Sandra Weitz

563 total citations
14 papers, 462 citations indexed

About

Sandra Weitz is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sandra Weitz has authored 14 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Genetics. Recurrent topics in Sandra Weitz's work include Genomics and Chromatin Dynamics (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Chronic Lymphocytic Leukemia Research (3 papers). Sandra Weitz is often cited by papers focused on Genomics and Chromatin Dynamics (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Chronic Lymphocytic Leukemia Research (3 papers). Sandra Weitz collaborates with scholars based in Germany, United Kingdom and Switzerland. Sandra Weitz's co-authors include Peter Lichter, Stephan Stilgenbauer, Hartmut Döhner, Martin Bentz, Stephan Wolf, Thomas Boehm, Konstanze Döhner, J. Wilhelm, Peter H. Krammer and Iris Behrmann and has published in prestigious journals such as Journal of Biological Chemistry, Blood and Oncogene.

In The Last Decade

Sandra Weitz

14 papers receiving 452 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sandra Weitz Germany 10 290 133 104 104 87 14 462
Peter Lichter Germany 5 230 0.8× 122 0.9× 81 0.8× 56 0.5× 153 1.8× 6 378
H.L. Drwinga United States 6 340 1.2× 86 0.6× 111 1.1× 83 0.8× 141 1.6× 10 598
J. Thick United Kingdom 8 486 1.7× 115 0.9× 122 1.2× 129 1.2× 257 3.0× 9 688
Giuliano Crispatzu Germany 10 238 0.8× 118 0.9× 93 0.9× 101 1.0× 61 0.7× 20 388
Paul Biggs United Kingdom 7 359 1.2× 85 0.6× 64 0.6× 44 0.4× 136 1.6× 8 495
Vadim Dyomin United States 11 197 0.7× 178 1.3× 217 2.1× 126 1.2× 190 2.2× 13 491
Danièle Lantoine France 12 546 1.9× 109 0.8× 158 1.5× 198 1.9× 187 2.1× 15 839
C Barletta Italy 12 268 0.9× 64 0.5× 55 0.5× 66 0.6× 63 0.7× 28 452
Hélène Dastot France 14 328 1.1× 161 1.2× 129 1.2× 302 2.9× 191 2.2× 26 789
IR Kirsch United States 9 304 1.0× 111 0.8× 120 1.2× 146 1.4× 123 1.4× 17 603

Countries citing papers authored by Sandra Weitz

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Sandra Weitz

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Weitz. A scholar is included among the top collaborators of Sandra Weitz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sandra Weitz. Sandra Weitz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

14 of 14 papers shown
1.
Bridger, Joanna M., Claudia Kalla, Harald Wodrich, et al.. (2004). Nuclear RNAs confined to a reticular compartment between chromosome territories. Experimental Cell Research. 302(2). 180–193. 24 indexed citations
2.
3.
Koesters, Robert, David R. Betts, Mirka Schmid, et al.. (1999). Human Eukaryotic Initiation Factor EIF2C1 Gene: cDNA Sequence, Genomic Organization, Localization to Chromosomal Bands 1p34–p35, and Expression. Genomics. 61(2). 210–218. 37 indexed citations
4.
Wolf, Stephan, Lindsay T. Sharpe, Holger Knau, et al.. (1999). Direct visual resolution of gene copy number in the human photopigment gene array.. PubMed. 40(7). 1585–9. 14 indexed citations
5.
Stilgenbauer, Stephan, J. Wilhelm, Stephan Wolf, et al.. (1998). Expressed sequences as candidates for a novel tumor suppressor gene at band 13q14 in B-cell chronic lymphocytic leukemia and mantle cell lymphoma. Oncogene. 16(14). 1891–1897. 124 indexed citations
6.
7.
Bruyns, Eddy, Antoaneta Mincheva, Henning Kirchgessner, et al.. (1996). Sequence, Genomic Organization, and Chromosomal Localization of the Human LPAP (PTPRCAP) and Mouse CD45-AP/LSM-1 Genes. Genomics. 38(1). 79–83. 5 indexed citations
8.
Kaestner, Klaus H., A. Paula Monaghan, Heidrun Kern, et al.. (1995). The Mouse fkh-2 Gene. Journal of Biological Chemistry. 270(50). 30029–30035. 37 indexed citations
9.
Solinas‐Toldo, Sabina, Regina B. Troyanovsky, Sandra Weitz, et al.. (1995). Bovine desmocollin genes (DSC1, DSC2, DSC3) cluster on Chromosome 24q21/q22. Mammalian Genome. 6(7). 484–486. 1 indexed citations
10.
Stilgenbauer, Stephan, et al.. (1993). High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics. Blood. 81(8). 2118–2124. 99 indexed citations
11.
Stilgenbauer, Stephan, et al.. (1993). High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics. Blood. 81(8). 2118–2124. 2 indexed citations
12.
Lichter, Peter, Henning Walczak, Sandra Weitz, Iris Behrmann, & Peter H. Krammer. (1992). The human APO-1 (APT) antigen maps to 10q23, a region that is syntenic with mouse chromosome 19. Genomics. 14(1). 179–180. 43 indexed citations
13.
Wirkner, Ute, Hartmut Voss, Peter Lichter, et al.. (1992). Human casein kinase II subunit α: Sequence of a processed (pseudo) gene and its localization on chromosome 11. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1131(2). 220–222. 33 indexed citations
14.
Fink, Thomas, Michael Zimmer, Sandra Weitz, et al.. (1992). Human perforin (PRF1) maps to 10q22, a region that is syntenic with mouse chromosome 10. Genomics. 13(4). 1300–1302. 20 indexed citations

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.

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