Stefan J Rietmann

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 8

Top Topics

Induced Pluripotent Stem Cells

Intellectual Disability

Top Venues

Animal genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Stefan J Rietmann, Anja Lange, Sara Soto, Nina Thom, Eberhard Manz, Vidhya Jagannathan, Ursula Mayer, Tosso Leeb
KRT5 in-frame deletion in a family of German Shepherd dogs with split paw pad disease resembling localized epidermolysis bullosa simplex in human patients. Animal genetics (2024)
Stefan J Rietmann, Noëlle Cochet-Faivre, Helene Dropsy, Vidhya Jagannathan, Lucie Chevallier, Tosso Leeb
EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia. Genes 15 (7) (2024)
Stefan J Rietmann, Noëlle Cochet-Faivre, Helene Dropsy, Vidhya Jagannathan, Lucie Chevallier, Tosso Leeb
EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia. Genes 15 (7) (2024)
Stefan J Rietmann, Noëlle Cochet-Faivre, Helene Dropsy, Vidhya Jagannathan, Lucie Chevallier, Tosso Leeb
EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia. Genes 15 (7) (2024)
Stefan J Rietmann, Sarah Nowell, M Kelly Keating, Cynthia Bauer, Vidhya Jagannathan, Tosso Leeb
Heterozygous COL5A1 deletion in a cat with classical Ehlers-Danlos syndrome. Animal genetics 55 (4) (2024)
Stefan J Rietmann, Noëlle Cochet-Faivre, Helene Dropsy, Vidhya Jagannathan, Lucie Chevallier, Tosso Leeb
EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia. Genes 15 (7) (2024)
Stefan J Rietmann, Sarah Nowell, M Kelly Keating, Cynthia Bauer, Vidhya Jagannathan, Tosso Leeb
Heterozygous COL5A1 deletion in a cat with classical Ehlers-Danlos syndrome. Animal genetics (2024)
Stefan J Rietmann, Anja Lange, Sara Soto, Nina Thom, Eberhard Manz, Vidhya Jagannathan, Ursula Mayer, Tosso Leeb
KRT5 in-frame deletion in a family of German Shepherd dogs with split paw pad disease resembling localized epidermolysis bullosa simplex in human patients. Animal genetics 55 (4) (2024)