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Paper Details

Improved Diagnosis and Care for Rare Diseases through Implementation of Precision Public Health Framework.
Adv Exp Med Biol
15
2017
Patient, Rare Diseases, patients, people, person, protein-coding gene, rare, rare diseases
Genetic Predisposition to Disease, Genomics, Health Policy, Humans, Phenotype, Policy Making, Precision Medicine, Predictive Value of Tests, Prognosis, Program Development, Program Evaluation, Public Health, Rare Diseases
Author NameAffiliation
Gareth BaynamKing Edward Memorial Hospital
Gareth Baynam
Gareth Baynam
Gareth BaynamKing Edward Memorial Hospital
Gareth Baynam
Gareth Baynam
Faye L Bowman
Karla J Lister
Caroline E Walker
Nicholas Pachter
Nicholas PachterUniversity of Western Australia
Nicholas PachterUniversity of Western Australia
Jack GoldblattUniversity of Western Australia
Jack Goldblatt
Kym M BoycottChildren's Hospital of Eastern Ontario Research Institute, University of Ottawa
William A GahlNational Institutes of Health
William A GahlNational Human Genome Research Institute, National Institutes of Health
William A GahlNational Institutes of Health
William A GahlNational Human Genome Research Institute, National Institutes of Health
Kenjiro KosakiKeio University School of Medicine
Takeya Adachi
Ken Ishii
Trinity Mahede
Fiona McKenzieUniversity of Western Australia
Fiona McKenzie
Sharron Townshend
Jennie Slee
Cathy Kiraly-Borri
Cathy Kiraly-Borri
Anand Vasudevan
Anne Hawkins
Stephanie Broley
Lyn Schofield
Lyn Schofield
Hedwig VerhoefCurtin University
Hedwig VerhoefCooperative Research Centre for Spatial Information
Tudor GrozaKinghorn Centre for Clinical Genomics, Garvan Institute for Medical Research
Tudor GrozaSt. Vincent's Clinical School, University of New South Wales (UNSW)
Tudor GrozaKinghorn Centre for Clinical Genomics, Garvan Institute for Medical Research
Tudor GrozaSt. Vincent's Clinical School, University of New South Wales (UNSW)
Andreas ZanklSydney Medical School, The University of Sydney
Andreas ZanklSydney Childrens Hospitals Network (Westmead)
Peter N Robinson
Peter N RobinsonInstitute for Systems Genomics, University of Connecticut
Peter N Robinson
Peter N RobinsonInstitute for Systems Genomics, University of Connecticut
Melissa A HaendelLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Melissa A HaendelLibrary and Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University
Michael BrudnoUniversity of Toronto
Michael BrudnoHospital for Sick Children
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