S P Robertson
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Explore the profile of S P Robertson including associated specialties, affiliations and a list of published articles.
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Articles
37
Citations
739
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Recent Articles
1.
Halliday B, Baynam G, Ewans L, Greenhalgh L, Leventer R, Pilz D, et al.
AJNR Am J Neuroradiol
. 2022 Oct;
43(11):1660-1666.
PMID: 36229163
Background And Purpose: Zhu-Tokita-Takenouchi-Kim syndrome is a severe multisystem malformation disorder characterized by developmental delay and a diverse array of congenital abnormalities. However, these currently identified phenotypic components provide limited...
2.
Narang A, Trieu J, Radwan N, Ram A, Robertson S, He P, et al.
Prostate Cancer Prostatic Dis
. 2017 Jan;
20(2):203-209.
PMID: 28094250
Background: In men undergoing definitive radiation for prostate cancer, it is unclear whether early biochemical response can provide additional prognostic value beyond pre-treatment risk stratification. Methods: Prostate cancer patients consecutively...
3.
Glendining K, Markie D, Gardner R, Franz E, Robertson S, Jasoni C
Sci Rep
. 2017 Jan;
7:39823.
PMID: 28057929
Mutations in RAD51 have recently been linked to human Congenital Mirror Movements (CMM), a developmental disorder of the motor system. The only gene previously linked to CMM encodes the Netrin-1...
4.
Shalev I, Moffitt T, Braithwaite A, Danese A, Fleming N, Goldman-Mellor S, et al.
Mol Psychiatry
. 2014 Jan;
19(11):1163-70.
PMID: 24419039
There is evidence that persistent psychiatric disorders lead to age-related disease and premature mortality. Telomere length has emerged as a promising biomarker in studies that test the hypothesis that internalizing...
5.
Petit F, Escande F, Jourdain A, Porchet N, Amiel J, Doray B, et al.
Clin Genet
. 2013 Sep;
86(3):246-51.
PMID: 24003905
Nager syndrome belongs to the group of acrofacial dysostosis, which are characterized by the association of craniofacial and limb malformations. Recently, exome sequencing studies identified the SF3B4 gene as the...
6.
Holman S, Morgan T, Baujat G, Cormier-Daire V, Cho T, Lees M, et al.
Clin Genet
. 2012 Jun;
83(3):251-6.
PMID: 22670894
Osteopathia striata congenita with cranial sclerosis (OSCS) is a skeletal dysplasia caused by germline deletions of or truncating point mutations in the X-linked gene WTX (FAM123B, AMER1). Females present with...
7.
Foley C, Roberts K, Tchrakian N, Morgan T, Fryer A, Robertson S, et al.
Mol Syndromol
. 2010 Oct;
1(3):121-126.
PMID: 21031081
Melnick-Needles syndrome (MNS) is a rare X-linked bone dysplasia characterised by facial dysmorphology and radiographic abnormalities [Melnick and Needles, 1966;97:39-48]. Previously, all published cases of MNS were associated with only...
8.
van Kogelenberg M, Ghedia S, McGillivray G, Bruno D, Leventer R, Macdermot K, et al.
Mol Syndromol
. 2010 Jul;
1(1):35-41.
PMID: 20648244
Periventricular heterotopia (PH) is a brain malformation characterised by heterotopic nodules of neurons lining the walls of the cerebral ventricles. Mutations in FLNA account for 20-24% of instances but a...
9.
10.
Robertson S, Hull L, Calvin D
J Econ Entomol
. 2005 Sep;
98(4):1229-35.
PMID: 16156575
Sixteen years of archived tufted apple bud moth, Platynota idaeusalis (Walker), trap capture data were compared with archived fruit injury data collected at the Penn State University Fruit Research and...