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Genes|June 24, 2022
State of the Science for Kidney Disorders in Phelan-McDermid Syndrome: UPK3A, FBLN1, WNT7B, and CELSR1 as Candidate GenesMegan D McCoy, Sara M Sarasua, Jane M DeLuca, et al.
American Journal of Medical Genetics. Part A|June 29, 2021
Comprehensive investigation of the phenotype of MEF2C-related disorders in human patients: A systematic reviewJessica A Cooley Coleman, Sara M Sarasua, Luigi Boccuto, et al.
Pediatric Nephrology (Berlin, Germany)|September 21, 2023
Genetics of kidney disorders in Phelan-McDermid syndrome: evidence from 357 registry participantsMegan D McCoy, Sara M Sarasua, Jane M DeLuca, et al.
Nursing Open|April 2, 2021
Tremors: A concept analysisJessica A Cooley Coleman, Sara M Sarasua, Luigi Boccuto, et al.
BMC Geriatrics|August 13, 2022
TOMM40 genetic variants associated with healthy aging and longevity: a systematic reviewSunny Chen, Sara M Sarasua, Nicole J Davis, et al.
Genes|March 29, 2023
Head Size in Phelan-McDermid Syndrome: A Literature Review and Pooled Analysis of 198 Patients Identifies Candidate Genes on 22q13Sara M Sarasua, Jane M DeLuca, Curtis Rogers, et al.
Molecular Genetics & Genomic Medicine|April 13, 2022
Clinical findings from the landmark MEF2C-related disorders natural history studyJessica A Cooley Coleman, Sara M Sarasua, Hannah Warren Moore, et al.
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