| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Access to genetic testing and genetic counseling in vulnerable populations: the d/Deaf and hard of hearing population
|
Cooke-Hubley, Sandra
|
|
2011
|
|
3 |
p. 117-125
|
artikel
|
| 2 |
A comparative study of patients’ perceptions of genetic and genomic medicine services in California and Malaysia
|
Qian, Emily
|
|
2018
|
|
3 |
p. 351-361
|
artikel
|
| 3 |
A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings
|
Rana, Huma Q.
|
|
2017
|
|
3 |
p. 233-241
|
artikel
|
| 4 |
A content analysis of direct-to-consumer DNA testing on TikTok
|
Basch, Corey H.
|
|
|
|
3 |
p. 489-492
|
artikel
|
| 5 |
A cost analysis of a cancer genetic service model in the UK
|
Slade, Ingrid
|
|
2016
|
|
3 |
p. 185-194
|
artikel
|
| 6 |
A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka
|
Black, M. L.
|
|
2010
|
|
3 |
p. 149-157
|
artikel
|
| 7 |
African American mothers’ attitudes towards genetic testing in the InterGEN study
|
Wright, Michelle L.
|
|
|
|
3 |
p. 285-290
|
artikel
|
| 8 |
A large family with CYLD cutaneous syndrome: medical genetics at the community level
|
Arruda, Anderson Pontes
|
|
|
|
3 |
p. 279-284
|
artikel
|
| 9 |
ALOX5AP gene variants show differential association with coronary artery disease in different populations
|
Alwan, Ahmad
|
|
2010
|
|
3 |
p. 107-115
|
artikel
|
| 10 |
Analysis of pre-test interviews in a cohort of Brazilian patients with movement disorders
|
Nascimento Marinho, Alice Salgueiro do
|
|
2015
|
|
3 |
p. 259-264
|
artikel
|
| 11 |
An Internet support group for parents of children with neurofibromatosis type 1: a qualitative analysis
|
Martin, Staci
|
|
2018
|
|
3 |
p. 327-334
|
artikel
|
| 12 |
Applying Rogers’ framework to evaluate public awareness and knowledge of medical genetics in a developing country
|
Asadollahi, Hamid
|
|
|
|
3 |
p. 367-375
|
artikel
|
| 13 |
A review of key terminology and definitions used for birth defects globally
|
Malherbe, HL
|
|
|
|
3 |
p. 241-262
|
artikel
|
| 14 |
A short history of the first 3 years of the Community Genetics Network and its newsletter
|
Kate, Leo P. ten
|
|
2011
|
|
3 |
p. 111-115
|
artikel
|
| 15 |
Attitudes and beliefs among high- and low-risk population groups towards β-thalassemia prevention: a cross-sectional descriptive study from India
|
Chawla, Swati
|
|
2017
|
|
3 |
p. 159-166
|
artikel
|
| 16 |
Attitudes and interest in incorporating BRCA1/2 cancer susceptibility testing into reproductive carrier screening for Ashkenazi Jewish men and women
|
Hardy, Melanie W.
|
|
|
|
3 |
p. 281-292
|
artikel
|
| 17 |
Barriers and strategies to integrate medical genetics and primary care in underserved populations: a scoping review
|
Chou, Ann F.
|
|
|
|
3 |
p. 291-309
|
artikel
|
| 18 |
Baseline knowledge and receptiveness to genetic testing for hereditary breast and ovarian cancer syndromes in Chinese high-risk females
|
Chu, Annie Tsz-Wai
|
|
|
|
3 |
p. 431-438
|
artikel
|
| 19 |
“Before Facebook and before social media…we did not know anybody else that had this”: parent perspectives on internet and social media use during the pediatric clinical genetic testing process
|
Barton, Krysta S.
|
|
2018
|
|
3 |
p. 375-383
|
artikel
|
| 20 |
Between personal and relational privacy: understanding the work of informed consent in cancer genetics in Brazil
|
Goldim, José Roberto
|
|
2015
|
|
3 |
p. 287-293
|
artikel
|
| 21 |
Bioethics, population studies, and geneticophobia
|
Salzano, Francisco M.
|
|
2015
|
|
3 |
p. 197-200
|
artikel
|
| 22 |
Birth defects surveillance: experiences in Argentina and Colombia
|
Groisman, Boris
|
|
2019
|
|
3 |
p. 385-393
|
artikel
|
| 23 |
Birth prevalence of congenital anomalies in Argentina, according to socioeconomic level
|
Bronberg, Ruben
|
|
|
|
3 |
p. 345-355
|
artikel
|
| 24 |
Birth prevalence of congenital anomalies in the City of Buenos Aires, Argentina, according to socioeconomic level
|
Bronberg, Ruben
|
|
|
|
3 |
p. 303-311
|
artikel
|
| 25 |
Brazilian legal and bioethical approach about donation for research and patents of human body parts
|
Fernandes, Márcia Santana
|
|
2017
|
|
3 |
p. 199-208
|
artikel
|
| 26 |
Cancer genetic counseling communication with low-income Chinese immigrants
|
Cheng, Janice Ka Yan
|
|
2017
|
|
3 |
p. 263-276
|
artikel
|
| 27 |
“CAPABILITY” and “Genetic testing in emerging economies” (GenTEE)
|
Nippert, I
|
|
2013
|
|
3 |
p. 293-296
|
artikel
|
| 28 |
Carrier screening for beta-thalassemia in the Maldives: perceptions of parents of affected children who did not take part in screening and its consequences
|
Waheed, Fazeela
|
|
2016
|
|
3 |
p. 243-253
|
artikel
|
| 29 |
Carrier screening for inherited haemoglobin disorders among secondary school students and young adults in Latium, Italy
|
Amato, Antonio
|
|
2013
|
|
3 |
p. 265-268
|
artikel
|
| 30 |
Carrier screening in preconception consultation in primary care
|
Metcalfe, Sylvia A.
|
|
2011
|
|
3 |
p. 193-203
|
artikel
|
| 31 |
CHACO outreach project: the development of a primary health care-based medical genetic service in an Argentinean province
|
Barreiro, C. Z.
|
|
2013
|
|
3 |
p. 321-334
|
artikel
|
| 32 |
Challenges for providing genetic counselling in Colombian genetic clinics: the viewpoint of the physicians providing genetic consultations
|
Rodas-Pérez, Clemencia
|
|
2015
|
|
3 |
p. 301-311
|
artikel
|
| 33 |
Characteristics predicting recommendation for familial breast cancer referral in a cohort of women from primary care
|
Lee, Siang Ing
|
|
|
|
3 |
p. 331-338
|
artikel
|
| 34 |
Clinical and community genetics services in the Dutch Caribbean
|
Verberne, Eline A.
|
|
|
|
3 |
p. 497-501
|
artikel
|
| 35 |
Co-designing interventions to ‘live well’: experiences and perceptions of the Genetic, Undiagnosed and Rare Disease (GUaRD) community
|
Beadell, Inez
|
|
|
|
3 |
p. 295-305
|
artikel
|
| 36 |
Co-designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom
|
Costa, Alessia
|
|
|
|
3 |
p. 313-327
|
artikel
|
| 37 |
Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who?
|
Aliberti, L.
|
|
|
|
3 |
p. 271-280
|
artikel
|
| 38 |
Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana
|
Anie, Kofi A.
|
|
2016
|
|
3 |
p. 195-202
|
artikel
|
| 39 |
Confidentiality and data sharing: vulnerabilities of the Mexican Genomics Sovereignty Act
|
Rojas-Martínez, Augusto
|
|
2015
|
|
3 |
p. 313-319
|
artikel
|
| 40 |
Congenital and genetic disorders in the Sultanate of Oman. First attempt to assess healthcare needs
|
Rajab, A.
|
|
2014
|
|
3 |
p. 283-289
|
artikel
|
| 41 |
Consanguineous marriages
|
Hamamy, Hanan
|
|
2011
|
|
3 |
p. 185-192
|
artikel
|
| 42 |
Consanguinity and its association with visual impairment in southern India: the Pavagada Pediatric Eye Disease Study 2
|
Kemmanu, Vasudha
|
|
2018
|
|
3 |
p. 345-350
|
artikel
|
| 43 |
Considerations for bio-specimen collection among black women residing in the rural Deep South participating in a cancer prevention study
|
Carson, Tiffany L.
|
|
2013
|
|
3 |
p. 257-263
|
artikel
|
| 44 |
Correction to: Co‑designing models for the communication of genomic results for rare diseases: a comparative study in the Czech Republic and the United Kingdom
|
Costa, Alessia
|
|
|
|
3 |
p. 365-369
|
artikel
|
| 45 |
Correction to: Geographic distribution of live births and infant mortality from congenital anomalies in Brazil, 2012–2017
|
Reis, Luzivan Costa
|
|
|
|
3 |
p. 387
|
artikel
|
| 46 |
Counsellee’s experience of cancer genetic counselling with pedigrees that automatically incorporate genealogical and cancer database information
|
Stefansdottir, Vigdis
|
|
2016
|
|
3 |
p. 229-235
|
artikel
|
| 47 |
Cultivating inclusivity in precision medicine research: disability, diversity, and cultural competence
|
Sabatello, Maya
|
|
2018
|
|
3 |
p. 363-373
|
artikel
|
| 48 |
De-identified genomic data sharing: the research participant perspective
|
Goodman, Deborah
|
|
2017
|
|
3 |
p. 173-181
|
artikel
|
| 49 |
Digital interventions for genomics and genetics education, empowerment, and service engagement: A systematic review
|
Gasteiger, Norina
|
|
|
|
3 |
p. 227-240
|
artikel
|
| 50 |
Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication
|
Makhnoon, Sukh
|
|
|
|
3 |
p. 439-447
|
artikel
|
| 51 |
Does personal genome testing drive service utilization in an adult preventive medicine clinic?
|
Hoang, Ny
|
|
2017
|
|
3 |
p. 151-158
|
artikel
|
| 52 |
Editorial: genetic aspects of preconception consultation in primary care
|
Emery, Jon D.
|
|
2012
|
|
3 |
p. 155-157
|
artikel
|
| 53 |
Education for fathers about newborn screening and leftover dried blood spots
|
Rothwell, Erin
|
|
2017
|
|
3 |
p. 239-241
|
artikel
|
| 54 |
Empowering newborn screening programs in African countries through establishment of an international collaborative effort
|
Therrell, Bradford L.
|
|
|
|
3 |
p. 253-268
|
artikel
|
| 55 |
Engaging a state: Facebook comments on a large population biobank
|
Platt, Tevah
|
|
2017
|
|
3 |
p. 183-197
|
artikel
|
| 56 |
Engaging rural communities in genetic research: challenges and opportunities
|
Dean, Caress
|
|
2017
|
|
3 |
p. 209-219
|
artikel
|
| 57 |
Enhancing recruitment of African-American families into genetic research: lessons learned from Project SuGar
|
Spruill, Ida J.
|
|
2010
|
|
3 |
p. 125-132
|
artikel
|
| 58 |
Erratum to: Genetic services and testing in Brazil
|
Horovitz, Dafne Dain Gandelman
|
|
2012
|
|
3 |
p. 377-378
|
artikel
|
| 59 |
Erratum to: Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in Brazil
|
Ashton-Prolla, Patrícia
|
|
2015
|
|
3 |
p. 285
|
artikel
|
| 60 |
Ethical issues in genetics and public health in Latin America with a focus on Argentina
|
Penchaszadeh, Victor B.
|
|
2015
|
|
3 |
p. 223-230
|
artikel
|
| 61 |
Ethical, legal and social issues in restoring genetic identity after forced disappearance and suppression of identity in Argentina
|
Penchaszadeh, Victor B.
|
|
2015
|
|
3 |
p. 207-213
|
artikel
|
| 62 |
Ethical problems in health research with indigenous or originary peoples in Peru
|
Minaya, Gabriela
|
|
2015
|
|
3 |
p. 201-206
|
artikel
|
| 63 |
Ethics, genetics and public policies in Uruguay: newborn and infant screening as a paradigm
|
Larrandaburu, Mariela
|
|
2015
|
|
3 |
p. 241-249
|
artikel
|
| 64 |
Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project
|
Okuyama, Sonia
|
|
|
|
3 |
p. 329-336
|
artikel
|
| 65 |
Experience of Asian males communicating cardiac genetic risk within the family
|
Kam, Sylvia
|
|
2018
|
|
3 |
p. 293-303
|
artikel
|
| 66 |
Exploring the impact of the reclassification of a hereditary cancer syndrome gene variant: emerging themes from a qualitative study
|
Wedd, Laura
|
|
|
|
3 |
p. 307-317
|
artikel
|
| 67 |
Factors influencing use of telegenetic counseling: perceptions of health care professionals in Sweden
|
Pestoff, Rebecka
|
|
2019
|
|
3 |
p. 407-415
|
artikel
|
| 68 |
Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives
|
Firdous, Naila
|
|
2011
|
|
3 |
p. 173-189
|
artikel
|
| 69 |
Families with complex needs: an inside perspective from young people, their carers, and healthcare providers
|
Radu, Mădălina
|
|
|
|
3 |
p. 293-302
|
artikel
|
| 70 |
Family history of cancer associated with breast tumor clinicopathological features
|
Ricks, Luisel J.
|
|
2014
|
|
3 |
p. 233-240
|
artikel
|
| 71 |
From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionals
|
Augusto, Bianca M.
|
|
2017
|
|
3 |
p. 209-215
|
artikel
|
| 72 |
Fundamental knowledge taught in compulsory education for effective genetic counseling: a qualitative study of descriptions in textbooks
|
Sakai, Eri
|
|
|
|
3 |
p. 263-274
|
artikel
|
| 73 |
Gene editing and disabled people: a response to Felicity Boardman
|
de Miguel Beriain, Iñigo
|
|
|
|
3 |
p. 241-243
|
artikel
|
| 74 |
GenEthics and religion
|
Cornel, Martina C.
|
|
2010
|
|
3 |
p. 159-160
|
artikel
|
| 75 |
Genetic diversity of hemoglobinopathies, G6PD deficiency, and ABO and Rhesus blood groups in two isolates of a primitive Kharia Tribe in Sundargarh District of Northwestern Orissa, India
|
Balgir, R. S.
|
|
2010
|
|
3 |
p. 117-123
|
artikel
|
| 76 |
Genetic information and biobanking: a Brazilian perspective on biological and biographical issues
|
Fernandes, Márcia Santana
|
|
2015
|
|
3 |
p. 295-299
|
artikel
|
| 77 |
Genetic risk
|
ten Kate, Leo P.
|
|
2011
|
|
3 |
p. 159-166
|
artikel
|
| 78 |
Genetics and ethics: a possible and necessary dialogue
|
Goldim, José Roberto
|
|
2015
|
|
3 |
p. 193-196
|
artikel
|
| 79 |
Genetics and ethics in Latin America
|
Sequeiros, Jorge
|
|
2015
|
|
3 |
p. 185-187
|
artikel
|
| 80 |
Genetic services and testing in Brazil
|
Horovitz, Dafne Dain Gandelman
|
|
2012
|
|
3 |
p. 355-375
|
artikel
|
| 81 |
Genetic services and testing in China
|
Zhao, Xinliang
|
|
2013
|
|
3 |
p. 379-390
|
artikel
|
| 82 |
Genetic services and testing in South Africa
|
Kromberg, Jennifer G. R.
|
|
2012
|
|
3 |
p. 413-423
|
artikel
|
| 83 |
Genetic services and testing in South Africa
|
Kromberg, Jennifer G. R.
|
|
|
|
3 |
p. 413-423
|
artikel
|
| 84 |
Genetic services and testing in the Philippines
|
Padilla, Carmencita David
|
|
2012
|
|
3 |
p. 399-411
|
artikel
|
| 85 |
Genetic services and testing in the Sultanate of Oman. Sultanate of Oman steps into modern genetics
|
Rajab, Anna
|
|
2013
|
|
3 |
p. 391-397
|
artikel
|
| 86 |
Genetics in primary health care and the National Policy on Comprehensive Care for People with Rare Diseases in Brazil: opportunities and challenges for professional education
|
Melo, Débora Gusmão
|
|
2015
|
|
3 |
p. 231-240
|
artikel
|
| 87 |
Genetic testing and services in Argentina
|
Penchaszadeh, Victor B.
|
|
2012
|
|
3 |
p. 343-354
|
artikel
|
| 88 |
Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in Brazil
|
Ashton-Prolla, Patrícia
|
|
2015
|
|
3 |
p. 275-283
|
artikel
|
| 89 |
Geographic distribution of live births and infant mortality from congenital anomalies in Brazil, 2012–2017
|
Reis, Luzivan Costa
|
|
|
|
3 |
p. 377-386
|
artikel
|
| 90 |
Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study: experiences from re-contacting mutation carriers and relatives
|
Nilsson, Martin P.
|
|
2017
|
|
3 |
p. 201-208
|
artikel
|
| 91 |
Healthcare providers attitudes towards risk stratification of adopted patients with limited family history information: a cross-sectional survey
|
Saltzman, Barbara
|
|
|
|
3 |
p. 485-488
|
artikel
|
| 92 |
Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations
|
Christianson, A.
|
|
2013
|
|
3 |
p. 297-308
|
artikel
|
| 93 |
Hereditary diseases and child wish: exploring motives, considerations, and the (joint) decision-making process of genetically at-risk couples
|
Severijns, Y.
|
|
|
|
3 |
p. 325-335
|
artikel
|
| 94 |
How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners
|
Evans, W. R. H.
|
|
|
|
3 |
p. 377-386
|
artikel
|
| 95 |
Identifying opportunities for collaboration and growth of genetic counseling services in the Asia Region
|
Laurino, Mercy Y.
|
|
2017
|
|
3 |
p. 243-248
|
artikel
|
| 96 |
Increased family history documentation in internal medicine resident continuity clinic at a community hospital through resident-led structured genetic education program
|
Chenbhanich, Jirat
|
|
|
|
3 |
p. 347-354
|
artikel
|
| 97 |
Increased prevalence of inherited neuromuscular disorders due to endogamy in Northeast Brazil: the need of community genetics services
|
Santos, Silvana
|
|
2013
|
|
3 |
p. 199-203
|
artikel
|
| 98 |
Influence of genetic variants in the apolipoprotein A5 and C3 gene on lipids, lipoproteins, and its association with coronary artery disease in Indians
|
Bhanushali, Aparna A.
|
|
2010
|
|
3 |
p. 139-148
|
artikel
|
| 99 |
Interpretation and management of genetic test results by Canadian family physicians: a multiple choice survey of performance
|
Skinner, Stephanie J.
|
|
|
|
3 |
p. 479-484
|
artikel
|
| 100 |
“I would like to discuss it further with an expert”: a focus group study of Finnish adults’ perspectives on genetic secondary findings
|
Vornanen, M.
|
|
2018
|
|
3 |
p. 305-314
|
artikel
|
| 101 |
Knowledge and perceptions of BRCA1/2 genetic testing and needs of diverse women with a personal or family history of breast cancer in South Florida
|
Jones, Tarsha
|
|
|
|
3 |
p. 415-429
|
artikel
|
| 102 |
Knowledge, attitude, and perceptions about cancer genetic testing in clinical practice in Karachi, Pakistan
|
Shafqat, Shameel
|
|
|
|
3 |
p. 337-344
|
artikel
|
| 103 |
Knowledge, attitudes, and barriers to carrier screening for the Ashkenazi Jewish panel: a Florida experience
|
Warsch, Jessica R. L.
|
|
2014
|
|
3 |
p. 223-231
|
artikel
|
| 104 |
Knowledge, attitudes, and perceived barriers towards genetic testing across three rural Illinois communities
|
Fogleman, A. J.
|
|
2019
|
|
3 |
p. 417-423
|
artikel
|
| 105 |
Letter to the editor. Gene editing and disabled people: a response to Iñigo de Miguel Beriain
|
Boardman, Felicity
|
|
|
|
3 |
p. 245-247
|
artikel
|
| 106 |
Letter to the Editor: Time to update the language of genetics from the nineteenth to the twenty-first century: a response to Schmidtke and Cornel
|
Small, Neil
|
|
|
|
3 |
p. 249-251
|
artikel
|
| 107 |
Mainstreaming genetics in palliative care: barriers and suggestions for clinical genetic services
|
Dearing, A.
|
|
2017
|
|
3 |
p. 243-256
|
artikel
|
| 108 |
Modelled epidemiological data for selected congenital disorders in South Africa
|
Malherbe, Helen L.
|
|
|
|
3 |
p. 357-376
|
artikel
|
| 109 |
Modernizing family health history: achievable strategies to reduce implementation gaps
|
Wildin, Robert S.
|
|
|
|
3 |
p. 493-496
|
artikel
|
| 110 |
Neonatal screening program for five conditions in Honduras
|
Buckley, Michelle Melissa Miralda
|
|
|
|
3 |
p. 389-395
|
artikel
|
| 111 |
Neurogenetics in Peru: clinical, scientific and ethical perspectives
|
Cornejo-Olivas, Mario
|
|
2015
|
|
3 |
p. 251-257
|
artikel
|
| 112 |
Never “totally prepared”: Support groups on helping families prepare for a child with a genetic condition
|
Craig, Kaitlynn P.
|
|
|
|
3 |
p. 319-327
|
artikel
|
| 113 |
Newborn screening education on the internet: a content analysis of North American newborn screening program websites
|
Araia, Makda H.
|
|
2011
|
|
3 |
p. 127-134
|
artikel
|
| 114 |
Oncologists’ perspectives of telephone genetic counseling to facilitate germline BRCA1/2 testing for their patients with high-grade serous ovarian cancer
|
Hemming, Pierre
|
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Online BRCA1/2 screening in the Australian Jewish community: a qualitative study
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Yuen, Jeanette
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On the future of genetic risk assessment
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Ropers, Hans-Hilger
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Opinions of hearing parents about the causes of hearing impairment of their children with biallelic GJB2 mutations
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Solovyev, Aisen V.
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2017
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Pakistani healthcare professionals’ perceptions of communication with patients and their relatives about hereditary breast cancer: a qualitative study in a LMIC
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Ahmed, Shenaz
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Parent and child perspectives on family interactions related to melanoma risk and prevention after CDKN2A/p16 testing of minor children
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Wu, Yelena P.
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Parenthood among individuals with Turner syndrome: results of an online survey of attitudes towards pregnancy, adoption, and surrogacy
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Falsey, Erin
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Participation of low-income women in genetic cancer risk assessment and BRCA 1/2 testing: the experience of a safety-net institution
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Komenaka, Ian K.
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2015
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Patentability of human genes: the conceptual differences between the industrialised and Latin American countries
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Bergel, Salvador Darío
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Patient and provider perspectives on the development of personalized medicine: a mixed-methods approach
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Puryear, Lauren
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Perceptions of parents of children with hearing loss of genetic origin in South Africa
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Gardiner, Sinead Amber
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2018
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Peripheral health workers’ knowledge and experience related to sickle cell disease: an in-depth interview study in six tribal-dominated districts of India
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Babu, Bontha V.
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Perspectives on communication and engagement with regard to collecting biospecimens and family health histories for cancer research in a rural Alaska Native community
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Dirks, Lisa G.
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2019
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Preconception care and genetic risk: ethical issues
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Wert, Guido M. W. R. De
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Preconception expanded carrier screening: a focus group study with relatives of mucopolysaccharidosis type III patients and the general population
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Conijn, Thirsa
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Preconception exposure to mutagens: medical and other exposures to radiation and chemicals
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Mulvihill, John J.
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Predictors of adverse psychological experiences surrounding genome-wide profiling for disease risk
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Broady, K. M.
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Prenatal detection of congenital anomalies and related factors in Argentina
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Bidondo, Maria Paz
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Prevalence of mutations in a diverse cohort of 3162 women tested via the same multigene cancer panel in a managed care health plan
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Alvarado, Mónica
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Primary care physician experiences utilizing a family health history tool with electronic health record–integrated clinical decision support: an implementation process assessment
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Lemke, Amy A.
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Project REENCONTRO: ethical aspects of genetic identification in families separated by the compulsory isolation of leprosy patients in Brazil
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Fonseca, Claudia Lee Williams
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2015
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Prospective experience with contingent screening strategy for Down syndrome in Estonia
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Muru, Kai
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Psychiatric symptoms in a Spanish sample with hereditary cancer risk
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Costa-Requena, Gema
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Psychosocial aspects of preconception consultation in primary care: lessons from our experience in clinical genetics
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Riedijk, S.
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Public attitudes regarding the use of electronic health information and residual clinical tissues for research
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Botkin, Jeffrey R.
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Public attitudes towards the genetic testing in Georgia
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Kvaratskhelia, Eka
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Public–private partnership as a solution for integrating genetic services into health care of countries with low and middle incomes
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Meier, Florian
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Public’s awareness of biobanks and willingness to participate in biobanking: the moderating role of social value orientation
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Grežo, Matúš
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QF-PCR: a valuable first-line prenatal and postnatal test for common aneuploidies in South Africa
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Cottino, Laura
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Quality of life and comprehensive health supervision for children with Down syndrome in Thailand
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Rojnueangnit, Kitiwan
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Random inbreeding, isonymy, and population isolates in Argentina
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Dipierri, José
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Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study
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Streicher, Samantha A.
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Recruiting for diversity: a pilot test of recruitment strategies for a national alcohol survey with mail-in genetic data collection
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Chartier, Karen G.
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Reproductive decision making: interviews with mothers of children with undiagnosed developmental delay
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Pond, Emily
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Responding to the increased genetic risk associated with customary consanguineous marriage among minority ethnic populations: lessons from local innovations in England
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Salway, Sarah
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Responsiveness and adaptability in community engaged biobanking research: experiences from a Hispanic community
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Mosavel, Maghboeba
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Risk stratification, genomic data and the law
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Hall, Alison
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Role of older generations in the family’s adjustment to Huntington disease
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Oliveira, Carla Roma
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SCA2 predictive testing in Cuba: challenging concepts and protocol evolution
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Cruz-Mariño, Tania
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Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem
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Patra, Pradeep K.
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Self-reported race and ethnicity of US biobank participants compared to the US Census
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Cohn, Elizabeth Gross
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Spatial and temporal analysis of infant mortality from congenital malformations in Brazil (1996–2010)
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Bronberg, Rubén
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Students’ attitudes towards somatic genome editing versus genome editing of the germline using an example of familial leukemia
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Vajen, Beate
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Successful implementation of Lynch syndrome screening in a safety net institution
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Swedish healthcare providers’ perceptions of preconception expanded carrier screening (ECS)—a qualitative study
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Matar, A.
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Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups
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Nguyen, Nga Thi
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Thalassemia: a prevalent disease yet unknown term among college students in Saudi Arabia
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Olwi, Duaa Ibrahim
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The accessibility and utilization of genetic testing for inherited heart rhythm disorders: a Canadian cross-sectional survey study
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Roston, Thomas M.
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The effect of parental age on NF1 patients in Turkey
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The family medical history as a tool in preconception consultation
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The Greater Sekhukhune-CAPABILITY outreach project
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The impact of participation in genetic research for families with cleft lip with and without cleft palate: a qualitative study
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The implementation of pharmacogenomics into UK general practice: a qualitative study exploring barriers, challenges and opportunities
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The Latin American School of Human and Medical Genetics: promoting education and collaboration in genetics and ethics applied to health sciences across the continent
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Giugliani, Roberto
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The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophies
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“To perpetuate blindness!”: attitudes of UK patients with inherited retinal disease towards genetic testing
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Undiagnosed haemoglobinopathies among pregnant women attending antenatal care clinics in Pune, India
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Universal tumor screening for Lynch syndrome: perspectives of Canadian pathologists and genetic counselors
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Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year period
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Users’ motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories
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What can be offered to couples at (possibly) increased genetic risk?
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Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market
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Borry, Pascal
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Why do pregnant women accept or decline prenatal diagnosis for Down syndrome?
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Young smokers’ views of genetic susceptibility testing for lung cancer risk: minding unintended consequences
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Docherty, Sharron L.
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