Andreas Tzschach

10.4k citations

145 papers · 7.9k · 2 hit papers · h-index 44

Impact in

Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Molecular Biology top 2%
- RNA modifications and cancer
- Epigenetics and DNA Methylation
- Congenital heart defects research
- RNA Research and Splicing

Papers in

Genetics 96
- Genetics and Neurodevelopmental Disorders 54
- Genomic variations and chromosomal abnormalities 45
- Genomics and Rare Diseases 25
Molecular Biology 77
- Congenital heart defects research 12
- Genomics and Chromatin Dynamics 11
- RNA modifications and cancer 10
- Ubiquitin and proteasome pathways 7

Co-authors: Hans‐Hilger Ropers (32 shared papers)Andreas Walter Kuss (21 shared papers)Reinhard Ullmann (21 shared papers)Vera M. Kalscheuer (24 shared papers)Masoud Garshasbi (15 shared papers)Kimia Kahrizi (17 shared papers)Hossein Najmabadi (17 shared papers)Wei Chen (8 shared papers)
Journals: European Journal of Human Genetics (15 papers)The American Journal of Human Genetics (11 papers)Human Mutation (8 papers)Clinical Genetics (8 papers)Human Genetics (6 papers)
Partner nations: Germany Iran Netherlands

In The Last Decade

Andreas Tzschach

143 papers receiving 7.7k citations

Andreas Tzschach's Hit Papers

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study 2012 · 841 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2012 The Lancet
2011 Nature

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 145 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study The Lancet ·Anita M. Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine U. Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi Hit paper breakdown →	2012	841
2	Deep sequencing reveals 50 novel genes for recessive cognitive disorders Nature ·Hossein Najmabadi, Hao Yu Hu, Masoud Garshasbi, Tomasz Żemojtel, Seyedeh Sedigheh Abedini, Wei Chen, Masoumeh Hosseini, Farkhondeh Behjati Hit paper breakdown →	2011	807
3	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	2005	324
4	STXBP1 encephalopathy Neurology ·Hannah Stamberger, Marina Nikanorova, Marjolein H. Willemsen, Patrizia Accorsi, Marco Angriman, Hartmut Baier, Ira Benkel-Herrenbrueck, Valérie Benoît	2016	250
5	X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes Molecular Psychiatry ·Hao Yu Hu, Stefan A. Haas, Jamel Chelly, Hilde Van Esch, Martine Raynaud, Arjan P.M. de Brouwer, Stefanie Weinert, Guy Froyen	2015	244
6	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	2012	240
7	Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly The American Journal of Human Genetics ·Maila Giannandrea, Veronica Bianchi, Maria Lidia Mignogna, Alessandra Sirri, Salvatore Carrabino, Errico D’Elia, Matteo L. Vecellio, Silvia P. Russo	2010	204
8	Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene The American Journal of Human Genetics ·Joanna Walczak‐Sztulpa, Jonathan T. Eggenschwiler, Daniel P. S. Osborn, Desmond A. Brown, Francesco Emma, Claus Klingenberg, Raoul C. M. Hennekam, Giuliano Torre	2010	171
9	Genetics of intellectual disability in consanguineous families Molecular Psychiatry ·Hao Yu Hu, Kimia Kahrizi, Luciana Musante, Zohreh Fattahi, Ralf Herwig, Masoumeh Hosseini, Cornelia Oppitz, Seyedeh Sedigheh Abedini	2018	158
10	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	2006	154
11	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	2008	143
12	Mutation Update for Kabuki Syndrome GenesKMT2DandKDM6Aand Further Delineation of X-Linked Kabuki Syndrome Subtype 2 Human Mutation ·Nina Bögershausen, Vincent Gâtinois, Vera Riehmer, Hülya Kayserili, Jutta Becker, Michaela Thoenes, Pelin Özlem Şimşek‐Kiper, Mouna Barat‐Houari	2016	142
13	Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation Nature Genetics ·Vera M. Kalscheuer, Kristine Freude, Luciana Musante, Lars Riff Jensen, Helger G. Yntema, Jozef Gécz, Abdelaziz Sefiani, Kirsten Hoffmann	2003	132
14	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 B. Hucho, Masoud Garshasbi, Kimia Kahrizi, Reinhard Ullmann, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh	2007	131
15	Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP Biological Psychiatry ·Anke Van Dijck, Anneke T. Vulto‐van Silfhout, Elisa Cappuyns, Ilse M. van der Werf, Grazia M. S. Mancini, Andreas Tzschach, Raphael Bernier, Illana Gozes	2018	123
16	Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy European Journal of Human Genetics ·Dorien Lugtenberg, Tjitske Kleefstra, Astrid R. Oudakker, Willy M. Nillesen, Helger G. Yntema, Andreas Tzschach, Martine Raynaud, D. Rating	2008	123
17	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	2008	120
18	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 Rahman Noor, M. Mahdi Motazacker, Talal Jamil, Matloob Azam, Kimia Kahrizi, Muhammad Rafiq	2009	117
19	Next-generation sequencing in X-linked intellectual disability European Journal of Human Genetics ·Andreas Tzschach, Ute Grasshoff, Stefanie Beck‐Woedl, Claudia Dufke, Claudia Bauer, Martin Kehrer, Christina Evers, Ute Moog	2015	114
20	Aberrant phase separation and nucleolar dysfunction in rare genetic diseases Nature ·Martin A. Mensah, Henri Niskanen, Alexandre Papadopoulos Magalhães, Shaon Basu, Martin Kircher, Henrike L. Sczakiel, Alisa Maria Vittoria Reiter, Jonas Elsner	2023	108

About Andreas Tzschach

Andreas Tzschach is a scholar working on Genetics, Molecular Biology, Cell Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 145 papers that have together received 7.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (54 papers), Genomic variations and chromosomal abnormalities (45 papers), Genomics and Rare Diseases (25 papers), Congenital heart defects research (12 papers), Chromosomal and Genetic Variations (11 papers), Genomics and Chromatin Dynamics (11 papers), RNA modifications and cancer (10 papers) and Ubiquitin and proteasome pathways (7 papers). The work is most often cited by research in Genetics (4.2k citations), Molecular Biology (4.4k citations), Cell Biology (747 citations), Cellular and Molecular Neuroscience (607 citations) and Cancer Research (358 citations). Andreas Tzschach has collaborated with scholars based in Germany, Iran and Netherlands. Frequent co-authors include Hans‐Hilger Ropers, Andreas Walter Kuss, Reinhard Ullmann, Vera M. Kalscheuer, Masoud Garshasbi, Kimia Kahrizi, Hossein Najmabadi, Wei Chen, Lars Riff Jensen and Fikret Erdogan. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Human Mutation, Clinical Genetics and Human 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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Andreas Tzschach

Andreas Tzschach's Hit Papers

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Fields of papers citing papers by Andreas Tzschach

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About Andreas Tzschach

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