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K. Tucker · SciRah

Researcher profile · Semantic Scholar

K. Tucker

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K. Tucker — researcher profile on SciRah

h-index: 49
Works: 185
Citations: 9,090

Most-cited papers

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
R. Milne, Karoline B. Kuchenbaecker, K. Michailidou, J. Beesley +466 more
2017Nature Genetics379 citations Open access
Semantic Scholar
Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.
Aung Ko Win, J. Young, N. Lindor, K. Tucker +21 more
2012Journal of Clinical Oncology323 citations Open access
Semantic Scholar
Identification of a recurrent germline PAX5 mutation and susceptibility to pre-B cell acute lymphoblastic leukemia
Sohela Shah, K. Schrader, E. Waanders, A. Timms +66 more
2013Nature Genetics289 citations Open access
Semantic Scholar
Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study
E. Bancroft, E. Page, E. Castro, H. Lilja +111 more
2014European Urology252 citations Open access
Semantic Scholar
Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome.
Aung Ko Win, N. Lindor, J. Young, F. Macrae +20 more
2012Journal of the National Cancer Institute240 citations Open access
Semantic Scholar
Risk of Colorectal Cancer for Carriers of Mutations in MUTYH, with and without a Family History of Cancer
Aung Ko Win, J. Dowty, S. Cleary, Hyeja Kim +22 more
2014Gastroenterology203 citations Open access
Semantic Scholar
Risk of extracolonic cancers for people with biallelic and monoallelic mutations in MUTYH
Aung Ko Win, J. Reece, J. Dowty, D. Buchanan +21 more
2016International Journal of Cancer134 citations Open access
Semantic Scholar
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
A. Osorio, R. Milne, Karoline B. Kuchenbaecker, Tereza Vaclová +193 more
2014PLoS Genetics123 citations Open access
Semantic Scholar
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk
A. Spurdle, P. Whiley, B. Thompson, Bing Feng +30 more
2012Journal of Medical Genetics118 citations Open access
Semantic Scholar
Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome.
Aung Ko Win, N. Lindor, I. Winship, K. Tucker +17 more
2013Journal of the National Cancer Institute111 citations Open access
Semantic Scholar
The psychological impact of genetic information on children: a systematic review
C. Wakefield, Lucy V. Hanlon, K. Tucker, A. Patenaude +3 more
2016Genetics in Medicine107 citations Open access
Semantic Scholar
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.
Huong D. Meeks, Hong-Lin Song, K. Michailidou, M. Bolla +249 more
2016Journal of the National Cancer Institute82 citations Open access
Semantic Scholar
Psychosocial and behavioral outcomes of genomic testing in cancer: a systematic review
T. Yanes, A. Willis, B. Meiser, K. Tucker +1 more
2018European Journal of Human Genetics66 citations Open access
Semantic Scholar
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium
S. Moghadasi, Huong D. Meeks, M. Vreeswijk, L. A. Janssen +36 more
2017Journal of Medical Genetics66 citations Open access
Semantic Scholar
Bayesian approach to determining penetrance of pathogenic SDH variants
Diana E. Benn, Ying Zhu, Katrina A. Andrews, M. Wilding +20 more
2018Journal of Medical Genetics62 citations Open access
Semantic Scholar
Therapeutic implications of germline genetic findings in cancer
S. Thavaneswaran, E. Rath, K. Tucker, A. Joshua +4 more
2019Nature Reviews Clinical Oncology54 citations
Semantic Scholar
Family Communication, Risk Perception and Cancer Knowledge of Young Adults from BRCA1/2 Families: a Systematic Review
A. Young, P. Butow, J. Vetsch, V. Quinn +3 more
2017Journal of Genetic Counseling51 citations Open access
Semantic Scholar
Multiplicity and Molecular Heterogeneity of Colorectal Carcinomas in Individuals with Serrated Polyposis
C. Rosty, M. Walsh, Rhiannon J. Walters, M. Clendenning +18 more
2013American Journal of Surgical Pathology46 citations Open access
Semantic Scholar
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
G. Figlioli, M. Bogliolo, Irene Catucci, Laura Caleca +473 more
2019npj Breast Cancer41 citations Open access
Semantic Scholar
Children and young people's understanding of inherited conditions and their attitudes towards genetic testing: A systematic review
B. McGill, C. Wakefield, J. Vetsch, K. Barlow-Stewart +5 more
2019Clinical Genetics40 citations Open access
Semantic Scholar
“I remember how I felt, but I don't remember the gene”: Families’ experiences of cancer‐related genetic testing in childhood
B. McGill, C. Wakefield, J. Vetsch, Qishan Lim +5 more
2019Pediatric Blood & Cancer39 citations
Semantic Scholar
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
V. Quinn, B. Meiser, J. Kirk, K. Tucker +14 more
2016Genetics in Medicine39 citations Open access
Semantic Scholar
Communication and information needs of women diagnosed with ovarian cancer regarding treatment-focused genetic testing.
M. Gleeson, B. Meiser, K. Barlow-Stewart, A. Trainer +4 more
2013Oncology Nursing Forum39 citations Open access
Semantic Scholar
There is no decision to make: experiences and attitudes toward treatment-focused genetic testing among women diagnosed with ovarian cancer.
B. Meiser, M. Gleeson, N. Kasparian, K. Barlow-Stewart +5 more
2012Gynecologic Oncology38 citations Open access
Semantic Scholar
Atypical Teratoid Rhabdoid Tumor: Two Case Reports and an Analysis of Adult Cases with Implications for Pathophysiology and Treatment
C. Dardis, J. Yeo, K. Milton, L. Ashby +9 more
2017Frontiers in Neurology36 citations Open access
Semantic Scholar
Role of Engrailed-2 (EN2) as a prostate cancer detection biomarker in genetically high risk men
E. Killick, R. Morgan, F. Launchbury, E. Bancroft +21 more
2013Scientific Reports36 citations Open access
Semantic Scholar
An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers
Dana Madorsky-Feldman, M. Sklair-Levy, T. Perri, Y. Laitman +34 more
2016Breast Cancer Research and Treatment35 citations Open access
Semantic Scholar
Knowledge, attitudes and beliefs of Arabic‐Australians concerning cancer
Mona Saleh, K. Barlow-Stewart, B. Meiser, K. Tucker +2 more
2012Psycho-Oncology35 citations Open access
Semantic Scholar
Challenges and strategies proposed by genetic health professionals to assist with family communication
A. Young, P. Butow, K. Tucker, C. Wakefield +2 more
2019European Journal of Human Genetics34 citations Open access
Semantic Scholar
Through the looking glass: an exploratory study of the lived experiences and unmet needs of families affected by Von Hippel–Lindau disease
N. A. Kasparian, A. Rutstein, U. Sansom-Daly, S. Mireskandari +3 more
2014European Journal of Human Genetics33 citations Open access
Semantic Scholar
Facilitating decision-making in women undergoing genetic testing for hereditary breast cancer: BRECONDA randomized controlled trial results.
K. Sherman, C. Kilby, Laura-Kate E. Shaw, C. Winch +3 more
2017Breast32 citations
Semantic Scholar
Are we being overly cautious? A qualitative inquiry into the experiences and perceptions of treatment-focused germline BRCA genetic testing amongst women recently diagnosed with breast cancer
Elvira Zilliacus, B. Meiser, M. Gleeson, K. Watts +3 more
2012Supportive Care in Cancer32 citations Open access
Semantic Scholar
“Balancing Expectations with Actual Realities”: Conversations with Clinicians and Scientists in the First Year of a High-Risk Childhood Cancer Precision Medicine Trial
B. McGill, C. Wakefield, Kate Hetherington, L. J. Munro +10 more
2020Journal of Personalized Medicine29 citations Open access
Semantic Scholar
Healthcare professionals' attitudes toward cancer precision medicine: A systematic review.
J. Vetsch, C. Wakefield, P. Techakesari, M. Warby +5 more
2019Seminars in Oncology29 citations
Semantic Scholar
Lost in translation: returning germline genetic results in genome-scale cancer research
A. Johns, S. McKay, J. Humphris, M. Pinese +22 more
2017Genome Medicine29 citations Open access
Semantic Scholar
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
K. Watts, B. Meiser, G. Mitchell, J. Kirk +9 more
2012BMC Cancer28 citations Open access
Semantic Scholar
Aligning intuition and theory: enhancing the replicability of behaviour change interventions in cancer genetics
N. Taylor, E. Healey, A. Morrow, Sian Greening +4 more
2020Implementation Science Communications27 citations Open access
Semantic Scholar
Women's preferences for selective estrogen reuptake modulators: an investigation using protection motivation theory.
A. Ralph, B. Ager, M. Bell, I. Collins +4 more
2014Patient Education and Counseling26 citations Open access
Semantic Scholar
Pilot study of an online training program to increase genetic literacy and communication skills in oncology healthcare professionals discussing BRCA1/2 genetic testing with breast and ovarian cancer patients
B. Meiser, P. Woodward, M. Gleeson, M. Kentwell +8 more
2021Familial Cancer25 citations Open access
Semantic Scholar
New Approaches to Continuing Medical Education: a QStream (spaced education) Program for Research Translation in Ovarian Cancer
T. Robinson, A. Janssen, J. Kirk, A. deFazio +3 more
2015Journal of Cancer Education25 citations Open access
Semantic Scholar
Multifactorial Likelihood Assessment of BRCA1 and BRCA2 Missense Variants Confirms That BRCA1:c.122A>G(p.His41Arg) Is a Pathogenic Mutation
P. Whiley, M. Parsons, J. Leary, K. Tucker +7 more
2014PLoS ONE25 citations Open access
Semantic Scholar
Cancer-Related Genetic Testing and Personalized Medicine for Adolescents: A Narrative Review of Impact and Understanding
J. Vetsch, C. Wakefield, M. Warby, K. Tucker +5 more
2018Journal of Adolescent and Young Adult Oncology24 citations Open access
Semantic Scholar
A quantitative model to predict pathogenicity of missense variants in the TP53 gene
Cristina Fortuno, A. Cipponi, M. Ballinger, S. Tavtigian +9 more
2019Human Mutation23 citations Open access
Semantic Scholar
Health professionals’ evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer
Kirsten F. L. Douma, B. Meiser, J. Kirk, G. Mitchell +6 more
2014Familial Cancer23 citations Open access
Semantic Scholar
Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma
T. Dwight, U. Na, Edward J. Kim, Ying Zhu +7 more
2017BMC Cancer21 citations Open access
Semantic Scholar
Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing
M. Southey, J. Dowty, M. Riaz, Jason A. Steen +28 more
2021npj Breast Cancer20 citations Open access
Semantic Scholar
The development and evaluation of a nationwide training program for oncology health professionals in the provision of genetic testing for ovarian cancer patients.
M. Gleeson, M. Kentwell, B. Meiser, J. Do +17 more
2020Gynecologic Oncology20 citations
Semantic Scholar
Lynch Syndrome and Cervical Cancer
Y. Antill, J. Dowty, Aung Ko Win, T. Thompson +14 more
2015International Journal of Cancer20 citations Open access
Semantic Scholar
Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: a cluster randomised trial protocol
A. Morrow, Emily Hogden, Yoon-Jung Kang, J. Steinberg +12 more
2019Trials19 citations Open access
Semantic Scholar
Psychological outcomes and surgical decisions after genetic testing in women newly diagnosed with breast cancer with and without a family history
B. Meiser, V. Quinn, G. Mitchell, K. Tucker +14 more
2018European Journal of Human Genetics17 citations Open access
Semantic Scholar

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