Maria Bitner‐Glindzicz
Impact in
- Sensory Systems top 0.1%
- Hearing, Cochlea, Tinnitus, Genetics
- Otorhinolaryngology top 0.5%
- Ear Surgery and Otitis Media
Papers in
-
- Hearing, Cochlea, Tinnitus, Genetics 39
-
- Ear Surgery and Otitis Media 8
- Co-authors
- Shamima RahmanLinda LuxonAndrew R. WebsterMarcus PembreyZubin SaihanGuy Van CampAn BoudewynsJess Tyson
- Journals
- Human Molecular Genetics (9 papers)European Journal of Human Genetics (4 papers)Human Genetics (4 papers)Clinical Genetics (4 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesNorway
In The Last Decade
Maria Bitner‐Glindzicz
93 papers receiving 5.1k citations
Hit Papers
Peers
Comparison fields: 5 of 134
- Sensory Systems 1.8k
- Otorhinolaryngology 443
- Neurology 617
- Clinical Biochemistry 347
- Molecular Biology 3.2k
Countries citing papers authored by Maria Bitner‐Glindzicz
This map shows the geographic impact of Maria Bitner‐Glindzicz'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 Maria Bitner‐Glindzicz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Bitner‐Glindzicz more than expected).
Fields of papers citing papers by Maria Bitner‐Glindzicz
This network shows the impact of papers produced by Maria Bitner‐Glindzicz. 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 Maria Bitner‐Glindzicz. The network helps show where Maria Bitner‐Glindzicz may publish in the future.
Co-authors
The 25 scholars most cited alongside Maria Bitner‐Glindzicz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 8 | |
| 2 | 2018 | 89 | |
| 3 | 2015 | 42 | |
| 4 | 2014 | 37 | |
| 5 | 2014 | 23 | |
| 6 | A comprehensive screen of the USH2A gene in 185 patients with autosomal recessive retinal disease | 2013 | 1 |
| 7 | 2013 | 21 | |
| 8 | 2012 | 18 | |
| 9 | 2012 | 38 | |
| 10 | 2010 | 78 | |
| 11 | 2010 | 8 | |
| 12 | 2010 | 41 | |
| 13 | 2010 | 31 | |
| 14 | 2007 | 13 | |
| 15 | 2005 | 241 | |
| 16 | 2004 | 4 | |
| 17 | 2001 | 92 | |
| 18 | Mapping of a locus for autosomal dominant Hemifacial Microsomia | 2000 | 1 |
| 19 | Hyperinsulinism (HI) associated with sensorineural hearing loss and an inflammatory enteropathy | 2000 | 1 |
| 20 | 2000 | 12 |
About Maria Bitner‐Glindzicz
Maria Bitner‐Glindzicz is a scholar working on Sensory Systems, Otorhinolaryngology, Neurology, Molecular Biology and Ophthalmology, having authored 94 papers that have together received 5.1k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (39 papers), Vestibular and auditory disorders (13 papers), Retinal Development and Disorders (11 papers), Ion channel regulation and function (10 papers), RNA and protein synthesis mechanisms (10 papers), Hearing Loss and Rehabilitation (9 papers), Ear Surgery and Otitis Media (8 papers) and Mitochondrial Function and Pathology (8 papers). The work is most often cited by research in Sensory Systems (1.8k citations), Otorhinolaryngology (443 citations), Neurology (617 citations), Clinical Biochemistry (347 citations) and Molecular Biology (3.2k citations). Maria Bitner‐Glindzicz has collaborated with scholars based in United Kingdom, United States and Norway. Frequent co-authors include Shamima Rahman, Linda Luxon, Andrew R. Webster, Marcus Pembrey, Zubin Saihan, Guy Van Camp, An Boudewyns, Jess Tyson, Frans P.M. Cremers and Hans‐Hilger Ropers. Their work appears in journals such as Human Molecular Genetics, European Journal of Human Genetics, Human Genetics, Clinical Genetics and The American Journal of Human Genetics.
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.