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Author Details
Full Name
Ruth Jamieson
Affiliation
Newcastle University
ORCID
Career Start Year
1992
Papers
12
H Index
10
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
28393292
Comparisons of the Factor Structure and Measurement Invariance of the Spence Children's Anxiety Scale-Parent Version in Children with Autism Spectrum Disorder and Typically Developing Anxious Children.
J Autism Dev Disord
2017
21851754
Individual therapy attrition rates in a low-intensity service: a comparison of cognitive behavioural and person-centred therapies and the impact of deprivation.
Behav Cogn Psychother
2012
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
11067780
Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32.
Am J Hum Genet
2000
11135492
Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
Ophthalmic Genet
2000
10521316
Primary autosomal recessive microcephaly: homozygosity mapping of MCPH4 to chromosome 15.
Am J Hum Genet
1999
10636744
Clinical and molecular findings in a patient with a deletion on the long arm of chromosome 12.
J Med Genet
1999
9312674
Molecular basis of the long-QT syndrome.
N Engl J Med
1997
9412792
Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12.
Eur J Hum Genet
1997
7894486
Mapping a gene for Noonan syndrome to the long arm of chromosome 12.
Nat Genet
1994
1346223
Long QT and Harvey-ras.
Lancet
1992
1 - 12 of 12
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