Chaya Miller

1.5k total citations
20 papers, 1.2k citations indexed

About

Chaya Miller is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Chaya Miller has authored 20 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 3 papers in Genetics. Recurrent topics in Chaya Miller's work include Mitochondrial Function and Pathology (14 papers), RNA and protein synthesis mechanisms (7 papers) and RNA modifications and cancer (5 papers). Chaya Miller is often cited by papers focused on Mitochondrial Function and Pathology (14 papers), RNA and protein synthesis mechanisms (7 papers) and RNA modifications and cancer (5 papers). Chaya Miller collaborates with scholars based in Israel, United States and United Kingdom. Chaya Miller's co-authors include Ann Saada, Orly Elpeleg, Avraham Shaag, Eli Hershkovitz, Simon Edvardson, Efrat Ben‐Shalom, Maria Bitner‐Glindzicz, Alistair T. Pagnamenta, Shamima Rahman and Linda Spremulli and has published in prestigious journals such as Molecular and Cellular Biology, Analytical Biochemistry and Annals of Neurology.

In The Last Decade

Chaya Miller

19 papers receiving 1.2k citations

Peers

Countries citing papers authored by Chaya Miller

Since Specialization

Citations

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

Fields of papers citing papers by Chaya Miller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chaya Miller

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Variable effects of omaveloxolone (RTA408) on primary fibroblasts with mitochondrial defects 2022 ·Frontiers in Molecular Biosciences ·(unknown), David Arkadir, Liza Douiev, (unknown), Chaya Miller, Ann Saada	7
2	Replicative Stress Coincides with Impaired Nuclear DNA Damage Response in COX4-1 Deficiency 2022 ·International Journal of Molecular Sciences ·Liza Douiev, Chaya Miller, (unknown), Hadar Benyamini, Bassam Abu‐Libdeh, Ann Saada	6
3	The effect of mutated mitochondrial ribosomal proteins S16 and S22 on the assembly of the small and large ribosomal subunits in human mitochondria 2020 ·UNC Libraries ·Emdadul Haque, Chaya Miller, Ann Saada, (unknown), Linda Spremulli	0
4	Mutation in the COX4I1 gene is associated with short stature, poor weight gain and increased chromosomal breaks, simulating Fanconi anemia 2017 ·European Journal of Human Genetics ·Bassam Abu‐Libdeh, Liza Douiev, (unknown), Maher Shahrour, Asaf Ta‐Shma, Chaya Miller, Orly Elpeleg, Ann Saada	40
5	Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy 2014 ·European Journal of Human Genetics ·(unknown), Devorah Soiferman, Ora Schueler‐Furman, Chaya Miller, Avraham Shaag, Orly Elpeleg, Simon Edvardson, Ann Saada	75
6	Human granulosa luteal cell oxidative phosphorylation function is not affected by age or ovarian response 2012 ·Fertility and Sterility ·Yoel Shufaro, (unknown), Einat Aizenman, Chaya Miller, Alex Simon, Neri Laufer, Ann Saada	22
7	The interplay between SUCLA2, SUCLG2, and mitochondrial DNA depletion 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Chaya Miller, Liya Wang, Elsebet Østergaard, Phyllis Dan, Ann Saada	40
8	Combined OXPHOS complex I and IV defect, due to mutated complex I assembly factor C20ORF7 2011 ·Journal of Inherited Metabolic Disease ·Ann Saada, Simon Edvardson, Avraham Shaag, Wendy K. Chung, Reeval Segel, Chaya Miller, Chaim Jalas, Orly Elpeleg	42
9	Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy 2010 ·European Journal of Human Genetics ·P. Smits, Ann Saada, Saskia B. Wortmann, Angelien Heister, (unknown), Rolph Pfundt, Chaya Miller, Dorothea Haas, (unknown), Richard J. Rodenburg, (unknown), (unknown)	77
10	Antibiotic effects on mitochondrial translation and in patients with mitochondrial translational defects 2009 ·Mitochondrion ·(unknown), Chaya Miller, Ariel Tenenbaum, Linda Spremulli, Ann Saada	33
11	The effect of mutated mitochondrial ribosomal proteins S16 and S22 on the assembly of the small and large ribosomal subunits in human mitochondria 2008 ·Mitochondrion ·Md. Emdadul Haque, (unknown), Chaya Miller, Linda Spremulli, Ann Saada	58
12	C6ORF66 Is an Assembly Factor of Mitochondrial Complex I 2008 ·The American Journal of Human Genetics ·Ann Saada, Simon Edvardson, (unknown), Avraham Shaag, (unknown), Chaya Miller, Haya Lorberboum‐Galski, Orly Elpeleg	134
13	Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion 2005 ·The American Journal of Human Genetics ·Orly Elpeleg, Chaya Miller, Eli Hershkovitz, Maria Bitner‐Glindzicz, (unknown), Shamima Rahman, Alistair T. Pagnamenta, (unknown), Ann Saada	241
14	Evaluation of enzymatic assays and compounds affecting ATP production in mitochondrial respiratory chain complex I deficiency 2004 ·Analytical Biochemistry ·Ann Saada, Maskit Bar‐Meir, (unknown), Chaya Miller, Orly Elpeleg	50
15	Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation 2004 ·Annals of Neurology ·Chaya Miller, Ann Saada, (unknown), (unknown), Efrat Ben‐Shalom, Avraham Shaag, Eli Hershkovitz, Orly Elpeleg	175
16	Mitochondrial deoxyribonucleoside triphosphate pools in thymidine kinase 2 deficiency 2003 ·Biochemical and Biophysical Research Communications ·Ann Saada, Efrat Ben‐Shalom, (unknown), Chaya Miller, Hanna Mandel, Orly Elpeleg	39
17	The trithorax Group Gene moira Encodes a Brahma-Associated Putative Chromatin-Remodeling Factor in Drosophila melanogaster 1999 ·Molecular and Cellular Biology ·Madeline A. Crosby, Chaya Miller, Tamir Alon, Kellie L. Watson, C. Peter Verrijzer, (unknown), Naomi B. Zak	109
18	Frameshifting in the expression of the Escherichia coli trpR gene is modulated by translation initiation 1993 ·Journal of Bacteriology ·Itai Benhar, Chaya Miller, Hanna Engelberg–Kulka	6
19	Frameshifting in the expression of the Escherichia coli trpR gene 1992 ·Molecular Microbiology ·Itai Benhar, Chaya Miller, (unknown)	20
20	Studies on the involvement of the UGA readthrough process in the mechanism of attenuation of the tryptophan operon of Escherichia coli 1982 ·Molecular and General Genetics MGG ·Hanna Engelberg–Kulka, Aliza Amiel, Chaya Miller, (unknown)	9

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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