American Psychiatric Association (2013) Diagnostic and Statistical Manual of Mental Disorders. Diagnostic and Statistical Manual of Mental Disorders, 5(5). https://doi.org/10.1176/appi.books.9780890425596
Ault R, Morales A, Ault R, Spitale A, Martinez GA (2019) Communication pitfalls in interpreted genetic counseling sessions. J Genet Couns 28(4):897–907. https://doi.org/10.1002/jgc4.1132
Cragun D, Weidner A, Tezak A, Zuniga B, Wiesner GL, Pal T (2020) A Web-Based tool to Automate portions of pretest genetic counseling for inherited Cancer. J Natl Compr Cancer Netw J Natl Compr Canc Netw 18(7):841–847. https://doi.org/10.6004/jnccn.2020.7546
Cragun D, Manso G, Arcusa SA, Zuniga B, Dutil J, Cruz M, Pal T (2023) Piloting a Spanish-Language Web-Based tool for hereditary Cancer genetic testing. Curr Oncol 30(9):8352–8362. https://doi.org/10.3390/curroncol30090606
Article PubMed PubMed Central Google Scholar
Genovese A, Butler MG (2020) Clinical assessment, genetics, and treatment approaches in autism spectrum disorder (ASD). Int J Mol Sci 21(13):4726. https://doi-org.ezproxy.bu.edu/https://doi.org/10.3390/ijms21134726
Article CAS PubMed PubMed Central Google Scholar
Li M, Amuta A, Xu L, Dhar SU, Talwar D, Jung E, Chen L-S (2016) Autism genetic testing information needs among parents of affected children: A qualitative study. Patient Educ Couns 99(6):1011–1016. https://doi.org/10.1016/j.pec.2015.12.023
Maiese DR, Keehn A, Lyon M, Flannery D, Watson M, Working Groups of the National Coordinating Center for Seven Regional Genetics Service Collaboratives (2019) Current conditions in medical genetics practice. Genet Sci 21(8):1874–1877. https://doi.org/10.1038/s41436-018-0417-6
Manickam K, McClain MR, Demmer LA, Biswas S, Kearney HM, Malinowski J, Massingham LJ, Miller D, Yu TW, Hisama FM; ACMG Board of Directors (2021) Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG). Genet Med 23(11):2029–2037. https://doi.org/10.1038/s41436-021-01242-6
National Society of Genetic Counselors (2024) Professional Status Survey. https://www.nsgc.org/Policy-Research-and-Publications/Professional-Status-Survey
Sandin S, Lichtenstein P, Kuja-Halkola R, Hultman C, Larsson H, Reichenberg A (2017) The heritability of autism spectrum disorder. JAMA 318(12):1182–1184. https://doi.org/10.1001/jama.2017.12141
Article PubMed PubMed Central Google Scholar
Savatt JM, Myers SM (2021) Genetic testing in neurodevelopmental disorders. Front Pead 9:526779. https://doi.org/10.3389/fped.2021.526779
Schaefer GB, Mendelsohn NJ, Professional Practice and Guidelines Committee (2013) Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions. Genet Medicine: Official J Am Coll Med Genet 15(5):399–407. https://doi.org/10.1038/gim.2013.32
Shaw KA, Williams S, Patrick ME, Valencia-Prado M, Durkin MS, Howerton EM, Ladd-Acosta CM, Pas ET, Bakian AV, Bartholomew P, Nieves-Muñoz N, Sidwell K, Alford A, Bilder DA, DiRienzo M, Fitzgerald RT, Furnier SM, Hudson AE, Pokoski OM, Shea L, Maenner MJ (2025) Prevalence and early identification of autism spectrum disorder among children aged 4 and 8 Years - autism and developmental disabilities monitoring network, 16 sites, united states, 2022. Morbidity Mortal Wkly Rep Surveillance Summaries (Washington D C: 2002) 74(2):1–22. https://doi.org/10.15585/mmwr.ss7402a1
Stefanski A, Calle-López Y, Leu C, Pérez-Palma E, Pestana-Knight E, Lal D (2021) Clinical sequencing yield in epilepsy, autism spectrum disorder, and intellectual disability: A systematic review and meta-analysis. Epilepsia 62(1):143–151. https://doi.org/10.1111/epi.16755
Sundjaja JH, Shrestha R, Krishan K (2023) McNemar And Mann-Whitney U Tests. National Library of Medicine National Center for Biotechnology Information. Retrieved January 10, 2025, from https://www.ncbi.nlm.nih.gov/books/NBK560699/
Wang C, Gonzalez R, Milliron KJ, Strecher VJ, Merajver SD (2005) Genetic counseling for BRCA1/2: a randomized controlled trial of two strategies to facilitate the education and counseling process. Am J Med Genet: A 134A(1):66–73. https://doi.org/10.1002/ajmg.a.30577
Comments (0)