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HJ Menzel

Research Profile

Geographic Areas

Austria

Chemicals & Drugs

Physiology

Phenomena

Polymorphism, Single-Stranded Conformational

Procedures

DNA Mutational Analysis

Genes & Molecular Sequences

Alleles

Disorders

Concepts & Ideas

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Co-author Network

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Publications

TOP 3
HJ Menzel; J Sarmanova; Pavel Soucek; R Berberich; Kurt Grünewald; Margot Haun; Hans Georg Kraft
Association of NQO1 polymorphism with spontaneous breast cancer in two independent populations.
Martina Witsch-Baumgartner; J Loeffler; HJ Menzel; Gerd Utermann; C Neuhaus
Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorder.
Jürgen Löffler; D Nekahm; Almut Hirst-Stadlmann; Barbara Günther; HJ Menzel; Gerd Utermann; Andreas R Janecke
Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.

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All Publications

2004: HJ Menzel; J Sarmanova; Pavel Soucek; R Berberich; Kurt Grünewald; Margot Haun; Hans Georg Kraft
Association of NQO1 polymorphism with spontaneous breast cancer in two independent populations.
British journal of cancer 2004;90(10):1989-94.
2001: Martina Witsch-Baumgartner; J Loeffler; HJ Menzel; Gerd Utermann; C Neuhaus
Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorder.
American journal of medical genetics 2001;102(1):106-7.
2001: Jürgen Löffler; D Nekahm; Almut Hirst-Stadlmann; Barbara Günther; HJ Menzel; Gerd Utermann; Andreas R Janecke
Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.
European journal of human genetics : EJHG 2001;9(3):226-30.
2001: Martina Witsch-Baumgartner; Elzbieta Ciara; Jürgen Löffler; HJ Menzel; U Seedorf; J Burn; Gabriele Gillessen-Kaesbach; G F Hoffmann; Barbara U Fitzky; H Mundy; P Clayton; Richard I Kelley; Malgorzata Krajewska-Walasek; Gerd Utermann
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations.
European journal of human genetics : EJHG 2001;9(1):45-50.
1999: M F Kronenberg; HJ Menzel; Georg Ebersbach; Gregor Wenning; Elisabeth Luginger; M Gollner; Gerhard Ransmayr; Gerd Utermann; Werner Poewe; Florian Kronenberg
Dopamine D4 receptor polymorphism and idiopathic Parkinson's disease.
European journal of human genetics : EJHG 1999;7(3):397-400.
1998: Hans Georg Kraft; M Windegger; HJ Menzel; Gerd Utermann
Significant impact of the +93 C/T polymorphism in the apolipoprotein(a) gene on Lp(a) concentrations in Africans but not in Caucasians: confounding effect of linkage disequilibrium.
Human molecular genetics 1998;7(2):257-64.

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