Barbara Utermann

649 total citations
18 papers, 336 citations indexed

About

Barbara Utermann is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Barbara Utermann has authored 18 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Barbara Utermann's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (6 papers) and Hedgehog Signaling Pathway Studies (3 papers). Barbara Utermann is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (6 papers) and Hedgehog Signaling Pathway Studies (3 papers). Barbara Utermann collaborates with scholars based in Austria, Germany and Switzerland. Barbara Utermann's co-authors include Gerd Utermann, Martin Erdel, Hans‐Christoph Duba, Judith Löffler, Andreas Janecke, Andreas Th. Müller, Barbara Günther, Doris Nekahm-Heis, Helga Weirich‐Schwaiger and Dieter Kotzot and has published in prestigious journals such as The Journal of Pediatrics, Movement Disorders and Journal of Medical Genetics.

In The Last Decade

Barbara Utermann

18 papers receiving 307 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barbara Utermann Austria 13 177 128 100 64 62 18 336
Babett Heye Germany 7 206 1.2× 147 1.1× 21 0.2× 18 0.3× 29 0.5× 7 365
Jennifer McCallum United States 5 112 0.6× 280 2.2× 23 0.2× 41 0.6× 36 0.6× 5 355
Charles Schwartz United States 6 150 0.8× 185 1.4× 30 0.3× 41 0.6× 19 0.3× 8 317
Jolanda Gyftodimou Greece 10 136 0.8× 125 1.0× 56 0.6× 54 0.8× 21 0.3× 13 270
Alisha Wilkens United States 13 255 1.4× 239 1.9× 104 1.0× 61 1.0× 67 1.1× 20 438
Beatriz R. Versiani Brazil 10 149 0.8× 126 1.0× 19 0.2× 38 0.6× 9 0.1× 16 335
Carol Hardy United Kingdom 9 314 1.8× 297 2.3× 105 1.1× 9 0.1× 18 0.3× 11 500
Y. Fukushima Japan 8 197 1.1× 249 1.9× 59 0.6× 15 0.2× 28 0.5× 15 349
Rita Teek Estonia 9 124 0.7× 126 1.0× 36 0.4× 27 0.4× 10 0.2× 14 221
Abigail L. D. Tadenev United States 11 98 0.6× 284 2.2× 10 0.1× 120 1.9× 15 0.2× 21 426

Countries citing papers authored by Barbara Utermann

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Utermann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Utermann

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Utermann. A scholar is included among the top collaborators of Barbara Utermann 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 Barbara Utermann. Barbara Utermann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Guilherme, Roberta Santos, Claudio Castellan, Andrew Green, et al.. (2013). Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18. The Journal of Pediatrics. 163(4). 1174–1178.e3. 5 indexed citations
2.
Haberlandt, Edda, Werner Judmaier, Albert Schinzel, et al.. (2012). Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype. American Journal of Medical Genetics Part A. 158A(9). 2239–2244. 3 indexed citations
3.
Höckner, Martina, Barbara Utermann, Martin Erdel, et al.. (2008). Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman. American Journal of Medical Genetics Part A. 146A(7). 925–929. 14 indexed citations
4.
Utermann, Barbara, Mariluce Riegel, Dru F. Leistritz, et al.. (2006). Pre‐ and postnatal findings in trisomy 17 mosaicism. American Journal of Medical Genetics Part A. 140A(15). 1628–1636. 17 indexed citations
5.
Seppi, Klaus, Michael Schocke, Katherina Mair, et al.. (2006). Diffusion‐weighted imaging in Huntington's disease. Movement Disorders. 21(7). 1043–1047. 38 indexed citations
6.
Walter, Sabine, Georg Klaus Hinkel, Beate Mitulla, et al.. (2004). Subtelomere FISH in 50 children with mental retardation and minor anomalies, identified by a checklist, detects 10 rearrangements including a de novo balanced translocation of chromosomes 17p13.3 and 20q13.33. American Journal of Medical Genetics Part A. 128A(4). 364–373. 26 indexed citations
7.
Hübner, Christian A., Barbara Utermann, Sigrid Tinschert, et al.. (2004). Intronic mutations in theL1CAMgene may cause X-linked hydrocephalus by aberrant splicing. Human Mutation. 23(5). 526–526. 12 indexed citations
8.
Sass, Jörn Oliver, Daniela Skladal, Bernhard Zelger, Nikolaus Romani, & Barbara Utermann. (2004). Trichothiodystrophy: quantification of cysteine in human hair and nails by application of sodium azide-dependent oxidation to cysteic acid. Archives of Dermatological Research. 296(4). 188–91. 13 indexed citations
9.
Janecke, Andreas, Andreas Th. Müller, Ingmar Gaßner, et al.. (2004). Joubert-like syndrome unlinked to known candidate loci. The Journal of Pediatrics. 144(2). 264–269. 13 indexed citations
10.
Janecke, Andreas, Barbara Günther, Barbara Utermann, et al.. (2002). Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria. Human Genetics. 111(2). 145–153. 62 indexed citations
11.
Erdel, Martin, et al.. (2002). Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism. American Journal of Medical Genetics Part A. 116A(3). 290–294. 20 indexed citations
12.
Utermann, Barbara, et al.. (2000). Mental and psychomotoric retardation in two brothers with pure partial trisomy 7q32-q34 due to a maternal insertion (14;7). American Journal of Medical Genetics. 91(4). 291–297. 4 indexed citations
13.
Duba, Hans‐Christoph, Martin Erdel, Judith Löffler, et al.. (1998). Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrier. European Journal of Human Genetics. 6(1). 75–79. 12 indexed citations
14.
Erdel, Martin, Hans‐Christoph Duba, Irmgard Verdorfer, et al.. (1997). Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations: delineation of the phenotype. Human Genetics. 99(5). 596–601. 28 indexed citations
15.
Duba, Hans‐Christoph, Harald G. Weirich, Helga Weirich‐Schwaiger, et al.. (1997). Chromosomal instability in a woman with infertility and two unaffected brothers: a new familial chromosomal breakage syndrome?. Human Genetics. 100(3-4). 431–440. 16 indexed citations
16.
17.
Erdel, Martin, Silvano Köchl, Barbara Utermann, et al.. (1996). Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10). Human Genetics. 97(6). 784–793. 6 indexed citations
18.
Utermann, Barbara, et al.. (1990). Trisomy 18 mosaicism in an adult woman with normal intelligence and history of miscarriage. Human Genetics. 84(3). 298–9. 18 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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