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12 in total

1. The potential social impact of predictive genetic testing for susceptibility to common chronic diseases: a review and proposed research agenda.

Authors: Charlie Davison; Sally Macintyre; George Davey Smith
Journal: Sociol Health Illn Date: 1994-06

2. Nuffield Council on Bioethics.

Authors: David Shapiro
Journal: Politics Life Sci Date: 1995-08

3. Diffusion of information about genetic risk within families.

Authors: Ségolène Ayme; Geneviève Macquart-Moulin; Claire Julian-Reynier; Françoise Chabal; Francis Giraud
Journal: Neuromuscul Disord Date: 1993 Sep-Nov Impact factor: 4.296

4. Recent advances in the clinical management of autosomal-dominant polycystic kidney disease.

Authors: Y Pirson
Journal: QJM Date: 1996-11

5. Alpha 1-antitrypsin deficiency--diagnosis, treatment, and control: identification of patients.

Authors: A S Buist
Journal: Lung Date: 1990 Impact factor: 2.584

6. alpha 1-antitrypsin deficiency in early childhood.

Authors: T Sveger
Journal: Pediatrics Date: 1978-07 Impact factor: 7.124

7. Proposed: an international code of ethics for medical genetics.

Authors: D C Wertz; J C Fletcher
Journal: Clin Genet Date: 1993-07 Impact factor: 4.438

8. Decline in FEV1 among patients with severe hereditary alpha 1-antitrypsin deficiency type PiZ.

Authors: N Seersholm; A Kok-Jensen; A Dirksen
Journal: Am J Respir Crit Care Med Date: 1995-12 Impact factor: 21.405

9. Right not to know or duty to know? Prenatal screening for polycystic renal disease.

Authors: R Kielstein; H M Sass
Journal: J Med Philos Date: 1992-08

10. Survival of patients with severe alpha 1-antitrypsin deficiency with special reference to non-index cases.

Authors: N Seersholm; A Kok-Jensen; A Dirksen
Journal: Thorax Date: 1994-07 Impact factor: 9.139

8 in total

1. Expanding the role of the family history in primary care.

Authors: J Emery; P Rose
Journal: Br J Gen Pract Date: 1999-04 Impact factor: 5.386

2. Revalidation.

Authors: M Pringle
Journal: Br J Gen Pract Date: 1999-04 Impact factor: 5.386

3. Comparison of genetic services with and without genetic registers: access and attitudes to genetic counselling services among relatives of genetic clinic patients.

Authors: L Kerzin-Storrar; C Wright; P R Williamson; A Fryer; A Njindou; O Quarrell; D Donnai; D Craufurd
Journal: J Med Genet Date: 2002-12 Impact factor: 6.318

4. Facilitating family communication about predictive genetic testing: probands' perceptions.

Authors: Clara L Gaff; Veronica Collins; Tiffany Symes; Jane Halliday
Journal: J Genet Couns Date: 2005-04 Impact factor: 2.537

5. Comparison of genetic services with and without genetic registers: knowledge, adjustment, and attitudes about genetic counselling among probands referred to three genetic clinics.

Authors: C Wright; L Kerzin-Storrar; P R Williamson; A Fryer; A Njindou; O Quarrell; D Donnai; D Craufurd
Journal: J Med Genet Date: 2002-12 Impact factor: 6.318

6. Transmitting genetic risk information in families: attitudes about disclosing the identity of relatives.

Authors: J T Wilcke; N Seersholm; A Kok-Jensen; A Dirksen
Journal: Am J Hum Genet Date: 1999-09 Impact factor: 11.025

7. The importance of written information packages in support of case-finding within families at risk for inherited high cholesterol.

Authors: Hélène W P van den Nieuwenhoff; Ilse Mesters; Joyce J T M Nellissen; Anton F Stalenhoef; Nanne K de Vries
Journal: J Genet Couns Date: 2006-02 Impact factor: 2.537

Review 8. Guidelines for disclosing genetic information to family members: from development to use.

Authors: Béatrice Godard; Thierry Hurlimann; Martin Letendre; Nathalie Egalité
Journal: Fam Cancer Date: 2006 Impact factor: 2.375

8 in total