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Publications by Margit Schraders

Novel and Recurrent CIB2 Variants, Associated With Nonsyndromic Deafness, Do Not Affect Calcium Buffering and Localization in Hair Cells

European Journal of Human Genetics

English

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Variants in WFS1 and Other Mendelian Deafness Genes Are Associated With Cisplatin-Associated Ototoxicity

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Nonsyndromic Deafness - Molecular Update

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Do Variants Associated With Susceptibility to Pancreatic Cancer and Type 2 Diabetes Reciprocally Affect Risk?

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Genetic Variants in Cellular Transport Do Not Affect Mesalamine Response in Ulcerative Colitis

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Novel Calmodulin Mutations Associated With Congenital Long QT Syndrome Affect Calcium Current in Human Cardiomyocytes

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Novel Cav2.1 Splice Variants Isolated From Purkinje Cells Do Not Generate P-Type Ca2+Current

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Comprehensive Analysis of Deafness Genes in Families With Autosomal Recessive Nonsyndromic Hearing Loss

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Mapping of a Novel Autosomal Recessive Nonsyndromic Deafness Locus (DFNB46) to Chromosome 18p11.32-P11.31

American Journal of Medical Genetics, Part A

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Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic Variants

Frontiers in Neurology

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