E A Janssen

Author PubWeight™ 8.44^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.	Am J Hum Genet	1997	1.37
2	De-novo mutation in hereditary motor and sensory neuropathy type I.	Lancet	1992	1.30
3	X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060).	J Inherit Metab Dis	1999	1.29
4	Trypsin in colorectal cancer: molecular biological mechanisms of proliferation, invasion, and metastasis.	J Pathol	2006	1.13
5	Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb region.	Hum Mol Genet	1996	0.95
6	The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2.	Hum Genet	1991	0.93
7	Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a).	Neurology	1993	0.84
8	Quantitative measurement of duplicated DNA as a diagnostic test for Charcot-Marie-Tooth disease type 1a.	Clin Chem	1993	0.83
9	Transepidermal water vapour loss is not increased during and following dithranol irritation.	Br J Dermatol	1995	0.75