Paper Details

Paper Title

Optimising clinical care through <i>CDH1</i>-specific germline variant curation: improvement of clinical assertions and updated curation guidelines.

Paper Journal Title

J Med Genet

Paper Citation Count

Paper Publication Year

2023

Bio Mention

VUS, clinically actionable gene, diffuse gastric cancer, germline variants, germline variant, lobular breast cancer, translation initiation codon

Mesh Descriptor

Author Name	Affiliation
Xi Luo	Baylor College of Medicine
Huei San Leong	Peter MacCallum Cancer Centre
Kristy Lee	The University of North Carolina at Chapel Hill
Amanda B Spurdle	QIMR Berghofer Medical Research Institute
Amanda B Spurdle	QIMR Berghofer Medical Research Institute
Chimene Kesserwan	National Institutes of Health
Brian H Shirts	University of Washington
Carla Oliveira	Instituto de Investigacao e Inovacao em Saude - (i3S), University of Porto
Carla Oliveira	University of Porto
Carla Oliveira	Institute of Molecular Pathology and Immunology - (IPATIMUP), University of Porto
Sharon E Plon	Baylor College of Medicine
Kasmintan A Schrader	The University of British Columbia
Kasmintan A Schrader
Kasmintan A Schrader	The University of British Columbia
Kasmintan A Schrader

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Dataset	Description	Source Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.	Link
ClinVar	ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publ	Link

1 - 15

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