Anne Rochtus

741 total citations
26 papers, 379 citations indexed

About

Anne Rochtus is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Anne Rochtus has authored 26 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in Anne Rochtus's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (4 papers) and Genetic Syndromes and Imprinting (4 papers). Anne Rochtus is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (4 papers) and Genetic Syndromes and Imprinting (4 papers). Anne Rochtus collaborates with scholars based in Belgium, United States and United Kingdom. Anne Rochtus's co-authors include Annapurna Poduri, Kathleen Freson, Chris Van Geet, Katrien Jansen, Beth Rosen Sheidley, Benedetta Izzi, Alan Taylor, Sonal Mahida, McKenna Kelly and Lacey Smith and has published in prestigious journals such as Annals of Neurology, Diabetologia and International Journal of Obesity.

In The Last Decade

Anne Rochtus

25 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Rochtus Belgium 10 217 189 98 75 31 26 379
Enrico Alfei Italy 11 160 0.7× 140 0.7× 35 0.4× 58 0.8× 15 0.5× 25 333
Rosario Berardi Italy 14 189 0.9× 146 0.8× 84 0.9× 108 1.4× 33 1.1× 29 422
Dawn Cordeiro Canada 10 233 1.1× 200 1.1× 145 1.5× 55 0.7× 43 1.4× 15 484
Dimitar N. Azmanov Australia 12 122 0.6× 191 1.0× 41 0.4× 53 0.7× 8 0.3× 23 336
Jaina Patel Canada 8 193 0.9× 118 0.6× 109 1.1× 37 0.5× 91 2.9× 17 389
Andrea Guerin Canada 8 103 0.5× 99 0.5× 19 0.2× 69 0.9× 24 0.8× 30 336
Tomohiro Kumada Japan 13 46 0.2× 168 0.9× 65 0.7× 51 0.7× 22 0.7× 44 398
Luis González Gutiérrez-Solana Spain 12 54 0.2× 155 0.8× 71 0.7× 38 0.5× 67 2.2× 59 458
Christine Makowski Germany 10 51 0.2× 229 1.2× 116 1.2× 94 1.3× 37 1.2× 18 480
Chiemi Hayakawa Japan 10 119 0.5× 145 0.8× 29 0.3× 52 0.7× 15 0.5× 20 350

Countries citing papers authored by Anne Rochtus

Since Specialization
Citations

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

Fields of papers citing papers by Anne Rochtus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Rochtus

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Rochtus. A scholar is included among the top collaborators of Anne Rochtus 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 Anne Rochtus. Anne Rochtus is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Rochtus, Anne, et al.. (2024). Hypogonadotropic Hypogonadism as First Presentation of the Severe Neuroendocrine Disorder Caused by RNF216. JCEM Case Reports. 2(11). luae195–luae195. 1 indexed citations
2.
Maslin, Kate, Lieveke Ameye, Anne Rochtus, et al.. (2024). Interpregnancy maternal weight change is not associated with offspring weight and obesity at age 2 years. International Journal of Obesity. 48(10). 1402–1413. 3 indexed citations
3.
Weiß, Andreas, Thekla von dem Berge, Kristina Casteels, et al.. (2024). Infection episodes and islet autoantibodies in children at increased risk for type 1 diabetes before and during the COVID-19 pandemic. Infection. 52(6). 2465–2473. 2 indexed citations
4.
Schepper, Jean De, Muriel Thomas, Koen Huysentruyt, et al.. (2024). Near Adult Height and Body Mass Index Changes in Growth Hormone Treated Short Children with Noonan Syndrome: The Belgian Experience. Hormone Research in Paediatrics. 98(2). 1–13. 1 indexed citations
5.
Hummel, Sandra, Thekla von dem Berge, Rachel Besser, et al.. (2024). Early-childhood body mass index and its association with the COVID-19 pandemic, containment measures and islet autoimmunity in children with increased risk for type 1 diabetes. Diabetologia. 67(4). 670–678. 3 indexed citations
6.
Casteels, Kristina, et al.. (2024). Systemic Adverse Events Associated with Locally Administered Corticosteroids. Children. 11(8). 951–951. 2 indexed citations
7.
Meulemans, Sandra, Lieven Thorrez, Patrizia Agostinis, et al.. (2024). Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870(5). 167175–167175. 3 indexed citations
8.
Jacobs, Sandra, et al.. (2024). Endocrine sequelae after pediatric craniopharyngioma treatment: a single-center retrospective cohort study. Journal of Pediatric Endocrinology and Metabolism. 37(11). 954–961. 2 indexed citations
9.
Rochtus, Anne, Lieven Lagae, Katrien Jansen, et al.. (2023). Reversible Hypothalamic Obesity in a Girl with Suprasellar Tuberculoma. Hormone Research in Paediatrics. 97(2). 165–171. 2 indexed citations
10.
Charleer, Sara, et al.. (2023). The Relationship Between Glycated Hemoglobin and Time in Range in a Pediatric Population. Diabetes Technology & Therapeutics. 26(5). 346–350. 2 indexed citations
11.
Rochtus, Anne, et al.. (2022). Behavioral Changes in Patients With Prader-Willi Syndrome Can Mask Severe Physical Illness. JCEM Case Reports. 1(1). luac034–luac034.
12.
Rodero, Mathieu P., et al.. (2020). Expanding the clinical spectrum of Fowler syndrome: Three siblings with survival into adulthood and systematic review of the literature. Clinical Genetics. 98(5). 423–432. 3 indexed citations
13.
Rochtus, Anne, et al.. (2020). Hypothalamic lipoma and growth hormone deficiency. International Journal of Pediatric Endocrinology. 2020(1). 4–4. 3 indexed citations
14.
Rochtus, Anne, Richard D. Goldstein, Ingrid A. Holm, et al.. (2020). The role of sodium channels in sudden unexpected death in pediatrics. Molecular Genetics & Genomic Medicine. 8(8). e1309–e1309. 17 indexed citations
15.
Scheffer, Ingrid E., Katja Boysen, Amy Schneider, et al.. (2019). BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures. Developmental Medicine & Child Neurology. 62(9). 1096–1099. 14 indexed citations
16.
Rochtus, Anne, Richard E. Goldstein, Beth Rosen Sheidley, et al.. (2019). Mutations in NRXN1 and NRXN2 in a patient with early-onset epileptic encephalopathy and respiratory depression. Molecular Case Studies. 5(1). a003442–a003442. 16 indexed citations
17.
Burgess, Rosemary, Amy McTague, Katja Boysen, et al.. (2019). The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures. Annals of Neurology. 86(6). 821–831. 79 indexed citations
18.
Rochtus, Anne, Alejandro Martin-Trujillo, Benedetta Izzi, et al.. (2016). Genome-wide DNA methylation analysis of pseudohypoparathyroidism patients with GNAS imprinting defects. Clinical Epigenetics. 8(1). 10–10. 38 indexed citations
19.
Rochtus, Anne, Raf Winand, Griet Laenen, et al.. (2016). Methylome analysis for spina bifida shows SOX18 hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development. Clinical Epigenetics. 8(1). 108–108. 18 indexed citations
20.
Rochtus, Anne, Benedetta Izzi, Christine Wittevrongel, et al.. (2015). DNA methylation analysis of Homeobox genes implicatesHOXB7hypomethylation as risk factor for neural tube defects. Epigenetics. 10(1). 92–101. 35 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Enrico Alfei Breakdown of academic impact, for papers by Rosario Berardi Breakdown of academic impact, for papers by Dawn Cordeiro Breakdown of academic impact, for papers by Dimitar N. Azmanov Breakdown of academic impact, for papers by Jaina Patel Breakdown of academic impact, for papers by Andrea Guerin Breakdown of academic impact, for papers by Tomohiro Kumada Breakdown of academic impact, for papers by Luis González Gutiérrez-Solana Breakdown of academic impact, for papers by Christine Makowski Breakdown of academic impact, for papers by Chiemi Hayakawa
Rankless by CCL
2026