Chieko Chijiwa

409 total citations
9 papers, 147 citations indexed

About

Chieko Chijiwa is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Chieko Chijiwa has authored 9 papers receiving a total of 147 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Chieko Chijiwa's work include RNA modifications and cancer (2 papers), Connective tissue disorders research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Chieko Chijiwa is often cited by papers focused on RNA modifications and cancer (2 papers), Connective tissue disorders research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Chieko Chijiwa collaborates with scholars based in Canada, Spain and Portugal. Chieko Chijiwa's co-authors include Evica Rajcan‐Separovic, M. E. Suzanne Lewis, Christine Tyson, Barbara McGillivray, William T. Gibson, Sally Martell, M. I. Van Allen, William B. Dobyns, Mélanie Fradin and María A. Ramos‐Arroyo and has published in prestigious journals such as Journal of Medical Genetics, Human Mutation and Genes.

In The Last Decade

Chieko Chijiwa

9 papers receiving 134 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chieko Chijiwa Canada	6	110	89	16	15	11	9	147
Ágnes Baross Canada	5	98 0.9×	106 1.2×	18 1.1×	10 0.7×	15 1.4×	5	155
Hugo Hernán Abarca-Barriga Peru	7	88 0.8×	86 1.0×	8 0.5×	15 1.0×	9 0.8×	30	159
Meron Azage United States	4	91 0.8×	81 0.9×	8 0.5×	10 0.7×	11 1.0×	6	129
Mala Isrie Belgium	6	90 0.8×	99 1.1×	17 1.1×	11 0.7×	5 0.5×	7	149
Xiaowei Zhan United States	5	146 1.3×	75 0.8×	5 0.3×	7 0.5×	7 0.6×	6	202
Faezeh Mojahedi Iran	6	64 0.6×	82 0.9×	12 0.8×	15 1.0×	4 0.4×	8	160
Eloi Mercier Canada	7	76 0.7×	89 1.0×	16 1.0×	35 2.3×	7 0.6×	9	152
Samantha L.P. Schilit United States	6	64 0.6×	89 1.0×	18 1.1×	19 1.3×	6 0.5×	13	151
Androniki Menelaou Netherlands	3	180 1.6×	155 1.7×	38 2.4×	14 0.9×	4 0.4×	3	269
Sarah M. Brotman United States	5	68 0.6×	41 0.5×	23 1.4×	11 0.7×	6 0.5×	6	105

Countries citing papers authored by Chieko Chijiwa

Since Specialization

Citations

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

Fields of papers citing papers by Chieko Chijiwa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chieko Chijiwa

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

All Works

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9 of 9 papers shown

Chijiwa, Chieko, et al.. (2024). Clinical and Molecular Characterization of a Novel Homozygous Frameshift Variant in AEBP1-Related Classical-like Ehlers Danlos Syndrome Type 2 with Comparison to Previously Reported Rare Cases. Genes. 15(4). 461–461. 2 indexed citations

Qiao, Ying, Kristina Calli, Sally Martell, et al.. (2021). Contribution of Multiple Inherited Variants to Autism Spectrum Disorder (ASD) in a Family with 3 Affected Siblings. Genes. 12(7). 1053–1053. 14 indexed citations

Chijiwa, Chieko, Christopher Dunham, Douglas H. Jamieson, et al.. (2020). Pathologic Skull Fracture in a Near-Term Neonate with Arthrochalasia Type Ehlers-Danlos Syndrome: A Case Report. Fetal and Pediatric Pathology. 41(1). 149–154. 1 indexed citations

Peñaherrera, Maria S., Christèle du Souich, Lijia Huang, et al.. (2019). Renpenning syndrome in a female. American Journal of Medical Genetics Part A. 182(3). 498–503. 5 indexed citations

Chijiwa, Chieko, et al.. (2016). Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication. BMC Medical Genetics. 17(1). 78–78. 24 indexed citations

Karnebeek, Clara D.M. van, Xin Ye, Mena Abdelsayed, et al.. (2015). MG-115 Compound heterozygous SCN4A mutation underlies severe congenital hypotonia and biophysical alteration in the encoded voltage-gated NAV1.4 sodium channel. Journal of Medical Genetics. 52(Suppl 1). A3.2–A4. 1 indexed citations

Cohen, Ana S.A., Damian Yap, M. E. Suzanne Lewis, et al.. (2015). Weaver Syndrome‐Associated EZH2 Protein Variants Show Impaired Histone Methyltransferase Function In Vitro. Human Mutation. 37(3). 301–307. 61 indexed citations

Chijiwa, Chieko, Saadet Mercimek‐Mahmutoglu, Laura Stewart, et al.. (2010). Pseudohypoparathyroidism type 1a and the GNAS p.R231H mutation: Somatic mosaicism in a mother with two affected sons. American Journal of Medical Genetics Part A. 152A(11). 2784–2790. 12 indexed citations

Tyson, Christine, Barbara McGillivray, Chieko Chijiwa, & Evica Rajcan‐Separovic. (2004). Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array‐CGH. American Journal of Medical Genetics Part A. 129A(3). 254–260. 27 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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