| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
An integrative review of factors that influence reproductive decisions in women with sickle cell disease
|
Rance, Josephine Claire
|
|
2018
|
10 |
2 |
p. 161-169
|
article
|
| 2 |
“A perfect society”— Swedish policymakers’ ethical and social views on preconception expanded carrier screening
|
Matar, Amal
|
|
2018
|
10 |
2 |
p. 267-280
|
article
|
| 3 |
Barriers to the identification of familial hypercholesterolemia among primary care providers
|
Zimmerman, John
|
|
2018
|
10 |
2 |
p. 229-236
|
article
|
| 4 |
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
|
10 |
2 |
p. 321
|
article
|
| 5 |
Correction to: EUROCAT: an update on its functions and activities
|
Tucker, F. D.
|
|
2018
|
10 |
2 |
p. 323
|
article
|
| 6 |
Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation
|
Holtkamp, Kim C. A.
|
|
2018
|
10 |
2 |
p. 249-257
|
article
|
| 7 |
Disclosure of diagnosis to at-risk relatives by individuals diagnosed with hypertrophic cardiomyopathy (HCM)
|
Hudson, Janella
|
|
2018
|
10 |
2 |
p. 207-217
|
article
|
| 8 |
Experiences of patients seeking to participate in variant of uncertain significance reclassification research
|
Makhnoon, Sukh
|
|
2018
|
10 |
2 |
p. 189-196
|
article
|
| 9 |
Exploring the perceived self-efficacy of genetic counselors as teachers
|
Gasparini, Justin
|
|
2018
|
10 |
2 |
p. 313-319
|
article
|
| 10 |
Family health history and genetic services—the East Baltimore community stakeholder interview project
|
Sanghavi, Kunal
|
|
2018
|
10 |
2 |
p. 219-227
|
article
|
| 11 |
Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome
|
Henriksson, Isabelle
|
|
2018
|
10 |
2 |
p. 259-266
|
article
|
| 12 |
High-risk women’s risk perception after receiving personalized polygenic breast cancer risk information
|
Forrest, Laura Elenor
|
|
2018
|
10 |
2 |
p. 197-206
|
article
|
| 13 |
Information exchange between patients with Lynch syndrome and their genetic and non-genetic health professionals: whose responsibility?
|
Douma, Kirsten F. L.
|
|
2018
|
10 |
2 |
p. 237-247
|
article
|
| 14 |
Risk perception and screening behavior of Filipino women at risk for breast cancer: implications for cancer genetic counseling
|
Lagarde, John Benedict B.
|
|
2018
|
10 |
2 |
p. 281-289
|
article
|
| 15 |
“This could be me”: exploring the impact of genetic risk for Huntington’s disease young caregivers
|
Dondanville, Danielle S.
|
|
2018
|
10 |
2 |
p. 291-302
|
article
|
| 16 |
Uncertainty related to multigene panel testing for cancer: a qualitative study on counsellors’ and counselees’ views
|
Medendorp, Niki M.
|
|
2018
|
10 |
2 |
p. 303-312
|
article
|
| 17 |
What do people think about genetics? A systematic review
|
LePoire, Erin
|
|
2018
|
10 |
2 |
p. 171-187
|
article
|
Journal description