Shane McCarthy

10.0k citations
16 papers · 1.5k · 1 hit paper · h-index 10

Impact in

Papers in

    • Pluripotent Stem Cells Research 3
    • Congenital heart defects research 3
    • Genomic variations and chromosomal abnormalities 4
    • Genetics and Neurodevelopmental Disorders 3
    • Genetic Associations and Epidemiology 3
    • Genomics and Rare Diseases 2

Shane McCarthy

15 papers receiving 1.5k citations

Shane McCarthy's Hit Papers

Modelling schizophrenia using human induced pluripotent stem cells 2011 · 1.0k citations
1.0k0+5+10Years since publication2505007501000

Peers

Shane McCarthy
Comparison fields: 5 of 81
  • Developmental Neuroscience 159
  • Biological Psychiatry 59
  • Aging 36
  • Cellular and Molecular Neuroscience 316
  • Genetics 436
Replace Brady J. Maher with:
Brady J. Maher United States
Trygve E. Bakken United States
Gabriele Lignani United Kingdom
Hanoch Kaphzan Israel
Kazue Hashimoto‐Torii United States
Geeske M. van Woerden Netherlands
Jonathan E. Ploski United States
Marc P. Forrest United States
Kaijie Ma United States
Kristen R. Maynard United States
Shane McCarthy relative to Brady J. Maher United States Brady J. Maher's profile →
Citations per field
00.5×2.6×
Brady J. Maher · 1×
Citations per year

Countries citing papers authored by Shane McCarthy

Since Specialization
Citations

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

Fields of papers citing papers by Shane McCarthy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Shane McCarthy, 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 Shane McCarthy Line = papers co-authored together Shane McCarthy links everyone, so they are left out of the graph.

All Works

16 of 16 papers shown
#Work
1
Modelling schizophrenia using human induced pluripotent stem cells
Hit paper breakdown →
20111033
2 2009190
3 201196
4 201086
5 201545
6 201824
7 201815
8 202012
9 202110
10 20189
11 20228
12 20227
13 20177
14 20192
15 20171
16 20190

About Shane McCarthy

Shane McCarthy is a scholar working on Molecular Biology, Genetics, Infectious Diseases, Cognitive Neuroscience and Epidemiology, having authored 16 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Pluripotent Stem Cells Research (3 papers), Congenital heart defects research (3 papers), Genetic Associations and Epidemiology (3 papers), Genomics and Rare Diseases (2 papers), Autism Spectrum Disorder Research (2 papers) and SARS-CoV-2 and COVID-19 Research (2 papers). The work is most often cited by research in Developmental Neuroscience (159 citations), Biological Psychiatry (59 citations), Aging (36 citations), Cellular and Molecular Neuroscience (316 citations) and Genetics (436 citations). Shane McCarthy has collaborated with scholars based in United States, United Kingdom and Switzerland. Frequent co-authors include Jonathan Sebat, Kristen Brennand, Fred H. Gage, Diana Yu, Yangling Mu, Ngoc Tran, Gong Chen, Anthony Simone, Chelsea Gelboin-Burkhart and Yan Li. Their work appears in journals such as Schizophrenia, G3 Genes Genomes Genetics, Trends in Genetics, Molecular Psychiatry and The American Journal of Human Genetics.

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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