Anne Gregor
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Lung Cancer Treatments and Mutations
- Lung Cancer Diagnosis and Treatment
Papers in
- Genetics 15
- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 10
- Genomic variations and chromosomal abnormalities 3
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- Genomics and Chromatin Dynamics 4
- RNA Research and Splicing 4
- Ubiquitin and proteasome pathways 4
- Mitochondrial Function and Pathology 3
- Co-authors
- Alan B. Sandler (1 shared paper)Ulrich Gatzemeier (1 shared paper)Clet Niyikiza (1 shared paper)Claude A. Denham (1 shared paper)Yvon F. Cormier (1 shared paper)Ch. Manegold (1 shared paper)Joachim von Pawel (1 shared paper)Martin Palmer (1 shared paper)
- Journals
- The American Journal of Human Genetics (7 papers)Genetics in Medicine (5 papers)Scientific Reports (3 papers)Clinical Radiology (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
Anne Gregor
37 papers receiving 1.8k citations
Anne Gregor's Hit Papers
Peers
Comparison fields: 5 of 102
- Genetics 440
- Pulmonary and Respiratory Medicine 459
- Oncology 321
- Molecular Biology 647
- Cancer Research 95
Countries citing papers authored by Anne Gregor
This map shows the geographic impact of Anne Gregor'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 Gregor with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anne Gregor more than expected).
Fields of papers citing papers by Anne Gregor
This network shows the impact of papers produced by Anne Gregor. 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 Gregor. The network helps show where Anne Gregor may publish in the future.
Co-authors
The 25 scholars most cited alongside Anne Gregor, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Phase III Trial of Gemcitabine Plus Cisplatin Versus Cisplatin Alone in Patients With Locally Advanced or Metastatic Non–Small-Cell Lung Cancer Hit paper breakdown → | 2000 | 626 |
| 2 | 2010 | 142 | |
| 3 | 2013 | 125 | |
| 4 | 2011 | 105 | |
| 5 | 2017 | 74 | |
| 6 | 2020 | 73 | |
| 7 | 2019 | 63 | |
| 8 | 2021 | 58 | |
| 9 | 2017 | 58 | |
| 10 | 2016 | 51 | |
| 11 | 2017 | 50 | |
| 12 | 2019 | 49 | |
| 13 | A Phase I study of gemcitabine with concurrent radiotherapy in stage III, locally advanced non-small cell lung cancer. | 2003 | 46 |
| 14 | 2018 | 39 | |
| 15 | 2014 | 28 | |
| 16 | 1981 | 26 | |
| 17 | 2004 | 22 | |
| 18 | 2018 | 22 | |
| 19 | 2020 | 21 | |
| 20 | 2020 | 16 |
About Anne Gregor
Anne Gregor is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health and Immunology, having authored 40 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers), Fetal and Pediatric Neurological Disorders (4 papers), Genomics and Chromatin Dynamics (4 papers), RNA Research and Splicing (4 papers), Ubiquitin and proteasome pathways (4 papers), Mitochondrial Function and Pathology (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (440 citations), Pulmonary and Respiratory Medicine (459 citations), Oncology (321 citations), Molecular Biology (647 citations) and Cancer Research (95 citations). Anne Gregor has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Alan B. Sandler, Ulrich Gatzemeier, Clet Niyikiza, Claude A. Denham, Yvon F. Cormier, Ch. Manegold, Joachim von Pawel, Martin Palmer, Binh Thanh Nguyen and Lawrence H. Einhorn. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Scientific Reports, Clinical Radiology and European Journal of Human 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.