Andrew Cuthbert

3.6k citations

45 papers · 2.8k indexed · 2 hit papers · h-index 19

Impact in

Genetics top 1%
- Inflammatory Bowel Disease
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders

Papers in ⓘ

Aging 2
Oncology 13
- Cancer-related Molecular Pathways 6

Co-authors: Christopher G. Mathew (13 shared papers)Cathryn M. Lewis (10 shared papers)Muddassar M. Mirza (8 shared papers)Sheila Fisher (9 shared papers)Jochen Hampe (7 shared papers)Stefan Schreiber (6 shared papers)Robert F. Newbold (21 shared papers)Alastair Forbes (7 shared papers)
Journals: Oncogene (3 papers)Annals of Human Genetics (2 papers)Carcinogenesis (2 papers)The American Journal of Human Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Andrew Cuthbert

44 papers receiving 2.7k citations

Hit Papers

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The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease 2002 · 523 citations

Peers

Countries citing papers authored by Andrew Cuthbert

Since Specialization

Citations

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

Fields of papers citing papers by Andrew Cuthbert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Andrew Cuthbert, 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 Andrew Cuthbert Line = papers co-authored together Andrew Cuthbert links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 45 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations The Lancet ·Jochen Hampe, Andrew Cuthbert, Peter J.P. Croucher, Muddassar M. Mirza, Silvia Mascheretti, Sheila Fisher, H Frenzel, Kathy King, Anja Hasselmeyer, Andrew JS MacPherson, Stephen Bridger, Sander van Deventer, Alastair Forbes, Susanna Nikolaus, John Edward Lennard-Jones, Ulrich R. Foelsch, Michael Krawczak, Cathryn M. Lewis, Stefan Schreiber, Christopher G. Mathew Hit paper breakdown →	2001	837
2	The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease Gastroenterology ·Andrew Cuthbert, Sheila Fisher, Muddassar M. Mirza, Kathy King, Jochen Hampe, Peter J.P. Croucher, Silvia Mascheretti, Jeremy Sanderson, Alastair Forbes, John Mansfield, Stefan Schreiber, Cathryn M. Lewis, Christopher G. Mathew Hit paper breakdown →	2002	523
3	SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome Nature Genetics ·Zhiqing Zhu, Jianbo Yao, Timothy Johns, Katherine Fu, Isabelle De Bie, Carol Macmillan, Andrew Cuthbert, Robert F. Newbold, J Wang, Mario Chevrette, Garry K. Brown, Ruth M. Brown, Eric A. Shoubridge	1998	474
4	Telomere length abnormalities in mammalian radiosensitive cells. PubMed ·Joanne McIlrath, Simon Bouffler, Enrique Samper, Andrew Cuthbert, A. Wojcik, I. Szumiel, Peter E. Bryant, Andrew Riches, Ann M. Thompson, Marı́a A. Blasco, R. F. Newbold, Predrag Slijepčević	2001	128
5	Evidence for a NOD2 -independent susceptibility locus for inflammatory bowel disease on chromosome 16p Proceedings of the National Academy of Sciences ·Jochen Hampe, H Frenzel, Muddassar M. Mirza, Peter J.P. Croucher, Andrew Cuthbert, Silvia Mascheretti, Klaus Huse, Matthias Platzer, Stephen Bridger, Birgit Meyer, Peter Nürnberg, Pieter Stokkers, Michael Krawczak, Christopher G. Mathew, Mark Curran, Stefan Schreiber	2001	82
6	Genetic Evidence for Interaction of the 5q31 Cytokine Locus and the CARD15 Gene in Crohn Disease The American Journal of Human Genetics ·Muddassar M. Mirza, Sheila Fisher, Kathy King, Andrew Cuthbert, Jochen Hampe, Jeremy Sanderson, John Mansfield, Peter T. Donaldson, Janet S. Macpherson, Alastair Forbes, Stefan Schreiber, Cathryn M. Lewis, Christopher G. Mathew	2003	82
7	Mechanisms involved in the immortalization of mammalian cells by ionizing radiation and chemical carcinogens Carcinogenesis ·Deborah A. Trott, Andrew Cuthbert, Robert W. Overell, Ivana Russo, Robert F. Newbold	1995	61
8	A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13 The American Journal of Human Genetics ·Agnieszka Seyda, Robert F. Newbold, Thomas J. Hudson, Andrei Verner, Neviana MacKay, Susan Winter, Annette Feigenbaum, Suzann Malaney, Diego González‐Halphen, Andrew Cuthbert, Brian H. Robinson	2001	57
9	Telomerase Suppression by Chromosome 6 in a Human Papillomavirus Type 16-Immortalized Keratinocyte Cell Line and in a Cervical Cancer Cell Line JNCI Journal of the National Cancer Institute ·Renske D.M. Steenbergen, Duco Kramer, C J Meijer, J. M. M. Walboomers, D. A. Trott, Andrew Cuthbert, Robert F. Newbold, Wilhelmina J. I. Overkamp, Małgorzata Z. Zdzienicka, Peter J.F. Snijders	2001	55
10	A telomere-independent senescence mechanism is the sole barrier to Syrian hamster cell immortalization Oncogene ·I H Russo, Andrew Silver, Andrew Cuthbert, Darren K. Griffin, Debbie A. Trott, Robert F. Newbold	1998	35
11	ACCELERATED PAPER: Identification of human tumour suppressor genes by monochromosome transfer: rapid growth-arrest response mapped to 9p21 is mediated solely by the cyclin-D-dependent kinase inhibitor gene, CDKN2A(p16^INK4A) Carcinogenesis ·Nicole L. England, Andrew Cuthbert, Deborah A. Trott, Sarah Jezzard, Tsutomu Nobori, Dennis A. Carson, Robert F. Newbold	1996	35
12	54th Annual Meeting of the American Society of Human Genetics Katherine Y. King, Mobeen A. Sheikh, Andrew Cuthbert, Sheila Fisher, C M Onnie, Maheen Mirza, J Sanderson, Alison Catherine Forbes, Jennifer Mansfield, Cathryn M. Lewis, Roland Roberts, Christopher G. Mathew	2004	35
13	Human chromosome 16 suppresses metastasis but not tumorigenesis in rat prostatic tumor cells. PubMed ·Tomoyuki Mashimo, Misako Watabe, Andrew Cuthbert, Robert F. Newbold, Carrie Rinker‐Schaeffer, Emmanuèle Helfer, Kenji Watabe	1998	32
14	Substrate conformational dynamics facilitate structure-specific recognition of gapped DNA by DNA polymerase Nucleic Acids Research ·Timothy D. Craggs, Marko Sustarsic, Anne Plochowietz, Majid Mosayebi, Hendrik Kaju, Andrew Cuthbert, Johannes Hohlbein, Laura Domicevica, Philip C. Biggin, Jonathan P. K. Doye, Achillefs N. Kapanidis	2019	27
15	Mutation, selection, and evolution of the Crohn disease susceptibility geneCARD15 Human Mutation ·Kathy King, Mohammed Sheikh, Andrew Cuthbert, Sheila Fisher, Clive M. Onnie, Muddassar M. Mirza, Reenal Pattni, Jeremy Sanderson, Alastair Forbes, John Mansfield, Cathryn M. Lewis, Roland G. Roberts, Christopher G. Mathew	2005	27
16	Similar regions of human chromosome 3 are eliminated from or retained in human/human and human/mouse microcell hybrids during tumor growth in severe combined immunodeficient (SCID) mice Proceedings of the National Academy of Sciences ·Ying Yang, Maria Kost‐Alimova, Sigurður Ingvarsson, Qianhui Qiu, Hajnalka Kiss, Anna Szeles, Irina Kholodnyuk, Andrew Cuthbert, George Klein, Stephan Imreh	2001	26
17	SNP Subset Selection for Genetic Association Studies Annals of Human Genetics ·Martyn C Byng, John C. Whittaker, Andrew Cuthbert, Christopher G. Mathew, Cathryn M. Lewis	2003	25
18	A Crohn's disease‐associated insertion polymorphism (3020insC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo‐plantar pustular psoriasis or guttate psoriasis Experimental Dermatology ·Celia N. Young, Michael H. Allen, Andrew Cuthbert, M. Ameen, Colin Veal, J. Leman, A. David Burden, Brian Kirby, C.E.M. Griffiths, Richard C. Trembath, Christopher G. Mathew, Juliet N. Barker	2003	23
19	Functional evidence of novel tumor suppressor genes for cutaneous malignant melanoma. PubMed ·Christopher N. Parris, Julian D. Harris, Darren K. Griffin, Andrew Cuthbert, Andrew Silver, Robert F. Newbold	1999	19
20	Cell immortalization as a key, rate-limiting event in malignant transformation: approaches toward a molecular genetic analysis Toxicology Letters ·Robert F. Newbold, Andrew Cuthbert, Michael Themis, Debbie A. Trott, Andrea L. Blair, Wei Li	1993	16

About Andrew Cuthbert

Andrew Cuthbert is a scholar working on Aging, Oncology, Genetics, Physiology and Molecular Biology, having authored 45 papers that have together received 2.8k indexed citations. Recurring topics across this work include Telomeres, Telomerase, and Senescence (9 papers), Inflammatory Bowel Disease (9 papers), Cancer-related Molecular Pathways (6 papers), DNA Repair Mechanisms (6 papers), Genomics and Chromatin Dynamics (6 papers), Helicobacter pylori-related gastroenterology studies (4 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and Microscopic Colitis (3 papers). The work is most often cited by research in Genetics (1.3k citations), Clinical Biochemistry (264 citations), Immunology (748 citations), Aging (54 citations) and Epidemiology (641 citations). Andrew Cuthbert has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Christopher G. Mathew, Cathryn M. Lewis, Muddassar M. Mirza, Sheila Fisher, Jochen Hampe, Stefan Schreiber, Robert F. Newbold, Alastair Forbes, Kathy King and Peter J.P. Croucher. Their work appears in journals such as Oncogene, Annals of Human Genetics, Carcinogenesis, The American Journal of Human Genetics and Proceedings of the National Academy of Sciences.

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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