Jürgen Kohlhase

7.4k total citations
91 papers, 2.7k citations indexed

About

Jürgen Kohlhase is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Jürgen Kohlhase has authored 91 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 44 papers in Genetics and 16 papers in Cell Biology. Recurrent topics in Jürgen Kohlhase's work include Renal and related cancers (24 papers), Genomic variations and chromosomal abnormalities (16 papers) and Skin and Cellular Biology Research (15 papers). Jürgen Kohlhase is often cited by papers focused on Renal and related cancers (24 papers), Genomic variations and chromosomal abnormalities (16 papers) and Skin and Cellular Biology Research (15 papers). Jürgen Kohlhase collaborates with scholars based in Germany, United States and United Kingdom. Jürgen Kohlhase's co-authors include Cristina Has, Leena Bruckner‐Tuderman, Wiktor Borozdin, Christian Wilhelm, Johann Böhm, Leticia Fröhlich Archangelo, Wolfgang Engel, Johannes S. Kern, Walter Schulz‐Schaeffer and Hauke Schumann and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

In The Last Decade

Jürgen Kohlhase

89 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jürgen Kohlhase Germany 33 1.7k 1.0k 463 287 270 91 2.7k
Millan S. Patel Canada 19 2.6k 1.5× 802 0.8× 247 0.5× 239 0.8× 147 0.5× 54 3.9k
Rika Kosaki Japan 25 1.3k 0.7× 846 0.8× 379 0.8× 297 1.0× 75 0.3× 113 2.3k
Beyhan Tüysüz Türkiye 24 1.4k 0.8× 988 1.0× 469 1.0× 231 0.8× 127 0.5× 139 2.5k
Wim Wuyts Belgium 34 1.6k 0.9× 866 0.9× 521 1.1× 244 0.9× 167 0.6× 108 3.7k
David Geneviève France 24 1.3k 0.8× 1.1k 1.1× 233 0.5× 285 1.0× 136 0.5× 80 2.3k
Hirofumi Ohashi Japan 36 3.1k 1.8× 2.5k 2.5× 356 0.8× 370 1.3× 283 1.0× 165 4.8k
Anthonie J. van Essen Netherlands 27 1.4k 0.8× 920 0.9× 277 0.6× 221 0.8× 122 0.5× 49 2.3k
Andreas H. Kottmann United States 16 1.6k 1.0× 698 0.7× 334 0.7× 168 0.6× 91 0.3× 19 3.8k
Sigrid Tinschert Germany 31 1.3k 0.8× 985 1.0× 232 0.5× 345 1.2× 340 1.3× 94 3.1k
Francesca Gualandi Italy 32 2.1k 1.2× 531 0.5× 252 0.5× 247 0.9× 99 0.4× 115 2.8k

Countries citing papers authored by Jürgen Kohlhase

Since Specialization
Citations

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

Fields of papers citing papers by Jürgen Kohlhase

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jürgen Kohlhase

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

All Works

20 of 20 papers shown
1.
He, Yinghong, Philipp R. Esser, Kerstin Thriene, et al.. (2016). Single Amino Acid Deletion in Kindlin-1 Results in Partial Protein Degradation Which Can Be Rescued by Chaperone Treatment. Journal of Investigative Dermatology. 136(5). 920–929. 12 indexed citations
2.
Kelberman, Daniel, Lily Islam, Jörn Lakowski, et al.. (2014). Mutation of SALL2 causes recessive ocular coloboma in humans and mice. Human Molecular Genetics. 23(10). 2511–2526. 37 indexed citations
3.
Wehner, Peter, Lennart Opitz, Gabriela Salinas-Riester, et al.. (2014). CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance. Human Genetics. 133(8). 997–1009. 88 indexed citations
4.
Ramantani, Georgia, Louis Maillard, Thomas Bast, et al.. (2013). Epilepsy in Aicardi–Goutières syndrome. European Journal of Paediatric Neurology. 18(1). 30–37. 18 indexed citations
5.
Demeer, Bénédicte, Cédric Le Caignec, Bertrand Isidor, et al.. (2012). A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features. European Journal of Medical Genetics. 56(3). 163–170. 41 indexed citations
6.
Pauli, Silke, et al.. (2011). CHD7 mutations causing CHARGE syndrome are predominantly of paternal origin. Clinical Genetics. 81(3). 234–239. 19 indexed citations
7.
Pigors, Manuela, Dimitra Kiritsi, Nicola Wagner, et al.. (2011). Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity. Human Molecular Genetics. 20(9). 1811–1819. 55 indexed citations
8.
Has, Cristina, Bettina Burger, A. Volz‐Thomas, et al.. (2010). Mild Clinical Phenotype of Kindler Syndrome Associated with Late Diagnosis and Skin Cancer. Dermatology. 221(4). 309–312. 16 indexed citations
9.
Arnold, Andreas, Peter Itin, Manuela Pigors, et al.. (2010). Poikiloderma with neutropenia: a novelC16orf57mutation and clinical diagnostic criteria. British Journal of Dermatology. 163(4). 866–869. 36 indexed citations
10.
Salchow, Daniel J., Jürgen Kohlhase, Marijean M. Miller, et al.. (2010). Absent Optic Chiasm Presenting With Horizontal Nystagmus. Journal of Pediatric Ophthalmology & Strabismus. 47(3). 187–191. 1 indexed citations
11.
Schlachetzki, Johannes C. M., Klaus Schmidtke, Jan Beckervordersandforth, et al.. (2009). Frequency of progranulin mutations in a German cohort of 79 frontotemporal dementia patients. Journal of Neurology. 256(12). 2043–2051. 6 indexed citations
12.
Kohlhase, Jürgen, et al.. (2008). New Recognized Ophthalmic Morphologic Anomalies in CHARGE Syndrome Caused by the R2319C Mutation in theCHD7Gene. Ophthalmic Genetics. 29(2). 79–84. 7 indexed citations
13.
Ala‐Mello, Sirpa, Carola Saloranta, Maila Penttinen, et al.. (2007). Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions. Genetics in Medicine. 9(10). 690–694. 38 indexed citations
14.
Wieczorek, Dagmar, Charles Shaw‐Smith, Jürgen Kohlhase, et al.. (2007). Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup‐shaped ears, congenital heart defect, and mental retardation—New MCA/MR syndrome in two affected sibs and a mildly affected mother?. American Journal of Medical Genetics Part A. 143A(11). 1135–1142. 12 indexed citations
15.
Böhm, Johann, Claudio Sustmann, Christian Wilhelm, & Jürgen Kohlhase. (2006). SALL4 is directly activated by TCF/LEF in the canonical Wnt signaling pathway. Biochemical and Biophysical Research Communications. 348(3). 898–907. 66 indexed citations
16.
Borozdin, Wiktor, Michael J. Bamshad, Elke Botzenhart, et al.. (2006). Expanding the spectrum ofTBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutations. Human Mutation. 27(9). 975–976. 33 indexed citations
17.
Netzer, Christian, et al.. (2006). Defining the heterochromatin localization and repression domains of SALL1. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1762(3). 386–391. 26 indexed citations
18.
Has, Cristina, Vesarat Wessagowit, Monica Pascucci, et al.. (2006). Molecular Basis of Kindler Syndrome in Italy: Novel and Recurrent Alu/Alu Recombination, Splice Site, Nonsense, and Frameshift Mutations in the KIND1 Gene. Journal of Investigative Dermatology. 126(8). 1776–1783. 47 indexed citations
19.
McCann, Emma, Alan Fryer, William Newman, Richard Appleton, & Jürgen Kohlhase. (2005). A family with Duane anomaly and distal limb abnormalities: A further family with the arthrogryposis‐ophthalmoplegia syndrome. American Journal of Medical Genetics Part A. 139A(2). 123–126. 5 indexed citations
20.
Salerno, Ann E., Jürgen Kohlhase, & B. S. Kaplan. (2000). Townes-Brocks syndrome and renal dysplasia: a novel mutation in the SALL1 gene. Pediatric Nephrology. 14(1). 25–28. 24 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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