David R. Betts

2.7k total citations
70 papers, 1.6k citations indexed

About

David R. Betts is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, David R. Betts has authored 70 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 20 papers in Genetics and 19 papers in Public Health, Environmental and Occupational Health. Recurrent topics in David R. Betts's work include Acute Lymphoblastic Leukemia research (17 papers), Genomic variations and chromosomal abnormalities (11 papers) and Acute Myeloid Leukemia Research (10 papers). David R. Betts is often cited by papers focused on Acute Lymphoblastic Leukemia research (17 papers), Genomic variations and chromosomal abnormalities (11 papers) and Acute Myeloid Leukemia Research (10 papers). David R. Betts collaborates with scholars based in Switzerland, United States and Ireland. David R. Betts's co-authors include Felix Niggli, Robert Koesters, Anthony W. Chow, Lucien B. Guze, Arnold S. Bayer, Matthew McKenzie, Hyunah Cho, Sharon L. Foster, Sidney E. Chang and Magnus von Knebel Doeberitz and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Clinical Cancer Research.

In The Last Decade

David R. Betts

67 papers receiving 1.6k citations

Peers

Countries citing papers authored by David R. Betts

Since Specialization

Citations

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

Fields of papers citing papers by David R. Betts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David R. Betts. 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 David R. Betts. The network helps show where David R. Betts may publish in the future.

Co-authorship network of co-authors of David R. Betts

This figure shows the co-authorship network connecting the top 25 collaborators of David R. Betts. A scholar is included among the top collaborators of David R. Betts 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 David R. Betts. David R. Betts 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	Paediatric lymphoblastic lymphoma: a national review of 20 years of clinical and biological data in Ireland 2025 ·Annals of Hematology ·Amélie Trinquand, David R. Betts, Seán Rooney, (unknown), Peter McCarthy, (unknown), Jonathan Bond, Aengus O’Marcaigh, (unknown), Owen Smith	0
2	A systematic review of research on empathy in health care 2022 ·Health Services Research ·Ingrid M. Nembhard, Guy David, (unknown), David R. Betts, Jennifer M. Radin	77
3	Nicolaides–Baraitser syndrome in a patient with hypertrophic cardiomyopathy and SMARCA2 gene deletion 2021 ·Cardiology in the Young ·(unknown), Sophie Duignan, (unknown), David R. Betts, Andrew Green, Colin J. McMahon	3
4	A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder 2015 ·BMC Medical Genetics ·Jillian P. Casey, Patricia Goggin, Jennifer McDaid, (unknown), Sean Ennis, David R. Betts, Jane S. Lucas, B. Elnazir, Sally Ann Lynch	10
5	Vocal cord paralysis in association with 9q34 duplication 2014 ·Clinical Dysmorphology ·(unknown), Jillian P. Casey, John Russell, Jennifer McDaid, David R. Betts, Sally Ann Lynch	14
6	High-resolution Genome-wide Copy-number Analyses Identify Localized Copy-number Alterations in Ewing Sarcoma 2013 ·Diagnostic Molecular Pathology ·Miriam A. Lynn, Yuexiang Wang, (unknown), Naisha Shah, Judith Conroy, Sean Ennis, T.J. Morris, David R. Betts, Jonathan A. Fletcher, Maureen J. O’Sullivan	14
7	A t(12;17)(p13;q12) identifies a distinct TEL rearrangement-negative subtype of precursor-B acute lymphoblastic leukemia 2006 ·Cancer Genetics and Cytogenetics ·Alistair Reid, (unknown), Nicolas von der Weid, Felix Niggli, David R. Betts	6
8	ATM alterations in childhood non-Hodgkin lymphoma 2006 ·Cancer Genetics and Cytogenetics ·Fabienne Gumy‐Pause, Pierre Wacker, Philippe Maillet, David R. Betts, André‐Pascal Sappino	10
9	Array comparative genomic hybridization reveals unbalanced gain of the MYCN region in Wilms tumors 2006 ·Cancer Genetics and Cytogenetics ·(unknown), Alexa Burger, (unknown), Felix Niggli, Beat W. Schäfer, David R. Betts	19
10	Cytogenetics of pineoblastoma: four new cases and a literature review 2006 ·Cancer Genetics and Cytogenetics ·(unknown), Kurt Leibundgut, Felix Niggli, David R. Betts	11
11	Favorable outcome of triploid neuroblastomas: a contribution to the special oncogenesis of neuroblastoma 2006 ·Cancer Genetics and Cytogenetics ·Ruediger Spitz, David R. Betts, Thorsten Simon, (unknown), (unknown), Felix Niggli, Karen Ernestus, Frank Berthold, Barbara Hero	26
12	ATM gene alterations in childhood acute lymphoblastic leukemias 2003 ·Human Mutation ·(unknown), Pierre Wacker, Philippe Maillet, David R. Betts, André‐Pascal Sappino	27
13	Clonal expansion and not cell interconversion is the basis for the neuroblast and nonneuronal types of the SK-N-SH neuroblastoma cell line 2003 ·Cancer Genetics and Cytogenetics ·Ninette Cohen, David R. Betts, Gideon Rechavi, Ninette Amariglio, Luba Trakhtenbrot	28
14	Co-occurrence of neuroblastoma and nephroblastoma in an infant with Fanconi's anemia 2002 ·Human Pathology ·Heidi Bissig, (unknown), Markus Tolnay, (unknown), Jan Richter, David R. Betts, Elisabeth Bruder, Thomas Kühne	13
15	Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY) 2001 ·Genes Chromosomes and Cancer ·Ninette Cohen, David R. Betts, Luba Trakhtenbrot, Felix Niggli, Ninette Amariglio, F. Brok‐Simoni, Gideon Rechavi, Dafna Meitar	19
16	The Investigation of Karyotypic Instability in the High-Hyperdiploidy Subgroup of Acute Lymphoblastic Leukemia 2001 ·Leukemia & lymphoma ·David R. Betts, (unknown), Michael A. Grotzer, Felix Niggli	9
17	Loss of X chromosome in childhood acute lymphoblastic leukemia 2001 ·Cancer Genetics and Cytogenetics ·(unknown), Felix Niggli, Kurt Leibundgut, Ueli Caflisch, David R. Betts	14
18	Human Eukaryotic Initiation Factor EIF2C1 Gene: cDNA Sequence, Genomic Organization, Localization to Chromosomal Bands 1p34–p35, and Expression 1999 ·Genomics ·Robert Koesters, (unknown), David R. Betts, (unknown), Mirka Schmid, (unknown), (unknown), Sandra Weitz, Peter Lichter, Philipp U. Heitz, Magnus von Knebel Doeberitz, J. Briner	37
19	Cytogenetic analysis in a case of intraocular medulloepithelioma 1996 ·Cancer Genetics and Cytogenetics ·David R. Betts, Kurt Leibundgut, Felix Niggli	12
20	A 45,X/69,XXY fetus 1989 ·Clinical Genetics ·David R. Betts, Claudine Fear, Teresa Barby, Mary J. Seller	1

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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