Ulrike Thies

545 total citations
19 papers, 357 citations indexed

About

Ulrike Thies is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Ulrike Thies has authored 19 papers receiving a total of 357 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Ulrike Thies's work include Genetic Neurodegenerative Diseases (6 papers), Genomics and Chromatin Dynamics (4 papers) and Prenatal Screening and Diagnostics (3 papers). Ulrike Thies is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), Genomics and Chromatin Dynamics (4 papers) and Prenatal Screening and Diagnostics (3 papers). Ulrike Thies collaborates with scholars based in Germany, France and Canada. Ulrike Thies's co-authors include Christine Zühlke, Derek Murphy, Stefan Wiese, Peter Burfeind, Marie‐Geneviève Mattéi, Walter Schulz‐Schaeffer, Karl Heinz Grzeschik, Renate Kirschner‐Schwabe, C. Schirren and André Reis and has published in prestigious journals such as Nucleic Acids Research, Human Molecular Genetics and Genomics.

In The Last Decade

Ulrike Thies

18 papers receiving 350 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ulrike Thies Germany	10	258	141	126	67	30	19	357
Carolyn Robbins United States	9	203 0.8×	139 1.0×	111 0.9×	30 0.4×	11 0.4×	9	330
J. Hewitt Canada	6	249 1.0×	226 1.6×	82 0.7×	104 1.6×	14 0.5×	8	410
Angelika Köhler Germany	10	222 0.9×	36 0.3×	134 1.1×	27 0.4×	34 1.1×	12	321
Jacques J. P. van de Kamp Netherlands	7	102 0.4×	139 1.0×	149 1.2×	43 0.6×	38 1.3×	9	313
Liudmila Romanova United States	9	198 0.8×	77 0.5×	25 0.2×	39 0.6×	25 0.8×	21	323
Naohiro Kurotaki Japan	12	223 0.9×	67 0.5×	312 2.5×	32 0.5×	76 2.5×	20	446
Sabine Schwemmle Germany	8	248 1.0×	134 1.0×	106 0.8×	39 0.6×	9 0.3×	13	309
Shirley McQuaid Ireland	9	140 0.5×	43 0.3×	83 0.7×	90 1.3×	10 0.3×	11	270
Shino Shimada Japan	15	315 1.2×	68 0.5×	318 2.5×	19 0.3×	62 2.1×	36	545
Wout H. Deelen Netherlands	11	232 0.9×	41 0.3×	256 2.0×	46 0.7×	69 2.3×	16	413

Countries citing papers authored by Ulrike Thies

Since Specialization

Citations

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

Fields of papers citing papers by Ulrike Thies

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrike Thies

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

All Works

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19 of 19 papers shown

Zühlke, Christine, et al.. (2008). PCR analysis of a three-allelic PvuII-RFLP at D4S127 closely linked to the Huntington disease locus. Clinical Genetics. 43(6). 321–323. 1 indexed citations

Thies, Ulrike, Iris Bartels, Karin Bink, et al.. (1998). Prenatal Diagnosis and Fetopathological Findings in a Fetus with Ring Chromosome 18. Fetal Diagnosis and Therapy. 13(5). 315–320. 1 indexed citations

Murphy, Derek, et al.. (1997). The Human Hepatocyte Nuclear Factor 3/Fork Head Gene FKHL13: Genomic Structure and Pattern of Expression. Genomics. 40(3). 462–469. 35 indexed citations

Wiese, Stefan, Bernd Schröder, Derek Murphy, et al.. (1997). The Novel Human UNF-3/ fork head -like 5 Gene: Chromosomal Localization and Expression Pattern. DNA and Cell Biology. 16(2). 165–171. 5 indexed citations

Zühlke, Christine & Ulrike Thies. (1996). [Huntington chorea. Molecular genetic principles, mutation detection and predictive diagnosis].. PubMed. 67(1). 25–35.

Wiese, Stefan, et al.. (1995). The genes for human brain factor 1 and 2, members of the fork head gene family, are clustered on chromosome 14q. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1262(2-3). 105–112. 28 indexed citations

Krawczak, Michael, Jörg Schmidtke, Jörg T. Epplen, I. Hansmann, & Ulrike Thies. (1994). 2. A Multilocus DNA Fingerprint with Built-in Security Devices. Medicine Science and the Law. 34(3). 256–262. 1 indexed citations

Rieß, Olaf, Ulrike Thies, Jane Theilmann, et al.. (1994). Precise Mapping of the Brain α2-Adrenergic Receptor Gene within Chromosome 4p16. Genomics. 19(2). 298–302. 9 indexed citations

Zühlke, Christine, et al.. (1994). Down syndrome and male fertility: PCR‐derived fingerprinting, serological and andrological investigations. Clinical Genetics. 46(4). 324–326. 32 indexed citations

10.

Murphy, Derek, Stefan Wiese, Peter Burfeind, et al.. (1994). Human Brain Factor 1, a New Member of the Fork Head Gene Family. Genomics. 21(3). 551–557. 64 indexed citations

11.

Zühlke, Christine, et al.. (1993). Mitotic stability and meiotic variability of the (CAG)_n repeat in the Huntington disease gene. Human Molecular Genetics. 2(12). 2063–2067. 118 indexed citations

12.

Thies, Ulrike, et al.. (1993). Attitudes of neurologists, psychiatrists, and psychotherapists towards predictive testing for Huntington's disease in Germany.. Journal of Medical Genetics. 30(12). 1023–1027. 13 indexed citations

13.

Thies, Ulrike, et al.. (1992). Clinical, cytogenetic and molecular investigations in three patients with Wolf‐Hirschhorn syndrome. Clinical Genetics. 42(4). 201–205. 11 indexed citations

14.

Thies, Ulrike, et al.. (1992). Prenatal diagnosis of Huntington's disease (HD): Experiences with six cases and PCR. Prenatal Diagnosis. 12(12). 1055–1061. 4 indexed citations

15.

Herzog, S., et al.. (1991). Holt‐Oram syndrome in four half‐siblings with unaffected parents: brief clinical report. Clinical Genetics. 39(4). 241–244. 8 indexed citations

16.

Thies, Ulrike, V.V.N. Gopal Rao, Wolfgang Engel, & Jörg Schmidtke. (1991). Physical mapping of two Xp markers DXS16 and DXS143. Human Genetics. 86(4). 418–20. 10 indexed citations

17.

Krawczak, Michael, et al.. (1991). Covariate-dependent age-at-onset distributions for Huntington disease.. PubMed. 49(4). 735–45. 12 indexed citations

18.

Pruggmayer, M., Barbara Zoll, M. Leipoldt, & Ulrike Thies. (1990). Prenatal diagnosis and postnatal follow‐up of a child with two de novo unrelated balanced reciprocal translocations. Prenatal Diagnosis. 10(5). 337–342. 4 indexed citations

19.

Wagner, Michael J., et al.. (1989). MspI RFLP for Duchenne muscular dystrophy cDNA subclone 9. Nucleic Acids Research. 17(8). 3328–3328. 1 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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