UCL School of Life and Medical Sciences

2013

• Moore GE, Stanier P (2013). Fat dads must not be blamed for their children's health problems.. BMC Med, 11, 30 - . doi:10.1186/1741-7015-11-30
• Pauws E, Peskett E, Boissin C, Hoshino A, Mengrelis K, Carta E, Abruzzo MA, Lees M, Moore GE, Erickson RP, Stanier P (2013). X-linked CHARGE-like Abruzzo-Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations.. Clin Genet, 83(4), 352 - 358. doi:10.1111/j.1399-0004.2012.01930.x
• Kinsler VA, Thomas AC, Ishida M, Bulstrode NW, Loughlin S, Hing S, Chalker J, McKenzie K, Abu-Amero S, Slater O, Chanudet E, Palmer R, Morrogh D, Stanier P, Healy E, Sebire NJ, Moore GE (2013). Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS.. J Invest Dermatol, , - . doi:10.1038/jid.2013.70

2012

• Kinsler VA, Thomas AC, Ishida M, Bulstrode NW, Loughlin S, Hing S, Chalker J, Mckenzie K, Abu-Amero S, Slater O, Chanudet E, Palmer R, Morrogh D, Stanier P, Healy E, Sebire NJ, Moore GE (2012). Multiple congenital melanocytic naevi and neurocutaneous melanosis are caused by mosaicism for NRAS codon 61 mutations, leading to an increased risk of melanoma in affected tissues.
• Thomas AC, Frost JM, Ishida M, Vargha-Khadem F, Moore GE, Stanier P (2012). The speech gene FOXP2 is not imprinted.. J Med Genet, 49(11), 669 - 670. doi:10.1136/jmedgenet-2012-101242
• Kinsler V, Abu-Amero S, Budd P, Jackson I, Stanier P, Hennekam R, Sebire N, Moore G, Healy E (2012). Association between melanocortin-1-receptor (MC1R) genotype and phenotype of congenital melanocytic naevi reveals a wider role for MC1R in utero.
• Kinsler VA, Abu-Amero S, Budd P, Jackson IJ, Ring SM, Northstone K, Atherton DJ, Bulstrode NW, Stanier P, Hennekam RC, Sebire NJ, Moore GE, Healy E (2012). Germline melanocortin-1-receptor genotype is associated with severity of cutaneous phenotype in congenital melanocytic nevi: a role for MC1R in human fetal development.. Journal of Investigative Dermatology, doi: 10.1038/jid.2012.95. [Epub ahead of print], - .
• Robinson A, Escuin S, Doudney K, Vekemans M, Stevenson RE, Greene ND, Copp AJ, Stanier P (2012). Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis.. Hum Mutat, 33(2), 440 - 447. doi:10.1002/humu.21662
• Carta E, Pauws E, Thomas AC, Mengrelis K, Moore GE, Lees M, Stanier P (2012). Investigation of SUMO pathway genes in the etiology of nonsyndromic cleft lip with or without cleft palate.. Birth Defects Res A Clin Mol Teratol, 94(6), 459 - 463. doi:10.1002/bdra.23008
• Ishida M, Monk D, Duncan AJ, Abu-Amero S, Chong J, Ring SM, Pembrey ME, Hindmarsh PC, Whittaker JC, Stanier P, Moore GE (2012). Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight. American Journal of Human Genetics, 90(4), 715 - 719.
• Narisawa A, Komatsuzaki S, Kikuchi A, Niihori T, Aoki Y, Fujiwara K, Tanemura M, Hata A, Suzuki Y, Relton CL, Grinham J, Leung K-Y, Partridge D, Robinson A, Stone V, Gustavsson P, Stanier P, Copp AJ, Greene NDE, Tominaga T, Matsubara Y, Kure S (2012). Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans. Human Molecular Genetics, 21(7), 1496 - 1503.
• Stanier P, Pauws E (2012). Development of the lip and palate: FGF signalling.. In (Ed.), (pp. 71 - 80). : . doi:10.1159/000337618

2011

• Ishida M, Monk D, Duncan A, Abu-Amero S, Chong J, Ring S, Pembrey M, Hindmarsh P, Whittaker J, Stanier P, Moore GE (2011). Inheritance of a copy number variant in the imprinted PHLDA2 gene promoter significantly increases fetal birth weight.
• Kinsler V, Hennekam R, Sebire N, Abu-Amero S, Stanier P, Budd P, Jackson I, Moore G, Healy E (2011). Germline melanocortin-1 receptor variants are associated with severity of phenotype in individuals with congenital melanocytic naevi.
• Frost J, Monk D, Moschidou D, Guillot PV, Stanier P, Minger SL, Fisk NM, Moore HD, Moore GE (2011). The effects of culture on genomic imprinting profiles in human embryonic and fetal mesenchymal stem cells.. Epigenetics, 6(1), 52 - 62. doi:10.4161/epi.6.1.13361
• Kantaputra PN, Paramee M, Kaewkhampa A, Hoshino A, Lees M, McEntagart M, Masrour N, Moore GE, Pauws E, Stanier P (2011). Cleft lip with cleft palate, ankyloglossia, and hypodontia are associated with TBX22 mutations.. J Dent Res, 90(4), 450 - 455. doi:10.1177/0022034510391052
• Rooryck C, Diaz-Font A, Osborn DP, Chabchoub E, Hernandez-Hernandez V, Shamseldin H, Kenny J, Waters A, Jenkins D, Kaissi AA, Leal GF, Dallapiccola B, Carnevale F, Bitner-Glindzicz M, Lees M, Hennekam R, Stanier P, Burns AJ, Peeters H, Alkuraya FS, Beales PL (2011). Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome.. Nat Genet, 43(3), 197 - 203. doi:10.1038/ng.757
• GREENE N, Stanier P, Moore GE (2011). The emerging role of epigenetic mechanisms in the aetiology of neural tube defects.. Epigenetics, 6, 875 - 883.

2010

• Kinsler V, Hennekam R, Sebire N, Abu-Amero S, Stanier P, Budd P, Jackson I, Moore G, Healy E (2010). Germline melanocortin-1-receptor variants are associated with severity of phenotype in individuals with congenital melanocytic naevi.
• Frost JM, Monk D, Stojilkovic-Mikic T, Woodfine K, Chitty LS, Murrell A, Stanier P, Moore GE (2010). Evaluation of allelic expression of imprinted genes in adult human blood.. PLoS One, 5(10), e13556 - . doi:10.1371/journal.pone.0013556
• Robinson A, Doudney K, Greene NDE, Stanier P, Copp AJ (2010). Identification of putative neural tube defect-causing mutations in planar cell polarity genes.
• Abu-Amero S, Wakeling EL, Preece M, Whittaker J, Stanier P, Moore GE (2010). Epigenetic signatures of Silver Russell syndrome. Journal of Medical Genetics, 47(3), 150 - 154.
• Acevedo AC, da Fonseca JAC, Grinham J, Doudney K, Gomes RR, de Paula LM, Stanier P (2010). Autosomal-dominant Ankyloglossia and Tooth Number Anomalies. J DENT RES, 89(2), 128 - 132. doi:10.1177/0022034509356401
• Daelemans C, Ritchie ME, Smits G, Abu-Amero S, Sudbery IM, Forrest MS, Campino S, Clark TG, Stanier P, Kwiatkowski D, Deloukas P, Dermitzakis ET, Tavaré S, Moore GE, Dunham I (2010). High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.. BMC Genet, 11, 25 - . doi:10.1186/1471-2156-11-25

2009

• Pauws E, Hoshino A, Bentley L, Prajapati S, Keller C, Hammond P, Martinez-Barbera JP, Moore GE, Stanier P (2009). Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes.. Hum Mol Genet, 18(21), 4171 - 4179. doi:10.1093/hmg/ddp368
• Greene ND, Stanier P, Copp AJ (2009). Genetics of human neural tube defects. Human Molecular Genetics, 18, R113 - R129.
• Daelemans C, Ritchie ME, Abu-Amero S, Sudbery IM, Stanier P, Forrest MS, Deloukas P, Tavare S, Moore GE, Dunham I (2009). Assessment of candidate imprinted genes in the human term placenta.
• Monk D, Arnaud P, Frost J, Hills FA, Stanier P, Feil R, Moore GE (2009). Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression. Human Molecular Genetics, 18(16), 3066 - 3074.
• Pauws E, Stanier P (2009). Sumoylation in craniofacial disorders. In Wilson V (Ed.), SUMO Regulation of Cellular Processes (pp. - ). : Springer Publishing.
• Pauws E, Hoshino A, Bentley L, Prajapati S, Keller C, Martinez-Barbera JP, Moore GE, Stanier P (2009). Loss of Tbx22 causes submucous cleft palate, ankyloglossia and choanal atresia.
• Doudney K, Grinham J, Whittaker J, Lynch SA, Thompson D, Moore GE, Copp AJ, Greene ND, Stanier P (2009). Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defects.. American Journal of Medical Genetics Part A, 149A(7), 1585 - 1589.
• Pauws E, Stanier P (2009). Loss of Tbx22 causes submucous cleft palate and ankyloglossia.
• Daelemans C, Ritchie M, Abu-Amero S, Susbury IM, Stanier P, Forrest MS, Deloukas P, Tavare S, Moore GE, Dunham I (2009). Assessment of candidate imprinted genes in the human term placenta.
• Pauws E, Moore GE, Stanier P (2009). A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia.. Journal of Medical Genetics, 46(8), 555 - 561.

2008

• Abu-Amero S, Monk D, Frost J, Preece M, Stanier P, Moore G (2008). The genetic aetiology of Silver-Russell syndrome1. Journal of Medical Genetics, 45(4), 193 - 199.
• Liu W, Lan Y, Pauws E, Meester-Smoor MA, Stanier P, Zwarthoff EC, Jiang R (2008). The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice.. Development, 135(23), 3959 - 3968.
• Pauws E, Stanier P (2008). TBX22 and X-linked cleft palate and ankyloglossia. In Epstein CG, Erickson RP, Wynshaw-Boris A (Ed.), Inborn Errors of Development (pp. 878 - 882). : Oxford University Press.
• Monk D, Wagschal A, Arnaud P, Iglelias-Platas I, Muller P, Parker-Katiraee L, Bourc his D, Scherer SW, Stanier P, Moore GE (2008). Evolutionary comparison of epigenetic profiles at large imprinted domains reveals differing mechanisms of allelic silencing.
• Monk D, Wagschal A, Arnaud P, Muller PS, Parker-Katiraee L, Bourc'his D, Scherer SW, Feil R, Stanier P, Moore GE (2008). Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing. Genome Research, 18(8), 1270 - 1281.

2007

• Pauws E, Stanier P (2007). FGF signalling and SUMO modification: new players in the aetiology of cleft lip and/or palate2. Trends Genet., 23(12), 631 - 640.
• Gustavsson P, Greene NDE, Lad D, Pauws E, de Castro SC, Stanier P, Copp AJ (2007). Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model. Human Molecular Genetics, 16(21), 2640 - 2646. doi:10.1093/hmg/ddm221
• Andreou AM, Pauws E, Jones MC, Singh MK, Bussen M, Doudney K, Moore GE, Kispert A, Brosens JJ, Stanier P (2007). TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression. The American Journal of Human Genetics, 81(4), 700 - 712. doi:10.1086/521033
• Apostolidou S, Abu-Amero S, O Donoghue K, Frost J, Olofsdottir O, Chavele KM, Whittaker JC, Loughna P, Stanier P, Moore GE (2007). Elevated maternal expression of the imprinted PHLDA2 gene is associated with low birth weight.. Journal of Molecular Medicine, 85(4), 379 - 387.
• Pauws E, Andreou A, Moore GE, Stanier P (2007). Characterisation and regulation of the human TBX22 promoter.
• Dunlevy LP, Chitty LS, Burren KA, Doudney K, Stojilkovic-Mikic T, Stanier P, Scott R, Copp AJ, Greene ND (2007). Abnormal folate metabolism in foetuses affected by neural tube defects. Brain, 130(Pt 4), 1043 - 1049. doi:10.1093/brain/awm028
• Iglesias-Platas I, Monk D, Jebbink J, Buimer M, Boer K, van der Post J, Hills F, Apostolidou S, Ris-Stalpers C, Stanier P, Moore GE (2007). STOX1 is not imprinted and is not likely to be involved in preeclampsia.. Nat Genet, 39(3), 279 - 280. doi:10.1038/ng0307-279
• Abu-Amero S, Apostolidou S, O'Donaghue K, Frost J, Olafsdottir O, Chavele K, Whittaker J, Loughna P, Stanier P, Moore G (2007). Elevated maternal expression of the imprinted PHLDA2 gene is associated with low birth weight.

2006

• Apostolidou S, bu-Amero S, O 'donoghue K, Frost J, Olafsdottir O, Chavele KM, Whittaker JC, Loughna P, Stanier P, Moore GE (2006). Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight.
• Zhou H, Brockington M, Jungbluth H, Monk D, Stanier P, Sewry CA, Moore GE, Muntoni F (2006). Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies. The American Journal of Human Genetics, 79(5), 859 - 868. doi:10.1086/508500
• Monk D, Arnaud P, Apostolidou S, Kelsey G, Stanier P, Feil R, Moore G (2006). Dynamics of placental imprinting: a comparison between mouse and humans.
• Monk D, Sanches R, Arnaud P, Apostolidou S, Hills F, Abu-Amero S, Murrell A, Friess H, G R, W S, P C, M M, G E (2006). ). Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human. Human Molecular Genetics, 15(8), 1259 - 1269.
• Monk D, Arnaud P, Apostolidou S, Hills FA, Kelsey G, Stanier P, Feil R, Moore GE (2006). Limited evolutionary conservation of imprinting in the human placenta.. Proc Natl Acad Sci U S A, 103(17), 6623 - 6628. doi:10.1073/pnas.0511031103
• Abu-Amero S, Monk D, Apostolidou S, Stanier P, Moore G (2006). Imprinted genes and their role in human fetal growth. CYTOGENET GENOME RES, 113(1-4), 262 - 270.
• Stanier P, Moore GE (2006). The relationship between genotype and phenotype: some basic concepts. In GE FPCATCM (Ed.), Embryos, genes and birth defects (pp. 1 - 18). : John Wiley & Sons Inc.

2005

• Gavriel G, Modi N, Stanier P, Moore GE (2005). Neonatal buccal cell collection for DNA analysis. ARCH DIS CHILD, 90(2), F187 - F187. doi:10.1136/adc.2004.062661
• Doudney K, Ybot-Gonzalez P, Paternotte C, Stevenson RE, Greene ND, Moore GE, Copp AJ, Stanier P (2005). Analysis of the planar cell polarity gene VANGL2 and its co- expressed paralogue VANGL1 in neural tube defect patients. American Journal of Medical Genetics Part A, 136A(1), 90 - 92.
• Doudney K, Moore GE, Stanier P, Ybot-Gonzalez P, Paternotte C, Greene NDE, Copp AJ, Stevenson RE (2005). Erratum: Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralog Vangl1 in neural tube defect patients (American Journal of Genetics (2005) 136A (90-92) DOI: 10.1002/ajmg.a.30766). American Journal of Medical Genetics, 138 A(4), 415 - 415.
• Doudney K, Stanier P (2005). Epithelial cell polarity genes are required for neural tube closure.. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 135, 42 - 47.
• Doudney K, Moore GE, Stanier P, Ybot-Gonzalez P, Paternotte C, Greene NDE, Copp AJ, Stevenson RE (2005). Analysis of the planar cell polarity gene Vangl2 and its, co-expressed paralog Vangl1 in neural tube defect patients (vol 136A, pg 90, 2005). American Journal of Medical Genetics Part A, 138A(4), 415 - 415.

2004

• Nakabayashi K, Makino S, Minagawa S, Smith AC, Bamforth JS, Stanier P, Preece M, Parker-Katiraee L, Paton T, Oshimura M, Mill P, Yoshikawa Y, Hui C-C, Monk D, Moore GE, Scherer SW (2004). Genomic Imprinting of PPP1R9A Encoding Neurabin 1 in Skeletal Muscle and Extra-Embryonic Tissues. Journal of Medical Genetics, 41, 601 - 608.
• Murdoch J, Quint E, Curtin J, Henderson D, Greene N, Arkell R, Bogani D, Gerrelli D, Doudney K, Paternotte C, Cattanach B, Nolan P, Spurr N, Fisher E, Stanier P, Gray I, Steel K, Brown S, Copp A (2004). Mechanisms regulating the initiation of neural tube closure.
• Arnaud P, Monk D, Hitchins M, Gordon E, Dean W, Beechey C, Peters J, Craigen W, Preece M, Stanier P, Moore G, Kelsey G (2004). Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark.
• Stanier P, Moore GE (2004). Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts. Human Molecular Genetics, 13, R73 - R81.
• Marcano AC, Doudney K, Braybrook C, Squires R, Patton MA, Lees MM, Richieri-Costa A, Lidral AC, Murray JC, Moore GE, Stanier P (2004). TBX22 mutations are a frequent cause of cleft palate.. Journal of Medical Genetics, 41, 68 - 74.

2003

• Monk D, Bentley L, Beechey C, Smith R, Arnaud P, Peters J, Preece M, Stanier P, Kelsey G, Moore G (2003). The use of Me-RDA to identify novel DMRs on mouse Chr 6 and 11..
• Apostolidou S, Williams A, O'Donoghue K, Birjandi Z, Stanier P, Loughna P, Moore GE (2003). Intrauterine growth restriction and analysis of imprinted genes on 1IP15.5..
• Arnaud P, Monk D, Hitchins M, Gordon E, Dean W, Beechey CV, Peters J, Craigen W, Preece MA, Stanier P, Moore GE, Kelsey G (2003). Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark. Human Molecular Genetics, 12(9), 1005 - 1009. doi:10.1093/hmg/ddg110
• Murdoch JN, Henderson DJ, Doudney K, Gaston-Massuet C, Phillips HM, Paternotte C, Arkell R, Stanier P, Copp AJ (2003). Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse. Human Molecular Genetics, 12(2), 87 - 98.
• Bentley L, Nakabayashi K, Monk D, Beechey CV, Peters J, Birjandi Z, Khayat FE, Patel M, Preece MA, Stanier P, Scherer S, Moore GE (2003). The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome. Journal of Medical Genetics, 40, 249 - 256.
• Apostolidou S, Williams A, O'Donoghue K, Birjandi Z, Stanier P, Loughna P, Moore GE (2003). Intrauterine growth restriction and analysis of imprinted genes on 1IP15.5.
• Monk D, Smith R, Arnaud P, Preece MA, Stanier P, Beechey CV, Peters J, Kelsey G, Moore GE (2003). Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis.. Mamm Genome, 14, 805 - 816.
• Murdoch JN, Doudney K, Gerrelli D, Wortham N, Paternotte C, Stanier P, Copp AJ (2003). Genomic organization and embryonic expression of Igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia. Molecular and Cellular Neuroscience, 22(1), 62 - 74. doi:10.1016/S1044-7431(02)00021-0
• Monk D, Beechey C, Smith R, Arnaud P, Peters J, Preece M, Stanier P, Kelsey G, Moore G (2003). The use of methylation-sensitive representation difference analysis (Me-RDA) to identify novel differentially methylated regions/imprinted regions on proximal chromosome 11.
• Bentley L, Monk D, Beechey C, Peters J, Birjandi Z, Preece MA, Stanier P, Moore GE (2003). The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster..
• Curtin JA, Quint E, Tsipouri V, Arkell RM, Cattanach B, Copp AJ, Henderson DJ, Spurr N, Stanier P, EMC F, Nolan PM, Steel KP, SDM B, Gray IC, Murdoch JN (2003). Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse. CURR BIOL, 12(13), 1129 - 1133. doi:10.1016/S0960-9822(03)00374-9

2002

• Braybrook C, Lisgo S, Doudney K, Henderson D, Marcano AC, Strachan T, Patton MA, Villard L, Moore GE, Stanier P, Lindsay S (2002). Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.. Human Molecular Genetics, 11(22), 2793 - 2804. doi:10.1093/hmg/11.22.2793
• Bentley L, Nakabayashi K, Montamedi Z, Preece M, Scherer S, Stanier P, Moore GE (2002). Carboxypeptidase A5: an imprinted member of the CPA gene family..
• Apostolidou S, Williams A, O'Donoghue K, Montamedi Z, Stanier P, Loughna P, Moore GE (2002). Analysis of imprinted genes on 11p15.5 associated with intrauterine growth.
• Monk D, Bentley L, Beechey C, Hitchins M, Peters J, Preece MA, Stanier P, Moore GE (2002). Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome.. Journal of Medical Genetics, 39(8), 575 - 581. doi:10.1136/jmg.39.8.575
• Braybrook C, Doudney K, Marçano ACB, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P (2002). The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia..
• Doudney K, Murdoch JN, Braybrook C, Paternotte C, Bentley L, Copp AJ, Stanier P (2002). Cloning and characterisation of Igsf9 in mouse and human: a new member of the IgCAM superfamily expressed in the developing nervous system. Genomics, 79, 663 - 670.
• Murdoch JN, Doudney K, Paternotte C, Stanier P, Copp AJ (2002). Identification of the gene mutated in the loop-tail mouse, a model for severe neural tube defects..
• Hitchins MP, Bentley L, Monk D, Beechey C, Peters J, Kelsey G, Ishino F, Preece MA, Stanier P, Moore GE (2002). DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed.. Mamm Genome, 13, 686 - 691.
• Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE (2002). Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region. Human Genetics, 111(4-5), 376 - 387. doi:10.1007/s00439-002-0777-4
• Rogner UC, Danoy P, Matsuda F, Moore GE, Stanier P, Avner P (2002). SNPs in the CpG island of NAP1L2: a possible link between DNA methylation and neural tube defects?. American Journal of Medical Genetics Part A, 110(3), 208 - 214. doi:10.1002/ajmg.10453
• Nakabayashi K, Bentley L, Hitchins MP, Mitsuya K, Meguro M, Minagawa S, Bamforth JS, Stanier P, Preece M, Weksberg R, Oshimura M, Moore GE, Scherer SW (2002). Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.. Human Molecular Genetics, 111, 1743 - 1756.
• Hitchins MP, Abu-Amero S, Apostolidou S, Monk D, Stanier P, Preece MA, Moore GE (2002). Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q.. Journal of Medical Genetics, 39, E13 - . doi:10.1136/jmg.38.12.810
• Bentley L, Nakebayashi K, Montameni Z, Preece M, Scherer S, Stanier P, Moore GE (2002). Carboxypeptidase A5: an imprinted member of the CPA gene family.
• Apostolidou S, Williams A, O Donoghue K, Montamedi Z, Stanier P, Loughna P, Moore GE (2002). Analysis of imprinted genes on 11p15.5 associated with interuterine growth.

2001

• Doudney K, Murdoch JN, Patternotte C, Bently L, Gregory S, Copp AJ, Stanier P (2001). Comparative physical and transcript maps of similar to 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23. Genomics, 72(2), 180 - 192.
• Hichins M, Stanier P, Preece MA, Moore GE (2001). Silver-Russell Syndrome: a dissection of the genetic aetiology and candidate chromosomal regions. Journal of Medical Genetics, 38, 810 - 819.
• Murdoch JN, Rachel RA, Shah S, Beermann F, Stanier P, Mason CA, Copp AJ (2001). Circletail, a new mouse mutant with severe neural tube defects: Chromosomal localization and interaction with the loop-tail mutation. Genomics, 78(1-2), 55 - 63.
• Moore GE, Abu-Amero SN, Bell G, Wakeling EL, Kingsnorth A, Stanier P, Jauniaux E, Bennett ST (2001). Evidence that insulin is imprinted in the human yolk sac. DIABETES, 50(1), 199 - 203.
• Braybrook C, Doudney K, Marcano ACB, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P (2001). Identification and mutation screening of candidate genes for X-linked cleft palate and ankyloglossia (CPX).
• Monk D, Hitchens M, Ismail I, Temple K, Sharp A, Clayton-Smith J, Preece M, Stanier P, Moore GE (2001). Detailed FISH analysis of Silver-Russell syndrome (SRS) patients with cytogenetic disruption of chromosome 7p11.2-p13 define a candidate region for SRS.
• Paternotte C, Murdoch JN, Doudney K, Stanier P, Copp AJ (2001). Severe neural tube defects in the loop-tail mouse result from mutations of loopin, a novel transmembrane protein..
• Murdoch J, Rivka RA, Shah SS, Beerman F, Stanier P, Mason CA, Copp AJ (2001). Circletail, a new mouse mutant with a severe neural tube defect, maps to Chromosome 15..
• Doudney K, Murdoch J, Paternotte C, Copp AJ, Stanier P (2001). Fine mapping of the locus underlying the severe neural tube defect loop-tail.
• Paternotte C, Murdoch JN, Doudney K, Stanier P, Copp AJ (2001). Severe neural tube defects in the loop-tail mouse result from mutation of loopin, a novel transmembrane protein..
• Bentley L, Monk D, Smith E, Edmonds R, Hitchins M, Preece MA, Stanier P, Moore GE (2001). Analysis of imprinting in the Silver Russell Syndrome candidate gene region at 7q31-qter..
• Braybrook C, Doudney K, Marcano ACB, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P (2001). Identification and mutation screening of candidate genes for X-linked cleft palate and ankyloglossia (CPX)..
• Monk D, Hitchins M, Russo S, Preece M, Stanier P, Moore GE (2001). No evidence for mosaicism in Silver-Russell syndrome.. J Med Genet, 38(4), E11 - .
• Mergenthaler S, Hitchins MP, Blagitko-Dorfs N, Monk D, Wollmann HA, Ranke MB, Ropers HH, Apostolidou S, Stanier P, Preece MA, Eggermann T, Kalscheuer VM, Moore GE (2001). Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?. The American Journal of Human Genetics, 68(543), 543 - 545. doi:10.1086/318192
• Hitchins MP, Monk D, Bell GM, Ali Z, Preece MA, Stanier P, Moore GE (2001). Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB70 in Silver-Russell syndrome. EUR J HUM GENET, 9(2), 82 - 90.
• Murdoch JN, Rachel RA, Shah S, Beermann F, Stanier P, Mason CA, Copp AJ (2001). Circletail, a new mouse mutant with severe neural tube defects: Chromosomal localization and interaction with the loop-tail mutation. Genomics, 78(1-2), 55 - 63.
• Murdoch JN, Doudney K, Paternotte C, Copp AJ, Stanier P (2001). Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification. Human Molecular Genetics, 10(22), 2593 - 2601. doi:10.1093/hmg/10.22.2593
• Braybrook C, Doudney K, Marcano AC, Arnason A, Bjornsson A, Patton MA, Goodfellow PJ, Moore GE, Stanier P (2001). The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia.. Nature Genetics, 29(2), 179 - 183. doi:10.1038/ng730
• Braybrook C, Warry G, Howell G, Mandryko V, Arnason A, Bjornsson A, Ross MT, Moore GE, Stanier P (2001). Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region.. Human Genetics, 108, 537 - 545.
• Braybrook C, Warry G, Howell G, Arnason A, Bjornsson A, Moore GE, Ross MT, Stanier P (2001). Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical region.. Genomics, 72, 128 - 136.
• Carrel T, Herman GE, Moore GE, Stanier P (2001). Lack of mutations in ZIC3 in three families with neural tube defects.. American Journal of Medical Genetics Part A, 98(3), 283 - 285. doi:10.1002/1096-8628(20010122)98:3<283::AID-AJMG1089>3.0.CO;2-G
• Bentley L, Monk D, Smith E, Edmonds R, Hitchins M, Preece MA, Stanier P, Moore GE (2001). Analysis of imprinting in the Silver Russell Syndrome candidate gene region at 7q31-qter.

2000

• Monk DN, Hitchins M, Wassal M, Temple K, Sharp A, Preece M, Stanier P, Moore G (2000). Detailed FISH analyses of Silver-Russell Syndrome (SRS) patients with cytogenetic disruptions of chromosome 7p11.2-p13 define a candidate region for SRS.. AM J HUM GENET, 67(4), 146 - 146.
• Hitchens MP, Monk D, Bell G, Stanier P, Preece MA, Moore GE (2000). Analysis and imprinting status of GRB10, a prime candidate for Silver-Russell syndrome, in human fetal development..
• Paternotte C, Murdoch J, Doudney K, Eddleston J, Stanier P, Copp A (2000). Genetic mapping of loop-tail, a mouse mutant with a severe neural tube defect.
• Wakeling EL, Hitchins MP, Monk D, Stanier PM, Moore GE, Preece MA (2000). Silver-Russell syndrome and ring chromosome 7. Journal of Medical Genetics, 37, 380 - .
• Wakeling EL, Hitchins MP, Abu-Amero SN, Stanier P, Moore GE, Preece MA (2000). Biallelic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndrome. Journal of Medical Genetics, 37(1), 65 - 67.
• Murdoch JN, Rachel RA, Shah SS, Beermann F, Stanier P, Mason CA, Copp AJ (2000). Genetic mapping of circletail, a new mouse mutant with a severe neural tube defect.
• Monk D, Wakeling EL, Proud V, Hitchins M, Abu-Amero SN, Stanier P, Preece MA, Moore GE (2000). Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome. The American Journal of Human Genetics, 66(1), 36 - 46.
• Monk D, Hitchens M, Temple K, Sharp A, Clayton-Smith J, Stanier P, Preece M, Moore GE (2000). Detailed FISH analyses of three Silver-Russell syndrome (SRS) patients with cytogenetic disruptions of chromosome 7p11.2-p13 define a candidate region for SRS.

1999

• Moore GE, Abu-Amero S, Wakeling E, Hitchins M, Monk D, Stanier P, Preece M (1999). The search for the gene for Silver-Russell syndrome.. Acta Paediatr Suppl, 88(433), 42 - 48.
• Hitchins MP, Monk D, Wakeling EL, Proud V, Stanier P, Preece MA, Moore GE (1999). De novo tandem duplication of 7p11.2-p12 in a patient with Silver-Russell syndrome and asynchronous replication timing further implicates GRB10 as a candidate gene..
• Eddleston J, Murdoch JN, Copp AJ, Stanier P (1999). Physical and transcriptional map of a 3-Mb region of mouse chromosome 1 containing the gene for the neural tube defect mutant loop-tail (Lp). Genomics, 56(2), 149 - 159.
• Wakeling E, Monk D, Hitchins M, Proud V, Stanier P, Preece MA, Moore GE (1999). Duplication of 7p11.2-p12, including GRB10, in Silver-Russell syndrome.
• Murdoch JN, Eddleston J, Leblond-Bourget N, Stanier P, Copp AJ (1999). Sequence and expression analysis of Nhlh1: a basic helix-loop-helix gene implicated in neurogenesis. Developmental Genetics, 24(1-2), 165 - 177.
• Braybrook C, Moore GE, Stanier P (1999). Identification of candidate genes for X-linked cleft palate and ankyloglossia in an Icelandic kindred.
• Ahmet Z, Stanier P, Harvey D, Holt D (1999). New PCR primers for the sensitive detection and specific identification of group B beta-hemolytic streptococci in cerebrospinal fluid.. Molecular and Cellular Probes, 13, 349 - 357.
• Abu-Amero SN, Ali Z, Abu-Amero KK, Stanier P, Moore GE (1999). An analysis of common isodisomic regions in five mUPD 16 probands.. Journal of Medical Genetics, 36, 204 - 207.
• Preece MA, Abu-Amero SN, Ali Z, Abu-Amero KK, Wakeling EL, P Moore GE (1999). An analysis of the distribution of heterodisomic and isodisomic regions of chromosome 7 in five mUPD 7 Silver Russell syndrome probands. Journal of Medical Genetics, 36, 457 - 460.
• Moore GE, Abu-Amero SN, Wakeling EL, Hitchins M, Monk D, Stanier P, Preece MA (1999). The search for the gene for Silver Russell syndrome.. Acta Paediatrica, 88(42), 48 - .
• White PS, Forus A, Matise TC, Schutte BC, Spieker N, Stanier P, Vance JM, Gregory SG (1999). Report of the Fifth International Workshop on Human Chromosome 1 Mapping 1999. Cytogenetics and Cell Genetics, 87, 143 - 171.

1998

• Wakeling EL, Abu-Amero SN, Stanier P, Preece MA, Moore GE (1998). Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues. (vol 6, pg 158, 1998).
• Stanier P, Abu-Hayyeh S, Murdoch JN, Eddleston J, Copp AJ (1998). Paralogous sm22alpha (Tagln) genes map to mouse chromosomes 1 and 9: further evidence for a paralogous relationship.. Genomics, 51, 144 - 147.
• Wakeling E, Abu-Amero SN, Stanier P, Preece MA, Moore GE (1998). Imprinted genes on chromosome 7: their role in Silver-Russell syndrome..
• Wakeling EL, Abu-Amero S, Price SM, Stanier P, Trembath RC, Moore GE, Preece MA (1998). Genetics of Silver-Russell syndrome.. Hormone Research, 49, 32 - 36.
• Abu-Hayyeh S, Eddleston J, Murdoch JN, Tham M, Copp AJ, Stanier P (1998). Linkage mapping of Lims1, the murine homolog of the human LIM domain gene PINCH, to mouse chromosome 10.. Cytogenetics and Cell Genetics, 82, 46 - 48.
• Wakeling EL, Abu-Amero SN, Stanier P, Preece MA, Moore GE (1998). Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.. European Journal of Human Genetics, 68, 158 - 164.
• Abu-Amero SN, Wakeling EL, Stanier P, Preece MA, Moore GE (1998). Search for imprinted genes involved in Silver Russell syndrome.
• Richardson MP, Braybrook C, Tham M, Moore GE, Stanier P (1998). Molecular cloning and characterization of a highly conserved human 67-kDa laminin receptor pseudogene mapping to Xq21.3.. Gene, 206, 145 - 150.

1997

• Wakeling EL, Abu-Amero S, Price SM, Stanier P, Preece MA, Moore GE (1997). Imprinted genes on chromosome 7: their role in Silver-Russell syndrome.
• Abu-Amero S, Preece M, Wakeling E, Moore G, Stanier P (1997). A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R).. Molecular and Cellular Probes, 11, 381 - 383.
• Preece MA, Price SM, Davies V, Clough L, Stanier P, Trembath RC, Moore GE (1997). Maternal uniparental disomy 7 in the Silver-Russell syndrome. Journal of Medical Genetics, 34(1), 6 - 9.
• Murdoch JN, Eddleston J, Stanier P, Copp AJ (1997). Localisation of the mouse gene encoding tyrosine kinase receptor type 10 on distal Chromosome 1. Mammalian Genome, 8, 941 - 952.
• Abu-Amero S, Price SM, Wakeling E, Stanier P, Trembath RC, Preece MA, Moore GE (1997). Lack of hemizygosity for the insulin-like growth factor I receptor gene in a quantitative study of 33 Silver-Russell syndrome probands and their families. European Journal of Human Genetics, 5(4), 235 - 241.

1996

• Fisk NH, Ware M, Stanier P, Moore G, Bennett P (1996). Molecular genetic etiology of twin reversed arterial perfusion sequence. AM J OBSTET GYNECOL, 174(3), 891 - 894.
• Forbes SA, Brennan L, Richardson M, Coffey A, Cole CG, Gregory SG, Bentley DR, Mumm S, Moore GE, Stanier P (1996). Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3. GENOMICS, 31(1), 36 - 43.

1995

• STANIER P, HENSON JN, EDDLESTON J, MOORE GE, COPP AJ (1995). GENETIC-BASIS OF NEURAL-TUBE DEFECTS - THE MOUSE GENE LOOP-TAIL MAPS TO A REGION OF CHROMOSOME-1 SYNTENIC WITH HUMAN 1Q21-Q23. GENOMICS, 26(3), 473 - 478.
• FORBES SA, RICHARDSON M, BRENNAN L, ARNASON A, BJORNSSON A, CAMPBELL L, MOORE G, STANIER P (1995). REFINEMENT OF THE X-LINKED CLEFT-PALATE AND ANKYLOGLOSSIA (CPX) LOCALIZATION BY GENETIC-MAPPING IN AN ICELANDIC KINDRED. HUM GENET, 95(3), 342 - 346.

1994

• NEWTON R, STANIER P, LOUGHNA S, HENDERSON DJ, FORBES SA, FARRALL M, JENSSON O, MOORE GE (1994). LINKAGE ANALYSIS OF 62 X-CHROMOSOMAL LOCI EXCLUDES THE X-CHROMOSOME IN AN ICELANDIC FAMILY SHOWING APPARENT X-LINKED RECESSIVE INHERITANCE OF NEURAL-TUBE DEFECTS. CLIN GENET, 45(5), 241 - 249.
• NEWTON R, STANIER P, FORBES S, MOORE GE (1994). NOVEL RFLPS AND MICROSATELLITE REPEATS INCREASE INFORMATIVITY AT 4 LOCI MAPPING TO XQ22-Q25. HUM GENET, 93(2), 218 - 221.
• STANIER P, FORBES S, RICHARDSON M, BRENNAN L, COLE CG, BENTLEY DR, MOORE GE (1994). PHYSICAL MAPPING OF THE X-LINKED CLEFT-PALATE LOCUS. CYTOGENET CELL GENET, 67(4), 351 - 352.

1993

• STANIER P, FORBES SA, ARNASON A, BJORNSSON A, SVEINBJORNSDOTTIR E, WILLIAMSON R, MOORE G (1993). THE LOCALIZATION OF A GENE CAUSING X-LINKED CLEFT-PALATE AND ANKYLOGLOSSIA (CPX) IN AN ICELANDIC KINDRED IS BETWEEN DXS326 AND DXYS1X. GENOMICS, 17(3), 549 - 555.
• BENNETT P, SLATER D, STANIER P, MOORE G (1993). EXPRESSION OF A COMMON CELLULAR PHOSPHOLIPASE-A2 BY HUMAN INTRAUTERINE TISSUES. PROSTAGLANDINS, 45(2), 121 - 127.
• STANIER P, FORBES S, RICHARDSON M, ARNASON A, MOORE G (1993). LINKAGE ANALYSIS OF X-LINKED CLEFT-PALATE IN AN ICELANDIC PEDIGREE.

1992

• BENNETT P, HENDERSON D, STANIER P, VAUGHAN J, MOORE G (1992). DETERMINATION OF TWIN ZYGOSITY BY DNA HYBRIDIZATION TO WILD-TYPE BACTERIOPHAGE M13. BRIT J OBSTET GYNAEC, 99(10), 858 - 860.
• STANIER P, KITCHEN AD, TAYLOR DL, TYMS AS (1992). DETECTION OF HUMAN CYTOMEGALOVIRUS IN PERIPHERAL MONONUCLEAR-CELLS AND URINE SAMPLES USING PCR. MOL CELL PROBE, 6(1), 51 - 58.
• Jones SM, Boobis AR, Moore GE, Stanier PM (1992). Expression of CYP2E1 during human fetal development: methylation of the CYP2E1 gene in human fetal and adult liver samples.. Biochem Pharmacol, 43(8), 1876 - 1879.

1991

• STANIER P, NEWTON R, MOORE GE (1991). A NEW POLYMORPHISM AT THE DXS178 LOCUS. NUCLEIC ACIDS RES, 19(24), 6972 - 6972.
• Tata F, Stanier P, Wicking C, Halford S, Kruyer H, Lench NJ, Scambler PJ, Hansen C, Braman JC, Williamson R (1991). Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene.. Genomics, 10(2), 301 - 307.
• STANIER P, NEWTON R, FORBES SA, IVENS A, MOORE GE (1991). POLYMORPHIC DINUCLEOTIDE REPEAT AT THE DXS3 LOCUS. NUCLEIC ACIDS RES, 19(17), 4793 - 4793.
• STANIER PM, NEWTON R, IVENS A, ARNASON A, BJORNSSON A, MOORE GE (1991). NEW POLYMORPHISMS IN THE REGION OF X-LINKED CLEFT-PALATE AND ANKYLOGLOSSIA.

1990

• RAMSAY M, WAINWRIGHT BJ, FARRALL M, ESTIVILL X, SUTHERLAND H, HO MF, DAVIES R, HALFORD S, TATA F, WICKING C, LENCH N, BAUER I, FEREC C, FARNDON P, KRUYER H, STANIER P, WILLIAMSON R, SCAMBLER PJ (1990). A NEW POLYMORPHIC LOCUS, D7S411, ISOLATED BY CLONING FROM PREPARATIVE PULSE-FIELD GELS IS CLOSE TO THE MUTATION CAUSING CYSTIC-FIBROSIS. GENOMICS, 6(1), 39 - 47.

1989

• STANIER P, TAYLOR DL, KITCHEN AD, WALES N, TRYHORN Y, TYMS AS (1989). PERSISTENCE OF CYTOMEGALO-VIRUS IN MONONUCLEAR-CELLS IN PERIPHERAL-BLOOD FROM BLOOD-DONORS. BRIT MED J, 299(6704), 897 - 898.

1988

• STANIER P, ESTIVILL X, LENCH N, WILLIAMSON R (1988). DETECTION OF A RARE-CUTTER RFLP IN A CPG-RICH ISLAND NEAR THE CYSTIC-FIBROSIS LOCUS. HUM GENET, 80(3), 309 - 310.
• LENCH N, STANIER P, WILLIAMSON R (1988). SIMPLE NON-INVASIVE METHOD TO OBTAIN DNA FOR GENE ANALYSIS. LANCET, 1(8599), 1356 - 1358.
• Wainwright BJ, Scambler PJ, Stanier P, Watson EK, Bell G, Wicking C, Estivill X, Courtney M, Boue A, Pedersen PS (1988). Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless.. EMBO J, 7(6), 1743 - 1748.

1987

• Estivill X, Farrall M, Scambler PJ, Bell GM, Hawley KM, Lench NJ, Bates GP, Kruyer HC, Frederick PA, Stanier P (1987). A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands.. Nature, 326(6116), 840 - 845. doi:10.1038/326840a0
• STANIER P, WILLIAMSON R (1987). DETECTION OF THE SICKLE-CELL MUTATION USING SYNTHETIC OLIGONUCLEOTIDE PROBES. BIOCHEM SOC T, 15(3), 543 - 544.
• LAW HY, STANIER P, WILLIAMSON R, MODELL B, WARD RHT, PETROU M, OLD J, FARRALL M (1987). 2 UNUSUAL CASES OF 1ST TRIMESTER PRENATAL-DIAGNOSIS OF CYSTIC-FIBROSIS USING DNA PROBES. PRENATAL DIAG, 7(3), 215 - 221.
• Estivill X, Bates G, Bell G, Farrall M, Frederick P, Hawley K, Kruyer H, Lench N, Scambler P, Stanier P, Wainwright B, Williamson R (1987). The application of molecular genetics to the study of the basic defect causing cystic fibrosis. In Riordan JR, Buchwald M (Ed.), Genetics and epithelial cell dysfunction in cystic fibrosis. Progress in CLinical and Biological Research (pp. 181 - 190). : .

1986

• FARRALL M, WATSON E, BATES G, BELL G, BELL J, DAVIES KA, ESTIVILL X, KRUYER H, LAW HY, LENCH N, LISSENS W, SIMON P, SCAMBLER P, STANIER P, VASSART G, WORRALL C, WILLIAMSON R, WAINWRIGHT BJ (1986). FURTHER DATA SUPPORTING LINKAGE BETWEEN CYSTIC-FIBROSIS AND THE MET ONCOGENE AND HAPLOTYPE ANALYSIS WITH MET AND PJ3.11. AM J HUM GENET, 39(6), 713 - 719.
• FARRALL M, RODECK C, STANIER P, LISSENS W, WATSON E, LAW H, WARREN R, SUPER M, SCAMBLER P, WAINWRIGHT B, WILLIAMSON R (1986). FIRST-TRIMESTER PRENATAL-DIAGNOSIS OF CYSTIC-FIBROSIS WITH LINKED DNA PROBES. LANCET, 327(8495), 1402 - 1405.
• WILLIAMSON R, BELL G, BELL J, BATES G, DAVIES KA, ESTIVILL X, FARRALL M, KRUYER H, LAW HY, LENCH N, SCAMBLER P, STANIER P, WAINWRIGHT B, WATSON E, WORRALL C (1986). MOLECULAR-GENETICS AND THE BASIC DEFECT CAUSING CYSTIC-FIBROSIS. COLD SPRING HARB SYM, 51, 309 - 315.

1985

• Scambler PJ, Wainwright BJ, Farrall M, Bell J, Stanier P, Lench NJ, Bell G, Kruyer H, Ramirez F, Williamson R (1985). Linkage of COL1A2 collagen gene to cystic fibrosis, and its clinical implications.. Lancet, 326(8466), 1241 - 1242.

1983

• STANIER P, BLACKMORE DJ (1983). MOLYBDENUM CONCENTRATIONS IN EQUINE SERUM. VET REC, 113(22), 518 - 518.
• STANIER P, BLACKMORE DJ (1983). ANTIMONY CONCENTRATIONS IN EQUINE SERUM. VET REC, 113(7), 157 - 157.