Madeline Couse

520 citations
16 papers · 187 · h-index 7

Impact in

    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
    • Genetics and Neurodevelopmental Disorders 3
    • Genomics and Rare Diseases 3
    • Genetic and Kidney Cyst Diseases 2
    • Hedgehog Signaling Pathway Studies 2
    • Genomics and Chromatin Dynamics 2

Madeline Couse

14 papers receiving 185 citations

Peers

Madeline Couse
Comparison fields: 5 of 59
  • Genetics 89
  • Physiology 12
  • Molecular Biology 90
  • Atmospheric Science 20
  • Cellular and Molecular Neuroscience 20
Replace Muhammad Nasim Khan with:
Muhammad Nasim Khan Pakistan
Arjan PM de Brouwer Netherlands
Anneke T. Vulto‐van Silfhout Netherlands
M. Lourdes Sampietro Netherlands
Tyler Schwend United States
Jennifer Heeley United States
Ursula‐Friederike Habenicht Germany
Elizabeth N. Schock United States
Boyan Dimitrov Bulgaria
Felicia S.H. Cheah Singapore
Madeline Couse relative to Muhammad Nasim Khan Pakistan Muhammad Nasim Khan's profile →
Citations per field
00.5×1.5×2.1×
Muhammad Nasim Khan · 1×
Citations per year

Countries citing papers authored by Madeline Couse

Since Specialization
Citations

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

Fields of papers citing papers by Madeline Couse

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

16 of 16 papers shown
#Work
1 201948
2 201936
3 202133
4 201421
5 201715
6 202213
7 20236
8 20146
9 20233
10 20232
11 20231
12 20251
13 20221
14 20191
15 20250
16 20140

About Madeline Couse

Madeline Couse is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Immunology and Biomedical Engineering, having authored 16 papers that have together received 187 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (3 papers), Genetic and Kidney Cyst Diseases (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Genomics and Chromatin Dynamics (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Microfluidic and Capillary Electrophoresis Applications (2 papers). The work is most often cited by research in Genetics (89 citations), Physiology (12 citations), Molecular Biology (90 citations), Atmospheric Science (20 citations) and Cellular and Molecular Neuroscience (20 citations). Madeline Couse has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Melissa A. Wilson, Phillip A. Richmond, Bruno M. Grande, Timothy H. Webster, Eric Karlins, Tanya N. Phung, Clara van Karnebeek, Jan M. Friedman, Roland I. Hall and Derek J. Taylor. Their work appears in journals such as The Journal of Rheumatology, Journal of Chromatography A, BMC Genomics, Molecular Genetics and Metabolism and PLoS 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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