Publications by authors named "Clausen Marc"

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Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study.
Sebastian Lunke, Lilian Downie, Jade Caruana, Nathasha Kugenthiran, Paul De Fazio, Marc Clausen

Nat Med· December 2025

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Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdens.
Chloe Mighton, Emma Reble, Jordan Sam, Rita Kodida, Salma Shickh, Marc Clausen

Genet Med· October 2025

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The development and usability of 'The Genetics Navigator': a digital solution for adult and paediatric clinical genetics services.
Saumeh Saeedi, Daena Hirijkaka, Marc Clausen, Stephanie Luca, Emma Reble

Eur J Hum Genet· September 2025

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What are patient perspectives on privacy and trust in digital genomic tools? A qualitative study.
Vedika Jha, Saumeh Saeedi, Marc Clausen, Daniel Assamad, Sonya Grewal

J Genet Couns· June 2025

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Opportunistic genomic screening has clinical utility: An interventional cohort study.
Chloe Mighton, Rita Kodida, Salma Shickh, Marc Clausen, Emma Reble

Genet Med· February 2025

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Offering complex genomic screening in acute pediatric settings: Family decision-making and outcomes.
Melissa Martyn, Ling Lee, Alli Jan, Rigan Tytherleigh, Fiona Lynch, Marc Clausen

Genet Med· February 2025

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A Genomic Counseling Model for Population-Based Sequencing: A Pre-Post Intervention Study.
Selina Casalino, Chloe Mighton, Marc Clausen, Erika Frangione, Navneet Aujla, Marc Dagher, Steven Marc Friedman

Genet Med· December 2024

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"Should I Let Them Know I Have This?": Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes.
Ridhi Gopalakrishnan, Jordan Sam, Carly Butkowsky, Emma Reble, Marc Clausen

Public Health Genomics· December 2024

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Clinical Utility of Genomic Sequencing for Hereditary Cancer Syndromes: An Observational Cohort Study.
Salma Shickh, Chloe Mighton, Marc Clausen, Jordan Sam, Daena Hirjikaka

JCO Precis Oncol· December 2024

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Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations.
Guylaine D'Amours, Marc Clausen, Stephanie Luca, Emma Reble, Rita Kodida

BMJ Open· September 2024

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Genetics providers' perspectives on the use of digital tools in clinical practice.
Whiwon Lee, Daena Hirjikaka, Sonya Grewal, Angela Shaw, Stephanie Luca, Marc Clausen

Genet Med· June 2024

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Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol.
Sebastian Lunke, Sophie E Bouffler, Lilian Downie, Jade Caruana, David J Amor, Marc Clausen

BMJ Open· April 2024

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"I just wanted more": Hereditary cancer syndromes patients' perspectives on the utility of circulating tumour DNA testing for cancer screening.
Ella Adi-Wauran, Marc Clausen, Salma Shickh, Anna R Gagliardi, Avram Denburg

Eur J Hum Genet· February 2024

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Parents' attitudes towards research involving genome sequencing of their healthy children: a qualitative study.
Christina Di Carlo, Chloe Mighton, Marc Clausen, Esha Joshi, Selina Casalino

Eur J Hum Genet· February 2024

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Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing.
Marc Clausen, Suvetha Krishnapillai, Daena Hirjikaka, Rita Kodida, Salma Shickh

Genet Med Open· January 2024

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"I don't need any more unknowns hanging over my head": Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing.
Salma Shickh, Chloe Mighton, Marc Clausen, Rita Kodida, Ella Adi-Wauran

Genet Med· December 2023

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Digital Health Tools in Genomics: Advancing Diversity, Equity, and Inclusion.
Daniel Assamad, Safa Majeed, Vernie Aguda, Sonya Grewal, Carly Butkowsky, Marc Clausen

Public Health Genomics· December 2023

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A model for the return and referral of all clinically significant secondary findings of genomic sequencing.
Rita Kodida, Emma Reble, Marc Clausen, Salma Shickh, Chloe Mighton

J Med Genet· August 2023

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Public knowledge of SARS-CoV-2 serological and viral lineage laboratory testing and result interpretation: A GENCOV study cross-sectional survey.
Gregory Morgan, Laurent Briollais, Marc Clausen, Selina Casalino, Chloe Mighton, Marc Dagher

Clin Biochem· August 2023

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Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol.
Sophie E Bouffler, Ling Lee, Fiona Lynch, Melissa Martyn, Elly Lynch, Marc Clausen

BMJ Open· June 2023

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How do members of the public expect to use variants of uncertain significance in their health care? A population-based survey.
Chloe Mighton, Marc Clausen, Salma Shickh, Nancy N Baxter, Adena Scheer

Genet Med· May 2023

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Great expectations: patients' preferences for clinically significant results from genomic sequencing.
Salma Shickh, Agnes Sebastian, Marc Clausen, Chloe Mighton, Christine Elser

Hum Genet· April 2023

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Finding the sweet spot: a qualitative study exploring patients' acceptability of chatbots in genetic service delivery.
Stephanie Luca, Marc Clausen, Angela Shaw, Whiwon Lee, Suvetha Krishnapillai

Hum Genet· March 2023

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Genome screening, reporting, and genetic counseling for healthy populations.
Selina Casalino, Erika Frangione, Monica Chung, Georgia MacDonald, Sunakshi Chowdhary, Marc Clausen, Marc Dagher, Steven Marc Friedman

Hum Genet· February 2023

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Patient-facing digital tools for delivering genetic services: a systematic review.
Lee Whiwon, Shickh Salma, Assamad Daniel, Luca Stephanie, Clausen Marc

J Med Genet· January 2023

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