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Author Details
Full Name
Matthew T Wheeler
Affiliation
Center for Undiagnosed Diseases, Stanford University
ORCID
Career Start Year
2019
Papers
9
H Index
7
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34374469
Genetic counselor roles in the undiagnosed diseases network research study: Clinical care, collaboration, and curation.
J Genet Couns
2022
36072659
Beyond race: Recruitment of diverse participants in clinical genomics research for rare disease.
Front Genet
2022
34981646
Perceived utility and disutility of genomic sequencing for pediatric patients: Perspectives from parents with diverse sociodemographic characteristics.
Am J Med Genet A
2022
35217565
Toward transcriptomics as a primary tool for rare disease investigation.
Cold Spring Harb Mol Case Stud
2022
34096130
"Doctors can read about it, they can know about it, but they've never lived with it": How parents use social media throughout the diagnostic odyssey.
J Genet Couns
2021
30476213
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources.
Nucleic Acids Res
2019
30964584
A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.
J Genet Couns
2019
30706981
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students.
J Genet Couns
2019
31478310
Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing.
J Genet Couns
2019
1 - 9 of 9
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