Gundula Leschik

795 total citations
11 papers, 608 citations indexed

About

Gundula Leschik is a scholar working on Molecular Biology, Developmental Biology and Oncology. According to data from OpenAlex, Gundula Leschik has authored 11 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Developmental Biology and 3 papers in Oncology. Recurrent topics in Gundula Leschik's work include Congenital limb and hand anomalies (4 papers), Genomics and Chromatin Dynamics (3 papers) and Bone health and treatments (2 papers). Gundula Leschik is often cited by papers focused on Congenital limb and hand anomalies (4 papers), Genomics and Chromatin Dynamics (3 papers) and Bone health and treatments (2 papers). Gundula Leschik collaborates with scholars based in Germany, Netherlands and Finland. Gundula Leschik's co-authors include Stefan Mundlos, Wolfgang Höhne, Hölger Thiele, Peter Nürnberg, Dieter Kotzot, Georg C. Schwabe, Hiroshi Kitagawa, Anna Rajab, Kazuyuki Sugahara and Michael L. Cunningham and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Gundula Leschik

11 papers receiving 597 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gundula Leschik Germany	9	380	234	123	104	94	11	608
Meena Balasubramanian United Kingdom	18	310 0.8×	555 2.4×	143 1.2×	64 0.6×	63 0.7×	74	802
Claudia Mischung Germany	6	234 0.6×	119 0.5×	133 1.1×	63 0.6×	47 0.5×	6	565
Chalurmpon Srichomthong Thailand	16	342 0.9×	356 1.5×	116 0.9×	29 0.3×	35 0.4×	49	676
Margaret Huskey United States	12	439 1.2×	152 0.6×	101 0.8×	136 1.3×	60 0.6×	17	685
Jinling Wu China	11	606 1.6×	204 0.9×	93 0.8×	55 0.5×	104 1.1×	22	833
Hiroya Takami Japan	11	369 1.0×	127 0.5×	92 0.7×	71 0.7×	306 3.3×	16	724
Janine Wagenstaller Germany	7	283 0.7×	419 1.8×	191 1.6×	124 1.2×	22 0.2×	9	842
Lauréane Mittaz Switzerland	10	211 0.6×	180 0.8×	76 0.6×	38 0.4×	93 1.0×	10	586
Mark L. Johnson United States	11	673 1.8×	166 0.7×	61 0.5×	164 1.6×	126 1.3×	16	938
Elke Piters Belgium	11	418 1.1×	190 0.8×	46 0.4×	154 1.5×	39 0.4×	19	543

Countries citing papers authored by Gundula Leschik

Since Specialization

Citations

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

Fields of papers citing papers by Gundula Leschik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gundula Leschik

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

1.

Ibrahim, Daniel M., Christian Rödelsperger, Asita C. Stiege, et al.. (2013). Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutations. Genome Research. 23(12). 2091–2102. 24 indexed citations

2.

Ott, Claus‐Eric, Gundula Leschik, Louise Brueton, et al.. (2010). Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Human Mutation. 31(8). E1587–E1593. 58 indexed citations

3.

Schwabe, Georg C., Anne Helmrich, Norbert Brieske, et al.. (2005). An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression. Journal of Clinical Investigation. 115(4). 900–909. 62 indexed citations

4.

Schwabe, Georg C., Anne Helmrich, Norbert Brieske, et al.. (2005). An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression. Journal of Clinical Investigation. 115(4). 900–909. 7 indexed citations

5.

Thiele, Hölger, Hiroshi Kitagawa, Kazuyuki Sugahara, et al.. (2004). Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement. Proceedings of the National Academy of Sciences. 101(27). 10155–10160. 131 indexed citations

6.

Schwabe, Georg C., Seval Türkmen, Gundula Leschik, et al.. (2003). Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1. American Journal of Medical Genetics Part A. 124A(4). 356–363. 51 indexed citations

7.

Sander, Thomas, Mohammad R. Toliat, Armin Heils, et al.. (2002). Association of the 867Asp variant of the human anion exchanger 3 gene with common subtypes of idiopathic generalized epilepsy. Epilepsy Research. 51(3). 249–255. 59 indexed citations

8.

Thiele, Hölger, Wolfgang Höhne, Michael L. Cunningham, et al.. (2001). Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nature Genetics. 28(1). 37–41. 182 indexed citations

9.

Nürnberg, Peter, Hölger Thiele, David Chandler, et al.. (2001). Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nature Genetics. 28(1). 37–41. 20 indexed citations

10.

Bollmann, R, Gundula Leschik, Jaakko Leisti, et al.. (1999). Rapid FMR1-protein analysis of fetal blood: an enhancement of prenatal diagnostics. Human Genetics. 105(3). 258–260. 11 indexed citations

11.

Peters, Harm, R. Bollmann, Gundula Leschik, et al.. (1999). Rapid FMR1-protein analysis of fetal blood: an enhancement of prenatal diagnostics. Human Genetics. 105(3). 258–260. 3 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.

Explore authors with similar magnitude of impact