Andreas W. Kuß

6.5k citations

87 papers · 3.2k indexed · h-index 33

Co-authors: Masoud Garshasbi Andreas Tzschach Kimia Kahrizi Hossein Najmabadi Hans‐Hilger Ropers Michael Nerlich Klaus von der Mark Thorsten Kirsch
Topics: Genetics and Neurodevelopmental Disorders (18 papers)RNA modifications and cancer (11 papers)RNA and protein synthesis mechanisms (7 papers)
Cited by: Genetics Cancer Research Molecular Biology
Journals: Journal of Clinical InvestigationSHILAP Revista de lepidopterologíaEnvironmental Science & Technology
Partner nations: Germany Iran United States

In The Last Decade

Andreas W. Kuß

85 papers receiving 3.2k citations

Peers

Countries citing papers authored by Andreas W. Kuß

Since Specialization

Citations

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

Fields of papers citing papers by Andreas W. Kuß

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas W. Kuß

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Winter Temperature Affects Fatty Acid Composition and Gene Expression, but Not Fat Content and Survival in a Northern Population of a Range‐Expanding Spider 2025 ·Ecology and Evolution ·(unknown),(unknown),Michael Klockmann,Andreas W. Kuß,Lars R. Jensen,Corinna Jensen,Alexander Wacker,George R. Uhl	0
2	Natural phenolic compounds as biofilm inhibitors of multidrug-resistant Escherichia coli – the role of similar biological processes despite structural diversity 2023 ·Frontiers in Microbiology ·(unknown),Michael Schwabe,(unknown),Andreas W. Kuß,Katharina Schaufler,Rabea Schlüter,Stefan Rödiger,Sebastian Guenther,(unknown)	17
3	MncR: Late Integration Machine Learning Model for Classification of ncRNA Classes Using Sequence and Structural Encoding 2023 ·International Journal of Molecular Sciences ·(unknown),(unknown),Lars R. Jensen,Andreas W. Kuß,Stefan Simm	4
4	Identification of sex chromosomes using genomic and cytogenetic methods in a range-expanding spider, Argiope bruennichi (Araneae: Araneidae) 2022 ·Biological Journal of the Linnean Society ·(unknown),Mathilde Cordellier,(unknown),(unknown),Katharina Hoffmann,Corinna Jensen,(unknown),Jiří Král,Andreas W. Kuß,Eva Líznarová,George R. Uhl	2
5	Chromosome-level reference genome of the European wasp spider Argiope bruennichi : a resource for studies on range expansion and evolutionary adaptation 2021 ·GigaScience ·(unknown),(unknown),Henrik Krehenwinkel,George R. Uhl,Andreas W. Kuß,Lars R. Jensen,Corinna Jensen,Rosemary G. Gillespie,Katharina J. Hoff,Stefan Prost	36
6	The C-Mannosylome of Human Induced Pluripotent Stem Cells Implies a Role for ADAMTS16 C-Mannosylation in Eye Development 2021 ·Molecular & Cellular Proteomics ·(unknown),(unknown),(unknown),Thomas Thumberger,(unknown),Stefan Weiß,Lars R. Jensen,(unknown),Daniel Tödt,Andreas W. Kuß,Thomas Ruppert,Joachim Wittbrodt,Hans Bakker,Falk F. R. Buettner	7
7	Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line 2018 ·Frontiers in Oncology ·(unknown),(unknown),Benjamin V. Becker,Chalid Assaf,Markus Möbs,Christian Schmidt,Piotr Grabarczyk,Lars Riff Jensen,Grzegorz K. Przybylski,Matthias Port,Andreas W. Kuß,Reinhard Ullmann	7
8	A t(3;9)(q25.1;q34.3) translocation leading to OLFM1 fusion transcripts in Gilles de la Tourette syndrome, OCD and ADHD 2014 ·Psychiatry Research ·Birgitte Bertelsen,Linea Cecilie Melchior,Lars R. Jensen,(unknown),(unknown),Nanette Mol Debes,Liselotte Skov,Gangcai Xie,Wei Sun,Karen Brøndum‐Nielsen,Andreas W. Kuß,Wei Chen,Zeynep Tümer	13
9	Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7 2014 ·BMC Genomics ·(unknown),(unknown),Robert Weißmann,(unknown),Allan Lind-Thomsen,(unknown),(unknown),(unknown),Matthias Peiser,(unknown),Lars R. Jensen,Ines Müller,Hao Hu,Peter F. Arndt,Andreas W. Kuß,(unknown),Reinhard Ullmann	5
10	Deciphering the Molecular Profile of Plaques, Memory Decline and Neuron Loss in Two Mouse Models for Alzheimerâ€™s Disease by Deep Sequencing 2014 ·Frontiers in Aging Neuroscience ·Yvonne Bouter,Tim Kacprowski,Robert Weißmann,Katharina Dietrich,(unknown),(unknown),Christian Sperling,Oliver Wirths,Mario Albrecht,Lars R. Jensen,Andreas W. Kuß,Thomas A. Bayer	70
11	CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling 2013 ·Journal of Clinical Investigation ·Petro Starokadomskyy,Nathan Gluck,Haiying Li,Baozhi Chen,Mathew Wallis,Gabriel N. Maine,Xicheng Mao,Iram Waris Zaidi,Marco Y. Hein,Fiona J. McDonald,Steffen Lenzner,(unknown),Hans‐Hilger Ropers,Andreas W. Kuß,Julie McGaughran,Jozef Gécz,Ezra Burstein	77
12	New kid on the ID block 2012 ·RNA Biology ·Seth M. Kelly,ChangHui Pak,Masoud Garshasbi,Andreas W. Kuß,Anita H. Corbett,Kenneth H. Moberg	17
13	Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability 2012 ·The American Journal of Human Genetics ·(unknown),Sara Mertel,(unknown),(unknown),Kimia Kahrizi,Sebahattin Çirak,Dagmar Wieczorek,Mohammad Mahdi Motazacker,(unknown),Kirsten Cremer,Robert Weißmann,Andreas Tzschach,Masoud Garshasbi,Seyedeh Sedigheh Abedini,Hossein Najmabadi,Hans‐Hilger Ropers,Stephan J. Sigrist,Andreas W. Kuß	218
14	A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family 2011 ·American Journal of Medical Genetics Part A ·Masoud Garshasbi,Kimia Kahrizi,Masoumeh Hosseini,(unknown),Masoumeh Falah,(unknown),Hao Hu,Andreas Tzschach,Hans Hilger Ropers,Hossein Najmabadi,Andreas W. Kuß	39
15	Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3 2010 ·European Journal of Human Genetics ·Kimia Kahrizi,(unknown),Masoud Garshasbi,Seyedeh Sedigheh Abedini,(unknown),Roxana Kariminejad,Reinhard Ullmann,Wei Chen,(unknown),Andreas W. Kuß,Hossein Najmabadi,Andreas Tzschach	49
16	An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4 2008 ·European Journal of Human Genetics ·Kimia Kahrizi,Hossein Najmabadi,Roxana Kariminejad,Payman Jamali,Mahdi Malekpour,Masoud Garshasbi,Hans Hilger Ropers,Andreas W. Kuß,Andreas Tzschach	16
17	A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation 2007 ·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,(unknown),Chandan Goswami,Andreas Tzschach,Lars Riff Jensen,Dietmar Schmitz,Hans Hilger Ropers,Hossein Najmabadi,Andreas W. Kuß	112
18	X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11 2006 ·European Journal of Human Genetics ·Lars Riff Jensen,Steffen Lenzner,Bettina A. Moser,Kristine Freude,Andreas Tzschach,Wei Chen,Jean‐Pierre Fryns,Jamel Chelly,Gillian Turner,Claude Moraine,Ben C.J. Hamel,Hans‐Hilger Ropers,Andreas W. Kuß	12
19	Associations of a Polymorphic AP-2 Binding Site in the 5′-Flanking Region of the Bovine β-Lactoglobulin Gene with Milk Proteins 2003 ·Journal of Dairy Science ·Andreas W. Kuß,(unknown),H. Geldermann	38
20	Mitochondria-Dependent Caspase-9 Activation Is Necessary for Antigen Receptor-Mediated Effector Caspase Activation and Apoptosis in WEHI 231 Lymphoma Cells 2002 ·The Journal of Immunology ·Marco J. Herold,Andreas W. Kuß,(unknown),Ingolf Berberich	41

About Andreas W. Kuß

Andreas W. Kuß is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 87 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (18 papers), RNA modifications and cancer (11 papers) and RNA and protein synthesis mechanisms (7 papers). The work is most often cited by research in Genetics (1.0k citations), Cancer Research (484 citations) and Molecular Biology (1.8k citations). Andreas W. Kuß has collaborated with scholars based in Germany, Iran and United States. Frequent co-authors include Masoud Garshasbi, Andreas Tzschach, Kimia Kahrizi, Hossein Najmabadi, Hans‐Hilger Ropers, Michael Nerlich, Klaus von der Mark, Thorsten Kirsch, G. Weseloh and H Stöß. Their work appears in journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Environmental Science & Technology.

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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