Matt Velinder

1.3k total citations
9 papers, 96 citations indexed

About

Matt Velinder is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Matt Velinder has authored 9 papers receiving a total of 96 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Cancer Research. Recurrent topics in Matt Velinder's work include Genomics and Rare Diseases (7 papers), Biomedical Text Mining and Ontologies (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Matt Velinder is often cited by papers focused on Genomics and Rare Diseases (7 papers), Biomedical Text Mining and Ontologies (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Matt Velinder collaborates with scholars based in United States, United Kingdom and Türkiye. Matt Velinder's co-authors include D. Hunter Best, Brent S. Pedersen, Joe Brown, Aaron R. Quinlan, Harriet Dashnow, Martin Tristani‐Firouzi, Pınar Bayrak‐Toydemir, Rong Mao, Joshua D. Schiffman and Tatiana Tvrdik and has published in prestigious journals such as Scientific Reports, BMC Bioinformatics and Journal of Medical Genetics.

In The Last Decade

Matt Velinder

7 papers receiving 96 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matt Velinder United States	5	56	52	10	9	9	9	96
Behrooz Torabi Moghadam Sweden	6	50 0.9×	38 0.7×	5 0.5×	10 1.1×	5 0.6×	7	101
Stéphane Liva France	3	78 1.4×	41 0.8×	5 0.5×	24 2.7×	17 1.9×	5	105
Richard P. Finney United States	4	116 2.1×	50 1.0×	8 0.8×	33 3.7×	5 0.6×	6	154
Giulia De Riso Italy	7	125 2.2×	32 0.6×	6 0.6×	25 2.8×	6 0.7×	13	164
William L. Macken United Kingdom	6	106 1.9×	40 0.8×	6 0.6×	12 1.3×	10 1.1×	11	146
Luca Stefanucci United Kingdom	4	77 1.4×	34 0.7×	6 0.6×	8 0.9×	11 1.2×	5	97
Ines F. Scheller Germany	4	120 2.1×	75 1.4×	7 0.7×	18 2.0×	8 0.9×	6	180
Nara L. M. Sobreira United States	5	44 0.8×	38 0.7×	9 0.9×	7 0.8×	13 1.4×	5	88
Setareh Moghadasi Netherlands	6	83 1.5×	78 1.5×	6 0.6×	18 2.0×	5 0.6×	8	126
Carey McDougall United States	5	43 0.8×	46 0.9×	11 1.1×	11 1.2×	4 0.4×	11	89

Countries citing papers authored by Matt Velinder

Since Specialization

Citations

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

Fields of papers citing papers by Matt Velinder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matt Velinder

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

1.

Carey, John C., Lorenzo D. Botto, Matt Velinder, et al.. (2023). SON -Related Zhu-Tokita-Takenouchi-Kim Syndrome With Recurrent Hemiplegic Migraine. Neurology Genetics. 9(3). e200062–e200062.

2.

Ward, Alistair, Matt Velinder, Barry Moore, et al.. (2022). Clin.iobio: A Collaborative Diagnostic Workflow to Enable Team-Based Precision Genomics. Journal of Personalized Medicine. 12(1). 73–73. 2 indexed citations

3.

Velinder, Matt, et al.. (2022). eP269: Reanalysis of commercial exome trio data reveals a de novo loss of function variant in KAT6A. Genetics in Medicine. 24(3). S170–S170.

4.

Velinder, Matt, Alistair Ward, 義行高橋, et al.. (2021). Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization. Scientific Reports. 11(1). 20307–20307. 11 indexed citations

5.

Pedersen, Brent S., Joe Brown, Harriet Dashnow, et al.. (2021). Effective variant filtering and expected candidate variant yield in studies of rare human disease. npj Genomic Medicine. 6(1). 60–60. 60 indexed citations

6.

Velinder, Matt, Dillon Lee, & Gábor Marth. (2020). ped_draw: pedigree drawing with ease. BMC Bioinformatics. 21(1). 569–569. 3 indexed citations

7.

Velinder, Matt, et al.. (2019). Genepanel.iobio - an easy to use web tool for generating disease- and phenotype-associated gene lists. BMC Medical Genomics. 12(1). 190–190. 4 indexed citations

8.

Wooderchak‐Donahue, Whitney, Jamie McDonald, Andrew Farrell, et al.. (2018). Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia. Journal of Medical Genetics. 55(12). 824–830. 12 indexed citations

9.

Ward, Alistair, Mary Anne Karren, Chase Miller, et al.. (2017). Rapid clinical diagnostic variant investigation of genomic patient sequencing data with iobio web tools. Journal of Clinical and Translational Science. 1(6). 381–386. 4 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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