Judith Brooks
Impact in
- Genetics top 2%
- Virus-based gene therapy research
- Genetics and Neurodevelopmental Disorders
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 11
- Genetics and Neurodevelopmental Disorders 8
- Virus-based gene therapy research 3
-
- Hematopoietic Stem Cell Transplantation 2
- Acute Myeloid Leukemia Research 1
- Co-authors
- William Ted Brown (5 shared papers)Erwin Friedman (3 shared papers)Joseph H. French (3 shared papers)Krystyna E. Wisniewski (2 shared papers)Edmund Charles Jenkins (1 shared paper)Edmund C. Jenkins (4 shared papers)EdmundC. Jenkins (3 shared papers)John M. Opitz (3 shared papers)
- Journals
- The Lancet (3 papers)Nature Medicine (2 papers)The Journal of Pediatrics (1 paper)Journal of Autism and Developmental Disorders (1 paper)American Journal of Medical Genetics (3 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Judith Brooks
15 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 74
- Genetics 1.0k
- Cognitive Neuroscience 290
- Hematology 133
- Oncology 282
- Genetics 108
Countries citing papers authored by Judith Brooks
This map shows the geographic impact of Judith Brooks'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 Judith Brooks with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judith Brooks more than expected).
Fields of papers citing papers by Judith Brooks
This network shows the impact of papers produced by Judith Brooks. 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 Judith Brooks. The network helps show where Judith Brooks may publish in the future.
Co-authors
The 25 scholars most cited alongside Judith Brooks, 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 | 1995 | 500 | |
| 2 | 1998 | 264 | |
| 3 | 1982 | 194 | |
| 4 | 1982 | 113 | |
| 5 | 1981 | 76 | |
| 6 | 1984 | 43 | |
| 7 | 1984 | 36 | |
| 8 | 1989 | 31 | |
| 9 | 1986 | 29 | |
| 10 | T cell depleted haploidentical bone marrow transplantation for the treatment of children with severe combined immunodeficiency. | 2000 | 25 |
| 11 | Autologous bone marrow transplantation with 4-hydroperoxycyclophosphamide purged marrows for children with acute non-lymphoblastic leukemia in second remission. | 1990 | 14 |
| 12 | 1984 | 10 | |
| 13 | 2011 | 5 | |
| 14 | 2010 | 5 | |
| 15 | 2008 | 1 |
About Judith Brooks
Judith Brooks is a scholar working on Genetics, Hematology, Astronomy and Astrophysics, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 15 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Virus-based gene therapy research (3 papers), Hematopoietic Stem Cell Transplantation (2 papers), Solar and Space Plasma Dynamics (2 papers), Prenatal Screening and Diagnostics (2 papers), Autism Spectrum Disorder Research (2 papers), Acute Myeloid Leukemia Research (1 paper) and Geomagnetism and Paleomagnetism Studies (1 paper). The work is most often cited by research in Genetics (1.0k citations), Cognitive Neuroscience (290 citations), Hematology (133 citations), Oncology (282 citations) and Genetics (108 citations). Judith Brooks has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include William Ted Brown, Erwin Friedman, Joseph H. French, Krystyna E. Wisniewski, Edmund Charles Jenkins, Edmund C. Jenkins, EdmundC. Jenkins, John M. Opitz, Joseph A. Church and Gertrude Costin. Their work appears in journals such as The Lancet, Nature Medicine, The Journal of Pediatrics, Journal of Autism and Developmental Disorders and American Journal of Medical 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.