Solveig Heide

2.1k total citations
17 papers, 187 citations indexed

About

Solveig Heide is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Solveig Heide has authored 17 papers receiving a total of 187 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Solveig Heide's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Solveig Heide is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Solveig Heide collaborates with scholars based in France, Germany and United Kingdom. Solveig Heide's co-authors include Jean‐Pierre Siffroi, Boris Keren, Sandra Chantot‐Bastaraud, Alexandra Afenjar, Alinoë Lavillaureix, Christel Depienne, Capucine Hyon, Diane Doummar, Nino Guy Cassuto and Delphine Héron and has published in prestigious journals such as The American Journal of Human Genetics, Neurobiology of Disease and Journal of Medical Genetics.

In The Last Decade

Solveig Heide

17 papers receiving 175 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Solveig Heide France 8 94 88 49 20 19 17 187
Frédérique Sloan‐Béna Switzerland 9 87 0.9× 123 1.4× 30 0.6× 6 0.3× 26 1.4× 23 263
A. Saad Tunisia 9 130 1.4× 97 1.1× 42 0.9× 9 0.5× 71 3.7× 24 255
Haruka Hamanoue Japan 10 84 0.9× 118 1.3× 33 0.7× 6 0.3× 29 1.5× 23 220
Margit Nõukas Estonia 9 111 1.2× 104 1.2× 30 0.6× 5 0.3× 30 1.6× 16 216
Talia Litmanovitch Israel 10 130 1.4× 197 2.2× 33 0.7× 9 0.5× 10 0.5× 11 294
Diane Hu‐Lince United States 7 144 1.5× 143 1.6× 22 0.4× 5 0.3× 6 0.3× 7 253
Alexandre Z. Daly United States 6 86 0.9× 157 1.8× 14 0.3× 8 0.4× 12 0.6× 9 282
Sara Nuovo Italy 8 68 0.7× 77 0.9× 38 0.8× 15 0.8× 7 0.4× 12 168
Deepika Puri India 7 27 0.3× 135 1.5× 26 0.5× 3 0.1× 20 1.1× 14 189
Angelika Köhler Germany 10 134 1.4× 222 2.5× 34 0.7× 27 1.4× 10 0.5× 12 321

Countries citing papers authored by Solveig Heide

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Solveig Heide

This figure shows the co-authorship network connecting the top 25 collaborators of Solveig Heide. A scholar is included among the top collaborators of Solveig Heide based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Solveig Heide. Solveig Heide is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

17 of 17 papers shown
1.
Lefebvre, Mathilde, A. Gélot, Solveig Heide, et al.. (2023). First reports of fetal SMARCC1 related hydrocephalus. European Journal of Medical Genetics. 66(8). 104797–104797. 1 indexed citations
2.
Heide, Solveig, Claire-Sophie Davoine, Clarisse Scherer‐Gagou, et al.. (2023). IRF2BPL Causes Mild Intellectual Disability Followed by Late-Onset Ataxia. Neurology Genetics. 9(6). e200096–e200096. 2 indexed citations
3.
Montcel, Sophie Tézenas du, Anna Heinzmann, Giulia Coarelli, et al.. (2022). Reproductive choices and intrafamilial communication in neurogenetic diseases with different self-estimated severities. Journal of Medical Genetics. 60(4). 346–351. 6 indexed citations
4.
Doummar, Diane, Thierry Bienvenu, Perrine Charles, et al.. (2021). Tremor-like subcortical myoclonus in STXBP1 encephalopathy. European Journal of Paediatric Neurology. 34. 62–66. 4 indexed citations
5.
Tosca, Lucie, Laure Lecerf, Sophie Brisset, et al.. (2021). Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C. Molecular Genetics & Genomic Medicine. 9(11). e1645–e1645. 3 indexed citations
6.
Clède, Sylvain, Aliénor de Chalus, Solveig Heide, et al.. (2020). Simple FISH-based evaluation of spermatic nuclear architecture shows an abnormal chromosomal organization in balanced chromosomal rearrangement carriers. Journal of Assisted Reproduction and Genetics. 37(4). 803–809. 5 indexed citations
7.
Chalus, Aliénor de, Solveig Heide, Nathalie Lédée, et al.. (2019). Double chromosomal translocation in an infertile man: one-step FISH meiotic segregation analysis and reproductive prognosis. Journal of Assisted Reproduction and Genetics. 36(5). 973–978. 3 indexed citations
8.
Heide, Solveig, Sandrine Poëa‐Guyon, Véronique Rousseau, et al.. (2019). PAK3 mutations responsible for severe intellectual disability and callosal agenesis inhibit cell migration. Neurobiology of Disease. 136. 104709–104709. 14 indexed citations
9.
Nixon, Kevin C., Justine Rousseau, Sophie Ehresmann, et al.. (2019). A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies. The American Journal of Human Genetics. 104(4). 596–610. 27 indexed citations
10.
Ader, Flavie, Solveig Heide, Pauline Marzin, et al.. (2019). A 14q distal chromoanagenesis elucidated by whole genome sequencing. European Journal of Medical Genetics. 63(4). 103776–103776. 3 indexed citations
11.
Heide, Solveig, Sandra Chantot‐Bastaraud, Boris Keren, et al.. (2017). Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences. Journal of Medical Genetics. 55(3). 205–213. 34 indexed citations
12.
Heide, Solveig, Matthieu Egloff, Pauline Marzin, et al.. (2017). Potential selection of genetically balanced spermatozoa based on the hypo-osmotic swelling test in chromosomal rearrangement carriers. Reproductive BioMedicine Online. 35(4). 372–378. 17 indexed citations
13.
Lavillaureix, Alinoë, Caroline Nava, Cyril Mignot, et al.. (2017). New generation sequencing for the diagnosis of intellectual disabilities: Exome sequencing or large panel?. European Journal of Paediatric Neurology. 21. e155–e155. 2 indexed citations
14.
Sternberg, Damien, Sandra Whalen, Alexandra Afenjar, et al.. (2017). How chromosomal deletions can unmask recessive mutations? Deletions in 10q11.2 associated with CHAT or SLC18A3 mutations lead to congenital myasthenic syndrome. American Journal of Medical Genetics Part A. 176(1). 151–155. 16 indexed citations
15.
Heide, Solveig, Alexandra Afenjar, Patrick Edery, et al.. (2015). Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature. European Journal of Medical Genetics. 58(6-7). 341–345. 28 indexed citations
16.
Heide, Solveig, Julien Masliah‐Planchon, Bertrand Isidor, et al.. (2015). Oncologic Phenotype of Peripheral Neuroblastic Tumors Associated With PHOX2B Non‐Polyalanine Repeat Expansion Mutations. Pediatric Blood & Cancer. 63(1). 71–77. 15 indexed citations
17.
Lavillaureix, Alinoë, Capucine Hyon, Solveig Heide, et al.. (2014). Nuclear volume differences between balanced and unbalanced spermatozoa in chromosomal translocation carriers. Reproductive BioMedicine Online. 30(3). 290–295. 7 indexed citations

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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