Kathy Tucker - Concepedia

Author

Kathy Tucker

Also Known As

Alicja Wolk, Alison Trainer, Georgia Trench, Hermela Shimelis, Kathleen Claes, Kathy Tucker, Marina Wallace, Mona Saleh, Renea Taylor, Rob A E M Tollenaar

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

Prince of Wales Hospital UNSW Sydney The University of Sydney The Royal Melbourne Hospital Royal North Shore Hospital

About

Kathy Tucker is an author at Prince of Wales Hospital specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	520
2	Arts	1	1	34
3	Public Health	1	1	21
4	Biology	1	1	108
5	Communication	1	1	34

Kathy Tucker

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Clinical Presentation and Penetrance of Pheochromocytoma/Paraganglioma Syndromes Diana E. Benn, Anne‐Paule Gimenez‐Roqueplo, Jennifer Reilly, The Journal of Clinical Endocrinology & Metabolism	2006	566
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia Sohela Shah, Kasmintan A. Schrader, Esmé Waanders, Nature Genetics Hematological MalignancyLymphoid NeoplasiaMixed-phenotype Acute LeukemiaGeneticsHematology	2013	320
Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study Elizabeth Bancroft, Elizabeth Page, Elena Castro, European Urology	2014	247
Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas Diana E. Benn, Michael Croxson, Kathy Tucker, Oncogene BiologySporadic PhaeochromocytomasSomatic VariantSomatic Sdhb MutationsGenetic Disorder	2003	108
Mutation analysis of the <i>MYH</i> gene in an Australian series of colorectal polyposis patients with or without germline <i>APC</i> mutations Carla F. Kairupan, Cliff Meldrum, Renee Crooks, International Journal of Cancer	2005	45
Atypical Teratoid Rhabdoid Tumor: Two Case Reports and an Analysis of Adult Cases with Implications for Pathophysiology and Treatment Christopher Dardis, Jared Jue Ying Yeo, Kelly Milton, Frontiers in Neurology Tumoral PathologyMedicineHistopathologyPathologyGynecology	2017	37
An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations Paboda Ratnayake, Claire E. Wakefield, Bettina Meiser, Familial Cancer Genetic TestingCommunication PreferencesHealth CommunicationGenetic CounselingBreast Cancer	2010	34
Role of Engrailed-2 (EN2) as a prostate cancer detection biomarker in genetically high risk men Emma Killick, Richard Morgan, Francesca Launchbury, Scientific Reports	2013	33
Comparing theory and non-theory based implementation approaches to improving referral practices in cancer genetics: a cluster randomised trial protocol April Morrow, Emily Hogden, Yoon‐Jung Kang, Trials	2019	27
Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome) Aedan Roberts, Derek J. Nancarrow, Mark Clendenning, Familial Cancer CytogeneticsGeneticsCrc Susceptibility LociGenetic EpidemiologyPathology	2010	21

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