Matthew J. Ferber

673 total citations
6 papers, 175 citations indexed

About

Matthew J. Ferber is a scholar working on Genetics, Pathology and Forensic Medicine and Health, Toxicology and Mutagenesis. According to data from OpenAlex, Matthew J. Ferber has authored 6 papers receiving a total of 175 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Pathology and Forensic Medicine and 2 papers in Health, Toxicology and Mutagenesis. Recurrent topics in Matthew J. Ferber's work include Cancer Genomics and Diagnostics (2 papers), Genetic factors in colorectal cancer (2 papers) and BRCA gene mutations in cancer (2 papers). Matthew J. Ferber is often cited by papers focused on Cancer Genomics and Diagnostics (2 papers), Genetic factors in colorectal cancer (2 papers) and BRCA gene mutations in cancer (2 papers). Matthew J. Ferber collaborates with scholars based in United States, Australia and Netherlands. Matthew J. Ferber's co-authors include Eric W. Klee, Kristy M. Kegley, Mark W. Johnson, Roshan Shrestha, Robert M. Jacobson, John Sherwin, George Cunningham, Piero Rinaldo, Brittany Dawson and Fred Lorey and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Transplantation and Genetics in Medicine.

In The Last Decade

Matthew J. Ferber

6 papers receiving 174 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matthew J. Ferber United States	6	75	54	54	50	29	6	175
Vanessa Bach Spain	9	116 1.5×	74 1.4×	52 1.0×	55 1.1×	106 3.7×	12	260
Sharon A. Ross United States	9	78 1.0×	85 1.6×	20 0.4×	29 0.6×	3 0.1×	12	225
Mirunalini Ravichandran Germany	7	33 0.4×	259 4.8×	15 0.3×	38 0.8×	10 0.3×	14	329
S.N. Wickramasinghe United Kingdom	11	28 0.4×	55 1.0×	6 0.1×	26 0.5×	139 4.8×	27	304
Alexandra Griffith United States	4	8 0.1×	82 1.5×	19 0.4×	49 1.0×	13 0.4×	6	227
Man	7	9 0.1×	65 1.2×	6 0.1×	21 0.4×	32 1.1×	38	206
K. Sigvard Olsson Sweden	12	172 2.3×	30 0.6×	10 0.2×	27 0.5×	336 11.6×	20	434
Yael Haberman Israel	10	40 0.5×	93 1.7×	6 0.1×	61 1.2×	4 0.1×	22	238
Andrew J. Pellatt United States	10	21 0.3×	182 3.4×	14 0.3×	33 0.7×	3 0.1×	20	331
Erik Waldenström Sweden	6	167 2.2×	34 0.6×	118 2.2×	13 0.3×	93 3.2×	6	222

Countries citing papers authored by Matthew J. Ferber

Since Specialization

Citations

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

Fields of papers citing papers by Matthew J. Ferber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew J. Ferber. 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 Matthew J. Ferber. The network helps show where Matthew J. Ferber may publish in the future.

Co-authorship network of co-authors of Matthew J. Ferber

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

All Works

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6 of 6 papers shown

1.

Bolze, Alexandre, Kelly M. Schiabor Barrett, Gai Elhanan, et al.. (2024). Combining rare and common genetic variants improves population risk stratification for breast cancer. SHILAP Revista de lepidopterología. 2. 101826–101826. 5 indexed citations

2.

Seifert, Bryce A., Jennifer McGlaughon, Sarah A. Jackson, et al.. (2018). Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework. Genetics in Medicine. 21(7). 1507–1516. 17 indexed citations

3.

Klee, Eric W., et al.. (2011). Expanding DNA diagnostic panel testing: is more better?. Expert Review of Molecular Diagnostics. 11(7). 703–709. 35 indexed citations

4.

Kegley, Kristy M., et al.. (2010). Fulminant Wilson's Disease Requiring Liver Transplantation in One Monozygotic Twin Despite Identical Genetic Mutation. American Journal of Transplantation. 10(5). 1325–1329. 45 indexed citations

5.

Ferber, Matthew J., Brittany Dawson, Robert M. Jacobson, et al.. (2006). Retrospective determination of ceruloplasmin in newborn screening blood spots of patients with Wilson disease. Molecular Genetics and Metabolism. 89(1-2). 134–138. 41 indexed citations

6.

Ferber, Matthew J., Paul H.C. Eilers, Ed Schuuring, et al.. (2004). Positioning of cervical carcinoma and Burkitt lymphoma translocation breakpoints with respect to the human papillomavirus integration cluster in FRA8C at 8q24.13. Cancer Genetics and Cytogenetics. 154(1). 1–9. 32 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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