L Side

Author PubWeight™ 7.60^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation.	Am J Hum Genet	2006	2.23
2	SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype.	J Med Genet	2009	1.32
3	Outcome of risk-reducing salpingo-oophorectomy in BRCA carriers and women of unknown mutation status.	BJOG	2011	1.23
4	Factors influencing uptake and timing of risk reducing salpingo-oophorectomy in women at risk of familial ovarian cancer: a competing risk time to event analysis.	BJOG	2012	0.86
5	Population-based, risk-stratified genetic testing for ovarian cancer risk: a focus group study.	Public Health Genomics	2013	0.81
6	Intramedullary tumours in patients with neurofibromatosis type 2: MRI features associated with a favourable prognosis.	Clin Radiol	2007	0.76
7	Varicella-zoster vaccination for health care workers.	Lancet	1994	0.75