Jutta Wirth

2.4k total citations · 1 hit paper
26 papers, 1.8k citations indexed

About

Jutta Wirth is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Jutta Wirth has authored 26 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Jutta Wirth's work include Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Jutta Wirth is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Jutta Wirth collaborates with scholars based in Germany, Denmark and Netherlands. Jutta Wirth's co-authors include Gerd Scherer, W. Schempp, Jobst Meyer, Niels Tommerup, Thomas Wagner, U. Wolf, Juan J. Pasantes, F. Dagna Bricarelli, Bernhard Zabel and Elisabeth Hustert and has published in prestigious journals such as Cell, Gastroenterology and Human Molecular Genetics.

In The Last Decade

Jutta Wirth

26 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

1994 1.2k citations Thomas Wagner, Jutta Wirth et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jutta Wirth Germany	13	1.4k	1.3k	230	209	195	26	1.8k
Cheni Kwok United Kingdom	12	1.3k 0.9×	1.4k 1.1×	331 1.4×	248 1.2×	113 0.6×	14	2.0k
M. Dominguez-Steglich Germany	11	1.2k 0.9×	1.1k 0.9×	278 1.2×	203 1.0×	135 0.7×	15	1.6k
Polly Weller United Kingdom	10	1.1k 0.8×	1.2k 1.0×	273 1.2×	211 1.0×	124 0.6×	10	1.7k
S. M. Darling United Kingdom	20	1.1k 0.8×	1.2k 0.9×	197 0.9×	55 0.3×	323 1.7×	32	1.8k
M.H. Breuning Netherlands	16	1.7k 1.3×	1.4k 1.1×	65 0.3×	57 0.3×	160 0.8×	26	2.1k
Stefan Bagheri‐Fam Australia	20	1.1k 0.8×	1.1k 0.9×	436 1.9×	162 0.8×	80 0.4×	38	1.5k
Annemiek Beverdam Australia	17	677 0.5×	974 0.8×	182 0.8×	71 0.3×	49 0.3×	28	1.3k
Vincenzo Zappavigna Italy	31	706 0.5×	2.4k 1.9×	26 0.1×	190 0.9×	106 0.5×	49	2.8k
P Jalbert France	19	1.1k 0.8×	735 0.6×	118 0.5×	59 0.3×	263 1.3×	59	1.7k
Edwina M. Wright Australia	11	942 0.7×	1.5k 1.2×	142 0.6×	742 3.6×	68 0.3×	14	2.6k

Countries citing papers authored by Jutta Wirth

Since Specialization

Citations

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

Fields of papers citing papers by Jutta Wirth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jutta Wirth

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

Wilhelm, Kerstin, et al.. (2017). Affairs happen—to whom? A study on extrapair paternity in common nightingales. Current Zoology. 63(4). 421–431. 7 indexed citations

Maass, Philipp G., Jutta Wirth, Atakan Aydın, et al.. (2009). A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E. Human Molecular Genetics. 19(5). 848–860. 47 indexed citations

Schreiber, Stefanie, et al.. (2004). Endoscopic Injection of Mitomycin Adsorbed on Carbon Particles for Advanced Esophageal Cancer: a Pilot Study. Endoscopy. 36(5). 421–425. 1 indexed citations

Kennerknecht, Ingo, Rita Exeler, J. Horst, et al.. (2004). Mild phenotype in two unrelated patients with a partial deletion of 21q22.2‐q22.3 defined by FISH and molecular studies. American Journal of Medical Genetics Part A. 131A(3). 265–372. 27 indexed citations

Gläser, Birgitta, Katayoon Shirneshan, Karin Bink, et al.. (2003). Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations. American Journal of Medical Genetics Part A. 126A(3). 229–236. 10 indexed citations

Rickes, S, et al.. (2002). Improved Accuracy in the Diagnosis of Intrahepatic Bile Duct Ectasia in Caroli's Disease by Combination of Ultrasound and Endoscopic Retrograde Cholangiography. Ultraschall in der Medizin - European Journal of Ultrasound. 21(5). 223–225. 4 indexed citations

Zhu, Guanshan, Gabriele Gillessen‐Kaesbach, Jutta Wirth, Eberhard Passarge, & Oliver Bartsch. (2001). Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2). American Journal of Medical Genetics. 98(4). 317–319. 6 indexed citations

Vollmer, Martin, Rainer Ruf, Sylvie Miot, et al.. (2000). Molecular Cloning of the Critical Region for Glomerulopathy with Fibronectin Deposits (GFND) and Evaluation of Candidate Genes. Genomics. 68(2). 127–135. 8 indexed citations

Scheer, Maurice, Silvère M. van der Maarel, Angela Schulz, et al.. (2000). DXS6673E Encodes a Predominantly Nuclear Protein, and Its Mouse Ortholog DXHXS6673E Is Alternatively Spliced in a Developmental- and Tissue-Specific Manner. Genomics. 63(1). 123–132. 7 indexed citations

10.

Kirchhoff, Maria, Hanne Rose, Jan Maahr, et al.. (2000). High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes. European Journal of Human Genetics. 8(9). 661–668. 38 indexed citations

11.

Nothwang, Hans Gerd, Andreas Schröer, Silvère M. van der Maarel, et al.. (2000). Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations. Cytogenetic and Genome Research. 90(1-2). 126–133. 2 indexed citations

12.

Silahtaroglu, Asli, Frans A. Hol, Martin Erdel, et al.. (1999). Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome. European Journal of Human Genetics. 7(1). 68–76. 16 indexed citations

13.

Caubit, Xavier, et al.. (1999). Mouse Dac, a novel nuclear factor with homology toDrosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud. Developmental Dynamics. 214(1). 66–80. 70 indexed citations

14.

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

15.

Silahtaroglu, Asli, et al.. (1998). Not para-, not peri-, but centric inversion of chromosome 12.. Journal of Medical Genetics. 35(8). 682–684. 6 indexed citations

16.

Wagner, Thomas, Niels Tommerup, Jutta Wirth, et al.. (1997). A somatic cell hybrid panel for distal 17q: GDIA1 maps to 17q25.3. Cytogenetic and Genome Research. 76(3-4). 172–175. 8 indexed citations

17.

Nothwang, Hans Gerd, Jutta Wirth, Thomas Haaf, et al.. (1997). Identification of positional candidates for neurological disorders on chromosome 13q14→q22. Cytogenetic and Genome Research. 79(3-4). 293–297. 2 indexed citations

18.

Meyer, Jobst, et al.. (1996). SOX20, a new member of the SOX gene family, is located on chromosome 17p13. Cytogenetic and Genome Research. 72(2-3). 246–249. 19 indexed citations

19.

Wirth, Jutta, Thomas Wagner, Jobst Meyer, et al.. (1996). Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9. Human Genetics. 97(2). 186–193. 82 indexed citations

20.

Wagner, Thomas, Jutta Wirth, Jobst Meyer, et al.. (1994). Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell. 79(6). 1111–1120. 1236 indexed citations breakdown →

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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