Iris Schrijver

5.3k total citations
98 papers, 3.1k citations indexed

About

Iris Schrijver is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Iris Schrijver has authored 98 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 28 papers in Genetics and 19 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Iris Schrijver's work include Hearing, Cochlea, Tinnitus, Genetics (17 papers), Cystic Fibrosis Research Advances (14 papers) and Connexins and lens biology (14 papers). Iris Schrijver is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (17 papers), Cystic Fibrosis Research Advances (14 papers) and Connexins and lens biology (14 papers). Iris Schrijver collaborates with scholars based in United States, Estonia and United Kingdom. Iris Schrijver's co-authors include James L. Zehnder, Uta Francke, Heinz Furthmayr, Thomas Brenn, Phyllis Gardner, Juan Rodriguez‐Paris, Teri A. Longacre, Wei Liu, Kay W. Chang and Jason D. Merker and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Clinical Oncology.

In The Last Decade

Iris Schrijver

98 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Iris Schrijver United States 33 984 819 616 550 431 98 3.1k
Jean‐Jacques Cassiman Belgium 37 2.0k 2.0× 990 1.2× 673 1.1× 247 0.4× 538 1.2× 185 4.9k
R Harris United Kingdom 38 2.1k 2.1× 1.5k 1.9× 792 1.3× 898 1.6× 432 1.0× 174 7.2k
Sonia Abdelhak Tunisia 26 1.7k 1.7× 953 1.2× 186 0.3× 247 0.4× 187 0.4× 206 3.3k
Jonathan S. T. Sham Hong Kong 38 1.6k 1.6× 499 0.6× 849 1.4× 634 1.2× 271 0.6× 80 4.1k
Peter Farndon United Kingdom 24 1.4k 1.4× 969 1.2× 173 0.3× 210 0.4× 281 0.7× 63 3.0k
Yuval Yaron Israel 35 1.2k 1.2× 1.2k 1.5× 243 0.4× 162 0.3× 155 0.4× 182 4.8k
Marta E. Alarcón‐Riquelme Sweden 49 2.2k 2.2× 2.0k 2.5× 312 0.5× 605 1.1× 695 1.6× 218 9.4k
Robert M. Verdijk Netherlands 36 1.2k 1.2× 244 0.3× 340 0.6× 248 0.5× 139 0.3× 194 4.7k
Deborah Phippard United States 26 773 0.8× 857 1.0× 221 0.4× 85 0.2× 263 0.6× 42 4.1k
Koh-ichiro Yoshiura Japan 31 1.8k 1.9× 1.2k 1.5× 272 0.4× 469 0.9× 168 0.4× 159 3.4k

Countries citing papers authored by Iris Schrijver

Since Specialization
Citations

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

Fields of papers citing papers by Iris Schrijver

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iris Schrijver

This figure shows the co-authorship network connecting the top 25 collaborators of Iris Schrijver. A scholar is included among the top collaborators of Iris Schrijver 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 Iris Schrijver. Iris Schrijver 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.
Rosenbaum, Jason N., Anna B. Berry, Alanna J. Church, et al.. (2021). A Curriculum for Genomic Education of Molecular Genetic Pathology Fellows. Journal of Molecular Diagnostics. 23(10). 1218–1240. 2 indexed citations
2.
Brennan, Marie‐Luise & Iris Schrijver. (2015). Cystic Fibrosis. Journal of Molecular Diagnostics. 18(1). 3–14. 51 indexed citations
3.
Lyon, Elaine, Iris Schrijver, Karen E. Weck, et al.. (2014). Molecular genetic testing for cystic fibrosis: laboratory performance on the College of American Pathologists external proficiency surveys. Genetics in Medicine. 17(3). 219–225. 9 indexed citations
4.
Schrijver, Iris, Yasodha Natkunam, Stephen J. Galli, & Scott D. Boyd. (2013). Integration of Genomic Medicine into Pathology Residency Training. Journal of Molecular Diagnostics. 15(2). 141–148. 14 indexed citations
5.
Kalman, Lisa V., Jay Leonard, Norman P. Gerry, et al.. (2011). Quality Assurance for Duchenne and Becker Muscular Dystrophy Genetic Testing. Journal of Molecular Diagnostics. 13(2). 167–174. 18 indexed citations
6.
Tian, Lü, et al.. (2011). Cystic Fibrosis Carrier Screening in Obstetric Clinical Practice: Knowledge, Practices, and Barriers, a Decade After Publication of Screening Guidelines. Genetic Testing and Molecular Biomarkers. 15(7-8). 517–523. 26 indexed citations
7.
Mojtahed, Amirkaveh, Iris Schrijver, James M. Ford, Teri A. Longacre, & Reetesh K. Pai. (2011). A two-antibody mismatch repair protein immunohistochemistry screening approach for colorectal carcinomas, skin sebaceous tumors, and gynecologic tract carcinomas. Modern Pathology. 24(7). 1004–1014. 87 indexed citations
8.
Beck, Andrew H., Juan Rodriguez‐Paris, James L. Zehnder, & Iris Schrijver. (2011). Evaluation of a Gene Expression Microarray-based Assay to Determine Tissue Type of Origin on a Diverse Set of 49 Malignancies. The American Journal of Surgical Pathology. 35(7). 1030–1037. 7 indexed citations
9.
Matsukuma, Karen, Franklin M. Mullins, James L. Zehnder, et al.. (2010). Hereditary diffuse gastric cancer due to a previously undescribed CDH1 splice site mutation. Human Pathology. 41(8). 1200–1203. 10 indexed citations
10.
Chan, Owen, et al.. (2010). Comprehensive and EfficientHBBMutation Analysis for Detection of β-Hemoglobinopathies in a Pan-Ethnic Population. American Journal of Clinical Pathology. 133(5). 700–707. 28 indexed citations
11.
Gardner, Phyllis, et al.. (2009). The role of the cytoskeleton in the formation of gap junctions by Connexin 30. Experimental Cell Research. 315(10). 1683–1692. 56 indexed citations
12.
13.
Teek, Rita, Eneli Oitmaa, Riina Žordania, et al.. (2008). Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss. International Journal of Pediatric Otorhinolaryngology. 73(1). 103–107. 8 indexed citations
14.
15.
Schrijver, Iris, et al.. (2006). Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis. Journal of Cystic Fibrosis. 6(2). 111–116. 22 indexed citations
16.
Schrijver, Iris, Marla Lay, & James L. Zehnder. (2004). Rapid Combined Genotyping Assay for Four Achondroplasia and Hypochondroplasia Mutations by Real-Time PCR with Multiple Detection Probes. Genetic Testing. 8(2). 185–189. 10 indexed citations
17.
Nagy, Péter L., Iris Schrijver, & James L. Zehnder. (2004). Molecular Diagnosis of Hypercoagulable States. Laboratory Medicine. 35(4). 214–221. 2 indexed citations
18.
Schrijver, Iris, et al.. (2003). Prothrombin Gene Variants in Non-Caucasians with Fetal Loss and Intrauterine Growth Retardation. Journal of Molecular Diagnostics. 5(4). 250–253. 16 indexed citations
19.
20.
Schrijver, Iris, Wanguo Liu, & Uta Francke. (1997). The pathogenicity of the Pro1148Ala substitution in the FBN1 gene: causing or predisposing to Marfan syndrome and aortic aneurysm, or clinically innocent?. Human Genetics. 99(5). 607–607. 15 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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