Sayeda Abu‐Amero

2.6k total citations
31 papers, 1.5k citations indexed

About

Sayeda Abu‐Amero is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sayeda Abu‐Amero has authored 31 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 20 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sayeda Abu‐Amero's work include Genetic Syndromes and Imprinting (20 papers), Prenatal Screening and Diagnostics (15 papers) and Epigenetics and DNA Methylation (12 papers). Sayeda Abu‐Amero is often cited by papers focused on Genetic Syndromes and Imprinting (20 papers), Prenatal Screening and Diagnostics (15 papers) and Epigenetics and DNA Methylation (12 papers). Sayeda Abu‐Amero collaborates with scholars based in United Kingdom, United States and Saudi Arabia. Sayeda Abu‐Amero's co-authors include Gudrun E. Moore, Philip Stanier, Emma Wakeling, Mohamed Al-Khtib, P. Coullin, A. Lefèvre, Jérôme Cavaillé, Jennifer M. Frost, David Monk and Michael A. Preece and has published in prestigious journals such as PLoS ONE, Neurology and Diabetes.

In The Last Decade

Sayeda Abu‐Amero

31 papers receiving 1.5k citations

Peers

Countries citing papers authored by Sayeda Abu‐Amero

Since Specialization

Citations

This map shows the geographic impact of Sayeda Abu‐Amero's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sayeda Abu‐Amero with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sayeda Abu‐Amero more than expected).

Fields of papers citing papers by Sayeda Abu‐Amero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sayeda Abu‐Amero. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sayeda Abu‐Amero. The network helps show where Sayeda Abu‐Amero may publish in the future.

Co-authorship network of co-authors of Sayeda Abu‐Amero

This figure shows the co-authorship network connecting the top 25 collaborators of Sayeda Abu‐Amero. A scholar is included among the top collaborators of Sayeda Abu‐Amero based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sayeda Abu‐Amero. Sayeda Abu‐Amero is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genome-wide methylation analysis in Silver–Russell syndrome patients 2015 ·Human Genetics ·(unknown), Miho Ishida, Stefanie Böhm, Jennifer M. Frost, William Puszyk, Sayeda Abu‐Amero, Philip Stanier, Reiner Schulz, Gudrun E. Moore, Rebecca J. Oakey	17
2	Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortion 2015 ·Reproductive BioMedicine Online ·Charalambos Demetriou, Sayeda Abu‐Amero, (unknown), Emma Peskett, Arseni Markoff, Philip Stanier, Gudrun E. Moore, Lesley Regan	12
3	Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS 2013 ·Journal of Investigative Dermatology ·Veronica A. Kinsler, Anna Thomas, Miho Ishida, Neil Bulstrode, Sam Loughlin, Sandra Hing, Jane Chalker, Kathryn J. McKenzie, Sayeda Abu‐Amero, Olga Slater, Estelle Chanudet, Rodger Palmer, Deborah Morrogh, Philip Stanier, Eugene Healy, Neil J. Sebire, Gudrun E. Moore	196
4	Germline Melanocortin-1-Receptor Genotype Is Associated with Severity of Cutaneous Phenotype in Congenital Melanocytic Nevi: A Role for MC1R in Human Fetal Development 2012 ·Journal of Investigative Dermatology ·Veronica A. Kinsler, Sayeda Abu‐Amero, Peter S. Budd, Ian J. Jackson, Susan M. Ring, Kate Northstone, David J. Atherton, Neil Bulstrode, Philip Stanier, Raoul C. M. Hennekam, Neil J. Sebire, Gudrun E. Moore, Eugene Healy	36
5	Inheritance of a copy number variant in the imprinted PHLDA2 gene promoter significantly increases fetal birth weight 2011 ·UCL Discovery (University College London) ·Miho Ishida, David Monk, (unknown), Sayeda Abu‐Amero, Jer Pin Chong, (unknown), Marcus Pembrey, (unknown), J. R. Whittaker, Philip Stanier, (unknown)	1
6	The growth hormone receptor gene deleted for exon three (GHRd3) polymorphism is associated with birth and placental weight 2011 ·Clinical Endocrinology ·Raja Padidela, (unknown), Sayeda Abu‐Amero, (unknown), John C. Achermann, Gudrun E. Moore, Peter C. Hindmarsh	13
7	Placental Bed Disorders 2010 ·Cambridge University Press eBooks ·Robert Pijnenborg, Sayeda Abu‐Amero, Jan J. Brosens, Brianna Cloke, Ashley Moffett, Christophe Depoix, Eric Jauniaux, S.R. Killick, Ernest Hung Yu Ng, Anthony Michael Carter, Judith E. Cartwright, Robert H. Lane, David Haig, Linda Morgan	41
8	The primate-specific microRNA gene cluster (C19MC) is imprinted in the placenta 2010 ·Human Molecular Genetics ·(unknown), Sayeda Abu‐Amero, Mohamed Al-Khtib, A. Lefèvre, P. Coullin, Gudrun E. Moore, Jérôme Cavaillé	257
9	Epigenetic signatures of Silver–Russell syndrome: Table 1 2010 ·Journal of Medical Genetics ·Sayeda Abu‐Amero, Emma Wakeling, Michael Preece, John C. Whittaker, Philip Stanier, Gudrun E. Moore	17
10	High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta 2010 ·BMC Genetics ·Caroline Daelemans, Matthew E. Ritchie, Guillaume Smits, Sayeda Abu‐Amero, Ian Sudbery, Matthew S. Forrest, Susana Campino, Taane G. Clark, Philip Stanier, Dominic Kwiatkowski, Panos Deloukas, Emmanouil T. Dermitzakis, Simon Tavaré, Gudrun E. Moore, Ian Dunham	48
11	Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution 2007 ·PLoS Genetics ·(unknown), Andrew R. Carson, Takahiro Yamada, Philippe Arnaúd, Robert Feil, Sayeda Abu‐Amero, (unknown), Masahiro Kaneda, George H. Perry, Anne C. Stone, Charles Lee, Makiko Meguro‐Horike, Hiroyuki Sasaki, Keiko Kobayashi, Kazuhiko Nakabayashi, Stephen W. Scherer	66
12	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 2007 ·Acta Dermato Venereologica ·Kristian Thestrup‐Pedersen, Ranjit S. Parhar, Kaida Wu, (unknown), Brian F. Meyer, Sayeda Abu‐Amero, Bo Hainau, (unknown), (unknown), (unknown), Abdulmajeed Alajlan, Khaled Al‐Hussein, Futwan Al‐Mohanna	4
13	The genetic aetiology of Silver–Russell syndrome 2007 ·Journal of Medical Genetics ·Sayeda Abu‐Amero, David Monk, Jennifer M. Frost, Michael Preece, Philip Stanier, Gudrun E. Moore	126
14	Elevated maternal expression of the imprinted PHLDA2 gene is associated with low birth weight 2006 ·UCL Discovery (University College London) ·Sophia Apostolidou, Sayeda Abu‐Amero, Keelin O’Donoghue, Ólöf Birna Ólafsdóttir, (unknown), Jennifer M. Frost, (unknown), P. T. Loughna, Philip Stanier, (unknown)	6
15	Imprinted genes and their role in human fetal growth 2006 ·Cytogenetic and Genome Research ·Sayeda Abu‐Amero, David Monk, Sophia Apostolidou, Philip Stanier, Gudrun E. Moore	35
16	Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight 2006 ·Journal of Molecular Medicine ·Sophia Apostolidou, Sayeda Abu‐Amero, Keelin O’Donoghue, Jennifer M. Frost, Ólöf Birna Ólafsdóttir, (unknown), John C. Whittaker, P. T. Loughna, Philip Stanier, Gudrun E. Moore	107
17	Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome 2000 ·The American Journal of Human Genetics ·David Monk, Emma Wakeling, Virginia K. Proud, Megan P. Hitchins, Sayeda Abu‐Amero, Philip Stanier, Michael A. Preece, Gudrun E. Moore	107
18	Expression of the insulin-like growth factors and their receptors in term placentas: A comparison between normal and IUGR births 1998 ·Molecular Reproduction and Development ·Sayeda Abu‐Amero, Zehra Ali, Phillip R. Bennett, Janet I. Vaughan, Gudrun E. Moore	69
19	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. 1998 ·PubMed ·Sayeda Abu‐Amero, Susan Price, Emma Wakeling, Philip Stanier, Richard C. Trembath, Michael A. Preece, Gudrun E. Moore	16
20	A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R) 1997 ·Molecular and Cellular Probes ·Sayeda Abu‐Amero, Michael Preece, Emma Wakeling, Gudrun E. Moore, Philip Stanier	3

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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