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Author Details
Full Name
Malcolm Fisher
Affiliation
Cincinnati Children's Hospital Medical Center
ORCID
Career Start Year
2002
Papers
24
H Index
16
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36755307
Xenbase: key features and resources of the Xenopus model organism knowledgebase.
Genetics
2023
36866529
The Gene Ontology knowledgebase in 2023.
Genetics
2023
31733057
Xenbase: deep integration of GEO & SRA RNA-seq and ChIP-seq data in a model organism database.
Nucleic Acids Res
2020
30863320
Xenbase: Facilitating the Use of <i>Xenopus</i> to Model Human Disease.
Front Physiol
2019
29059324
Xenbase: a genomic, epigenomic and transcriptomic model organism database.
Nucleic Acids Res
2018
30586382
Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice.
PLoS Genet
2018
29761462
Navigating Xenbase: An Integrated Xenopus Genomics and Gene Expression Database.
Methods Mol Biol
2018
28850106
FANTOM5 CAGE profiles of human and mouse samples.
Sci Data
2017
25678556
Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells.
Science
2015
24670764
A promoter-level mammalian expression atlas.
Nature
2014
23540693
Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinoma.
Cell
2013
24348270
A trans-acting protein effect causes severe eye malformation in the Mp mouse.
PLoS Genet
2013
21138943
Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla.
Hum Mol Genet
2011
21526123
Comparative analysis of 3D expression patterns of transcription factor genes and digit fate maps in the developing chick wing.
PLoS One
2011
21509900
3D expression patterns of cell cycle genes in the developing chick wing and comparison with expression patterns of genes implicated in digit specification.
Dev Dyn
2011
21565291
Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.
Am J Hum Genet
2011
21750680
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice.
PLoS Genet
2011
19767607
EMAGE mouse embryo spatial gene expression database: 2010 update.
Nucleic Acids Res
2010
20708683
Identification of genes downstream of the Shh signalling in the developing chick wing and syn-expressed with Hoxd13 using microarray and 3D computational analysis.
Mech Dev
2010
19843505
Disruption of ST5 is associated with mental retardation and multiple congenital anomalies.
J Med Genet
2010
19234473
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence.
Nat Genet
2009
18355805
Integrating technologies for comparing 3D gene expression domains in the developing chick limb.
Dev Biol
2008
14630393
Cloning and characterisation of Myf5 and MyoD orthologues in Xenopus tropicalis.
Biol Cell
2003
11880340
eFGF is required for activation of XmyoD expression in the myogenic cell lineage of Xenopus laevis.
Development
2002
1 - 24 of 24
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6
Christina James-Zorn
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Peter D Vize
University of Calgary
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5
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University of Calgary
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Piero Carninci
RIKEN Center for Integrative Medical Sciences
Co-authored papers
4
John Kenneth Baillie
Roslin Institute, University of Edinburgh
Co-authored papers
4
Geoffrey J Faulkner
Mater Research Institute - University of Queensland
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Carsten O Daub
International Institute of Molecular and Cell Biology in Warsaw
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3
Miki Kojima
Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology
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Sayaka Nagao-Sato
Ochanomizu University
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3
Alistair R R Forrest
RIKEN Center for Integrative Medical Sciences
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Hideya Kawaji
RIKEN Center for Integrative Medical Sciences
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3
Robert Passier
University of Twente
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Akira Hasegawa
RIKEN Center for Integrative Medical Sciences
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3
Sugata Roy
RIKEN Center for Integrative Medical Sciences
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Beatrice Bodega
University of Milan
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