Andreas Tzschach

10.1k total citations
104 papers, 3.3k citations indexed

About

Andreas Tzschach is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Andreas Tzschach has authored 104 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Genetics, 68 papers in Molecular Biology and 10 papers in Plant Science. Recurrent topics in Andreas Tzschach's work include Genomic variations and chromosomal abnormalities (39 papers), Genetics and Neurodevelopmental Disorders (38 papers) and Genomics and Rare Diseases (16 papers). Andreas Tzschach is often cited by papers focused on Genomic variations and chromosomal abnormalities (39 papers), Genetics and Neurodevelopmental Disorders (38 papers) and Genomics and Rare Diseases (16 papers). Andreas Tzschach collaborates with scholars based in Germany, Iran and Netherlands. Andreas Tzschach's co-authors include Hans‐Hilger Ropers, Andreas W. Kuß, Reinhard Ullmann, Vera M. Kalscheuer, Masoud Garshasbi, Kimia Kahrizi, Hossein Najmabadi, Wei Chen, Fikret Erdogan and Lars Riff Jensen and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Genome Research.

In The Last Decade

Andreas Tzschach

103 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Tzschach Germany 30 2.1k 1.8k 266 255 238 104 3.3k
Yoshinori Tsurusaki Japan 37 2.6k 1.2× 1.6k 0.9× 392 1.5× 197 0.8× 357 1.5× 146 3.9k
Benoı̂t Arveiler France 33 1.7k 0.8× 1.2k 0.7× 693 2.6× 182 0.7× 235 1.0× 137 3.1k
Takeshi Mizuguchi Japan 28 1.6k 0.8× 1.2k 0.6× 266 1.0× 198 0.8× 381 1.6× 126 2.7k
David Geneviève France 24 1.3k 0.6× 1.1k 0.6× 233 0.9× 202 0.8× 95 0.4× 80 2.3k
Fen Zhou China 12 2.0k 0.9× 886 0.5× 229 0.9× 208 0.8× 121 0.5× 47 2.5k
Tayfun Özçelık Türkiye 30 1.5k 0.7× 859 0.5× 317 1.2× 225 0.9× 541 2.3× 59 3.1k
Kimia Kahrizi Iran 30 1.8k 0.8× 835 0.5× 252 0.9× 105 0.4× 203 0.9× 141 3.0k
Patrick Edery France 33 2.4k 1.1× 1.6k 0.9× 326 1.2× 250 1.0× 304 1.3× 117 4.5k
Christophe Philippe France 30 1.5k 0.7× 1.6k 0.9× 152 0.6× 207 0.8× 135 0.6× 77 2.7k
Christopher J. Schoenherr United States 12 3.2k 1.5× 1.4k 0.8× 176 0.7× 528 2.1× 658 2.8× 14 3.7k

Countries citing papers authored by Andreas Tzschach

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Tzschach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Tzschach

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Tzschach. A scholar is included among the top collaborators of Andreas Tzschach 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 Andreas Tzschach. Andreas Tzschach 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.
Maier, Alexander, Kimon Runge, Kathrin Nickel, et al.. (2023). Obsessive–compulsive symptoms and 15q11.2q13.1 duplication syndrome. European Neuropsychopharmacology. 78. 67–69. 1 indexed citations
2.
Deniz, Miriam, Ulrike Faust, Cristiana Roggia, et al.. (2023). ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways—lessons from breast cancer patients. Cell Death and Disease. 14(5). 328–328. 1 indexed citations
3.
Beck‐Woedl, Stefanie, Katalin Komlósi, Matthias Eckenweiler, et al.. (2023). Novel homozygous LAMB1 in‐frame deletion in a pediatric patient with brain anomalies and cerebrovascular event. American Journal of Medical Genetics Part A. 191(10). 2656–2663. 1 indexed citations
4.
Runge, Kimon, Marco Reisert, Bernd Feige, et al.. (2023). Deep clinical phenotyping of patients with obsessive-compulsive disorder: an approach towards detection of organic causes and first results. Translational Psychiatry. 13(1). 83–83. 11 indexed citations
5.
Komlósi, Katalin, Jürgen Neesen, Paul Dremsek, et al.. (2021). Marfan Syndrome Caused by Disruption of the FBN1 Gene due to A Reciprocal Chromosome Translocation. Genes. 12(11). 1836–1836. 16 indexed citations
6.
Endres, Dominique, Niels Decher, Katharina Domschke, et al.. (2020). New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel CACNA1C Loss-of-Function Mutation. International Journal of Molecular Sciences. 21(22). 8611–8611. 15 indexed citations
7.
Niceta, Marcello, Domenico Barbuti, Neerja Gupta, et al.. (2019). Skeletal abnormalities are common features in Aymé‐Gripp syndrome. Clinical Genetics. 97(2). 362–369. 10 indexed citations
8.
Rump, Andreas, et al.. (2018). PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome. European Journal of Medical Genetics. 62(12). 103587–103587. 7 indexed citations
9.
Porrmann, Joseph, Andreas Rump, Karl Hackmann, et al.. (2018). Novel truncating PPM1D mutation in a patient with intellectual disability. European Journal of Medical Genetics. 62(1). 70–72. 6 indexed citations
10.
Porrmann, Joseph, Martin Smitka, Evelin Schröck, et al.. (2018). Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion. Ophthalmic Genetics. 39(5). 645–647. 1 indexed citations
11.
Alter, Svenja, Alrun Hotz, Arne Jahn, et al.. (2018). Novel VPS33B mutation in a patient with autosomal recessive keratoderma‐ichthyosis‐deafness syndrome. American Journal of Medical Genetics Part A. 176(12). 2862–2866. 8 indexed citations
12.
Ufartes, Roser, Christiane Neuhofer, Janika Möller, et al.. (2018). Sema3a plays a role in the pathogenesis of CHARGE syndrome. Human Molecular Genetics. 27(8). 1343–1352. 20 indexed citations
13.
Porrmann, Joseph, Nataliya Di Donato, Anne‐Karin Kahlert, et al.. (2017). Novel PRPS1 gain‐of‐function mutation in a patient with congenital hyperuricemia and facial anomalies. American Journal of Medical Genetics Part A. 173(10). 2736–2742. 11 indexed citations
14.
Gieldon, Laura, Luisa Mackenroth, Andreas Rump, et al.. (2017). Skewed X‐inactivation in a family with DLG3‐associated X‐linked intellectual disability. American Journal of Medical Genetics Part A. 173(9). 2545–2550. 12 indexed citations
15.
Hackmann, Karl, Andreas Rump, Stefan A. Haas, et al.. (2015). Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?. American Journal of Medical Genetics Part A. 170(1). 94–102. 8 indexed citations
16.
Oehl‐Jaschkowitz, Barbara, Olivier Vanakker, Anne De Paepe, et al.. (2013). Deletions in 14q24.1q24.3 are associated with congenital heart defects, brachydactyly, and mild intellectual disability. American Journal of Medical Genetics Part A. 164(3). 620–626. 17 indexed citations
17.
Czeschik, Johanna Christina, Peter Bauer, Karin Buiting, et al.. (2013). X-linked intellectual disability type Nascimento is a clinically distinct, probably underdiagnosed entity. Orphanet Journal of Rare Diseases. 8(1). 146–146. 17 indexed citations
18.
Chen, Wei, Vera M. Kalscheuer, Andreas Tzschach, et al.. (2008). Mapping translocation breakpoints by next-generation sequencing. Genome Research. 18(7). 1143–1149. 102 indexed citations
19.
Motazacker, Mohammad Mahdi, Benjamin R. Rost, Tim Hucho, et al.. (2007). A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation. The American Journal of Human Genetics. 81(4). 792–798. 112 indexed citations
20.
Budny, Bartłomiej, Wei Chen, Heymut Omran, et al.. (2006). A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome. Human Genetics. 120(2). 171–178. 122 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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