Amanda J. Walne

4.9k citations

36 papers · 3.0k indexed · h-index 26

Physiology top 1%
Molecular Biology top 5%
Genetics top 5%
Immunology top 10%
Hematology top 5%

Co-authors: Inderjeet Dokal Tom Vulliamy Anna Marrone Michael Kirwan Richard Beswick Philip J. Mason Vincent Plagnol Richard Szydlo
Topics: Telomeres, Telomerase, and Senescence (28 papers)DNA Repair Mechanisms (7 papers)Neutrophil, Myeloperoxidase and Oxidative Mechanisms (5 papers)
Cited by: Aging Physiology Hematology
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences Journal of Clinical Investigation
Partner nations: United Kingdom United States Germany

In The Last Decade

Amanda J. Walne

36 papers receiving 3.0k citations

Peers

Countries citing papers authored by Amanda J. Walne

Since Specialization

Citations

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

Fields of papers citing papers by Amanda J. Walne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amanda J. Walne. 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 Amanda J. Walne. The network helps show where Amanda J. Walne may publish in the future.

Co-authorship network of co-authors of Amanda J. Walne

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda J. Walne. A scholar is included among the top collaborators of Amanda J. Walne 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 Amanda J. Walne. Amanda J. Walne 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	Germline thymidylate synthase deficiency impacts nucleotide metabolism and causes dyskeratosis congenita 2022 ·The American Journal of Human Genetics ·Hemanth Tummala,Amanda J. Walne,Roberto Buccafusca,(unknown),(unknown),Peter N. Robinson,Allyn McConkie‐Rosell,Meredith Wilson,(unknown),Veronica A. Kinsler,(unknown),(unknown),Manthan Patel,Nikolas Pontikos,Veryan Codd,Tom Vulliamy,Inderjeet Dokal	13
2	High-throughput STELA provides a rapid test for the diagnosis of telomere biology disorders 2021 ·Human Genetics ·Kevin Norris,Amanda J. Walne,Mark Ponsford,Kez Cleal,Julia W. Grimstead,Alicia Ellison,(unknown),Inderjeet Dokal,Tom Vulliamy,Duncan M. Baird	16
3	A frameshift variant in specificity protein 1 triggers superactivation of Sp1-mediated transcription in familial bone marrow failure 2020 ·Proceedings of the National Academy of Sciences ·Hemanth Tummala,Amanda J. Walne,Findlay Bewicke‐Copley,Alicia Ellison,Nikolas Pontikos,(unknown),Ana Rio‐Machín,Jasmin Sidhu,Jun Wang,Henrik Hasle,Jude Fitzgibbon,Tom Vulliamy,Inderjeet Dokal	4
4	DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit Maturation 2016 ·The American Journal of Human Genetics ·Hemanth Tummala,Amanda J. Walne,Mike Williams,Nicholas Bockett,Laura C. Collopy,Shirleny Cardoso,Alicia Ellison,Robert Wynn,Thierry Leblanc,Jude Fitzgibbon,David P. Kelsell,David A. van Heel,Elspeth Payne,Vincent Plagnol,Inderjeet Dokal,Tom Vulliamy	73
5	Triallelic and epigenetic-like inheritance in human disorders of telomerase 2015 ·Blood ·Laura C. Collopy,Amanda J. Walne,Shirleny Cardoso,Josu de la Fuente,Mahfuzah Mohamed,Helga V. Toriello,Hannah Tamary,(unknown),(unknown),(unknown),Hemanth Tummala,(unknown),Inderjeet Dokal	33
6	Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita 2015 ·Journal of Clinical Investigation ·Hemanth Tummala,Amanda J. Walne,Laura C. Collopy,Shirleny Cardoso,Josu de la Fuente,Sarah Lawson,James Powell,Nicola Cooper,Alison Foster,Shehla Mohammed,Vincent Plagnol,(unknown),Inderjeet Dokal	134
7	ERCC6L2 Mutations Link a Distinct Bone-Marrow-Failure Syndrome to DNA Repair and Mitochondrial Function 2014 ·The American Journal of Human Genetics ·Hemanth Tummala,Michael Kirwan,Amanda J. Walne,Upal Hossain,Nicholas Jackson,Corinne Pondarré,Vincent Plagnol,Tom Vulliamy,Inderjeet Dokal	43
8	Exome Sequencing Identifies Autosomal-Dominant SRP72 Mutations Associated with Familial Aplasia and Myelodysplasia 2012 ·The American Journal of Human Genetics ·Michael Kirwan,Amanda J. Walne,Vincent Plagnol,Mark Velangi,Aloysius Ho,Upal Hossain,Tom Vulliamy,Inderjeet Dokal	71
9	Inflammatory Skin and Bowel Disease Linked toADAM17Deletion 2011 ·New England Journal of Medicine ·Diana C. Blaydon,Paolo Biancheri,Wei‐Li Di,Vincent Plagnol,Rita Cabral,Matthew A. Brooke,David A. van Heel,Franz Rüschendorf,Mark Toynbee,Amanda J. Walne,Edel A. O’Toole,Joanne E. Martin,Keith Lindley,Tom Vulliamy,Dominic J. Abrams,Thomas T. MacDonald,John Harper,David P. Kelsell	235
10	Dyskeratosis congenita and the DNA damage response 2011 ·British Journal of Haematology ·Michael Kirwan,Richard Beswick,Amanda J. Walne,Upal Hossain,Colin Casimir,Tom Vulliamy,Inderjeet Dokal	26
11	Differences in Disease Severity but Similar Telomere Lengths in Genetic Subgroups of Patients with Telomerase and Shelterin Mutations 2011 ·PLoS ONE ·Tom Vulliamy,Michael Kirwan,Richard Beswick,Upal Hossain,(unknown),(unknown),Judith Marsh,Amanda J. Walne,Inderjeet Dokal	70
12	Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome 2010 ·Human Molecular Genetics ·Amanda J. Walne,Tom Vulliamy,Richard Beswick,Michael Kirwan,Inderjeet Dokal	68
13	Advances in the understanding of dyskeratosis congenita 2009 ·British Journal of Haematology ·Amanda J. Walne,Inderjeet Dokal	126
14	Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia 2009 ·Human Mutation ·Michael Kirwan,Tom Vulliamy,Anna Marrone,Amanda J. Walne,Richard Beswick,Peter Hillmen,Richard J. Kelly,Andrew Stewart,David Bowen,Stefan Schönland,(unknown),(unknown),Maria Gilleece,Inderjeet Dokal	88
15	Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita 2008 ·Proceedings of the National Academy of Sciences ·Tom Vulliamy,Richard Beswick,Michael Kirwan,Anna Marrone,Martin Digweed,Amanda J. Walne,Inderjeet Dokal	235
16	Exogenous TERC alone can enhance proliferative potential, telomerase activity and telomere length in lymphocytes from dyskeratosis congenita patients 2008 ·British Journal of Haematology ·Michael Kirwan,Richard Beswick,Tom Vulliamy,Amit Nathwani,Amanda J. Walne,Colin Casimir,Inderjeet Dokal	29
17	Dyskeratosis Congenita: A historical perspective 2007 ·Mechanisms of Ageing and Development ·Amanda J. Walne,Inderjeet Dokal	54
18	Dyskeratosis Congenita: A Disorder of Defective Telomere Maintenance? 2005 ·International Journal of Hematology ·Amanda J. Walne,Anna Marrone,Inderjeet Dokal	34
19	Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure 2005 ·Blood Cells Molecules and Diseases ·Tom Vulliamy,Amanda J. Walne,Aroon Baskaradas,Philip J. Mason,Anna Marrone,Inderjeet Dokal	148
20	Pyridinium crosslinks in the monitoring of patients with bone metastases from carcinoma of the breast 1997 ·Clinical Oncology ·Amanda J. Walne,Paul J. Jenkins,Ian James,P.N. Plowman	5

About Amanda J. Walne

Amanda J. Walne is a scholar working on Physiology, Dermatology and Immunology, having authored 36 papers that have together received 3.0k indexed citations. Recurring topics across this work include Telomeres, Telomerase, and Senescence (28 papers), DNA Repair Mechanisms (7 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (5 papers). The work is most often cited by research in Aging (171 citations), Physiology (1.9k citations) and Hematology (350 citations). Amanda J. Walne has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Inderjeet Dokal, Tom Vulliamy, Anna Marrone, Michael Kirwan, Richard Beswick, Philip J. Mason, Vincent Plagnol, Richard Szydlo, S. W. Knight and Hemanth Tummala. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

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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