Urielle Ullmann

647 total citations
7 papers, 357 citations indexed

About

Urielle Ullmann is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Urielle Ullmann has authored 7 papers receiving a total of 357 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Surgery and 2 papers in Genetics. Recurrent topics in Urielle Ullmann's work include Pluripotent Stem Cells Research (3 papers), Tissue Engineering and Regenerative Medicine (2 papers) and Prenatal Screening and Diagnostics (2 papers). Urielle Ullmann is often cited by papers focused on Pluripotent Stem Cells Research (3 papers), Tissue Engineering and Regenerative Medicine (2 papers) and Prenatal Screening and Diagnostics (2 papers). Urielle Ullmann collaborates with scholars based in Belgium, Netherlands and Italy. Urielle Ullmann's co-authors include H. Van de Velde, I. Liebærs, Karen Sermon, Martine De Rycke, A. Van Steirteghem, Christine Gilles, G. Cauffman, Niels De Temmerman, Ileana Mateizel and Paul Devroey and has published in prestigious journals such as Human Reproduction, Molecular Human Reproduction and European Journal of Human Genetics.

In The Last Decade

Urielle Ullmann

7 papers receiving 352 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Urielle Ullmann Belgium	6	306	73	71	41	40	7	357
Alison Venable United States	5	461 1.5×	68 0.9×	77 1.1×	31 0.8×	49 1.2×	6	525
Zongyong Ai China	11	441 1.4×	66 0.9×	84 1.2×	29 0.7×	47 1.2×	18	547
Anne‐Marie Strömberg Sweden	9	403 1.3×	107 1.5×	96 1.4×	51 1.2×	29 0.7×	9	470
Roksana Moraghebi Sweden	7	279 0.9×	65 0.9×	41 0.6×	47 1.1×	28 0.7×	8	349
Suchitra Muenthaisong Hungary	10	262 0.9×	79 1.1×	70 1.0×	34 0.8×	15 0.4×	19	375
Jinglei Zhai China	9	348 1.1×	74 1.0×	39 0.5×	81 2.0×	29 0.7×	14	488
Yanting Xue China	7	625 2.0×	128 1.8×	85 1.2×	66 1.6×	77 1.9×	9	709
Shiran Bar Israel	7	514 1.7×	40 0.5×	43 0.6×	30 0.7×	29 0.7×	9	583
Hotae Lim United States	6	345 1.1×	76 1.0×	48 0.7×	28 0.7×	63 1.6×	11	394
Sebastian Knöbel Germany	8	231 0.8×	98 1.3×	72 1.0×	27 0.7×	58 1.4×	14	352

Countries citing papers authored by Urielle Ullmann

Since Specialization

Citations

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

Fields of papers citing papers by Urielle Ullmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Urielle Ullmann

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

All Works

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7 of 7 papers shown

1.

Ullmann, Urielle, L. D'Argenzio, Shrey Mathur, et al.. (2018). ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspects. Neuromuscular Disorders. 28(9). 741–749. 10 indexed citations

2.

Grisart, Bernard, et al.. (2016). Trisomy rescue mechanism: the case of concomitant mosaic trisomy 14 and maternal uniparental disomy 14 in a 15‐year‐old girl. Clinical Case Reports. 4(3). 265–271. 19 indexed citations

3.

Seneca, Sara, Willy Lissens, M Bonduelle, et al.. (2012). Reliable and Sensitive Detection of Fragile X (Expanded) Alleles in Clinical Prenatal DNA Samples with a Fast Turnaround Time. Journal of Molecular Diagnostics. 14(6). 560–568. 7 indexed citations

4.

Ullmann, Urielle, David Unuane, Brigitte Velkeniers, et al.. (2012). A new double substitution mutation in the MEN1 gene: a limited penetrance and a specific phenotype. European Journal of Human Genetics. 21(6). 695–697. 5 indexed citations

5.

Ullmann, Urielle, Christine Gilles, Martine De Rycke, et al.. (2008). GSK-3-specific inhibitor-supplemented hESC medium prevents the epithelial-mesenchymal transition process and the up-regulation of matrix metalloproteinases in hESCs cultured in feeder-free conditions. Molecular Human Reproduction. 14(3). 169–179. 39 indexed citations

6.

Ullmann, Urielle, Pieter In 'T Veld, Christine Gilles, et al.. (2006). Epithelial–mesenchymal transition process in human embryonic stem cells cultured in feeder-free conditions. Molecular Human Reproduction. 13(1). 21–32. 107 indexed citations

7.

Mateizel, Ileana, Niels De Temmerman, Urielle Ullmann, et al.. (2005). Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders. Human Reproduction. 21(2). 503–511. 170 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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