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Publications

Publications
Rg score: 23.22
h-index: 10

Bakkeren I, Diderich KEM, Mattemaker E, Galjaard RJ, Smith E, Knapen M, Van Opstal D, Go ATJI, Riedijk SR (2018). A training for midwives to counsel the decision between invasive and non-invasive prenatal testing: development and pilot testing. Submitted.

Van der Steen SL*, Houtman D*, Bakkeren I, Galjaard RJ, Polak MG, van Busschbach JJ, Tibben A, Riedijk SR (2018). Offering a choice between NIPT and invasive PND in prenatal genetic counseling: the impact of counselor characteristics on patients test uptake'. Submitted

Van der Steen SL,  Riedijk SR, Bakkeren I, Galjaard RJ, Polak MG, Knapen MFCM, Go ATJI, Tibben A, van Busschbach JJ (2018). Non-invasive or invasive prenatal testing: safety for the fetus overrules ‘the need to know’. Resubmitted.

Van der Steen SL, Diderich KEM, Verhagen-Visser J, Govaerts LCP, Joosten M, Knapen MFCM, et al., Riedijk SR (2017). Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude? J Genet couns². doi: 10.1007/s10897-017-0124-5. [Epub ahead of print]

Govaerts LCP, Srebniak MI, Diderich KEM, Joosten M, Riedijk SR, Knapen MFCM, Go ATJI, Papatsonis D, de Graaf K, Toolenaar T, van der Steen SL, Huijbregts G, Knijnenburg J, de Vries FAT, Van Opstal D, Galjaard RJ. (2017). Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders - genetic counseling and pregnancy outcome in 57 cases. Prenat Diagn². 37(1):73-80.

Van der Steen SL*, Riedijk, SR*, Verhagen-Visser J, Govaerts LCP, Van Opstal A, De Vries FAT, et al. (2016). Receiving a susceptibility locus as a result from SNP array in prenatal genetic testing: quick recovery after initial shock. J Genet Couns². 25(6):1227-1234.
* van der Steen and Riedijk are joint first authors

Joosten M, Diderich KEM, Van Opstal D, Govaerts LCP, Riedijk SR, Prinsen AK, De Vries FAT, Go ATJI, Galjaard RJ, Srebniak MI. (2016) Clinical experience of unexpected findings in prenatal array testing. Biomark Med. 10(8):831-40.

Srebniak MI, Van Opstal D, Joosten M, Diderich KEM, de Vries FAT, Riedijk SR, Knapen MFCM, Go ATJI, Govaerts LCP, Galjaard RJ.( 2015) Whole-genome array as a first-line cytogenetic test in prenatal diagnosis. Ultrasound Obstet Gynecol¹. 45(4):363-72.

Van der Steen SL*, Diderich KEM*, Riedijk SR, Verhagen-Visser J, Govaerts LCP, Joosten M, et al. (2014). Pregnant Couples at Increased Risk for Common Aneuploidies Prefer Maximal Information From Invasive Genetic Testing. Clin Genet². 88(1):25-31
*Diderich and van der Steen are joint first authors

Srebniak MI, Diderich KEM, Govaerts LCP, Joosten M, Riedijk SR, Galjaard RJ, Van Opstal D. (2014). Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification. Eur J Hum Genet¹. 22(7):856-8.

Riedijk SR, Diderich, KEM, van der Steen SL, Govaerts LCP, Joosten M, Knapen MFCM, et al. (2014). The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array
Analysis in Prenatal Testing. J. Clin. Med, 3(3): 713-723. Special issue "Prenatal Genetic Screening and Diagnosis-Part 2" Invited publication

Srebniak MI, Diderich KEM, Govaerts LCP, Joosten M, Riedijk SR, Galjaard RJ, et al. (2013).Types of array findings detectable in cytogenetic diagnosis: a
proposal for a generic classification. Eur J Hum Genet¹, 22(7): 856-858.

Riedijk SR, Oudesluijs G & Tibben A. (2012). Psychosocial aspects of preconception consultation in primary care: lessons from our experience in clinical genetics. J Community Genet, 3(3): 213-219. Special issue “Genetic Aspects of Preconception Consultation in Primary Care Invited publication

Riedijk SR, Niermeijer MF, Dooijes D, & Tibben A. (2009 ). A decade of genetic counseling in frontotemporal dementia affected families: few counseling requests and much familial opposition to testing. J Genet Couns², 18(4):350-356.

Riedijk SR, Duivenvoorden HJ, van Oostrom I, Rosso SM, van Swieten JC, Niermeijer MF, et al. (2009). Frontotemporal dementia (FTD) patients living at home and their spousal caregivers compared with institutionalized FTD patients and their spousal caregivers; Which characteristics are associated with in-home care? Dementia, 8(1):61-77.

Riedijk SR, Duivenvoorden HJ, van Swieten JC, Niermeijer MF & Tibben A. (2009). Sense of Competence in a Dutch Sample of informal Caregivers of Frontotemporal Dementia Patients. Dement Geriatr Cogn Disord¹, 27(4):337-343.

Riedijk SR, Duivenvoorden HJ, Rosso S, Van Swieten JC, Niermeijer MF & Tibben A. (2008). Frontotemporal Dementia: Change of Familial Caregiver Burden and Partner Relation in a Dutch Cohort of 63 Patients. Dement Geriatr Cogn Disord¹, 26(5):398-406.

van Oostrom I, Meijers-Heijboer H, Duivenvoorden HJ, Bröcker-Vriends AH, van Asperen CJ, Sijmons RH, Seynaeve C, Van Gool AR, Klijn JG, Riedijk SR, van Dooren S, Tibben A. (2007). A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships. Psychooncology¹. 16(4):320-8.

De Vugt M, Riedijk SR, Aalten P, Tibben A, Van Swieten JC & Verhey FR (2006). Impact of behavioural problems on spousal caregivers: A comparison between Alzheimer's disease and Frontotemporal Dementia. Dement Geriatr Cogn Disord¹, 22(1), 35-41.

Riedijk SR, De Snoo FA, Van Dijk S, Bergman W, Van Haeringen A, Silberg S et al. (2005). Hereditary melanoma and predictive genetic testing: Why not? Psychooncology¹, 14(9):738-745.
*De Snoo and Riedijk are joint first authors