Jessica L. Mester - Concepedia

Author

Jessica L. Mester

Also Known As

Hatton, Jessica N., J Mester, J. Mester, J.L. Mester, JESSICA MESTER, James Harraway, Jessica L Mester, Jessica L. Mester, Jessica Mester, Jessica L. Mester

Publications

5.4K

Citations

H-Index

Concepts

All Affiliations

Cleveland Clinic Case Western Reserve University Cleveland Clinic Lerner College of Medicine University School Ambry Genetics (United States)

About

Jessica L. Mester is an author at Cleveland Clinic specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	22	2.5K
2	Public Health	4	4	804
3	Health Sciences	3	3	125
4	Engineering	2	2	459
5	Nursing	1	1	15

Jessica L. Mester

Publications

4.9K

Citations

H-Index

Page 1

	Year	Citations
Lifetime Cancer Risks in Individuals with Germline<i>PTEN</i>Mutations Min-Han Tan, Jessica L. Mester, Joanne Ngeow, Clinical Cancer Research	2012	861
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
A Clinical Scoring System for Selection of Patients for PTEN Mutation Testing Is Proposed on the Basis of a Prospective Study of 3042 Probands Min-Han Tan, Jessica L. Mester, Charissa Peterson, The American Journal of Human Genetics Genetic TestingMutation-based TestingGenetic DisorderClinical Scoring SystemGenetics	2010	403
Frequent Gastrointestinal Polyps and Colorectal Adenocarcinomas in a Prospective Series of PTEN Mutation Carriers Brandie Heald, Jessica L. Mester, Lisa Rybicki, Gastroenterology	2010	267
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
ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene‐level specification of the ACMG/AMP guidelines for sequence variant interpretation E. Andres Rivera-Munoz, Laura V. Milko, Steven M. Harrison, Human Mutation Clinical Genome ResourceEngineeringGeneticsGenetic EpidemiologyPathology	2018	205
Incidence and Clinical Characteristics of Thyroid Cancer in Prospective Series of Individuals with Cowden and Cowden-Like Syndrome Characterized by Germline PTEN, SDH, or KLLN Alterations Joanne Ngeow, Jessica L. Mester, Lisa Rybicki, The Journal of Clinical Endocrinology & Metabolism MedicineGermline PtenThyroid DiseasePathologyManganese Superoxide Dismutase	2011	195
Germline PIK3CA and AKT1 Mutations in Cowden and Cowden-like Syndromes Mohammed S. Orloff, Xin He, Charissa Peterson, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathogenesisPathology	2012	189
Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism Thomas Frazier, Rebecca Embacher, Amanda K. Tilot, Molecular Psychiatry Neurodevelopmental DisordersDevelopmental BiologyMendelian DisorderSyndromic AutismGenetic Disorder	2014	170
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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