| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adoptees’ views and experiences of direct-to-consumer (DTC) genomic testing: an exploratory interview study from the UK
|
Kay, Alison C.
|
|
|
|
2 |
p. 149-162
|
artikel
|
| 2 |
A family genetic risk communication framework: guiding tool development in genetics health services
|
Wiens, Miriam E.
|
|
2013
|
|
2 |
p. 233-242
|
artikel
|
| 3 |
A framework for youth-friendly genetic counseling
|
Young, Mary-Anne
|
|
|
|
2 |
p. 161-170
|
artikel
|
| 4 |
A holistic approach to education programs in thalassemia for a multi-ethnic population: consideration of perspectives, attitudes, and perceived needs
|
Wong, Li Ping
|
|
2011
|
|
2 |
p. 71-79
|
artikel
|
| 5 |
Altered incidence of meiotic errors and Down syndrome birth under extreme low socioeconomic exposure in the Sundarban area of India
|
Ghosh, Sujoy
|
|
2013
|
|
2 |
p. 119-124
|
artikel
|
| 6 |
An exemplary model of genetic counselling for highly specialised services
|
Harris, Juliette
|
|
|
|
2 |
p. 115-119
|
artikel
|
| 7 |
An integrative review of factors that influence reproductive decisions in women with sickle cell disease
|
Rance, Josephine Claire
|
|
2018
|
|
2 |
p. 161-169
|
artikel
|
| 8 |
Anticipating the arrival of low-penetrance genetic testing to primary care medicine
|
Tarini, Beth A.
|
|
2013
|
|
2 |
p. 285-288
|
artikel
|
| 9 |
“A perfect society”— Swedish policymakers’ ethical and social views on preconception expanded carrier screening
|
Matar, Amal
|
|
2018
|
|
2 |
p. 267-280
|
artikel
|
| 10 |
Applying theory to characterize impediments to dissemination of community-facing family health history tools: a review of the literature
|
Allen, Caitlin G.
|
|
|
|
2 |
p. 147-159
|
artikel
|
| 11 |
Assessing patient-level knowledge of precision medicine in a community health center setting
|
Stallings, Sarah C.
|
|
|
|
2 |
p. 197-210
|
artikel
|
| 12 |
Assessment of in silico protein sequence analysis in the clinical classification of variants in cancer risk genes
|
Kerr, Iain D.
|
|
2016
|
|
2 |
p. 87-95
|
artikel
|
| 13 |
A study of consanguineous marriage as a risk factor for developing comitant strabismus
|
Bagheri, Mansooreh
|
|
2015
|
|
2 |
p. 177-180
|
artikel
|
| 14 |
Attitudes towards prenatal diagnosis and abortion in a multi-ethnic country: a survey among parents of children with thalassaemia major in Malaysia
|
Ngim, Chin Fang
|
|
2013
|
|
2 |
p. 215-221
|
artikel
|
| 15 |
“Awakening to” a new meaning of being at-risk for arrhythmogenic right ventricular cardiomyopathy: a grounded theory study
|
Manuel, April
|
|
2015
|
|
2 |
p. 167-175
|
artikel
|
| 16 |
Awareness of risks of biobank research may affect public attitudes toward consent
|
Nurmsoo, Sean
|
|
2015
|
|
2 |
p. 181-182
|
artikel
|
| 17 |
Barriers to the identification of familial hypercholesterolemia among primary care providers
|
Zimmerman, John
|
|
2018
|
|
2 |
p. 229-236
|
artikel
|
| 18 |
Beliefs on the causes of birth defects as perceived by mothers of children with birth defects in a tertiary care hospital in the Philippines
|
Felipe-Dimog, Eva Belingon
|
|
|
|
2 |
p. 183-191
|
artikel
|
| 19 |
Biobank governance: heterogeneous modes of ordering and democratization
|
Gottweis, Herbert
|
|
2011
|
|
2 |
p. 61-72
|
artikel
|
| 20 |
BRCA sequencing and large rearrangement testing in young Black women with breast cancer
|
Pal, Tuya
|
|
2013
|
|
2 |
p. 157-165
|
artikel
|
| 21 |
Breast and ovarian cancer risk evaluation in families with a disease-causing mutation in BRCA1/2
|
Beristain, Elena
|
|
2010
|
|
2 |
p. 91-99
|
artikel
|
| 22 |
Breast cancer genetic counseling among Dutch patients from Turkish and Moroccan descent: participation determinants and perspectives of patients and healthcare professionals
|
Baars, J.E.
|
|
2017
|
|
2 |
p. 97-108
|
artikel
|
| 23 |
Clinical genetics in transition—a comparison of genetic services in Estonia, Finland, and the Netherlands
|
Vrijenhoek, T.
|
|
|
|
2 |
p. 277-290
|
artikel
|
| 24 |
Colorectal Cancer Survivors’ Receptivity toward Genomic Testing and Targeted Use of Non-Steroidal Anti-Inflammatory Drugs to Prevent Cancer Recurrence
|
O’Malley, Denalee M.
|
|
|
|
2 |
p. 201-214
|
artikel
|
| 25 |
Communicating risk and the landscape of cancer prevention — an exploratory study that examines perceptions of cancer-related genetic counseling and testing among African Americans and Latinos in the Midwest
|
Lumpkins, Crystal Y.
|
|
|
|
2 |
p. 121-133
|
artikel
|
| 26 |
Community perspectives on public health biobanking: an analysis of community meetings on the Michigan BioTrust for Health
|
Thiel, Daniel B.
|
|
2013
|
|
2 |
p. 125-138
|
artikel
|
| 27 |
Components of genetic counsellor education: A systematic review of the peer-reviewed literature
|
Ingvoldstad, C.
|
|
2015
|
|
2 |
p. 107-118
|
artikel
|
| 28 |
Consanguinity, endogamy, and genetic disorders in Tunisia
|
Ben Halim, Nizar
|
|
2012
|
|
2 |
p. 273-284
|
artikel
|
| 29 |
Consenting postpartum women for use of routinely collected biospecimens and/or future biospecimen collection
|
Kozinetz, Claudia A.
|
|
2016
|
|
2 |
p. 153-158
|
artikel
|
| 30 |
Considerations for developing regulations for direct-to-consumer genetic testing: a scoping review using the 3-I framework
|
Cernat, Alexandra
|
|
|
|
2 |
p. 155-170
|
artikel
|
| 31 |
Correction to: Behavioural changes, sharing behaviour and psychological responses after receiving direct-to-consumer genetic test results:a systematic review and meta-analysis
|
Stewart, Kelly F. J.
|
|
2017
|
|
2 |
p. 321
|
artikel
|
| 32 |
Correction to: EUROCAT: an update on its functions and activities
|
Tucker, F. D.
|
|
2018
|
|
2 |
p. 323
|
artikel
|
| 33 |
Correction to: Mothers’ knowledge and attitudes about newborn screening in Jordan
|
Kasem, Abedallah
|
|
|
|
2 |
p. 227
|
artikel
|
| 34 |
Correction to: Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience
|
Suwannachat, Sukrit
|
|
|
|
2 |
p. 239
|
artikel
|
| 35 |
Cost-effectiveness of a gene sequencing test for Alzheimer’s disease in Ontario
|
Iragorri, Nicolas
|
|
|
|
2 |
p. 135-147
|
artikel
|
| 36 |
Curative gene therapies for rare diseases
|
Maldonado, Rocio
|
|
|
|
2 |
p. 267-276
|
artikel
|
| 37 |
Definitions of genetic testing in European legal documents
|
Varga, Orsolya
|
|
2012
|
|
2 |
p. 125-141
|
artikel
|
| 38 |
Definitions of genetic testing in Italian legal documents
|
Battistuzzi, Linda
|
|
2012
|
|
2 |
p. 289-291
|
artikel
|
| 39 |
Desiderata for digital consent in genomic research
|
Parra-Calderón, Carlos Luis
|
|
2018
|
|
2 |
p. 191-194
|
artikel
|
| 40 |
Determining accurate costs for genomic sequencing technologies—a necessary prerequisite
|
Jegathisawaran, Jathishinie
|
|
|
|
2 |
p. 235-238
|
artikel
|
| 41 |
Developing and evaluating a culturally appropriate genetic service for consanguineous South Asian families
|
Khan, Nasaim
|
|
2010
|
|
2 |
p. 73-81
|
artikel
|
| 42 |
Development of multidisciplinary committees for decision making and care management in hereditary colon cancer: the French state of the art
|
Aissaoui, Souria
|
|
2013
|
|
2 |
p. 185-189
|
artikel
|
| 43 |
Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation
|
Holtkamp, Kim C. A.
|
|
2018
|
|
2 |
p. 249-257
|
artikel
|
| 44 |
Direct-to-consumer genomic testing from the perspective of the health professional: a systematic review of the literature
|
Goldsmith, Lesley
|
|
2013
|
|
2 |
p. 169-180
|
artikel
|
| 45 |
Disclosure of diagnosis to at-risk relatives by individuals diagnosed with hypertrophic cardiomyopathy (HCM)
|
Hudson, Janella
|
|
2018
|
|
2 |
p. 207-217
|
artikel
|
| 46 |
Editorial: Genetics and Democracy
|
Hedlund, Maria
|
|
2012
|
|
2 |
p. 57-59
|
artikel
|
| 47 |
Engaging Hmong adults in genomic and pharmacogenomic research: Toward reducing health disparities in genomic knowledge using a community-based participatory research approach
|
Culhane-Pera, Kathleen A.
|
|
2017
|
|
2 |
p. 117-125
|
artikel
|
| 48 |
Epidemiological profile of common haemoglobinopathies in Arab countries
|
Hamamy, Hanan A.
|
|
2012
|
|
2 |
p. 147-167
|
artikel
|
| 49 |
Ethnicity, educational level and attitudes contribute to parental intentions about genetic testing for child obesity
|
Kocken, Paul L.
|
|
2013
|
|
2 |
p. 243-250
|
artikel
|
| 50 |
European Reference Networks: challenges and opportunities
|
Tumiene, Birute
|
|
|
|
2 |
p. 217-229
|
artikel
|
| 51 |
Evaluation of cortisol and telomere length measurements in ethnically diverse women with breast cancer using culturally sensitive methods
|
Ramirez, Julio
|
|
2016
|
|
2 |
p. 75-86
|
artikel
|
| 52 |
Evaluation of two-year Jewish genetic disease screening program in Atlanta: insight into community genetic screening approaches
|
Shao, Yunru
|
|
2015
|
|
2 |
p. 137-145
|
artikel
|
| 53 |
Expanded carrier screening panels—does bigger mean better?
|
Wienke, Sara
|
|
2013
|
|
2 |
p. 191-198
|
artikel
|
| 54 |
Experiences of patients seeking to participate in variant of uncertain significance reclassification research
|
Makhnoon, Sukh
|
|
2018
|
|
2 |
p. 189-196
|
artikel
|
| 55 |
Exploring Asian Indian views about cancer and participation in cancer research: an evaluation of a culturally tailored educational intervention
|
Giri, Veda N.
|
|
|
|
2 |
p. 193-203
|
artikel
|
| 56 |
Exploring perceptions of consanguineous unions with women from an East London community: analysis of discussion groups
|
Cupp, Meghan A.
|
|
|
|
2 |
p. 225-234
|
artikel
|
| 57 |
Exploring the perceived self-efficacy of genetic counselors as teachers
|
Gasparini, Justin
|
|
2018
|
|
2 |
p. 313-319
|
artikel
|
| 58 |
Family health history and genetic services—the East Baltimore community stakeholder interview project
|
Sanghavi, Kunal
|
|
2018
|
|
2 |
p. 219-227
|
artikel
|
| 59 |
Frequency of single nucleotide platelet receptor gene polymorphism (P2Y12-i744T>C) in coronary artery disease patients among Tamilian population
|
Priyadharsini, R.
|
|
2017
|
|
2 |
p. 127-132
|
artikel
|
| 60 |
Funding of rare disease research in Germany: a pilot study
|
Reinecke, Martin
|
|
2011
|
|
2 |
p. 101-105
|
artikel
|
| 61 |
General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices
|
Challen, Kirsty
|
|
2010
|
|
2 |
p. 83-90
|
artikel
|
| 62 |
Genetic counseling of patients with ovarian carcinoma: acceptance, timing, and psychological wellbeing
|
Van de Beek, I.
|
|
|
|
2 |
p. 183-191
|
artikel
|
| 63 |
Genetics and democracy—what is the issue?
|
Hagen, Niclas
|
|
2012
|
|
2 |
p. 181-188
|
artikel
|
| 64 |
Genetic screening and democracy: lessons from debating genetic screening criteria in the Netherlands
|
El, Carla Geertruida van
|
|
2011
|
|
2 |
p. 79-89
|
artikel
|
| 65 |
Genetic susceptibility testing for chronic disease and intention for behavior change in healthy young adults
|
Vassy, Jason L.
|
|
2013
|
|
2 |
p. 263-271
|
artikel
|
| 66 |
Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany
|
Gadzicki, Dorothea
|
|
2011
|
|
2 |
p. 53-69
|
artikel
|
| 67 |
Genetic testing legislation in Western Europe—a fluctuating regulatory target
|
Soini, Sirpa
|
|
2012
|
|
2 |
p. 143-153
|
artikel
|
| 68 |
Genetic variants at the APOE, lipoprotein lipase (LpL), cholesteryl ester transfer protein (CETP), and endothelial nitric oxide (eNOS) genes and coronary artery disease (CAD): CETP Taq1 B2B2 associates with lower risk of CAD in Asian Indians
|
Bhanushali, Aparna Amarendra
|
|
2010
|
|
2 |
p. 55-62
|
artikel
|
| 69 |
Genuine participation in participant-centred research initiatives: the rhetoric and the potential reality
|
Feeney, Oliver
|
|
2017
|
|
2 |
p. 133-142
|
artikel
|
| 70 |
Health in Our Hands: diabetes and substance use education through a new genomic framework for schools and communities
|
Modell, Stephen M.
|
|
|
|
2 |
p. 211-225
|
artikel
|
| 71 |
Health needs assessment for congenital anomalies in middle-income countries: Examining the case for neural tube defects in Brazil
|
Schuler-Faccini, Lavinia
|
|
2013
|
|
2 |
p. 147-155
|
artikel
|
| 72 |
Health research: working with Indigenous People in Peru
|
Zavaleta, Carol
|
|
2016
|
|
2 |
p. 173-174
|
artikel
|
| 73 |
Health, wealth and behavioural change: an exploration of role responsibilities in the wake of epigenetics
|
Vears, Danya F.
|
|
2017
|
|
2 |
p. 153-167
|
artikel
|
| 74 |
“He didn’t say that thalassaemia might come up” — β-thalassaemia carriers’ experiences and attitudes
|
Cousens, Nicole E.
|
|
2013
|
|
2 |
p. 223-232
|
artikel
|
| 75 |
Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome
|
Henriksson, Isabelle
|
|
2018
|
|
2 |
p. 259-266
|
artikel
|
| 76 |
Hereditary thrombophilic risk factors for recurrent pregnancy loss
|
Bogdanova, Nadja
|
|
2010
|
|
2 |
p. 47-53
|
artikel
|
| 77 |
High-risk women’s risk perception after receiving personalized polygenic breast cancer risk information
|
Forrest, Laura Elenor
|
|
2018
|
|
2 |
p. 197-206
|
artikel
|
| 78 |
High school Tay–Sachs disease carrier screening: 5 to 11-year follow-up
|
Curd, Helen
|
|
2013
|
|
2 |
p. 139-146
|
artikel
|
| 79 |
How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry
|
Keogh, Louise A.
|
|
2013
|
|
2 |
p. 99-108
|
artikel
|
| 80 |
How to responsibly acknowledge research work in the era of big data and biobanks: ethical aspects of the Bioresource Research Impact Factor (BRIF)
|
Howard, Heidi Carmen
|
|
2017
|
|
2 |
p. 169-176
|
artikel
|
| 81 |
Human genetics education as part of the Japanese Cancer Education Comprehensive Support Project
|
Yamada-Kurebayashi, Fumi
|
|
|
|
2 |
p. 163-174
|
artikel
|
| 82 |
Human genome editing and the identity politics of genetic disability
|
Boardman, Felicity
|
|
|
|
2 |
p. 125-127
|
artikel
|
| 83 |
Human germline genome editing is illegal in Canada, but could it be desirable for some members of the rare disease community?
|
Kleiderman, Erika
|
|
|
|
2 |
p. 129-138
|
artikel
|
| 84 |
Hypothesis: epigenetic effects will require a review of the genetics of child development
|
Kosztolányi, György
|
|
2011
|
|
2 |
p. 91-96
|
artikel
|
| 85 |
Identification of psychoeducation needs and an intervention response for pre-symptomatic Huntington’s disease
|
Gluyas, Cathy
|
|
|
|
2 |
p. 175-183
|
artikel
|
| 86 |
Impact of consanguinity on cardio-metabolic health and other diseases: findings from an Afro-Indian tribal community
|
Bhasin, Prerna
|
|
2014
|
|
2 |
p. 129-135
|
artikel
|
| 87 |
Implementing genetic education in primary care: the Gen-Equip programme
|
Paneque, Milena
|
|
2017
|
|
2 |
p. 147-150
|
artikel
|
| 88 |
Improving diagnostics of rare genetic diseases with NGS approaches
|
Vinkšel, Mateja
|
|
|
|
2 |
p. 247-256
|
artikel
|
| 89 |
Information exchange between patients with Lynch syndrome and their genetic and non-genetic health professionals: whose responsibility?
|
Douma, Kirsten F. L.
|
|
2018
|
|
2 |
p. 237-247
|
artikel
|
| 90 |
Intrafamilial disclosure of risk for hereditary breast and ovarian cancer: points to consider
|
Black, Lee
|
|
2012
|
|
2 |
p. 203-214
|
artikel
|
| 91 |
Is there a doctor in the house?
|
Howard, Heidi Carmen
|
|
2011
|
|
2 |
p. 105-112
|
artikel
|
| 92 |
“It gives them more options”: preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare
|
Archibald, Alison D.
|
|
2016
|
|
2 |
p. 159-171
|
artikel
|
| 93 |
Knowledge and attitudes towards genetic testing in those affected with Parkinson’s disease
|
Scuffham, Tracey M
|
|
2013
|
|
2 |
p. 167-177
|
artikel
|
| 94 |
Legal issues in governing genetic biobanks: the Italian framework as a case study for the implications for citizen’s health through public-private initiatives
|
Piciocchi, Cinzia
|
|
2017
|
|
2 |
p. 177-190
|
artikel
|
| 95 |
Legislation of direct-to-consumer genetic testing in Europe: a fragmented regulatory landscape
|
Kalokairinou, L.
|
|
2017
|
|
2 |
p. 117-132
|
artikel
|
| 96 |
Lost in print: difficulty in reading online information pertaining to phenylketonuria
|
Samuel, Lalitha
|
|
|
|
2 |
p. 185-188
|
artikel
|
| 97 |
Mothers’ knowledge and attitudes about newborn screening in Jordan
|
Kasem, Abedallah
|
|
|
|
2 |
p. 215-225
|
artikel
|
| 98 |
Mothers of children with Down syndrome: a clinical and epidemiological study
|
Aprigio, Joissy
|
|
|
|
2 |
p. 189-195
|
artikel
|
| 99 |
Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide
|
Cornel, Martina C.
|
|
|
|
2 |
p. 257-265
|
artikel
|
| 100 |
‘No thanks’—reasons why pregnant women declined an offer of cystic fibrosis carrier screening
|
Ioannou, L.
|
|
2013
|
|
2 |
p. 109-117
|
artikel
|
| 101 |
Opinions and experiences of recontacting patients: a survey of Australasian genetic health professionals
|
Vora, Bhavya Bhupen
|
|
|
|
2 |
p. 193-199
|
artikel
|
| 102 |
Our greatest untapped resource: our patients
|
Bolz-Johnson, Matt
|
|
|
|
2 |
p. 241-246
|
artikel
|
| 103 |
Participant views on consent in cancer genetics research: preparing for the precision medicine era
|
Edwards, Karen L.
|
|
2016
|
|
2 |
p. 133-143
|
artikel
|
| 104 |
Patient-facing genetic and genomic mobile apps in the UK: a systematic review of content, functionality, and quality
|
Gasteiger, Norina
|
|
|
|
2 |
p. 171-182
|
artikel
|
| 105 |
Patient-reported hereditary breast and ovarian cancer in a primary care practice
|
Quillin, John M.
|
|
2013
|
|
2 |
p. 179-183
|
artikel
|
| 106 |
Patients’ views on variants of uncertain significance across indications
|
Clift, Kristin
|
|
|
|
2 |
p. 139-145
|
artikel
|
| 107 |
Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience
|
Suwannachat, Sukrit
|
|
|
|
2 |
p. 171-181
|
artikel
|
| 108 |
Power, expertise and the limits of representative democracy: genetics as scientific progress or political legitimation in carcinogenic risk assessment of pharmaceuticals?
|
Abraham, John
|
|
2011
|
|
2 |
p. 91-103
|
artikel
|
| 109 |
Prevalence of Bardet–Biedl syndrome in Tunisia
|
M’hamdi, Oussama
|
|
2011
|
|
2 |
p. 97-99
|
artikel
|
| 110 |
Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica
|
Mason, Karlene
|
|
2015
|
|
2 |
p. 127-132
|
artikel
|
| 111 |
Psychosocial approaches to participation in BRCA1/2 genetic risk assessment among African American women: a systematic review
|
Sherman, Kerry A.
|
|
2013
|
|
2 |
p. 89-98
|
artikel
|
| 112 |
Public attitudes regarding the use of electronic health information and residual clinical tissues for research
|
Botkin, Jeffrey R.
|
|
2015
|
|
2 |
p. 183
|
artikel
|
| 113 |
Public concerns regarding the storage and secondary uses of residual newborn bloodspots: an analysis of print media, legal cases, and public engagement activities
|
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