Heidi Mateus

480 citations
32 papers · 362 · h-index 11

Impact in

    • Ovarian function and disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

Heidi Mateus

30 papers receiving 360 citations

Peers

Heidi Mateus
Comparison fields: 5 of 70
  • Reproductive Medicine 41
  • Genetics 119
  • Psychiatry and Mental health 54
  • Public Health, Environmental and Occupational Health 91
  • Cellular and Molecular Neuroscience 45
Replace Alenka Hodžić with:
Alenka Hodžić Slovenia
Caroline Nava France
Valérie Nalesso France
Victoria Harrison United Kingdom
Miguel Tapia‐Rodríguez Mexico
Cecilia Anichini Italy
Dimitris Avramopoulos Greece
Alain Y. Dury Canada
Ali Al‐Odaib Saudi Arabia
Shinji Ono Japan
Heidi Mateus relative to Alenka Hodžić Slovenia Alenka Hodžić's profile →
Citations per field
00.5×10×13.5×
Alenka Hodžić · 1×
Citations per year

Countries citing papers authored by Heidi Mateus

Since Specialization
Citations

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

Fields of papers citing papers by Heidi Mateus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201761
2 201547
3 200935
4 201534
5 201330
6 201315
7 201115
8 201514
9 201713
10 201411
11 200611
12 201210
13 201510
14 20048
15
Deficiencia de glucosa 6-fosfato deshidrogenasa: Aspectos generales de la eritroenzimopatía más frecuente en el mundo
20058
16 20156
17 20196
18 20184
19 20134
20 20213

About Heidi Mateus

Heidi Mateus is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Cardiology and Cardiovascular Medicine and Epidemiology, having authored 32 papers that have together received 362 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (8 papers), Attention Deficit Hyperactivity Disorder (5 papers), Cardiomyopathy and Myosin Studies (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Cystic Fibrosis Research Advances (3 papers), Neurotransmitter Receptor Influence on Behavior (3 papers), Lysosomal Storage Disorders Research (3 papers) and Neural and Behavioral Psychology Studies (3 papers). The work is most often cited by research in Reproductive Medicine (41 citations), Genetics (119 citations), Psychiatry and Mental health (54 citations), Public Health, Environmental and Occupational Health (91 citations) and Cellular and Molecular Neuroscience (45 citations). Heidi Mateus has collaborated with scholars based in Colombia, Netherlands and France. Frequent co-authors include Paul Laissue, Dora Janeth Fonseca, Liliana Catherine Patiño, Carlos Martín Restrepo, Oscar Ortega‐Recalde, Alberto Vélez-van-Meerbeke, Claudia Talero‐Gutiérrez, Maëva Elzaïat, Reiner A. Veitia and Diego A. Forero. Their work appears in journals such as Fertility and Sterility, ADHD Attention Deficit and Hyperactivity Disorders, Gene, Human Molecular Genetics and Immunogenetics.

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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