All Stories

  1. Genetic biomarkers in the VEGF pathway predicting response to anti-VEGF therapy in age-related macular degeneration

    Article • BMJ Open Ophthalmology, December 2019, BMJ

    irina Balikova

  2. Truncating RAX Mutations: Anophthalmia, Hypopituitarism, Diabetes Insipidus, and Cleft Palate in Mice and Men

    Article • The Journal of Clinical Endocrinology & Metabolism, February 2019, Endocrine Society

    irina Balikova

  3. Analysis of KERA in four families with cornea plana identifies two novel mutations

    Article • Acta Ophthalmologica, July 2017, Wiley

    Dr Petra Liskova, irina Balikova

  4. Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations inKIF11

    Article • Acta Ophthalmologica, May 2015, Wiley

    irina Balikova

  5. High Frequency Of Submicroscopic Chromosomal Deletions in Patients with Idiopathic Congenital Eye Malformations

    Article • American Journal of Ophthalmology, June 2011, Elsevier

    Dr Bernard Thienpont, irina Balikova

  6. FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish

    Article • Molecular Syndromology, January 2010, Karger Publishers

    irina Balikova

  7. Deletions in theVPS13B(COH1) gene as a cause of Cohen syndrome

    Article • Human Mutation, September 2009, Wiley

    irina Balikova

  8. Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16

    Article • The American Journal of Human Genetics, January 2008, Elsevier

    irina Balikova

  9. Acrofacial dysostosis type Rodríguez

    Article • American Journal of Medical Genetics Part A, March 2005, Wiley

    irina Balikova