Sandra Imholz

1.3k total citations
35 papers, 683 citations indexed

About

Sandra Imholz is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Epidemiology. According to data from OpenAlex, Sandra Imholz has authored 35 papers receiving a total of 683 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Pediatrics, Perinatology and Child Health and 6 papers in Epidemiology. Recurrent topics in Sandra Imholz's work include Prenatal Screening and Diagnostics (5 papers), DNA Repair Mechanisms (4 papers) and Genetics, Aging, and Longevity in Model Organisms (4 papers). Sandra Imholz is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), DNA Repair Mechanisms (4 papers) and Genetics, Aging, and Longevity in Model Organisms (4 papers). Sandra Imholz collaborates with scholars based in Netherlands, United States and Germany. Sandra Imholz's co-authors include Martijn E.T. Dollé, Jolanda M.A. Boer, Edith J. M. Feskens, W. M. Monique Verschuren, Yingchang Lu, Michael Müller, Jeroen L. A. Pennings, Annemieke de Vries, Peter C. J. I. Schielen and Cisca Wijmenga and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and American Journal of Clinical Nutrition.

In The Last Decade

Sandra Imholz

35 papers receiving 660 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra Imholz Netherlands 18 230 162 125 105 98 35 683
Sobha Puppala United States 17 198 0.9× 239 1.5× 80 0.6× 100 1.0× 38 0.4× 35 691
R. Lance Miller United States 19 588 2.6× 90 0.6× 95 0.8× 85 0.8× 67 0.7× 26 946
Yasunori Shibutani Japan 18 139 0.6× 66 0.4× 68 0.5× 226 2.2× 133 1.4× 35 828
Brian Van Yserloo United States 13 218 0.9× 166 1.0× 141 1.1× 159 1.5× 38 0.4× 21 705
Eva Fisher Germany 18 307 1.3× 207 1.3× 151 1.2× 170 1.6× 31 0.3× 41 898
Kwang‐Jen Hsiao Taiwan 18 478 2.1× 152 0.9× 111 0.9× 109 1.0× 21 0.2× 43 1.1k
J.S.H. Tay Singapore 19 121 0.5× 166 1.0× 80 0.6× 148 1.4× 44 0.4× 66 952
Gen Isshiki Japan 19 267 1.2× 164 1.0× 141 1.1× 86 0.8× 17 0.2× 70 858
Michael Traurig United States 18 370 1.6× 272 1.7× 186 1.5× 111 1.1× 27 0.3× 31 808
Isabel Sousa Portugal 7 540 2.3× 396 2.4× 236 1.9× 139 1.3× 31 0.3× 8 1.0k

Countries citing papers authored by Sandra Imholz

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Imholz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Imholz

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Imholz. A scholar is included among the top collaborators of Sandra Imholz 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 Sandra Imholz. Sandra Imholz 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.
Brandt, Renata M. C., Sander Barnhoorn, Sandra Imholz, et al.. (2025). High protein intake causes gene-length-dependent transcriptional decline, shortens lifespan and accelerates ageing in progeroid DNA repair-deficient mice. PubMed. 3(1). 20–20. 1 indexed citations
2.
Imholz, Sandra, Bhawani Nagarajah, Conny T. van Oostrom, et al.. (2021). Compromised DNA Repair Promotes the Accumulation of Regulatory T Cells With an Aging-Related Phenotype and Responsiveness. Frontiers in Aging. 2. 7 indexed citations
3.
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5.
Bouwman, Freek G., Jolanda M.A. Boer, Sandra Imholz, et al.. (2014). Gender-specific genetic associations of polymorphisms in ACE, AKR1C2, FTO and MMP2 with weight gain over a 10-year period. Genes & Nutrition. 9(6). 434–434. 13 indexed citations
6.
Choi, Yong Jun, Li Han, Mi‐Young Son, et al.. (2014). Deletion of Individual Ku Subunits in Mice Causes an NHEJ-Independent Phenotype Potentially by Altering Apurinic/Apyrimidinic Site Repair. PLoS ONE. 9(1). e86358–e86358. 20 indexed citations
7.
Lu, Yingchang, Anika A. M. Vaarhorst, Audrey H. H. Merry, et al.. (2012). Markers of Endogenous Desaturase Activity and Risk of Coronary Heart Disease in the CAREMA Cohort Study. PLoS ONE. 7(7). e41681–e41681. 47 indexed citations
8.
Rodenburg, Wendy, Johan Reimerink, Sandra Imholz, et al.. (2011). Quantitative performance of antibody array technology in a prenatal screening setting. Clinical Chemistry and Laboratory Medicine (CCLM). 50(2). 325–32. 2 indexed citations
9.
Reiling, Erwin, Valeriya Lyssenko, Jolanda M.A. Boer, et al.. (2011). Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time. European Journal of Human Genetics. 20(6). 696–700. 20 indexed citations
10.
Pennings, Jeroen L. A., Wendy Rodenburg, Sandra Imholz, et al.. (2011). Gene Expression Profiling in a Mouse Model Identifies Fetal Liver- and Placenta-Derived Potential Biomarkers for Down Syndrome Screening. PLoS ONE. 6(4). e18866–e18866. 18 indexed citations
11.
Boer, Jolanda M.A., et al.. (2011). Genetic variants in lipid metabolism are independently associated with multiple features of the metabolic syndrome. Lipids in Health and Disease. 10(1). 118–118. 14 indexed citations
12.
Lu, Yingchang, Edith J. M. Feskens, Martijn E.T. Dollé, et al.. (2010). Dietary n−3 and n−6 polyunsaturated fatty acid intake interacts with FADS1 genetic variation to affect total and HDL-cholesterol concentrations in the Doetinchem Cohort Study. American Journal of Clinical Nutrition. 92(1). 258–265. 77 indexed citations
13.
Koster, Maria P. H., Jeroen L. A. Pennings, Sandra Imholz, et al.. (2010). Proteomics and Down syndrome screening: a validation study. Prenatal Diagnosis. 30(11). 1039–1043. 23 indexed citations
14.
Feskens, Edith J. M., et al.. (2010). Glucose levels and genetic variants across transcriptional pathways: interaction effects with BMI. International Journal of Obesity. 34(5). 840–845. 20 indexed citations
15.
Berg, Sophie, Martijn E.T. Dollé, Sandra Imholz, et al.. (2009). Genetic variations in regulatory pathways of fatty acid and glucose metabolism are associated with obesity phenotypes: a population-based cohort study. International Journal of Obesity. 33(10). 1143–1152. 42 indexed citations
16.
Lu, Yingchang, Martijn E.T. Dollé, Sandra Imholz, et al.. (2008). Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations. Journal of Lipid Research. 49(12). 2582–2589. 49 indexed citations
17.
Imholz, Sandra, et al.. (2006). Assessment of collagen genes involved in fragmented medial coronoid process development in Labrador Retrievers as determined by affected sibling-pair analysis. American Journal of Veterinary Research. 67(10). 1713–1718. 7 indexed citations
18.
Stabej, Polona Le Quesne, Sandra Imholz, Serge A. Versteeg, et al.. (2004). Characterization of the canine desmin (DES) gene and evaluation as a candidate gene for dilated cardiomyopathy in the Dobermann. Gene. 340(2). 241–249. 21 indexed citations
19.
Berg, Linda van den, Sandra Imholz, Serge A. Versteeg, et al.. (2003). Isolation and characterization of the canine serotonin receptor 1B gene (htr1B). Gene. 326. 131–139. 12 indexed citations
20.
Oost, Bernard A. van, Serge A. Versteeg, Sandra Imholz, & H.S. Kooistra. (2002). Exclusion of the lim homeodomain gene LHX4 as a candidate gene for pituitary dwarfism in German shepherd dogs. Molecular and Cellular Endocrinology. 197(1-2). 57–62. 9 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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