PDE3A mutations cause autosomal dominant hypertension with brachydactyly
2015 · Nature Genetics · 169 citations
https://doi.org/10.1038/ng.3302
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Anja Weise
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Anja Weise is an academic researcher from Jena University Hospital. The author has contributed to research in topics: Genomic variations and chromosomal abnormalities & Chromosomal and Genetic Variations & Prenatal Screening and Diagnostics. The author has an h-index of 39, co-authored 224 publications.
ORCID: 0000-0003-3988-8919Papers by this author
worksChromosome distribution in human sperm – a 3D multicolor banding-study
2008 · Molecular Cytogenetics · 87 citations
https://doi.org/10.1186/1755-8166-1-25
Heteromorphic variants of chromosome 9
2013 · Molecular Cytogenetics · 47 citations
https://doi.org/10.1186/1755-8166-6-14
Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report
2012 · Molecular Cytogenetics · 40 citations
https://doi.org/10.1186/1755-8166-5-30
Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon
2008 · Molecular Cytogenetics · 32 citations
https://doi.org/10.1186/1755-8166-1-9
Parental origin of deletions and duplications – about the necessity to check for cryptic inversions
2018 · Molecular Cytogenetics · 19 citations
https://doi.org/10.1186/s13039-018-0369-1
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