Katherine Rose Smith
Katherine Rose Smith
Verified email at astrazeneca.com
Title
Cited by
Cited by
Year
Whole-body hypothermia for term and near-term newborns with hypoxic-ischemic encephalopathy: a randomized controlled trial
SE Jacobs, CJ Morley, TE Inder, MJ Stewart, KR Smith, PJ McNamara, ...
Archives of Pediatrics and Adolescent Medicine 165 (8), 692, 2011
5552011
Preschooler obesity and parenting styles of mothers and fathers: Australian national population study
M Wake, JM Nicholson, P Hardy, K Smith
Pediatrics 120 (6), e1520-e1527, 2007
3912007
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage
KR Smith, J Damiano, S Franceschetti, S Carpenter, L Canafoglia, ...
The American Journal of Human Genetics 90 (6), 1102-1107, 2012
3732012
DNA methylation analysis of multiple tissues from newborn twins reveals both genetic and intrauterine components to variation in the human neonatal epigenome
M Ollikainen, KR Smith, EJH Joo, HK Ng, R Andronikos, B Novakovic, ...
Human molecular genetics 19 (21), 4176, 2010
3152010
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy
SE Heron, KR Smith, M Bahlo, L Nobili, E Kahana, L Licchetta, KL Oliver, ...
Nature Genetics 44 (11), 1188-1190, 2012
2912012
Prospects for epigenetic epidemiology
DL Foley, JM Craig, R Morley, CJ Olsson, T Dwyer, K Smith, R Saffery
American journal of epidemiology 169 (4), 389-400, 2009
2752009
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
C Turnbull, RH Scott, E Thomas, L Jones, N Murugaesu, FB Pretty, ...
Bmj 361, 2018
2212018
The prevalence of hypoxaemia among ill children in developing countries: a systematic review
R Subhi, M Adamson, H Campbell, M Weber, K Smith, T Duke
The Lancet infectious diseases 9 (4), 219-227, 2009
1862009
Pharyngeal pressure with high-flow nasal cannulae in premature infants
DJ Wilkinson, CC Andersen, K Smith, J Holberton
Journal of Perinatology 28 (1), 42-47, 2007
1552007
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6
T Arsov, KR Smith, J Damiano, S Franceschetti, L Canafoglia, ...
The American Journal of Human Genetics, 2011
1482011
Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features
D Lessel, B Vaz, S Halder, PJ Lockhart, I Marinovic-Terzic, ...
Nature genetics 46 (11), 1239-1244, 2014
1402014
Proximal femoral geometry in cerebral palsy: a population-based cross sectional study
J Robin, K Graham, P Selber, F Dobson, K Smith, R Baker
Developmental Medicine & Child Neurology 51, 6, 2009
1342009
IV acetaminophen pharmacokinetics in neonates after multiple doses
GM Palmer, M Atkins, BJ Anderson, KR Smith, TJ Culnane, CM McNally, ...
British journal of anaesthesia 101 (4), 523, 2008
1342008
Proximal femoral geometry in cerebral palsy: a population-based cross-sectional study
J Robin, HK Graham, P Selber, F Dobson, K Smith, R Baker
Journal of Bone and Joint Surgery-British Volume 90 (10), 1372, 2008
1332008
Proximal femoral geometry in cerebral palsy
HK Graham, K Smith, R Baker, P Selber, F Dobson, J Robin
United Kingdom: British Editorial Society of Bone and Joint Surgery,, 2008
133*2008
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis
KR Smith, HHM Dahl, L Canafoglia, E Andermann, J Damiano, M Morbin, ...
Human molecular genetics 22 (7), 1417-1423, 2013
1162013
Prenatal probiotic administration can influence Bifidobacterium microbiota development in infants at high risk of allergy
SJ Lahtinen, RJ Boyle, S Kivivuori, F Oppedisano, KR Smith, ...
Journal of Allergy and Clinical Immunology 123 (2), 499-501. e8, 2009
1082009
Germline selection shapes human mitochondrial DNA diversity
W Wei, S Tuna, MJ Keogh, KR Smith, TJ Aitman, PL Beales, DL Bennett, ...
Science 364 (6442), eaau6520, 2019
902019
Systemic adverse events following botulinum toxin A therapy in children with cerebral palsy
K NAIDU, K SMITH, M SHEEDY, B ADAIR, X YU, HK GRAHAM
Developmental Medicine & Child Neurology 52 (2), 139-144, 2010
892010
Reducing the exome search space for Mendelian diseases using genetic linkage analysis of exome genotypes
KR Smith, CJ Bromhead, MS Hildebrand, AE Shearer, PJ Lockhart, ...
Genome Biology 12 (9), R85, 2011
882011
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