Kristina Gervin

Author PubWeight™ 8.92^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease.	Eur J Hum Genet	2008	1.10
2	Limitations and possibilities of low cell number ChIP-seq.	BMC Genomics	2012	1.09
3	Multiple loci in the HLA complex are associated with Addison's disease.	J Clin Endocrinol Metab	2011	0.94
4	T cell-specific T-box transcription factor haplotype is associated with allergic asthma in children.	J Allergy Clin Immunol	2007	0.91
5	A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult.	Hum Mol Genet	2012	0.87
6	CD14 polymorphisms and serum CD14 levels through childhood: a role for gene methylation?	J Allergy Clin Immunol	2010	0.85
7	The Norwegian Twin Registry from a public health perspective: a research update.	Twin Res Hum Genet	2012	0.84
8	Rapid and efficient FBN1 mutation detection using automated sample preparation and direct sequencing as the primary strategy.	Genet Test	2006	0.83
9	X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene.	J Clin Endocrinol Metab	2009	0.81
10	Pet keeping and tobacco exposure influence CD14 methylation in childhood.	Pediatr Allergy Immunol	2012	0.79