Ester Garne

12.5k total citations · 2 hit papers
149 papers, 5.8k citations indexed

About

Ester Garne is a scholar working on Surgery, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Ester Garne has authored 149 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Surgery, 61 papers in Pediatrics, Perinatology and Child Health and 32 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Ester Garne's work include Congenital Anomalies and Fetal Surgery (34 papers), Congenital Heart Disease Studies (27 papers) and Prenatal Screening and Diagnostics (25 papers). Ester Garne is often cited by papers focused on Congenital Anomalies and Fetal Surgery (34 papers), Congenital Heart Disease Studies (27 papers) and Prenatal Screening and Diagnostics (25 papers). Ester Garne collaborates with scholars based in Denmark, United Kingdom and Italy. Ester Garne's co-authors include Helen Dolk, Maria Loane, Claude Stoll, Ingeborg Barišić, Massimo Clementi, Joan K. Morris, Janneke Jentink, Lolkje T.W. de Jong‐van den Berg, Babak Khoshnood and Elisa Calzolari and has published in prestigious journals such as New England Journal of Medicine, The Lancet and Circulation.

In The Last Decade

Ester Garne

143 papers receiving 5.6k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The Prevalence of Congenital Anomalies in Europe

2010 462 citations Helen Dolk, Maria Loane et al. profile →
Congenital Heart Defects in Europe

2011 448 citations Helen Dolk, Maria Loane et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Ester Garne	2.3k	2.0k	1.2k	1.2k	978	149	5.8k
Helen Dolk	3.4k 1.5×	2.1k 1.1×	1.1k 0.9×	1.6k 1.3×	786 0.8×	176	8.2k
Charlotte M. Druschel	2.1k 0.9×	1.8k 0.9×	1.0k 0.8×	1.1k 0.9×	594 0.6×	160	6.6k
Mark A. Canfield	2.7k 1.2×	2.8k 1.4×	1.3k 1.1×	1.8k 1.4×	864 0.9×	212	8.7k
Charlotte A. Hobbs	2.2k 0.9×	1.6k 0.8×	1.3k 1.0×	986 0.8×	711 0.7×	127	6.1k
Richard S. Olney	1.4k 0.6×	1.3k 0.7×	778 0.6×	983 0.8×	643 0.7×	104	4.7k
Heidi J. Kalkwarf	1.3k 0.6×	1.5k 0.8×	1.2k 1.0×	2.1k 1.7×	504 0.5×	178	9.7k
Paul Merlob	1.9k 0.8×	1.3k 0.6×	497 0.4×	1.4k 1.2×	573 0.6×	248	5.2k
Philip J. Lupo	1.4k 0.6×	1.3k 0.7×	706 0.6×	1.0k 0.8×	1.1k 1.1×	305	5.9k
Janine F. Felix	1.6k 0.7×	869 0.4×	714 0.6×	1.0k 0.8×	1.1k 1.2×	231	6.3k
Suzan L. Carmichael	3.0k 1.3×	2.0k 1.0×	1.0k 0.8×	2.0k 1.6×	662 0.7×	309	9.2k

Countries citing papers authored by Ester Garne

Since Specialization

Citations

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

Fields of papers citing papers by Ester Garne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ester Garne

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

All Works

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20 of 20 papers shown

Santoro, Michele, Ingeborg Barišić, Alessio Coi, et al.. (2025). Health outcomes and drug utilisation in children with Noonan syndrome: a European cohort study. Orphanet Journal of Rare Diseases. 20(1). 76–76.

Loane, Maria, Joan K. Morris, & Ester Garne. (2025). Recommendations for Improving Surveillance of Congenital Anomalies in Europe Using Healthcare Databases. Paediatric and Perinatal Epidemiology. 39(3). 277–284. 1 indexed citations

Seaton, Sarah E, Judith Rankin, Clara Cavero‐Carbonell, et al.. (2025). The Healthcare Needs of Children With Down Syndrome in the First Year of Life: An Analysis of the EUROlinkCAT Data Linkage Study. Paediatric and Perinatal Epidemiology. 39(5). 394–401. 1 indexed citations

Urhøj, Stine Kjær, Joan K. Morris, Maria Loane, et al.. (2024). Higher risk of cerebral palsy, seizures/epilepsy, visual‐ and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT study. Acta Paediatrica. 113(5). 1024–1031. 1 indexed citations

Damkjær, Mads, Joachim Tan, Joan K. Morris, et al.. (2024). Children with Hirschsprung's disease have high morbidity in the first 5 years of life. Birth Defects Research. 116(5). e2338–e2338. 1 indexed citations

Bergman, Jorieke E. H., Ingeborg Barišić, Agnieszka Kinsner‐Ovaskainen, et al.. (2024). Updated EUROCAT guidelines for classification of cases with congenital anomalies. Birth Defects Research. 116(2). e2314–e2314. 8 indexed citations

Olesen, Annette Wind, et al.. (2023). Prenatal detection of major congenital malformations in a cohort of 19 367 Danish fetuses with a complete follow‐up six months after birth. Acta Obstetricia Et Gynecologica Scandinavica. 102(8). 1115–1124. 5 indexed citations

Urhøj, Stine Kjær, Joachim Tan, Clara Cavero‐Carbonell, et al.. (2023). The burden of disease for children born alive with Turner syndrome—A European cohort study. Birth Defects Research. 115(16). 1459–1468. 1 indexed citations

Glinianaia, Svetlana V., Judith Rankin, Joachim Tan, et al.. (2023). Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study. Archives of Disease in Childhood. 108(6). 461–467. 6 indexed citations

10.

Heino, Anna, Sonja Kiuru‐Kuhlefelt, Joan K. Morris, et al.. (2023). Educational achievement of children with selected major congenital anomalies and associated factors: a Finnish registry-based study. European Journal of Public Health. 33(6). 1027–1034. 1 indexed citations

11.

Garne, Ester, Joachim Tan, Mads Damkjær, et al.. (2023). Hospital Length of Stay and Surgery among European Children with Rare Structural Congenital Anomalies—A Population-Based Data Linkage Study. International Journal of Environmental Research and Public Health. 20(5). 4387–4387. 2 indexed citations

12.

Damkjær, Mads, Ester Garne, Maria Loane, et al.. (2023). Timing of Cardiac Surgical Interventions and Postoperative Mortality in Children With Severe Congenital Heart Defects Across Europe: Data From the EUROlinkCAT Study. Journal of the American Heart Association. 12(24). e029871–e029871. 6 indexed citations

13.

Given, Joanne, Joan K. Morris, Ester Garne, et al.. (2023). Prescriptions for insulin and insulin analogues in children with and without major congenital anomalies: a data linkage cohort study across six European regions. European Journal of Pediatrics. 182(5). 2235–2244.

14.

Garne, Ester, Joachim Tan, Maria Loane, et al.. (2022). Gastrostomy and congenital anomalies: a European population-based study. BMJ Paediatrics Open. 6(1). e001526–e001526. 3 indexed citations

15.

Damkjær, Mads, Stine Kjær Urhøj, Joachim Tan, et al.. (2022). Prescription of cardiovascular medication in children with congenital heart defects across six European Regions from 2000 to 2014: data from the EUROlinkCAT population-based cohort study. BMJ Open. 12(4). e057400–e057400. 5 indexed citations

16.

Latos‐Bieleńska, Anna, Elena Marcus, Judith Rankin, et al.. (2022). COVID-19 and children with congenital anomalies: a European survey of parents’ experiences of healthcare services. BMJ Open. 12(7). e061428–e061428. 3 indexed citations

17.

Damkjær, Mads, Maria Loane, Stine Kjær Urhøj, et al.. (2022). Preterm birth and prescriptions for cardiovascular, antiseizure, antibiotics and antiasthmatic medication in children up to 10 years of age: a population-based data linkage cohort study across six European regions. BMJ Open. 12(10). e061746–e061746. 3 indexed citations

18.

Morris, Joan K., Ester Garne, Maria Loane, et al.. (2021). EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies. BMJ Open. 11(6). e047859–e047859. 24 indexed citations

19.

Dolk, Helen, Maria Loane, Karen Casson, et al.. (2021). Macrolide and lincosamide antibiotic exposure in the first trimester of pregnancy and risk of congenital anomaly: A European case-control study. Reproductive Toxicology. 100. 101–108. 12 indexed citations

20.

Wender-Ożegowska, Ewa, Ester Garne, Margery Morgan, et al.. (2015). Use of insulin analogs in pregestational diabetes and risk of congenital anomalies. University of Southern Denmark Research Portal (University of Southern Denmark). 1 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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