Solveig Heide
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
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- Fetal and Pediatric Neurological Disorders
- Prenatal Screening and Diagnostics
Papers in
- Genetics 46
- Genetics and Neurodevelopmental Disorders 25
- Genomics and Rare Diseases 20
- Genomic variations and chromosomal abnormalities 9
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- Fetal and Pediatric Neurological Disorders 10
- Co-authors
- Jean‐Pierre Siffroi (9 shared papers)Boris Keren (8 shared papers)Sandra Chantot‐Bastaraud (6 shared papers)Delphine Héron (8 shared papers)Alexandra Afenjar (4 shared papers)Alinoë Lavillaureix (4 shared papers)Christel Depienne (3 shared papers)Capucine Hyon (2 shared papers)
- Journals
- Genetics in Medicine (10 papers)The American Journal of Human Genetics (7 papers)Clinical Genetics (6 papers)Journal of Medical Genetics (6 papers)European Journal of Medical Genetics (4 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Solveig Heide
63 papers receiving 1.5k citations
Solveig Heide's Hit Papers
Peers
Comparison fields: 5 of 76
- Genetics 806
- Pediatrics, Perinatology and Child Health 160
- Developmental Neuroscience 33
- Cellular and Molecular Neuroscience 151
- Clinical Biochemistry 28
Countries citing papers authored by Solveig Heide
This map shows the geographic impact of Solveig Heide'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 Solveig Heide with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Solveig Heide more than expected).
Fields of papers citing papers by Solveig Heide
This network shows the impact of papers produced by Solveig Heide. 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 Solveig Heide. The network helps show where Solveig Heide may publish in the future.
Co-authors
The 25 scholars most cited alongside Solveig Heide, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 66 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 231 | |
| 2 | 2017 | 88 | |
| 3 | 2018 | 83 | |
| 4 | 2017 | 77 | |
| 5 | 2017 | 75 | |
| 6 | 2019 | 64 | |
| 7 | 2019 | 63 | |
| 8 | 2018 | 60 | |
| 9 | 2018 | 50 | |
| 10 | 2020 | 42 | |
| 11 | 2017 | 37 | |
| 12 | 2019 | 37 | |
| 13 | 2020 | 37 | |
| 14 | 2021 | 33 | |
| 15 | 2015 | 32 | |
| 16 | 2016 | 28 | |
| 17 | 2017 | 28 | |
| 18 | PFMG2025–integrating genomic medicine into the national healthcare system in France Hit paper breakdown → | 2025 | 26 |
| 19 | 2020 | 23 | |
| 20 | 2021 | 21 |
About Solveig Heide
Solveig Heide is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Reproductive Medicine, Cellular and Molecular Neuroscience and Clinical Biochemistry, having authored 66 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (25 papers), Genomics and Rare Diseases (20 papers), Fetal and Pediatric Neurological Disorders (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Sperm and Testicular Function (4 papers), Epigenetics and DNA Methylation (3 papers), Metabolism and Genetic Disorders (3 papers) and Genetic Neurodegenerative Diseases (3 papers). The work is most often cited by research in Genetics (806 citations), Pediatrics, Perinatology and Child Health (160 citations), Developmental Neuroscience (33 citations), Cellular and Molecular Neuroscience (151 citations) and Clinical Biochemistry (28 citations). Solveig Heide has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Jean‐Pierre Siffroi, Boris Keren, Sandra Chantot‐Bastaraud, Delphine Héron, Alexandra Afenjar, Alinoë Lavillaureix, Christel Depienne, Capucine Hyon, Damien Sanlaville and Diane Doummar. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Clinical Genetics, Journal of Medical Genetics and European Journal of Medical 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.