Published in J Genet Couns on February 13, 2007
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Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing. Genet Med (2015) 0.84
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An exploration of how psychotic-like symptoms are experienced, endorsed, and understood from the National Latino and Asian American Study and National Survey of American Life. Ethn Health (2014) 0.81
Telegenetics use in presymptomatic genetic counselling: patient evaluations on satisfaction and quality of care. Eur J Hum Genet (2015) 0.80
A pre-visit tailored website enhances counselees' realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling. Fam Cancer (2012) 0.80
Linking genetic counseling content to short-term outcomes in individuals at elevated breast cancer risk. J Genet Couns (2014) 0.80
A group approach to genetic counselling of cardiomyopathy patients: satisfaction and psychological outcomes sufficient for further implementation. Eur J Hum Genet (2015) 0.80
A tailored approach to family-centered genetic counseling for cystic fibrosis newborn screening: the Wisconsin model. J Genet Couns (2010) 0.79
Implementation and outcomes of telephone disclosure of clinical BRCA1/2 test results. Patient Educ Couns (2013) 0.79
The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes. Fam Cancer (2016) 0.78
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Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study. J Med Internet Res (2016) 0.76
Assessment and model guided cancer screening promotion by village doctors in China: a randomized controlled trial protocol. BMC Cancer (2015) 0.75
Anxiety and depression symptoms among women attending group-based patient education courses for hereditary breast and ovarian cancer. Hered Cancer Clin Pract (2017) 0.75
Communication patterns of primary care physicians. JAMA (1997) 6.88
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Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients. Am J Med Genet A (2003) 1.86
Long-term psychological impact of carrying a BRCA1/2 mutation and prophylactic surgery: a 5-year follow-up study. J Clin Oncol (2003) 1.68
Psychological impact of genetic counseling for familial cancer: a systematic review and meta-analysis. J Natl Cancer Inst (2004) 1.55
Doctor-patient communication and cancer patients' quality of life and satisfaction. Patient Educ Couns (2000) 1.50
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Doctor-patient communication patterns in breast cancer adjuvant therapy discussions. Health Expect (2000) 1.35
Nondirectiveness in genetic counseling: an empirical study. Am J Hum Genet (1997) 1.32
What is the impact of genetic counselling in women at increased risk of developing hereditary breast cancer? A meta-analytic review. Soc Sci Med (2002) 1.29
Psychological consequences of predictive genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a prospective follow-up study. Int J Cancer (2001) 1.23
Process studies in genetic counseling: peering into the black box. Am J Med Genet (2001) 1.20
Initial cancer genetic counseling consultation: change in counselees' cognitions and anxiety, and association with addressing their needs and preferences. Am J Med Genet A (2005) 1.16
Goals of genetic counseling. Clin Genet (2001) 1.16
Patient satisfaction with two different models of cancer genetic services in south-east Scotland. Br J Cancer (2004) 1.15
Communication in cancer genetic counselling: does it reflect counselees' previsit needs and preferences? Br J Cancer (2005) 1.13
Perceived personal control (PPC): a new concept in measuring outcome of genetic counseling. Am J Med Genet (1999) 1.13
Analyzing the process and content of genetic counseling in familial breast cancer consultations. J Genet Couns (2004) 1.11
Communication and information-giving in high-risk breast cancer consultations: influence on patient outcomes. Br J Cancer (2004) 1.07
The perceived personal control (PPC) questionnaire as an outcome of genetic counseling: reliability and validity of the instrument. Am J Med Genet A (2006) 1.06
Communication analysis of BRCA1 genetic counseling. J Genet Couns (2005) 1.03
Assessment of genetic testing and related counseling services: current research and future directions. Soc Sci Med (2004) 1.01
QUOTE-gene(ca): development of a counselee-centered instrument to measure needs and preferences in genetic counseling for hereditary cancer. Psychooncology (2005) 1.00
Genetic counselling: information given, recall and satisfaction. Patient Educ Couns (1997) 0.95
Uncertainty in the information provided during genetic counseling. Patient Educ Couns (1997) 0.92
Communicating risk information in genetic counseling: an observational study. Health Educ Behav (2005) 0.92
What do women really want to know? Motives for attending familial breast cancer clinics. J Med Genet (2002) 0.90
Changes in physician-patient communication from initial to return visits: a prospective study in a haematology outpatient clinic. Patient Educ Couns (2005) 0.89
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Counseling families with hereditary breast and ovarian cancer: A psychosocial perspective. J Genet Couns (1995) 0.86
Genetic counselling for those with a family history of breast or ovarian cancer--current practice and ethical issues. Acta Oncol (1999) 0.84
Psychological aspects of genetic counseling. II: Quantitative analysis of a transcript of a genetic counseling session. Am J Med Genet (1982) 0.84
The standard of neutrality during genetic counselling: an empirical investigation. Patient Educ Couns (1997) 0.83
Differences in individual approaches: communication in the familial breast cancer consultation and the effect on patient outcomes. J Genet Couns (2005) 0.81
Assessment of education and counselling offered by a familial colorectal cancer clinic. Clin Genet (2000) 0.81
The relevance of lowered personal control for patients who have stoma surgery to treat cancer. Br J Clin Psychol (2001) 0.81
Does indirect speech promote nondirective genetic counseling? Results of a sociolinguistic investigation. Am J Med Genet (2001) 0.80
Research directions in genetic counselling: a review of the literature. Patient Educ Couns (2001) 0.80
Counselor-counselee interaction in reproductive genetic counseling: Does a pregnancy in the counselee make a difference? Patient Educ Couns (2006) 0.80
Certainty and uncertainty in genetic counselling: a qualitative case study. Psychol Health (2000) 0.76
The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms. J Am Acad Child Adolesc Psychiatry (2006) 3.86
Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK). BMJ (2012) 2.44
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk. PLoS Genet (2013) 2.39
Online focus groups as a tool to collect data in hard-to-include populations: examples from paediatric oncology. BMC Med Res Methodol (2009) 2.38
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. Nat Genet (2008) 2.28
Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors. Hum Mol Genet (2005) 2.06
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome). Nat Genet (2005) 2.04
Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy. Hum Mol Genet (2004) 1.94
The workload of general practitioners does not affect their awareness of patients' psychological problems. Patient Educ Couns (2007) 1.91
Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk. PLoS Genet (2013) 1.88
Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf-Hirschhorn syndrome. Eur J Hum Genet (2007) 1.83
Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome. Gastroenterology (2008) 1.79
Early recognition of basal cell naevus syndrome. Eur J Pediatr (2004) 1.75
Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer. Clin Cancer Res (2004) 1.68
Factors associated with adolescent mental health service need and utilization. J Am Acad Child Adolesc Psychiatry (2003) 1.55
Help seeking for emotional and behavioural problems in children and adolescents: a review of recent literature. Eur Child Adolesc Psychiatry (2003) 1.54
Retracted Effects of a pre-visit educational website on information recall and needs fulfilment in breast cancer genetic counselling, a randomized controlled trial. Breast Cancer Res (2012) 1.54
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes. J Med Genet (2010) 1.54
The effectiveness of a computer-assisted instruction programme on communication skills of medical specialists in oncology. Med Educ (2002) 1.49
Health beliefs and perceived need for mental health care of anxiety and depression--the patients' perspective explored. Clin Psychol Rev (2008) 1.47
Does the attention General Practitioners pay to their patients' mental health problems add to their workload? A cross sectional national survey. BMC Fam Pract (2006) 1.44
The introduction of a nursing guideline on depression at psychogeriatric nursing home wards: effects on certified nurse assistants. Int J Nurs Stud (2010) 1.44
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. J Natl Cancer Inst (2010) 1.41
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. Breast Cancer Res (2012) 1.38
Psychological outcomes of patients with screen-detected type 2 diabetes: the influence of time since diagnosis and treatment intensity. Diabetes Care (2006) 1.35
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting. Hum Mutat (2006) 1.34
Stickler syndrome caused by COL2A1 mutations: genotype-phenotype correlation in a series of 100 patients. Eur J Hum Genet (2010) 1.27
Has patients' involvement in the decision-making process changed over time? Health Expect (2006) 1.27
The workload of GPs: consultations of patients with psychological and somatic problems compared. Br J Gen Pract (2005) 1.26
Reproductive and hormonal factors, and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers: results from the International BRCA1/2 Carrier Cohort Study. Cancer Epidemiol Biomarkers Prev (2009) 1.25
Does age really matter? Recall of information presented to newly referred patients with cancer. J Clin Oncol (2008) 1.25
Deficient knowledge of genetics relevant for daily practice among medical students nearing graduation. Genet Med (2005) 1.25
Young patients', parents', and survivors' communication preferences in paediatric oncology: results of online focus groups. BMC Pediatr (2007) 1.24
Tailored information about cancer risk and screening: a systematic review. Patient Educ Couns (2009) 1.24
Gene-network analysis identifies susceptibility genes related to glycobiology in autism. PLoS One (2009) 1.23
A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history. Breast Cancer Res (2009) 1.22
Body weight and risk of breast cancer in BRCA1/2 mutation carriers. Breast Cancer Res Treat (2010) 1.22
Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autism. Neurogenetics (2011) 1.21
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. Cancer Epidemiol Biomarkers Prev (2012) 1.17
Initial cancer genetic counseling consultation: change in counselees' cognitions and anxiety, and association with addressing their needs and preferences. Am J Med Genet A (2005) 1.16
Patient risk profiles and practice variation in nonadherence to antidepressants, antihypertensives and oral hypoglycemics. BMC Health Serv Res (2007) 1.16
Manipulation of patient-provider interaction: discussing illness representations or action plans concerning adherence. Patient Educ Couns (2003) 1.15
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk. J Med Genet (2012) 1.13
Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer. Genet Med (2007) 1.12
Identification of CANT1 mutations in Desbuquois dysplasia. Am J Hum Genet (2009) 1.12
Electronic momentary assessment in chronic pain I: psychological pain responses as predictors of pain intensity. Clin J Pain (2006) 1.11
Cognitive development in children with 22q11.2 deletion syndrome. Br J Psychiatry (2012) 1.08
The perceived personal control (PPC) questionnaire as an outcome of genetic counseling: reliability and validity of the instrument. Am J Med Genet A (2006) 1.06
Bridging the gap: how traditional healers interact with their patients. A comparative study in Cameroon. Trop Med Int Health (2010) 1.06
A literature review of the psychological impact of genetic testing on breast cancer patients. Patient Educ Couns (2005) 1.06
Receiving treatment for common mental disorders. Gen Hosp Psychiatry (2008) 1.05
Effects of an intervention promoting proactive coping competencies in middle and late adulthood. Gerontologist (2007) 1.04
A review of successful aging models: proposing proactive coping as an important additional strategy. Clin Psychol Rev (2007) 1.03
Association of the PIK4CA schizophrenia-susceptibility gene in adults with the 22q11.2 deletion syndrome. Am J Med Genet B Neuropsychiatr Genet (2009) 1.02
Consultation for and identification of child and adolescent psychological problems in Dutch general practice. Fam Pract (2005) 1.02
Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations. J Med Genet (2013) 1.01
Demand and supply for psychological help in general practice in different European countries: access to primary mental health care in six European countries. Eur J Public Health (2004) 1.01
Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: a prospective analysis. Int J Cancer (2014) 1.01
Proline affects brain function in 22q11DS children with the low activity COMT 158 allele. Neuropsychopharmacology (2008) 1.01
Patient factors associated with guideline-concordant treatment of anxiety and depression in primary care. J Gen Intern Med (2010) 1.00
Primary care patients with anxiety and depression: need for care from the patient's perspective. J Affect Disord (2009) 0.99
Help-seeking for child psychopathology: pathways to informal and professional services in the Netherlands. J Am Acad Child Adolesc Psychiatry (2005) 0.99
A pre-visit website with question prompt sheet for counselees facilitates communication in the first consultation for breast cancer genetic counseling: findings from a randomized controlled trial. Genet Med (2012) 0.98
CDH1-related hereditary diffuse gastric cancer syndrome: clinical variations and implications for counseling. Int J Cancer (2011) 0.98
Older cancer patients' information and support needs surrounding treatment: An evaluation through the eyes of patients, relatives and professionals. BMC Nurs (2009) 0.97
BRCA1/2 mutation testing in breast cancer patients: a prospective study of the long-term psychological impact of approach during adjuvant radiotherapy. Breast Cancer Res Treat (2007) 0.97
The workload of GPs: patients with psychological and somatic problems compared. Fam Pract (2005) 0.97
Behavioral and mood effects of snoezelen integrated into 24-hour dementia care. J Am Geriatr Soc (2005) 0.97
Communicating with child patients in pediatric oncology consultations: a vignette study on child patients', parents', and survivors' communication preferences. Psychooncology (2011) 0.97
Fatigue in multiple sclerosis: reciprocal relationships with physical disabilities and depression. J Psychosom Res (2002) 0.96
The validity of using analogue patients in practitioner-patient communication research: systematic review and meta-analysis. J Gen Intern Med (2012) 0.96
Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences. J Clin Oncol (2010) 0.95
Morphological features in children with autism spectrum disorders: a matched case-control study. J Autism Dev Disord (2011) 0.95
Breast cancer genetic counseling after diagnosis but before treatment: a pilot study on treatment consequences and psychological impact. Patient Educ Couns (2012) 0.94
The role of companions in aiding older cancer patients to recall medical information. Psychooncology (2010) 0.94
Quantification of sequence exchange events between PMS2 and PMS2CL provides a basis for improved mutation scanning of Lynch syndrome patients. Hum Mutat (2010) 0.94
Physical activity and the risk of breast cancer in BRCA1/2 mutation carriers. Breast Cancer Res Treat (2009) 0.94
Pediatric generalized joint hypermobility with and without musculoskeletal complaints: a localized or systemic disorder? Pediatrics (2003) 0.93
Short term psychological distress in patients actively approached for genetic counselling after diagnosis of breast cancer. Eur J Cancer (2006) 0.93
Effects of communication skills training and a Question Prompt Sheet to improve communication with older cancer patients: a randomized controlled trial. Crit Rev Oncol Hematol (2010) 0.93
Genotype-phenotype correlation in patients suspected of having Sotos syndrome. Horm Res (2004) 0.93
Explaining variation in Down's syndrome screening uptake: comparing the Netherlands with England and Denmark using documentary analysis and expert stakeholder interviews. BMC Health Serv Res (2014) 0.93
Behavioral and psychosocial effects of rapid genetic counseling and testing in newly diagnosed breast cancer patients: design of a multicenter randomized clinical trial. BMC Cancer (2011) 0.92
Infant mortality, ethnicity, and genetically determined disorders in The Netherlands. Eur J Public Health (2005) 0.91
Comorbid depression in dementia on psychogeriatric nursing home wards: which symptoms are prominent? Am J Geriatr Psychiatry (2009) 0.91
The different stages and actors involved in the process leading to the use of adolescent mental health services. Clin Child Psychol Psychiatry (2007) 0.90
Development of E-info gene(ca): a website providing computer-tailored information and question prompt prior to breast cancer genetic counseling. J Genet Couns (2009) 0.89
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers. Hum Mol Genet (2011) 0.89
Effects of snoezelen, integrated in 24 h dementia care, on nurse-patient communication during morning care. Patient Educ Couns (2005) 0.88
Tailoring communication in cancer genetic counseling through individual video-supported feedback: a controlled pretest-posttest design. Patient Educ Couns (2005) 0.88