I. López

586 total citations
23 papers, 336 citations indexed

About

I. López is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, I. López has authored 23 papers receiving a total of 336 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in I. López's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (4 papers). I. López is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (4 papers). I. López collaborates with scholars based in Spain, Canada and United States. I. López's co-authors include G. Glóver, Pablo Carbonell, Ági K. Gedeon, Danuta Z. Loesch, David Hay, Encarna Guillén‐Navarro, John C. Mulley, Shuancang Yu, Andrew J. Donnelly and Robert K. Koenekoop and has published in prestigious journals such as Scientific Reports, Gene and Investigative Ophthalmology & Visual Science.

In The Last Decade

I. López

21 papers receiving 332 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
I. López Spain	10	207	202	57	39	30	23	336
Raffaella Stallone Italy	9	147 0.7×	110 0.5×	32 0.6×	20 0.5×	7 0.2×	16	312
D Robinson United Kingdom	10	410 2.0×	269 1.3×	95 1.7×	28 0.7×	10 0.3×	14	534
Claudine Fear United Kingdom	10	229 1.1×	147 0.7×	74 1.3×	16 0.4×	6 0.2×	16	312
Martha Schatz United States	6	91 0.4×	56 0.3×	29 0.5×	20 0.5×	16 0.5×	8	236
Olaya Villa Spain	9	237 1.1×	150 0.7×	126 2.2×	49 1.3×	10 0.3×	17	336
Emma McCann United Kingdom	6	177 0.9×	153 0.8×	80 1.4×	14 0.4×	18 0.6×	10	315
Sheila Margolis United States	10	105 0.5×	195 1.0×	36 0.6×	50 1.3×	48 1.6×	14	363
Atsushi Ieshima Japan	11	205 1.0×	153 0.8×	66 1.2×	26 0.7×	37 1.2×	29	393
Sarah Dugan United States	7	132 0.6×	127 0.6×	21 0.4×	29 0.7×	11 0.4×	14	272
Isabella Borg Malta	10	133 0.6×	102 0.5×	16 0.3×	35 0.9×	25 0.8×	20	315

Countries citing papers authored by I. López

Since Specialization

Citations

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

Fields of papers citing papers by I. López

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. López

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

López, I., et al.. (2018). A complete, homozygous CRX deletion causing nullizygosity is a new genetic mechanism for Leber congenital amaurosis. Scientific Reports. 8(1). 5034–5034. 24 indexed citations

Suela, Javier, I. López, Lluı́s Armengol, et al.. (2017). Recomendaciones para el uso de microarrays en el diagnóstico prenatal. Medicina Clínica. 148(7). 328.e1–328.e8. 9 indexed citations

Silva, Ma Victoria de Rojas, et al.. (2014). Keratometric index in keratoconic eyes before and after intracorneal ring segment implantation. 5(1). 9–13.

Coussa, Razek Georges, Edgar A. Otto, Heon Yung Gee, et al.. (2013). WDR19 : An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior‐Loken syndrome. Clinical Genetics. 84(2). 150–159. 49 indexed citations

Silva, Ma Victoria de Rojas, et al.. (2012). Anterior segment optical coherence tomography in corneal and conjunctival pathology. 3(4). 177–192. 1 indexed citations

Vílchez, Juan Ignacio, et al.. (2012). Performance Evaluation of Biochemical and Ultrasound Markers for the Screening of Chromosomal Numerical Abnormalities in the First Trimester of Pregnancy. Clinical Laboratory. 59(01+02/2013). 45–50. 1 indexed citations

Sánchez-Ferrer, María Luisa, et al.. (2012). Management of a Dichorionic Twin Pregnancy with a Normal Fetus and an Androgenetic Diploid Complete Hydatidiform Mole. Fetal Diagnosis and Therapy. 33(3). 194–200. 7 indexed citations

Moya‐Quiles, María Rosa, et al.. (2012). Rapp–Hodgkin syndrome and SHFM1 patients: Delineating the p63–Dlx5/Dlx6 pathway. Gene. 497(2). 292–297. 14 indexed citations

López, I.. (2011). (Re)composición del cuerpo/texto en "Diario del dolor". Dialnet (Universidad de la Rioja). 44(44). 233–253.

10.

Sánchez-Ferrer, María Luisa, et al.. (2009). Partial Mole with a Diploid Fetus: Case Study and Literature Review. Fetal Diagnosis and Therapy. 25(3). 354–358. 11 indexed citations

11.

Ebermann, Inga, Martin H. J. Wiesen, Eberhart Zrenner, et al.. (2009). GPR98 mutations cause Usher syndrome type 2 in males. Journal of Medical Genetics. 46(4). 277–280. 28 indexed citations

12.

López, I., et al.. (2006). Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects. Prenatal Diagnosis. 26(6). 577–580. 32 indexed citations

13.

López, I., et al.. (2006). Duplication 19q13-qter and deletion 19p13-pter arising from an inversion (19)(p13.3q13.3) of maternal origin. European Journal of Medical Genetics. 49(6). 511–515. 4 indexed citations

14.

López, I., Gerald A. Fishman, Julie Racine, et al.. (2005). The Phenotypes of Patients and Heterozygous Carriers With RDH12 Mutations Are Different From Those With RPE65 Mutations. Investigative Ophthalmology & Visual Science. 46(13). 528–528. 1 indexed citations

15.

López, I., et al.. (2004). RPGRIP1 mutations in juvenile retinitis pigmentosa: a linkage and mutation study.. Investigative Ophthalmology & Visual Science. 45(13). 4727–4727. 1 indexed citations

16.

López, I., et al.. (2000). Phylogenetic Comparison of the DEN-2 Mexican Isolate with Other Flaviviruses. Intervirology. 43(1). 48–54. 7 indexed citations

17.

Carbonell, Pablo, et al.. (1996). FRAXE mutation analysis in three spanish families. American Journal of Medical Genetics. 64(2). 434–440. 20 indexed citations

18.

Romero, M. Carolina, et al.. (1996). De novo interstitial tandem duplication of chromosome 4(q21-q28). American Journal of Medical Genetics. 62(3). 297–299. 16 indexed citations

19.

López, I., et al.. (1992). Fragile X screening program in a spanish region. American Journal of Medical Genetics. 43(1-2). 333–338. 8 indexed citations

20.

Glóver, G., et al.. (1988). Partial monosomy 6q(q15q21) by de novo interstitial deletion. Clinical Genetics. 33(4). 308–310. 15 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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