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Heide Hellebrand

Research Profile

Procedures

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Physiology

Chemicals & Drugs

Anatomy

X Chromosome

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Genes & Molecular Sequences

Amino Acid Sequences

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Infants

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Publications

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Kari Hemminki; Bertram Müller-Myhsok; Peter Lichtner; Christoph Engel; Bowang Chen; Barbara Burwinkel; Asta Försti; Christian Sutter; Barbara Wappenschmidt; Heide Hellebrand; Thomas Illig; Norbert Arnold; Dieter Niederacher; Bernd Dworniczak; Helmut Deissler; Karin Kast; Dorothea Gadzicki; Thomas Meitinger; H-Erich Wichmann; Marion Kiechle; Claus R Bartram; Rita K Schmutzler; Alfons Meindl
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients.
Alfons Meindl; Heide Hellebrand; Constanze Wiek; Verena Erven; Barbara Wappenschmidt; Dieter Niederacher; Marcel Freund; Peter Lichtner; Linda Hartmann; Heiner Schaal; Juliane Ramser; Ellen Honisch; Christian Kubisch; Hans E Wichmann; Karin Kast; Helmut Deissler; Christoph Engel; Bertram Müller-Myhsok; Kornelia Neveling; Marion Kiechle; Christopher G Mathew; Detlev Schindler; Rita K Schmutzler; Helmut Hanenberg
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
Guenther Rudolph; Michael Nentwich; Heide Hellebrand; Katharina Pollack; Roswitha Gordes; Viktoria Bau; Anselm Kampik; Alfons Meindl
KIF21A variant R954W in familial or sporadic cases of CFEOM1.

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All Publications

2010: Kari Hemminki; Bertram Müller-Myhsok; Peter Lichtner; Christoph Engel; Bowang Chen; Barbara Burwinkel; Asta Försti; Christian Sutter; Barbara Wappenschmidt; Heide Hellebrand; Thomas Illig; Norbert Arnold; Dieter Niederacher; Bernd Dworniczak; Helmut Deissler; Karin Kast; Dorothea Gadzicki; Thomas Meitinger; H-Erich Wichmann; Marion Kiechle; Claus R Bartram; Rita K Schmutzler; Alfons Meindl
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients.
International journal of cancer. Journal international du cancer 2010;126(12):2858-62.
2010: Alfons Meindl; Heide Hellebrand; Constanze Wiek; Verena Erven; Barbara Wappenschmidt; Dieter Niederacher; Marcel Freund; Peter Lichtner; Linda Hartmann; Heiner Schaal; Juliane Ramser; Ellen Honisch; Christian Kubisch; Hans E Wichmann; Karin Kast; Helmut Deissler; Christoph Engel; Bertram Müller-Myhsok; Kornelia Neveling; Marion Kiechle; Christopher G Mathew; Detlev Schindler; Rita K Schmutzler; Helmut Hanenberg
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
Nature genetics 2010;42(5):410-4.
2009: Guenther Rudolph; Michael Nentwich; Heide Hellebrand; Katharina Pollack; Roswitha Gordes; Viktoria Bau; Anselm Kampik; Alfons Meindl
KIF21A variant R954W in familial or sporadic cases of CFEOM1.
European journal of ophthalmology 2009;19(4):667-74.
2009: Ariane Sadr-Nabavi; Juliane Ramser; Juliane Volkmann; Joerg Naehrig; Frank Wiesmann; Beate Betz; Heide Hellebrand; Stefanie Engert; Susanne Seitz; Rene Kreutzfeld; Takako Sasaki; Norbert Arnold; Rita K Schmutzler; Marion Kiechle; Dieter Niederacher; Nadia Harbeck; Edgar Dahl; Alfons Meindl
Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker.
International journal of cancer. Journal international du cancer 2009;124(7):1727-35.
2008: Stefanie Engert; Barbara Wappenschmidt; Beate Betz; Karin Kast; Michael Kutsche; Heide Hellebrand; Timm O Goecke; Marion Kiechle; Dieter Niederacher; Rita K Schmutzler; Alfons Meindl
MLPA screening in the BRCA1 gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases.
Human mutation 2008;29(7):948-58.
2008: Juliane Ramser; Mary Ellen Ahearn; Claus Lenski; Kemal O Yariz; Heide Hellebrand; Michael von Rhein; Robin D Clark; Rita K Schmutzler; Peter Lichtner; Eric Hoffman; Alfons Meindl; Lisa Baumbach
Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy.
American journal of human genetics 2008;82(1):188-93.
2007: Claus Lenski; R Frank Kooy; Edwin Reyniers; Daniela Loessner; Ronald J A Wanders; Birgitta Winnepenninckx; Heide Hellebrand; Stefanie Engert; Charles E Schwartz; Alfons Meindl; Juliane Ramser
The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior.
American journal of human genetics 2007;80(2):372-7.
2007: Volker O Melichar; Sabine Guth; Heide Hellebrand; Alfons Meindl; Katharina von der Hardt; Cornelia Kraus; Udo Trautmann; Wolfgang Rascher; Anita Rauch; Martin Zenker
A male infant with a 9.6 Mb terminal Xp deletion including the OA1 locus: Limit of viability of Xp deletions in males.
American journal of medical genetics. Part A 2007;143(2):135-41.
2007: Razvan T Radulescu; Carla Hufnagel; Peter B Luppa; Heide Hellebrand; Wen-Liang Kuo; Marsha Rich Rosner; Nadia Harbeck; Cecylia Giersig; Alfons Meindl; Manfred Schmitt; Gregor Weirich
Immunohistochemical demonstration of the zinc metalloprotease insulin-degrading enzyme in normal and malignant human breast: correlation with tissue insulin levels.
International journal of oncology 2007;30(1):73-80.
2004: Boris Hügle; P Suchowerskyj; Heide Hellebrand; B Adler; Michael Borte; Ulrich Sack; U Schulte Overberg-Schmidt; N Strnad; J Otto; Alfons Meindl; Volker Schuster
Persistent hypogammaglobulinemia following mononucleosis in boys is highly suggestive of X-linked lymphoproliferative disease--report of three cases.
Journal of clinical immunology 2004;24(5):515-22.
2003: Eva Gross; Katharina Seck; Steffi Neubauer; Jutta Mayr; Heide Hellebrand; Adisorn Ratanaphan; Verena Lutz; Hubertus Stockinger; Marion Kiechle
High-throughput genotyping by DHPLC of the dihydropyrimidine dehydrogenase gene implicated in (fluoro)pyrimidine catabolism.
International journal of oncology 2003;22(2):325-32.
2002: Astrid Golla; Annette Jansson; Juliane Ramser; Heide Hellebrand; Robert Zahn; Thomas Meitinger; Bernd H Belohradsky; Alfons Meindl
Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22.
European journal of human genetics : EJHG 2002;10(3):217-21.
2002: Attila Braun; Attila Aszódi; Heide Hellebrand; Alejandro Berna; Reinhard Fässler; Oliver Brandau
Genomic organization of profilin-III and evidence for a transcript expressed exclusively in testis.
Gene 2002;283(1-2):219-25.
1999: Oliver Brandau; Volker Schuster; M Weiss; Heide Hellebrand; Franz-Martin Fink; Alfons Kreczy; W Friedrich; Brigitte Strahm; Charlotte Niemeyer; Bernd H Belohradsky; Alfons Meindl
Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP).
Human molecular genetics 1999;8(13):2407-13.
1998: Tim M Strom; Gerald Nyakatura; Eckart Apfelstedt-Sylla; Heide Hellebrand; Birgit Lorenz; Bernhard H F Weber; K Wutz; N Gutwillinger; K Rüther; Bernd Drescher; C Sauer; Eberhart Zrenner; Thomas Meitinger; André Rosenthal; Alfons Meindl
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
Nature genetics 1998;19(3):260-3.
1996: D Schindelhauer; Heide Hellebrand; L Grimm; I Bader; Thomas Meitinger; M Wehnert; M Ross; Alfons Meindl
Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval.
Genome research 1996;6(11):1056-69.
1996: D Schindelhauer; M Weiss; Heide Hellebrand; Astrid Golla; M Hergersberg; R Seger; Bernd H Belohradsky; Alfons Meindl
Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product.
Human genetics 1996;98(1):68-76.
1996: Alfons Meindl; K Dry; K Herrmann; F Manson; Alfredo Ciccodicola; A Edgar; M R Carvalho; H Achatz; Heide Hellebrand; A Lennon; Carmen Migliaccio; K Porter; Eberhart Zrenner; A Bird; MR Jay; B Lorenz; B Wittwer; Michele D'Urso; Thomas Meitinger; A Wright
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3).
Nature genetics 1996;13(1):35-42.
1995: Alfons Meindl; B Lorenz; H Achatz; Heide Hellebrand; P Schmitz-Valckenberg; Thomas Meitinger
Missense mutations in the NDP gene in patients with a less severe course of Norrie disease.
Human molecular genetics 1995;4(3):489-90.
1994: A Klink; Alfons Meindl; Heide Hellebrand; G A Rappold
A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval.
Human genetics 1994;93(4):463-6.
1992: Alfons Meindl; Wolfgang Berger; Thomas Meitinger; Dorien J R van De Pol; H Achatz; C Dörner; M Haasemann; Heide Hellebrand; Andreas Gal; Frans P M Cremers
Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.
Nature genetics 1992;2(2):139-43.