Tina Pesaran - Concepedia

Author

Tina Pesaran

Also Known As

Kesserwan, Chimene, Kyong Soo Park, Maurizio Genuardi, Sarah Richards, Sean V. Tavtigian, T Pesaran, T. Pesaran, Tina F. Pesaran, Tina Pesaran

130

Publications

Citations

H-Index

Concepts

All Affiliations

Ambry Genetics (United States)University of Utah QIMR Berghofer Medical Research Institute Huntsman Cancer Institute Peter MacCallum Cancer Centre

About

Tina Pesaran is an author at Ambry Genetics (United States) specializing in medicine, molecular diagnostics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	16	2.5K
2	Public Health	8	8	1.5K
3	Engineering	2	3	625
4	Health Sciences	1	1	15
5	Management	1	1	55

Tina Pesaran

Publications

5.3K

Citations

H-Index

Page 1

	Year	Citations
Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion Ahmad Abou Tayoun, Tina Pesaran, Marina T. DiStefano, Human Mutation GeneticsGenetic EpidemiologyHuman PolymorphismPathologyDisease Gene Identification	2018	821
Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer Fergus J. Couch, Hermela Shimelis, Chunling Hu, JAMA Oncology	2017	615
Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria Vikas Pejaver, Alicia B. Byrne, Bing Feng, The American Journal of Human Genetics	2022	471
Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients Holly LaDuca, Aaron J. Stuenkel, Jill S. Dolinsky, Genetics in Medicine	2014	335
Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing Hermela Shimelis, Holly LaDuca, Chunling Hu, JNCI Journal of the National Cancer Institute	2018	312
Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup Logan C. Walker, Miguel de la Hoya, George A. R. Wiggins, The American Journal of Human Genetics Acmg/amp FrameworkSystems BiologyFunctional GenomicsEngineeringMedicine	2023	254
Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar Steven M. Harrison, Jill S. Dolinsky, Amy E. Knight Johnson, Genetics in Medicine Allelic VariantVariant InterpretationsClinical TranslationMedicinePathology	2017	242
A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients Holly LaDuca, Eric C. Polley, Amal Yussuf, Genetics in Medicine	2019	212
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline <i>CDH1</i> sequence variants Kristy Lee, Kate Krempely, Maegan E. Roberts, Human Mutation Cancer PathologyGeneticsGenetic EpidemiologyPathologyMolecular Genetics	2018	167
Gene‐specific criteria for <i>PTEN</i> variant curation: Recommendations from the ClinGen PTEN Expert Panel Jessica L. Mester, Rajarshi Ghosh, Tina Pesaran, Human Mutation Gene‐specific CriteriaGeneticsGenetic EpidemiologyPathologyPten Expertise	2018	165

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