Remschmidt, 2005, Journal of Neural Transmission.

Molecular genetic aspects of attention-deficit/hyperactivity disorder

B. Herpertz-Dahlmann, K. Konrad, J. Hebebrand, 2004, Neuroscience & Biobehavioral Reviews.

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

F. Poustka, J. Hebebrand, A. Hinney, 1999, American journal of medical genetics.

Evidence for linkage of spelling disability to chromosome 15.

S. Cichon, M. Nöthen, B. Müller-Myhsok, 1998, American journal of human genetics.

Systematic mutation screening of the estrogen receptor beta gene in probands of different weight extremes: identification of several genetic variants.

J. Hebebrand, A. Hinney, J. K. Young, 1998, The Journal of clinical endocrinology and metabolism.

5-HT2A promoter polymorphism −1438G/A in children and adolescents with obsessive-compulsive disorders

B. Herpertz-Dahlmann, J. Hebebrand, A. Hinney, 2002, Molecular Psychiatry.

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder

K Konrad, A Dempfle, H Remschmidt, 2005, Molecular Psychiatry.

White blood cells and cortisol after sleep deprivation and recovery sleep in humans

J. Hennig, H. Remschmidt, W. Wesemann, 2000, European Archives of Psychiatry and Clinical Neuroscience.

Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor gene.

J. Hebebrand, A. Hinney, H. Remschmidt, 1999, American journal of human genetics.

Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample

B. Herpertz-Dahlmann, K. Konrad, J. Hebebrand, 2006, Journal of Neural Transmission.

Body weight gain induced by atypical antipsychotics: an extension of the monocygotic twin and sib pair study

P. Wehmeier, M. Haberhausen, F. Theisen, 2010, Journal of clinical pharmacy and therapeutics.

No evidence for binding of clozapine, olanzapine and/or haloperidol to selected receptors involved in body weight regulation

H Remschmidt, J. Hebebrand, H. Remschmidt, 2007, The Pharmacogenomics Journal.

Serum leptin levels increase rapidly after initiation of clozapine therapy

J. Hebebrand, H. Remschmidt, W. Blum, 1998, Molecular Psychiatry.

Rates for tic disorders and obsessive compulsive symptomatology in families of children and adolescents with Gilles de la Tourette syndrome.

F. Poustka, R. Fimmers, M. Baur, 1997, Journal of psychiatric research.

Speech perception deficit in dyslexic adults as measured by mismatch negativity (MMN).

H. Remschmidt, G. Schulte-Körne, J. Bartling, 2001, International journal of psychophysiology : official journal of the International Organization of Psychophysiology.

Epidemiology and Pathogenesis

Helmut Remschmidt, Michael Schmidt, 2001 .

Objective measurement of hyperactivity, impulsivity, and inattention in children with hyperkinetic disorders before and after treatment with methylphenidate

J. Hebebrand, H. Remschmidt, P. Wehmeier, 2004, European Child & Adolescent Psychiatry.

Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method.

S. Cichon, M. Nöthen, F. Poustka, 1994, American journal of medical genetics.

Candidate gene polymorphisms in eating disorders.

J. Hebebrand, A. Hinney, H. Remschmidt, 2000, European journal of pharmacology.

Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15

M. Nöthen, G. Schulte-Körne, P. Propping, 2009, European Child & Adolescent Psychiatry.

Association and linkage of allelic variants of the dopamine transporter gene in ADHD

K. Lesch, N. Hübner, B. Herpertz-Dahlmann, 2007, Molecular Psychiatry.

Further lack of association between the 5-HT2A gene promoter polymorphism and susceptibility to eating disorders and a meta-analysis pertaining to anorexia nervosa

B. Herpertz-Dahlmann, J. Hebebrand, A. Hinney, 1999, Molecular Psychiatry.

Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene.

S. Cichon, W. Maier, J. Erdmann, 1995, American journal of medical genetics.