Elizabeth Illingworth

965 total citations
21 papers, 700 citations indexed

About

Elizabeth Illingworth is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Elizabeth Illingworth has authored 21 papers receiving a total of 700 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 6 papers in Pulmonary and Respiratory Medicine and 6 papers in Genetics. Recurrent topics in Elizabeth Illingworth's work include Congenital heart defects research (18 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Developmental Biology and Gene Regulation (4 papers). Elizabeth Illingworth is often cited by papers focused on Congenital heart defects research (18 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Developmental Biology and Gene Regulation (4 papers). Elizabeth Illingworth collaborates with scholars based in Italy, United States and United Kingdom. Elizabeth Illingworth's co-authors include Stefania Martucciello, Antonio Baldini, Rosa Ferrentino, Peter Scambler, Filomena Gabriella Fulcoli, Sara Cioffi, Vanessa Kyriakopoulou, M. Albert Basson, Li Chen and Marchesa Bilio and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

Elizabeth Illingworth

20 papers receiving 692 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Elizabeth Illingworth Italy 12 557 169 145 141 84 21 700
Maila Penttinen Finland 19 383 0.7× 173 1.0× 128 0.9× 86 0.6× 114 1.4× 31 920
Lanying Song United States 16 557 1.0× 205 1.2× 67 0.5× 44 0.3× 80 1.0× 22 749
Kaari L. Linask United States 12 589 1.1× 115 0.7× 72 0.5× 79 0.6× 43 0.5× 22 708
Corina Anastasaki United States 19 448 0.8× 120 0.7× 132 0.9× 130 0.9× 70 0.8× 35 1.0k
Ali Jalali United States 12 302 0.5× 70 0.4× 94 0.6× 84 0.6× 37 0.4× 40 602
Emanuela Conti Italy 13 703 1.3× 189 1.1× 167 1.2× 92 0.7× 40 0.5× 18 831
Julia Pöschl Germany 10 263 0.5× 55 0.3× 120 0.8× 37 0.3× 68 0.8× 11 499
Thomas Schwarzbraun Austria 14 517 0.9× 252 1.5× 60 0.4× 45 0.3× 51 0.6× 26 852
Marry Markman Netherlands 8 524 0.9× 95 0.6× 46 0.3× 31 0.2× 107 1.3× 11 815
Guy A. Rouleau Canada 17 433 0.8× 139 0.8× 102 0.7× 26 0.2× 146 1.7× 36 835

Countries citing papers authored by Elizabeth Illingworth

Since Specialization
Citations

This map shows the geographic impact of Elizabeth Illingworth'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 Elizabeth Illingworth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elizabeth Illingworth more than expected).

Fields of papers citing papers by Elizabeth Illingworth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth Illingworth. 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 Elizabeth Illingworth. The network helps show where Elizabeth Illingworth may publish in the future.

Co-authorship network of co-authors of Elizabeth Illingworth

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth Illingworth. A scholar is included among the top collaborators of Elizabeth Illingworth 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 Elizabeth Illingworth. Elizabeth Illingworth is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bilio, Marchesa, Johannes Liebig, Katharina Jechow, et al.. (2025). Tbx1 stabilizes differentiation of the cardiopharyngeal mesoderm and drives morphogenesis in the pharyngeal apparatus. Development. 152(12).
2.
Caterino, Marianna, Debora Paris, Giulia Torromino, et al.. (2024). Brain and behavioural anomalies caused byTbx1haploinsufficiency are corrected by vitamin B12. Life Science Alliance. 8(2). e202403075–e202403075. 2 indexed citations
3.
Ferrentino, Rosa, et al.. (2024). Significant improvement of cardiac outflow tract septation defects in a DiGeorge syndrome model after minoxidil treatment. Biochemical and Biophysical Research Communications. 720. 150104–150104. 1 indexed citations
4.
Lania, Gabriella, et al.. (2024). Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation. Communications Biology. 7(1). 351–351. 1 indexed citations
5.
Cioffi, Sara, et al.. (2022). VEGFR3 modulates brain microvessel branching in a mouse model of 22q11.2 deletion syndrome. Life Science Alliance. 5(12). e202101308–e202101308. 2 indexed citations
6.
Cioffi, Sara, et al.. (2021). Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome. Frontiers in Molecular Neuroscience. 14. 663598–663598. 2 indexed citations
7.
Franzese, Monica, Gabriella Lania, Dario Righelli, et al.. (2020). Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells. Frontiers in Cell and Developmental Biology. 8. 571501–571501. 8 indexed citations
8.
Cioffi, Sara, et al.. (2016). Cortical Development Requires Mesodermal Expression ofTbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome. Cerebral Cortex. 27(3). bhw076–bhw076. 15 indexed citations
9.
Sannino, Sara, et al.. (2016). Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis. Cerebral Cortex. 27(2). bhv336–bhv336. 33 indexed citations
10.
Cioffi, Sara, Stefania Martucciello, Filomena Gabriella Fulcoli, et al.. (2013). Tbx1 regulates brain vascularization. Human Molecular Genetics. 23(1). 78–89. 49 indexed citations
11.
Toritsuka, Michihiro, Sohei Kimoto, Melissa A. Landek‐Salgado, et al.. (2013). Deficits in microRNA-mediated Cxcr4/Cxcl12 signaling in neurodevelopmental deficits in a 22q11 deletion syndrome mouse model. Proceedings of the National Academy of Sciences. 110(43). 17552–17557. 63 indexed citations
12.
Cegli, Rossella De, Simona Iacobacci, Gennaro Gambardella, et al.. (2012). Reverse engineering a mouse embryonic stem cell-specific transcriptional network reveals a new modulator of neuronal differentiation. Nucleic Acids Research. 41(2). 711–726. 19 indexed citations
13.
Chen, Li, Filomena Gabriella Fulcoli, Rosa Ferrentino, et al.. (2012). Transcriptional Control in Cardiac Progenitors: Tbx1 Interacts with the BAF Chromatin Remodeling Complex and Regulates Wnt5a. PLoS Genetics. 8(3). e1002571–e1002571. 90 indexed citations
14.
Kimoto, Sohei, Michihiro Toritsuka, Kagemasa Kajiwara, et al.. (2012). Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome. Translational Psychiatry. 2(8). e146–e146. 25 indexed citations
15.
Chen, Li, Annalisa Mupo, Tuong Huynh, et al.. (2010). Tbx1 regulates Vegfr3 and is required for lymphatic vessel development. The Journal of Cell Biology. 189(3). 417–424. 61 indexed citations
16.
Earls, Laurie R., Ildar T. Bayazitov, Raymond B. Berry, et al.. (2010). Dysregulation of Presynaptic Calcium and Synaptic Plasticity in a Mouse Model of 22q11 Deletion Syndrome. Journal of Neuroscience. 30(47). 15843–15855. 65 indexed citations
17.
McCue, Karen, Catherine Roberts, Vanessa Kyriakopoulou, et al.. (2009). Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice. Journal of Clinical Investigation. 119(11). 3301–10. 111 indexed citations
18.
McCue, Karen, Catherine Roberts, Vanessa Kyriakopoulou, et al.. (2009). 06-P038 Great vessel development requires dizygous expression of Chd7 and Tbx1 in pharyngeal ectoderm. Mechanisms of Development. 126. S131–S131. 1 indexed citations
19.
Calmont, Amélie, Sarah Ivins, Kelly Lammerts van Bueren, et al.. (2009). Tbx1 controls cardiac neural crest cell migration during arch artery development by regulatingGbx2expression in the pharyngeal ectoderm. Development. 136(18). 3173–3183. 109 indexed citations
20.
Sivagnanasundaram, Sinthuja, Danielle Fletcher, Michael Hubank, et al.. (2007). Differential gene expression in the hippocampus of the Df1/+ mice: A model for 22q11.2 deletion syndrome and schizophrenia. Brain Research. 1139. 48–59. 33 indexed citations

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