Christopher F. Hoth

1.2k total citations
9 papers, 912 citations indexed

About

Christopher F. Hoth is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Sensory Systems. According to data from OpenAlex, Christopher F. Hoth has authored 9 papers receiving a total of 912 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 2 papers in Cellular and Molecular Neuroscience and 2 papers in Sensory Systems. Recurrent topics in Christopher F. Hoth's work include Developmental Biology and Gene Regulation (3 papers), Genomics and Chromatin Dynamics (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Christopher F. Hoth is often cited by papers focused on Developmental Biology and Gene Regulation (3 papers), Genomics and Chromatin Dynamics (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). Christopher F. Hoth collaborates with scholars based in United States, Israel and Germany. Christopher F. Hoth's co-authors include Clinton T. Baldwin, Aubrey Milunsky, Jean Amos, Elias O. Da‐Silva, Sterling K. Clarren, Ruth Sheffer, Roberto A. Macina, Scott P. Kennedy, Joseph J. Oleynek and Roger J. Hill and has published in prestigious journals such as Nature, Nucleic Acids Research and Biochemical and Biophysical Research Communications.

In The Last Decade

Christopher F. Hoth

9 papers receiving 892 citations

Peers

Countries citing papers authored by Christopher F. Hoth

Since Specialization

Citations

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

Fields of papers citing papers by Christopher F. Hoth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher F. Hoth. 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 Christopher F. Hoth. The network helps show where Christopher F. Hoth may publish in the future.

Co-authorship network of co-authors of Christopher F. Hoth

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Expression of the Rat Adrenomedullin Receptor or a Putative Human Adrenomedullin Receptor Does Not Correlate with Adrenomedullin Binding or Functional Response 1998 ·Biochemical and Biophysical Research Communications ·Scott P. Kennedy, Dexue Sun, Joseph J. Oleynek, Christopher F. Hoth, Jimmy Kong, Roger J. Hill	80
2	Cloning, Expression and Pharmacological Characterization of Rabbit Adenosine A1 and A3 Receptors 1997 ·Journal of Pharmacology and Experimental Therapeutics ·Roger J. Hill, Joseph J. Oleynek, Christopher F. Hoth, (unknown), Weifan Weng, Ronald T. Wester, W. Ross Tracey, Delvin R. Knight, Richard Buchholz, Scott P. Kennedy	31
3	Mutations in PAX3 that cause Waardenburg syndrome type I: Ten new mutations and review of the literature 1995 ·American Journal of Medical Genetics ·Clinton T. Baldwin, Christopher F. Hoth, Roberto A. Macina, Aubrey Milunsky	97
4	Mutations in PAX3 associated with waardenburg syndrome type I 1994 ·Human Mutation ·Clinton T. Baldwin, (unknown), Christopher F. Hoth, Tirza Cohen, Wilfred Mamuya, Aubrey Milunsky	53
5	Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes. 1994 ·PubMed ·Lindsay A. Farrer, Kathleen S. Arnos, James H. Asher, Clinton T. Baldwin, Scott R. Diehl, Thomas B. Friedman, James M. Greenberg, (unknown), Christopher F. Hoth, Anil K. Lalwani	54
6	In Situ Hybridization applied to Waardenburg Syndrome 1993 ·Cytogenetic and Genome Research ·Bai‐Lin Wu, Aubrey Milunsky, (unknown), Christopher F. Hoth, Clinton T. Baldwin, James Skare	14
7	Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I). 1993 ·PubMed ·Christopher F. Hoth, Aubrey Milunsky, (unknown), Ruth Sheffer, Sterling K. Clarren, Clinton T. Baldwin	191
8	An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome 1992 ·Nature ·Clinton T. Baldwin, Christopher F. Hoth, Jean Amos, Elias O. Da‐Silva, Aubrey Milunsky	385
9	TWo RFLPs at the TNP1 locus 1991 ·Nucleic Acids Research ·Christopher F. Hoth, Wolfgang Engel	7

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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