Heide Hellebrand - Abteilung Pädiatrische Genetiky Kinderpoliklinik, der Universität München

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Beyond CHEK2 in breast cancer: Search for additional moderately penetrant risk gene variants by analyzing the oligogenic disease course in CHEK2 mutation carriers

E. Pohl,J. Borde,J. Hauke, S. Schmidt,K. Weber-Lassalle,C. Ernst,D. Niederacher,N. Arnold,H. Hellebrand,A. Meindl,A. Gehrig, G. Schmidt,V. Dutrannoy,K. Kast,E. Hahnen,R. Schmutzler

CANCER RESEARCH（2018）

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TP53 Mutations in the Subgroup of BRCA-negative Breast Cancer Families – a Clinical Challenge

S Grill,J Ramser,H Hellebrand,N Ditsch,E Groß,A Meindl,M Kiechle,A Quante

Senologie - Zeitschrift für Mammadiagnostik und -therapie Information und Programm wwwsenologiekongressde (2018)

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Compelling evidence for FANCM as a breast cancer susceptibility gene

G. Neidhardt,J. Hauke,S. Heilmann,H. Hellebrand,H. M. Surowy,K. Klaschik,E. Honisch,A. Gehrig,C. Sutter,A. Rump, N. Bogdanova-Markov,P. Bugert,E. Mangold,D. Steinemann,A. Ramirez,N. Ditsch,N. Arnold,D. Niederacher,B. Burwinkel,H. Thiele, I. Altmueller, P. Nuernberg,C. Engel,B. Wappenschmidt,K. Rhiem,A. Meindl,R. K. Schmutzler,E. Hahnen

ONCOLOGY RESEARCH AND TREATMENT（2016）

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Persistent Hypogammaglobulinemia Following Mononucleosis in Boys is Highly Suggestive of X-Linked Lymphoproliferative Disease—Report of Three Cases

B. Hügle,P. Suchowerskyj,H. Hellebrand, B. Adler,M. Borte,U. Sack, U. Schulte Overberg-Schmidt,N. Strnad, J. Otto,A. Meindl,V. Schuster

Journal of clinical immunologyno. 5 (2004): 515-522

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Genomic Organization of Profilin-Iii and Evidence for A Transcript Expressed Exclusively in Testis

A Braun,A Aszodi,H Hellebrand,A Berna,R Fassler,O Brandau

GENE（2002）

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A systematic mutation screening approach for syndromic and nonsyndromic forms of mental retardation in human Xp21.1-Xp11.23

J Ramser,G Wen, IM Garay, M Dufault,H Hellebrand,S Engert,C Schwartz,M Platzer,A Meindl

EUROPEAN JOURNAL OF HUMAN GENETICS（2002）

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Detection of 5FU-toxicity-related variants in the DPYD gene by denaturing HPLC

E Gross,K Seck, S Neubauer,H Hellebrand,A Meindl, S Riemer, J Mayr,V Lutz,M Kiechle

EUROPEAN JOURNAL OF HUMAN GENETICS（2002）

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Mutation Analysis Of The Sh2d1a/Sap Gene In 4 Families Affected By X-Linked Lymphoproliferative Disease (Xlp)

V Schuster,H Hellebrand, M Weiss,K Steppberger,U Sack,M Borte, G Henze,N Strnad, J Gierich,A Meindl

BLOOD（2000）

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Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)

O Brandau,V Schuster, M Weiss,H Hellebrand,F M Fink,A Kreczy, W Friedrich,B Strahm, C Niemeyer,B H Belohradsky,A Meindl

HUMAN MOLECULAR GENETICS（1999）

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Mutation Analysis Of A Novel Sh2-Domain Encoding Gene, Sh2d1a, In Five Patients With X-Linked Lymphoproliferative Disease (Xlp)

V Schuster,O Brandau, M Weiss,S Seidenspinner,H Hellebrand,Hw Kreth,A Meindl

BLOOD（1998）

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