Michael Yourshaw

2.2k citations
17 papers · 1.7k · 1 hit paper · h-index 14

Impact in

  • Genetics top 5%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Cancer Genomics and Diagnostics

Papers in

Michael Yourshaw

17 papers receiving 1.6k citations

Michael Yourshaw's Hit Papers

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders 2014 · 780 citations
7800+4+8Years since publication250500750

Peers

Michael Yourshaw
Comparison fields: 5 of 80
  • Genetics 734
  • Cancer Research 178
  • Molecular Biology 643
  • Gastroenterology 46
  • Clinical Biochemistry 57
Replace Pavel N. Pichurin with:
Pavel N. Pichurin United States
Susan L. Schelley United States
Maggie M. Williams United Kingdom
Hester Y. Kroes Netherlands
Katrina A. Rack United Kingdom
Susan J. Allen United States
Linlea Armstrong Canada
Fatema Alzahrani Saudi Arabia
Elisa Rahikkala Finland
Lynette S. Penney Canada
Michael Yourshaw relative to Pavel N. Pichurin United States Pavel N. Pichurin's profile →
Citations per field
00.5×2×3×3.6×
Pavel N. Pichurin · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Michael Yourshaw, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Michael Yourshaw Line = papers co-authored together Michael Yourshaw links everyone, so they are left out of the graph.

All Works

17 of 17 papers shown
#Work
1
Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders
Hit paper breakdown →
2014780
2 2012207
3 2019130
4 2013117
5 201376
6 201675
7 201859
8 201535
9 201335
10 201435
11 201331
12 201625
13 201323
14 201422
15 20188
16 20257
17 20151

About Michael Yourshaw

Michael Yourshaw is a scholar working on Gastroenterology, Genetics, Cancer Research, Pediatrics, Perinatology and Child Health and Infectious Diseases, having authored 17 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Cancer Genomics and Diagnostics (3 papers), Celiac Disease Research and Management (3 papers), Fungal Infections and Studies (2 papers), Genomics and Phylogenetic Studies (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Antifungal resistance and susceptibility (2 papers) and Peptidase Inhibition and Analysis (2 papers). The work is most often cited by research in Genetics (734 citations), Cancer Research (178 citations), Molecular Biology (643 citations), Gastroenterology (46 citations) and Clinical Biochemistry (57 citations). Michael Yourshaw has collaborated with scholars based in United States, Israel and Germany. Frequent co-authors include Dara L. Aisner, Kurtis D. Davies, D. Ross Camidge, Aliz R. Rao, Stanley F. Nelson, Martı́n G. Martı́n, Stanley F. Nelson, Berit Kerner, Iris Lindberg and S. Paige Taylor. Their work appears in journals such as PLoS ONE, Briefings in Bioinformatics, Nature Genetics, Neurology and Molecular Psychiatry.

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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