| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acceptability of prenatal testing and termination of pregnancy in Pakistan
|
Jafri, H.
|
|
2014
|
|
1 |
p. 29-37
|
artikel
|
| 2 |
A collaborative genetic carrier screening model for the British Ashkenazi Jewish community
|
Ziff, Monica
|
|
|
|
1 |
p. 133-135
|
artikel
|
| 3 |
Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis
|
Darr, A.
|
|
2015
|
|
1 |
p. 65-79
|
artikel
|
| 4 |
A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments
|
Mudau, Maria Mabyalwa
|
|
|
|
1 |
p. 39-48
|
artikel
|
| 5 |
A heartfelt "thank you" to all the reviewers of the Journal of Community Genetics in 2010
|
|
|
2011
|
|
1 |
p. 51
|
artikel
|
| 6 |
A novel approach to screening for familial hypercholesterolemia in a large public venue
|
Campbell, Megan
|
|
2016
|
|
1 |
p. 35-44
|
artikel
|
| 7 |
A profile of the genetic counsellor and genetic nurse profession in European countries
|
Cordier, Cristophe
|
|
2011
|
|
1 |
p. 19-24
|
artikel
|
| 8 |
A qualitative study of patients’ perceptions of the value of molecular diagnosis for familial hypercholesterolemia (FH)
|
Hallowell, Nina
|
|
2016
|
|
1 |
p. 45-52
|
artikel
|
| 9 |
A review of 5-HT transporter linked promoter region (5-HTTLPR) polymorphism and associations with alcohol use problems and sexual risk behaviors
|
Rubens, Muni
|
|
2015
|
|
1 |
p. 1-10
|
artikel
|
| 10 |
A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services
|
Nakouzi, Ghunwa
|
|
2014
|
|
1 |
p. 83-105
|
artikel
|
| 11 |
Assessing patient readiness for personalized genomic medicine
|
Frost, Caren J.
|
|
2018
|
|
1 |
p. 109-120
|
artikel
|
| 12 |
Assessing the risks and benefits of diagnosing genetic conditions with variable phenotypes through population screening: Klinefelter syndrome as an example
|
Herlihy, Amy Simone
|
|
2010
|
|
1 |
p. 41-46
|
artikel
|
| 13 |
Association of DD genotype of angiotensin-converting enzyme gene (I/D) polymorphism with hypertension among a North Indian population
|
Rana, Garima
|
|
2017
|
|
1 |
p. 51-55
|
artikel
|
| 14 |
A study of the practice of individual genetic counsellors and genetic nurses in Europe
|
Skirton, Heather
|
|
2012
|
|
1 |
p. 69-75
|
artikel
|
| 15 |
A systematic review of the views of healthcare professionals on the scope of preimplantation genetic testing
|
Siermann, Maria
|
|
|
|
1 |
p. 1-11
|
artikel
|
| 16 |
Attitudes among South African university staff and students towards disclosing secondary genetic findings
|
Spies, Georgina
|
|
|
|
1 |
p. 171-184
|
artikel
|
| 17 |
Attitudes and impact among people with abnormal premarital screening test results in Muscat governorate’s primary healthcare centers in 2018
|
Al Zeedi, Manar Al Sanaa Ali
|
|
|
|
1 |
p. 163-169
|
artikel
|
| 18 |
Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literature
|
Janssens, S.
|
|
2012
|
|
1 |
p. 13-29
|
artikel
|
| 19 |
Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes
|
Kate, Leo P. ten
|
|
2010
|
|
1 |
p. 37-40
|
artikel
|
| 20 |
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
|
|
1 |
p. 1-18
|
artikel
|
| 21 |
Birth defect mortality in India 1990–2017: estimates from the Global Burden of Disease data
|
Ujagare, Dhammasagar
|
|
|
|
1 |
p. 81-90
|
artikel
|
| 22 |
Cancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK: general practitioners' and breast surgeons' current practice and preferred practice responsibilities
|
Nippert, Irmgard
|
|
2013
|
|
1 |
p. 69-79
|
artikel
|
| 23 |
Captious certainties: makings, meanings and misreadings of consumer-oriented genetic testing
|
Paul, Norbert W.
|
|
2013
|
|
1 |
p. 81-87
|
artikel
|
| 24 |
Challenges in recruiting Mexican women for cancer genetics research
|
Quinn, Gwendolyn P.
|
|
2010
|
|
1 |
p. 43-47
|
artikel
|
| 25 |
Challenges in the management of patients with maple syrup urine disease diagnosed by newborn screening in a developing country
|
De Castro-Hamoy, Leniza G.
|
|
2016
|
|
1 |
p. 9-15
|
artikel
|
| 26 |
Clinicians’ use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey
|
Brédart, Anne
|
|
2018
|
|
1 |
p. 61-71
|
artikel
|
| 27 |
Clusters of genetic diseases in Brazil
|
Cardoso, Gabriela Costa
|
|
2018
|
|
1 |
p. 121-128
|
artikel
|
| 28 |
Coming to terms with the imperfectly normal child: attitudes of Israeli parents of screen-positive infants regarding subsequent prenatal diagnosis
|
Raz, Aviad E.
|
|
2018
|
|
1 |
p. 41-50
|
artikel
|
| 29 |
Commentary: a sociologist's view on community genetics
|
Raz, Aviad E.
|
|
2010
|
|
1 |
p. 3-10
|
artikel
|
| 30 |
Communication about breast cancer genetic counseling with patients with limited health literacy or a migrant background: evaluation of a training program for healthcare professionals
|
van der Giessen, Jeanine
|
|
|
|
1 |
p. 91-99
|
artikel
|
| 31 |
Community genetics. Its definition 2010
|
Kate, Leo P. ten
|
|
2010
|
|
1 |
p. 19-22
|
artikel
|
| 32 |
Comprehension of skin cancer genetic risk feedback in primary care patients
|
Khan, Erva
|
|
|
|
1 |
p. 113-119
|
artikel
|
| 33 |
Conceptions on genetics in a group of college students
|
Correia, Patrícia Santana
|
|
2012
|
|
1 |
p. 115-123
|
artikel
|
| 34 |
Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1
|
Nippert, Irmgard
|
|
2010
|
|
1 |
p. 1-11
|
artikel
|
| 35 |
Consolidating newborn screening efforts in the Asia Pacific region
|
Padilla, Carmencita David
|
|
2012
|
|
1 |
p. 35-45
|
artikel
|
| 36 |
Consumer attitudes towards the establishment of a national Australian familial cancer research database by the Inherited Cancer Connect (ICCon) Partnership
|
Forrest, Laura
|
|
2017
|
|
1 |
p. 57-64
|
artikel
|
| 37 |
Correction to: Treatment decision‑making in sickle cell disease patients
|
Booth, A.
|
|
|
|
1 |
p. 153-154
|
artikel
|
| 38 |
Correction to: Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling
|
Jodarski, Colleen
|
|
|
|
1 |
p. 27
|
artikel
|
| 39 |
Cross-sectional survey on genetic testing utilization and perceptions in Wisconsin Amish and Mennonite communities
|
Williams, Katie B.
|
|
|
|
1 |
p. 41-49
|
artikel
|
| 40 |
Development and pilot testing of an online decision aid for women considering risk-stratified breast screening
|
Lippey, Jocelyn
|
|
|
|
1 |
p. 137-141
|
artikel
|
| 41 |
Diagnosis of rare diseases under focus: impacts for Canadian patients
|
Esquivel-Sada, Daphne
|
|
2017
|
|
1 |
p. 37-50
|
artikel
|
| 42 |
Differences in preferences for models of consent for biobanks between Black and White women
|
Brown, Katherine M.
|
|
2015
|
|
1 |
p. 41-49
|
artikel
|
| 43 |
Direct-to-consumer genetic testing in the news: a descriptive analysis
|
Basch, Corey H.
|
|
|
|
1 |
p. 63-69
|
artikel
|
| 44 |
Discussion of photoprotection, screening, and risk behaviors with children and grandchildren after melanoma genetic testing
|
Wu, Yelena P.
|
|
2015
|
|
1 |
p. 21-31
|
artikel
|
| 45 |
Dying to see you? Deaths on a clinical genetics waiting list in the Republic of Ireland; what are the consequences?
|
Bradley, Lisa
|
|
|
|
1 |
p. 121-127
|
artikel
|
| 46 |
Electronic informed consent information for residual newborn specimen research: findings from focus groups with diverse populations
|
Frost, Caren J.
|
|
|
|
1 |
p. 199-203
|
artikel
|
| 47 |
Erratum to: Perceptions of genetic research in three rural Appalachian Ohio communities
|
Fullenkamp, A. N.
|
|
2012
|
|
1 |
p. 19
|
artikel
|
| 48 |
Ethics in genetic counselling
|
Clarke, Angus J.
|
|
2018
|
|
1 |
p. 3-33
|
artikel
|
| 49 |
Ethics of artificial intelligence in prenatal and pediatric genomic medicine
|
Coghlan, Simon
|
|
|
|
1 |
p. 13-24
|
artikel
|
| 50 |
Evaluating and improving the implementation of a community-based hereditary cancer screening program
|
Greenberg, Samantha
|
|
2018
|
|
1 |
p. 51-60
|
artikel
|
| 51 |
Evaluating the model of offering expanded genetic carrier screening to high school students within the Sydney Jewish community
|
Barlow-Stewart, Kristine
|
|
|
|
1 |
p. 121-131
|
artikel
|
| 52 |
Evaluating visual imagery for participant understanding of research concepts in genomics research
|
Rothwell, Erin
|
|
|
|
1 |
p. 51-62
|
artikel
|
| 53 |
Evaluation findings from genetics and family health history community-based workshops for African Americans
|
Manswell Butty, Jo-Anne
|
|
2011
|
|
1 |
p. 1-12
|
artikel
|
| 54 |
Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective
|
Darr, A.
|
|
2012
|
|
1 |
p. 49-57
|
artikel
|
| 55 |
Experiences of parents with a child with Down syndrome in Pakistan and their views on termination of pregnancy
|
Ahmed, Shenaz
|
|
2012
|
|
1 |
p. 107-114
|
artikel
|
| 56 |
Exploring approaches to facilitate family communication of genetic risk information after cystic fibrosis population carrier screening
|
Gorrie, Anita
|
|
2017
|
|
1 |
p. 71-80
|
artikel
|
| 57 |
Exploring Asian Indian and Pakistani views about cancer and participation in cancer genetics research: toward the development of a community genetics intervention
|
Leader, Amy E.
|
|
2017
|
|
1 |
p. 27-35
|
artikel
|
| 58 |
Extended family thalassemia screening as a feasible alternative method to be implemented in identifying carriers in West Java, Indonesia
|
Susanah, Susi
|
|
|
|
1 |
p. 103-112
|
artikel
|
| 59 |
Factors influencing consultation to discuss family history of cancer by asymptomatic patients in primary care
|
Lim, Jennifer N. W.
|
|
2011
|
|
1 |
p. 19-26
|
artikel
|
| 60 |
Family health information sharing among older adults: reaching more family members
|
Ashida, Sato
|
|
2014
|
|
1 |
p. 17-27
|
artikel
|
| 61 |
Feasibility of establishing a network of community health workers to support care of people with sickle cell disease in Kumasi, Ghana
|
Buser, Julie M.
|
|
|
|
1 |
p. 155-161
|
artikel
|
| 62 |
Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification
|
Fridman, Alma Levin
|
|
|
|
1 |
p. 13-18
|
artikel
|
| 63 |
Frequency distribution of the single-nucleotide -108C/T polymorphism at the promoter region of the PON1 gene in Asian Indians and its relationship with coronary artery disease
|
Ahmad, Imteyaz
|
|
2011
|
|
1 |
p. 27-32
|
artikel
|
| 64 |
Frequency of sickle cell genotype among the Yorubas in Lagos: implications for the level of awareness and genetic counseling for sickle cell disease in Nigeria
|
Taiwo, Idowu A.
|
|
2011
|
|
1 |
p. 13-18
|
artikel
|
| 65 |
Genetic counseling in an indigenous Filipino community with a high prevalence of A2ML1-related otitis media
|
Paz, Eva Maria Cutiongco-de la
|
|
2018
|
|
1 |
p. 143-151
|
artikel
|
| 66 |
Genetic epidemiology of hemoglobinopathies among Iraqi Kurds
|
Al-Allawi, Nasir
|
|
|
|
1 |
p. 5-14
|
artikel
|
| 67 |
Genetic professionals’ views on genetic counsellors: a French survey
|
Cordier, Christophe
|
|
2015
|
|
1 |
p. 51-55
|
artikel
|
| 68 |
Genetics and ethics
|
Ormond, Kelly E.
|
|
2018
|
|
1 |
p. 1-2
|
artikel
|
| 69 |
Genetics and public health: the experience of a reference center for diagnosis of 22q11.2 deletion in Brazil and suggestions for implementing genetic testing
|
Vieira, Társis Paiva
|
|
2012
|
|
1 |
p. 99-106
|
artikel
|
| 70 |
Genetic testing and counseling for hereditary neurological diseases in Mali
|
Meilleur, Katherine Gloria
|
|
2011
|
|
1 |
p. 33-42
|
artikel
|
| 71 |
Geographic clusters of congenital anomalies in Argentina
|
Groisman, Boris
|
|
2016
|
|
1 |
p. 1-7
|
artikel
|
| 72 |
Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results
|
Hylind, Robyn
|
|
2017
|
|
1 |
p. 19-26
|
artikel
|
| 73 |
Growth in perceived clinical genetics competency among primary care providers participating in genomic population health screening
|
Hansen, Christina A.
|
|
|
|
1 |
p. 33-37
|
artikel
|
| 74 |
Haemoglobinopathies in eastern Indian states: a demographic evaluation
|
Nagar, Rachana
|
|
2014
|
|
1 |
p. 1-8
|
artikel
|
| 75 |
Healthcare and support experiences of adolescents and young adults diagnosed with 47,XXY, 47,XXX, and 48,XXYY
|
Ahlawat, Nivedita
|
|
|
|
1 |
p. 75-83
|
artikel
|
| 76 |
Hereditary cancer panel testing challenges and solutions for the latinx community: costs, access, and variants
|
Douglas, Michael P.
|
|
|
|
1 |
p. 75-80
|
artikel
|
| 77 |
Hmong participants’ reactions to return of individual and community pharmacogenetic research results: “A positive light for our community”
|
Holzer, K.
|
|
|
|
1 |
p. 53-65
|
artikel
|
| 78 |
How obedience of marriage rules may counteract genetic drift
|
Krawczak, Michael
|
|
2010
|
|
1 |
p. 23-28
|
artikel
|
| 79 |
How people in Benin assess a couple’s risk of having a baby with sickle cell disease
|
Zounon, Ornheilia
|
|
2014
|
|
1 |
p. 77-82
|
artikel
|
| 80 |
Identification of familial clustering for cancer through the family health strategy program in the municipality of Angra dos Reis, Rio de Janeiro, Brazil
|
Vieira, Daniela Koeller Rodrigues
|
|
2014
|
|
1 |
p. 9-16
|
artikel
|
| 81 |
Identifying the current status and future needs of clinical, educational, and laboratory genetics services in Pakistan: a web-based panel discussion
|
Ashfaq, Myla
|
|
|
|
1 |
p. 71-80
|
artikel
|
| 82 |
Impacts of personal DNA ancestry testing
|
Rubanovich, Caryn Kseniya
|
|
|
|
1 |
p. 37-52
|
artikel
|
| 83 |
IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy
|
Christian, Susan
|
|
|
|
1 |
p. 81-89
|
artikel
|
| 84 |
Inclusion of medical genetics in primary health care: report of a pilot project in Brazil
|
Vieira, Taiane Alves
|
|
2012
|
|
1 |
p. 137-145
|
artikel
|
| 85 |
Increased ease of access to genetic counseling for low-income women with breast cancer using a point of care screening tool
|
Rao, Smita K.
|
|
|
|
1 |
p. 129-136
|
artikel
|
| 86 |
Inequities in genetic testing for hereditary breast cancer: implications for public health practice
|
Sayani, Ambreen
|
|
2018
|
|
1 |
p. 35-39
|
artikel
|
| 87 |
Influence of gender norms in relation to child’s quality of care: follow-up of families of children with SCD identified through NBS in Tanzania
|
Bukini, Daima
|
|
|
|
1 |
p. 143-154
|
artikel
|
| 88 |
In memoriam Prof. Dr. Leo P. ten Kate
|
Cornel, Martina C.
|
|
|
|
1 |
p. 1-3
|
artikel
|
| 89 |
Interventions addressing genetic disease burdens within selected countries in the MENA region: a scoping review
|
Grant, Madison
|
|
|
|
1 |
p. 29-39
|
artikel
|
| 90 |
Issues concerning the evaluation and regulation of predictive genetic testing
|
Zimmern, R. L.
|
|
2012
|
|
1 |
p. 49-57
|
artikel
|
| 91 |
“It takes a village”: multilevel approaches to recruit African Americans and their families for genetic research
|
Ochs-Balcom, Heather M.
|
|
2014
|
|
1 |
p. 39-45
|
artikel
|
| 92 |
Knowing, relationships and trust—citizens’ perceptions of whole genome sequencing for the Genetics Clinic of the Future
|
Schumann, Simone
|
|
|
|
1 |
p. 67-80
|
artikel
|
| 93 |
Latina immigrants’ breast and colon cancer causal attributions: genetics is key
|
Fiallos, Katie
|
|
|
|
1 |
p. 59-73
|
artikel
|
| 94 |
Leaves imitate trees: Minnesota Hmong concepts of heredity and applications to genomics research
|
Culhane-Pera, Kathleen A.
|
|
2016
|
|
1 |
p. 23-34
|
artikel
|
| 95 |
Life experiences of individuals with hereditary hemorrhagic telangiectasia and disclosing outside the family: a qualitative analysis
|
Higa, Leigh Ann
|
|
2015
|
|
1 |
p. 81-89
|
artikel
|
| 96 |
Life paths of patients with transthyretin-related familial amyloid polyneuropathy Val30Met: a descriptive study
|
Lopes, Alice
|
|
2017
|
|
1 |
p. 93-99
|
artikel
|
| 97 |
Neither as harmful as feared by critics nor as empowering as promised by providers: risk information offered direct to consumer by personal genomics companies
|
Nordgren, Anders
|
|
2012
|
|
1 |
p. 59-68
|
artikel
|
| 98 |
Newborn screening for sickle cell disease in Jamaica: logistics and experience with umbilical cord samples
|
Serjeant, G. R.
|
|
2016
|
|
1 |
p. 17-22
|
artikel
|
| 99 |
New literacy challenge for the twenty-first century: genetic knowledge is poor even among well educated
|
Chapman, Robert
|
|
2018
|
|
1 |
p. 73-84
|
artikel
|
| 100 |
New year, new goals for the journal?
|
Cornel, Martina C.
|
|
|
|
1 |
p. 1-3
|
artikel
|
| 101 |
Ophthalmic genetic counselling: emerging trends in practice perspectives in Asia
|
Hui, Esther K. Y.
|
|
|
|
1 |
p. 81-89
|
artikel
|
| 102 |
Pakistani mothers’ and fathers’ experiences and understandings of the diagnosis of Down syndrome for their child
|
Ahmed, Kiran Jan
|
|
2014
|
|
1 |
p. 47-53
|
artikel
|
| 103 |
Parents’ experiences of caring for a young person with neurofibromatosis type 1 (NF1): a qualitative study
|
Barke, Jenny
|
|
2015
|
|
1 |
p. 33-39
|
artikel
|
| 104 |
Parents’ perspectives, experiences, and need for support when communicating with their children about the psychiatric manifestations of 22q11.2 deletion syndrome (22q11DS)
|
Cook, Courtney B.
|
|
|
|
1 |
p. 91-101
|
artikel
|
| 105 |
Parents’ views of genetic testing and treatment of familial hypercholesterolemia in children: a qualitative study
|
Keenan, Karen Forrest
|
|
2018
|
|
1 |
p. 129-141
|
artikel
|
| 106 |
Patient compliance based on genetic medicine: a literature review
|
Schneider, Kai Insa
|
|
2013
|
|
1 |
p. 31-48
|
artikel
|
| 107 |
Patients’ decision to contribute to a biobank in the light of the patient-recruiter relationship—a qualitative study of broad consent in a hospital setting
|
Bosisio, Francesca
|
|
|
|
1 |
p. 15-25
|
artikel
|
| 108 |
Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making
|
Archibald, Alison D.
|
|
2011
|
|
1 |
p. 47-54
|
artikel
|
| 109 |
Perceptions of genetic research in three rural Appalachian Ohio communities
|
Fullenkamp, Amy N.
|
|
2012
|
|
1 |
p. 9-17
|
artikel
|
| 110 |
Predictive genetic testing, risk communication, and risk perception: an international expert meeting in Berlin, Germany
|
Fisher, Eva
|
|
2013
|
|
1 |
p. 1-5
|
artikel
|
| 111 |
Preferences for multigene panel testing for hereditary breast cancer risk among ethnically diverse BRCA-uninformative families
|
Vicuña, Belinda
|
|
2017
|
|
1 |
p. 81-92
|
artikel
|
| 112 |
Prenatal diagnosis and termination of pregnancy: perspectives of South African parents of children with Down syndrome
|
Scott, Chantelle Jennifer
|
|
2012
|
|
1 |
p. 87-97
|
artikel
|
| 113 |
Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study
|
Mohanty, D.
|
|
2012
|
|
1 |
p. 33-42
|
artikel
|
| 114 |
Primary care providers’ lived experiences of genetics in practice
|
Harding, Brittany
|
|
2018
|
|
1 |
p. 85-93
|
artikel
|
| 115 |
Primary prevention of neural tube defects in Brazil: insights into anencephaly
|
Bronberg, Rubén
|
|
2015
|
|
1 |
p. 97-105
|
artikel
|
| 116 |
Property and human genetic information
|
Nielsen, Morten Ebbe Juul
|
|
2018
|
|
1 |
p. 95-107
|
artikel
|
| 117 |
Public engagement with genomic medicine: a summary of town hall discussions
|
Etchegary, Holly
|
|
|
|
1 |
p. 27-35
|
artikel
|
| 118 |
Quality issues in clinical genetic services edited by Ulf Kristofferson, Jörg Schmidtke, and Jean-Jacques Cassiman
|
Leter, Edward M.
|
|
2011
|
|
1 |
p. 49-50
|
artikel
|
| 119 |
Receiving de novo genetic diagnoses for autism with intellectual disability: parents’ views of impacts on families’ reproductive decisions
|
Klitzman, Robert
|
|
|
|
1 |
p. 85-96
|
artikel
|
| 120 |
Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population
|
Ungvári, Ildikó
|
|
2011
|
|
1 |
p. 25-33
|
artikel
|
| 121 |
Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making
|
Reumkens, Kelly
|
|
|
|
1 |
p. 101-110
|
artikel
|
| 122 |
Retrospective chart analysis to determine the impact of a patient-facing digital risk stratification tool combined with a clinical screener for hereditary cancer genetic risk assessment triage in a community oncology clinic
|
Shane-Carson, Kate P.
|
|
|
|
1 |
p. 25-31
|
artikel
|
| 123 |
“Right diet for the right person”: a focus group study of nutritionist-dietitians’ perspectives on nutritional genomics and gene-based nutrition advice
|
Nacis, Jacus S.
|
|
|
|
1 |
p. 49-57
|
artikel
|
| 124 |
Rural Mexican-Americans’ perceptions of family health history, genetics, and disease risk: implications for disparities-focused research dissemination
|
Malen, Rachel
|
|
2015
|
|
1 |
p. 91-96
|
artikel
|
| 125 |
Scope of definitions of genetic testing: evidence from a EuroGentest survey
|
Pinto-Basto, Jorge
|
|
2010
|
|
1 |
p. 29-35
|
artikel
|
| 126 |
Screening criteria: the need to deal with new developments and ethical issues in newborn metabolic screening
|
Forman, John
|
|
2012
|
|
1 |
p. 59-67
|
artikel
|
| 127 |
Screening for the beta-thalassaemia trait: hazards among populations of West African Ancestry
|
Gibson, Felicea
|
|
2011
|
|
1 |
p. 13-18
|
artikel
|
| 128 |
Screening for the sickle cell gene in Gujarat, India: a village-based model
|
Patel, Jyotish
|
|
2012
|
|
1 |
p. 43-47
|
artikel
|
| 129 |
Service provision of genetics health care in Portugal
|
Costa, C.
|
|
|
|
1 |
p. 101-113
|
artikel
|
| 130 |
Short Communication: Lived experience perspectives on genetic testing for a rare eye disease
|
Tam, Mallorie T.
|
|
|
|
1 |
p. 97-101
|
artikel
|
| 131 |
Sickle cell trait newborn screen results: disclosure and management
|
Lilley, Margaret
|
|
|
|
1 |
p. 137-142
|
artikel
|
| 132 |
Social determinants of family health history collection
|
Hughes Halbert, Chanita
|
|
2015
|
|
1 |
p. 57-64
|
artikel
|
| 133 |
Specialist recommendation for chemoprevention medications in patients at familial risk of breast cancer: a cross-sectional survey in England
|
Lee, Siang Ing
|
|
|
|
1 |
p. 111-120
|
artikel
|
| 134 |
Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study
|
Meiser, Bettina
|
|
|
|
1 |
p. 59-73
|
artikel
|
| 135 |
Study of stillbirth and major congenital anomaly among newborns in the high-level natural radiation areas of Kerala, India
|
Jaikrishan, G.
|
|
2012
|
|
1 |
p. 21-31
|
artikel
|
| 136 |
Survey of attitude to human genome modification in Nigeria
|
Jibrilla, Maryam
|
|
|
|
1 |
p. 1-11
|
artikel
|
| 137 |
Telehealth in genetic counselling consultations: the impact of COVID-19 in a Portuguese genetic healthcare service
|
Dantas, Mayla A. A.
|
|
|
|
1 |
p. 91-100
|
artikel
|
| 138 |
The challenge of implementing genetic tests with clinical utility while avoiding unsound applications
|
Cornel, Martina C.
|
|
2012
|
|
1 |
p. 7-12
|
artikel
|
| 139 |
The clinical and genetic Spectrum of Maroteaux-Lamy syndrome (Mucopolysaccharidosis VI) in the Eastern Province of Saudi Arabia
|
Al-Sannaa, Nouriya Abbas
|
|
2017
|
|
1 |
p. 65-70
|
artikel
|
| 140 |
The Dutch national summit on preconception care: a summary of definitions, evidence and recommendations
|
Temel, Sevilay
|
|
2014
|
|
1 |
p. 107-115
|
artikel
|
| 141 |
The impact of insurance on equitable access to non-invasive prenatal screening (NIPT): private insurance may not pay
|
Benoy, Megan E.
|
|
|
|
1 |
p. 185-197
|
artikel
|
| 142 |
The importance and value of EQA for diagnostic genetic laboratories
|
Hastings, Ros J.
|
|
2010
|
|
1 |
p. 11-17
|
artikel
|
| 143 |
The journal of community genetics
|
Schmidtke, Jörg
|
|
2010
|
|
1 |
p. 1-2
|
artikel
|
| 144 |
The M2 haplotype of ANXA5 gene in the context of unexplained recurrent miscarriages
|
Markoff, Arseni
|
|
2017
|
|
1 |
p. 101-102
|
artikel
|
| 145 |
“There should be one spot that you can go:” BRCA mutation carriers’ perspectives on cancer risk management and a hereditary cancer registry
|
Hynes, J.
|
|
|
|
1 |
p. 49-58
|
artikel
|
| 146 |
The scope of prenatal diagnosis for women at increased risk for aneuploidies: views and preferences of professionals and potential users
|
Jong, Antina de
|
|
2012
|
|
1 |
p. 125-135
|
artikel
|
| 147 |
The use of a Toolkit for health needs assessment on neural tube defects in Argentina
|
Groisman, Boris
|
|
2012
|
|
1 |
p. 77-86
|
artikel
|
| 148 |
The use of genealogy databases for risk assessment in genetic health service: a systematic review
|
Stefansdottir, Vigdis
|
|
2012
|
|
1 |
p. 1-7
|
artikel
|
| 149 |
Timing and context: important considerations in the return of genetic results to research participants
|
McBride, Kate A.
|
|
2015
|
|
1 |
p. 11-20
|
artikel
|
| 150 |
To worry or not to worry: breast cancer genetic counseling communication with low-income Latina immigrants
|
Joseph, Galen
|
|
2014
|
|
1 |
p. 63-76
|
artikel
|
| 151 |
Transgender and gender-diverse (TGD) individuals’ perspectives on research seeking genetic variants associated with TGD identities: a qualitative study
|
Rajkovic, Antoine
|
|
|
|
1 |
p. 31-48
|
artikel
|
| 152 |
Translation and adaptation of skin cancer genomic risk education materials for implementation in primary care
|
Rodríguez, Vivian M.
|
|
2016
|
|
1 |
p. 53-63
|
artikel
|
| 153 |
Treatment decision-making in sickle cell disease patients
|
Booth, A.
|
|
|
|
1 |
p. 143-151
|
artikel
|
| 154 |
Understanding how educational interventions improve treatment adherence in patients with familial hypercholesterolaemia: a systematic review
|
Massey, Hannah
|
|
|
|
1 |
p. 5-15
|
artikel
|
| 155 |
Understanding the phenotypic spectrum and family experiences of XYY syndrome: Important considerations for genetic counseling
|
Jodarski, Colleen
|
|
|
|
1 |
p. 17-25
|
artikel
|
| 156 |
Usefulness of fragile X checklist and CGG distribution in specialized institutions in Kinshasa, DR Congo
|
Lumaka, Aimé
|
|
2018
|
|
1 |
p. 153-159
|
artikel
|
| 157 |
When guidelines face reality — Lynch syndrome screening in the setting of public health system in a developing country
|
Kozak, Vanessa Nascimento
|
|
|
|
1 |
p. 19-29
|
artikel
|
| 158 |
Women’s concerns about the emotional impact of awareness of heritable breast cancer risk and its implications for their children
|
O’Neill, Suzanne C.
|
|
2014
|
|
1 |
p. 55-62
|
artikel
|
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