Janet Marcadier

1.2k citations
8 papers · 247 · h-index 6

Impact in

    • Genomics and Rare Diseases
    • Neurogenetic and Muscular Disorders Research
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Prenatal Screening and Diagnostics

Papers in

Janet Marcadier

8 papers receiving 240 citations

Peers

Janet Marcadier
Comparison fields: 5 of 41
  • Genetics 42
  • Genetics 94
  • Pediatrics, Perinatology and Child Health 41
  • Psychiatry and Mental health 20
  • Molecular Biology 100
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Citations per field
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Citations per year

Countries citing papers authored by Janet Marcadier

Since Specialization
Citations

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

Fields of papers citing papers by Janet Marcadier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

8 of 8 papers shown
#Work
1 201182
2 201464
3 201137
4 202027
5 201020
6 202112
7 20144
8 20111

About Janet Marcadier

Janet Marcadier is a scholar working on Molecular Biology, Surgery, Genetics, Genetics and Infectious Diseases, having authored 8 papers that have together received 247 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Parvovirus B19 Infection Studies (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Congenital Anomalies and Fetal Surgery (1 paper), Gestational Trophoblastic Disease Studies (1 paper), Hedgehog Signaling Pathway Studies (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Genetics (42 citations), Genetics (94 citations), Pediatrics, Perinatology and Child Health (41 citations), Psychiatry and Mental health (20 citations) and Molecular Biology (100 citations). Janet Marcadier has collaborated with scholars based in Canada and United States. Frequent co-authors include Kym M. Boycott, Jeremy Schwartzentruber, Jacek Majewski, Mark A. Tarnopolsky, Lysanne Patry, Hilde Van Esch, Jacques L. Michaud, Jean‐Pierre Fryns, Aurore Caqueret and Mark E. Samuels. Their work appears in journals such as Clinical Genetics, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, BMJ Open, Journal of Obstetrics and Gynaecology Canada and Canadian Journal of Cardiology.

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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