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| Open Access“Uninsurable because of a genetic test”: a qualitative study of consumer views about the use of genetic test results in Australian life insurance
- Cassandra Muller
- , Lyndon Gallacher
- & Jane Tiller
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Clinical impact of preemptive pharmacogenomic testing on antiplatelet therapy in a real-world setting
- Amanda Massmann
- , Kurt D. Christensen
- & Tomasz P. Stys
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Viewpoint
| Open AccessA framework for evaluating long-term impact of newborn screening
- Shona Kalkman
- , Ron A. Wevers
- & Mariska M. G. Leeflang
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Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients
- Nandana D. Rao
- , Kristine M. King
- & Brian H. Shirts
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Article
| Open AccessConsanguinity and willingness to perform premarital genetic screening in Sudan
- Yasir Ahmed Mohammed Elhadi
- , Salma S. Alrawa
- & Ashraf Yahia
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Viewpoint
| Open AccessUnderrepresentation of racial and ethnic minorities in cascade testing for hereditary cancer syndromes
- Muhammad Danyal Ahsan
- , Emily M. Webster
- & Melissa K. Frey
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Uncertainties experienced by parents of children diagnosed with severe combined immunodeficiency through newborn screening
- Melissa Raspa
- , Oksana Kutsa
- & Barbara B. Biesecker
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| Open AccessExpanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?
- Stephanie White
- , Tamara Mossfield
- & Veronica Wiley
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Viewpoint
| Open AccessCommunity Genetics screening in a pandemic: solutions for pre-test education, informed consent, and specimen collection
- Bronwyn Terrill
- , Lauren McKnight
- & Leslie Burnett
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Viewpoint
| Open AccessResearch priorities in psychiatric genetic counselling: how to talk to children and adolescents about genetics and psychiatric disorders
- Jessica Mundy
- , Helena L. Davies
- & Ramona Moldovan
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| Open AccessThe more you do it, the easier it gets: using behaviour change theory to support health care professionals offering reproductive genetic carrier screening
- Stephanie Best
- , Janet C. Long
- & Jeffrey Braithwaite
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Exome sequencing for structurally normal fetuses—yields and ethical issues
- Hagit Daum
- , Tamar Harel
- & Hagar Mor-Shaked
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| Open AccessHemoglobinopathy screening in primary care in the Netherlands: exploring the problems and needs of patients and general practitioners
- Margo E. van Vliet
- , Jean-Louis H. Kerkhoffs
- & Elisa. J. F. Houwink
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Article
| Open AccessHealth professionals’ views and experiences of the Australian moratorium on genetic testing and life insurance: A qualitative study
- Grace Dowling
- , Jane Tiller
- & Paul Lacaze
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Review Article
| Open AccessIncorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: a sequential systematic review
- Ebony Richardson
- , Alison McEwen
- & Chris Jacobs
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| Open AccessHemoglobinopathy prevention in primary care: a reflection of underdetection and difficulties with accessibility of medical care, a quantitative study
- Margo E. van Vliet
- , Jean-Louis H. Kerkhoffs
- & Elisa J. F. Houwink
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Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants
- Liis Leitsalu
- , Marili Palover
- & Neeme Tõnisson
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Regulatory landscape of providing information on newborn screening to parents across Europe
- Věra Franková
- , Riona O. Driscoll
- & Katrin Õunap
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Viewpoint |
COVID-19 and Down’s syndrome: are we heading for a disaster?
- Rodolphe Dard
- , Nathalie Janel
- & François Vialard
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Gene selection for the Australian Reproductive Genetic Carrier Screening Project (“Mackenzie’s Mission”)
- Edwin P. Kirk
- , Royston Ong
- & Martin B. Delatycki
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National Newborn Screening for cystic fibrosis in the Republic of Ireland: genetic data from the first 6.5 years
- Erina Sasaki
- , Marija Kostocenko
- & Sally Ann Lynch
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Attitudes of relatives of mucopolysaccharidosis type III patients toward preconception expanded carrier screening
- Stephanie C. M. Nijmeijer
- , Thirsa Conijn
- & Lotte Haverman
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Development and validation of a measure of comprehension of genomic screening—negative results (CoG-NR)
- Gail E. Henderson
- , Molly Ewing
- & Teresa P. Edwards
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| Open AccessSelf-reported hearing loss questions provide a good measure for genetic studies: a polygenic risk score analysis from UK Biobank
- Stacey S. Cherny
- , Gregory Livshits
- & Frances M. K. Williams
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Knowledge and views about genetics: a public-based cross-sectional study
- Basima A. Almomani
- , Maha S. Al-Keilani
- & Nour A. Al-Sawalha
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| Open AccessGP-provided couple-based expanded preconception carrier screening in the Dutch general population: who accepts the test-offer and why?
- Juliette Schuurmans
- , Erwin Birnie
- & Mirjam Plantinga
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| Open AccessRethinking the ethical principles of genomic medicine services
- Stephanie B. Johnson
- , Ingrid Slade
- & Mackenzie Graham
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What do cancer patients’ relatives think about addressing cancer family history and performing genetic testing in palliative care?
- Jude E. Cléophat
- , Ana Marin
- & Michel Dorval
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Review Article |
Implementation of public health genomics in Pakistan
- Moeen Riaz
- , Jane Tiller
- & Paul Lacaze
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Viewpoint |
Population genetic screening: current issues in a European country
- Laurent Pasquier
- , Bertrand Isidor
- & Grégoire Moutel
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Estimating the prevalence of allelic variants in the transthyretin gene by analysing large-scale sequencing data
- Carmen Lahuerta Pueyo
- , Miguel Ángel Aibar Arregui
- & Sebastián Menao Guillén
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Differences in attitudes toward genetic testing among the public, patients, and health-care professionals in Korea
- Heesang Eum
- , Mangyeong Lee
- & Yoon Jung Chang
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Distress, uncertainty, and positive experiences associated with receiving information on personal genomic risk of melanoma
- Amelia K Smit
- , Ainsley J Newson
- & Anne E Cust
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Review Article
| Open AccessHow is genetic testing evaluated? A systematic review of the literature
- Erica Pitini
- , Corrado De Vito
- & Paolo Villari
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Psychosocial impact on mothers receiving expanded newborn screening results
- Kathleen O’Connor
- , Tara Jukes
- & Chitra Prasad
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| Open AccessPatient experience and utility of genetic information: a cross-sectional study among patients tested for cancer susceptibility and thrombophilia
- Elvira D’Andrea
- , Tyra Lagerberg
- & Paolo Villari
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| Open AccessOlder mothers and increased impact of prenatal screening: stable livebirth prevalence of trisomy 21 in the Netherlands for the period 2000–2013
- Maurike D. de Groot- van der Mooren
- , Saskia Tamminga
- & Martina C. Cornel
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Preconception carrier screening for multiple disorders: evaluation of a screening offer in a Dutch founder population
- Inge B. Mathijssen
- , Kim C. A. Holtkamp
- & Lidewij Henneman
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Letter |
UK National Screening Committee Criteria: clarification of two misunderstandings
- Anne Mackie
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Review |
International differences in the evaluation of conditions for newborn bloodspot screening: a review of scientific literature and policy documents
- Marleen E Jansen
- , Selina C Metternick-Jones
- & Karla J Lister
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Review |
Role of pharmacogenetics in public health and clinical health care: a SWOT analysis
- Ritika Kapoor
- , Wei Chuen Tan-Koi
- & Yik-Ying Teo
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Neonatal screening for profound biotinidase deficiency in the Netherlands: consequences and considerations
- Rachel C Wiltink
- , Michelle E Kruijshaar
- & Monique Williams
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The effect of a decision aid on informed decision-making in the era of non-invasive prenatal testing: a randomised controlled trial
- Lean Beulen
- , Michelle van den Berg
- & Mireille N Bekker
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Letter |
Why do we pay for information that we won’t use? A cognitive-based explanation for genetic information seeking
- Alessandra Gorini
- & Gabriella Pravettoni
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Compare and contrast: a cross-national study across UK, USA and Greek experts regarding return of incidental findings from clinical sequencing
- Elli G Gourna
- , Natalie Armstrong
- & Susan E Wallace
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| Open AccessImproved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’
- Patrick Deelen
- , Androniki Menelaou
- & Morris A Swertz