Paper Details

Paper Title

ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.

Paper Journal Title

Blood Adv

Paper Citation Count

Paper Publication Year

2019

Bio Mention

ACMG/AMP, Myeloid Malignancy, RUNX1, RUNX1 variants, VUS variants, familial platelet disorder, functional domains, germline, hematologic malignancies, inherited disorders, inherited myeloid malignancies, minor, mutational hotspots, myeloid leukemia, patients, thrombocytopenia

Mesh Descriptor

Clinical Decision-Making, Core Binding Factor Alpha 2 Subunit, Disease Management, Genetic Association Studies, Genetic Predisposition to Disease, Genetic Testing, Genetic Variation, Genomics, Germ-Line Mutation, Humans, Leukemia, Myeloid, Phenotype, Reproducibility of Results

Author Name	Affiliation
Xi Luo	Baylor College of Medicine
Simone Feurstein	Section of Hematology/Oncology and Center for Clinical Cancer Genetics, The University of Chicago
Shruthi Mohan	University of North Carolina School of Medicine
Christopher C Porter	Emory University School of Medicine
Sarah A Jackson
Siob??n B Keel	University of Washington
Michael Chicka
Anna L Brown	SA Pathology & University of South Australia
Chimene Kesserwan	St. Jude Children's Research Hospital
Anupriya Agarwal	Knight Cancer Institute, Oregon Health & Science University
Minjie Luo	The Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Minjie Luo	The Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
Zejuan Li	Houston Methodist Research Institute and Houston Methodist Hospital
Zejuan Li	Weill Cornell Medical College
Justyne E Ross	University of North Carolina School of Medicine
Panagiotis Baliakas	Uppsala University
Daniel E Pineda-Alvarez
Courtney D DiNardo	University of Texas MD Anderson Cancer Center
Alison A Bertuch	Baylor College of Medicine
Nikita Mehta	Mayo Clinic
Tom Vulliamy	Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University London
Ying Wang	Johns Hopkins University School of Medicine
Kim E Nichols	St. Jude Children's Research Hospital
Luca Malcovati	University of Pavia and Istituto di Ricovero e Cura a Carattere Scientifico Policlinico S. Matteo Foundation
Michael F Walsh	Memorial Sloan Kettering Cancer Center
Lesley Rawlings
Shannon K McWeeney	Oregon Health & Science University
Jean Soulier	INSERM/CNRS U/7212, Universite de Paris and Hematology Laboratory Assistance Publique-Hopitaux de Paris
Anna Raimbault	INSERM/CNRS U/7212, Universite de Paris and Hematology Laboratory Assistance Publique-Hopitaux de Paris
Mark J Routbort	University of Texas MD Anderson Cancer Center
Liying Zhang	Memorial Sloan Kettering Cancer Center
Gabriella Ryan
Nancy A Speck	Perelman School of Medicine, University of Pennsylvania
Sharon E Plon	Baylor College of Medicine
David Wu	University of Washington
Lucy A Godley	Section of Hematology/Oncology and Center for Clinical Cancer Genetics, The University of Chicago

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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

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