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Andreas Volz

Research Profile

Disorders

Physiology

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Publications

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Heike Olbrich; Manfred Fliegauf; Julia Hoefele; Andreas Kispert; Edgar Otto; Andreas Volz; Matthias T F Wolf; Gürsel Sasmaz; Ute Trauer; Richard Reinhardt; Ralf Sudbrak; Corinne Antignac; Norbert Gretz; Gerd Walz; Bernhard Schermer; Thomas Benzing; Friedhelm Hildebrandt; Heymut Omran
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.
Andreas Kispert; Marianne Petry; Heike Olbrich; Andreas Volz; Uwe-Peter Ketelsen; Judit Horvath; Rachid Melkaoui; Heymut Omran; Maimoona A Zariwala; Peadar G Noone; Michael Knowles
Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations.
Heike Olbrich; Karsten Häffner; Andreas Kispert; Alexander Völkel; Andreas Volz; Gürsel Sasmaz; Richard Reinhardt; Steffen Hennig; Hans Lehrach; Nikolaus Konietzko; Maimoona A Zariwala; Peadar G Noone; Michael Knowles; Hannah M Mitchison; Maggie Meeks; Eddie M K Chung; Friedhelm Hildebrandt; Ralf Sudbrak; Heymut Omran
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.

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All Publications

2003: Heike Olbrich; Manfred Fliegauf; Julia Hoefele; Andreas Kispert; Edgar Otto; Andreas Volz; Matthias T F Wolf; Gürsel Sasmaz; Ute Trauer; Richard Reinhardt; Ralf Sudbrak; Corinne Antignac; Norbert Gretz; Gerd Walz; Bernhard Schermer; Thomas Benzing; Friedhelm Hildebrandt; Heymut Omran
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.
Nature genetics 2003;34(4):455-9.
2003: Andreas Kispert; Marianne Petry; Heike Olbrich; Andreas Volz; Uwe-Peter Ketelsen; Judit Horvath; Rachid Melkaoui; Heymut Omran; Maimoona A Zariwala; Peadar G Noone; Michael Knowles
Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations.
Thorax 2003;58(6):552-4.
2002: Heike Olbrich; Karsten Häffner; Andreas Kispert; Alexander Völkel; Andreas Volz; Gürsel Sasmaz; Richard Reinhardt; Steffen Hennig; Hans Lehrach; Nikolaus Konietzko; Maimoona A Zariwala; Peadar G Noone; Michael Knowles; Hannah M Mitchison; Maggie Meeks; Eddie M K Chung; Friedhelm Hildebrandt; Ralf Sudbrak; Heymut Omran
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.
Nature genetics 2002;30(2):143-4.
2002: Andreas Volz; Rachid Melkaoui; Friedhelm Hildebrandt; Heymut Omran
Candidate gene analysis of KIAA0678 encoding a DnaJ-like protein for adolescent nephronophthisis and Senior-Løken syndrome type 3.
Cytogenetic and genome research 2002;97(3-4):163-6.
2002: Heymut Omran; Gürsel Sasmaz; Karsten Häffner; Andreas Volz; Heike Olbrich; Rachid Melkaoui; Edgar Otto; Thomas F Wienker; Rudolf Korinthenberg; Matthias Brandis; Corinne Antignac; Friedhelm Hildebrandt
Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 gene.
Journal of the American Society of Nephrology : JASN 2002;13(1):75-9.