Solveig Heide
Impact in
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- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 8
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 2
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- Chromatin Remodeling and Cancer 2
- Co-authors
- Jean‐Pierre Siffroi (8 shared papers)Boris Keren (7 shared papers)Sandra Chantot‐Bastaraud (5 shared papers)Alexandra Afenjar (4 shared papers)Alinoë Lavillaureix (3 shared papers)Capucine Hyon (2 shared papers)Diane Doummar (2 shared papers)Patrick Edery (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)Reproductive BioMedicine Online (2 papers)Journal of Assisted Reproduction and Genetics (2 papers)Journal of Medical Genetics (2 papers)European Journal of Paediatric Neurology (2 papers)
- Partner nations
- FranceGermanyUnited States
In The Last Decade
Solveig Heide
17 papers receiving 186 citations
Peers
Comparison fields: 5 of 44
- Genetics 87
- Pediatrics, Perinatology and Child Health 36
- Reproductive Medicine 14
- Endocrine and Autonomic Systems 9
- Neurology 18
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
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 36 | |
| 2 | 2015 | 32 | |
| 3 | 2019 | 30 | |
| 4 | 2017 | 18 | |
| 5 | 2017 | 16 | |
| 6 | 2015 | 16 | |
| 7 | 2019 | 14 | |
| 8 | 2014 | 7 | |
| 9 | 2022 | 6 | |
| 10 | 2020 | 5 | |
| 11 | 2021 | 4 | |
| 12 | 2021 | 4 | |
| 13 | 2023 | 3 | |
| 14 | 2019 | 3 | |
| 15 | 2019 | 3 | |
| 16 | 2017 | 2 | |
| 17 | 2023 | 2 |
About Solveig Heide
Solveig Heide is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Neurology, having authored 17 papers that have together received 201 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Sperm and Testicular Function (2 papers), Chromatin Remodeling and Cancer (2 papers) and Reproductive Biology and Fertility (2 papers). The work is most often cited by research in Genetics (87 citations), Pediatrics, Perinatology and Child Health (36 citations), Reproductive Medicine (14 citations), Endocrine and Autonomic Systems (9 citations) and Neurology (18 citations). Solveig Heide has collaborated with scholars based in France, Germany and United States. Frequent co-authors include Jean‐Pierre Siffroi, Boris Keren, Sandra Chantot‐Bastaraud, Alexandra Afenjar, Alinoë Lavillaureix, Capucine Hyon, Diane Doummar, Patrick Edery, Christel Depienne and Nino Guy Cassuto. Their work appears in journals such as European Journal of Medical Genetics, Reproductive BioMedicine Online, Journal of Assisted Reproduction and Genetics, Journal of Medical Genetics and European Journal of Paediatric Neurology.
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.