Robert D Nicholls

Author PubWeight™ 27.41^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences.	Nature	2007	7.91
2	Development of type 2 diabetes following intrauterine growth retardation in rats is associated with progressive epigenetic silencing of Pdx1.	J Clin Invest	2008	3.02
3	The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing.	Hum Mol Genet	2010	1.83
4	Possible genomic imprinting of three human obesity-related genetic loci.	Am J Hum Genet	2005	1.54
5	NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).	Am J Hum Genet	2003	1.54
6	Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models.	Mamm Genome	2005	1.22
7	Recent assembly of an imprinted domain from non-imprinted components.	PLoS Genet	2006	1.17
8	The putatively functional Mkrn1-p1 pseudogene is neither expressed nor imprinted, nor does it regulate its source gene in trans.	Proc Natl Acad Sci U S A	2006	1.15
9	Recommendations for the investigation of animal models of Prader-Willi syndrome.	Mamm Genome	2013	1.01
10	Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus.	Nucleic Acids Res	2005	1.00
11	The gene encoding the fragile X RNA-binding protein is controlled by nuclear respiratory factor 2 and the CREB family of transcription factors.	Nucleic Acids Res	2006	0.87
12	In vivo evolution of tumor-derived endothelial cells.	PLoS One	2012	0.86
13	A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.	Genomics	2005	0.86
14	Genetic mapping of putative Chrna7 and Luzp2 neuronal transcriptional enhancers due to impact of a transgene-insertion and 6.8 Mb deletion in a mouse model of Prader-Willi and Angelman syndromes.	BMC Genomics	2005	0.85
15	Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia.	PLoS One	2012	0.83
16	Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome.	Am J Physiol Endocrinol Metab	2011	0.80
17	What have rare genetic syndromes taught us about the pathophysiology of the common forms of obesity?	Curr Diab Rep	2004	0.79
18	Anorexigenic melanocortin signaling in the hypothalamus is augmented in association with failure-to-thrive in a transgenic mouse model for Prader-Willi syndrome.	Brain Res	2002	0.77
19	Physical mapping of the pink-eyed dilution complex in mouse chromosome 7 shows that Atp10c is the only transcript between Gabrb3 and Ube3a.	DNA Seq	2004	0.75