Anna Wawrocka

11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia

Anna Wawrocka, Agata Sikora, Łukasz Kuszel et al. · Journal of Applied Genetics · 2013 · 63 citations · Full text

Medicine, Genetics, Ophthalmology +15

Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 gene

Anna Skorczyk‐Werner, Wei‐Chieh Chiang, Anna Wawrocka et al. · European Journal of Human Genetics · 2017 · 36 citations · Full text

Life Sciences, Genetics, Molecular Genetics +5

<i>PAX6</i>3′ deletion in a family with aniridia

Anna Wawrocka, Bartłomiej Budny, Szymon Dębicki et al. · Ophthalmic Genetics · 2011 · 30 citations

Medicine, Genetics, Molecular Genetics +17

Novel variants identified with next-generation sequencing in Polish patients with cone-rod dystrophy.

Anna Wawrocka, Anna Skorczyk‐Werner, Katarzyna Wicher et al. · PubMed · 2018 · 25 citations

Medicine, Genetics, Molecular Genetics +14

Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease

Joanna Walczak‐Sztulpa, Renata Posmyk, Ewelina Bukowska‐Olech et al. · Orphanet Journal of Rare Diseases · 2020 · 24 citations · Full text

Medicine, Genetics, Molecular Genetics +16