Anat Blumenfeld

3.4k total citations
71 papers, 2.4k citations indexed

About

Anat Blumenfeld is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Anat Blumenfeld has authored 71 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 22 papers in Cell Biology and 20 papers in Cellular and Molecular Neuroscience. Recurrent topics in Anat Blumenfeld's work include Retinal Development and Disorders (18 papers), Hereditary Neurological Disorders (14 papers) and melanin and skin pigmentation (11 papers). Anat Blumenfeld is often cited by papers focused on Retinal Development and Disorders (18 papers), Hereditary Neurological Disorders (14 papers) and melanin and skin pigmentation (11 papers). Anat Blumenfeld collaborates with scholars based in Israel, United States and Germany. Anat Blumenfeld's co-authors include Maria Idelson, James F. Gusella, Felicia B. Axelrod, Channa Maayan, Susan A. Slaugenhaupt, Rivka Dresner Pollak, Christopher B. Liebert, James Mull, Sandra Gill and Maire Leyne and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Anat Blumenfeld

68 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anat Blumenfeld Israel 25 1.2k 692 354 268 262 71 2.4k
Éliane Chouery Lebanon 29 1.7k 1.5× 277 0.4× 205 0.6× 224 0.8× 111 0.4× 130 2.8k
Bernd Wollnik Germany 36 2.8k 2.4× 306 0.4× 304 0.9× 368 1.4× 395 1.5× 138 4.3k
Elizabeth C. Engle United States 39 1.9k 1.6× 631 0.9× 799 2.3× 117 0.4× 74 0.3× 112 4.4k
Annick Toutain France 36 2.5k 2.1× 469 0.7× 343 1.0× 120 0.4× 87 0.3× 138 4.0k
Alar Karis Estonia 24 2.0k 1.7× 479 0.7× 255 0.7× 52 0.2× 318 1.2× 33 3.3k
Shigemi Hayashi United States 11 3.2k 2.7× 460 0.7× 384 1.1× 57 0.2× 73 0.3× 12 4.1k
Rebecca A. Ihrie United States 25 1.5k 1.3× 476 0.7× 200 0.6× 62 0.2× 53 0.2× 54 2.7k
Claude A. Dechesne France 29 1.4k 1.2× 157 0.2× 224 0.6× 63 0.2× 123 0.5× 53 2.2k
Patrick Edery France 33 2.4k 2.1× 304 0.4× 326 0.9× 153 0.6× 175 0.7× 117 4.5k
Maria Grigoriou Greece 16 1.7k 1.4× 1.5k 2.1× 200 0.6× 66 0.2× 42 0.2× 42 3.4k

Countries citing papers authored by Anat Blumenfeld

Since Specialization
Citations

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

Fields of papers citing papers by Anat Blumenfeld

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anat Blumenfeld

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

All Works

20 of 20 papers shown
1.
Markowitz, S, Dekel Shilo, Shaul Beyth, et al.. (2025). Amelogenin Null Mice Develop Osteoarthritis, While Its Application Mitigates Disease Phenotypes in a Rat Model. The FASEB Journal. 39(14). e70838–e70838.
2.
Markowitz, S, et al.. (2023). Regeneration of injured articular cartilage using the recombinant human amelogenin protein. Bone and Joint Research. 12(10). 615–623. 4 indexed citations
3.
Yahalom, Claudia, et al.. (2021). Childhood visual impairment and blindness: 5-year data from a tertiary low vision center in Israel. Eye. 36(10). 2052–2056. 4 indexed citations
4.
Zelinger, Lina, Artur V. Cideciyan, Susanne Kohl, et al.. (2015). Genetics and Disease Expression in the CNGA3 Form of Achromatopsia. Ophthalmology. 122(5). 997–1007. 53 indexed citations
5.
Blumenfeld, Anat, et al.. (2013). Prenatal Molecular Diagnosis of Oculocutaneous Albinism (OCA) in a Large Cohort of Israeli Families. Investigative Ophthalmology & Visual Science. 54(15). 1358–1358.
6.
Yahalom, Claudia, et al.. (2011). Refractive profile in oculocutaneous albinism and its correlation with final visual outcome. British Journal of Ophthalmology. 96(4). 537–539. 42 indexed citations
7.
Rosenmann, Ada, et al.. (2009). Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli families. Prenatal Diagnosis. 29(10). 939–946. 12 indexed citations
8.
Blumenfeld, Anat, Genia Maftzir, Liliana Mizrahi‐Meissonnier, et al.. (2008). Strong Founder Effect in Israeli Oculocutaneous Albinism Type I (OCAI) Populations. Investigative Ophthalmology & Visual Science. 49(13). 1298–1298. 1 indexed citations
9.
Leiser, Yoav, Anat Blumenfeld, Amir Haze, et al.. (2007). Localization, quantification, and characterization of tuftelin in soft tissues. The Anatomical Record. 290(5). 449–454. 22 indexed citations
10.
Anteby, Eyal Y., et al.. (2003). Fetal inherited thrombophilias influence the severity of preeclampsia, IUGR and placental abruption. European Journal of Obstetrics & Gynecology and Reproductive Biology. 113(1). 31–35. 17 indexed citations
11.
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
12.
13.
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
14.
Chadwick, Brian P., James Mull, Sandra Gill, et al.. (1999). Cloning, Mapping, and Expression of Two Novel Actin Genes, Actin-like-7A (ACTL7A) and Actin-like-7B (ACTL7B), from the Familial Dysautonomia Candidate Region on 9q31. Genomics. 58(3). 302–309. 32 indexed citations
15.
Menon, Anil G., Joni L. Rutter, Anat Blumenfeld, et al.. (1997). Frequent loss of chromosome 14 in atypical and malignant meningioma: identification of a putative `tumor progression' locus. Oncogene. 14(5). 611–616. 92 indexed citations
16.
Mitrani‐Rosenbaum, Stella, Zohar Argov, Anat Blumenfeld, Christine E. Seidman, & J G Seidman. (1996). Hereditary Inclusion Body Myopathy Maps to Chromosome 9p1-q1. Human Molecular Genetics. 5(1). 159–163. 84 indexed citations
17.
Davar, Gudarz, Christo Shalish, Anat Blumenfeld, & Xandra O. Breakefield. (1996). Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy Type II. Pain. 67(1). 135–139. 6 indexed citations
18.
Slaugenhaupt, Susan A., Anat Blumenfeld, Christopher B. Liebert, et al.. (1995). The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene. Genomics. 25(3). 730–732. 8 indexed citations
19.
Blumenfeld, Anat, Diane Lucente, James A. Trofatter, et al.. (1995). Peripherin gene is linked to keratin 18 gene on human chromosome 12. Somatic Cell and Molecular Genetics. 21(1). 83–88. 7 indexed citations
20.
Blumenfeld, Anat, Susan Slaugenhaupt, Diane Lucente, et al.. (1993). The gene for familial dysautonomia is linked to chromosome 9 and shows strong linkage disequilibrium with D9S58. The Society for Neuroscience Abstracts. 19. 1463. 7 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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