|
1
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Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.
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Pediatrics
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2004
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1.81
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2
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Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?
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J Autism Dev Disord
|
2004
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1.14
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3
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Autism Genetic Database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites.
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BMC Med Genet
|
2009
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1.11
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4
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snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions.
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Gene
|
2007
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1.07
|
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5
|
Genetic studies of complex human diseases: characterizing SNP-disease associations using Bayesian networks.
|
BMC Syst Biol
|
2012
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1.00
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6
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Plasma peptide YY and ghrelin levels in infants and children with Prader-Willi syndrome.
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J Pediatr Endocrinol Metab
|
2004
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0.98
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7
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Body composition and fatness patterns in Prader-Willi syndrome: comparison with simple obesity.
|
Obesity (Silver Spring)
|
2006
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0.96
|
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8
|
Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.
|
Genomics
|
2005
|
0.93
|
|
9
|
X-chromosome inactivation patterns in females with Prader-Willi syndrome.
|
Am J Med Genet A
|
2007
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0.91
|
|
10
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DFNA2/KCNQ4 and its manifestations.
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Adv Otorhinolaryngol
|
2002
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0.90
|
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11
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FEPI-MB: identifying SNPs-disease association using a Markov Blanket-based approach.
|
BMC Bioinformatics
|
2011
|
0.85
|