PubRank

Journal of community genetics (J Community Genet)

Journal PubWeight™ 231.10‹?›

Top papers

Rank Title Year PubWeight™‹?›
1 Consanguineous marriages : Preconception consultation in primary health care settings. 2011 2.19
2 Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study. 2012 1.58
3 Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study. 2011 1.55
4 Confidence of primary care physicians in their ability to carry out basic medical genetic tasks-a European survey in five countries-Part 1. 2010 1.47
5 A profile of the genetic counsellor and genetic nurse profession in European countries. 2011 1.46
6 Community genetics. Its definition 2010. 2010 1.42
7 Using a community of practice to develop standards of practice and education for genetic counsellors in Europe. 2010 1.32
8 Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market. 2010 1.28
9 Users' motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories. 2011 1.28
10 Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem. 2011 1.27
11 Is there a doctor in the house? : The presence of physicians in the direct-to-consumer genetic testing context. 2011 1.25
12 Genetic testing for familial/hereditary breast cancer-comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany. 2011 1.23
13 Public attitudes regarding the use of electronic health information and residual clinical tissues for research. 2013 1.22
14 Biobanking for research: a survey of patient population attitudes and understanding. 2013 1.20
15 The wide variation of definitions of genetic testing in international recommendations, guidelines and reports. 2012 1.19
16 Ethical problems in health research with indigenous or originary peoples in Peru. 2015 1.18
17 Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes. 2010 1.17
18 Preconception care and genetic risk: ethical issues. 2011 1.13
19 Engaging African-Americans about biobanks and the return of research results. 2012 1.12
20 On the future of genetic risk assessment. 2012 1.12
21 Awareness and interest in biospecimen donation for cancer research: views from gatekeepers and prospective participants in the Latino community. 2013 1.11
22 Scope of definitions of genetic testing: evidence from a EuroGentest survey. 2010 1.11
23 The disclosure of incidental genomic findings: an "ethically important moment" in pediatric research and practice. 2013 1.10
24 Definitions of genetic testing in European legal documents. 2012 1.10
25 Biobank governance: heterogeneous modes of ordering and democratization. 2011 1.07
26 Carrier screening in preconception consultation in primary care. 2011 1.07
27 The journal of community genetics. 2010 1.06
28 Willingness to participate in genomics research and desire for personal results among underrepresented minority patients: a structured interview study. 2013 1.05
29 Genetic screening and democracy: lessons from debating genetic screening criteria in the Netherlands. 2011 1.04
30 Patient compliance based on genetic medicine: a literature review. 2013 1.04
31 Issues concerning the evaluation and regulation of predictive genetic testing. 2012 1.02
32 Genetic services and testing in Brazil. 2012 1.02
33 Engaging diverse populations about biospecimen donation for cancer research. 2014 1.02
34 Public health approach to birth defects: the Argentine experience. 2015 1.01
35 Consolidating newborn screening efforts in the Asia Pacific region : Networking and shared education. 2012 1.01
36 A study of the practice of individual genetic counsellors and genetic nurses in Europe. 2012 1.01
37 Using a "genomics tool" to develop disease prevention strategy in a low-income setting: lessons from the podoconiosis research project. 2012 0.99
38 Genetic testing legislation in Western Europe-a fluctuating regulatory target. 2012 0.98
39 Neither as harmful as feared by critics nor as empowering as promised by providers: risk information offered direct to consumer by personal genomics companies. 2012 0.97
40 Health research: working with Indigenous People in Peru. 2016 0.96
41 Genetic risk. 2012 0.96
42 Community perspectives on public health biobanking: an analysis of community meetings on the Michigan BioTrust for Health. 2013 0.96
43 Disparities in knowledge and willingness to donate research biospecimens: a mixed-methods study in an underserved urban community. 2014 0.96
44 The use of a Toolkit for health needs assessment on neural tube defects in Argentina. 2012 0.95
45 The family medical history as a tool in preconception consultation. 2012 0.95
46 Finding people who will tell you their thoughts on genomics-recruitment strategies for social sciences research. 2014 0.95
47 Comparison of locus-specific databases for BRCA1 and BRCA2 variants reveals disparity in variant classification within and among databases. 2015 0.94
48 The promises of genomic screening: building a governance infrastructure. Special issue: genetics and democracy. 2011 0.92
49 Epidemiological profile of common haemoglobinopathies in Arab countries. 2012 0.92
50 "You don't have to keep everything on paper": African American women's use of family health history tools. 2013 0.92
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