Aimée Paulussen

3.4k total citations · 1 hit paper
65 papers, 1.9k citations indexed

About

Aimée Paulussen is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Aimée Paulussen has authored 65 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 25 papers in Pediatrics, Perinatology and Child Health and 21 papers in Genetics. Recurrent topics in Aimée Paulussen's work include Prenatal Screening and Diagnostics (20 papers), Hedgehog Signaling Pathway Studies (7 papers) and Cardiac electrophysiology and arrhythmias (6 papers). Aimée Paulussen is often cited by papers focused on Prenatal Screening and Diagnostics (20 papers), Hedgehog Signaling Pathway Studies (7 papers) and Cardiac electrophysiology and arrhythmias (6 papers). Aimée Paulussen collaborates with scholars based in Netherlands, Belgium and United States. Aimée Paulussen's co-authors include Andrea Romano, Marinus J. Blok, B.J.C. van den Bosch, Rita D. Brandão, Rick Kamps, Sofia Xanthoulea, Jeroen Aerssens, Maurice P. Zeegers, Christine de Die‐Smulders and Nicole Y. Souren and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Aimée Paulussen

62 papers receiving 1.8k citations

Hit Papers

align trajectories

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.

Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification

2017 321 citations Rita D. Brandão, B.J.C. van den Bosch et al. profile →

Peers

Aimée Paulussen

GENET

PPCH

PHEOH

Christopher J. McCabe United Kingdom

R G Rosenfeld United States

Kara L. Cushing‐Haugen United States

Csaba Szalai Hungary

Jean Guibourdenche France

Teresa Ferreira Portugal

Qurratulain Hasan India

Helen V. New United Kingdom

V. Kerlan France

Letizia Schreiber Israel

Christopher J. McCabe United Kingdom

Aimée Paulussen

848 ×1.0

329 ×0.6

GENET

478 ×1.0

PPCH

475 ×1.8

139 ×0.7

PHEOH

Citations per year, relative to Aimée Paulussen Aimée Paulussen (= 1×) peers Christopher J. McCabe

Countries citing papers authored by Aimée Paulussen

Since Specialization

Citations

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

Fields of papers citing papers by Aimée Paulussen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aimée Paulussen

This figure shows the co-authorship network connecting the top 25 collaborators of Aimée Paulussen. A scholar is included among the top collaborators of Aimée Paulussen 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 Aimée Paulussen. Aimée Paulussen 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

Cao, Ping, Aimée Paulussen, Robert A. C. Ruiter, et al.. (2025). Artificial intelligence-simplified information to advance reproductive genetic literacy and health equity. Human Reproduction. 40(9). 1681–1688. 1 indexed citations

Roemen, Guido M.J.M., Tom E. J. Theunissen, Anja Steyls, et al.. (2024). Detection of PTCH1 Copy-Number Variants in Mosaic Basal Cell Nevus Syndrome. Biomedicines. 12(2). 330–330.

Derks, Kasper, Marion Drüsedau, J. Dreesen, et al.. (2022). Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing. Human Reproduction. 37(11). 2700–2708. 3 indexed citations

Stoep, Nienke van der, Aimée Paulussen, Karlien Mul, et al.. (2021). Facioscapulohumeral muscular dystrophy—Reproductive counseling, pregnancy, and delivery in a complex multigenetic disease. Clinical Genetics. 101(2). 149–160. 8 indexed citations

Benoit‐Pilven, Clara, Audrey Putoux, Amandine Campan-Fournier, et al.. (2019). New insights into minor splicing—a transcriptomic analysis of cells derived from TALS patients. RNA. 25(9). 1130–1149. 26 indexed citations

Coenen, Marieke J. H., Aimée Paulussen, Martijn Lindhout, et al.. (2018). Evolution of Dihydropyrimidine Dehydrogenase Diagnostic Testing in a Single Center during an 8-Year Period of Time. Current Therapeutic Research. 90. 1–7. 10 indexed citations

Montfoort, Aafke P.A. van, M. Meijer‐Hoogeveen, Frank J. Broekmans, et al.. (2018). Perinatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014. Journal of Assisted Reproduction and Genetics. 35(11). 1995–2002. 17 indexed citations

Paulussen, Aimée, Anja Steyls, Jo Vanoevelen, et al.. (2016). Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. European Journal of Human Genetics. 24(12). 1783–1791. 16 indexed citations

Sallevelt, Suzanne C.E.H., J. Dreesen, Marion Drüsedau, et al.. (2016). PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy. Human Reproduction. 32(3). 698–703. 16 indexed citations

10.

Drüsedau, Marion, Jos Dreesen, I. A. P. Derks-Smeets, et al.. (2013). PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers. European Journal of Human Genetics. 21(12). 1361–1368. 16 indexed citations

11.

Bakker, Jaap, Martijn Lindhout, Daphna D.J. Habets, et al.. (2011). The Effect ofITPAPolymorphisms on the Enzyme Kinetic Properties of Human Erythrocyte Inosine Triphosphatase Toward its Substrates ITP and 6-Thio-ITP. Nucleosides Nucleotides & Nucleic Acids. 30(11). 839–849. 11 indexed citations

12.

Borst, Bram van den, Nicole Y. Souren, Ruth J. F. Loos, et al.. (2011). Genetics of maximally attained lung function: A role for leptin?. Respiratory Medicine. 106(2). 235–242. 14 indexed citations

13.

Souren, Nicole Y., Aimée Paulussen, Anja Steyls, et al.. (2009). Parent-of-origin specific linkage and association of the IGF2 gene region with birth weight and adult metabolic risk factors. International Journal of Obesity. 33(9). 962–970. 11 indexed citations

14.

Harssel, J. J. T. van, Rita D. Brandão, Aimée Paulussen, et al.. (2009). Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection. Familial Cancer. 9(2). 193–201. 8 indexed citations

15.

Roessler, Erich, Kênia Balbi El-Jaick, Christèle Dubourg, et al.. (2009). The mutational spectrum of holoprosencephaly-associated changes within theSHHgene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis. Human Mutation. 30(10). E921–E935. 68 indexed citations

16.

Gielen, Marij, Patrick Lindsey, Cathérine Derom, et al.. (2008). Twin-Specific Intrauterine ‘Growth’ Charts Based on Cross-Sectional Birthweight Data. Twin Research and Human Genetics. 11(2). 224–235. 42 indexed citations

17.

Moonen, Rob, Aimée Paulussen, Nicole Y. Souren, et al.. (2007). Carbamoyl Phosphate Synthetase Polymorphisms as a Risk Factor for Necrotizing Enterocolitis. Pediatric Research. 62(2). 188–190. 53 indexed citations

18.

Chi, Dennis, Nadeem R. Abu‐Rustum, Yukio Sonoda, et al.. (2005). Papers to Appear in Forthcoming Issues. Gynecologic Oncology. 100(1). 221–221. 1 indexed citations

19.

Paulussen, Aimée, Ann Raes, R. J. E. Jongbloed, et al.. (2005). HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency. Cardiovascular Research. 67(3). 467–475. 18 indexed citations

20.

Paulussen, Aimée, Gert Matthijs, Marc Gewillig, et al.. (2003). Mutation Analysis in Congenital Long QT Syndrome—A Case with Missense Mutations in KCNQ1 and SCN5A. Genetic Testing. 7(1). 57–61. 20 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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