Patrick Rump

4.5k total citations
39 papers, 1.2k citations indexed

About

Patrick Rump is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Patrick Rump has authored 39 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 13 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Patrick Rump's work include Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Fatty Acid Research and Health (6 papers). Patrick Rump is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (6 papers) and Fatty Acid Research and Health (6 papers). Patrick Rump collaborates with scholars based in Netherlands, United States and Germany. Patrick Rump's co-authors include Gerard Hornstra, Anthonie J. van Essen, Arnold D.M. Kester, Ronald P. Mensink, Conny M.A. van Ravenswaaij‐Arts, Birgit Sikkema‐Raddatz, Yvonne J. Vos, Joanne Verheij, Oebele F. Brouwer and Richard J. Sinke and has published in prestigious journals such as American Journal of Clinical Nutrition, PEDIATRICS and Annals of Neurology.

In The Last Decade

Patrick Rump

38 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patrick Rump Netherlands	21	547	487	314	164	140	39	1.2k
Inge François Belgium	23	592 1.1×	405 0.8×	631 2.0×	59 0.4×	173 1.2×	45	1.7k
Laura Bernardini Italy	27	797 1.5×	1.0k 2.1×	317 1.0×	51 0.3×	124 0.9×	126	2.1k
Sandra Janssens Belgium	20	483 0.9×	430 0.9×	293 0.9×	40 0.2×	74 0.5×	66	1.5k
W. F. Blum Germany	18	387 0.7×	232 0.5×	209 0.7×	207 1.3×	89 0.6×	31	1.6k
Werner F. Blum Germany	16	299 0.5×	242 0.5×	213 0.7×	63 0.4×	51 0.4×	20	1.1k
Bessie E. Spiliotis Greece	17	452 0.8×	368 0.8×	310 1.0×	46 0.3×	135 1.0×	65	1.5k
Andrea D. Praticò Italy	23	396 0.7×	427 0.9×	254 0.8×	30 0.2×	71 0.5×	116	1.3k
Vandana Rai India	22	266 0.5×	224 0.5×	269 0.9×	37 0.2×	71 0.5×	79	1.3k
Elizabeth Forsythe United Kingdom	14	715 1.3×	892 1.8×	156 0.5×	54 0.3×	53 0.4×	23	1.2k
Edward C. Frackelton United States	19	474 0.9×	1.0k 2.1×	92 0.3×	72 0.4×	162 1.2×	23	1.6k

Countries citing papers authored by Patrick Rump

Since Specialization

Citations

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

Fields of papers citing papers by Patrick Rump

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Rump

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

Chung, Hyung-Lok, Patrick Rump, Jawid M. Fatih, et al.. (2022). De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in Drosophila. Human Molecular Genetics. 31(19). 3231–3244. 13 indexed citations

Dingemans, Alexander J.M., Lisenka E.L.M. Vissers, David A. Koolen, et al.. (2021). Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndrome. European Journal of Human Genetics. 29(9). 1418–1423. 6 indexed citations

Muir, Alison M., Jennifer L. Cohen, Sarah E. Sheppard, et al.. (2020). Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities. The American Journal of Human Genetics. 106(5). 623–631. 19 indexed citations

Chia, Poh Hui, Ariana Kariminejad, Patrick Rump, & Bruno Reversade. (2017). Increased Endoplasmic Reticulum Stress in patients with Congenital Liver Fibrosis caused by germline mutations in a Protein Disulfide Isomerase. Mechanisms of Development. 145. S27–S27. 1 indexed citations

Lange, Iris, Patrick Rump, Rinze F. Neuteboom, et al.. (2017). Male patients affected by mosaic PCDH19 mutations: five new cases. Neurogenetics. 18(3). 147–153. 36 indexed citations

Bandsma, Robert, Harry van Goor, Michael Yourshaw, et al.. (2015). Loss of ADAM17 is associated with severe multiorgan dysfunction. Human Pathology. 46(6). 923–928. 31 indexed citations

Vries, Paul S. de, Marij Gielen, Dimitris Rizopoulos, et al.. (2014). Association between polyunsaturated fatty acid concentrations in maternal plasma phospholipids during pregnancy and offspring adiposity at age 7: The MEFAB cohort. Prostaglandins Leukotrienes and Essential Fatty Acids. 91(3). 81–85. 48 indexed citations

Rump, Patrick, Nicole de Leeuw, Anthonie J. van Essen, et al.. (2014). Central 22q11.2 deletions. American Journal of Medical Genetics Part A. 164(11). 2707–2723. 43 indexed citations

Chehadeh-Djebbar, Salima El, Edward Blair, Muriel Holder‐Espinasse, et al.. (2012). Changing facial phenotype in Cohen syndrome: towards clues for an earlier diagnosis. European Journal of Human Genetics. 21(7). 736–742. 22 indexed citations

10.

Boogerd, Cornelis J., Dennis Dooijes, Aho Ilgun, et al.. (2011). Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome (vol 88, pg 130, 2010). Cardiovascular Research. 89(1).

11.

Rump, Patrick, Jan D.H. Jongbloed, Birgit Sikkema‐Raddatz, et al.. (2011). Madelung deformity in a girl with a novel and de novo mutation in the GNAS gene. American Journal of Medical Genetics Part A. 155(10). 2566–2570. 4 indexed citations

12.

Daalen, Emma van, Chantal Kemner, Nienke E. Verbeek, et al.. (2011). Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism. Neurogenetics. 12(4). 315–323. 62 indexed citations

13.

Hogervorst, Janneke, et al.. (2009). Prenatal arachidonic acid exposure and selected immune-related variables in childhood. British Journal Of Nutrition. 102(3). 387–397. 6 indexed citations

14.

Breda, Eric van, et al.. (2007). Insulin resistance, physical fitness, body composition and leptin concentration in 7–8 year-old children. Journal of science and medicine in sport. 11(2). 132–138. 16 indexed citations

15.

Rump, Patrick, P.M. Grootscholten, Johanna M. Fock, et al.. (2005). A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect. Neurogenetics. 6(4). 201–207. 14 indexed citations

16.

Rump, Patrick, et al.. (2005). Tumor risk in Beckwith–Wiedemann syndrome: A review and meta‐analysis. American Journal of Medical Genetics Part A. 136A(1). 95–104. 110 indexed citations

17.

Rump, Patrick & Gerard Hornstra. (2002). The n-3 and n-6 Polyunsaturated Fatty Acid Composition of Plasma Phospholipids in Pregnant Women and Their Infants. Relationship with Maternal Linoleic Acid Intake. Clinical Chemistry and Laboratory Medicine (CCLM). 40(1). 32–9. 20 indexed citations

18.

Rump, Patrick, F. Verstappen, Willem J.M. Gerver, & Gerard Hornstra. (2002). Body Composition and Cardiorespiratory Fitness Indicators in Prepubescent Boys and Girls. International Journal of Sports Medicine. 23(1). 50–54. 32 indexed citations

19.

Rump, Patrick, C. Popp‐Snijders, R.J. Heine, & Gerard Hornstra. (2002). Components of the insulin resistance syndrome in seven-year-old children: relations with birth weight and the polyunsaturated fatty acid content of umbilical cord plasma phospholipids. Diabetologia. 45(3). 349–355. 32 indexed citations

20.

Rump, Patrick, Ronald P. Mensink, Arnold D.M. Kester, & Gerard Hornstra. (2001). Essential fatty acid composition of plasma phospholipids and birth weight: a study in term neonates. American Journal of Clinical Nutrition. 73(4). 797–806. 78 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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