Sara Benito‐Sanz

1.0k total citations
22 papers, 637 citations indexed

About

Sara Benito‐Sanz is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Sara Benito‐Sanz has authored 22 papers receiving a total of 637 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 18 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Sara Benito‐Sanz's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Genomics and Chromatin Dynamics (9 papers) and Ubiquitin and proteasome pathways (4 papers). Sara Benito‐Sanz is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers), Genomics and Chromatin Dynamics (9 papers) and Ubiquitin and proteasome pathways (4 papers). Sara Benito‐Sanz collaborates with scholars based in Spain, United States and United Kingdom. Sara Benito‐Sanz's co-authors include Karen E. Heath, Ángel Campos‐Barros, Miriam Aza‐Carmona, Jesús Argente, Darya Gorbenko del Blanco, Alfonso Hisado-Oliva, Eva Barroso, Pablo Lapunzina, Ricardo Gracía and Valérie Cormier‐Daire and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Sara Benito‐Sanz

22 papers receiving 629 citations

Peers

Countries citing papers authored by Sara Benito‐Sanz

Since Specialization

Citations

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

Fields of papers citing papers by Sara Benito‐Sanz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sara Benito‐Sanz. 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 Sara Benito‐Sanz. The network helps show where Sara Benito‐Sanz may publish in the future.

Co-authorship network of co-authors of Sara Benito‐Sanz

This figure shows the co-authorship network connecting the top 25 collaborators of Sara Benito‐Sanz. A scholar is included among the top collaborators of Sara Benito‐Sanz 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 Sara Benito‐Sanz. Sara Benito‐Sanz 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

#	Work	Indexed citations
1	Novel variant in HHAT as a cause of different sex development with partial gonadal dysgenesis associated with microcephaly, eye defects, and distal phalangeal hypoplasia of both thumbs: Case report 2022 ·Frontiers in Endocrinology ·(unknown), (unknown), Mónica Fernández‐Cancio, Sara Benito‐Sanz, (unknown), Teresa Moliné, María Clemente, Núria Camats, (unknown)	5
2	Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR : Expanding the PORD Phenotype 2020 ·The Journal of Clinical Endocrinology & Metabolism ·Shaheena Parween, Mónica Fernández‐Cancio, Sara Benito‐Sanz, Núria Camats, (unknown), (unknown), Sameer S. Udhane, Norio Kagawa, Christa E. Flück, Laura Audı́, Amit V. Pandey	13
3	A Novel Homozygous <b><i>AMRH2</i></b> Gene Mutation in a Patient with Persistent Müllerian Duct Syndrome 2019 ·Sexual Development ·Mónica Fernández‐Cancio, (unknown), (unknown), Praveen V. Pavithran, (unknown), Núria Camats, Laura Audí, Sara Benito‐Sanz	8
4	Heterozygous aggrecan variants are associated with short stature and brachydactyly: Description of 16 probands and a review of the literature 2018 ·Clinical Endocrinology ·Lucia Sentchordi, Miriam Aza‐Carmona, Sara Benito‐Sanz, (unknown), (unknown), Pablo Prieto‐Matos, (unknown), Alfonso M. Lechuga‐Sancho, Atilano Carcavilla, (unknown), Gabriel Ángel Martos‐Moreno, Ángela del Pozo, Elena Vallespín, Amaka C Offiah, Manuel Parrón, Isabel Dinis, Sérgio B. Sousa, (unknown), I. González Casado, Karen E. Heath	35
5	Identification of a limb enhancer that is removed by pathogenic deletions downstream of the SHOX gene 2018 ·Scientific Reports ·(unknown), Sara Benito‐Sanz, Jessica M. Rosin, Brent E. Bobick, Karen E. Heath, John Cobb	13
6	Mutations in C-natriuretic peptide (NPPC): a novel cause of autosomal dominant short stature 2017 ·Genetics in Medicine ·Alfonso Hisado-Oliva, (unknown), Lucia Sentchordi, Mariana F.A. Funari, (unknown), (unknown), (unknown), (unknown), Antônio Marcondes Lerário, Sara Benito‐Sanz, Miriam Aza‐Carmona, Ángel Campos‐Barros, Alexander A.L. Jorge, Karen E. Heath	50
7	Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot region 2016 ·Journal of Human Genetics ·Sara Benito‐Sanz, (unknown), Miriam Aza‐Carmona, Carolina de la Torre, Céline Huber, I. González Casado, Judith L. Ross, N. Simon Thomas, Andrew R. Zinn, Valérie Cormier‐Daire, Karen E. Heath	9
8	Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape 2015 ·Scientific Reports ·Hannah Verdin, Ana Fernández‐Miñán, Sara Benito‐Sanz, Sandra Janssens, Bert Callewaert, Kathleen De Waele, Jean De Schepper, Inge François, Björn Menten, Karen E. Heath, José Luis Gómez-Skármeta, Elfride De Baere	19
9	HeterozygousNPR2Mutations Cause Disproportionate Short Stature, Similar to Léri-Weill Dyschondrosteosis 2015 ·The Journal of Clinical Endocrinology & Metabolism ·Alfonso Hisado-Oliva, (unknown), (unknown), (unknown), (unknown), Gabriela A. Vasques, (unknown), (unknown), (unknown), I. González Casado, Sara Benito‐Sanz, Alexander A.L. Jorge, Ángel Campos‐Barros, Karen E. Heath	51
10	Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants 2014 ·European Journal of Human Genetics ·Beatriz Paumard‐Hernández, (unknown), Eva Barroso, (unknown), (unknown), Sara Benito‐Sanz, (unknown), Fernando Santos, (unknown), A. Romance, (unknown), Vanesa López‐González, Ángel Campos‐Barros, Jaime Cruz‐Rojo, Encarna Guillén‐Navarro, Jaime Sánchez del Pozo, Pablo Lapunzina, Sixto García‐Miñáur, Karen E. Heath	41
11	NPPB and ACAN, Two Novel SHOX2 Transcription Targets Implicated in Skeletal Development 2014 ·PLoS ONE ·Miriam Aza‐Carmona, (unknown), Alfonso Hisado-Oliva, (unknown), Darya Gorbenko del Blanco, José Ignacio Rodrı́guez, Sara Benito‐Sanz, Ángel Campos‐Barros, Karen E. Heath	15
12	Identification of the first recurrent PAR1 deletion in Léri-Weill dyschondrosteosis and idiopathic short stature reveals the presence of a novel SHOX enhancer 2012 ·Journal of Medical Genetics ·Sara Benito‐Sanz, José Luís Royo, Eva Barroso, Beatriz Paumard‐Hernández, (unknown), Pengfei Liu, Ricardo Gracía, James R. Lupski, Ángel Campos‐Barros, José Luis Gómez-Skármeta, Karen E. Heath	55
13	Clinical utility gene card for: Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD) 2012 ·European Journal of Human Genetics ·Juliette Albuisson, Sébastien Schmitt, S. Baron, Stéphane Bezieau, Sara Benito‐Sanz, Karen E. Heath	9
14	Identification of a Gypsy SHOX mutation (p.A170P) in Léri-Weill dyschondrosteosis and Langer mesomelic dysplasia 2011 ·European Journal of Human Genetics ·(unknown), Miriam Aza‐Carmona, Eva Barroso, Damián Heine‐Suñer, Dimitar N. Azmanov, Jordi Rosell, Begoña Ezquieta, (unknown), (unknown), Jaime Cruz‐Rojo, Fernando Santos, José Ignacio Rodrı́guez, (unknown), Jesús Argente, Luba Kalaydjieva, Ricardo Gracía, Ángel Campos‐Barros, Sara Benito‐Sanz, Karen E. Heath	8
15	SHOX interacts with the chondrogenic transcription factors SOX5 and SOX6 to activate the aggrecan enhancer 2011 ·Human Molecular Genetics ·Miriam Aza‐Carmona, Deborah Shears, Patricia Yuste‐Checa, (unknown), Alfonso Hisado-Oliva, (unknown), Sara Benito‐Sanz, José Ignacio Rodrı́guez, Jesús Argente, Ángel Campos‐Barros, Peter Scambler, Karen E. Heath	43
16	Identification of the first PAR1 deletion encompassing upstream SHOX enhancers in a family with idiopathic short stature 2011 ·European Journal of Human Genetics ·Sara Benito‐Sanz, Miriam Aza‐Carmona, (unknown), (unknown), Ricardo Gracía, Ángel Campos‐Barros, Karen E. Heath	39
17	Identification of the first de novo PAR1 deletion downstream of SHOX in an individual diagnosed with Léri–Weill dyschondrosteosis (LWD) 2010 ·European Journal of Medical Genetics ·Eva Barroso, Sara Benito‐Sanz, (unknown), Patricia Yuste‐Checa, Ricardo Gracía, (unknown), Ángel Campos‐Barros, Karen E. Heath	6
18	Compound heterozygosity of SHOX‐encompassing and downstream PAR1 deletions results in Langer mesomelic dysplasia (LMD) 2007 ·American Journal of Medical Genetics Part A ·Ángel Campos‐Barros, Sara Benito‐Sanz, Judith L. Ross, Andrew R. Zinn, Karen E. Heath	15
19	PAR1 deletions downstream ofSHOX are the most frequent defect in a Spanish cohort of Léri-Weill dyschondrosteosis (LWD) probands 2006 ·Human Mutation ·Sara Benito‐Sanz, Darya Gorbenko del Blanco, Miriam Aza‐Carmona, (unknown), Pablo Lapunzina, Jesús Argente, Ángel Campos‐Barros, Karen E. Heath	44
20	A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis 2005 ·The American Journal of Human Genetics ·Sara Benito‐Sanz, N. Simon Thomas, Céline Huber, Darya Gorbenko del Blanco, Miriam Aza‐Carmona, John A. Crolla, V.K. Maloney, Jesús Argente, Ángel Campos‐Barros, Valérie Cormier‐Daire, Karen E. Heath	96

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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