Ryland D Mortlock
7PUBLICATIONS
25CO-AUTHORS
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Publications (7)
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|Oct 15, 2025
Erythrokeratodermia-Cardiomyopathy Syndrome: Expanding the DSP Mutational Spectrum Beyond Proline Substitutions.Sepideh Hamzehlou, Ryland D Mortlock, Caroline Echeandia-Francis
|Aug 30, 2025
LZTR1 is a melanoma oncogene that promotes invasion and suppresses apoptosis.Antonella Bacchiocchi, Michael Mak, Zerin Mahzabin Khan
|Aug 04, 2025
A recurrent de novo damaging variant in EMP2 causes progressive symmetric erythrokeratoderma.Xingyuan Jiang, Ryland D Mortlock, Nathalie Pironon
|May 30, 2025
Linear epidermal naevus associated with a novel mosaic heterozygous PTPN11 variant.Xingyuan Jiang, Tiffany X Chen, Ronghua Hu
|Feb 06, 2025
Autosomal dominant SLURP1 variants cause palmoplantar keratoderma and progressive symmetric erythrokeratoderma.Xingyuan Jiang, Ryland D Mortlock, Ivan B Lomakin
|May 18, 2024
Enhancing in vivo cell and tissue targeting by modulation of polymer nanoparticles and macrophage decoys.Alexandra S Piotrowski-Daspit, Laura G Bracaglia, David A Eaton
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Frequent Collaborators
2 joint publications
Xingyuan Jiang
2 joint publications
Keith A Choate
1 joint publications
Stacey D Finley
1 joint publications
Alexandra S Piotrowski-Daspit
1 joint publications
David A Eaton
1 joint publications
Thomas C Binns
1 joint publications
Jordan S Pober
1 joint publications
W Mark Saltzman
1 joint publications
Ivan B Lomakin
1 joint publications
Christopher G Bunick
