PubRank

Bernhard G Herrmann

Author PubWeight™ 34.55‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Minimum information specification for in situ hybridization and immunohistochemistry experiments (MISFISHIE). Nat Biotechnol 2008 3.43
2 Wnt3a plays a major role in the segmentation clock controlling somitogenesis. Dev Cell 2003 3.15
3 The tissue-specific lncRNA Fendrr is an essential regulator of heart and body wall development in the mouse. Dev Cell 2013 3.14
4 A gene expression map of human chromosome 21 orthologues in the mouse. Nature 2002 2.76
5 Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis. PLoS One 2010 2.10
6 The t complex-encoded GTPase-activating protein Tagap1 acts as a transmission ratio distorter in mice. Nat Genet 2005 1.87
7 WNT signaling, in synergy with T/TBX6, controls Notch signaling by regulating Dll1 expression in the presomitic mesoderm of mouse embryos. Genes Dev 2004 1.74
8 Segmentation in vertebrates: clock and gradient finally joined. Genes Dev 2004 1.52
9 Multiple roles for neurofibromin in skeletal development and growth. Hum Mol Genet 2007 1.29
10 The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation. Genes Dev 2004 1.17
11 Expression of Msgn1 in the presomitic mesoderm is controlled by synergism of WNT signalling and Tbx6. EMBO Rep 2007 1.17
12 DNA-methylome analysis of mouse intestinal adenoma identifies a tumour-specific signature that is partly conserved in human colon cancer. PLoS Genet 2013 1.13
13 The t-complex-encoded guanine nucleotide exchange factor Fgd2 reveals that two opposing signaling pathways promote transmission ratio distortion in the mouse. Genes Dev 2007 1.06
14 Wnt and BMP signals control intestinal adenoma cell fates. Int J Cancer 2012 0.98
15 An inducible RNA interference system for the functional dissection of mouse embryogenesis. Nucleic Acids Res 2010 0.95
16 In vivo knockdown of Brachyury results in skeletal defects and urorectal malformations resembling caudal regression syndrome. Dev Biol 2012 0.88
17 Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract. Hum Genet 2015 0.84
18 Retention of gene products in syncytial spermatids promotes non-Mendelian inheritance as revealed by the t complex responder. Genes Dev 2009 0.84
19 Cloning and expression of the mouse dual-specificity mitogen-activated protein (MAP) kinase phosphatase Mkp3 during mouse embryogenesis. Mech Dev 2002 0.84
20 De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association. Eur J Hum Genet 2013 0.84
21 Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region. Birth Defects Res A Clin Mol Teratol 2014 0.83
22 An RNA interference phenotypic screen identifies a role for FGF signals in colon cancer progression. PLoS One 2011 0.83
23 The nucleoside diphosphate kinase gene Nme3 acts as quantitative trait locus promoting non-Mendelian inheritance. PLoS Genet 2012 0.82
24 Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12. Birth Defects Res A Clin Mol Teratol 2013 0.81