A group approach to genetic counselling of cardiomyopathy patients: satisfaction and psychological outcomes sufficient for further implementation

por Otten, Ellen, Birnie, Erwin, Ranchor, Adelita V, van Tintelen, J Peter, van Langen, Irene M
Publicado 2015

Actual Use of Medications Prescribed During Pregnancy: A Cross-Sectional Study Using Data from a Population-Based Congenital Anomaly Registry

por de Jonge, Linda, de Walle, Hermien E. K., de Jong-van den Berg, Lolkje T. W., van Langen, Irene M., Bakker, Marian K.
Publicado 2015

Maximising the efficiency of clinical screening programmes: balancing predictive genetic testing with a right not to know

por Schuurman, Agnes G, van der Kolk, Dorina M, Verkerk, Marian A, Birnie, Erwin, Ranchor, Adelita V, Plantinga, Mirjam, van Langen, Irene M
Publicado 2015

The impact of national prenatal screening on the time of diagnosis and outcome of pregnancies affected with common trisomies, a cohort study in the Northern Netherlands

por Bouman, Katelijne, Bakker, Marian K., Birnie, Erwin, ter Beek, Lies, Bilardo, Caterina M., van Langen, Irene M., de Walle, Hermien E. K.
Publicado 2017

Reinterpretation, reclassification, and its downstream effects: challenges for clinical laboratory geneticists

por El Mecky, Julia, Johansson, Lennart, Plantinga, Mirjam, Fenwick, Angela, Lucassen, Anneke, Dijkhuizen, Trijnie, van der Hout, Annemieke, Lyle, Kate, van Langen, Irene
Publicado 2019

Cognitive and affective outcomes of genetic counselling in the Netherlands at group and individual level: a personalized approach seems necessary

por Voorwinden, Jan S., Plantinga, Mirjam, Ausems, Margreet, Knoers, Nine, Velthuizen, Mary, Birnie, Erwin, Lucassen, Anneke M., Ranchor, Adelita V., van Langen, Irene M.
Publicado 2020

Couple-based expanded carrier screening provided by general practitioners to couples in the Dutch general population: psychological outcomes and reproductive intentions

por Birnie, Erwin, Schuurmans, Juliette, Plantinga, Mirjam, Abbott, Kristin M., Fenwick, Angela, Lucassen, Anneke, Berger, Marjolein Y., van Langen, Irene M., Ranchor, Adelita V.
Publicado 2021

Expanded carrier screening for autosomal recessive conditions in health care: Arguments for a couple‐based approach and examination of couples' views

por Plantinga, Mirjam, Birnie, Erwin, Schuurmans, Juliette, Buitenhuis, Anne H., Boersma, Elise, Lucassen, Anneke M., Verkerk, Marian A., van Langen, Irene M., Ranchor, Adelita V.
Publicado 2019

GP-provided couple-based expanded preconception carrier screening in the Dutch general population: who accepts the test-offer and why?

por Schuurmans, Juliette, Birnie, Erwin, Ranchor, Adelita V., Abbott, Kristin M., Fenwick, Angela, Lucassen, Anneke, Berger, Marjolein Y., Verkerk, Marian, van Langen, Irene M., Plantinga, Mirjam
Publicado 2019

Views of patients and parents of children with genetic disorders on population‐based expanded carrier screening

por Woudstra, Anke J., van den Heuvel, Lieke M., van Vliet‐Lachotzki, Elsbeth H., Dondorp, Wybo, Lakeman, Phillis, Haverman, Lotte, van Langen, Irene M., Henneman, Lidewij
Publicado 2022

Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases

por Plantinga, Mirjam, Birnie, Erwin, Abbott, Kristin M, Sinke, Richard J, Lucassen, Anneke M, Schuurmans, Juliette, Kaplan, Seyma, Verkerk, Marian A, Ranchor, Adelita V, van Langen, Irene M
Publicado 2016

Long-Term Follow-Up Study on the Uptake of Genetic Counseling and Predictive DNA Testing in Inherited Cardiac Conditions

por van den Heuvel, Lieke M., van Teijlingen, Maxiem O., van der Roest, Wilma, van Langen, Irene M., Smets, Ellen M.A., van Tintelen, J. Peter, Christiaans, Imke
Publicado 2020

Societal implications of expanded universal carrier screening: a scoping review

por van den Heuvel, Lieke M., van den Berg, Nina, Janssens, A. Cecile J. W., Birnie, Erwin, Henneman, Lidewij, Dondorp, Wybo J., Plantinga, Mirjam, van Langen, Irene M.
Publicado 2022

Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancy

por Plantinga, Mirjam, Zwienenberg, Lauren, van Dijk, Eva, Breet, Hanna, Diphoorn, Janouk, El  Mecky, Julia, Bouman, Katelijne, Verheij, Joke, Birnie, Erwin, Ranchor, Adelita V., Corsten‐Janssen, Nicole, van Langen, Irene M.
Publicado 2021

Feasibility of couple-based expanded carrier screening offered by general practitioners

por Schuurmans, Juliette, Birnie, Erwin, van den Heuvel, Lieke M., Plantinga, Mirjam, Lucassen, Anneke, van der Kolk, Dorina M., Abbott, Kristin M., Ranchor, Adelita V., Diemers, Agnes D., van Langen, Irene M.
Publicado 2019

NIPTRIC: an online tool for clinical interpretation of non-invasive prenatal testing (NIPT) results

por Sikkema-Raddatz, Birgit, Johansson, Lennart F., de Boer, Eddy N., Boon, Elles M. J., Suijkerbuijk, Ron F., Bouman, Katelijne, Bilardo, Catia M., Swertz, Morris A., Dijkstra, Martijn, van Langen, Irene M., Sinke, Richard J., te Meerman, Gerard J.
Publicado 2016

Practical Barriers and Facilitators Experienced by Patients, Pharmacists and Physicians to the Implementation of Pharmacogenomic Screening in Dutch Outpatient Hospital Care—An Expl...

por Lanting, Pauline, Drenth, Evelien, Boven, Ludolf, van Hoek, Amanda, Hijlkema, Annemiek, Poot, Ellen, van der Vries, Gerben, Schoevers, Robert, Horwitz, Ernst, Gans, Reinold, Kosterink, Jos, Plantinga, Mirjam, van Langen, Irene, Ranchor, Adelita, Wijmenga, Cisca, Franke, Lude, Wilffert, Bob, Sijmons, Rolf
Publicado 2020

Trial by Dutch laboratories for evaluation of non‐invasive prenatal testing. Part II—women's perspectives

por van Schendel, Rachèl V., Page‐Christiaens, G. C. (Lieve), Beulen, Lean, Bilardo, Catia M., de Boer, Marjon A., Coumans, Audrey B. C., Faas, Brigitte H., van Langen, Irene M., Lichtenbelt, Klaske D., van Maarle, Merel C., Macville, Merryn V. E., Oepkes, Dick, Pajkrt, Eva, Henneman, Lidewij
Publicado 2016

Women’s Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results

por van Schendel, Rachèl V., Page-Christiaens, G. C. M. Lieve, Beulen, Lean, Bilardo, Caterina M., de Boer, Marjon A., Coumans, Audrey B. C., Faas, Brigitte H. W., van Langen, Irene M., Lichtenbelt, Klaske D., van Maarle, Merel C., Macville, Merryn V. E., Oepkes, Dick, Pajkrt, Eva, Henneman, Lidewij
Publicado 2017

A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound

por Corsten‐Janssen, Nicole, Bouman, Katelijne, Diphoorn, Janouk C. D., Scheper, Arjen J., Kinds, Rianne, el Mecky, Julia, Breet, Hanna, Verheij, Joke B. G. M., Suijkerbuijk, Ron, Duin, Leonie K., Manten, Gwendolyn T. R., van Langen, Irene M., Sijmons, Rolf H., Sikkema‐Raddatz, Birgit, Westers, Helga, van Diemen, Cleo C.
Publicado 2020