J. Horváth

A. Meindl, R. Schmutzler, H. Hellebrand, 2017, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

DNAI 2 mutations can cause primary ciliary dyskinesia with outer dynein arm defects

Chung, H. Blau, R. Reinhardt, 2009 .

Cellular and molecular mechanisms of the IL-12-induced increase in allospecific murine cytolytic T cell activity. Implications for the age-related decline in CTL.

J. Horváth, E. Bloom, 1994, Journal of immunology.

Four Novel NR5A1 Mutations in 46,XY Gonadal Dysgenesis Patients Including Frameshift Mutations with Altered Subcellular SF-1 Localization

P. Wieacker, G. Scherer, J. Horváth, 2017, Sexual Development.

Generation of a Porcine Antibody Fab Fragment Using Protein Engineering to Facilitate the Evaluation of Ocular Sustained Delivery Technology.

R. Kelley, Joyce Chan, L. Comps-Agrar, 2022, Molecular pharmaceutics.

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

D. Steinemann, F. Couch, B. Bonanni, 2020, Genetics in Medicine.

Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 families from the German Hereditary Breast and Ovarian Cancer Consortium

E. Schröck, A. Antoniou, A. Meindl, 2013, Journal of Medical Genetics.

The Immunosenescence of Cytolytic T Lymphocytes (CTL): Reduction of Pore-Forming Protein and Granzyme Levels

J. Horváth, E. Bloom, 1993 .

BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer

J. Ramser, A. Meindl, R. Schmutzler, 2018, Breast Cancer Research.

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Katherine M. Tucker, Sebastian A. Wagner, Kelly J. Sullivan, 2019, Human Mutation.

Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

W. Chung, T. Fehm, T. Rebbeck, 2022, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer

Tanja Fehm, Nina Ditsch, Dieter Niederacher, 2016, Journal of Medical Genetics.

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

F. Couch, O. Olopade, J. Benítez, 2021, Journal of the National Cancer Institute.

Phosphorylation by casein kinase 2 induces PACS‐1 binding of nephrocystin and targeting to cilia

H. Zentgraf, H. Omran, B. Schermer, 2005, The EMBO journal.

CADMIUM AND SOFT LASER RADIATION EFFECTS ON HUMAN T CELLS VIABILITY AND DEATH STYLE CHOICES

C. Davila, J. Horváth, É. Katona, 2008 .

MEMBRANE EFFECTS OF LOW LEVEL INFRARED LASER IRRADIATION, AS SEEN IN METABOLICALLY INTACT AND IMPAIRED HUMAN BLOOD CELLS

C. Davila, J. Horváth, É. Katona, 2004 .

Gene panel testing of 5589 BRCA1/2‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer

Nina Ditsch, Peter Nürnberg, Dieter Niederacher, 2018, Cancer medicine.

Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia.

H. Omran, M. Fliegauf, J. Wildhaber, 2005, American journal of respiratory and critical care medicine.

Validation of the Manchester scoring system for predicting BRCA1/2 mutations in 9,390 families suspected of having hereditary breast and ovarian cancer

A. Meindl, R. Schmutzler, M. Kiechle, 2014, International journal of cancer.

Performance of breast cancer polygenic risk scores in 760 female CHEK2 germline mutation carriers.

A. Antoniou, A. Rump, M. Schmidt, 2020, Journal of the National Cancer Institute.

Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility

H. Omran, P. Pennekamp, H. Olbrich, 2021, PLoS genetics.

Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients.

R. Reinhardt, H. Omran, R. Sudbrak, 2005, American journal of respiratory cell and molecular biology.

Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia.

H. Zentgraf, H. Omran, G. Pazour, 2006, Journal of the American Society of Nephrology : JASN.

LOW LEVEL LONG WAVELENGTH LASER IRRADIATION EFFECTS ON HUMAN T LEUKEMIC LYMPHOBLASTS MITOCHONDRIAL MEMBRANE POTENTIAL

C. Davila, J. Horváth, É. Katona, 2008 .

Mutations in ACY 1 , the Gene Encoding Aminoacylase 1 , Cause a Novel Inborn Error of Metabolism

H. Omran, A. Kispert, U. Engelke, 2007 .

Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism.

H. Omran, A. Kispert, U. Engelke, 2006, American journal of human genetics.

Is (99m)Tc-sestamibi scintimammography complementary to conventional mammography for detecting breast cancer in patients with palpable masses?

T. Massardo, J. Horváth, O. Alonso, 2001, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

Possible genotype-phenotype correlations in children with mild clinical course of Canavan disease.

D. Zafeiriou, H. Omran, J. Sass, 2005, Neuropediatrics.

Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer

A. Meindl, R. Schmutzler, Jan Hauke, 2019, Breast Cancer Research.

Identification of a novel LAMP2 mutation responsible for X-chromosomal dominant Danon disease.

H. Omran, H. Olbrich, N. Boehm, 2003, Neuropediatrics.