Bernhard Suter (Bernard Suter)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 5

Top Topics

Community Dwelling

Genetic Diversity

Top Venues

American journal of medical genetics. Part A

Disability and rehabilitation

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

Publications

Isabel Haviland, Ralph D Hector, Lindsay C Swanson, Aubrie Soucy Verran, Emma Sherrill, Zoë Frazier, AnneMarie M Denny, Jenna Lucash, Bo Zhang, Holly A Dubbs, Eric D Marsh, Judith L Weisenberg, Helen Leonard, Milena Crippa, Francesca Cogliati, Silvia Russo, Bernhard Suter, Rajsekar Rajaraman, Alan K Percy, John M Schreiber, Scott T Demarest, Timothy A Benke, Maya Chopra, Timothy W Yu, Heather E Olson
Deletions in the CDKL5 5' untranslated region lead to CDKL5 deficiency disorder. American journal of medical genetics. Part A (2024)
Jacinta M Saldaris, Peter Jacoby, Jennepher Anne Downs, Eric D Marsh, Helen Margaret Leonard, Elia M Pestana Knight, Rajsekar Rajaraman, Judith Weisenberg, Bernhard Suter, Heather E Olson, Dana Price, William Hong, Erin Prange, Timothy A Benke, Scott T Demarest
Psychometric evaluation of clinician- and caregiver-reported clinical severity assessments for individuals with CDKL5 deficiency disorder. Epilepsia (2024)
Sarika U Peters, Cary Fu, Eric D Marsh, Tim A Benke, Bernhard Suter, Steve A Skinner, David N Lieberman, Shannon Standridge, Mary Jones, Arthur Beisang, Timothy Feyma, Peter Heydeman, Robin Ryther, Daniel G Glaze, Alan K Percy, Jeffrey L Neul
Phenotypic features in MECP2 duplication syndrome: Effects of age. American journal of medical genetics. Part A 185 (2) (2020)
David R Young, Bernhard Suter, Jackson T Levine, Daniel G Glaze, Charles S Layne
Characteristic behaviors associated with gait of individuals with Rett syndrome. Disability and rehabilitation (2020)
Manar Zaghlula, Daniel G Glaze, Gregory M Enns, Lorraine Potocki, Aloysia L Schwabe, Bernhard Suter
Current clinical evidence does not support a link between TBL1XR1 and Rett syndrome: Description of one patient with Rett features and a novel mutation in TBL1XR1, and a review of TBL1XR1 phenotypes. American journal of medical genetics. Part A 176 (7) (2018)