S. Abu-Amero

发表

Genome-wide methylation analysis in Silver–Russell syndrome patients

P. Stanier, W. Puszyk, R. Oakey, 2015, Human Genetics.

Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS

N. Sebire, E. Healy, V. Kinsler, 2013, The Journal of investigative dermatology.

Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight

K. Nicolaides, D. Peebles, P. Stanier, 2013, PloS one.

An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands

P. Stanier, K. Abu-Amero, M. Preece, 1999, Journal of medical genetics.

High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta

Matthew E. Ritchie, P. Deloukas, S. Tavaré, 2010, BMC Genetics.

Genetic Analyses in Small-for-Gestational-Age Newborns

R. Hennekam, J. Wit, N. Solanky, 2018, The Journal of clinical endocrinology and metabolism.

Expression of the insulin‐like growth factors and their receptors in term placentas: A comparison between normal and IUGR births

P. Bennett, G. Moore, P. Bennett, 1998, Molecular reproduction and development.

The growth hormone receptor gene deleted for exon three (GHRd3) polymorphism is associated with birth and placental weight

P. Hindmarsh, J. Achermann, G. Moore, 2012, Clinical endocrinology.

articleHigh-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta

Matthew E. Ritchie, P. Deloukas, S. Tavaré, 2019 .

Epigenetic signatures of Silver–Russell syndrome

J. Whittaker, M. Preece, P. Stanier, 2010, Journal of Medical Genetics.

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues

P. Stanier, E. Wakeling, G. Moore, 1998, European Journal of Human Genetics.

A new biological and clinical resource for research into pregnancy complications: The Baby Bio Bank

N. Solanky, P. Stanier, L. Regan, 2016, Placenta.

Exploring the spectrum of 3‐M syndrome, a primordial short stature disorder of disrupted ubiquitination

D. Hanson, P. Clayton, P. Murray, 2012, Clinical endocrinology.

Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q

S. Apostolidou, M. Preece, P. Stanier, 2002, Journal of medical genetics.

Investigation of the GRB 2 , GRB 7 , and CSH 1 genes as candidates for the Silver-Russell syndrome ( SRS ) on chromosome 17 q

S. Apostolidou, M. Preece, P. Stanier, 2002 .

Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer

James D. Brenton, Maja Jagodic, Sayeda Abu-Amero, 2008, Human molecular genetics.

The search for the gene for Silver‐Russell syndrome

M. Preece, P. Stanier, D. Monk, 1999, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution

Charles Lee, S. Scherer, A. Carson, 2007, PLoS genetics.

Author and Subject Index

P. Czernichow, S. Bernasconi, R. Trembath, 1998, Hormone Research in Paediatrics.

The Baby Bio Bank-A Legacy for Researchers Worldwide into Common Complications of Pregnancy

N. Solanky, S. Stanier, L. Regan, 2014 .

Genome-wide methylation analysis in Silver–Russell syndrome patients

P. Stanier, W. Puszyk, R. Oakey, 2015, Human Genetics.

An analysis of common isodisomic regions in five mUPD 16 probands

P. Stanier, K. Abu-Amero, G. Moore, 1999, Journal of medical genetics.

A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R).

P. Stanier, M. Preece, E. Wakeling, 1997, Molecular and Cellular Probes.

Skin-homing CD8+ T lymphocytes show preferential growth in vitro and suppress CD4+ T-cell proliferation in patients with early stages of cutaneous T-cell lymphoma.

F. Al-Mohanna, B. Hainau, B. Meyer, 2007, Acta dermato-venereologica.

Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development

S. Ring, I. Jackson, R. Hennekam, 2012, The Journal of investigative dermatology.

Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy

B. Lach, S. Bohlega, S. Wakil, 2004, Neurology.

The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta.

J. Cavaille, G. Moore, P. Coullin, 2010, Human molecular genetics.

Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

J. Whittaker, S. Apostolidou, P. Stanier, 2007, Journal of Molecular Medicine.

Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models

J. Wegiel, B. Tycko, W. Silverman, 2015, Genome Biology.

Biallelic expression of IGFBP1 andIGFBP3, two candidate genes for the Silver-Russell syndrome

P Stanier, M. Preece, P. Stanier, 2000, Journal of medical genetics.

Genetics of Silver-Russell Syndrome

R. Trembath, M. Preece, P. Stanier, 1998, Hormone Research in Paediatrics.

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

R. Trembath, P. Stanier, E. Wakeling, 1997, European journal of human genetics : EJHG.

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.

P Stanier, D Monk, E L Wakeling, 1999, American journal of human genetics.

Maternal inheritance of a promoter variant in the imprinted PHLDA2 gene significantly increases birth weight.

Philip Stanier, Sayeda Abu-Amero, David Monk, 2012, American journal of human genetics.

Evidence that insulin is imprinted in the human yolk sac.

P Stanier, E. Jauniaux, G. Bell, 2001, Diabetes.

Investigation of the Annexin A 5 M 2 haplotype in 500 white European recurrent miscarriage couples

P. Stanier, L. Regan, G. Moore, 2016 .

Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortion.

P. Stanier, L. Regan, G. Moore, 2015, Reproductive biomedicine online.

Imprinted chromatin around DIRAS3 regulates alternative splicing of GNG12-AS1, a long noncoding RNA.

Yoko Ito, C. Caldas, A. Git, 2013, American journal of human genetics.

The role and interaction of imprinted genes in human fetal growth

K. Nicolaides, J. Whittaker, S. Apostolidou, 2015, Philosophical Transactions of the Royal Society B: Biological Sciences.

A novel form of autosomal recessive pure hereditary spastic paraplegia maps to chromosome 13q14

C. Hodgkinson, B. Meyer, S. Bohlega, 2002, Neurology.

Faculty Opinions recommendation of Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.

S. Malcolm, S. Abu-Amero, 2008 .

The genetic aetiology of Silver–Russell syndrome

P. Stanier, D. Monk, M. Preece, 2007, Journal of Medical Genetics.

Faculty Opinions recommendation of Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

S. Malcolm, S. Abu-Amero, 2011 .

Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human.

S Apostolidou, P Stanier, D Monk, 2006, Human molecular genetics.

Imprinted genes and their role in human fetal growth

S. Apostolidou, P. Stanier, D. Monk, 2006, Cytogenetic and Genome Research.

Expression of the insulin‐like growth factors and their receptors in term placentas: A comparison between normal and IUGR births

G. Moore, P. Bennett, S. Abu-Amero, 1998, Molecular reproduction and development.

High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta

Matthew E. Ritchie, P. Deloukas, S. Tavaré, 2010, BMC Genetics.

The genetic aetiology of Silver–Russell syndrome

P. Stanier, D. Monk, G. Moore, 2007, Journal of Medical Genetics.