Ute Knoll

547 total citations
12 papers, 167 citations indexed

About

Ute Knoll is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, Ute Knoll has authored 12 papers receiving a total of 167 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Ute Knoll's work include Prenatal Screening and Diagnostics (10 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Congenital Anomalies and Fetal Surgery (3 papers). Ute Knoll is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Congenital Anomalies and Fetal Surgery (3 papers). Ute Knoll collaborates with scholars based in Germany, United States and Netherlands. Ute Knoll's co-authors include Rolf Becker, Rolf‐Dieter Wegner, Michael Entezami, Markus Stümm, Han G. Brunner, Sheila Unger, Mohandas Nair, Antonio Rossi, Lisenka E.L.M. Vissers and Denise Horn and has published in prestigious journals such as The American Journal of Human Genetics, Ultrasound in Obstetrics and Gynecology and Prenatal Diagnosis.

In The Last Decade

Ute Knoll

12 papers receiving 138 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ute Knoll Germany	7	94	57	56	29	18	12	167
Ann‐Leslie Zaslav United States	9	138 1.5×	99 1.7×	46 0.8×	34 1.2×	6 0.3×	24	214
Michelle Steinraths Canada	8	104 1.1×	60 1.1×	60 1.1×	12 0.4×	6 0.3×	12	168
Bai-Lin Wu United States	6	163 1.7×	51 0.9×	142 2.5×	15 0.5×	6 0.3×	7	228
Sonja A. de Munnik Netherlands	7	121 1.3×	23 0.4×	104 1.9×	14 0.5×	7 0.4×	9	209
Myriam Châabouni Tunisia	9	114 1.2×	33 0.6×	113 2.0×	32 1.1×	7 0.4×	21	202
Sally Martell Canada	10	178 1.9×	83 1.5×	131 2.3×	12 0.4×	7 0.4×	12	289
Céline Pebrel‐Richard France	7	91 1.0×	39 0.7×	69 1.2×	26 0.9×	6 0.3×	20	138
Anne Bazin France	8	119 1.3×	90 1.6×	74 1.3×	12 0.4×	7 0.4×	16	195
Jennifer M. Feenstra United States	6	88 0.9×	22 0.4×	94 1.7×	50 1.7×	8 0.4×	8	200
Anne-Marie Van Der Kevie-Kersemaekers Netherlands	7	124 1.3×	61 1.1×	92 1.6×	9 0.3×	6 0.3×	13	212

Countries citing papers authored by Ute Knoll

Since Specialization

Citations

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

Fields of papers citing papers by Ute Knoll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ute Knoll

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

All Works

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12 of 12 papers shown

Knoll, Ute, et al.. (2019). EP16.28: Prenatal diagnosis of a Swyer syndrome as a result of gender discrepancy in NIPT and ultrasound. Ultrasound in Obstetrics and Gynecology. 54(S1). 333–333. 1 indexed citations

Becker, Rolf, Thomas Keller, Rolf‐Dieter Wegner, et al.. (2014). Consanguinity and pregnancy outcomes in a multi-ethnic, metropolitan European population. Prenatal Diagnosis. 35(1). 81–89. 23 indexed citations

Vissers, Lisenka E.L.M., Ekkehart Lausch, Sheila Unger, et al.. (2011). Chondrodysplasia and Abnormal Joint Development Associated with Mutations in IMPAD1, Encoding the Golgi-Resident Nucleotide Phosphatase, gPAPP. The American Journal of Human Genetics. 88(5). 608–615. 66 indexed citations

Becker, Rolf, Denise Horn, Ute Knoll, et al.. (2010). First-Trimester Prenatal Diagnosis of Okihiro Syndrome. Fetal Diagnosis and Therapy. 27(4). 222–226. 4 indexed citations

Hagen, Anke, et al.. (2010). The Impact of First Trimester Screening and Early Fetal Anomaly Scan on Invasive Testing Rates in Women with Advanced Maternal Age. Ultraschall in der Medizin - European Journal of Ultrasound. 32(3). 302–306. 11 indexed citations

Wegner, Rolf‐Dieter, Rolf Becker, Markus Stümm, et al.. (2009). Fetal 46,XX/69,XXY mixoploidy: origin and confirmation by analysis of fetal urine cells. Prenatal Diagnosis. 29(3). 287–289. 14 indexed citations

Stümm, Markus, Eva Klopocki, Ute Knoll, et al.. (2007). Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis. Prenatal Diagnosis. 27(5). 475–478. 10 indexed citations

Entezami, Michael, et al.. (2006). OP03.14: Different degrees of ventriculomegaly: frequency of chromosomal anomalies, associated malformations and congenital infections. Ultrasound in Obstetrics and Gynecology. 28(4). 436–436. 1 indexed citations

Hagen, Anke, et al.. (2006). OP03.15: Isolated mild cerebral ventriculomegaly: cytogenetic findings and pregnancy outcome. Ultrasound in Obstetrics and Gynecology. 28(4). 436–437. 1 indexed citations

10.

Becker, Rolf, et al.. (2005). The potential of first trimester anomaly scan and first trimester fetal echocardiography as screening procedures in a medium risk population. 2 indexed citations

11.

Entezami, Michael, et al.. (2004). Ultrasound Diagnosis of Fetal Anomalies. 13 indexed citations

12.

Wegner, Rolf‐Dieter, et al.. (2003). Prenatal diagnosis of fetal trisomy 6 mosaicism and phenotype of the affected newborn. American Journal of Medical Genetics Part A. 124A(1). 85–88. 21 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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