Shannon Nees, MD

Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study; Circulation: Genomic and Precision Medicine; (2023).

Cyproheptadine and atrioventricular block in a patient with congenital heart disease; Progress in Pediatric Cardiology; (2021).

The genetics of isolated congenital heart disease; American Journal of Medical Genetics Part C: Seminars in Medical Genetics; (2020).

Genetic Basis of Human Congenital Heart Disease.; Cold Spring Harbor perspectives in biology; (2020).

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes.; Genetics in medicine : official journal of the American College of Medical Genetics; (2020).

Targeted Therapy for Pulmonary Hypertension in Premature Infants. ; Children (Basel, Switzerland); (2020).

Assessment of Anomalous Coronary Arteries by Imagers and Surgeons: Comparison of Imaging Modalities.; The Annals of thoracic surgery; (2020).

Patients with anomalous aortic origin of the coronary artery remain at risk after surgical repair.; The Journal of thoracic and cardiovascular surgery; (2018).

Pulmonary hypertension in patients with 9q34.3 microdeletion-associated Kleefstra syndrome.; American journal of medical genetics. Part A; (2018).

Sildenafil Use in Children with Pulmonary Hypertension.; The Journal of pediatrics; (2018).

Outcomes of targeted treatment for vesicoureteral reflux in children with nonneurogenic lower urinary tract dysfunction.; The Journal of urology; (2013).

Incidence, significance and natural history of persistent retrograde venous flow after varicocelectomy in children and adolescents: correlation with catch-up growth.; The Journal of urology; (2013).

Use of complementary and alternative medicine among children, adolescent, and young adult cancer survivors: a survey study.; Journal of pediatric hematology/oncology; (2013).

Proprotein convertase subtilisin/kexin type 9 potentially influences cholesterol uptake in macrophages and reverse cholesterol transport.; FEBS letters; (2013).

Mutations in DSTYK and dominant urinary tract malformations.; The New England journal of medicine; (2013).

Outcomes of vesicoureteral reflux in children with non-neurogenic lower urinary tract dysfunction treated with dextranomer/hyaluronic acid copolymer (Deflux).; Journal of pediatric urology; (2013).

Adolescent varicocelectomy: does artery sparing influence recurrence rate and/or catch-up growth?; Andrology; (2013).

Physical exam and ultrasound characteristics of right varicocoeles in adolescents with left varicocoeles.; Andrology; (2013).

Intratesticular varicoceles: are they significant?; Journal of pediatric urology; (2012).

Copy-number disorders are a common cause of congenital kidney malformations.; American journal of human genetics; (2012).

Testicular symmetry and adolescent varicocele--does it need followup?; The Journal of urology; (2011).

Observations on hydroceles following adolescent varicocelectomy.; The Journal of urology; (2011).

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.; Kidney international; (2011).