Daniela S. Gerhard
Impact in
- Cancer Research top 2%
- Cancer-related molecular mechanisms research
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
Papers in
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- Genomics and Chromatin Dynamics 8
- Epigenetics and DNA Methylation 7
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- Cancer Genomics and Diagnostics 13
- Co-authors
- David E. Housman (11 shared papers)Janice A. Egeland (7 shared papers)David L. Pauls (5 shared papers)Kenneth K. Kídd (3 shared papers)Abram M. Hostetter (2 shared papers)Jon Sussex (1 shared paper)David L. Stern (1 shared paper)Dione K. Bailey (1 shared paper)
- Journals
- Blood (11 papers)Genomics (6 papers)Cancer Research (6 papers)Proceedings of the National Academy of Sciences (5 papers)Cytogenetic and Genome Research (5 papers)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
Daniela S. Gerhard
81 papers receiving 3.8k citations
Hit Papers
Peers
Comparison fields: 5 of 135
- Cancer Research 777
- Genetics 1.1k
- Molecular Biology 2.3k
- Hematology 322
- Biological Psychiatry 56
Countries citing papers authored by Daniela S. Gerhard
This map shows the geographic impact of Daniela S. Gerhard'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 Daniela S. Gerhard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela S. Gerhard more than expected).
Fields of papers citing papers by Daniela S. Gerhard
This network shows the impact of papers produced by Daniela S. Gerhard. 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 Daniela S. Gerhard. The network helps show where Daniela S. Gerhard may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniela S. Gerhard, 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 82 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Transcriptional Maps of 10 Human Chromosomes at 5-Nucleotide Resolution Hit paper breakdown → | 2005 | 881 |
| 2 | Bipolar affective disorders linked to DNA markers on chromosome 11 Hit paper breakdown → | 1987 | 565 |
| 3 | 1989 | 303 | |
| 4 | 2011 | 190 | |
| 5 | 1985 | 166 | |
| 6 | 1981 | 136 | |
| 7 | 1989 | 114 | |
| 8 | 2016 | 104 | |
| 9 | 2019 | 77 | |
| 10 | 2018 | 76 | |
| 11 | 1981 | 76 | |
| 12 | 1987 | 65 | |
| 13 | Loss of heterozygosity of markers on chromosome 11 in tumors from patients with multiple endocrine neoplasia syndrome type 1. | 1990 | 59 |
| 14 | 1995 | 58 | |
| 15 | 2006 | 57 | |
| 16 | 1985 | 56 | |
| 17 | 1991 | 56 | |
| 18 | Polymorphisms in the prostate cancer susceptibility gene HPC2/ELAC2 in multiplex families and healthy controls. | 2001 | 50 |
| 19 | 2007 | 46 | |
| 20 | 1997 | 43 |
About Daniela S. Gerhard
Daniela S. Gerhard is a scholar working on Molecular Biology, Cancer Research, Genetics, Hematology and Oncology, having authored 82 papers that have together received 3.9k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (11 papers), Acute Myeloid Leukemia Research (10 papers), Genomics and Chromatin Dynamics (8 papers), Epigenetics and DNA Methylation (7 papers), Acute Lymphoblastic Leukemia research (6 papers), Chromosomal and Genetic Variations (6 papers) and Cancer-related Molecular Pathways (5 papers). The work is most often cited by research in Cancer Research (777 citations), Genetics (1.1k citations), Molecular Biology (2.3k citations), Hematology (322 citations) and Biological Psychiatry (56 citations). Daniela S. Gerhard has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include David E. Housman, Janice A. Egeland, David L. Pauls, Kenneth K. Kídd, Abram M. Hostetter, Jon Sussex, David L. Stern, Dione K. Bailey, Srinka Ghosh and Jörg Drenkow. Their work appears in journals such as Blood, Genomics, Cancer Research, Proceedings of the National Academy of Sciences and Cytogenetic and Genome 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.