Dimah Saade

7PUBLICATIONS
105CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cancer geneticsMicroelectromechanical systems (MEMS)Neurology and neuromuscular diseasesPsychophysiology
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Publications (7)

|Jul 03, 2026
Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.

|Apr 08, 2024
The recurrent deep intronic pseudoexon-inducing variant COL6A1 c.930+189C>T results in a consistently severe phenotype of COL6-related dystrophy: Towards clinical trial readiness for splice-modulating therapy.

A Reghan Foley, Véronique Bolduc, Fady Guirguis

|Aug 24, 2023
PIEZO2 and perineal mechanosensation are essential for sexual function.

Ruby M Lam, Lars J von Buchholtz, Melanie Falgairolle

|Jun 01, 2021
Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis.

Payam Mohassel, Sandra Donkervoort, Museer A Lone

|Jan 29, 2021
Innocuous pressure sensation requires A-type afferents but not functional ΡΙΕΖΟ2 channels in humans.

Laura K Case, Jaquette Liljencrantz, Nicholas Madian

|Jul 09, 2019
An ultrafast system for signaling mechanical pain in human skin.

Saad S Nagi, Andrew G Marshall, Adarsh Makdani

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Frequent Collaborators

5 joint publications

Carsten G Bönnemann

3 joint publications

M Catherine Bushnell

2 joint publications

Jaquette Liljencrantz

2 joint publications

Payam Mohassel