Katharina Hopp, Ph.D.

Affiliations: 
2013 Biochemistry and Molecular Biology College of Medicine - Mayo Clinic 
Area:
Genetics, Molecular Biology, Oncology
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"Katharina Hopp"

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Peter C. Harris grad student 2013 College of Medicine - Mayo Clinic
 (Genetic dissection of ciliopathy pedigrees with unusual disease presentation or unresolved etiology.)
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Publications

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Olson RJ, Hopp K, Wells H, et al. (2019) Synergistic Genetic Interactions between and Result in an ARPKD-Like Phenotype in Murine Models. Journal of the American Society of Nephrology : Jasn
Kleczko EK, Marsh KH, Tyler LC, et al. (2018) CD8 T cells modulate autosomal dominant polycystic kidney disease progression. Kidney International
Boczek NJ, Hopp K, Benoit L, et al. (2018) Characterization of three ciliopathy pedigrees expands the phenotype associated with biallelic C2CD3 variants. European Journal of Human Genetics : Ejhg
Cornec-Le Gall E, Olson RJ, Besse W, et al. (2018) Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease. American Journal of Human Genetics
Porath B, Gainullin VG, Cornec-Le Gall E, et al. (2016) Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease. American Journal of Human Genetics. 98: 1193-1207
Heyer CM, Sundsbak JL, Abebe KZ, et al. (2016) Predicted Mutation Strength of Nontruncating PKD1 Mutations Aids Genotype-Phenotype Correlations in Autosomal Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology : Jasn
Warner G, Hein KZ, Nin V, et al. (2015) Food Restriction Ameliorates the Development of Polycystic Kidney Disease. Journal of the American Society of Nephrology : Jasn
Ye H, Wang X, Sussman CR, et al. (2015) Modulation of Polycystic Kidney Disease Severity by Phosphodiesterase 1 and 3 Subfamilies. Journal of the American Society of Nephrology : Jasn
Kline TL, Irazabal MV, Ebrahimi B, et al. (2015) Utilizing magnetization transfer imaging to investigate tissue remodeling in a murine model of autosomal dominant polycystic kidney disease. Magnetic Resonance in Medicine : Official Journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine
Hopp K, Cogal AG, Bergstralh EJ, et al. (2015) Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria. Journal of the American Society of Nephrology : Jasn
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