I Huber

607 total citations
7 papers, 439 citations indexed

About

I Huber is a scholar working on Sensory Systems, Molecular Biology and Genetics. According to data from OpenAlex, I Huber has authored 7 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Sensory Systems, 3 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in I Huber's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Cancer-related molecular mechanisms research (1 paper). I Huber is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Cancer-related molecular mechanisms research (1 paper). I Huber collaborates with scholars based in Netherlands, United Kingdom and Spain. I Huber's co-authors include Silvère M. van der Maarel, Frans P.M. Cremers, Hans‐Hilger Ropers, Anthony P. Monaco, Marcus Pembrey, Yvette J.M. de Kok, S Malcolm, Maria Bitner‐Glindzicz, H.-H. Ropers and S Malcolm and has published in prestigious journals such as Science, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

I Huber

7 papers receiving 431 citations

Peers

Countries citing papers authored by I Huber

Since Specialization

Citations

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

Fields of papers citing papers by I Huber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I Huber

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Cytogenetic mapping and orientation of the rhesus macaque MHC 2003 ·Cytogenetic and Genome Research ·I Huber, Lutz Walter, (unknown), Juan J. Pasantes, E. Günther, W. Schempp	4
2	Cloning of candidate genes for X-linked mental retardation by use of chromosome aberrations 1995 ·American Journal of Medical Genetics Part A ·Silvère M. van der Maarel, (unknown), D. Olde Weghuis, I Huber, Dan Röhme, S Gilgenkrantz, Juha Kere, Jean‐Pierre Fryns, Dvorah Abeliovich, Anne Smits, F.P.M. Cremers, HH Ropers	1
3	A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene 1995 ·Human Molecular Genetics ·(unknown), Gerard Merkx, Silvère M. van der Maarel, I Huber, S Malcolm, H.-H. Ropers, Frans P.M. Cremers	60
4	Yeast Artificial Chromosome Cloningof the Xq13.3-q21.31 Region and FineMapping of a Deletion Associated withChoroideremia and NonspecificMental Retardation 1995 ·European Journal of Human Genetics ·Silvère M. van der Maarel, (unknown), J A Maat-Kievit, I Huber, (unknown), (unknown), (unknown), Hans van Bokhoven, Johan T. den Dunnen, G J van Ommen, (unknown), (unknown), (unknown), (unknown), (unknown)	13
5	Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene POU3F4 1995 ·Science ·Yvette J.M. de Kok, Silvère M. van der Maarel, Maria Bitner‐Glindzicz, I Huber, Anthony P. Monaco, S Malcolm, Marcus Pembrey, Hans‐Hilger Ropers, Frans P.M. Cremers	326
6	X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions 1994 ·Human Molecular Genetics ·I Huber, (unknown), Yvette J.M. de Kok, Silvère M. van der Maarel, Yumiko Ishikawa-Brush, Anthony P. Monaco, David Robinson, S Malcolm, Marcus Pembrey, Han G. Brunner, Frans P.M. Cremers, Hans‐Hilger Ropers	28
7	Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families. 1994 ·Journal of Medical Genetics ·Maria Bitner‐Glindzicz, (unknown), (unknown), I Huber, Frans P.M. Cremers, Hans‐Hilger Ropers, William Reardon, Marcus Pembrey, S Malcolm	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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