Amit Kawalia

768 total citations
7 papers, 112 citations indexed

About

Amit Kawalia is a scholar working on Molecular Biology, Neurology and Immunology. According to data from OpenAlex, Amit Kawalia has authored 7 papers receiving a total of 112 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Neurology and 2 papers in Immunology. Recurrent topics in Amit Kawalia's work include Barrier Structure and Function Studies (1 paper), Hearing, Cochlea, Tinnitus, Genetics (1 paper) and interferon and immune responses (1 paper). Amit Kawalia is often cited by papers focused on Barrier Structure and Function Studies (1 paper), Hearing, Cochlea, Tinnitus, Genetics (1 paper) and interferon and immune responses (1 paper). Amit Kawalia collaborates with scholars based in Germany, Egypt and United Arab Emirates. Amit Kawalia's co-authors include Peter Nürnberg, Raoul Heller, Susanne Motameny, Janine Altmüller, Michaela Thoenes, Rolf Kaiser, Birgit Budde, Maha S. Zaki, Hölger Thiele and Markus Pfister and has published in prestigious journals such as PLoS ONE, Frontiers in Genetics and Immunogenetics.

In The Last Decade

Amit Kawalia

7 papers receiving 110 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Amit Kawalia Germany	6	59	34	23	23	14	7	112
Céline Poirsier France	5	64 1.1×	5 0.1×	36 1.6×	29 1.3×	13 0.9×	6	125
Manuela Oppo Italy	8	90 1.5×	10 0.3×	13 0.6×	52 2.3×	5 0.4×	8	129
Joyce B. Kang United States	6	86 1.5×	69 2.0×	7 0.3×	22 1.0×	9 0.6×	11	168
Sebastian Röner Germany	3	84 1.4×	12 0.4×	11 0.5×	68 3.0×	6 0.4×	5	160
Rachel Hardisty United Kingdom	5	90 1.5×	10 0.3×	54 2.3×	29 1.3×	9 0.6×	7	162
Theresa Mihalic Mosher United States	7	76 1.3×	5 0.1×	12 0.5×	65 2.8×	11 0.8×	11	115
Abdullah Üzümcü Türkiye	4	55 0.9×	5 0.1×	32 1.4×	13 0.6×	19 1.4×	5	87
Mariet W. Elting Netherlands	3	44 0.7×	10 0.3×	12 0.5×	26 1.1×	4 0.3×	3	94
Suzanne E. de Bruijn Netherlands	5	46 0.8×	8 0.2×	13 0.6×	15 0.7×	7 0.5×	13	64
Ramona Gerhards Germany	6	21 0.4×	29 0.9×	4 0.2×	5 0.2×	11 0.8×	7	142

Countries citing papers authored by Amit Kawalia

Since Specialization

Citations

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

Fields of papers citing papers by Amit Kawalia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amit Kawalia

This figure shows the co-authorship network connecting the top 25 collaborators of Amit Kawalia. A scholar is included among the top collaborators of Amit Kawalia 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 Amit Kawalia. Amit Kawalia 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

1.

Budde, Birgit, Janine Altmüller, Susanne Motameny, et al.. (2020). Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clinical Genetics. 98(1). 32–42. 24 indexed citations

2.

Dafsari, Hormos Salimi, Amit Kawalia, Rosanne Sprute, et al.. (2019). Novel mutations in SLC6A5 with benign course in hyperekplexia. Molecular Case Studies. 5(6). a004465–a004465. 10 indexed citations

3.

Zaki, Maha S., Michaela Thoenes, Amit Kawalia, et al.. (2017). Recurrent and Prolonged Infections in a Child with a Homozygous IFIH1 Nonsense Mutation. Frontiers in Genetics. 8. 130–130. 28 indexed citations

4.

Altmüller, Janine, Britta Haenisch, Amit Kawalia, et al.. (2017). Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing. Immunogenetics. 69(6). 359–369. 10 indexed citations

5.

Khan, Arif O., Birgit Budde, Peter Nürnberg, et al.. (2017). Genome‐wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1‐related fundus phenotype. Clinical Genetics. 93(1). 149–154. 13 indexed citations

6.

Kawalia, Amit, et al.. (2017). Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia. Molecular Case Studies. 4(1). a002139–a002139. 5 indexed citations

7.

Kawalia, Amit, Susanne Motameny, Hölger Thiele, et al.. (2015). Leveraging the Power of High Performance Computing for Next Generation Sequencing Data Analysis: Tricks and Twists from a High Throughput Exome Workflow. PLoS ONE. 10(5). e0126321–e0126321. 22 indexed citations

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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