Maria Idelson

2.5k total citations
15 papers, 1.7k citations indexed

About

Maria Idelson is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Orthopedics and Sports Medicine. According to data from OpenAlex, Maria Idelson has authored 15 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Orthopedics and Sports Medicine. Recurrent topics in Maria Idelson's work include Retinal Development and Disorders (5 papers), Pluripotent Stem Cells Research (4 papers) and CRISPR and Genetic Engineering (3 papers). Maria Idelson is often cited by papers focused on Retinal Development and Disorders (5 papers), Pluripotent Stem Cells Research (4 papers) and CRISPR and Genetic Engineering (3 papers). Maria Idelson collaborates with scholars based in Israel, United States and Australia. Maria Idelson's co-authors include Benjamin Reubinoff, Anat Blumenfeld, Hanita Khaner, Tamir Ben‐Hur, Rivka Dresner Pollak, Etti Reinhartz, Anna Itzik, Martín F. Pera, Alexey Obolensky and Eyal Banin and has published in prestigious journals such as PLoS ONE, Journal of Bacteriology and Cell stem cell.

In The Last Decade

Maria Idelson

15 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maria Idelson Israel	12	1.2k	616	229	132	129	15	1.7k
Stefan A. Hoyng Netherlands	13	765 0.7×	407 0.7×	208 0.9×	134 1.0×	184 1.4×	18	1.4k
Justine D. Miller United States	10	2.5k 2.2×	264 0.4×	151 0.7×	62 0.5×	314 2.4×	14	2.8k
R. Toro Spain	16	894 0.8×	351 0.6×	83 0.4×	175 1.3×	75 0.6×	23	1.6k
Sabine Conrad Germany	24	603 0.5×	615 1.0×	361 1.6×	122 0.9×	57 0.4×	37	1.6k
Marina Scarlato Italy	22	491 0.4×	493 0.8×	191 0.8×	140 1.1×	48 0.4×	43	1.3k
Benjamin Ellezam Canada	18	647 0.6×	734 1.2×	425 1.9×	121 0.9×	39 0.3×	51	1.9k
Mehrdad Khajavi United States	21	1.5k 1.3×	984 1.6×	119 0.5×	219 1.7×	596 4.6×	31	2.6k
Toby A. Ferguson United States	16	382 0.3×	650 1.1×	180 0.8×	228 1.7×	33 0.3×	32	1.2k
Cassandre Labelle‐Dumais United States	17	533 0.5×	223 0.4×	53 0.2×	111 0.8×	253 2.0×	29	1.2k

Countries citing papers authored by Maria Idelson

Since Specialization

Citations

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

Fields of papers citing papers by Maria Idelson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Idelson

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

All Works

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15 of 15 papers shown

David, Ahuvit, Maria Idelson, Yamit Cohen‐Tayar, et al.. (2023). The LHX2-OTX2 transcriptional regulatory module controls retinal pigmented epithelium differentiation and underlies genetic risk for age-related macular degeneration. PLoS Biology. 21(1). e3001924–e3001924. 4 indexed citations

Blinder, Pablo, et al.. (2016). Pax6 role in the regulation of retinal pigmented epithelium maturation. Investigative Ophthalmology & Visual Science. 57(12). 6055–6055. 1 indexed citations

Raviv, S., Kapil Bharti, Sigal Rencus‐Lazar, et al.. (2014). PAX6 Regulates Melanogenesis in the Retinal Pigmented Epithelium through Feed-Forward Regulatory Interactions with MITF. PLoS Genetics. 10(5). e1004360–e1004360. 71 indexed citations

Gropp, Michal, Vitali Shilo, Gilad W. Vainer, et al.. (2012). Standardization of the Teratoma Assay for Analysis of Pluripotency of Human ES Cells and Biosafety of Their Differentiated Progeny. PLoS ONE. 7(9). e45532–e45532. 92 indexed citations

Idelson, Maria, Ruslana Alper, Alexey Obolensky, et al.. (2009). Directed Differentiation of Human Embryonic Stem Cells into Functional Retinal Pigment Epithelium Cells. Cell stem cell. 5(4). 396–408. 346 indexed citations

Banin, Eyal, Alexey Obolensky, Maria Idelson, et al.. (2005). Retinal Incorporation and Differentiation of Neural Precursors Derived from Human Embryonic Stem Cells. Stem Cells. 24(2). 246–257. 140 indexed citations

Ben‐Hur, Tamir, Maria Idelson, Hanita Khaner, et al.. (2004). Transplantation of Human Embryonic Stem Cell–Derived Neural Progenitors Improves Behavioral Deficit in Parkinsonian Rats. Stem Cells. 22(7). 1246–1255. 281 indexed citations

Slaugenhaupt, Susan A., Anat Blumenfeld, Sandra Gill, et al.. (2001). Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia. The American Journal of Human Genetics. 68(3). 598–605. 448 indexed citations

Pollak, Rivka Dresner, et al.. (2001). The <i>BsmI</i> Vitamin D Receptor Gene Polymorphism in Israeli Populations and in Perimenopausal and Osteoporotic Ashkenazi Women. American Journal of Nephrology. 21(3). 185–188. 7 indexed citations

10.

Pollak, Rivka Dresner, et al.. (2000). Ethnic Differences in the Frequency of the C677T Mutation in the Methylenetetrahydrofolate Reductase ( MTHFR ) Gene in Healthy Israeli Populations. Genetic Testing. 4(3). 309–311. 15 indexed citations

11.

Pollak, Rivka Dresner, et al.. (2000). The C677T Mutation in the Methylenetetrahydrofolate Reductase (MTHFR) Gene and Vascular Dementia. Journal of the American Geriatrics Society. 48(6). 664–668. 47 indexed citations

12.

Pollak, Rivka Dresner, Eliezer A. Rachmilewitz, Anat Blumenfeld, Maria Idelson, & Ada Goldfarb. (2000). Bone mineral metabolism in adults with β‐thalassaemia major and intermedia. British Journal of Haematology. 111(3). 902–907. 113 indexed citations

13.

Pollak, Rivka Dresner, Eliezer A. Rachmilewitz, Anat Blumenfeld, Maria Idelson, & Ada Goldfarb. (2000). Bone mineral metabolism in adults with beta-thalassaemia major and intermedia. British Journal of Haematology. 111(3). 902–907. 58 indexed citations

14.

Blumenfeld, Anat, Susan A. Slaugenhaupt, Christopher B. Liebert, et al.. (1999). Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31. The American Journal of Human Genetics. 64(4). 1110–1118. 53 indexed citations

15.

Idelson, Maria & Orna Amster‐Choder. (1998). SacY, a Transcriptional Antiterminator fromBacillus subtilis, Is Regulated by Phosphorylation In Vivo. Journal of Bacteriology. 180(3). 660–666. 28 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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