Cecilia W. Lo

Department of Developmental Biology, University of Pittsburgh

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 1	2022

Other Publications

Article	Year
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies. Human molecular genetics\| PubMed ID: 25877302	2015
Establishing normative nasal nitric oxide values in infants. Respiratory medicine\| PubMed ID: 26233707	2015
Automated identification of abnormal respiratory ciliary motion in nasal biopsies. Science translational medicine\| PubMed ID: 26246169	2015
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects. Biology open\| PubMed ID: 26883626	2016
Brain Dysplasia Associated with Ciliary Dysfunction in Infants with Congenital Heart Disease. The Journal of pediatrics\| PubMed ID: 27574995	2016
Cilia and Ciliopathies in Congenital Heart Disease. Cold Spring Harbor perspectives in biology\| PubMed ID: 28159874	2017
Reply. The Journal of pediatrics\| PubMed ID: 28283257	2017
Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography. JCI insight\| PubMed ID: 28289722	2017
The complex genetics of hypoplastic left heart syndrome. Nature genetics\| PubMed ID: 28530678	2017
Phenotyping cardiac and structural birth defects in fetal and newborn mice. Birth defects research\| PubMed ID: 28544620	2017
Diverse application of MRI for mouse phenotyping. Birth defects research\| PubMed ID: 28544650	2017
Loss of function in is associated with tetralogy of Fallot and septal defects. Journal of medical genetics\| PubMed ID: 28592524	2017
Airway ciliary dysfunction: Association with adverse postoperative outcomes in nonheterotaxy congenital heart disease patients. The Journal of thoracic and cardiovascular surgery\| PubMed ID: 29056267	2018
Low Nasal NO in Congenital Heart Disease With Systemic Right Ventricle and Postcardiac Transplantation. Journal of the American Heart Association\| PubMed ID: 29212650	2017
Airway ciliary dysfunction and respiratory symptoms in patients with transposition of the great arteries. PloS one\| PubMed ID: 29444099	2018
Wdpcp promotes epicardial EMT and epicardium-derived cell migration to facilitate coronary artery remodeling. Science signaling\| PubMed ID: 29487191	2018
The Genetic Landscape of Hypoplastic Left Heart Syndrome. Pediatric cardiology\| PubMed ID: 29569026	2018
A computational framework for the detection of subcortical brain dysmaturation in neonatal MRI using 3D Convolutional Neural Networks. NeuroImage\| PubMed ID: 29793060	2018
Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes. Frontiers in pediatrics\| PubMed ID: 29963541	2018
Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome biology\| PubMed ID: 30012220	2018
Vertebrate myosin 1d regulates left-right organizer morphogenesis and laterality. Nature communications\| PubMed ID: 30139971	2018
Cardiac Targeting Peptide, a Novel Cardiac Vector: Studies in Bio-Distribution, Imaging Application, and Mechanism of Transduction. Biomolecules\| PubMed ID: 30441852	2018
Reply to 'Double-outlet right ventricle is not hypoplastic left heart syndrome'. Nature genetics\| PubMed ID: 30617253	2019
Deposition studies of aerosol delivery by nasal cannula to infants. Pediatric pulmonology\| PubMed ID: 30932345	2019
Left-right patterning in congenital heart disease beyond heterotaxy. American journal of medical genetics. Part C, Seminars in medical genetics\| PubMed ID: 31999049	2020
Role of cilia in the pathogenesis of congenital heart disease. Seminars in cell & developmental biology\| PubMed ID: 32418658	2021
Mutation of LRP1 in cardiac neural crest cells causes congenital heart defects by perturbing outflow lengthening. Communications biology\| PubMed ID: 32546759	2020
Rapid Ex-Vivo Ciliogenesis and Dose-Dependent Effect of Notch Inhibition on Ciliogenesis of Respiratory Epithelia. Biomolecules\| PubMed ID: 32823934	2020
A Membrane-Tethered Ubiquitination Pathway Regulates Hedgehog Signaling and Heart Development. Developmental cell\| PubMed ID: 32966817	2020
Cilia interactome with predicted protein-protein interactions reveals connections to Alzheimer's disease, aging and other neuropsychiatric processes. Scientific reports\| PubMed ID: 32973177	2020
Differential effect of anesthetics on mucociliary clearance in vivo in mice. Scientific reports\| PubMed ID: 33649513
Mucociliary Clearance Scans Show Infants Undergoing Congenital Cardiac Surgery Have Poor Airway Clearance Function. Frontiers in cardiovascular medicine\| PubMed ID: 33969015	2021
Cardiovascular Development and Congenital Heart Disease Modeling in the Pig. Journal of the American Heart Association\| PubMed ID: 34219463	2021
Mechanisms of Impaired Lung Development and Ciliation in Mannosidase-1-Alpha-2 () Mutants. Frontiers in physiology\| PubMed ID: 34366878	2021
Novel insights into the genetic landscape of congenital heart disease with systems genetics. Progress in pediatric cardiology\| PubMed ID: 34404969	2019
Gene-teratogen interactions influence the penetrance of birth defects by altering Hedgehog signaling strength. Development (Cambridge, England)\| PubMed ID: 34486668	2021
Mitochondrial Respiration Defects in Single-Ventricle Congenital Heart Disease. Frontiers in cardiovascular medicine\| PubMed ID: 34631832	2021
Relationships Between Regional Cerebral Blood Flow and Neurocognitive Outcomes in Children and Adolescents With Congenital Heart Disease. Seminars in thoracic and cardiovascular surgery\| PubMed ID: 34767938	2022
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. HGG advances\| PubMed ID: 34888534	2021
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract. Kidney international\| PubMed ID: 35227688	2022
Genetic resiliency associated with dominant lethal mutation causing atrial septal defect with high heritability. Cell reports. Medicine\| PubMed ID: 35243414	2022
Cerebellar and Prefrontal Structures Associated With Executive Functioning in Pediatric Patients With Congenital Heart Defects. Frontiers in neurology\| PubMed ID: 35356449	2022
Uncompensated mitochondrial oxidative stress underlies heart failure in an iPSC-derived model of congenital heart disease. Cell stem cell\| PubMed ID: 35395180	2022
Novel Protein-Protein Interactions Highlighting the Crosstalk between Hypoplastic Left Heart Syndrome, Ciliopathies and Neurodevelopmental Delays. Genes\| PubMed ID: 35456433	2022
Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta. Genes\| PubMed ID: 35456442	2022
Flow blockage disrupts cilia-driven fluid transport in the epileptic brain. Acta neuropathologica\| PubMed ID: 35980457	2022
Impaired Neurovascular Function Underlies Poor Neurocognitive Outcomes and Is Associated with Nitric Oxide Bioavailability in Congenital Heart Disease. Metabolites\| PubMed ID: 36144286	2022
Profiling development of abdominal organs in the pig. Scientific reports\| PubMed ID: 36171243	2022
Correction to: Flow blockage disrupts cilia-driven fluid transport in the epileptic brain. Acta neuropathologica\| PubMed ID: 36175669	2022
Clinical factors associated with microstructural connectome related brain dysmaturation in term neonates with congenital heart disease. Frontiers in neuroscience\| PubMed ID: 36466162	2022