Anne E. Wiktor
Impact in
- Hematology top 5%
- Acute Myeloid Leukemia Research
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 25
- Genomic variations and chromosomal abnormalities 17
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Chronic Lymphocytic Leukemia Research 6
- Co-authors
- Daniel L. Van Dyke (32 shared papers)William R. Sukov (12 shared papers)Robert B. Jenkins (10 shared papers)Rhett P. Ketterling (14 shared papers)Koichi Maeda (3 shared papers)Benjamin A. Rybicki (2 shared papers)Lester Weiss (4 shared papers)Kathryn E. Pearce (3 shared papers)
- Journals
- Genetics in Medicine (6 papers)Journal of Clinical Oncology (6 papers)American Journal of Clinical Pathology (4 papers)Genes Chromosomes and Cancer (3 papers)Leukemia Research (2 papers)
- Partner nations
- United StatesBelgiumPoland
In The Last Decade
Anne E. Wiktor
54 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 75
- Hematology 263
- Genetics 185
- Cancer Research 258
- Oncology 415
- Genetics 410
Countries citing papers authored by Anne E. Wiktor
This map shows the geographic impact of Anne E. Wiktor'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 Anne E. Wiktor with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anne E. Wiktor more than expected).
Fields of papers citing papers by Anne E. Wiktor
This network shows the impact of papers produced by Anne E. Wiktor. 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 Anne E. Wiktor. The network helps show where Anne E. Wiktor may publish in the future.
Co-authors
The 25 scholars most cited alongside Anne E. Wiktor, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 118 | |
| 2 | 2000 | 118 | |
| 3 | 2012 | 116 | |
| 4 | 2000 | 92 | |
| 5 | 2012 | 77 | |
| 6 | 1992 | 72 | |
| 7 | 2006 | 69 | |
| 8 | 2016 | 66 | |
| 9 | 2013 | 63 | |
| 10 | 2013 | 61 | |
| 11 | 2011 | 58 | |
| 12 | 2005 | 43 | |
| 13 | 2011 | 39 | |
| 14 | 1991 | 38 | |
| 15 | 2004 | 31 | |
| 16 | 2013 | 30 | |
| 17 | 1991 | 25 | |
| 18 | 2010 | 25 | |
| 19 | 2009 | 23 | |
| 20 | 2006 | 22 |
About Anne E. Wiktor
Anne E. Wiktor is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 55 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Acute Myeloid Leukemia Research (10 papers), Prenatal Screening and Diagnostics (10 papers), HER2/EGFR in Cancer Research (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Chromosomal and Genetic Variations (7 papers), Chronic Lymphocytic Leukemia Research (6 papers) and Cancer Genomics and Diagnostics (5 papers). The work is most often cited by research in Hematology (263 citations), Genetics (185 citations), Cancer Research (258 citations), Oncology (415 citations) and Genetics (410 citations). Anne E. Wiktor has collaborated with scholars based in United States, Belgium and Poland. Frequent co-authors include Daniel L. Van Dyke, William R. Sukov, Robert B. Jenkins, Rhett P. Ketterling, Koichi Maeda, Benjamin A. Rybicki, Lester Weiss, Kathryn E. Pearce, Jennelle C. Hodge and Harry H. Yoon. Their work appears in journals such as Genetics in Medicine, Journal of Clinical Oncology, American Journal of Clinical Pathology, Genes Chromosomes and Cancer and Leukemia Research.
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.