Inés Santisteban

1.5k total citations
38 papers, 1000 citations indexed

About

Inés Santisteban is a scholar working on Molecular Biology, Epidemiology and Immunology. According to data from OpenAlex, Inés Santisteban has authored 38 papers receiving a total of 1000 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 19 papers in Epidemiology and 17 papers in Immunology. Recurrent topics in Inés Santisteban's work include Cytomegalovirus and herpesvirus research (19 papers), Immunodeficiency and Autoimmune Disorders (17 papers) and Virus-based gene therapy research (11 papers). Inés Santisteban is often cited by papers focused on Cytomegalovirus and herpesvirus research (19 papers), Immunodeficiency and Autoimmune Disorders (17 papers) and Virus-based gene therapy research (11 papers). Inés Santisteban collaborates with scholars based in United States, United Kingdom and Türkiye. Inés Santisteban's co-authors include Michael S. Hershfield, Francisco X. Arredondo-Vega, F X Arredondo-Vega, Susan J. Kelly, Sue Povey, Howard M. Lederman, Elizabeth A. Shephard, Ian Phillips, S Kelly and Eva Richard and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Inés Santisteban

37 papers receiving 976 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Inés Santisteban United States	17	378	347	342	314	221	38	1000
N Livni Israel	16	242 0.6×	213 0.6×	54 0.2×	143 0.5×	143 0.6×	42	1.0k
Nobuya Yoshida United States	22	301 0.8×	117 0.3×	964 2.8×	67 0.2×	204 0.9×	38	1.4k
Minh Diem Vu United States	17	261 0.7×	52 0.1×	848 2.5×	93 0.3×	295 1.3×	26	1.4k
Ilana Chefetz United States	19	420 1.1×	184 0.5×	367 1.1×	71 0.2×	163 0.7×	30	1.6k
Anne‐Laure Mathieu France	15	322 0.9×	59 0.2×	444 1.3×	49 0.2×	134 0.6×	39	901
Susan B. Liu United States	9	339 0.9×	48 0.1×	124 0.4×	384 1.2×	138 0.6×	9	971
Lyle E. Pegg United States	11	431 1.1×	103 0.3×	217 0.6×	39 0.1×	162 0.7×	17	873
M Giralt Spain	19	522 1.4×	59 0.2×	198 0.6×	329 1.0×	96 0.4×	50	1.7k
Abdelaziz Gdoura France	8	253 0.7×	28 0.1×	361 1.1×	114 0.4×	178 0.8×	11	740
Justin A. Shyer United States	10	419 1.1×	97 0.3×	814 2.4×	90 0.3×	312 1.4×	16	1.3k

Countries citing papers authored by Inés Santisteban

Since Specialization

Citations

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

Fields of papers citing papers by Inés Santisteban

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inés Santisteban

This figure shows the co-authorship network connecting the top 25 collaborators of Inés Santisteban. A scholar is included among the top collaborators of Inés Santisteban 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 Inés Santisteban. Inés Santisteban 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

Santisteban, Inés, et al.. (2024). Evolving spectrum of adenosine deaminase (ADA) deficiency: Assessing genotype pathogenicity according to expressed ADA activity of 46 variants. Journal of Allergy and Clinical Immunology. 155(1). 166–175.

Çağdaş, Deniz, Pınar Gür Çetinkaya, Betül Karaatmaca, et al.. (2018). ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome. Journal of Clinical Immunology. 38(4). 484–493. 22 indexed citations

Genel, Ferah, et al.. (2015). Adenosine Deaminase-Deficient Severe Combined Immunodeficiency and Diffuse Large B-Cell Lymphoma. Pediatric Allergy Immunology and Pulmonology. 28(2). 138–142. 4 indexed citations

Notarangelo, Lucia Dora, Luisa Imberti, Michael S. Hershfield, et al.. (2015). Diagnosis, Treatment and Long-Term Follow Up of Patients with ADA Deficiency: a Single-Center Experience. Journal of Clinical Immunology. 35(7). 624–637. 17 indexed citations

Moncada‐Vélez, Marcela, A. Catalina Vélez-Ortega, Julio César Orrego, et al.. (2011). Somatic Mosaicism Caused by Monoallelic Reversion of a Mutation in T Cells of a Patient with ADA‐SCID and the Effects of Enzyme Replacement Therapy on the Revertant Phenotype. Scandinavian Journal of Immunology. 74(5). 471–481. 12 indexed citations

Hershfield, Michael S., L. Jackson Roberts, Nancy J. Ganson, et al.. (2010). Treating gout with pegloticase, a PEGylated urate oxidase, provides insight into the importance of uric acid as an antioxidant in vivo. Proceedings of the National Academy of Sciences. 107(32). 14351–14356. 104 indexed citations

Aytekin, Caner, Figen Doğu, Gönül Tanır, et al.. (2009). Purine nucleoside phosphorylase deficiency with fatal course in two sisters. European Journal of Pediatrics. 169(3). 311–314. 14 indexed citations

Artaç, Hasibe, Şefika Elmas Bozdemir, Hatice Toy, et al.. (2009). Late-onset adenosine deaminase deficiency presenting with Heck’s disease. European Journal of Pediatrics. 169(8). 1033–1036. 13 indexed citations

Santisteban, Inés, et al.. (2003). E. coli Expression System for Identifying Folding Mutations of Human Adenosine Deaminase. Humana Press eBooks. 232. 175–182. 1 indexed citations

10.

Richard, Eva, Francisco X. Arredondo-Vega, Inés Santisteban, et al.. (2000). The Binding Site of Human Adenosine Deaminase for Cd26/Dipeptidyl Peptidase IV. The Journal of Experimental Medicine. 192(9). 1223–1236. 54 indexed citations

11.

Arredondo-Vega, Francisco X., et al.. (1998). Adenosine Deaminase Deficiency: Genotype-Phenotype Correlations Based on Expressed Activity of 29 Mutant Alleles. The American Journal of Human Genetics. 63(4). 1049–1059. 83 indexed citations

12.

Bollinger, Mary E., Francisco X. Arredondo-Vega, Inés Santisteban, et al.. (1996). Hepatic Dysfunction as a Complication of Adenosine Deaminase Deficiency. New England Journal of Medicine. 334(21). 1367–1372. 77 indexed citations

13.

Santisteban, Inés, F X Arredondo-Vega, S Kelly, et al.. (1995). Three new adenosine deaminase mutations that define a splicing enhancer and cause severe and partial phenotypes: implications for evolution of a CpG hotspot and expression of a transduced ADA cDNA. Human Molecular Genetics. 4(11). 2081–2087. 45 indexed citations

14.

Arredondo-Vega, F X, et al.. (1994). Correct splicing despite mutation of the invariant first nucleotide of a 5' splice site: a possible basis for disparate clinical phenotypes in siblings with adenosine deaminase deficiency.. PubMed. 54(5). 820–30. 36 indexed citations

15.

Arredondo-Vega, F X, et al.. (1990). Paradoxical expression of adenosine deaminase in T cells cultured from a patient with adenosine deaminase deficiency and combine immunodeficiency.. Journal of Clinical Investigation. 86(2). 444–452. 27 indexed citations

16.

Shephard, Elizabeth A., Ian Phillips, Inés Santisteban, et al.. (1989). Isolation of a human cytochrome P‐450 reductase cDNA clone and localization of the corresponding gene to chromosome 7q11.2. Annals of Human Genetics. 53(4). 291–301. 32 indexed citations

17.

Bull, Peter C., et al.. (1989). Isolation and characterization of genes coding for cytochrome b5 and cytochrome- b5 reductase. Biochemical Society Transactions. 17(1). 194–195. 6 indexed citations

18.

Santisteban, Inés, Sue Povey, Elizabeth A. Shephard, & Ian Phillips. (1988). The major phenobarbital‐inducible cytochrome P‐450 gene subfamily (P450IIB) mapped to the long arm of human chromosome 19. Annals of Human Genetics. 52(2). 129–135. 24 indexed citations

19.

Bull, Peter C., Elizabeth A. Shephard, Sue Povey, Inés Santisteban, & Ian Phillips. (1988). Cloning and chromosomal mapping of human cytochrome b₅ reductase (DIA1). Annals of Human Genetics. 52(4). 263–268. 16 indexed citations

20.

Santisteban, Inés, Sue Povey, L. F. WEST, J M Parrington, & D. A. HOPKINSON. (1985). Chromosome assignment, biochemical and immunological studies on a human aldehyde dehydrogenase, ALDH3. Annals of Human Genetics. 49(2). 87–100. 47 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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