APA (7th ed.) Citation

Cooperstein, I. B., Marwaha, S., Ward, A., Kobren, S. N., Carter, J. N., Quinlan, A., . . . Vargas, A. (2025). An optimized variant prioritization process for rare disease diagnostics: Recommendations for Exomiser and Genomiser. Genome Medicine, 17(1), 1. https://doi.org/10.1186/s13073-025-01546-1

Chicago Style (17th ed.) Citation

Cooperstein, Isabelle B., et al. "An Optimized Variant Prioritization Process for Rare Disease Diagnostics: Recommendations for Exomiser and Genomiser." Genome Medicine 17, no. 1 (2025): 1. https://doi.org/10.1186/s13073-025-01546-1.

MLA (9th ed.) Citation

Cooperstein, Isabelle B., et al. "An Optimized Variant Prioritization Process for Rare Disease Diagnostics: Recommendations for Exomiser and Genomiser." Genome Medicine, vol. 17, no. 1, 2025, p. 1, https://doi.org/10.1186/s13073-025-01546-1.