Irmgard Nippert

914 total citations
44 papers, 592 citations indexed

About

Irmgard Nippert is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Irmgard Nippert has authored 44 papers receiving a total of 592 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 11 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Irmgard Nippert's work include BRCA gene mutations in cancer (21 papers), Prenatal Screening and Diagnostics (11 papers) and Ethics and Legal Issues in Pediatric Healthcare (7 papers). Irmgard Nippert is often cited by papers focused on BRCA gene mutations in cancer (21 papers), Prenatal Screening and Diagnostics (11 papers) and Ethics and Legal Issues in Pediatric Healthcare (7 papers). Irmgard Nippert collaborates with scholars based in Germany, France and United Kingdom. Irmgard Nippert's co-authors include Jörg Schmidtke, Ulf Kristoffersson, Claire Julian‐Reynier, Hilary Harris, Jorge Sequeiros, Helena Kääriäinen, D. Gareth Evans, Aad Tibben, Kirsty Challen and Caroline Benjamin and has published in prestigious journals such as PLoS ONE, Annals of the New York Academy of Sciences and European Journal of Cancer.

In The Last Decade

Irmgard Nippert

43 papers receiving 572 citations

Peers

Irmgard Nippert
Sherry Grumet United States
Laura DiGiovanni United States
Katherine S. Hunt United States
Belinda Rahman Australia
Y Aurran France
Christine Lasset France
Monica Marvin United States
Kara J. Milliron United States
Shanna Gustafson United States
Shelley R. McCormick United States
Sherry Grumet United States
Irmgard Nippert
Citations per year, relative to Irmgard Nippert Irmgard Nippert (= 1×) peers Sherry Grumet

Countries citing papers authored by Irmgard Nippert

Since Specialization
Citations

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

Fields of papers citing papers by Irmgard Nippert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irmgard Nippert

This figure shows the co-authorship network connecting the top 25 collaborators of Irmgard Nippert. A scholar is included among the top collaborators of Irmgard Nippert 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 Irmgard Nippert. Irmgard Nippert 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.
2.
Nippert, Irmgard. (2013). “CAPABILITY” and “Genetic testing in emerging economies” (GenTEE). Journal of Community Genetics. 4(3). 293–296. 6 indexed citations
3.
Nippert, Irmgard, Claire Julian‐Reynier, Hilary Harris, et al.. (2013). Cancer risk communication, predictive testing and management in France, Germany, the Netherlands and the UK: general practitioners' and breast surgeons' current practice and preferred practice responsibilities. Journal of Community Genetics. 5(1). 69–79. 19 indexed citations
4.
Christianson, Arnold L., R.L. Zimmern, Ulf Kristoffersson, et al.. (2013). Health needs assessment for medical genetic services for congenital disorders in middle- and low-income nations. Journal of Community Genetics. 4(3). 297–308. 9 indexed citations
5.
Varga, Orsolya, Sirpa Soini, Helena Kääriäinen, et al.. (2012). Definitions of genetic testing in European legal documents. Journal of Community Genetics. 3(2). 125–141. 12 indexed citations
6.
Kääriäinen, H, et al.. (2010). Genetic Screening in Europe. Public Health Genomics. 13(7-8). 524–537. 5 indexed citations
7.
Challen, Kirsty, Hilary Harris, Ulf Kristoffersson, et al.. (2010). General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices. Journal of Community Genetics. 1(2). 83–90. 6 indexed citations
8.
Nippert, Irmgard, Hilary Harris, Claire Julian‐Reynier, et al.. (2010). Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1. Journal of Community Genetics. 2(1). 1–11. 75 indexed citations
9.
Plass, Anne Marie, Marieke J.H. Baars, Martina C. Cornel, et al.. (2009). Testing the Children: Do Non-Genetic Health-Care Providers Differ in Their Decision to Advise Genetic Presymptomatic Testing on Minors? A Cross-Sectional Study in Five Countries in the European Union. Genetic Testing and Molecular Biomarkers. 13(3). 367–376. 6 indexed citations
10.
Kääriäinen, Helena, Ulf Kristoffersson, Irmgard Nippert, et al.. (2008). EuroGentest: DNA-Based Testing for Heritable Disorders in Europe. Public Health Genomics. 11(2). 75–120. 23 indexed citations
11.
Hietala, Marja, Ulf Kristoffersson, Irmgard Nippert, et al.. (2008). What is ideal genetic counselling? A survey of current international guidelines. European Journal of Human Genetics. 16(4). 445–452. 62 indexed citations
12.
Schmidtke, J., et al.. (2006). Education in Medical Genetics for Physicians: Germany. Public Health Genomics. 9(4). 235–239. 10 indexed citations
13.
Stuhrmann, Manfred, Ludwig Hoy, Irmgard Nippert, & Jörg Schmidtke. (2005). Genotype-based Screening for Hereditary Hemochromatosis: II. Attitudes Toward Genetic Testing and Psychosocial Impact—A Report from a German Pilot Study. Genetic Testing. 9(3). 242–254. 15 indexed citations
14.
Schmidtke, Jörg, Brigitte Pabst, & Irmgard Nippert. (2005). DNA-based Genetic Testing Is Rising Steeply in a National Health Care System with Open Access to Services: A Survey of Genetic Test Use in Germany, 1996–2002. Genetic Testing. 9(1). 80–84. 16 indexed citations
15.
Challen, Kirsty, Hilary Harris, Claire Julian‐Reynier, et al.. (2005). Genetic education and nongenetic health professionals: Educational providers and curricula in Europe. Genetics in Medicine. 7(5). 302–310. 32 indexed citations
16.
Wertz, Dorothy C., John C. Fletcher, Irmgard Nippert, G. Wolff, & Ségolène Aymé. (2002). In focus. Has patient autonomy gone to far? Geneticists' views in 36 nations.. PubMed. 2(4). W21–W21. 9 indexed citations
17.
Nippert, Irmgard. (2002). The pros and cons of human therapeutic cloning in the public debate. Journal of Biotechnology. 98(1). 53–60. 12 indexed citations
18.
Nippert, Irmgard, et al.. (2002). 40 Years Later: The Health Related Quality of Life of Women Affected by Thalidomide. Public Health Genomics. 5(4). 209–216. 13 indexed citations
19.
Meschede, Dieter, et al.. (1998). Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomies. American Journal of Medical Genetics. 80(4). 330–334. 29 indexed citations
20.
Holzgreve, Wolfgang, et al.. (1993). Immediate and Long- Term Applications of Technology. Clinical Obstetrics & Gynecology. 36(3). 476–484. 5 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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