Gemma Llort

1.8k total citations
32 papers, 638 citations indexed

About

Gemma Llort is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Gemma Llort has authored 32 papers receiving a total of 638 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 16 papers in Molecular Biology and 8 papers in Pathology and Forensic Medicine. Recurrent topics in Gemma Llort's work include BRCA gene mutations in cancer (20 papers), Genetic factors in colorectal cancer (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Gemma Llort is often cited by papers focused on BRCA gene mutations in cancer (20 papers), Genetic factors in colorectal cancer (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Gemma Llort collaborates with scholars based in Spain, United States and Palestinian Territory. Gemma Llort's co-authors include Ignacio Blanco, Teresa Ramón y Cajal, Javier Benı́tez, Trinidad Caldés, Miguel de la Hoya, Àlex Teulé, Joan Brunet, Conxi Lázaro, Ana Osório and Judith Balmañà and has published in prestigious journals such as Journal of Clinical Oncology, The American Journal of Human Genetics and British Journal of Cancer.

In The Last Decade

Gemma Llort

31 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gemma Llort Spain 14 435 314 161 149 144 32 638
Jean‐Pierre Fricker France 11 303 0.7× 252 0.8× 126 0.8× 145 1.0× 99 0.7× 15 576
Josef Herzog United States 11 584 1.3× 309 1.0× 183 1.1× 147 1.0× 104 0.7× 33 724
Helen Byers United Kingdom 14 429 1.0× 183 0.6× 144 0.9× 217 1.5× 71 0.5× 30 651
Susan Manley United States 11 436 1.0× 170 0.5× 223 1.4× 115 0.8× 151 1.0× 15 581
Jacqueline Mersch United States 3 333 0.8× 185 0.6× 148 0.9× 173 1.2× 123 0.9× 9 544
Betsy Bove United States 11 336 0.8× 311 1.0× 109 0.7× 97 0.7× 74 0.5× 14 633
Zoe Kemp United Kingdom 12 316 0.7× 225 0.7× 148 0.9× 258 1.7× 179 1.2× 27 580
Corinne Serruya Canada 5 310 0.7× 218 0.7× 172 1.1× 93 0.6× 94 0.7× 6 520
Anu Chittenden United States 12 328 0.8× 120 0.4× 212 1.3× 174 1.2× 231 1.6× 32 599
Sonia Nanda Canada 7 234 0.5× 190 0.6× 108 0.7× 141 0.9× 53 0.4× 8 426

Countries citing papers authored by Gemma Llort

Since Specialization
Citations

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

Fields of papers citing papers by Gemma Llort

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gemma Llort

This figure shows the co-authorship network connecting the top 25 collaborators of Gemma Llort. A scholar is included among the top collaborators of Gemma Llort 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 Gemma Llort. Gemma Llort 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.
Feliubadaló, Lídia, Jesús Del Valle, Sara González, et al.. (2024). Open-Source Bioinformatic Pipeline to Improve PMS2 Genetic Testing Using Short-Read NGS Data. Journal of Molecular Diagnostics. 26(8). 727–738. 1 indexed citations
2.
Stjepanovic, Neda, Guillermo Villacampa, Kevin T. Nead, et al.. (2020). Association of premenopausal risk-reducing salpingo-oophorectomy with breast cancer risk in BRCA1/2 mutation carriers: Maximising bias-reduction. European Journal of Cancer. 132. 53–60. 12 indexed citations
3.
Aragón, Isabel M., Heather Thorne, Urbano Anido, et al.. (2020). 612MO Clinical impact of somatic alterations in prostate cancer patients with and without previously known germline BRCA1/2 mutations: Results from PROREPAIR-A study. Annals of Oncology. 31. S509–S510. 4 indexed citations
4.
González-Santiago, Santiago, Teresa Ramón y Cajal, Elena Aguirre, et al.. (2019). SEOM clinical guidelines in hereditary breast and ovarian cancer (2019). Clinical & Translational Oncology. 22(2). 193–200. 48 indexed citations
5.
Andrés, Leire, Elena Aguirre, Judith Balmañà, et al.. (2016). Analysis of Lynch Syndrome Mismatch Repair Genes in Women with Endometrial Cancer. Oncology. 91(3). 171–176. 16 indexed citations
6.
Llort, Gemma, Isabel Chirivella, Rafael Morales, et al.. (2015). SEOM clinical guidelines in Hereditary Breast and ovarian cancer. Clinical & Translational Oncology. 17(12). 956–961. 81 indexed citations
7.
Hernán, Imma, Emma Borràs, Miguel Dias, et al.. (2015). Two novel frameshift mutations in BRCA2 gene detected by next generation sequencing in a survey of Spanish patients of breast cancer. Clinical & Translational Oncology. 17(7). 576–580. 3 indexed citations
8.
Ruiz, Anna, Gemma Llort, Neus Baena, et al.. (2014). Genetic Testing in Hereditary Breast and Ovarian Cancer Using Massive Parallel Sequencing. BioMed Research International. 2014. 1–8. 13 indexed citations
9.
Hernán, Imma, Emma Borràs, Miguel Dias, et al.. (2012). Detection of Genomic Variations in BRCA1 and BRCA2 Genes by Long-Range PCR and Next-Generation Sequencing. Journal of Molecular Diagnostics. 14(3). 286–293. 40 indexed citations
10.
Lasa, Adriana, Teresa Ramón y Cajal, Gemma Llort, et al.. (2010). Copy number variations are not modifiers of phenotypic expression in a pair of identical twins carrying a BRCA1 mutation. Breast Cancer Research and Treatment. 123(3). 901–905. 11 indexed citations
11.
Fernández‐Ramires, Ricardo, Gonzalo Goméz-López, Loris De Cecco, et al.. (2010). Transcriptional characteristics of familial non‐BRCA1/BRCA2 breast tumors. International Journal of Cancer. 128(11). 2635–2644. 10 indexed citations
12.
Rosa-Rosa, Juan Manuel, Guillermo Pita, Miguel Urioste, et al.. (2009). Genome-wide Linkage Scan Reveals Three Putative Breast-Cancer-Susceptibility Loci. The American Journal of Human Genetics. 84(2). 115–122. 25 indexed citations
13.
Fernández‐Ramires, Ricardo, Xavier Solé, Loris De Cecco, et al.. (2009). Gene expression profiling integrated into network modelling reveals heterogeneity in the mechanisms of BRCA1 tumorigenesis. British Journal of Cancer. 101(8). 1469–1480. 12 indexed citations
14.
García, María J., María Victoria Fernández, Ana Osório, et al.. (2008). Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families. Breast Cancer Research and Treatment. 113(3). 545–551. 68 indexed citations
15.
Pineda, Marta, Ester Castellsagué, Eva Musulén, et al.. (2008). Non‐Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 gene. Genes Chromosomes and Cancer. 47(4). 326–332. 15 indexed citations
16.
Llort, Gemma, Mercé Peris, & Ignacio Blanco. (2007). Cáncer de mama y ovario hereditario: prevención primaria y secundaria en mujeres portadoras de mutación en los genes BRCA1 y BRCA2. Medicina Clínica. 128(12). 468–476. 4 indexed citations
17.
Gutiérrez‐Enríquez, Sara, Miguel de la Hoya, Cristina Martínez-Bouzas, et al.. (2006). Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer. Breast Cancer Research and Treatment. 103(1). 103–107. 38 indexed citations
18.
Parés, David, Sebastiano Biondo, Ignacio Blanco, et al.. (2006). Estado actual del seguimiento del área gastroduodenal en la poliposis adenomatosa familiar. Gastroenterología y Hepatología. 29(1). 15–21. 2 indexed citations
19.
Blanco, Ignacio, et al.. (2005). Cáncer colorrectal hereditario. Hispana. 2(2). 213–228. 1 indexed citations
20.
Llort, Gemma, et al.. (2002). Low frequency of recurrent BRCA1 and BRCA2 mutations in Spain. Human Mutation. 19(3). 307–307. 36 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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