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Cardiology in the Young|January 28, 2020
Adolescents with congenital heart defects: a patient and parental perspective of genetic information and genetic riskChristopher A Crawford, Courtney E Vujakovich, Lindsey Elmore, et al.
Research Square|April 17, 2026
Provider Perceptions of the Impact of Rapid Whole Genome Sequencing on Care and ManagementRachel Palmquist, Chelsea Solorzano, Brian J Shayota, et al.
Plastic and Reconstructive Surgery|February 26, 2005
Female college students and cosmetic surgery: an investigation of experiences, attitudes, and body imageDavid B Sarwer, Thomas F Cash, Leanne Magee, et al.
Breast Cancer Research and Treatment|April 5, 2021
Incidence of cardiotoxicity and validation of the Heart Failure Association-International Cardio-Oncology Society risk stratification tool in patients treated with trastuzumab for HER2-positive early breast cancerNicolò Matteo Luca Battisti, Maria Sol Andres, Karla A Lee, et al.
Brain : a Journal of Neurology|December 21, 2023
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamicsRaffaella De Pace, Reza Maroofian, Adeline Paimboeuf, et al.
The American Journal of Medicine|January 3, 2015
Late Consequences of Acute Coronary Syndromes: Global Registry of Acute Coronary Events (GRACE) Follow-upSami M A Alnasser, Wei Huang, Joel M Gore, et al.
Medrxiv : the Preprint Server for Health Sciences|November 6, 2024
Basic helix-loop-helix transcription factor BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, tone and movement abnormalitiesCarolyn Le, Emanuela Argilli, Elizabeth George, et al.
American Journal of Human Genetics|July 30, 2019
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental DisordersBjörn Fischer-Zirnsak, Lara Segebrecht, Max Schubach, et al.
Molecular Psychiatry|November 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental conditionElizabeth E Palmer, Michael Pusch, Alessandra Picollo, et al.
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