Sandra Weitz
Impact in
- Genetics top 10%
- Chronic Lymphocytic Leukemia Research
- Genomic variations and chromosomal abnormalities
- Pathology and Forensic Medicine top 10%
- Lymphoma Diagnosis and Treatment
Papers in
- Genetics 3
- Chronic Lymphocytic Leukemia Research 3
- Animal Genetics and Reproduction 2
-
- Genomics and Chromatin Dynamics 4
- Glycosylation and Glycoproteins Research 3
- RNA Research and Splicing 3
- RNA and protein synthesis mechanisms 3
- Co-authors
- Peter Lichter (13 shared papers)Hartmut Doehner (3 shared papers)S. Stilgenbauer (3 shared papers)Martin Bentz (2 shared papers)Stephan Wolf (2 shared papers)Konstanze Döhner (1 shared paper)Thomas L. J. Boehm (1 shared paper)Jens Wilhelm (1 shared paper)
- Journals
- Genomics (4 papers)Blood (2 papers)Cytogenetic and Genome Research (1 paper)Mammalian Genome (1 paper)Journal of Biological Chemistry (1 paper)
- Partner nations
- GermanyUnited KingdomSwitzerland
In The Last Decade
Sandra Weitz
14 papers receiving 455 citations
Peers
Comparison fields: 5 of 52
- Genetics 136
- Pathology and Forensic Medicine 105
- Immunology 101
- Cancer Research 63
- Molecular Biology 288
Countries citing papers authored by Sandra Weitz
This map shows the geographic impact of Sandra Weitz'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 Sandra Weitz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra Weitz more than expected).
Fields of papers citing papers by Sandra Weitz
This network shows the impact of papers produced by Sandra Weitz. 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 Sandra Weitz. The network helps show where Sandra Weitz may publish in the future.
Co-authors
The 25 scholars most cited alongside Sandra Weitz, 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 | 1998 | 130 | |
| 2 | 1993 | 105 | |
| 3 | 1992 | 43 | |
| 4 | 1995 | 36 | |
| 5 | 1999 | 36 | |
| 6 | 1992 | 33 | |
| 7 | 2004 | 23 | |
| 8 | 1992 | 21 | |
| 9 | Direct visual resolution of gene copy number in the human photopigment gene array. | 1999 | 14 |
| 10 | 1998 | 14 | |
| 11 | 2000 | 9 | |
| 12 | 1996 | 5 | |
| 13 | 1995 | 3 | |
| 14 | 1993 | 2 |
About Sandra Weitz
Sandra Weitz is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Immunology and Genetics, having authored 14 papers that have together received 474 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (4 papers), Glycosylation and Glycoproteins Research (3 papers), Lymphoma Diagnosis and Treatment (3 papers), Chronic Lymphocytic Leukemia Research (3 papers), RNA Research and Splicing (3 papers), RNA and protein synthesis mechanisms (3 papers), Animal Genetics and Reproduction (2 papers) and Acute Lymphoblastic Leukemia research (2 papers). The work is most often cited by research in Genetics (136 citations), Pathology and Forensic Medicine (105 citations), Immunology (101 citations), Cancer Research (63 citations) and Molecular Biology (288 citations). Sandra Weitz has collaborated with scholars based in Germany, United Kingdom and Switzerland. Frequent co-authors include Peter Lichter, Hartmut Doehner, S. Stilgenbauer, Martin Bentz, Stephan Wolf, Konstanze Döhner, Thomas L. J. Boehm, Jens Wilhelm, Peter H. Krammer and Iris Behrmann. Their work appears in journals such as Genomics, Blood, Cytogenetic and Genome Research, Mammalian Genome and Journal of Biological Chemistry.
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.