Search Results - "Rahman, Belinda"

Awareness, knowledge, perceptions, and attitudes towards genetic testing for cancer risk among ethnic minority groups: a systematic review by Hann, Katie E J, Freeman, Madeleine, Fraser, Lindsay, Waller, Jo, Sanderson, Saskia C, Rahman, Belinda, Side, Lucy, Gessler, Sue, Lanceley, Anne

“…Genetic testing for risk of hereditary cancer can help patients to make important decisions about prevention or early detection. US and UK studies show that…”
Get full text

Impact of a decision aid about stratified ovarian cancer risk-management on women's knowledge and intentions: a randomised online experimental survey study by Meisel, Susanne F, Freeman, Maddie, Waller, Jo, Fraser, Lindsay, Gessler, Sue, Jacobs, Ian, Kalsi, Jatinderpal, Manchanda, Ranjit, Rahman, Belinda, Side, Lucy, Wardle, Jane, Lanceley, Anne, Sanderson, Saskia C

“…Risk stratification using genetic and other types of personal information could improve current best available approaches to ovarian cancer risk reduction,…”
Get full text

How should we discuss genetic testing with women newly diagnosed with breast cancer? Design and implementation of a randomized controlled trial of two models of delivering education about treatment-focused genetic testing to younger women newly diagnosed with breast cancer by Watts, Kaaren J, Meiser, Bettina, Mitchell, Gillian, Kirk, Judy, Saunders, Christobel, Peate, Michelle, Duffy, Jessica, Kelly, Patrick J, Gleeson, Margaret, Barlow-Stewart, Kristine, Rahman, Belinda, Friedlander, Michael, Tucker, Kathy

“…Germline BRCA1 and BRCA2 mutation testing offered shortly after a breast cancer diagnosis to inform women's treatment choices - treatment-focused genetic…”
Get full text

One size does not fit all: The case for targeted education in genetics and genomics for cancer nurses by Jacobs, Chris, Rahman, Belinda

Get full text

Mainstreamed genetic testing for women with ovarian cancer: first-year experience by Rahman, Belinda, Lanceley, Anne, Kristeleit, Rebecca S, Ledermann, Jonathan A, Lockley, Michelle, McCormack, Mary, Mould, Tim, Side, Lucy

“…Ovarian cancer is the fifth most common cause of cancer death for women in the UK. Up to 18% of cases can be attributed to germline mutations in and genes…”
Get more information

The narrative paradox of the BRCA gene: an ethnographic study in the clinical encounters of ovarian cancer patients by Therond, Clara, Lanceley, Anne, Gibbon, Sahra, Rahman, Belinda

“…In this era of personalisation a patient's molecular profile plays an increasingly central role in development and delivery of personalised medicine. This…”
Get full text

Genomic sequencing in oncology: Considerations for integration in routine cancer care by Rahman, Belinda, Lamb, Alastair, Protheroe, Andrew, Shah, Ketan, Solomons, Joyce, Williams, Jonathan, Ormondroyd, Elizabeth

Get full text

Genetic and genomic learning needs of oncologists and oncology nurses in the era of precision medicine: a scoping review by Rahman, Belinda, McEwen, Alison, Phillips, Jane L, Tucker, Katherine, Goldstein, David, Jacobs, Chris

“…Genetic and genomic data are increasingly guiding clinical care for cancer patients. To meet the growing demand for precision medicine, patient-facing oncology…”
Get more information

Mainstreamed genetic testing in ovarian cancer: patient experience of the testing process by McLeavy, Laura, Rahman, Belinda, Kristeleit, Rebecca, Ledermann, Jonathan, Lockley, Michelle, McCormack, Mary, Mould, Tim, Side, Lucy, Lanceley, Anne

“…Pathogenic variants account for 5.8-24.8% of ovarian cancers. The identification of such a variant can have a significant impact on the affected individual and…”
Get more information

Attitudes in Patients with Autosomal Dominant Polycystic Kidney Disease Toward Prenatal Diagnosis and Preimplantation Genetic Diagnosis by Swift, Oscar, Vilar, Enric, Rahman, Belinda, Side, Lucy, Gale, Daniel P

“…No recommendations currently exist regarding implementation of both prenatal diagnosis and preimplantation genetic diagnosis (PGD) for autosomal dominant…”
Get more information

Adjusting the frequency of mammography screening on the basis of genetic risk: Attitudes among women in the UK by Meisel, Susanne F, Pashayan, Nora, Rahman, Belinda, Side, Lucy, Fraser, Lindsay, Gessler, Sue, Lanceley, Anne, Wardle, Jane

“…Abstract Purpose To explore public attitudes towards modifying frequency of mammography screening based on genetic risk. Methods Home-based interviews were…”
Get full text

Acceptability of, and Information Needs Regarding, Next-Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study by Meiser, Bettina, Storey, Ben, Quinn, Veronica, Rahman, Belinda, Andrews, Lesley

“…Next generation sequencing (NGS) for patients at risk of hereditary cancer syndromes can also identify non-cancer related mutations, as well as variants of…”
Get full text

Mainstreamed genetic testing in ovarian cancer : a case study of BRCA1/2 tumour testing by Rahman, Belinda

“…Background: With the advent of targeted therapies in ovarian cancer (OC), there is an impetus to identify patients with a BRCA1/2 mutation. Germline testing…”
Get full text

Adolescents with Implantable Cardioverter Defibrillators: A Patient and Parent Perspective by RAHMAN, BELINDA, MACCIOCCA, IVAN, SAHHAR, MARGARET, KAMBERI, SULEMAN, CONNELL, VANESSA, DUNCAN, RONY E.

“…Background:  An implantable cardioverter defibrillator (ICD) is a device used in the treatment of individuals with life‐threatening cardiac conditions. These…”
Get full text

Genetic testing and personalized ovarian cancer screening: a survey of public attitudes by Meisel, Susanne F, Rahman, Belinda, Side, Lucy, Fraser, Lindsay, Gessler, Sue, Lanceley, Anne, Wardle, Jane

“…Advances in genetic technologies are expected to make population-wide genetic testing feasible. This could provide a basis for risk stratified cancer…”
Get full text

Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history by Meiser, Bettina, Quinn, Veronica F, Mitchell, Gillian, Tucker, Kathy, Watts, Kaaren J, Rahman, Belinda, Peate, Michelle, Saunders, Christobel, Geelhoed, Elizabeth, Gleeson, Margaret, Barlow-Stewart, Kristine, Field, Michael, Harris, Marion, Antill, Yoland C, Susman, Rachel, Bowen, Michael T, Mills, Llew, Kirk, Judy

“…In patients with early breast cancer, personal and tumour characteristics other than family history are increasingly used to prompt genetic testing to guide…”
Get full text

Streamlined genetic education is effective in preparing women newly diagnosed with breast cancer for decision making about treatment-focused genetic testing: a randomized controlled noninferiority trial by Quinn, Veronica F., Meiser, Bettina, Kirk, Judy, Tucker, Kathy M., Watts, Kaaren J., Rahman, Belinda, Peate, Michelle, Saunders, Christobel, Geelhoed, Elizabeth, Gleeson, Margaret, Barlow-Stewart, Kristine, Field, Michael, Harris, Marion, Antill, Yoland C., Cicciarelli, Linda, Crowe, Karen, Bowen, Michael T., Mitchell, Gillian

“…Increasingly, women newly diagnosed with breast cancer are being offered treatment-focused genetic testing (TFGT). As the demand for TFGT increases,…”
Get full text

Population-based genetic risk prediction and stratification for ovarian cancer: views from women at high risk by Rahman, Belinda, Meisel, Susanne F., Fraser, Lindsay, Side, Lucy, Gessler, Sue, Wardle, Jane, Lanceley, Anne

“…There is an opportunity to improve outcomes for ovarian cancer (OC) through advances in risk stratification, early detection and diagnosis. A population-based…”
Get full text

Health professionals’ evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer by Douma, Kirsten F. L., Meiser, Bettina, Kirk, Judy, Mitchell, Gillian, Saunders, Christobel, Rahman, Belinda, Sousa, Mariana S., Barlow-Stewart, Kristine, Gleeson, Margaret, Tucker, Kathy

“…Increasingly, women are offered genetic testing shortly after diagnosis of breast cancer to facilitate decision-making about treatment, often referred to as…”
Get full text

Long-term health and development of children diagnosed prenatally with a de novo apparently balanced chromosomal rearrangement by Sinnerbrink, Ingrid B., Sherwen, Amanda, Meiser, Bettina, Halliday, Jane, Amor, David J., Waters, Elizabeth, Rea, Felicity, Evans, Elizabeth, Rahman, Belinda, Kirk, Edwin P.

“…ABSTRACT Objective This study aimed to determine if liveborn children with prenatally detected de novo apparently balanced chromosome rearrangements (ABCR)…”
Get full text