Andreas Lux

1.3k total citations
26 papers, 907 citations indexed

About

Andreas Lux is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Andreas Lux has authored 26 papers receiving a total of 907 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Andreas Lux's work include Vascular Anomalies and Treatments (12 papers), Tracheal and airway disorders (6 papers) and TGF-β signaling in diseases (5 papers). Andreas Lux is often cited by papers focused on Vascular Anomalies and Treatments (12 papers), Tracheal and airway disorders (6 papers) and TGF-β signaling in diseases (5 papers). Andreas Lux collaborates with scholars based in Germany, United States and United Kingdom. Andreas Lux's co-authors include Douglas A. Marchuk, Mathias Hafner, Liliana Attisano, Ramin Naim, Karl Hörmann, Frank Riedel, Haneen Sadick, Ulrich Goessler, Calvin Vary and Carol J. Gallione and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Genome Research.

In The Last Decade

Andreas Lux

26 papers receiving 897 citations

Peers

Countries citing papers authored by Andreas Lux

Since Specialization

Citations

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

Fields of papers citing papers by Andreas Lux

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Lux

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Lux. A scholar is included among the top collaborators of Andreas Lux 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 Lux. Andreas Lux 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	Investigation of Endoglin Wild-Type and Missense Mutant Protein Heterodimerisation Using Fluorescence Microscopy Based IF, BiFC and FRET Analyses 2014 ·PLoS ONE ·(unknown), Mathias Hafner, Andreas Lux	18
2	HHT diagnosis by Mid-infrared spectroscopy and artificial neural network analysis 2013 ·Orphanet Journal of Rare Diseases ·Andreas Lux, (unknown), (unknown), Carla Olivieri, (unknown), (unknown), Bernhard Wirnitzer	18
3	The antibiotics roseoflavin and 8-demethyl-8-amino-riboflavin from Streptomyces davawensis are metabolized by human flavokinase and human FAD synthetase 2011 ·Biochemical Pharmacology ·Danielle Biscaro Pedrolli, S. Nakanishi, Maria Barile, Madina Mansurova, Eleonora Cano Carmona, Andreas Lux, Wolfgang Gärtner, Matthias Mack	39
4	Genetic and Molecular Analyses of PEG10 Reveal New Aspects of Genomic Organization, Transcription and Translation 2010 ·PLoS ONE ·(unknown), (unknown), Mathias Hafner, Andreas Lux	33
5	Identification of Tctex2β, a Novel Dynein Light Chain Family Member That Interacts with Different Transforming Growth Factor-β Receptors 2006 ·Journal of Biological Chemistry ·Qing‐Jun Meng, Andreas Lux, Andreas Holloschi, Jian Li, John M.X. Hughes, (unknown), John E.G. McCarthy, Anthony M. Heagerty, Petra Kioschis, Mathias Hafner, John M. Garland	36
6	ALK1 signalling analysis identifies angiogenesis related genes and reveals disparity between TGF-β and constitutively active receptor induced gene expression 2006 ·BMC Cardiovascular Disorders ·Andreas Lux, Fiona Salway, Holly K. Dressman, (unknown), Mathias Hafner, Philip J. Day, Douglas A. Marchuk, John M. Garland	35
7	High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients 2005 ·Human Mutation ·Claudia Schulte, Urban W. Geisthoff, Andreas Lux, Susan Kupka, Hans‐Peter Zenner, Nikolaus Blin, Markus Pfister	43
8	Peritoneal cancer treatment with CYP2B1 transfected, microencapsulated cells and ifosfamide 2005 ·Cancer Gene Therapy ·(unknown), Michael Keese, Andreas Lux, Ralf Jesnowski, R. L. Prosst, Robert Saller, Mathias Hafner, J. Sturm, Stefan Post, Matthias Löhr	14
9	Human Retroviral gag- and gag-pol-like Proteins Interact with the Transforming Growth Factor-β Receptor Activin Receptor-like Kinase 1 2004 ·Journal of Biological Chemistry ·Andreas Lux, Christian Beil, Meher Majety, (unknown), Carol J. Gallione, (unknown), Jonathan Berg, Petra Kioschis, Douglas A. Marchuk, Mathias Hafner	54
10	Cost-benefit analysis of a new health insurance card and electronic prescription in Germany 2002 ·Journal of Telemedicine and Telecare ·Andreas Lux	3
11	Cost—Benefit Analysis of a New Health Insurance Card and Electronic Prescription in Germany 2002 ·Journal of Telemedicine and Telecare ·Andreas Lux	3
12	Expression analysis of endoglin missense and truncation mutations: insights into protein structure and disease mechanisms 2000 ·Human Molecular Genetics ·Andreas Lux	56
13	Assignment of Transforming Growth Factor β1 and β3 and a Third New Ligand to the Type I Receptor ALK-1 1999 ·Journal of Biological Chemistry ·Andreas Lux, Liliana Attisano, Douglas A. Marchuk	120
14	Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles 1998 ·Human Mutation ·Carol J. Gallione, (unknown), (unknown), Timothy T. Stenzel, Yan Xue, Kara B. Anthony, Kimberly A. McAllister, (unknown), Jonathan Berg, Andreas Lux, Joshua D. Smith, Calvin Vary, William J. Craigen, (unknown), M. L. Warner, York E. Miller, Charles E. Jackson, Alan E. Guttmacher, Douglas A. Marchuk	77
15	Identification of novel 'expressed sequence tags' within the FHIT gene locus in human chromosome region 3p14.2 1997 ·Human Genetics ·Andreas Lux, Walter Bardenheuer, (unknown), (unknown), (unknown), (unknown), S Michaelis, S. Seeber, Bertram Opalka, J. Schütte	9
16	Genetic instability of 3p12‐p21‐specific microsatellite sequences in renal cell carcinoma 1996 ·British Journal of Urology ·(unknown), Reiner Siebert, Walter Bardenheuer, Andreas Lux, S Michaelis, S. Seeber, (unknown), Bertram Opalka, J. Schütte	15
17	Construction of a consistent YAC contig for human chromosome region 3p14.1. 1996 ·Genome Research ·Walter Bardenheuer, S Michaelis, Andreas Lux, (unknown), (unknown), (unknown), (unknown), Reiner Siebert, Jeremy C. Smith, Annemarie H. van der Hout, Charles H.C.M. Buys, J. Schütte, Bertram Opalka	7
18	Characterization and chromosomal assignment of yeast artificial chromosomes containing human 3p13-p21-specific sequence tagged sites 1995 ·Cancer Genetics and Cytogenetics ·S Michaelis, Walter Bardenheuer, Andreas Lux, Alexander Schramm, (unknown), Reiner Siebert, Christoph Willers, (unknown), (unknown), Annemarie H. van der Hout, Charles H.C.M. Buys, Amanda Heppell-Parton, Pamela Rabbitts, (unknown), Jeremy C. Smith, Denis Le Paslier, Daniel Cohen, Bertram Opalka, J. Schütte	20
19	Characterization of a Microdissection Library from Human Chromosome Region 3p14 1994 ·Genomics ·Walter Bardenheuer, (unknown), Andreas Lux, H.-J. Lüdecke, Bernhard Horsthemke, U. Claussen, Gabriele Senger, Jeremy C. Smith, (unknown), Denis Le Paslier, Daniel Cohen, Amanda Heppell-Parton, Pamela Rabbitts, J. Schütte, Bertram Opalka	13
20	Analysis of the p53 gene in patients with isochromosome 17q and Ph1-positive or -negative myeloid leukemia 1993 ·Leukemia Research ·J. Schütte, Bertram Opalka, R. Becher, Walter Bardenheuer, (unknown), Andreas Lux, S. Seeber	22

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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