Lisa Heinz

Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans

Lisa Heinz, Gwang-Jin Kim, Slaheddine Marrakchi et al. · The American Journal of Human Genetics · 2017 · 82 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +3

Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions

Manuela Pigors, Ofer Sarig, Lisa Heinz et al. · The American Journal of Human Genetics · 2016 · 36 citations · Full text

Protein Function, Bone Morphogenic Protein, Intercellular Adhesions +9

Strong fascin expression promotes metastasis independent of its F-actin bundling activity

Lisa Heinz, Stefanie Muhs, Johanna Schiewek et al. · Oncotarget · 2017 · 31 citations · Full text

A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation

Steffen Hörer, Slaheddine Marrakchi, Franz P.W. Radner et al. · Journal of Investigative Dermatology · 2019 · 31 citations

Monoallelic Two-hit Mechanism, Genetic Disorder, Genetics +9

Buccal swabs as a reliable non-invasive tissue sampling method for DNA analysis in the lacertid lizard Podarcis muralis

Ulrich Schulte, Felix Gebhard, Lisa Heinz et al. · 2011 · 21 citations

Biology, Dna Barcoding, Genetic Testing +15