Sue Richards
Impact in
- Genetics top 0.05%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Hematology top 0.2%
Papers in
- Genetics 36
- Chronic Lymphocytic Leukemia Research 33
- Hematology 31
- Chronic Myeloid Leukemia Treatments 19
- Acute Myeloid Leukemia Research 10
- Hematopoietic Stem Cell Transplantation 4
- Co-authors
- Wayne W. GrodySoma DasSherri J. BaleKarl V. VoelkerdingHeidi L. RehmJulie M. Gastier‐FosterDavid BickMadhuri Hegde
- Journals
- Blood (39 papers)British Journal of Haematology (11 papers)Journal of Clinical Oncology (4 papers)Genetics in Medicine (3 papers)Cochrane Database of Systematic Reviews (3 papers)
- Partner nations
- United KingdomUnited StatesIsrael
In The Last Decade
Sue Richards
83 papers receiving 22.1k citations
Hit Papers
Peers
Comparison fields: 5 of 153
- Genetics 8.7k
- Hematology 2.4k
- Genetics 2.2k
- Clinical Biochemistry 952
- Molecular Biology 9.6k
Countries citing papers authored by Sue Richards
This map shows the geographic impact of Sue Richards'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 Sue Richards with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sue Richards more than expected).
Fields of papers citing papers by Sue Richards
This network shows the impact of papers produced by Sue Richards. 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 Sue Richards. The network helps show where Sue Richards may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Sue Richards, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 44 | |
| 2 | Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology Hit paper breakdown → | 2015 | 18892 |
| 3 | Treatment reduction for children and young adults with low-risk acute lymphoblastic leukaemia defined by minimal residual disease (UKALL 2003): a randomised controlled trial Hit paper breakdown → | 2013 | 313 |
| 4 | 2013 | 1 | |
| 5 | 2012 | 26 | |
| 6 | 2012 | 66 | |
| 7 | 2011 | 16 | |
| 8 | 2010 | 50 | |
| 9 | 2009 | 51 | |
| 10 | 2009 | 2 | |
| 11 | 2008 | 40 | |
| 12 | 2007 | 92 | |
| 13 | 2006 | 132 | |
| 14 | Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial Hit paper breakdown → | 2006 | 502 |
| 15 | 2006 | 74 | |
| 16 | 2006 | 191 | |
| 17 | 2005 | 22 | |
| 18 | 2005 | 3 | |
| 19 | Thioguanine-Related Veno-Occlusive Disease of the Liver in Children with Acute Lymphoblastic Leukaemia Report from United Kingdom Medical Research Council Trial ALL97 | 2002 | 2 |
| 20 | 1995 | 5 |
About Sue Richards
Sue Richards is a scholar working on Genetics, Hematology, Public Health, Environmental and Occupational Health, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 85 papers that have together received 22.4k indexed citations. Recurring topics across this work include Acute Lymphoblastic Leukemia research (49 papers), Chronic Lymphocytic Leukemia Research (33 papers), Lymphoma Diagnosis and Treatment (26 papers), Chronic Myeloid Leukemia Treatments (19 papers), Childhood Cancer Survivors' Quality of Life (16 papers), Immunodeficiency and Autoimmune Disorders (11 papers), Acute Myeloid Leukemia Research (10 papers) and Hematopoietic Stem Cell Transplantation (4 papers). The work is most often cited by research in Genetics (8.7k citations), Hematology (2.4k citations), Genetics (2.2k citations), Clinical Biochemistry (952 citations) and Molecular Biology (9.6k citations). Sue Richards has collaborated with scholars based in United Kingdom, United States and Israel. Frequent co-authors include Wayne W. Grody, Soma Das, Sherri J. Bale, Karl V. Voelkerding, Heidi L. Rehm, Julie M. Gastier‐Foster, David Bick, Madhuri Hegde, Elaine Lyon and Nazneen Aziz. Their work appears in journals such as Blood, British Journal of Haematology, Journal of Clinical Oncology, Genetics in Medicine and Cochrane Database of Systematic Reviews.
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.