Malcolm E Fisher
TitleCited byYear
A promoter-level mammalian expression atlas
ARR Forrest, H Kawaji, M Rehli, JK Baillie, MJL De Hoon, V Haberle, ...
Nature 507 (7493), 462, 2014
6872014
Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells
E Arner, CO Daub, K Vitting-Seerup, R Andersson, B Lilje, F Drabl°s, ...
Science 347 (6225), 1010-1014, 2015
3372015
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
S Benko, JA Fantes, J Amiel, DJ Kleinjan, S Thomas, J Ramsay, ...
Nature genetics 41 (3), 359, 2009
3272009
Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinoma
R Shukla, KR Upton, M Mu˝oz-Lopez, DJ Gerhardt, ME Fisher, T Nguyen, ...
Cell 153 (1), 101-111, 2013
2662013
EMAGE mouse embryo spatial gene expression database: 2010 update
L Richardson, S Venkataraman, P Stevenson, Y Yang, N Burton, J Rao, ...
Nucleic acids research 38 (suppl_1), D703-D709, 2009
972009
Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies
L Southgate, RD Machado, KM Snape, M Primeau, D Dafou, DM Ruddy, ...
The American Journal of Human Genetics 88 (5), 574-585, 2011
952011
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice
J Rainger, E van Beusekom, JK Ramsay, L McKie, L Al-Gazali, R Pallotta, ...
PLoS genetics 7 (7), e1002114, 2011
702011
eFGF is required for activation of XmyoD expression in the myogenic cell lineage of Xenopus laevis
ME Fisher, HV Isaacs, ME Pownall
Development 129 (6), 1307-1315, 2002
662002
Integrating technologies for comparing 3D gene expression domains in the developing chick limb
ME Fisher, AK Clelland, A Bain, RA Baldock, P Murphy, H Downie, ...
Developmental biology 317 (1), 13-23, 2008
532008
FANTOM5 CAGE profiles of human and mouse samples
S Noguchi, T Arakawa, S Fukuda, M Furuno, A Hasegawa, F Hori, ...
Scientific data 4, 170112, 2017
292017
Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla
R Berry, L Harewood, L Pei, M Fisher, D Brownstein, A Ross, WA Alaynick, ...
Human molecular genetics 20 (5), 917-926, 2010
292010
Identification of genes downstream of the Shh signalling in the developing chick wing and syn-expressed with Hoxd13 using microarray and 3D computational analysis
F Bangs, M Welten, MG Davey, M Fisher, Y Yin, H Downie, B Paton, ...
Mechanisms of development 127 (9-12), 428-441, 2010
262010
Comparative analysis of 3D expression patterns of transcription factor genes and digit fate maps in the developing chick wing
M Fisher, H Downie, MCM Welten, I Delgado, A Bain, T Planzer, ...
PLoS One 6 (4), e18661, 2011
182011
3D expression patterns of cell cycle genes in the developing chick wing and comparison with expression patterns of genes implicated in digit specification
M Welten, G Pavlovska, Y Chen, Y Teruoka, M Fisher, F Bangs, M Towers, ...
Developmental Dynamics 240 (5), 1278-1288, 2011
162011
Disruption of ST5 is associated with mental retardation and multiple congenital anomalies
I G÷hring, A Tagariello, S Endele, CC Stolt, M GhassibÚ, M Fisher, ...
Journal of medical genetics 47 (2), 91-98, 2010
142010
Cloning and characterisation of Myf5 and MyoD orthologues in Xenopus tropicalis
ME Fisher, W Peck, PA Branney, ME Pownall
Biology of the Cell 95 (8), 555-561, 2003
92003
Navigating Xenbase: An Integrated Xenopus Genomics and Gene Expression Database
C James-Zorn, V Ponferrada, ME Fisher, K Burns, J Fortriede, E Segerdell, ...
Eukaryotic Genomic Databases, 251-305, 2018
62018
A trans-acting protein effect causes severe eye malformation in the Mp mouse
J Rainger, M Keighren, DR Keene, NL Charbonneau, JK Rainger, ...
PLoS genetics 9 (12), e1003998, 2013
52013
Xenbase: Facilitating the Use of Xenopus to Model Human Disease
MJ Nenni, ME Fisher, C James-Zorn, TJ Pells, V Ponferrada, S Chu, ...
Frontiers in physiology 10, 154, 2019
12019
Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice
J Rainger, E van Beusekom, JK Ramsay, L McKie, L Al-Gazali, R Pallotta, ...
PLoS genetics 14 (12), e1007866, 2018
2018
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