alessandra sironi
Laboratorio Sperimentale di Ricerche di Citogenetica Medica e Genetica Molecolare
Italy
- Frontiers in Genetics
- Human and Medical Genomics
- Research Topics
- The clinical utility of Long Read Sequencing (LRS) to improve diagnostic yield and uncover biological mechanisms in rare disease
The clinical utility of Long Read Sequencing (LRS) to improve diagnostic yield and uncover biological mechanisms in rare disease
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33 Authors
christopher m. watson
Institute of Medical Research, St James’s University Hospital, University of Leeds Faculty of Medicine and Health
United Kingdom
daniela turchetti
Department of Medical and Surgical Sciences (DIMEC)
Italy
dongjuan wang
Center for Clinical Molecular Medicine
China
emanuela iovino
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Italy
ferruccio ceriotti
SC Patologia Clinica
Italy
giovanni innella
Department of Medical and Surgical Sciences (DIMEC)
Italy
giulia olivucci
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Italy
hiroki ura
Center for Clinical Genomics
Japan
ilaria bestetti
SC Patologia Clinica
Italy
lidia larizza
Laboratorio Sperimentale di Ricerche di Citogenetica Medica e Genetica Molecolare
Italy
madelyn a. gillentine
Department of Laboratories, Seattle Children’s Hospital
United States
Published in
Frontiers in Genetics
- Human and Medical Genomics
- Epigenomics and Epigenetics
- Genetics of Common and Rare Diseases
Participating Journals
Frontiers in Cell and Developmental Biology
- 4.6 impact factor
- 9.7 citescore
Frontiers in Pediatrics
- 2.1 impact factor
- 3.6 citescore
Impact
- 14kTopic views
- 9,636Article views
- 2,949Article downloads