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Bridget Kiely, Sujit Vettam & Andrew Adesman. (2016) Utilization of genetic testing among children with developmental disabilities in the United States. The Application of Clinical Genetics 9, pages 93-100.
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Padraic J. Grattan-Smith & Russell C. Dale. 2023. Mechanisms and Emerging Therapies in Tremor Disorders. Mechanisms and Emerging Therapies in Tremor Disorders
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Gianmaria Miolo, Maria Grazia Giuffrida, Giuseppe Corona, Anna Capalbo, Barbara Pivetta, Giovanni Tessitori & Laura Bernardini. (2019) A novel mosaic 1q32.1 microduplication identified through Chromosome Microarray Analysis: narrowing the smallest critical region including KDM5B gene found associated with neurodevelopmetal disorders. European Journal of Medical Genetics 62:9, pages 103558.
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Alyson E. Hanish, Marlene Z. Cohen & Lois J. Starr. (2018) Autism spectrum disorder and genetic testing: Parental perceptions and decision-making. Journal for Specialists in Pediatric Nursing 23:2, pages e12211.
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Marian Reiff, Eva Bugos, Ellen Giarelli, Barbara A. Bernhardt, Nancy B. Spinner, Pamela L. Sankar & Surabhi Mulchandani. (2017) “Set in Stone” or “Ray of Hope”: Parents’ Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASD. Journal of Autism and Developmental Disorders 47:5, pages 1453-1463.
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Laila Y. AlAyadhi, Jamil A. Hashmi, Muhammad Iqbal, Alia M. Albalawi, Mohammad I. Samman, Nadra E. Elamin, Shahid Bashir & Sulman Basit. (2016) High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex families. Neuroscience 339, pages 561-570.
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Ming Li, Ann Amuta, Lei Xu, Shweta U. Dhar, Divya Talwar, Eunju Jung & Lei-Shih Chen. (2016) Autism genetic testing information needs among parents of affected children: A qualitative study. Patient Education and Counseling 99:6, pages 1011-1016.
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Michael L. Cuccaro, Kayla Czape, Michael Alessandri, Joycelyn Lee, Abigail Rupchock Deppen, Elise Bendik, Nicole Dueker, Laura Nations, Margaret Pericak-Vance & Susan Hahn. (2014) Genetic testing and corresponding services among individuals with autism spectrum disorder (ASD). American Journal of Medical Genetics Part A 164:10, pages 2592-2600.
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Lindsay Shea, Craig J. Newschaffer, Ming Xie, Scott M. Myers & David S. Mandell. (2013) Genetic testing and genetic counseling among medicaid-enrolled children with autism spectrum disorder in 2001 and 2007. Human Genetics 133:1, pages 111-116.
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Shruti GargJonathan GreenKathy LeadbitterRichard EmsleyAnnukka Lehtonen, D. Gareth Evans & Susan M. Huson. (2013) Neurofibromatosis Type 1 and Autism Spectrum Disorder. Pediatrics 132:6, pages e1642-e1648.
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Padraic J. Grattan-Smith & Russell C. Dale. 2013. Mechanisms and Emerging Therapies in Tremor Disorders. Mechanisms and Emerging Therapies in Tremor Disorders
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Susan G. McGrew, Brittany R. Peters, Julie A. Crittendon & Jeremy Veenstra-VanderWeele. (2011) Diagnostic Yield of Chromosomal Microarray Analysis in an Autism Primary Care Practice: Which Guidelines to Implement?. Journal of Autism and Developmental Disorders 42:8, pages 1582-1591.
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Isabel Filges, Anjeung Kang, Vanessa Klug, Friedel Wenzel, Karl Heinimann, Sevgi Tercanli & Peter Miny. (2012) Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies. Molecular Cytogenetics 5:1, pages 38.
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Jessica Roesser. (2011) Diagnostic Yield of Genetic Testing in Children Diagnosed With Autism Spectrum Disorders at a Regional Referral Center. Clinical Pediatrics 50:9, pages 834-843.
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