Clara Gaff - Concepedia

Author

Clara Gaff

The University of Melbourne ORCID

Also Known As

C Gaff, C. GAFF, C. Gaff, C. L. Gaff, C.L. Gaff, CL Gaff, Clara Gaff, Clara L Gaff, Clara L. Gaff, Clara Louise Gaff

250

Publications

9.9K

Citations

H-Index

152

Concepts

All Affiliations

The University of Melbourne Murdoch Children's Research Institute Melbourne Genomics Health Alliance Victorian Clinical Genetics Services The Royal Melbourne Hospital

About

Clara Gaff is an author at The University of Melbourne specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	45	2.6K
2	Nursing	9	9	380
3	Education	8	8	297
4	Arts	2	2	100
5	Natural Sciences	2	2	77

Clara Gaff

Publications

5.4K

Citations

H-Index

Page 1

	Year	Citations
A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders Zornitza Stark, Tiong Yang Tan, Belinda Chong, Genetics in Medicine Mendelian DisorderGenetic DisorderWhole-exome SequencingGeneticsMedicine	2016	399
Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions Tiong Yang Tan, Oliver James Dillon, Zornitza Stark, JAMA Pediatrics	2017	318
GA4GH: International policies and standards for data sharing across genomic research and healthcare Heidi L. Rehm, Angela Page, Lindsay Smith, Cell Genomics	2021	273
Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement Zornitza Stark, Deborah Schofield, Khurshid Alam, Genetics in Medicine InfertilityNext-generation SequencingUsual CareHealth Care ReimbursementClinical Whole-exome Sequencing	2017	237
Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness Zornitza Stark, Deborah Schofield, Melissa Martyn, Genetics in Medicine	2018	169
Meeting the challenges of implementing rapid genomic testing in acute pediatric care Zornitza Stark, Sebastian Lunke, Gemma R. Brett, Genetics in Medicine	2018	162
Communication and information-giving in high-risk breast cancer consultations: influence on patient outcomes Elizabeth Lobb, Phyllis Butow, Alexandra Barratt, British Journal of Cancer	2004	136
The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population William D. Foulkes, Isabelle Thiffault, Stephen B. Gruber, The American Journal of Human Genetics Somatic VariantGenetic DisorderGeneticsGenetic EpidemiologyColorectal Cancer	2002	131
Australian Genomics: A Federated Model for Integrating Genomics into Healthcare Zornitza Stark, Tiffany Boughtwood, Peta Phillips, The American Journal of Human Genetics Australian GenomicsFamily MedicineBiomedical Data IntegrationTranslational BioinformaticsHealth Policy	2019	125
Facilitating Family Communication About Predictive Genetic Testing: Probands’ Perceptions Clara Gaff, Veronica Collins, Tiffany Symes, Journal of Genetic Counseling	2005	124

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