M. Wirtenberger

发表

Aurora kinases A and B and familial breast cancer risk.

P. Bugert, K. Hemminki, A. Meindl, 2007, Cancer letters.

Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer.

Alfons Meindl, Barbara Burwinkel, Sandrine Tchatchou, 2006, Carcinogenesis.

Headliners: Smoking: The Role of the Parent in Deterring Child Smoking, as Seen by Rural Native American and White Parents

K. Hemminki, B. Burwinkel, A. Försti, 2005, Environmental Health Perspectives.

Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP 13 with familial breast cancer

K. Hemminki, A. Meindl, R. Schmutzler, 2006 .

c‐MYC Asn11Ser is associated with increased risk for familial breast cancer

P. Bugert, K. Hemminki, R. Schmutzler, 2005, International journal of cancer.

SNP microarray analysis for genome-wide detection of crossover regions

K. Hemminki, B. Burwinkel, M. Wirtenberger, 2005, Human Genetics.

Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer.

K. Hemminki, A. Meindl, R. Schmutzler, 2006, Carcinogenesis.

PPARGC1A, PPARGC1B and EP300 with familial breast cancer

K. Hemminki, A. Meindl, R. Schmutzler, 2006 .

The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancer.

K. Hemminki, A. Meindl, R. Schmutzler, 2006, Carcinogenesis.

A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults

P. Schirmacher, K. Hemminki, B. Burwinkel, 2008, Hepatology.

Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer.

Dieter Niederacher, Alfons Meindl, Barbara Burwinkel, 2005, Carcinogenesis.

factor AKAP13 with familial breast cancer

K. Hemminki, A. Meindl, B. Burwinkel, 2005 .

Association of NCOA3 Polymorphisms with Breast Cancer Risk

Barbara Burwinkel, Peter Bugert, Asta Försti, 2005, Clinical Cancer Research.

The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk

P. Bugert, K. Hemminki, B. Burwinkel, 2004, Breast Cancer Research.

Identification of frequent chromosome copy-number polymorphisms by use of high-resolution single-nucleotide-polymorphism arrays.

K. Hemminki, B. Burwinkel, M. Wirtenberger, 2006, American Journal of Human Genetics.

Trisomy 8q and partial trisomy 22 in a 43‐year‐old man with moderate intellectual disability, epilepsy and large cell non‐Hodgkin lymphoma

A. Jauch, K. Hemminki, B. Burwinkel, 2006, American journal of medical genetics. Part A.

Arthrogryposis multiplex with deafness, inguinal hernias, and early death: A family report of a probably autosomal recessive trait

B. Burwinkel, M. Wirtenberger, C. Hübner, 2005, American journal of medical genetics. Part A.

Allelotyping of pooled DNA with 250 K SNP microarrays

K. Hemminki, B. Burwinkel, A. Försti, 2007 .