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Parents, their children, whole exome sequencing and unsolicited findings: growing towards the child’s future autonomy
Author / Creator:Tibben, Aad ; Dondorp, Wybo ; Cornelis, Candice ; Knoers, Nine ; Brilstra, Eva ; van Summeren, Marieke ; Bolt, Ineke
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2021-06, Vol.29 (6), p.911-919
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Hope, but never expect? Comparing parents' pre‐ and post‐disclosure attitudes toward return of results from diagnostic exome sequencing for their child
Author / Creator:Cornelis, Candice ; Tibben, Aad ; Brilstra, Eva ; Bolt, Ineke ; Summeren, Marieke ; Knoers, Nine ; Bredenoord, Annelien L.
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2024-03, Vol.12 (3), p.e2341-n/a
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Most women recover from psychological distress after postoperative complications following implant or DIEP flap breast reconstruction: A prospective long-term follow-up study
Author / Creator:Timman, Reinier ; Gopie, Jessica P. ; Brinkman, J. Nick ; Kleijne, Annelies ; Seynaeve, Caroline ; Menke-Pluymers, Marian B. E. ; ter Kuile, Moniek M. ; Tibben, Aad ; Mureau, Marc A. M.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-03, Vol.12 (3), p.e0174455-e0174455
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Validation of a scale for assessing attitudes towards outcomes of genetic cancer testing among primary care providers and breast specialists
Author / Creator:Bouhnik, Anne-Deborah ; N’Diaye, Khadim ; Evans, D. Gareth ; Harris, Hilary ; Tibben, Aad ; van Asperen, Christi ; Schmidtke, Joerg ; Nippert, Irmgard ; Mancini, Julien ; Julian-Reynier, Claire
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-06, Vol.12 (6), p.e0178447-e0178447
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Frontotemporal Dementia: Change of Familial Caregiver Burden and Partner Relation in a Dutch Cohort of 63 Patients
Author / Creator:Riedijk, Samantha ; Duivenvoorden, Hugo ; Rosso, Sonia ; Van Swieten, John ; Niermeijer, Martinus ; Tibben, Aad
Publisher:Basel, Switzerland: Karger
Journal title:Dementia and geriatric cognitive disorders, 2008-01, Vol.26 (5), p.398-406
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A Counselling Model for BRCA1/2 Genetic Susceptibility Testing
Author / Creator:van Oostrom, Iris ; Tibben, Aad
Publisher:Poland: BioMed Central Ltd
Journal title:Hereditary cancer in clinical practice, 2004-02, Vol.2 (1), p.19-23, Article 19
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Quality in genetic counselling for presymptomatic testing — clinical guidelines for practice across the range of genetic conditions
Author / Creator:Skirton, Heather ; Goldsmith, Lesley ; Jackson, Leigh ; Tibben, Aad
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2013-03, Vol.21 (3), p.256-260
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Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
Author / Creator:Dondorp, Wybo ; de Wert, Guido ; Bombard, Yvonne ; Bianchi, Diana W ; Bergmann, Carsten ; Borry, Pascal ; Chitty, Lyn S ; Fellmann, Florence ; Forzano, Francesca ; Hall, Alison ; Henneman, Lidewij ; Howard, Heidi C ; Lucassen, Anneke ; Ormond, Kelly ; Peterlin, Borut ; Radojkovic, Dragica ; Rogowski, Wolf ; Soller, Maria ; Tibben, Aad ; Tranebjærg, Lisbeth ; van El, Carla G ; Cornel, Martina C
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2015-11, Vol.23 (11), p.1438-1450
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Mothers’ psychological adaptation to Duchenne/Becker muscular dystrophy
Author / Creator:Peay, Holly L ; Meiser, Bettina ; Kinnett, Kathleen ; Furlong, Pat ; Porter, Kathryn ; Tibben, Aad
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2016-05, Vol.24 (5), p.633-637
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Genetic discrimination in Huntington’s disease
Author / Creator:Tibben, Aad
Publisher:England: British Medical Journal Publishing Group
Journal title:BMJ, 2009-06, Vol.338 (jun08 3), p.b1281-b1281
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Whole-exome sequencing in pediatrics: parents’ considerations toward return of unsolicited findings for their child
Author / Creator:Cornelis, Candice ; Tibben, Aad ; Dondorp, Wybo ; van Haelst, Mieke ; Bredenoord, Annelien L ; Knoers, Nine ; Düwell, Marcus ; Bolt, Ineke ; van Summeren, Marieke
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2016-12, Vol.24 (12), p.1681-1687
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Offering a choice between NIPT and invasive PND in prenatal genetic counseling: the impact of clinician characteristics on patients’ test uptake
Author / Creator:van der Steen, Sanne L. ; Houtman, Diewertje ; Bakkeren, Iris M. ; Galjaard, Robert-Jan H. ; Polak, Marike G. ; Busschbach, Jan J. ; Tibben, Aad ; Riedijk, Sam R.
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2019-02, Vol.27 (2), p.235-243
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Developing a policy for paediatric biobanks: principles for good practice
Author / Creator:Hens, Kristien ; Van El, Carla E ; Borry, Pascal ; Cambon-Thomsen, Anne ; Cornel, Martina C ; Forzano, Francesca ; Lucassen, Anneke ; Patch, Christine ; Tranebjaerg, Lisbeth ; Vermeulen, Eric ; Salvaterra, Elena ; Tibben, Aad ; Dierickx, Kris
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2013-01, Vol.21 (1), p.2-7
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ArticlesPeer ReviewedFull Text
Psychosocial Needs and Facilitators of Mothers Caring for Children with Duchenne/Becker Muscular Dystrophy
Author / Creator:Peay, Holly L. ; Meiser, Bettina ; Kinnett, Kathleen ; Tibben, Aad
Publisher:New York: Springer US
Journal title:Journal of genetic counseling, 2018-02, Vol.27 (1), p.197-203
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Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations
Author / Creator:Dondorp, Wybo ; de Wert, Guido ; Bombard, Yvonne ; Bianchi, Diana W ; Bergmann, Carsten ; Borry, Pascal ; Chitty, Lyn S ; Fellmann, Florence ; Forzano, Francesca ; Hall, Alison ; Henneman, Lidewij ; Howard, Heidi C ; Lucassen, Anneke ; Ormond, Kelly ; Peterlin, Borut ; Radojkovic, Dragica ; Rogowski, Wolf ; Soller, Maria ; Tibben, Aad ; Tranebjærg, Lisbeth ; van El, Carla G ; Cornel, Martina C
Publisher:England
Journal title:European journal of human genetics : EJHG, 2015-04
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Expectations and experiences of investigators and parents involved in a clinical trial for Duchenne/Becker muscular dystrophy
Author / Creator:Peay, Holly L ; Tibben, Aad ; Fisher, Tyler ; Brenna, Ethan ; Biesecker, Barbara B
Publisher:London, England: SAGE Publications
Journal title:Clinical trials (London, England), 2014-02, Vol.11 (1), p.77-85
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Thinking about the end of life: a common issue for patients with Huntington’s disease
Author / Creator:Booij, Suzanne J. ; Tibben, Aad ; Engberts, Dick P. ; Marinus, Johan ; Roos, Raymund A. C.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2014-11, Vol.261 (11), p.2184-2191
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Body image issues after bilateral prophylactic mastectomy with breast reconstruction in healthy women at risk for hereditary breast cancer
Author / Creator:Gopie, Jessica P. ; Mureau, Marc A. M. ; Seynaeve, Caroline ; ter Kuile, Moniek M. ; Menke-Pluymers, Marian B. E. ; Timman, Reinier ; Tibben, Aad
Publisher:Dordrecht: Springer Netherlands
Journal title:Familial cancer, 2013-09, Vol.12 (3), p.479-487
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Diagnostic genetic testing for Huntington's disease
Author / Creator:Craufurd, David ; MacLeod, Rhona ; Frontali, Marina ; Quarrell, Oliver ; Bijlsma, Emilia K ; Davis, Mary ; Hjermind, Lena Elisabeth ; Lahiri, Nayana ; Mandich, Paola ; Martinez, Asunción ; Tibben, Aad ; Roos, Raymund A
Publisher:England: BMJ Publishing Group LTD
Journal title:Practical neurology, 2015-02, Vol.15 (1), p.80-84
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“Be an ambassador for change that you would like to see”: a call to action to all stakeholders for co-creation in healthcare and medical research to improve quality of life of people with a neuromuscu...
Author / Creator:Ambrosini, Anna ; Quinlivan, Ros ; Sansone, Valeria A. ; Meijer, Ingeborg ; Schrijvers, Guus ; Tibben, Aad ; Padberg, George ; de Wit, Maarten ; Sterrenburg, Ellen ; Mejat, Alexandre ; Breukel, Alexandra ; Rataj, Michal ; Lochmüller, Hanns ; Willmann, Raffaella
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2019-06, Vol.14 (1), p.126-126, Article 126
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Showing 1 to 20 of 62 results

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Parents, their children, whole exome sequencing and unsolicited findings: growing towards the child’s future autonomy

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Hope, but never expect? Comparing parents' pre‐ and post‐disclosure attitudes toward return of results from diagnostic exome sequencing for their child

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Most women recover from psychological distress after postoperative complications following implant or DIEP flap breast reconstruction: A prospective long-term follow-up study

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Validation of a scale for assessing attitudes towards outcomes of genetic cancer testing among primary care providers and breast specialists

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Frontotemporal Dementia: Change of Familial Caregiver Burden and Partner Relation in a Dutch Cohort of 63 Patients

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A Counselling Model for BRCA1/2 Genetic Susceptibility Testing

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Quality in genetic counselling for presymptomatic testing — clinical guidelines for practice across the range of genetic conditions

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Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

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Mothers’ psychological adaptation to Duchenne/Becker muscular dystrophy

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Genetic discrimination in Huntington’s disease

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Whole-exome sequencing in pediatrics: parents’ considerations toward return of unsolicited findings for their child

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Offering a choice between NIPT and invasive PND in prenatal genetic counseling: the impact of clinician characteristics on patients’ test uptake

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Developing a policy for paediatric biobanks: principles for good practice

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Psychosocial Needs and Facilitators of Mothers Caring for Children with Duchenne/Becker Muscular Dystrophy

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Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

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Expectations and experiences of investigators and parents involved in a clinical trial for Duchenne/Becker muscular dystrophy

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Thinking about the end of life: a common issue for patients with Huntington’s disease

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Body image issues after bilateral prophylactic mastectomy with breast reconstruction in healthy women at risk for hereditary breast cancer

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Diagnostic genetic testing for Huntington's disease

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“Be an ambassador for change that you would like to see”: a call to action to all stakeholders for co-creation in healthcare and medical research to improve quality of life of people with a neuromuscu...

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