|
1
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Clinical and genetic aspects of craniofrontonasal syndrome: towards resolving a genetic paradox.
|
Mol Genet Metab
|
2005
|
1.14
|
|
2
|
The impact of CFNS-causing EFNB1 mutations on ephrin-B1 function.
|
BMC Med Genet
|
2010
|
0.93
|
|
3
|
Loss of heterozygosity on chromosome 5p13-12 predicts adverse prognosis in advanced bladder cancer independent of tumor stage and grade.
|
J Urol
|
2002
|
0.85
|
|
4
|
INTS6/DICE1 inhibits growth of human androgen-independent prostate cancer cells by altering the cell cycle profile and Wnt signaling.
|
Cancer Cell Int
|
2009
|
0.84
|
|
5
|
Clinical and genetic evaluation of patients with KATP channel mutations from the German registry for congenital hyperinsulinism.
|
Horm Res Paediatr
|
2014
|
0.83
|
|
6
|
Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer.
|
Oncogene
|
2005
|
0.83
|
|
7
|
Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype.
|
Am J Med Genet A
|
2013
|
0.82
|
|
8
|
Molecular interactions of B-CAM (basal-cell adhesion molecule) and laminin in epithelial skin cancer.
|
Arch Dermatol Res
|
2004
|
0.80
|
|
9
|
The heterozygous LMNA mutation p.R471G causes a variable phenotype with features of two types of familial partial lipodystrophy.
|
Am J Med Genet A
|
2007
|
0.79
|
|
10
|
A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation.
|
Neurogenetics
|
2005
|
0.77
|
|
11
|
Remission of congenital hyperinsulinism following conservative treatment: an exploratory study in patients with KATP channel mutations.
|
J Pediatr Endocrinol Metab
|
2016
|
0.76
|
|
12
|
Greig cephalopolysyndactyly (GCPS) contiguous gene syndrome in a boy with a 14 Mb deletion in region 7p13-14 caused by a paternal balanced insertion (5; 7).
|
Appl Clin Genet
|
2008
|
0.75
|
|
13
|
Genetic Variants of DICE1/INTS6 in German Prostate Cancer Families with Linkage to 13q14.
|
Urol Int
|
2015
|
0.75
|
|
14
|
Craniofrontonasal Syndrome: Atrial Septal Defect With a Novel EFNB1 Gene Mutation.
|
Cleft Palate Craniofac J
|
2014
|
0.75
|