J. Gannon

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

David T. Miller, L. Demmer, M. Scheuner, 2020, Genetics in Medicine.

Delayed diagnosis of holocarboxylase synthetase deficiency in three patients with prominent skin findings.

C. Saunders, B. Heese, J. Gannon, 2021, Pediatric dermatology.

Nutrition Management for the Preterm Infant With PAH Deficiency

B. Heese, K. Rowzer, J. Gannon, 2020 .

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

David T. Miller, L. Demmer, M. Scheuner, 2020, Genetics in Medicine.

Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes

Orion J. Buske, Nigel J. Price, Warren A. Cheung, 2021, medRxiv.

Diagnostic gene sequencing panels: from design to report—a technical standard of the American College of Medical Genetics and Genomics (ACMG)

Birgit Funke, Pinar Bayrak-Toydemir, Lora J H Bean, 2019, Genetics in Medicine.

Points to consider when assessing relationships (or suspecting misattributed relationships) during family-based clinical genomic testing: a statement of the American College of Medical Genetics and Genomics (ACMG)

Joshua L. Deignan, H. Greely, S. Topper, 2020, Genetics in Medicine.

Points to consider when assessing relationships (or suspecting misattributed relationships) during family-based clinical genomic testing: a statement of the American College of Medical Genetics and Genomics (ACMG)

Joshua L. Deignan, H. Greely, S. Topper, 2020, Genetics in Medicine.

Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.

Orion J. Buske, Neil A. Miller, J. Korlach, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.