Gillian Carpenter

933 total citations
17 papers, 706 citations indexed

About

Gillian Carpenter is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Gillian Carpenter has authored 17 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Gillian Carpenter's work include DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Gillian Carpenter is often cited by papers focused on DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Gillian Carpenter collaborates with scholars based in United Kingdom, United States and Japan. Gillian Carpenter's co-authors include Mark O’Driscoll, Rita Colnaghi, Virginia M. Pain, Simon Morley, Claudia Kerzendorfer, Marcel Volker, Martin Bushell, Wendy Wood, Michael J. Clemens and Emily Outwin and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Gillian Carpenter

17 papers receiving 694 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gillian Carpenter United Kingdom 13 568 217 133 87 72 17 706
Rebecca Cullum Canada 11 537 0.9× 151 0.7× 63 0.5× 45 0.5× 101 1.4× 18 700
Martin D. Burkhalter Germany 15 609 1.1× 133 0.6× 65 0.5× 117 1.3× 71 1.0× 29 715
Andrey Poleshko United States 15 779 1.4× 96 0.4× 75 0.6× 38 0.4× 47 0.7× 20 864
Erwan Watrin France 16 922 1.6× 159 0.7× 208 1.6× 88 1.0× 68 0.9× 28 1.0k
Deborah Nusskern United States 9 588 1.0× 220 1.0× 63 0.5× 112 1.3× 152 2.1× 9 880
Rohini Desetty United States 7 550 1.0× 104 0.5× 65 0.5× 80 0.9× 120 1.7× 10 601
Lidia Lopez‐Serra Spain 12 776 1.4× 194 0.9× 69 0.5× 68 0.8× 64 0.9× 12 861
Theodoros Kantidakis United Kingdom 11 769 1.4× 52 0.2× 79 0.6× 88 1.0× 113 1.6× 15 873
Daniel Stauffer United States 10 370 0.7× 133 0.6× 149 1.1× 89 1.0× 44 0.6× 10 539
Tomoyoshi Nakadai Japan 16 778 1.4× 101 0.5× 37 0.3× 85 1.0× 112 1.6× 36 939

Countries citing papers authored by Gillian Carpenter

Since Specialization
Citations

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

Fields of papers citing papers by Gillian Carpenter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gillian Carpenter

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

All Works

17 of 17 papers shown
1.
Carpenter, Gillian, Mariaevelina Alfieri, Rita Colnaghi, et al.. (2016). Oral-facial-digital syndrome type I cells exhibit impaired DNA repair; unanticipated consequences of defective OFD1 outside of the cilia network. Human Molecular Genetics. 26(1). ddw364–ddw364. 14 indexed citations
2.
Payne, Felicity, Rita Colnaghi, Nuno Rocha, et al.. (2014). Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance. Journal of Clinical Investigation. 124(9). 4028–4038. 72 indexed citations
3.
Mirzaa, Ghayda, Benjamin Vitre, Gillian Carpenter, et al.. (2014). Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism. Human Genetics. 133(8). 1023–1039. 73 indexed citations
5.
Qiao, Ying, Kajari Mondal, Valentina Trapani, et al.. (2013). Variant ATRX Syndrome with Dysfunction ofATRXandMAGT1Genes. Human Mutation. 35(1). 58–62. 8 indexed citations
6.
Tanaka, Akio, Nikoletta Nagy, Mark O’Driscoll, et al.. (2012). Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome. The American Journal of Human Genetics. 90(3). 511–517. 51 indexed citations
7.
Ogi, Tomoo, Sarah Walker, Tom Stiff, et al.. (2012). Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome. PLoS Genetics. 8(11). e1002945–e1002945. 79 indexed citations
8.
Kerzendorfer, Claudia, Femke Hannes, Rita Colnaghi, et al.. (2012). Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf–Hirschhorn syndrome. Human Molecular Genetics. 21(10). 2181–2193. 38 indexed citations
9.
Raffan, Eleanor, Liam A. Hurst, Saeed Al Turki, et al.. (2011). Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient. SHILAP Revista de lepidopterología. 2. 8–8. 9 indexed citations
10.
Outwin, Emily, Gillian Carpenter, Weimin Bi, et al.. (2011). Increased RPA1 Gene Dosage Affects Genomic Stability Potentially Contributing to 17p13.3 Duplication Syndrome. PLoS Genetics. 7(8). e1002247–e1002247. 22 indexed citations
11.
Colnaghi, Rita, Gillian Carpenter, Marcel Volker, & Mark O’Driscoll. (2011). The consequences of structural genomic alterations in humans: Genomic Disorders, genomic instability and cancer. Seminars in Cell and Developmental Biology. 22(8). 875–885. 73 indexed citations
12.
Kerzendorfer, Claudia, Rita Colnaghi, Gillian Carpenter, et al.. (2011). CUL4B-deficiency in humans: Understanding the clinical consequences of impaired Cullin 4-RING E3 ubiquitin ligase function. Mechanisms of Ageing and Development. 132(8-9). 366–373. 31 indexed citations
13.
Kerzendorfer, Claudia, Annabel Whibley, Gillian Carpenter, et al.. (2010). Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks. Human Molecular Genetics. 19(7). 1324–1334. 61 indexed citations
14.
Hinton, Tracey M., Mark J. Coldwell, Gillian Carpenter, Simon Morley, & Virginia M. Pain. (2006). Functional Analysis of Individual Binding Activities of the Scaffold Protein eIF4G. Journal of Biological Chemistry. 282(3). 1695–1708. 53 indexed citations
15.
Bushell, Martin, Wendy Wood, Gillian Carpenter, et al.. (2001). Disruption of the Interaction of Mammalian Protein Synthesis Eukaryotic Initiation Factor 4B with the Poly(A)-binding Protein by Caspase- and Viral Protease-mediated Cleavages. Journal of Biological Chemistry. 276(26). 23922–23928. 89 indexed citations
16.
Hopkins, Richard A., et al.. (1996). Ventricular Outflow Tract Reconstructions with Cryopreserved Cardiac Valve Homografts. Annals of Surgery. 223(5). 544–554. 11 indexed citations
17.
Carpenter, Gillian, et al.. (1992). Cardiac dysrhythmias before and after balloon aortic valvuloplasty in children. The American Journal of Cardiology. 70(6). 694–695. 1 indexed citations

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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