M Beis

519 total citations
6 papers, 376 citations indexed

About

M Beis is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Physiology. According to data from OpenAlex, M Beis has authored 6 papers receiving a total of 376 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Radiology, Nuclear Medicine and Imaging and 2 papers in Physiology. Recurrent topics in M Beis's work include Retinal Development and Disorders (2 papers), Retinal and Macular Surgery (2 papers) and Lysosomal Storage Disorders Research (2 papers). M Beis is often cited by papers focused on Retinal Development and Disorders (2 papers), Retinal and Macular Surgery (2 papers) and Lysosomal Storage Disorders Research (2 papers). M Beis collaborates with scholars based in Canada, United States and Austria. M Beis's co-authors include Issam A. Awad, Eric W. Johnson, Alan Fryer, R.A. Sabroe, Richard P. Lifton, Elisabeth Steichen‐Gersdorf, Steve Crawford, R. Michael Scott, Gabrielle Mettler and Claire Kennedy and has published in prestigious journals such as Human Molecular Genetics, Investigative Ophthalmology & Visual Science and British Journal of Ophthalmology.

In The Last Decade

M Beis

6 papers receiving 364 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M Beis Canada	5	229	115	35	31	29	6	376
Philippe Coubes France	4	310 1.4×	70 0.6×	32 0.9×	12 0.4×	26 0.9×	4	454
Sonja Stahl Germany	10	389 1.7×	128 1.1×	14 0.4×	25 0.8×	30 1.0×	13	582
Patrick Peschl Austria	7	316 1.4×	80 0.7×	28 0.8×	74 2.4×	16 0.6×	10	496
Abdulkadir Özkan Türkiye	9	89 0.4×	136 1.2×	14 0.4×	13 0.4×	30 1.0×	14	288
Setareh Sadat Banihosseini Iran	7	149 0.7×	97 0.8×	15 0.4×	88 2.8×	31 1.1×	8	288
Marshall J. Huang United States	6	153 0.7×	44 0.4×	59 1.7×	45 1.5×	101 3.5×	8	299
Emile Pinarbasi United States	8	162 0.7×	120 1.0×	30 0.9×	19 0.6×	42 1.4×	13	301
Joakim Bergman Sweden	6	145 0.6×	72 0.6×	23 0.7×	41 1.3×	26 0.9×	8	348
K. Fujihara Japan	8	170 0.7×	53 0.5×	12 0.3×	42 1.4×	7 0.2×	15	271
Erika Horta United States	6	267 1.2×	55 0.5×	14 0.4×	16 0.5×	13 0.4×	13	344

Countries citing papers authored by M Beis

Since Specialization

Citations

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

Fields of papers citing papers by M Beis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Beis

This figure shows the co-authorship network connecting the top 25 collaborators of M Beis. A scholar is included among the top collaborators of M Beis 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 M Beis. M Beis 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.

Bedard, Karen, Karin Wallace, Michael P. Mackley, et al.. (2025). Gene Variant Spectrum in Probands With Familial Exudative Vitreoretinopathy Using an Expanded Panel. Investigative Ophthalmology & Visual Science. 66(2). 23–23. 2 indexed citations

2.

Jarrett, Pamela, Alexander S. Easton, Kenneth Rockwood, et al.. (2017). Evidence for Cholinergic Dysfunction in Autosomal Dominant Kufs Disease. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45(2). 150–157. 8 indexed citations

3.

Robitaille, Johane M., Karin Wallace, M Beis, et al.. (2010). The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease. British Journal of Ophthalmology. 95(4). 574–579. 53 indexed citations

4.

Robitaille, Johane M., Karin Wallace, M Beis, et al.. (2009). Phenotypic Overlap of Familial Exudative Vitreoretinopathy (FEVR) with Persistent Fetal Vasculature (PFV) Caused byFZD4Mutations in two Distinct Pedigrees. Ophthalmic Genetics. 30(1). 23–30. 48 indexed citations

5.

Günel, Murat, Eric W. Johnson, Louis J. Ptáček, et al.. (1998). Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27. Human Molecular Genetics. 7(12). 1851–1858. 253 indexed citations

6.

Coulter-Mackie, Marion B., Liane Gagnier, M Beis, et al.. (1997). Metachromatic leucodystrophy in three families from Nova Scotia, Canada: a recurring mutation in the arylsulphatase A gene.. Journal of Medical Genetics. 34(6). 493–498. 12 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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