Elena Beristain

512 citations

18 papers · 284 indexed · h-index 11

Co-authors: María‐Isabel Tejada Cristina Martínez-Bouzas Berta Ibáñez Miguel Mínguez Arantza Sanz-Parra Manel Poch Guiomar Pérez de Nanclares Feliciano J. Ramos
Topics: Genetics and Neurodevelopmental Disorders (6 papers)Genomic variations and chromosomal abnormalities (6 papers)Cancer Genomics and Diagnostics (5 papers)
Cited by: Genetics Cognitive Neuroscience Developmental Biology
Journals: The Journal of Clinical Endocrinology & Metabolism Cancer Letters RNA
Partner nations: Spain United States Argentina

In The Last Decade

Elena Beristain

18 papers receiving 278 citations

Peers

Countries citing papers authored by Elena Beristain

Since Specialization

Citations

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

Fields of papers citing papers by Elena Beristain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Beristain

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	m6A levels and expression of its modification genes show significant differences in breast cancer molecular subtypes 2022 ·Genes & Diseases ·(unknown),Felix Olasagasti,Elena Beristain,(unknown),(unknown),(unknown),Marian M. de Pancorbo	1
2	In silico identification and in vitro expression analysis of breast cancer-related m⁶A-SNPs 2022 ·Epigenetics ·(unknown),Felix Olasagasti,(unknown),Elena Beristain,(unknown),(unknown),(unknown),Marian M. de Pancorbo	2
3	Germline c.1A>C heterozygous pathogenic variant in SDHA reported for the first time in a young adult with a gastric gastrointestinal stromal tumour (GIST): a case report 2019 ·Hereditary Cancer in Clinical Practice ·(unknown),Elena Beristain,(unknown),(unknown),María Pilar Rivero Gracia,(unknown),Guillermo López-Vivanco	4
4	Molecular and Clinical Characterization of a Novel Nonsense Variant in Exon 1 of the UPF3B Gene Found in a Large Spanish Basque Family (MRX82) 2019 ·Frontiers in Genetics ·María‐Isabel Tejada,Olatz Villate,(unknown),Ana B. de la Hoz,Cristina Martínez-Bouzas,Elena Beristain,Francisco Martı́nez,Michael J. Friez,Beatriz Sobrino,Francisco Barros	14
5	Luminal B breast cancer subtype displays a dicotomic epigenetic pattern 2016 ·SpringerPlus ·Naiara G. Bediaga,Elena Beristain,Borja Calvo,(unknown),(unknown),Ricardo Rezola,(unknown),Isabel Guerra,Marian M. de Pancorbo	13
6	Brachydactyly E: isolated or as a feature of a syndrome 2013 ·Orphanet Journal of Rare Diseases ·Arrate Pereda,Intza Garin,María García‐Barcina,Blanca Gener,Elena Beristain,(unknown),Guiomar Pérez de Nanclares	31
7	Disomy as the Genetic Underlying Mechanisms of Loss of Heterozigosity in SDHD-Paragangliomas 2013 ·The Journal of Clinical Endocrinology & Metabolism ·Elena Beristain,(unknown),Isabel Guerra,(unknown),Intza Garin,Guiomar Pérez de Nanclares	3
8	Breast and ovarian cancer risk evaluation in families with a disease-causing mutation in BRCA1/2 2010 ·Journal of Community Genetics ·Elena Beristain,Berta Ibáñez,Itziar Vergara,Cristina Martínez-Bouzas,Isabel Guerra,María‐Isabel Tejada	3
9	A study on MSH2 and MLH1 mutations in hereditary nonpolyposis colorectal cancer families from the Basque Country, describing four new germline mutations 2009 ·Familial Cancer ·Cristina Martínez-Bouzas,Elena Beristain,E Ojembarrena,José Errasti,(unknown),(unknown),María‐Isabel Tejada	4
10	BRCA1 5272‐1G>A and BRCA2 5374delTATG are founder mutations of high relevance for genetic counselling in breast/ovarian cancer families of Spanish origin 2009 ·Clinical Genetics ·Mar Infante,M. Durán,Alberto Acedo,Lucía Pérez‐Cabornero,David J. Sanz,Miguel A. García-González,Elena Beristain,Eva Esteban‐Cardeñosa,Miguel de la Hoya,Àlex Teulé,Ana Vega,María‐Isabel Tejada,(unknown),Cristina Miner,(unknown)	13
11	Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome 2008 ·Menopause The Journal of The North American Menopause Society ·María‐Isabel Tejada,(unknown),Amaia Bilbao,Cristina Martínez-Bouzas,Elena Beristain,(unknown),María A. Ramos-Arroyo,(unknown),(unknown),(unknown),Feliciano J. Ramos	45
12	Risk of cognitive impairment in female premutation carriers of fragile X premutation: Analysis by means of robust segmented linear regression models 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown),Berta Ibáñez,(unknown),Feliciano J. Ramos,(unknown),(unknown),(unknown),(unknown),Ángel Alonso,Cristina Martínez-Bouzas,Elena Beristain,María‐Isabel Tejada	16
13	Analysis of FMR1 gene expression in female premutation carriers using robust segmented linear regression models 2007 ·RNA ·(unknown),Berta Ibáñez,Miguel Mínguez,Manel Poch,(unknown),Arantza Sanz-Parra,Cristina Martínez-Bouzas,Elena Beristain,María‐Isabel Tejada	42
14	High proportion of large genomic rearrangements in hMSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families of the Basque Country 2007 ·Cancer Letters ·Cristina Martínez-Bouzas,E Ojembarrena,Elena Beristain,(unknown),(unknown),María‐Isabel Tejada	14
15	Differences in the frequency and distribution of BRCA1 and BRCA2 mutations in breast/ovarian cancer cases from the Basque country with respect to the Spanish population: implications for genetic counselling 2007 ·Breast Cancer Research and Treatment ·Elena Beristain,Cristina Martínez-Bouzas,Iván Guerra,(unknown),(unknown),Elena Ibáñez,(unknown),Fernándo Rodríguez,(unknown),S. Luján,(unknown),(unknown),Juan Mendizabal‐Zubiaga,María‐Isabel Tejada	25
16	Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer 2006 ·Breast Cancer Research and Treatment ·Sara Gutiérrez‐Enríquez,Miguel de la Hoya,Cristina Martínez-Bouzas,(unknown),Teresa Ramón y Cajal,Gemma Llort,Ignacio Blanco,Elena Beristain,Eduardo Díaz‐Rubio,Carmen Alonso,María‐Isabel Tejada,Trinidad Caldés,Orland Dı́ez	38
17	Screening for MECP2 mutations in Spanish patients with an unexplained mental retardation 2006 ·Clinical Genetics ·María‐Isabel Tejada,Olga Peñagarikano,Laia Rodríguez‐Revenga,Cristina Martínez-Bouzas,Begoña García,Célia Bádenas,Míriam Guitart,Miguel Mínguez,(unknown),Arantza Sanz-Parra,Elena Beristain,Montserrat Milà	14
18	Gene symbol: MECP2. Disease: Rett syndrome (atypical). 2005 ·PubMed ·Olga Peñagarikano,Cristina Martínez-Bouzas,(unknown),Arantza Sanz-Parra,(unknown),Elena Beristain,María‐Isabel Tejada	2

About Elena Beristain

Elena Beristain is a scholar working on Cancer Research, Genetics and Gastroenterology, having authored 18 papers that have together received 284 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Cancer Genomics and Diagnostics (5 papers). The work is most often cited by research in Genetics (220 citations), Cognitive Neuroscience (77 citations) and Developmental Biology (7 citations). Elena Beristain has collaborated with scholars based in Spain, United States and Argentina. Frequent co-authors include María‐Isabel Tejada, Cristina Martínez-Bouzas, Berta Ibáñez, Miguel Mínguez, Arantza Sanz-Parra, Manel Poch, Guiomar Pérez de Nanclares, Feliciano J. Ramos, Intza Garin and María García‐Barcina. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Cancer Letters and RNA.

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