Stanislawa Weremowicz

10.1k total citations
81 papers, 5.6k citations indexed

About

Stanislawa Weremowicz is a scholar working on Molecular Biology, Genetics and Obstetrics and Gynecology. According to data from OpenAlex, Stanislawa Weremowicz has authored 81 papers receiving a total of 5.6k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 21 papers in Genetics and 13 papers in Obstetrics and Gynecology. Recurrent topics in Stanislawa Weremowicz's work include Uterine Myomas and Treatments (12 papers), Genetic Syndromes and Imprinting (9 papers) and Sarcoma Diagnosis and Treatment (9 papers). Stanislawa Weremowicz is often cited by papers focused on Uterine Myomas and Treatments (12 papers), Genetic Syndromes and Imprinting (9 papers) and Sarcoma Diagnosis and Treatment (9 papers). Stanislawa Weremowicz collaborates with scholars based in United States, United Kingdom and France. Stanislawa Weremowicz's co-authors include Cynthia C. Morton, Matthias A. Hediger, Jonathan A. Fletcher, Hiroyasu Tsukaguchi, Paola Dal Cin, Kornélia Polyák, Marlena S. Fejzo, Bradley J. Quade, Kiran Chada and Jun Yao and has published in prestigious journals such as New England Journal of Medicine, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Stanislawa Weremowicz

81 papers receiving 5.5k citations

Peers

Stanislawa Weremowicz
Stanislawa Weremowicz
Citations per year, relative to Stanislawa Weremowicz Stanislawa Weremowicz (= 1×) peers Yasuteru Muragaki

Countries citing papers authored by Stanislawa Weremowicz

Since Specialization
Citations

This map shows the geographic impact of Stanislawa Weremowicz'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 Stanislawa Weremowicz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stanislawa Weremowicz more than expected).

Fields of papers citing papers by Stanislawa Weremowicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stanislawa Weremowicz. 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 Stanislawa Weremowicz. The network helps show where Stanislawa Weremowicz may publish in the future.

Co-authorship network of co-authors of Stanislawa Weremowicz

This figure shows the co-authorship network connecting the top 25 collaborators of Stanislawa Weremowicz. A scholar is included among the top collaborators of Stanislawa Weremowicz 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 Stanislawa Weremowicz. Stanislawa Weremowicz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Yoshida, Taku, Jee Hyun Kim, Kristopher Carver, et al.. (2015). CLK2 Is an Oncogenic Kinase and Splicing Regulator in Breast Cancer. Cancer Research. 75(7). 1516–1526. 84 indexed citations
2.
Sholl, Lynette M., Stanislawa Weremowicz, Stacy W. Gray, et al.. (2013). Combined Use of ALK Immunohistochemistry and FISH for Optimal Detection of ALK-Rearranged Lung Adenocarcinomas. Journal of Thoracic Oncology. 8(3). 322–328. 117 indexed citations
3.
Yao, Jun, Stanislawa Weremowicz, Bin Feng, et al.. (2006). Combined cDNA Array Comparative Genomic Hybridization and Serial Analysis of Gene Expression Analysis of Breast Tumor Progression. Cancer Research. 66(8). 4065–4078. 133 indexed citations
4.
Weremowicz, Stanislawa, et al.. (2006). Validation of DNA probes for preimplantation genetic diagnosis (PGD) by fluorescencein situ hybridization (FISH) R1. Prenatal Diagnosis. 26(11). 1042–1050. 1 indexed citations
5.
Weremowicz, Stanislawa, et al.. (2001). Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases†. Prenatal Diagnosis. 21(4). 262–269. 50 indexed citations
6.
Vaughan, Carl J., Stanislawa Weremowicz, Marsha M. Goldstein, et al.. (2000). A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosis. Genes Chromosomes and Cancer. 28(2). 133–137. 18 indexed citations
7.
Peng, Ji‐Bin, Xing-Zhen Chen, Urs V. Berger, et al.. (2000). Human Calcium Transport Protein CaT1. Biochemical and Biophysical Research Communications. 278(2). 326–332. 168 indexed citations
9.
Weremowicz, Stanislawa, Amy J. Williams, Bradley J. Quade, et al.. (1999). Expression of HMGIY in Three Uterine Leiomyomata with Complex Rearrangements of Chromosome 6. Cancer Genetics and Cytogenetics. 114(1). 9–16. 31 indexed citations
10.
Qiu, Xiao‐Bo, Yi‐Ling Lin, Kelly C. Thome, et al.. (1998). An Eukaryotic RuvB-like Protein (RUVBL1) Essential for Growth. Journal of Biological Chemistry. 273(43). 27786–27793. 114 indexed citations
11.
Saha, Partha, et al.. (1998). The Human Homolog of Saccharomyces cerevisiae CDC45. Journal of Biological Chemistry. 273(29). 18205–18209. 53 indexed citations
12.
Guo, Ning, Stanislawa Weremowicz, Nicholas J. Lynch, et al.. (1997). Assignment of C1QBP encoding the C1q globular domain binding protein (gC1q-R) to human chromosome 17 band p13.3 by in situ hybridization. Cytogenetic and Genome Research. 77(3-4). 283–284. 17 indexed citations
13.
Nomura, Hideki, et al.. (1997). Identification, Localization, and Expression of Two Novel Human Genes Similar to Deoxyribonuclease I. Genomics. 42(3). 507–513. 84 indexed citations
14.
Wilkins‐Haug, Louise, Mary Sandstrom, & Stanislawa Weremowicz. (1996). Fluorescence in situ hybridization for the detection of aneuploidy from archived fetal cells. Obstetrics and Gynecology. 88(4). 684–687. 2 indexed citations
15.
Schneider, Michael, Hideki Nomura, Jing Zhou, et al.. (1996). A Gene Similar to PKD1 Maps to Chromosome 4q22: A Candidate Gene for PKD2. Genomics. 38(1). 1–4. 20 indexed citations
16.
Fejzo, Marlena S., Xianjin Zhou, Jonathan A. Fletcher, et al.. (1995). Disruption of the architectural factor HMGI-C: DNA-binding AT hook motifs fused in lipomas to distinct transcriptional regulatory domains. Cell. 82(1). 57–65. 363 indexed citations
17.
Zhao, Yi, Christian Bjørbæk, Stanislawa Weremowicz, Cynthia C. Morton, & David E. Moller. (1995). RSK3 Encodes a Novel pp90 rsk Isoform with a Unique N-Terminal Sequence: Growth Factor-Stimulated Kinase Function and Nuclear Translocation. Molecular and Cellular Biology. 15(8). 4353–4363. 120 indexed citations
18.
Weremowicz, Stanislawa, Harry P. Kozakewich, Daniel A. Haber, et al.. (1994). Identification of genetically aberrant cell lineages in Wilms' tumors. Genes Chromosomes and Cancer. 10(1). 40–48. 7 indexed citations
19.
Weremowicz, Stanislawa, et al.. (1994). Localization of Serum Biotinidase (BTD) to Human Chromosome 3 in Band p25. Genomics. 22(3). 662–663. 34 indexed citations
20.
Ney, Paul A., Nancy C. Andrews, Stephen M. Jane, et al.. (1993). Purification of the Human NF-E2 Complex: cDNA Cloning of the Hematopoietic Cell-Specific Subunit and Evidence for an Associated Partner. Molecular and Cellular Biology. 13(9). 5604–5612. 42 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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