Publications by authors named "Rhona Macleod"

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Cascade counselling and testing. Recommendations of the European Society of Human Genetics.
Guido de Wert, Carla G van El, Angus Clarke, Christophe Cordier, Florence Fellmann, Rhona MacLeod

Eur J Hum Genet· December 2025

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Genetic testing for Huntington's disease: Past, present and future. How could genetic data be used to improve clinical practice?
Davina J Hensman Moss, Rhiannon Ireland, Guy Chapman, Rhona MacLeod, Robyn Labrum

J Huntingtons Dis· December 2025

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The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders.
Laynie Dratch, Kim Jenny, Kristiana Salmon, Ashley Crook, Wendy R Uhlmann, Rhona MacLeod

Neurology· November 2025

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The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders.
Laynie Dratch, Kim Jenny, Kristiana Salmon, Ashley Crook, Wendy R Uhlmann, Rhona MacLeod

Neurology· August 2025

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The use of genetic testing in amyotrophic lateral sclerosis (ALS): a practical approach.
Amina Chaouch, Ashley Crook, Andrew G L Douglas, Christopher J McDermott, Ammar Al-Chalabi, Rhona MacLeod

Amyotroph Lateral Scler Frontotemporal Degener· August 2025

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Counseling supervision for genetic counselors: A proposed outsider witness structure.
Mariangels Ferrer-Duch, Fiona Ulph, Elisabet Dachs Cabanas, Glenda Fredman, Rhona MacLeod

J Genet Couns· June 2025

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Perils of predictive testing for unaffected people from motor neuron disease families with no identified causal gene.
Alisdair Mcneill, Andrew G L Douglas, Rhona Macleod, Nayana Lahiri,

Amyotroph Lateral Scler Frontotemporal Degener· May 2025

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Genetic testing for monogenic forms of motor neuron disease/amyotrophic lateral sclerosis in unaffected family members.
Jade Howard, Amina Chaouch, Andrew G L Douglas, Rhona MacLeod, Jennifer Roggenbuck

Eur J Hum Genet· January 2025

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Exploring NICU nurses' views of a novel genetic point-of-care test identifying neonates at risk of antibiotic-induced ototoxicity: A qualitative study.
Georgia Brown, Natalie Warrington, Fiona Ulph, Nicola Booth, Karen Harvey, Rhona Macleod

J Adv Nurs· August 2024

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The global status of genetic counselors in 2023: What has changed in the past 5 years?
Kelly E Ormond, Peter James Abad, Rhona MacLeod, Masakazu Nishigaki, Tina-Marié Wessels

Genet Med Open· August 2024

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Informed consent for whole genome sequencing in mainstream clinics: logistical constraints and possible solutions.
Amina Chaouch, Fiona Ulph, James Alder, Hisham Hamdalla, John Ealing, Rhona Macleod

Eur J Hum Genet· March 2024

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Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research.
Faye Johnson, Fiona Ulph, Rhona MacLeod, Kevin W Southern

Eur J Hum Genet· May 2022

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Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care.
John H McDermott, Ajit Mahaveer, Rachel A James, Nicola Booth, Mark Turner, Rhona MacLeod

JAMA Pediatr· May 2022

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Pharmacogenetics to Avoid Loss of Hearing (PALOH) trial: a protocol for a prospective observational implementation trial.
John Henry McDermott, Rachel Mahood, Duncan Stoddard, Ajit Mahaveer, Mark A Turner, Rhona Macleod

BMJ Open· June 2021

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A family systems approach to genetic counseling: Development of narrative interventions.
Rhona MacLeod, Alison Metcalfe, Mariangels Ferrer-Duch

J Genet Couns· February 2021

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Evaluating a genetic counseling narrative group session for people who have tested positive for the Huntington's disease expansion: An interpretative phenomenological analysis.
Johanna Spiers, Jonathan A Smith, Mariangels Ferrer-Duch, Ramona Moldovan, Jay Roche, Rhona MacLeod

J Genet Couns· December 2020

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Letter in Response to Tibben et al., Risk Assessment for Huntington's Disease for (Future) Offspring Requires Offering Preconceptional CAG Analysis to Both Partners.
Oliver W Quarrell, Martin B Delatycki, Angus J Clarke, Nayana Lahiri, David Craufurd, Rhona MacLeod

J Huntingtons Dis· July 2020

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Diagnosing and Preventing Hearing Loss in the Genomic Age.
John H McDermott, Leslie P Molina-Ramírez, Iain A Bruce, Ajit Mahaveer, Mark Turner, Rhona MacLeod

Trends Hear· March 2020

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Improving follow up after predictive testing in Huntington's disease: evaluating a genetic counselling narrative group session.
Cheryl Stopford, Mariangels Ferrer-Duch, Ramona Moldovan, Rhona MacLeod

J Community Genet· January 2020

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Genetic Counselling and Narrative Practices: A Model of Support following a "Negative" Predictive Test for Huntington's Disease.
Rhona MacLeod, Ramona Moldovan, Cheryl Stopford, Mariangels Ferrer-Duch

J Huntingtons Dis· October 2019

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A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice.
Felicity Wadrup, Simon Holden, Rhona MacLeod, Zosia Miedzybrodzka, Andrea H Németh

Eur J Hum Genet· August 2019

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Delivering effective genetic services for patients and families affected by cleft lip and/or palate.
Nicola Marie Stock, Rhona MacLeod, Jill Clayton-Smith

Eur J Hum Genet· July 2019

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The Process of Disclosure: Mothers' Experiences of Communicating X-Linked Carrier Risk Information to At-Risk Daughters.
Amy Goldman, Alison Metcalfe, Rhona MacLeod

J Genet Couns· September 2018

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Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences.
Oliver W Quarrell, Angus J Clarke, Cecilia Compton, Christine E M de Die-Smulders, Alan Fryer, Rhona MacLeod

Am J Med Genet B Neuropsychiatr Genet· January 2018

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The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors.
Anna Middleton, Peter Marks, Anita Bruce, Liwsi K Protheroe-Davies, Cath King, Rhona Macleod

Eur J Hum Genet· March 2017

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