Gillian Carpenter

933 citations

17 papers · 706 · h-index 13

Impact in

Molecular Biology
- DNA Repair Mechanisms
- RNA and protein synthesis mechanisms
- Ubiquitin and proteasome pathways
- RNA Research and Splicing
- RNA modifications and cancer
Cell Biology top 10%
- Microtubule and mitosis dynamics

Papers in

Molecular Biology 14
- DNA Repair Mechanisms 8
- Genomics and Chromatin Dynamics 3
- Ubiquitin and proteasome pathways 3
- RNA and protein synthesis mechanisms 2
Genetics 10
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 4

Co-authors: Mark O’Driscoll (13 shared papers)Rita Colnaghi (6 shared papers)Virginia M. Pain (2 shared papers)Simon Morley (2 shared papers)Claudia Kerzendorfer (4 shared papers)Marcel Volker (1 shared paper)Wendy Wood (1 shared paper)Martin Bushell (1 shared paper)
Journals: Human Molecular Genetics (3 papers)Journal of Biological Chemistry (2 papers)PLoS Genetics (2 papers)Human Mutation (1 paper)The American Journal of Human Genetics (1 paper)
Partner nations: United Kingdom United States Japan

In The Last Decade

Gillian Carpenter

17 papers receiving 694 citations

Peers

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-authors

The 25 scholars most cited alongside Gillian Carpenter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Gillian Carpenter Line = papers co-authored together Gillian Carpenter links everyone, so they are left out of the graph.

All Works

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17 of 17 papers shown

#	Work
1	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 ·Martin Bushell, Wendy Wood, Gillian Carpenter, Virginia M. Pain, Simon Morley, Michael J. Clemens	2001	89
2	Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome PLoS Genetics ·Tomoo Ogi, Sarah Walker, Tom Stiff, Emma Hobson, Siripan Limsirichaikul, Gillian Carpenter, Katrina Prescott, Mohnish Suri, Philip J. Byrd, Michiko Matsuse, Norisato Mitsutake, Yuka Nakazawa, Pradeep Vasudevan, Margaret Barrow, Grant S. Stewart, A. Malcolm R. Taylor, Mark O’Driscoll, Penny A. Jeggo	2012	79
3	Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism Human Genetics ·Ghayda Mirzaa, Benjamin Vitre, Gillian Carpenter, I Abramowiçz, Joseph G. Gleeson, Alex R. Paciorkowski, Don W. Cleveland, William B. Dobyns, Mark O’Driscoll	2014	73
4	The consequences of structural genomic alterations in humans: Genomic Disorders, genomic instability and cancer Seminars in Cell and Developmental Biology ·Rita Colnaghi, Gillian Carpenter, Marcel Volker, Mark O’Driscoll	2011	73
5	Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance Journal of Clinical Investigation ·Felicity Payne, Rita Colnaghi, Nuno Rocha, Asha Seth, J. Ieuan Harris, Gillian Carpenter, William Bottomley, Eleanor Wheeler, Stephen Q. Wong, Vladimı́r Saudek, David B. Savage, Stephen O’Rahilly, Jean‐Claude Carel, Inês Barroso, Mark O’Driscoll, Robert K. Semple	2014	72
6	Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks Human Molecular Genetics ·Claudia Kerzendorfer, Annabel Whibley, Gillian Carpenter, Emily Outwin, Shih‐Chieh Chiang, Gillian Turner, Charles E. Schwartz, Sherif F. El‐Khamisy, F. Lucy Raymond, Mark O’Driscoll	2010	61
7	Functional Analysis of Individual Binding Activities of the Scaffold Protein eIF4G Journal of Biological Chemistry ·Tracey M. Hinton, Mark J. Coldwell, Gillian Carpenter, Simon Morley, Virginia M. Pain	2006	53
8	Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome The American Journal of Human Genetics ·Akio Tanaka, Sarah Weinel, Nikoletta Nagy, Mark O’Driscoll, Joey E. Lai‐Cheong, Carol L. Kulp‐Shorten, Alfred L. Knable, Gillian Carpenter, Sheila Fisher, Makiko Hiragun, Yuhki Yanase, Michihiro Hide, Jeffrey P. Callen, John A. McGrath	2012	51
9	Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf–Hirschhorn syndrome Human Molecular Genetics ·Claudia Kerzendorfer, Femke Hannes, Rita Colnaghi, I Abramowiçz, Gillian Carpenter, Joris Vermeesch, Mark O’Driscoll	2012	38
10	CUL4B-deficiency in humans: Understanding the clinical consequences of impaired Cullin 4-RING E3 ubiquitin ligase function Mechanisms of Ageing and Development ·Claudia Kerzendorfer, Lesley Hart, Rita Colnaghi, Gillian Carpenter, Diana Alcantara, Emily Outwin, Antony M. Carr, Mark O’Driscoll	2011	31
11	Increased RPA1 Gene Dosage Affects Genomic Stability Potentially Contributing to 17p13.3 Duplication Syndrome PLoS Genetics ·Emily Outwin, Gillian Carpenter, Weimin Bi, Marjorie Withers, James R. Lupski, Mark O’Driscoll	2011	22
12	Meier–Gorlin syndrome and Wolf–Hirschhorn syndrome: Two developmental disorders highlighting the importance of efficient DNA replication for normal development and neurogenesis DNA repair ·Claudia Kerzendorfer, Rita Colnaghi, I Abramowiçz, Gillian Carpenter, Mark O’Driscoll	2013	21
13	Oral-facial-digital syndrome type I cells exhibit impaired DNA repair; unanticipated consequences of defective OFD1 outside of the cilia network Human Molecular Genetics ·I Abramowiçz, Gillian Carpenter, Mariaevelina Alfieri, Rita Colnaghi, Emily Outwin, Philippe Parent, Christel Thauvin‐Robinet, Daniela Iaconis, Brunella Franco, Mark O’Driscoll	2016	14
14	Ventricular Outflow Tract Reconstructions with Cryopreserved Cardiac Valve Homografts Annals of Surgery ·Richard A. Hopkins, Aurelio A. de los Reyes V, Deborah A. Imperato, Gillian Carpenter, Jeffrey L. Myers, Kerry A. Murphy	1996	11
15	Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient SHILAP Revista de lepidopterología ·Eleanor Raffan, Liam A. Hurst, Saeed Al Turki, Gillian Carpenter, Carol Scott, Allan Daly, Alison J. Coffey, Sanjeev S. Bhaskar, Eleanor Howard, Naz Khan, Helen Kingston, Aarno Palotie, David B. Savage, Mark O’Driscoll, Claire E. L. Smith, Stephen O’Rahilly, Inês Barroso, Robert K. Semple	2011	9
16	Variant ATRX Syndrome with Dysfunction ofATRXandMAGT1Genes Human Mutation ·Ying Qiao, Kajari Mondal, Valentina Trapani, Jiadi Wen, Gillian Carpenter, Robert S. Wildin, E. Magda Price, Richard J. Gibbons, Jennifer N. Eichmeyer, Ruby Jiang, Barbara R. DuPont, Sally Martell, M. E. Suzanne Lewis, Wendy P. Robinson, Mark O’Driscoll, Federica I. Wolf, Michael E. Zwick, Evica Rajcan‐Separovic	2013	8
17	Cardiac dysrhythmias before and after balloon aortic valvuloplasty in children The American Journal of Cardiology ·Gillian Carpenter, Stephen R. Shapiro, John T. Cockerham, Stanley D. Beder	1992	1

About Gillian Carpenter

Gillian Carpenter is a scholar working on Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Rheumatology and Cell Biology, having authored 17 papers that have together received 706 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Chromatin Dynamics (3 papers), Ubiquitin and proteasome pathways (3 papers), Viral Infections and Immunology Research (2 papers), Moyamoya disease diagnosis and treatment (2 papers) and RNA and protein synthesis mechanisms (2 papers). The work is most often cited by research in Molecular Biology (568 citations), Cell Biology (133 citations), Genetics (217 citations), Cancer Research (72 citations) and Oncology (87 citations). Gillian Carpenter has collaborated with scholars based in United Kingdom, United States and Japan. Frequent co-authors include Mark O’Driscoll, Rita Colnaghi, Virginia M. Pain, Simon Morley, Claudia Kerzendorfer, Marcel Volker, Wendy Wood, Martin Bushell, Emily Outwin and Michael J. Clemens. Their work appears in journals such as Human Molecular Genetics, Journal of Biological Chemistry, PLoS Genetics, Human Mutation and The American Journal of Human Genetics.

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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