J Sowden

Author PubWeight™ 6.55^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.	Nat Genet	2000	2.87
2	The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27.	Genome Res	1996	1.13
3	The caudal-type homeobox protein Cdx-2 binds to the colon promoter of the carbonic anhydrase 1 gene.	Eur J Biochem	1996	0.94
4	Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida.	Hum Mol Genet	1996	0.88
5	Colon carbonic anhydrase 1: transactivation of gene expression by the homeodomain protein Cdx2.	FEBS Lett	1998	0.84
6	Regulation of the CA1, CA2 and CA3 genes.	EXS	2000	0.75
7	Basal cell carcinoma masquerading as habit tic.	Clin Exp Dermatol	2011	0.75
8	Malignant melanoma arising in the scar of lupus vulgaris and response to treatment with topical azelaic acid.	Clin Exp Dermatol	1988	0.75