Citation Impact
Citing Papers
Chromosome Abnormalities and Genetic Counseling
2011
The mitophagy activator urolithin A is safe and induces a molecular signature of improved mitochondrial and cellular health in humans
2019 Standout
Deubiquitylating enzymes and drug discovery: emerging opportunities
2017
Mechanotransduction and extracellular matrix homeostasis
2014 Standout
Dissection and Aneurysm in Patients With Fibromuscular Dysplasia
2016
A Cancer-Specific Ubiquitin Ligase Drives mRNA Alternative Polyadenylation by Ubiquitinating the mRNA 3′ End Processing Complex
2020
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents
2015 Standout
A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases
2017
The Role of the Reactive Oxygen Species and Oxidative Stress in the Pathomechanism of the Age‐Related Ocular Diseases and Other Pathologies of the Anterior and Posterior Eye Segments in Adults
2016 Standout
PROTAC targeted protein degraders: the past is prologue
2022 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline From the American Heart Association/American Stroke Association
2021 Standout
Fibromuscular Dysplasia: State of the Science and Critical Unanswered Questions
2014
Spontaneous Coronary Artery Dissection: Current State of the Science: A Scientific Statement From the American Heart Association
2018
Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF‐β expression and connective tissue features
2014
Cellular and disease functions of the Prader–Willi Syndrome geneMAGEL2
2017
Insights into keratoconus from a genetic perspective
2013
Clinical Utility of Contemporary Molecular Cytogenetics
2008
Works of Rocio Moran being referenced
Familial adenomatous polyposis in a patient with unexplained mental retardation
2007
USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder
2015
The Value of Keratometry and Central Corneal Thickness Measurements in the Clinical Diagnosis of Marfan Syndrome
2008
Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype
2011
Low yield of genetic testing for known vascular connective tissue disorders in patients with fibromuscular dysplasia
2012