|
1
|
Ensembl's 10th year.
|
Nucleic Acids Res
|
2009
|
10.82
|
|
2
|
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
|
Nat Genet
|
2009
|
8.30
|
|
3
|
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
|
Nat Genet
|
2007
|
2.35
|
|
4
|
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.
|
Am J Hum Genet
|
2007
|
2.07
|
|
5
|
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment.
|
Nat Genet
|
2008
|
1.95
|
|
6
|
Outcomes in patients who underwent both laparoscopic and open inguinal hernia repairs.
|
ANZ J Surg
|
2010
|
1.37
|
|
7
|
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.
|
Am J Hum Genet
|
2007
|
1.26
|
|
8
|
Assessment of cosmetic outcome after laparoscopic cholecystectomy among women 4 years after laparoscopic cholecystectomy: is there a problem?
|
Surg Endosc
|
2011
|
1.12
|
|
9
|
Laparoscopic Heller's myotomy for achalasia after gastric bypass: A case report.
|
Int J Surg Case Rep
|
2013
|
0.88
|
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10
|
Death of a proverb.
|
BMJ
|
2015
|
0.75
|