Sabine Uhrig

1.6k total citations
23 papers, 823 citations indexed

About

Sabine Uhrig is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Sabine Uhrig has authored 23 papers receiving a total of 823 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Sabine Uhrig's work include Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (4 papers). Sabine Uhrig is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (4 papers). Sabine Uhrig collaborates with scholars based in Germany, Austria and United Kingdom. Sabine Uhrig's co-authors include Michael R. Speicher, Roland Eils, Kaan Saracoglu, Christine Fauth, Iver Petersen, Claude Gaultier, Béatrice Laudier, Delphine Trochet, David Gozal and Louise M. O’Brien and has published in prestigious journals such as Nature Medicine, Neurology and Annals of Neurology.

In The Last Decade

Sabine Uhrig

23 papers receiving 800 citations

Peers

Sabine Uhrig

GENET

PPCH

EAS

Raquel Flores Spain

Virginia P. Johnson United States

Birgit Zirn Germany

Wissam A. AbouAlaiwi United States

Patrizia Ronchetto Italy

Bartolomeo Augello Italy

Laura Kasch United States

Maria Grigoriadou Greece

Suneeta Madan‐Khetarpal United States

Rebecca R. Majewski United States

Raquel Flores Spain

Sabine Uhrig

274 ×0.6

GENET

410 ×1.1

55 ×0.3

47 ×0.4

PPCH

23 ×0.2

EAS

Citations per year, relative to Sabine Uhrig Sabine Uhrig (= 1×) peers Raquel Flores

Countries citing papers authored by Sabine Uhrig

Since Specialization

Citations

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

Fields of papers citing papers by Sabine Uhrig

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine Uhrig

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

Schoch, Kelly, Sabine Uhrig, Saskia Biskup, et al.. (2024). A second hotspot for pathogenic exon-skipping variants in CDC45. European Journal of Human Genetics. 32(7). 786–794. 1 indexed citations

Feichtinger, René G., Michaela Brunner‐Krainz, Bader Alhaddad, et al.. (2017). Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. Oxidative Medicine and Cellular Longevity. 2017(1). 7202589–7202589. 33 indexed citations

Röeben, Benjamin, Sabine Uhrig, Benjamin Bender, & Matthis Synofzik. (2016). Teaching Neuro Images : When alopecia and disk herniations meet vascular leukoencephalopathy. Neurology. 86(15). e166–e167. 7 indexed citations

Kolanczyk, Mateusz, Peter Krawitz, Jochen Hecht, et al.. (2014). Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome. European Journal of Human Genetics. 23(5). 633–638. 43 indexed citations

Reiterer, F., et al.. (2014). Congenital pulmonary lymphangiectasis. Paediatric Respiratory Reviews. 15(3). 275–280. 20 indexed citations

Klopocki, Eva, Luitgard Graul‐Neumann, Sabine Uhrig, et al.. (2013). Novel mutations of the PRKAR1A gene in patients with acrodysostosis. Clinical Genetics. 84(6). 531–538. 21 indexed citations

Theiler‐Schwetz, Verena, et al.. (2012). Manifestations of juvenile polyposis syndrome in SMAD4 mutation carriers of a kindred. European Journal of Gastroenterology & Hepatology. 24(8). 988–994. 5 indexed citations

Nagel, Bert, U Gruber‐Sedlmayr, Sabine Uhrig, et al.. (2012). Left ventricular hypertrabeculation/noncompaction with epilepsy, other heart defects, minor facial anomalies and new copy number variants. BMC Medical Genetics. 13(1). 60–60. 2 indexed citations

Sperl, Daniela, Martin Benesch, Ch. Urban, et al.. (2012). Fatal EBV Infection and Variable Clinical Manifestations in an XLP-1 Pedigree – Rapid Diagnosis of Primary Immunodeficiencies may Save Lives. Klinische Pädiatrie. 224(6). 386–389. 3 indexed citations

10.

Sovinz, Petra, Christian Urban, Sabine Uhrig, et al.. (2010). Pheochromocytoma in a 2.75‐year‐old‐girl with a germline von Hippel–Lindau mutation Q164R. American Journal of Medical Genetics Part A. 152A(7). 1752–1755. 17 indexed citations

11.

Fauth, Christine, Susan Gribble, Keith Porter, et al.. (2006). Micro-array analyses decipher exceptional complex familial chromosomal rearrangement. Human Genetics. 119(1-2). 145–153. 17 indexed citations

12.

Geigl, Jochen B., Sabine Uhrig, & Michael R. Speicher. (2006). Multiplex-fluorescence in situ hybridization for chromosome karyotyping. Nature Protocols. 1(3). 1172–1184. 31 indexed citations

13.

Trochet, Delphine, Louise M. O’Brien, David Gozal, et al.. (2005). PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome. The American Journal of Human Genetics. 76(3). 421–426. 183 indexed citations

14.

Martin, Alastair J., Darrel Waggoner, Andrew Wong, et al.. (2002). “Molecular rulers” for calibrating phenotypic effects of telomere imbalance. Journal of Medical Genetics. 39(10). 734–740. 63 indexed citations

15.

Saracoglu, Kaan, Jill M. Brown, Robert E. Kearney, et al.. (2001). New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization. Cytometry. 44(1). 7–15. 33 indexed citations

16.

Brown, Jill M., Kaan Saracoglu, Sabine Uhrig, et al.. (2001). Subtelomeric chromosome rearrangements are detected using an innovative 12-color FISH assay (M-TEL). Nature Medicine. 7(4). 497–501. 49 indexed citations

17.

Speicher, Michael R., Simone Petersen, Sabine Uhrig, et al.. (2000). Analysis of Chromosomal Alterations in Non-Small Cell Lung Cancer by Multiplex-FISH, Comparative Genomic Hybridization, and Multicolor Bar Coding. Laboratory Investigation. 80(7). 1031–1041. 34 indexed citations

18.

Holinski‐Feder, Elke, Edwin Reyniers, Sabine Uhrig, et al.. (2000). Familial Mental Retardation Syndrome ATR-16 Due to an Inherited Cryptic Subtelomeric Translocation, t(3;16)(q29;p13.3). The American Journal of Human Genetics. 66(1). 16–25. 43 indexed citations

19.

Uhrig, Sabine, Simone Schuffenhauer, Christine Fauth, et al.. (1999). Multiplex-FISH for Pre- and Postnatal Diagnostic Applications. The American Journal of Human Genetics. 65(2). 448–462. 72 indexed citations

20.

Eils, Roland, Sabine Uhrig, Kaan Saracoglu, et al.. (1998). An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH). Cytogenetic and Genome Research. 82(3-4). 160–171. 95 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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