Cordula Neuner

656 total citations
11 papers, 482 citations indexed

About

Cordula Neuner is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Cordula Neuner has authored 11 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Sensory Systems. Recurrent topics in Cordula Neuner's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Congenital heart defects research (3 papers) and Developmental Biology and Gene Regulation (3 papers). Cordula Neuner is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Congenital heart defects research (3 papers) and Developmental Biology and Gene Regulation (3 papers). Cordula Neuner collaborates with scholars based in Germany, Netherlands and Austria. Cordula Neuner's co-authors include Thomas Haaf, Barbara Vona, Manfred Schartl, Indrajit Nanda, Christoph Winkler, Wafaa Shehata-Dieler, Jörg Schröder, Fabian Kraus, Michaela A. H. Hofrichter and Tobias Müller and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Developmental Biology and Mechanisms of Development.

In The Last Decade

Cordula Neuner

11 papers receiving 460 citations

Peers

Countries citing papers authored by Cordula Neuner

Since Specialization

Citations

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

Fields of papers citing papers by Cordula Neuner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cordula Neuner

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature 2014 ·BMC Medical Genetics ·Barbara Vona, Indrajit Nanda, Cordula Neuner, Jörg Schröder, Vera M. Kalscheuer, Wafaa Shehata-Dieler, Thomas Haaf	40
2	Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations 2014 ·Genetics in Medicine ·Barbara Vona, Tobias Müller, Indrajit Nanda, Cordula Neuner, Michaela A. H. Hofrichter, Jörg Schröder, Oliver Bartsch, (unknown), Annerose Keilmann, Sebastian P. Schraven, Fabian Kraus, Wafaa Shehata-Dieler, Thomas Haaf	75
3	Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss 2013 ·Molecular Syndromology ·Barbara Vona, Cordula Neuner, Nady El Hajj, E. Schneider, R. Farcas, Vera Beyer, Ulrich Zechner, Annerose Keilmann, Martin Poot, Oliver Bartsch, I. Nanda, Thomas Haaf	5
4	Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6 2013 ·European Journal of Human Genetics ·Simone Rost, (unknown), Cordula Neuner, Indrajit Nanda, (unknown), Reginald E. Bittner, Alexander Keller, Oliver Bartsch, Robert Mlynski, Thomas Haaf, Clemens R. Müller, Erdmute Kunstmann	50
5	A Boy with an LCR3/4-Flanked 10q22.3q23.2 Microdeletion and Uncommon Phenotypic Features 2013 ·Molecular Syndromology ·Ekaterina Petrova, Cordula Neuner, Thomas Haaf, Michael Schmid, Johannes Wirbelauer, (unknown), Kathleen Wermke, I. Nanda, Erdmute Kunstmann	5
6	Confirmation of GRHL2 as the gene for the DFNA28 locus 2013 ·American Journal of Medical Genetics Part A ·Barbara Vona, Indrajit Nanda, Cordula Neuner, Tobias Müller, Thomas Haaf	33
7	DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics 2013 ·Clinical Genetics ·Barbara Vona, Michaela A. H. Hofrichter, Cordula Neuner, Jörg Schröder, Andrea Gehrig, Julia B. Hennermann, Fabian Kraus, Wafaa Shehata-Dieler, Eva Klopocki, I. Nanda, Thomas Haaf	69
8	Sequential SDF1a and b-induced mobility guides Medaka PGC migration 2008 ·Developmental Biology ·Amaury Herpin, Peter Fischer, Daniel Liedtke, (unknown), Cordula Neuner, Erez Raz, Manfred Schartl	51
9	Developmentally regulated and non-sex-specific expression of autosomal dmrt genes in embryos of the Medaka fish (Oryzias latipes) 2004 ·Mechanisms of Development ·Christoph Winkler, Ute Hornung, Mariko Kondo, Cordula Neuner, Jutta Duschl, Akihiro Shima, Manfred Schartl	78
10	Hedgehog and retinoid signalling confines nkx2.2b expression to the lateral floor plate of the zebrafish trunk 2004 ·Mechanisms of Development ·Mathias Schäfer, (unknown), Cordula Neuner, Manfred Schartl, Jean‐Nicolas Volff, Christoph Winkler	31
11	The pro-opiomelanocortin gene of the zebrafish (Danio rerio) 2003 ·Biochemical and Biophysical Research Communications ·Immo A. Hansen, Thuy Thanh To, Sebastian Wortmann, Thorsten Burmester, Christoph Winkler, Susanne Meyer, Cordula Neuner, Martin Faßnacht, Bruno Allolio	45

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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