Moritz Meins

Author PubWeight™ 7.82^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.	Hum Mol Genet	2008	1.58
2	Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2).	BMC Med Genet	2006	1.31
3	A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?	Eur Neurol	2003	0.88
4	Mice deficient for RNA-binding protein brunol1 show reduction of spermatogenesis but are fertile.	Mol Reprod Dev	2007	0.88
5	Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease.	J Neurol	2003	0.83
6	Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10.	Hum Mutat	2003	0.80
7	Electrophoresis of DNA in human genetic diagnostics - state-of-the-art, alternatives and future prospects.	Electrophoresis	2006	0.80
8	Severe Guillain-Barré syndrome associated with chromosome 17p11.2-12 duplication.	Muscle Nerve	2008	0.75