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Stanier P
Stanier P
UCL Institute of Child Health
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Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse
JA Curtin, E Quint, V Tsipouri, RM Arkell, B Cattanach, AJ Copp, ...
Current Biology 13 (13), 1129-1133, 2003
7102003
Neural tube defects: recent advances, unsolved questions, and controversies
AJ Copp, P Stanier, NDE Greene
The Lancet Neurology 12 (8), 799-810, 2013
6692013
Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts
P Stanier, GE Moore
Human molecular genetics 13 (suppl_1), R73-R81, 2004
6152004
Genetics of human neural tube defects
NDE Greene, P Stanier, AJ Copp
Human molecular genetics 18 (R2), R113-R129, 2009
4222009
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands
X Estivill, M Farrall, PJ Scambler, GM Bell, KMF Hawley, NJ Lench, ...
Nature 326 (6116), 840-845, 1987
4101987
Simple non-invasive method to obtain DNA for gene analysis
N Lench, P Stanier, R Williamson
The Lancet 331 (8599), 1356-1358, 1988
3881988
Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification
JN Murdoch, K Doudney, C Paternotte, AJ Copp, P Stanier
Human molecular genetics 10 (22), 2593-2601, 2001
3682001
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse
JN Murdoch, DJ Henderson, K Doudney, C Gaston-Massuet, HM Phillips, ...
Human molecular genetics 12 (2), 87-98, 2003
3482003
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia
C Braybrook, K Doudney, ACB Marçano, A Arnason, A Bjornsson, ...
Nature genetics 29 (2), 179-183, 2001
3472001
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRAS
VA Kinsler, AC Thomas, M Ishida, NW Bulstrode, S Loughlin, S Hing, ...
Journal of Investigative Dermatology 133 (9), 2229-2236, 2013
3142013
Limited evolutionary conservation of imprinting in the human placenta
D Monk, P Arnaud, S Apostolidou, FA Hills, G Kelsey, P Stanier, R Feil, ...
Proceedings of the National Academy of Sciences 103 (17), 6623-6628, 2006
2962006
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome
C Rooryck, A Diaz-Font, DPS Osborn, E Chabchoub, ...
Nature genetics 43 (3), 197-203, 2011
2632011
The genetic aetiology of Silver–Russell syndrome
S Abu-Amero, D Monk, J Frost, M Preece, P Stanier, GE Moore
Journal of medical genetics 45 (4), 193-199, 2008
2292008
Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis
A Robinson, S Escuin, K Doudney, M Vekemans, RE Stevenson, ...
Human mutation 33 (2), 440-447, 2012
2102012
Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark
P Arnaud, D Monk, M Hitchins, E Gordon, W Dean, CV Beechey, J Peters, ...
Human molecular genetics 12 (9), 1005-1019, 2003
1782003
Genetics of cleft lip and/or cleft palate: association with other common anomalies
N Setó-Salvia, P Stanier
European journal of medical genetics 57 (8), 381-393, 2014
1752014
Maternal uniparental disomy 7 in Silver-Russell syndrome.
MA Preece, SM Price, V Davies, L Clough, P Stanier, RC Trembath, ...
Journal of medical genetics 34 (1), 6-9, 1997
1751997
Duplication of 7p11. 2-p13, including GRB10, in Silver-Russell syndrome
D Monk, EL Wakeling, V Proud, M Hitchins, SN Abu-Amero, P Stanier, ...
The American Journal of Human Genetics 66 (1), 36-46, 2000
1722000
Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight
S Apostolidou, S Abu-Amero, K O’donoghue, J Frost, O Olafsdottir, ...
Journal of molecular medicine 85, 379-387, 2007
1712007
Persistence of cytomegalovirus in mononuclear cells in peripheral blood from blood donors.
P Stanier, DL Taylor, AD Kitchen, N Wales, Y Tryhorn, AS Tyms
BMJ: British Medical Journal 299 (6704), 897, 1989
1701989
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