Katherine Siminovitch

12.5k total citations · 1 hit paper
49 papers, 3.5k citations indexed

About

Katherine Siminovitch is a scholar working on Immunology, Genetics and Molecular Biology. According to data from OpenAlex, Katherine Siminovitch has authored 49 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Immunology, 13 papers in Genetics and 12 papers in Molecular Biology. Recurrent topics in Katherine Siminovitch's work include Galectins and Cancer Biology (8 papers), Protein Tyrosine Phosphatases (7 papers) and Chronic Lymphocytic Leukemia Research (6 papers). Katherine Siminovitch is often cited by papers focused on Galectins and Cancer Biology (8 papers), Protein Tyrosine Phosphatases (7 papers) and Chronic Lymphocytic Leukemia Research (6 papers). Katherine Siminovitch collaborates with scholars based in Canada, United States and United Kingdom. Katherine Siminovitch's co-authors include Robert M. Plenge, Peter K. Gregersen, William G. Newman, Jane Worthington, Eli A. Stahl, Soumya Raychaudhuri, Paul I. W. de Bakker, Lars Alfredsson, Xiangdong Liu and Christopher I. Amos and has published in prestigious journals such as Nature, New England Journal of Medicine and Journal of Clinical Investigation.

In The Last Decade

Katherine Siminovitch

49 papers receiving 3.5k citations

Hit Papers

1 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis

2012 617 citations Soumya Raychaudhuri, Eli A. Stahl et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Katherine Siminovitch Canada	26	1.0k	934	917	761	514	49	3.5k
Pekka Kurki Finland	35	1.1k 1.1×	1.1k 1.2×	1.1k 1.2×	443 0.6×	379 0.7×	95	4.2k
Nicole Fabien France	35	894 0.9×	764 0.8×	740 0.8×	729 1.0×	930 1.8×	146	3.7k
Gerda Horst Netherlands	40	1.6k 1.6×	1.3k 1.4×	1.8k 2.0×	319 0.4×	368 0.7×	88	4.6k
Norbert Sepp Austria	35	1.2k 1.1×	824 0.9×	794 0.9×	231 0.3×	441 0.9×	115	3.5k
Karel J.M. Assmann Netherlands	34	1.3k 1.2×	613 0.7×	993 1.1×	301 0.4×	209 0.4×	98	4.0k
Yaakov Naparstek Israel	34	1.8k 1.8×	1.0k 1.1×	1.0k 1.1×	321 0.4×	276 0.5×	105	4.1k
Anne Spurkland Norway	35	1.8k 1.7×	346 0.4×	913 1.0×	777 1.0×	597 1.2×	116	3.9k
Miguel Ángel López‐Nevot Spain	38	2.6k 2.5×	724 0.8×	945 1.0×	661 0.9×	407 0.8×	152	4.4k
Anne Dubart‐Kupperschmitt France	35	573 0.6×	170 0.2×	2.2k 2.4×	708 0.9×	264 0.5×	109	3.8k
Frédérique Ponchel United Kingdom	36	1.6k 1.5×	1.4k 1.5×	1.1k 1.2×	293 0.4×	285 0.6×	108	4.3k

Countries citing papers authored by Katherine Siminovitch

Since Specialization

Citations

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

Fields of papers citing papers by Katherine Siminovitch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katherine Siminovitch

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

All Works

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20 of 20 papers shown

Gruner, Christiane, Raymond H. Chan, Andrew Crean, et al.. (2014). Significance of left ventricular apical–basal muscle bundle identified by cardiovascular magnetic resonance imaging in patients with hypertrophic cardiomyopathy. European Heart Journal. 35(39). 2706–2713. 56 indexed citations

Nam, Robert K., William Zhang, Katherine Siminovitch, et al.. (2011). New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort. Cancer Biology & Therapy. 12(11). 997–1004. 29 indexed citations

Martini, Maurizio, Anna Maria Ferrara, Manuela Giachelia, et al.. (2011). Association of the OCTN1/1672T variant with increased risk for colorectal cancer in young individuals and ulcerative colitis patients. Inflammatory Bowel Diseases. 18(3). 439–448. 23 indexed citations

Stahl, Eli A., Fina Kurreeman, Peter K. Gregersen, et al.. (2011). Fine mapping the TAGAP risk locus in rheumatoid arthritis. Genes and Immunity. 12(4). 314–318. 24 indexed citations

Kim, Dong Hwan, Wei Xu, Suzanne Kamel‐Reid, et al.. (2009). Clinical Relevance of a Pharmacogenetic Approach Using Multiple Candidate Genes to Predict Response and Resistance to Imatinib Therapy in Chronic Myeloid Leukemia. Clinical Cancer Research. 15(14). 4750–4758. 154 indexed citations

Newman, William G., et al.. (2009). Genetic Variants in IL-23R and ATG16L1 Independently Predispose to Increased Susceptibility to Crohn's Disease in a Canadian Population. Journal of Clinical Gastroenterology. 43(5). 444–447. 30 indexed citations

Gregersen, Peter K., C. I. Amos, Annette T. Lee, et al.. (2009). REL, encoding a member of the NF-κB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. Nature Genetics. 41(7). 820–823. 243 indexed citations

Pao, Lily, Karen Badour, Katherine Siminovitch, & Benjamin G. Neel. (2007). Nonreceptor Protein-Tyrosine Phosphatases in Immune Cell Signaling. Annual Review of Immunology. 25(1). 473–523. 148 indexed citations

Newman, William G., Qing Zhang, Xiangdong Liu, et al.. (2006). Rheumatoid arthritis association with the FCRL3 –169C polymorphism is restricted to PTPN22 1858T–homozygous individuals in a Canadian population. Arthritis & Rheumatism. 54(12). 3820–3827. 52 indexed citations

10.

Newman, William G., Richard F. Wintle, Mark Van Oene, et al.. (2005). SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian population. Arthritis & Rheumatism. 52(2). 425–429. 35 indexed citations

11.

Thompson, Miles D., Raffick A.R. Bowen, Betty Wong, et al.. (2005). Whole genome amplification of buccal cell DNA: genotyping concordance before and after multiple displacement amplification. Clinical Chemistry and Laboratory Medicine (CCLM). 43(2). 157–62. 20 indexed citations

12.

Newman, William G. & Katherine Siminovitch. (2005). Recent advances in the genetics of inflammatory bowel disease.. PubMed. 21(4). 401–7. 48 indexed citations

13.

Newman, William G., Mark S. Silverberg, Xiangjun Gu, et al.. (2004). CARD15 and HLA DRB1 Alleles Influence Susceptibility and Disease Localization in Crohn's Disease. The American Journal of Gastroenterology. 99(2). 306–315. 76 indexed citations

14.

Brown, Matthew A., S.H. Laval, Andrew E. Timms, et al.. (2000). Confirmation of non-MHC genetic loci by whole genome linkage studies in ankylosing spondylitis.. Queensland's institutional digital repository (The University of Queensland). 43(9). 1 indexed citations

15.

Cruz, L.A.G. da, et al.. (2000). Involvement of the Lymphocyte Cytoskeleton in Antigen-Receptor Signaling. Current topics in microbiology and immunology. 245(1). 135–167. 2 indexed citations

16.

Huang, D F, Katherine Siminovitch, Xiong Liu, et al.. (1995). Population and family studies of three disease-related polymorphic genes in systemic lupus erythematosus.. Journal of Clinical Investigation. 95(4). 1766–1772. 20 indexed citations

17.

Adams, Mark E., et al.. (1995). The role of viscosupplementation with hylan G-F 20 (Synvisc®) in the treatment of osteoarthritis of the knee: a Canadian multicenter trial comparing hylan G-F 20 alone, hylan G-F 20 with non-steroidal anti-inflammatory drugs (NSAIDs) and NSAIDs alone. Osteoarthritis and Cartilage. 3(4). 213–225. 293 indexed citations

18.

Wu, Yongjian, Giovambattista Pani, Katherine Siminovitch, & Nobumichi Hozumi. (1995). Antigen receptor‐triggered apoptosis in immature B cell lines is associated with the binding of a 44‐kDa phosphoprotein to the PTP1C tyrosine phosphatase. European Journal of Immunology. 25(8). 2279–2284. 14 indexed citations

19.

Greer, Wenda, Monica Peacocke, & Katherine Siminovitch. (1992). The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1. Human Genetics. 88(4). 453–456. 14 indexed citations

20.

Greer, Wenda, Melanie M. Mahtani, Pak C. Kwong, et al.. (1989). Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction. Human Genetics. 83(3). 227–230. 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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