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Yvonne Bombard on Muck Rack

Yvonne Bombard

As seen in: Nature, BMJ Open, Journal of Medical Genetics (JMG), MDPI, The Globe and Mail, Implementation Science, Cell Press, The American Journal of Human Genetics, Pediatrics, Canadian Medical Association Journal and
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Articles

Genomic newborn screening: a scoping review of the field’s evolution and associated ethical, legal, and social implications

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By Gemma Brown, Loren Walker, Mutiat Afolabi, Paul Bain, Ana Eliza Bonilha, Bimal P. Chaudhari, John Christodoulou, Ziyi Dai, Jan M Friedman, Amy Gaviglio, Robert Green, Subhashini Jagu, Bartha M. Knoppers, Zornitza Stark, Danya Vears, Yvonne Bombard, Anna Lewis, Aliza Wilson
| Nature Verified
Abstract The integration of genomic sequencing into newborn screening (genomic newborn screening; gNBS) has the potential to identify more presymptomatic babies who could benefit from early intervention compared to traditional universal newborn screening (NBS). Realizing these benefits requires careful navigation of ethical, legal, and social implications (ELSI) to minimize harms, promote equity, and maintain trust in NBS programs.
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Correction: The development and usability of ‘The Genetics Navigator’: a digital solution for adult and paediatric clinical genetics services

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By Saumeh Saeedi, Marc Clausen, Stephanie Luca, Emma Reble, Rita Kodida, Daniel Assamad, Lauren Chad, Gregory Costain, Hanna Faghfoury, Josh Silver, Maureen Smith, Robin Z. Hayeems, Yvonne Bombard, Daena Hirjikaka, Serena Shastri-Estrada
| Nature Verified
Correction to: European Journal of Human Genetics https://doi.org/10.1038/s41431-025-01871-4, published online 30 May 2025 In this article, the author Daena Hirjikaka’s family name was incorrectly written as Hirijkaka. The original article has been corrected. About this article Saeedi, S., Hirjikaka, D., Clausen, M. et al. Correction: The development and usability of ‘The Genetics Navigator’: a digital solution for adult and paediatric clinical genetics services. Eur J Hum Genet (2026).
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“Where do I go from here?” Navigating a lifelong road without a map: the care experiences of hereditary cancer patients - European Journal of Human Genetics

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By June C. Carroll, Melyssa Aronson, Emma Reble, Marc Clausen, Brooklyn Sparkes, Lesa Dawson, Andrea Eisen, Tracy Graham, JAne Green, Jane Green, Chloe Mighton, Cláudia Pavão, Petros Pechlivanoglou, Sophie Austin Sun, Teresa Tiano, Kevin Thorpe, Kasmintan A. Schrader, Holly Etchegary, Yvonne Bombard, Carly Butkowsky, Jordan Sam, Ridhi Gopalakrishnan, Sepideh Rajeziesfahani, Vernie Aguda, Derrick Bishop, Julee Pauling, Catriona Remocker, Angelina Tilley
| Nature Verified
Abstract Individuals with hereditary cancer syndromes (HCS) face significant healthcare challenges, as they require lifelong surveillance for a multitude of at-risk organs. Despite the existence of HCS programs, literature has not elucidated the patient perspective of living with an HCS and the care journey. This study aimed to inform clinical practice by exploring the care experiences of HCS patients.
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