Andrea M. Oza

2.0k citations
13 papers · 593 indexed · 1 hit paper · h-index 8
    • Hearing, Cochlea, Tinnitus, Genetics 8
  • Genetics top 10%
    • Genomics and Rare Diseases 5
    • Genomic variations and chromosomal abnormalities 2
    • Ear Surgery and Otitis Media 3
    • Vestibular and auditory disorders 3
    • Retinal Development and Disorders 2
    • CRISPR and Genetic Engineering 2
    • Genomics and Phylogenetic Studies 2

Andrea M. Oza

13 papers receiving 589 citations

Hit Papers

Recommendations for interpreting the loss of function PVS...4332018202620202023100200300400

Peers

Andrea M. Oza
Comparison fields: 5 of 60
  • Sensory Systems 132
  • Genetics 271
  • Otorhinolaryngology 34
  • Neurology 48
  • Molecular Biology 294
Replace Flavio Faletra with:
Flavio Faletra Italy
Ersan Kalay Türkiye
Zhijian Yang China
Nam Suk Sim South Korea
Christine Briggs United States
Magdalena Beneyto Spain
Paola Primignani Italy
Jo-Anne Herbrick Canada
Soo Kyung Koo South Korea
Andrea M. Oza relative to Flavio Faletra Italy Flavio Faletra's profile →
Citations per field
00.5×1.7×
Flavio Faletra · 1×
Citations per year

Countries citing papers authored by Andrea M. Oza

Since Specialization
Citations

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

Fields of papers citing papers by Andrea M. Oza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrea M. Oza. 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 Andrea M. Oza. The network helps show where Andrea M. Oza may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Andrea M. Oza, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Andrea M. Oza Line = papers co-authored together Andrea M. Oza links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 202211
2 20217
3 202122
4 20215
5 20212
6 202113
7 20216
8 20204
9 20188
10 201818
11
Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterionbreakdown →
2018433
12 201719
13 201545

About Andrea M. Oza

Andrea M. Oza is a scholar working on Sensory Systems, Otorhinolaryngology and Neurology, having authored 13 papers that have together received 593 indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (8 papers), Genomics and Rare Diseases (5 papers), Ear Surgery and Otitis Media (3 papers), Vestibular and auditory disorders (3 papers), Retinal Development and Disorders (2 papers), CRISPR and Genetic Engineering (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Sensory Systems (132 citations), Genetics (271 citations) and Otorhinolaryngology (34 citations). Andrea M. Oza has collaborated with scholars based in United States, United Arab Emirates and Switzerland. Frequent co-authors include Heidi L. Rehm, Ahmad Abou Tayoun, Marina T. DiStefano, Tina Pesaran, Steven M. Harrison, Leslie G. Biesecker, Sami S. Amr, Mark Bowser, Birgit Funke and Saeed Al Turki. Their work appears in journals such as Journal of Neuroscience, The Laryngoscope and Human Mutation.

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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