Brian E. Ward
Impact in
- Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 22
- Genomic variations and chromosomal abnormalities 14
- BRCA gene mutations in cancer 9
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- Prenatal Screening and Diagnostics 13
- Co-authors
- Thomas Scholl (11 shared papers)Amie M. Deffenbaugh (5 shared papers)Julia Reid (3 shared papers)Wayne W. Grody (1 shared paper)C. Sue Richards (1 shared paper)Sherri J. Bale (1 shared paper)Madhuri Hegde (1 shared paper)Soma Das (1 shared paper)
- Journals
- Prenatal Diagnosis (3 papers)PEDIATRICS (2 papers)American Journal of Obstetrics and Gynecology (2 papers)Fetal Diagnosis and Therapy (2 papers)Journal of Clinical Oncology (2 papers)
- Partner nations
- United StatesGermanyFrance
In The Last Decade
Brian E. Ward
40 papers receiving 2.8k citations
Brian E. Ward's Hit Papers
Peers
Comparison fields: 5 of 112
- Genetics 1.6k
- Cancer Research 378
- Pediatrics, Perinatology and Child Health 429
- Pathology and Forensic Medicine 381
- Oncology 295
Countries citing papers authored by Brian E. Ward
This map shows the geographic impact of Brian E. Ward'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 Brian E. Ward with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Brian E. Ward more than expected).
Fields of papers citing papers by Brian E. Ward
This network shows the impact of papers produced by Brian E. Ward. 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 Brian E. Ward. The network helps show where Brian E. Ward may publish in the future.
Co-authors
The 25 scholars most cited alongside Brian E. Ward, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 Hit paper breakdown → | 2008 | 689 |
| 2 | 2002 | 499 | |
| 3 | 2009 | 304 | |
| 4 | Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens. | 1993 | 178 |
| 5 | 2006 | 157 | |
| 6 | 1997 | 129 | |
| 7 | 1979 | 106 | |
| 8 | 1999 | 92 | |
| 9 | 1994 | 73 | |
| 10 | 2005 | 53 | |
| 11 | 1988 | 52 | |
| 12 | 1996 | 50 | |
| 13 | 1979 | 48 | |
| 14 | 2005 | 45 | |
| 15 | Cytogenetic studies in 100 couples with recurrent spontaneous abortions. | 1980 | 41 |
| 16 | Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH. | 1996 | 37 |
| 17 | 1990 | 37 | |
| 18 | 1989 | 36 | |
| 19 | 1997 | 35 | |
| 20 | 1989 | 35 |
About Brian E. Ward
Brian E. Ward is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine, Molecular Biology and Epidemiology, having authored 41 papers that have together received 3.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (13 papers), BRCA gene mutations in cancer (9 papers), CRISPR and Genetic Engineering (7 papers), Chromosomal and Genetic Variations (6 papers), Cervical Cancer and HPV Research (5 papers), Genetic factors in colorectal cancer (4 papers) and Molecular Biology Techniques and Applications (4 papers). The work is most often cited by research in Genetics (1.6k citations), Cancer Research (378 citations), Pediatrics, Perinatology and Child Health (429 citations), Pathology and Forensic Medicine (381 citations) and Oncology (295 citations). Brian E. Ward has collaborated with scholars based in United States, Germany and France. Frequent co-authors include Thomas Scholl, Amie M. Deffenbaugh, Julia Reid, Wayne W. Grody, C. Sue Richards, Sherri J. Bale, Madhuri Hegde, Soma Das, Elaine Lyon and Daniel B. Bellissimo. Their work appears in journals such as Prenatal Diagnosis, PEDIATRICS, American Journal of Obstetrics and Gynecology, Fetal Diagnosis and Therapy and Journal of Clinical Oncology.
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.