Anna Dı́az-Font

1.3k total citations
12 papers, 622 citations indexed

About

Anna Dı́az-Font is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Anna Dı́az-Font has authored 12 papers receiving a total of 622 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Physiology and 4 papers in Genetics. Recurrent topics in Anna Dı́az-Font's work include Lysosomal Storage Disorders Research (6 papers), Glycosylation and Glycoproteins Research (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Anna Dı́az-Font is often cited by papers focused on Lysosomal Storage Disorders Research (6 papers), Glycosylation and Glycoproteins Research (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Anna Dı́az-Font collaborates with scholars based in Spain, United Kingdom and United States. Anna Dı́az-Font's co-authors include Philip L. Beales, Erica E. Davis, Nicholas Katsanis, Norann A. Zaghloul, Suzanne Rix, Eyal Banin, Wafaa Eyaid, Carmen C. Leitch, Majid Alfadhel and Hélène Dollfus and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Human Molecular Genetics.

In The Last Decade

Anna Dı́az-Font

12 papers receiving 612 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Dı́az-Font Spain	10	443	398	127	109	45	12	622
Julie S. Trausch‐Azar United States	17	614 1.4×	78 0.2×	109 0.9×	104 1.0×	23 0.5×	20	741
Liza L. Cox Australia	10	292 0.7×	198 0.5×	48 0.4×	56 0.5×	33 0.7×	12	484
Thomas B. Nicholson United States	10	768 1.7×	136 0.3×	31 0.2×	43 0.4×	53 1.2×	14	867
Sarah E. Conduit Australia	11	373 0.8×	306 0.8×	147 1.2×	68 0.6×	32 0.7×	13	536
Elena Schiff United Kingdom	10	300 0.7×	107 0.3×	54 0.4×	57 0.5×	6 0.1×	29	418
Raphael Schiffmann United States	9	299 0.7×	53 0.1×	143 1.1×	261 2.4×	10 0.2×	10	539
Gandham SriLakshmi Bhavani India	13	277 0.6×	304 0.8×	61 0.5×	61 0.6×	10 0.2×	45	542
Athina Ganner Germany	10	806 1.8×	605 1.5×	170 1.3×	19 0.2×	58 1.3×	23	963
Salma Ben‐Salem United Arab Emirates	13	256 0.6×	209 0.5×	37 0.3×	21 0.2×	40 0.9×	26	470
Laura Baker United States	11	281 0.6×	99 0.2×	31 0.2×	16 0.1×	46 1.0×	17	405

Countries citing papers authored by Anna Dı́az-Font

Since Specialization

Citations

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

Fields of papers citing papers by Anna Dı́az-Font

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Dı́az-Font. 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 Anna Dı́az-Font. The network helps show where Anna Dı́az-Font may publish in the future.

Co-authorship network of co-authors of Anna Dı́az-Font

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

All Works

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12 of 12 papers shown

Munye, Mustafa M., Anna Dı́az-Font, Louise Ocaka, et al.. (2017). COLEC10 is mutated in 3MC patients and regulates early craniofacial development. PLoS Genetics. 13(3). e1006679–e1006679. 60 indexed citations

Hernández-Hernández, Víctor, Anna Dı́az-Font, Helen May‐Simera, et al.. (2013). Bardet–Biedl syndrome proteins control the cilia length through regulation of actin polymerization. Human Molecular Genetics. 22(19). 3858–3868. 91 indexed citations

Hernández-Hernández, Víctor, et al.. (2012). Bardet-Biedl syndrome proteins control cilia length through regulation of actin polymerisation. SHILAP Revista de lepidopterología. 1(S1). 1 indexed citations

Held, Swantje, Anna Dı́az-Font, Erica E. Davis, et al.. (2009). Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mapping. Journal of Medical Genetics. 47(4). 262–267. 60 indexed citations

Leitch, Carmen C., Norann A. Zaghloul, Erica E. Davis, et al.. (2008). Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome. Nature Genetics. 40(4). 443–448. 292 indexed citations

Dı́az-Font, Anna, Amparo Chabás, Daniel Grinberg, & Lluı̈sa Vilageliu. (2006). RNAi-mediated inhibition of the glucosylceramide synthase (GCS) gene: A preliminary study towards a therapeutic strategy for Gaucher disease and other glycosphingolipid storage diseases. Blood Cells Molecules and Diseases. 37(3). 197–203. 19 indexed citations

Chabás, Amparo, Laura Gort, Anna Dı́az-Font, et al.. (2005). Perinatal lethal phenotype with generalized ichthyosis in a type 2 Gaucher disease patient with the [L444P;E326K]/P182L genotype: Effect of the E326K change in neonatal and classic forms of the disease. Blood Cells Molecules and Diseases. 35(2). 253–258. 31 indexed citations

Dı́az-Font, Anna, Bru Cormand, Raül Santamaría, et al.. (2005). A mutation within the saposin D domain in a Gaucher disease patient with normal glucocerebrosidase activity. Human Genetics. 117(2-3). 275–277. 32 indexed citations

Dı́az-Font, Anna, Raül Santamaría, Mónica Cozar, et al.. (2005). Clinical and mutational characterization of three patients with multiple sulfatase deficiency: Report of a new splicing mutation. Molecular Genetics and Metabolism. 86(1-2). 206–211. 14 indexed citations

10.

Dı́az-Font, Anna, Bru Cormand, Mariana Blanco, et al.. (2003). Gene rearrangements in the glucocerebrosidase-metaxin region giving rise to disease-causing mutations and polymorphisms. Analysis of 25 RecNciI alleles in Gaucher disease patients. Human Genetics. 112(4). 426–429. 1 indexed citations

11.

Dı́az-Font, Anna, Bru Cormand, Amparo Chabás, Lluı̈sa Vilageliu, & Daniel Grinberg. (2003). Unsuccessful chimeraplast strategy for the correction of a mutation causing Gaucher disease. Blood Cells Molecules and Diseases. 31(2). 183–186. 12 indexed citations

12.

Rodríguez‐Marí, Adriana, Anna Dı́az-Font, Amparo Chabás, et al.. (2001). New Insights into the Origin of the Gaucher Disease-Causing Mutation N370S: Extended Haplotype Analysis Using the 5GC3.2, 5470 G/A, and ITG6.2 Polymorphisms. Blood Cells Molecules and Diseases. 27(5). 950–959. 9 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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