Meron Azage

417 total citations
6 papers, 129 citations indexed

About

Meron Azage is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Meron Azage has authored 6 papers receiving a total of 129 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Meron Azage's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Prenatal Screening and Diagnostics (2 papers). Meron Azage is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Prenatal Screening and Diagnostics (2 papers). Meron Azage collaborates with scholars based in United States, Canada and Belgium. Meron Azage's co-authors include Berivan Baskin, Dmitriy Niyazov, Megan T. Cho, Lindsay B. Henderson, Carolyn Applegate, Hans T. Björnsson, Jonathan Picker, Wendy K. Chung, Volkan Okur and Mark A. Tarnopolsky and has published in prestigious journals such as Neurology, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Meron Azage

5 papers receiving 118 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Meron Azage United States	4	91	81	11	10	8	6	129
Jessica Sebastian United States	6	92 1.0×	64 0.8×	13 1.2×	21 2.1×	7 0.9×	11	146
Alfonso Caro‐Llopis Spain	7	132 1.5×	102 1.3×	16 1.5×	16 1.6×	22 2.8×	14	190
Alessandro Calcia Italy	5	60 0.7×	41 0.5×	19 1.7×	10 1.0×	8 1.0×	8	100
Jūratė Kasnauskienė Lithuania	9	91 1.0×	104 1.3×	9 0.8×	22 2.2×	11 1.4×	16	160
Heidi Thiese United States	4	92 1.0×	66 0.8×	11 1.0×	9 0.9×	4 0.5×	4	113
M.P. Botella Spain	5	79 0.9×	80 1.0×	33 3.0×	6 0.6×	5 0.6×	7	135
Candace Muss United States	3	114 1.3×	58 0.7×	29 2.6×	13 1.3×	3 0.4×	3	149
Jakub Klapecki Poland	5	70 0.8×	76 0.9×	5 0.5×	12 1.2×	5 0.6×	5	114
Mira Kharbanda United Kingdom	5	70 0.8×	65 0.8×	4 0.4×	9 0.9×	4 0.5×	7	105
Nurit Assia Batzir Israel	5	43 0.5×	58 0.7×	8 0.7×	11 1.1×	4 0.5×	9	92

Countries citing papers authored by Meron Azage

Since Specialization

Citations

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

Fields of papers citing papers by Meron Azage

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meron Azage

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Azage, Meron, et al.. (2025). Patient‐reported outcomes for remote and in‐person visits for genetic counseling in adult neurology. Journal of Genetic Counseling. 34(3). e70040–e70040.

2.

Baldwin, Aaron F., et al.. (2023). Preimplantation Genetic Testing for Adult-Onset Neurodegenerative Disease. Neurology. 101(19). 836–841. 1 indexed citations

3.

Pilarowski, Genay, Hilary J. Vernon, Carolyn Applegate, et al.. (2017). Missense variants in the chromatin remodeler CHD1 are associated with neurodevelopmental disability. Journal of Medical Genetics. 55(8). 561–566. 38 indexed citations

4.

Okur, Volkan, Megan T. Cho, Lindsay B. Henderson, et al.. (2016). De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. Human Genetics. 135(7). 699–705. 53 indexed citations

5.

Hu, Jie, Malini Sathanoori, Meron Azage, et al.. (2015). A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders. American Journal of Medical Genetics Part A. 167(8). 1921–1926. 16 indexed citations

6.

Dijck, Anke Van, Ilse M. van der Werf, Edwin Reyniers, et al.. (2015). Five patients with a chromosome 1q21.1 triplication show macrocephaly, increased weight and facial similarities. European Journal of Medical Genetics. 58(10). 503–508. 21 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.

Explore authors with similar magnitude of impact