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Author Details
Full Name
Mathew W Wright
Affiliation
Stanford University School of Medicine
ORCID
Career Start Year
2001
Papers
38
H Index
30
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36541006
Accessing clinical-grade genomic classification data through the ClinGen Data Platform.
Pac Symp Biocomput
2023
34955381
Evaluating the impact of in silico predictors on clinical variant classification.
Genet Med
2022
34890165
An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease Genetics.
Pac Symp Biocomput
2022
30311373
The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics.
Hum Mutat
2018
30311390
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene.
Hum Mutat
2018
30311374
ClinGen Allele Registry links information about genetic variants.
Hum Mutat
2018
28552198
Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource.
Am J Hum Genet
2017
26842383
A review of the new HGNC gene family resource.
Hum Genomics
2016
26553804
Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation.
Nucleic Acids Res
2016
25352543
RNAcentral: an international database of ncRNA sequences.
Nucleic Acids Res
2015
26215545
Mouse genome annotation by the RefSeq project.
Mamm Genome
2015
25713288
International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors.
Pharmacol Rev
2015
25361968
Genenames.org: the HGNC resources in 2015.
Nucleic Acids Res
2015
24716852
A short guide to long non-coding RNA gene nomenclature.
Hum Genomics
2014
23161694
Genenames.org: the HGNC resources in 2013.
Nucleic Acids Res
2013
24172014
Update of the human and mouse SERPIN gene superfamily.
Hum Genomics
2013
23634723
Vive la différence: naming structural variants in the human reference genome.
Hum Genomics
2013
22298953
An updated nomenclature for keratin-associated proteins (KAPs).
Int J Biol Sci
2012
23245209
Gene family matters: expanding the HGNC resource.
Hum Genomics
2012
20929869
genenames.org: the HGNC resources in 2011.
Nucleic Acids Res
2011
22155607
Update of the human secretoglobin (SCGB) gene superfamily and an example of 'evolutionary bloom' of androgen-binding protein genes within the mouse Scgb gene superfamily.
Hum Genomics
2011
21940779
RNAcentral: A vision for an international database of RNA sequences.
RNA
2011
21296742
Naming 'junk': human non-protein coding RNA (ncRNA) gene nomenclature.
Hum Genomics
2011
20931200
Recommended nomenclature for five mammalian carboxylesterase gene families: human, mouse, and rat genes and proteins.
Mamm Genome
2010
18948278
IUPHAR-DB: the IUPHAR database of G protein-coupled receptors and ion channels.
Nucleic Acids Res
2009
18923155
New nomenclature for mammalian BSP genes.
Biol Reprod
2009
17984084
The HGNC Database in 2008: a resource for the human genome.
Nucleic Acids Res
2008
16951416
HCOP: a searchable database of human orthology predictions.
Brief Bioinform
2007
16641997
The DNA sequence, annotation and analysis of human chromosome 3.
Nature
2006
16831889
New consensus nomenclature for mammalian keratins.
J Cell Biol
2006
16431039
Human and orthologous gene nomenclature.
Gene
2006
16103133
A revised nomenclature for mammalian acyl-CoA thioesterases/hydrolases.
J Lipid Res
2005
16284797
HCOP: the HGNC comparison of orthology predictions search tool.
Mamm Genome
2005
15057823
The DNA sequence and analysis of human chromosome 13.
Nature
2004
15573121
Gene map of the extended human MHC.
Nat Rev Genet
2004
11944974
Guidelines for human gene nomenclature.
Genomics
2002
11163611
Retinal photoreceptors of paleognathous birds: the ostrich (Struthio camelus) and rhea (Rhea americana).
Vision Res
2001
11810281
The HUGO Gene Nomenclature Committee (HGNC).
Hum Genet
2001
1 - 38 of 38
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