Andreas Tzschach

10.2k citations

105 papers · 3.3k · h-index 31

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
Molecular Biology top 5%
- RNA modifications and cancer
- Epigenetics and DNA Methylation
- Congenital heart defects research
- RNA Research and Splicing

Papers in

Genetics 74
- Genomic variations and chromosomal abnormalities 38
- Genetics and Neurodevelopmental Disorders 37
- Genomics and Rare Diseases 16
Molecular Biology 64
- Congenital heart defects research 11
- Genomics and Chromatin Dynamics 10
- RNA modifications and cancer 7
- Ubiquitin and proteasome pathways 6

Co-authors: Hans‐Hilger Ropers (33 shared papers)Andreas W. Kuß (21 shared papers)Reinhard Ullmann (22 shared papers)Vera M. Kalscheuer (23 shared papers)Masoud Garshasbi (15 shared papers)Kimia Kahrizi (17 shared papers)Hossein Najmabadi (17 shared papers)Wei Chen (9 shared papers)
Journals: European Journal of Human Genetics (10 papers)The American Journal of Human Genetics (8 papers)Human Genetics (4 papers)Human Mutation (4 papers)Clinical Genetics (4 papers)
Partner nations: Germany Iran Netherlands

In The Last Decade

Andreas Tzschach

104 papers receiving 3.2k citations

Peers

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-authors

The 25 scholars most cited alongside Andreas Tzschach, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Andreas Tzschach Line = papers co-authored together Andreas Tzschach links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 105 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation The American Journal of Human Genetics ·Lars Riff Jensen, M Amende, Ulf Gurok, Bettina A. Moser, Verena Gimmel, Andreas Tzschach, Andreas Janecke, Gholamali Tariverdian, Jamel Chelly, Jean‐Pierre Fryns, Hilde Van Esch, Tjitske Kleefstra, B Hamel, Claude Moraine, Jozef Gécz, Gillian Turner, Richard Reinhardt, Vera M. Kalscheuer, Hans‐Hilger Ropers, Steffen Lenzner	2005	288
2	Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability The American Journal of Human Genetics ·Lia Abbasi‐Moheb, Sara Mertel, Melanie Gonsior, Leyla Nouri-Vahid, Kimia Kahrizi, Sebahattin Çirak, Dagmar Wieczorek, Mohammad Mahdi Motazacker, Sahar Esmaeeli-Nieh, Kirsten Cremer, Robert Weißmann, Andreas Tzschach, Masoud Garshasbi, Seyedeh Sedigheh Abedini, Hossein Najmabadi, Hans‐Hilger Ropers, Stephan J. Sigrist, Andreas W. Kuß	2012	220
3	Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene The American Journal of Human Genetics ·Joanna Walczak‐Sztulpa, Jonathan Eggenschwiler, Daniel P. S. Osborn, Desmond Brown, Francesco Emma, Claus Klingenberg, Raoul C. M. Hennekam, Giuliano Torre, Masoud Garshasbi, Andreas Tzschach, Małgorzata Szczepańska, Marian Krawczyński, Jacek Zachwieja, Danuta Zwołińska, Philip L. Beales, Hans‐Hilger Ropers, Anna Latos‐Bieleńska, Andreas W. Kuß	2010	152
4	A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome Human Genetics ·Bartłomiej Budny, Wei Chen, Heymut Omran, Manfred Fliegauf, Andreas Tzschach, Marzena Wiśniewska, Lars Riff Jensen, Martine Raynaud, Sarah A. Shoichet, Magda Badura, Steffen Lenzner, Anna Latos‐Bieleńska, Hans‐Hilger Ropers	2006	123
5	A balanced chromosomal translocation disruptingARHGEF9is associated with epilepsy, anxiety, aggression, and mental retardation Human Mutation ·Vera M. Kalscheuer, Luciana Musante, Cheng Fang, Kirsten Hoffmann, Céline Fuchs, Eloisa Carta, Emma Deas, Venkateswarlu Kanamarlapudi, Corinna Menzel, Reinhard Ullmann, Niels Tommerup, Leda Dalprà, Andreas Tzschach, Angelo Selicorni, Bernhard Lüscher, Hans‐Hilger Ropers, Kirsten Harvey, (unknown)	2008	120
6	A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation The American Journal of Human Genetics ·Mohammad Mahdi Motazacker, Benjamin R. Rost, Tim Hucho, Masoud Garshasbi, Kimia Kahrizi, Reinhard Ullmann, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saeid Hosseini Amini, Chandan Goswami, Andreas Tzschach, Lars Riff Jensen, Dietmar Schmitz, Hans Hilger Ropers, Hossein Najmabadi, Andreas W. Kuß	2007	112
7	A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation The American Journal of Human Genetics ·Masoud Garshasbi, Valeh Hadavi, Haleh Habibi, Kimia Kahrizi, Roxana Kariminejad, Farkhondeh Behjati, Andreas Tzschach, Hossein Najmabadi, Hans Hilger Ropers, Andreas W. Kuß	2008	106
8	Mapping translocation breakpoints by next-generation sequencing Genome Research ·Wei Chen, Vera M. Kalscheuer, Andreas Tzschach, Corinna Menzel, Reinhard Ullmann, Marcel H. Schulz, Fikret Erdogan, Na Li, Zofia Kijas, Ger J. A. Arkesteijn, I. López Pajares, Margret Goetz-Sothmann, Uwe Heinrich, Imma Rost, Andreas Dufke, Ute Grasshoff, Birgitta Glaeser, Martin Vingron, Hans‐Hilger Ropers	2008	103
9	Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation The American Journal of Human Genetics ·Asif Mir, Liana Kaufman, Abdul Noor, M. Mahdi Motazacker, Talal Jamil, Matloob Azam, Kimia Kahrizi, Muhammad Rafiq, Rosanna Weksberg, Tanveer Nasr, Farooq Naeem, Andreas Tzschach, Andreas W. Kuß, Gisele E. Ishak, Dan Doherty, Hans‐Hilger Ropers, A. James Barkovich, Hossein Najmabadi, Muhammad Ayub, John B. Vincent	2009	98
10	Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation Human Genetics ·Vera M. Kalscheuer, David Fitzpatrick, Niels Tommerup, Merete Bugge, E. Niebuhr, Luitgard M. Neumann, Andreas Tzschach, Sarah A. Shoichet, Corinna Menzel, Fikret Erdogan, Ger J. A. Arkesteijn, Hans‐Hilger Ropers, Reinhard Ullmann	2007	90
11	NovelJARID1C/SMCX mutations in patients with X-linked mental retardation Human Mutation ·Andreas Tzschach, Steffen Lenzner, Bettina A. Moser, Richard Reinhardt, Jamel Chelly, Jean‐Pierre Fryns, Tjitske Kleefstra, Martine Raynaud, Gillian Turner, Hans‐Hilger Ropers, Andreas W. Kuß, Lars Riff Jensen	2006	87
12	ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions The American Journal of Human Genetics ·Hao Hu, Katinka Eggers, Wei Chen, Masoud Garshasbi, M. Mahdi Motazacker, Klaus Wrogemann, Kimia Kahrizi, Andreas Tzschach, Masoumeh Hosseini, Ideh Bahman, Tim Hucho, Martina Mühlenhoff, Rita Gerardy‐Schahn, Hossein Najmabadi, Hans‐Hilger Ropers, Andreas W. Kuß	2011	87
13	High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease Journal of Medical Genetics ·Fikret Erdogan, Lars Allan Larsen, Litu Zhang, Zeynep Tümer, Niels Tommerup, Wei Chen, J. Ramsøe Jacobsen, Marei Schubert, Jan Jurkatis, Andreas Tzschach, HH Ropers, Reinhard Ullmann	2008	86
14	A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability The American Journal of Human Genetics ·Lingli Huang, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, Alison Gardner, Raman Kumar, Evelyn Douglas, Cheryl Shoubridge, Dagmar Wieczorek, Andreas Tzschach, Monika Cohen, Anna Hackett, Michael Field, Guy Froyen, Hao Hu, Stefan A. Haas, Hans‐Hilger Ropers, Vera M. Kalscheuer, Mark Corbett, Jozef Gécz	2012	75
15	Chromosome deletions in 13q33–34: Report of four patients and review of the literature American Journal of Medical Genetics Part A ·Joanna Walczak‐Sztulpa, Marzena Wiśniewska, Anna Latos‐Bieleńska, Maja Linné, Christina Kelbova, Britta Belitz, Lutz Pfeiffer, Vera M. Kalscheuer, Fikret Erdogan, Andreas W. Kuß, Hans‐Hilger Ropers, Reinhard Ullmann, Andreas Tzschach	2008	72
16	SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly Human Genetics ·Masoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, Farkhondeh Behjati, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saghar Ghasemi Firouzabadi, Christian Becker, Franz Rüschendorf, Peter Nürnberg, Andreas Tzschach, Reza Vazifehmand, Fikret Erdogan, Reinhard Ullmann, Steffen Lenzner, Andreas W. Kuß, Hans‐Hilger Ropers, Hossein Najmabadi	2005	60
17	Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing European Journal of Human Genetics ·Wei Chen, Reinhard Ullmann, Claudia Langnick, Corinna Menzel, Zofia Wotschofsky, Hao Hu, Andreas Gogol‐Döring, Yuhui Hu, Hui Kang, Andreas Tzschach, Maria Hoeltzenbein, Heidemarie Neitzel, Susanne Markus, Eberhard Wiedersberg, G Kistner, Conny M. A. van Ravenswaaij-Arts, Tjitske Kleefstra, Vera M. Kalscheuer, Hans‐Hilger Ropers	2009	50
18	Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3 European Journal of Human Genetics ·Kimia Kahrizi, Cougar Hao Hu, Masoud Garshasbi, Seyedeh Sedigheh Abedini, Shirin Ghadami, Roxana Kariminejad, Reinhard Ullmann, Wei Chen, H-Hilger Ropers, Andreas W. Kuß, Hossein Najmabadi, Andreas Tzschach	2010	49
19	Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability Human Mutation ·Luciana Musante, Lucia Püttmann, Kimia Kahrizi, Masoud Garshasbi, Hao Hu, Henning Stehr, Bettina Lipkowitz, Sabine Otto, Lars R. Jensen, Andreas Tzschach, Payman Jamali, Thomas F. Wienker, Hossein Najmabadi, Hans Hilger Ropers, Andreas W. Kuß	2017	48
20	Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome “tiling path” BAC array in a girl with heart defect, cleft palate, and developmental delay American Journal of Medical Genetics Part A ·Fikret Erdogan, Reinhard Ullmann, Wei Chen, Marei Schubert, S. Adolph, Claus Hultschig, Vera M. Kalscheuer, Hans‐Hilger Ropers, Christiane Spaich, Andreas Tzschach	2006	46

About Andreas Tzschach

Andreas Tzschach is a scholar working on Genetics, Molecular Biology, Plant Science, Cell Biology and Genetics, having authored 105 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (38 papers), Genetics and Neurodevelopmental Disorders (37 papers), Genomics and Rare Diseases (16 papers), Congenital heart defects research (11 papers), Chromosomal and Genetic Variations (10 papers), Genomics and Chromatin Dynamics (10 papers), RNA modifications and cancer (7 papers) and Ubiquitin and proteasome pathways (6 papers). The work is most often cited by research in Genetics (1.7k citations), Molecular Biology (2.0k citations), Cell Biology (248 citations), Cancer Research (188 citations) and Cellular and Molecular Neuroscience (224 citations). Andreas Tzschach has collaborated with scholars based in Germany, Iran and Netherlands. Frequent 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. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Human Genetics, Human Mutation and Clinical Genetics.

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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