Michael Yourshaw

2.1k total citations
10 papers, 347 citations indexed

About

Michael Yourshaw is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Michael Yourshaw has authored 10 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Oncology. Recurrent topics in Michael Yourshaw's work include Genomics and Rare Diseases (4 papers), Peptidase Inhibition and Analysis (3 papers) and Antifungal resistance and susceptibility (2 papers). Michael Yourshaw is often cited by papers focused on Genomics and Rare Diseases (4 papers), Peptidase Inhibition and Analysis (3 papers) and Antifungal resistance and susceptibility (2 papers). Michael Yourshaw collaborates with scholars based in United States, Netherlands and Australia. Michael Yourshaw's co-authors include Stanley F. Nelson, D. Ross Camidge, Dara L. Aisner, Kurtis D. Davies, Martı́n G. Martı́n, Stanley F. Nelson, Berit Kerner, Iris Lindberg, Lindsay A. Pickett and R. Sergio Solórzano-Vargas and has published in prestigious journals such as PLoS ONE, Brain and Molecular Psychiatry.

In The Last Decade

Michael Yourshaw

10 papers receiving 339 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael Yourshaw United States	9	166	86	83	49	48	10	347
Kei Shioda Japan	14	274 1.7×	82 1.0×	42 0.5×	30 0.6×	83 1.7×	25	517
Natsuko Arai‐Ichinoi Japan	10	160 1.0×	94 1.1×	45 0.5×	14 0.3×	94 2.0×	18	398
Tomoko Izaki Japan	11	246 1.5×	35 0.4×	60 0.7×	18 0.4×	116 2.4×	25	616
Ritesh Kaushal United States	10	198 1.2×	92 1.1×	72 0.9×	46 0.9×	29 0.6×	14	472
Simon Ling Singapore	6	113 0.7×	41 0.5×	67 0.8×	20 0.4×	93 1.9×	10	335
Mingfei Zhao China	11	168 1.0×	25 0.3×	31 0.4×	54 1.1×	26 0.5×	14	359
Runa Araya Japan	9	222 1.3×	60 0.7×	54 0.7×	34 0.7×	15 0.3×	9	381
Juntang Yang China	14	205 1.2×	38 0.4×	166 2.0×	92 1.9×	29 0.6×	28	436
Khalid Al‐Thihli Oman	13	219 1.3×	116 1.3×	17 0.2×	21 0.4×	28 0.6×	50	456
Riccardo Berutti Germany	12	215 1.3×	175 2.0×	11 0.1×	25 0.5×	17 0.4×	29	502

Countries citing papers authored by Michael Yourshaw

Since Specialization

Citations

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

Fields of papers citing papers by Michael Yourshaw

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Yourshaw

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

All Works

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10 of 10 papers shown

Davies, Kurtis D., et al.. (2019). DNA-Based versus RNA-Based Detection of MET Exon 14 Skipping Events in Lung Cancer. Journal of Thoracic Oncology. 14(4). 737–741. 104 indexed citations

Yourshaw, Michael, et al.. (2016). Rare deleterious mutations are associated with disease in bipolar disorder families. Molecular Psychiatry. 22(7). 1009–1014. 20 indexed citations

Wan, Jijun, Janos Steffen, Michael Yourshaw, et al.. (2016). Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia. Brain. 139(11). 2877–2890. 69 indexed citations

Bandsma, Robert, Harry van Goor, Michael Yourshaw, et al.. (2015). Loss of ADAM17 is associated with severe multiorgan dysfunction. Human Pathology. 46(6). 923–928. 31 indexed citations

Krogstad, Paul, et al.. (2015). Whole Exome Sequencing Identification of Human Genetic Polymorphisms Associated With Extrapulmonary Dissemination of Coccidioidomycosis. Open Forum Infectious Diseases. 2(suppl_1). 1 indexed citations

Wilschanski, Michael, Iris Lindberg, Michael Yourshaw, et al.. (2014). A Novel Familial Mutation in the PCSK1 Gene That Alters the Oxyanion Hole Residue of Proprotein Convertase 1/3 and Impairs Its Enzymatic Activity. PLoS ONE. 9(10). e108878–e108878. 19 indexed citations

Yourshaw, Michael, et al.. (2014). Rich annotation of DNA sequencing variants by leveraging the Ensembl Variant Effect Predictor with plugins. Briefings in Bioinformatics. 16(2). 255–264. 26 indexed citations

Kerner, Berit, et al.. (2013). Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways. Frontiers in Psychiatry. 4. 154–154. 31 indexed citations

Pickett, Lindsay A., Michael Yourshaw, Zijun Chen, et al.. (2013). Functional Consequences of a Novel Variant of PCSK1. PLoS ONE. 8(1). e55065–e55065. 19 indexed citations

10.

Yourshaw, Michael, R. Sergio Solórzano-Vargas, Lindsay A. Pickett, et al.. (2013). Exome Sequencing Finds a Novel PCSK1 Mutation in a Child With Generalized Malabsorptive Diarrhea and Diabetes Insipidus. Journal of Pediatric Gastroenterology and Nutrition. 57(6). 759–767. 27 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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