A. Mitri

994 total citations
9 papers, 741 citations indexed

About

A. Mitri is a scholar working on Pathology and Forensic Medicine, Oncology and Cancer Research. According to data from OpenAlex, A. Mitri has authored 9 papers receiving a total of 741 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pathology and Forensic Medicine, 5 papers in Oncology and 5 papers in Cancer Research. Recurrent topics in A. Mitri's work include Genetic factors in colorectal cancer (9 papers), Cancer Genomics and Diagnostics (5 papers) and Colorectal Cancer Screening and Detection (4 papers). A. Mitri is often cited by papers focused on Genetic factors in colorectal cancer (9 papers), Cancer Genomics and Diagnostics (5 papers) and Colorectal Cancer Screening and Detection (4 papers). A. Mitri collaborates with scholars based in Canada, Germany and United States. A. Mitri's co-authors include Bharati Bapat, Steven Gallinger, Andrew J. Smith, K Hay, Steven Gallinger, H. Štern, Mark Redston, H Griesser, Wolfgang G. Ballhausen and Tak W. Mak and has published in prestigious journals such as Nature Genetics, Gastroenterology and Gut.

In The Last Decade

A. Mitri

9 papers receiving 709 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Mitri Canada	7	535	327	326	229	103	9	741
Hansjakob Müller Switzerland	14	384 0.7×	220 0.7×	269 0.8×	164 0.7×	163 1.6×	42	647
Stefania Segditsas United Kingdom	13	401 0.7×	628 1.9×	425 1.3×	193 0.8×	180 1.7×	15	1.1k
Yuko Suemoto United States	8	267 0.5×	408 1.2×	322 1.0×	181 0.8×	41 0.4×	8	655
Victoria Valinluck Lao United States	9	256 0.5×	510 1.6×	288 0.9×	237 1.0×	50 0.5×	17	797
Hiroyuki Ohata Japan	9	241 0.5×	295 0.9×	152 0.5×	219 1.0×	117 1.1×	9	557
J G Guillem United States	10	134 0.3×	240 0.7×	370 1.1×	199 0.9×	54 0.5×	11	706
Kajsa Ericson Sweden	7	185 0.3×	427 1.3×	221 0.7×	110 0.5×	39 0.4×	7	678
Matthias Jungck Germany	11	495 0.9×	229 0.7×	322 1.0×	255 1.1×	111 1.1×	16	647
Simeen Malik United States	5	162 0.3×	432 1.3×	213 0.7×	188 0.8×	71 0.7×	5	605
Catherine Bond Australia	14	287 0.5×	233 0.7×	311 1.0×	144 0.6×	29 0.3×	20	521

Countries citing papers authored by A. Mitri

Since Specialization

Citations

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

Fields of papers citing papers by A. Mitri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Mitri

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

All Works

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9 of 9 papers shown

1.

Ramyar, Lily, A. Mitri, Aaron Pollett, et al.. (2009). A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome. Journal of Human Genetics. 55(1). 37–41. 8 indexed citations

2.

Bapat, Bharati, Hussein Z Noorani, Z. Cohen, et al.. (1999). Cost comparison of predictive genetic testing versus conventional clinical screening for familial adenomatous polyposis. Gut. 44(5). 698–703. 34 indexed citations

3.

Pal, Tuya, Lisa Madlensky, Christopher Sherman, et al.. (1999). Mismatch Repair Gene Defects Contribute to the Genetic Basis of Double Primary Cancers of the Colorectum and Endometrium. Human Molecular Genetics. 8(5). 823–829. 69 indexed citations

4.

Soravia, Claudio, Lisa Madlensky, A. Mitri, et al.. (1998). Genotype-phenotype correlations in patients with attenuated adenomatous polyposis coli. Gastroenterology. 114. A682–A682. 1 indexed citations

5.

Xia, Ling, Weiwei Shen, A. Mitri, et al.. (1996). A truncated hMSH2 transcript occurs as a common variant in the population: implications for genetic diagnosis.. PubMed. 56(10). 2289–92. 38 indexed citations

6.

Reitmair, Armin, Rudolf Schmits, Amy Ewel, et al.. (1995). MSH2 deficient mice are viable and susceptible to lymphoid tumours. Nature Genetics. 11(1). 64–70. 328 indexed citations

7.

Gallinger, Steven, et al.. (1995). Somatic APC and K-ras codon 12 mutations in periampullary adenomas and carcinomas from familial adenomatous polyposis patients.. PubMed. 10(9). 1875–8. 30 indexed citations

8.

Smith, Andrew J., H. Štern, K Hay, et al.. (1994). Somatic APC and K-ras codon 12 mutations in aberrant crypt foci from human colons.. PubMed. 54(21). 5527–30. 227 indexed citations

9.

Bapat, Bharati, A. Mitri, & Cheryl R. Greenberg. (1993). Improved predictive carrier testing for familial adenomatous polyposis using DNA from a single archival specimen and polymorphic markers with multiple alleles. Human Pathology. 24(12). 1376–1379. 6 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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