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Author Details

Malcolm Fisher
Cincinnati Children's Hospital Medical Center
2002
24
16
PMIDPaper TitleJournal TitlePublished Year
36755307Xenbase: key features and resources of the Xenopus model organism knowledgebase.Genetics2023
36866529The Gene Ontology knowledgebase in 2023.Genetics2023
31733057Xenbase: deep integration of GEO & SRA RNA-seq and ChIP-seq data in a model organism database.Nucleic Acids Res2020
30863320Xenbase: Facilitating the Use of <i>Xenopus</i> to Model Human Disease.Front Physiol2019
29059324Xenbase: a genomic, epigenomic and transcriptomic model organism database.Nucleic Acids Res2018
30586382Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice.PLoS Genet2018
29761462Navigating Xenbase: An Integrated Xenopus Genomics and Gene Expression Database.Methods Mol Biol2018
28850106FANTOM5 CAGE profiles of human and mouse samples.Sci Data2017
25678556Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells.Science2015
24670764A promoter-level mammalian expression atlas.Nature2014
23540693Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinoma.Cell2013
24348270A trans-acting protein effect causes severe eye malformation in the Mp mouse.PLoS Genet2013
21138943Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla.Hum Mol Genet2011
21526123Comparative analysis of 3D expression patterns of transcription factor genes and digit fate maps in the developing chick wing.PLoS One2011
215099003D expression patterns of cell cycle genes in the developing chick wing and comparison with expression patterns of genes implicated in digit specification.Dev Dyn2011
21565291Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.Am J Hum Genet2011
21750680Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice.PLoS Genet2011
19767607EMAGE mouse embryo spatial gene expression database: 2010 update.Nucleic Acids Res2010
20708683Identification of genes downstream of the Shh signalling in the developing chick wing and syn-expressed with Hoxd13 using microarray and 3D computational analysis.Mech Dev2010
19843505Disruption of ST5 is associated with mental retardation and multiple congenital anomalies.J Med Genet2010
19234473Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence.Nat Genet2009
18355805Integrating technologies for comparing 3D gene expression domains in the developing chick limb.Dev Biol2008
14630393Cloning and characterisation of Myf5 and MyoD orthologues in Xenopus tropicalis.Biol Cell2003
11880340eFGF is required for activation of XmyoD expression in the myogenic cell lineage of Xenopus laevis.Development2002
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Collaborators

Institute of Genetics and Cancer, The University of Edinburgh MRC Human Genetics Unit
Co-authored papers 7
Cincinnati Children's Hospital Medical Center
Co-authored papers 6
Cincinnati Children's Hospital Medical Center
Co-authored papers 6
Cincinnati Children's Hospital Medical Center
Co-authored papers 6
University of Calgary
Co-authored papers 5
University of Calgary
Co-authored papers 5
RIKEN Center for Integrative Medical Sciences
Co-authored papers 4
Roslin Institute, University of Edinburgh
Co-authored papers 4
Mater Research Institute - University of Queensland
Co-authored papers 4
International Institute of Molecular and Cell Biology in Warsaw
Co-authored papers 3
Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology
Co-authored papers 3
Ochanomizu University
Co-authored papers 3
RIKEN Center for Integrative Medical Sciences
Co-authored papers 3
RIKEN Center for Integrative Medical Sciences
Co-authored papers 3
University of Twente
Co-authored papers 3
RIKEN Center for Integrative Medical Sciences
Co-authored papers 3
RIKEN Center for Integrative Medical Sciences
Co-authored papers 3
University of Milan
Co-authored papers 3
Karolinska Institute
Co-authored papers 3
University of British Columbia
Co-authored papers 3
Institute of Pharmaceutical Sciences, ETH Zurich
Co-authored papers 3
Nagoya City University Graduate School of Medical Sciences
Co-authored papers 3
Child and Family Research Institute, University of British Columbia
Co-authored papers 3
RIKEN Research Center for Allergy and Immunology
Co-authored papers 3
Yokohama National University
Co-authored papers 3
International Centre for Genetic Engineering and Biotechnology
Co-authored papers 3
Australian Institute for Bioengineering and Nanotechnology, University of Queensland
Co-authored papers 3
South African Medical Research Council (SAMRC), University of Cape Town
Co-authored papers 3
Tohoku University Graduate School of Medicine
Co-authored papers 3
Leiden University Medical Center
Co-authored papers 3