Conxi Lázaro

17.9k total citations
147 papers, 3.6k citations indexed

About

Conxi Lázaro is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Conxi Lázaro has authored 147 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Genetics, 52 papers in Molecular Biology and 47 papers in Neurology. Recurrent topics in Conxi Lázaro's work include Neurofibromatosis and Schwannoma Cases (47 papers), Genetic factors in colorectal cancer (41 papers) and Cancer Genomics and Diagnostics (36 papers). Conxi Lázaro is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (47 papers), Genetic factors in colorectal cancer (41 papers) and Cancer Genomics and Diagnostics (36 papers). Conxi Lázaro collaborates with scholars based in Spain, United States and Germany. Conxi Lázaro's co-authors include Xavier Estivill, Eduard Serra, Gabriel Capellá, Ignacio Blanco, Antonia Gaona, Marta Pineda, Joan Brunet, Elisabet Ars, H. Kruyer and Anna Ravella and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Conxi Lázaro

142 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Conxi Lázaro Spain	35	1.5k	1.1k	1.0k	838	673	147	3.6k
Ludwine Messiaen United States	39	2.2k 1.5×	2.3k 2.1×	932 0.9×	661 0.8×	397 0.6×	145	5.0k
Masashi Sanada Japan	33	2.2k 1.5×	585 0.5×	733 0.7×	441 0.5×	920 1.4×	118	4.1k
Juan A. Rey Spain	36	2.1k 1.4×	1.1k 1.0×	415 0.4×	258 0.3×	883 1.3×	171	3.9k
Marcus B. Valentine United States	26	1.7k 1.1×	454 0.4×	303 0.3×	932 1.1×	415 0.6×	39	3.6k
Chantal Desmaze France	23	2.6k 1.8×	313 0.3×	489 0.5×	743 0.9×	597 0.9×	43	4.5k
Holger Christiansen Germany	29	1.9k 1.3×	1.9k 1.7×	429 0.4×	157 0.2×	921 1.4×	97	3.4k
Roland P. Kuiper Netherlands	35	2.6k 1.8×	195 0.2×	758 0.7×	1.1k 1.3×	1.1k 1.7×	123	5.4k
Sabine Strehl Austria	31	1.1k 0.8×	348 0.3×	263 0.3×	370 0.4×	251 0.4×	72	2.9k
Nicolas Sévenet France	20	2.3k 1.6×	311 0.3×	271 0.3×	1.1k 1.3×	329 0.5×	51	3.1k
Reiner Siebert Germany	34	1.6k 1.1×	340 0.3×	243 0.2×	1.5k 1.8×	377 0.6×	144	3.3k

Countries citing papers authored by Conxi Lázaro

Since Specialization

Citations

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

Fields of papers citing papers by Conxi Lázaro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Conxi Lázaro

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

Terradas, Mariona, Pilar Mur, Chiara Maria Lavinia Löffler, et al.. (2025). Constitutional epimutations in LTBP4, a component of the TGF-β signaling, and in BRCA1, as potential drivers of early-onset colorectal cancer. Clinical Epigenetics. 17(1). 183–183. 1 indexed citations

Fernández‐Rodríguez, Juana, Yvonne Richaud‐Patín, Ernest Terribas, et al.. (2022). Modeling iPSC-derived human neurofibroma-like tumors in mice uncovers the heterogeneity of Schwann cells within plexiform neurofibromas. Cell Reports. 38(7). 110385–110385. 24 indexed citations

Rodríguez, Anna Duat, Juan Luís Becerra, Sandra Bonache, et al.. (2022). Neurofibromatosis type 1 families with first-degree relatives harbouring distinct NF1 pathogenic variants. Genetic counselling and familial diagnosis: what should be offered?. Journal of Medical Genetics. 59(10). 1017–1023. 7 indexed citations

Fernández‐Rodríguez, Juana, María Martínez‐Iniesta, Rajarshi Guha, et al.. (2022). A High-Throughput Screening Platform Identifies Novel Combination Treatments for Malignant Peripheral Nerve Sheath Tumors. Molecular Cancer Therapeutics. 21(7). 1246–1258. 7 indexed citations

Galván‐Femenía, Iván, Juan Luís Becerra, Isabel Bielsa, et al.. (2021). Revisiting the UK Genetic Severity Score for NF2: a proposal for the addition of a functional genetic component. Journal of Medical Genetics. 59(7). 678–686. 7 indexed citations

Navarro, Matilde, Àlex Teulé, Ares Solanes, et al.. (2021). Correction: Dueñas et al. Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers 2020, 12, 3419. Cancers. 13(13). 3104–3104. 1 indexed citations

Fernández‐Rodríguez, Juana, Ernest Terribas, Cleofé Romagosa, et al.. (2021). Chromosomal translocations inactivating CDKN2A support a single path for malignant peripheral nerve sheath tumor initiation. Human Genetics. 140(8). 1241–1252. 12 indexed citations

Valle, Jesús Del, Elisabeth Castellanos, Lídia Feliubadaló, et al.. (2021). CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools. Bioinformatics. 37(22). 4227–4229. 2 indexed citations

Valle, Jesús Del, Lídia Feliubadaló, Marta Pineda, et al.. (2020). Screening of CNVs using NGS data improves mutation detection yield and decreases costs in genetic testing for hereditary cancer. Journal of Medical Genetics. 59(1). 75–78. 6 indexed citations

10.

Terradas, Mariona, Pilar Mur, Sami Belhadj, et al.. (2020). TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes. Gut. 70(6). 1139–1146. 11 indexed citations

11.

Terribas, Ernest, Marco A. Fernández, Juana Fernández‐Rodríguez, et al.. (2020). KIF11 and KIF15 mitotic kinesins are potential therapeutic vulnerabilities for malignant peripheral nerve sheath tumors. Neuro-Oncology Advances. 2(Supplement_1). i62–i74. 11 indexed citations

12.

Stradella, Agostina, Jesús Del Valle, Paula Rofes, et al.. (2020). ERCC3, a new ovarian cancer susceptibility gene?. European Journal of Cancer. 141. 1–8. 9 indexed citations

13.

Valle, Jesús Del, Elisabeth Castellanos, Lídia Feliubadaló, et al.. (2020). Evaluation of CNV detection tools for NGS panel data in genetic diagnostics. European Journal of Human Genetics. 28(12). 1645–1655. 76 indexed citations

14.

Navarro, Matilde, Àlex Teulé, Ares Solanes, et al.. (2020). Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers. 12(11). 3419–3419. 12 indexed citations

15.

Castellanos, Elisabeth, Bernat Gel, Andreu Alibés, et al.. (2019). Mutational spectrum by phenotype: panel‐based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café‐au‐lait macules. Clinical Genetics. 97(2). 264–275. 12 indexed citations

16.

Mur, Pilar, Ann‐Sofie Jemth, Nuno Amaral, et al.. (2018). Germline variation in the oxidative DNA repair genesNUDT1andOGG1is not associated with hereditary colorectal cancer or polyposis. Human Mutation. 39(9). 1214–1225. 5 indexed citations

17.

Hummel, Trent R., Walter J. Jessen, Shyra J. Miller, et al.. (2010). Gene Expression Analysis Identifies Potential Biomarkers of Neurofibromatosis Type 1 Including Adrenomedullin. Clinical Cancer Research. 16(20). 5048–5057. 37 indexed citations

18.

Laitinen, Tarja, Vesa Ollikainen, Conxi Lázaro, et al.. (2000). Association Study of the Chromosomal Region Containing the FCER2 Gene Suggests It Has a Regulatory Role in Atopic Disorders. American Journal of Respiratory and Critical Care Medicine. 161(3). 700–706. 33 indexed citations

19.

Ruiz, Anna, Susana Puig, Josep Malvehy, et al.. (1999). CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia. Journal of Medical Genetics. 36(6). 490–493. 41 indexed citations

20.

Soriano, Joan B., Guadalupe Ercilla, Jordi Sunyer, et al.. (1997). HLA Class II Genes in Soybean Epidemic Asthma Patients. American Journal of Respiratory and Critical Care Medicine. 156(5). 1394–1398. 26 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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