Silvia Parajes

915 total citations
20 papers, 641 citations indexed

About

Silvia Parajes is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Silvia Parajes has authored 20 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Endocrinology, Diabetes and Metabolism and 8 papers in Genetics. Recurrent topics in Silvia Parajes's work include Sexual Differentiation and Disorders (13 papers), Hormonal and reproductive studies (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Silvia Parajes is often cited by papers focused on Sexual Differentiation and Disorders (13 papers), Hormonal and reproductive studies (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Silvia Parajes collaborates with scholars based in United Kingdom, Spain and Germany. Silvia Parajes's co-authors include Nils Krone, Fernando Domı́nguez, Lourdes Loidi, Wiebke Arlt, Celsa Quinteiro, Ian T. Rose, Angela E. Taylor, Vivek Dhir, C. Souto and Ramón Martı́nez-Pacheco and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Endocrinology.

In The Last Decade

Silvia Parajes

20 papers receiving 630 citations

Peers

Countries citing papers authored by Silvia Parajes

Since Specialization

Citations

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

Fields of papers citing papers by Silvia Parajes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Parajes

This figure shows the co-authorship network connecting the top 25 collaborators of Silvia Parajes. A scholar is included among the top collaborators of Silvia Parajes 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 Silvia Parajes. Silvia Parajes 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	Characterization of the molecular genetic pathology in patients with 11β‐hydroxylase deficiency 2015 ·Clinical Endocrinology ·Christiaan F. Mooij, Silvia Parajes, Ian T. Rose, Angela E. Taylor, Taner Bayraktaroğlu, John Wass, John Connell, David Ray, Wiebke Arlt, Nils Krone	17
2	5α-Reductase Type 2 Regulates Glucocorticoid Action and Metabolic Phenotype in Human Hepatocytes 2015 ·Endocrinology ·Maryam Nasiri, Nikolaos Nikolaou, Silvia Parajes, Nils Krone, George Valsamakis, George Mastorakos, Beverly Hughes, Angela E. Taylor, Iwona Bujalska, Laura Gathercole, Jeremy Tomlinson	38
3	Ferredoxin 1b (Fdx1b) Is the Essential Mitochondrial Redox Partner for Cortisol Biosynthesis in Zebrafish 2015 ·Endocrinology ·Aliesha Griffin, Silvia Parajes, Meltem Weger, Andreas Zaucker, Angela E. Taylor, Donna O’Neil, Ferenc Müller, Nils Krone	31
4	Influence of 17-Hydroxyprogesterone, Progesterone and Sex Steroids on Mineralocorticoid Receptor Transactivation in Congenital Adrenal Hyperplasia 2015 ·Hormone Research in Paediatrics ·Christiaan F. Mooij, Silvia Parajes, (unknown), Wiebke Arlt, Nils Krone, Hedi L. Claahsen‐van der Grinten	18
5	Low estriol levels in the maternal marker screen as a predictor of X-linked adrenal hypoplasia congenita: Case report 2014 ·Srpski arhiv za celokupno lekarstvo ·(unknown), Tatjana Milenković, Nils Krone, Silvia Parajes, (unknown)	6
6	A Diagnosis Not to Be Missed: Nonclassic Steroid 11β-Hydroxylase Deficiency Presenting With Premature Adrenarche and Hirsutism 2013 ·The Journal of Clinical Endocrinology & Metabolism ·Nicole Reisch, Wolfgang Högler, Silvia Parajes, Ian T. Rose, Vivek Dhir, (unknown), Wiebke Arlt, Nils Krone	44
7	The zebrafish ferredoxin orthologue Fdx1b is essential for the redox regulation of interrenal steroidogenesis in larvae and adult fish 2013 ·Endocrine Abstracts ·Aliesha Griffin, Silvia Parajes, (unknown), Cedric Shackleton, (unknown), Nils Krone	1
8	Redefining the Initiation and Maintenance of Zebrafish Interrenal Steroidogenesis by Characterizing the Key Enzyme Cyp11a2 2013 ·Endocrinology ·Silvia Parajes, Aliesha Griffin, Angela E. Taylor, Ian T. Rose, Irene Miguel-Escalada, Yavor Hadzhiev, Wiebke Arlt, Cedric Shackleton, Ferenc Müller, Nils Krone	37
9	Genotype-Phenotype Correlation in 153 Adult Patients With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Analysis of the United Kingdom Congenital Adrenal Hyperplasia Adult Study Executive (CaHASE) Cohort 2013 ·The Journal of Clinical Endocrinology & Metabolism ·Nils Krone, Ian T. Rose, Debbie Willis, James Hodson, Sarah H. Wild, (unknown), Stefanie Hahner, Silvia Parajes, Roland H. Stimson, Thang S. Han, Paul Carroll, Gerry Conway, Brian R. Walker, Fiona MacDonald, Richard Ross, Wiebke Arlt, (unknown)	76
10	Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency - analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort 2012 ·UCL Discovery (University College London) ·Nils Krone, I.C. Rose, Debbie Willis, Sarah H. Wild, James Hodson, (unknown), Stefanie Hahner, Silvia Parajes, Roland H. Stimson, (unknown), Paul Carroll, Gerard S. Conway, Brian R. Walker, Fiona MacDonald, Richard Ross, Wiebke Arlt	1
11	Delayed diagnosis of adrenal insufficiency in a patient with severe penoscrotal hypospadias due to two novel P450 side-change cleavage enzyme (CYP11A1) mutations (p.R360W; p.R405X) 2012 ·European Journal of Endocrinology ·Silvia Parajes, (unknown), (unknown), (unknown), Angela E. Taylor, Vivek Dhir, Wiebke Arlt, Nils Krone	24
12	A Novel Entity of Clinically Isolated Adrenal Insufficiency Caused by a Partially Inactivating Mutation of the Gene Encoding for P450 Side Chain Cleavage Enzyme (CYP11A1) 2011 ·The Journal of Clinical Endocrinology & Metabolism ·Silvia Parajes, Clemens Kamrath, Ian T. Rose, Angela E. Taylor, Christiaan F. Mooij, Vivek Dhir, Joachim Grötzinger, Wiebke Arlt, Nils Krone	39
13	Genetic study of the hepcidin gene (HAMP) promoter and functional analysis of the c.-582A > G variant 2010 ·BMC Genetics ·Silvia Parajes, Arturo González‐Quintela, J. Campos Franco, Celsa Quinteiro, Fernando Domı́nguez, Lourdes Loidi	22
14	Functional Consequences of Seven Novel Mutations in theCYP11B1Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11β-Hydroxylase Deficiency 2010 ·The Journal of Clinical Endocrinology & Metabolism ·Silvia Parajes, Lourdes Loidi, Nicole Reisch, Vivek Dhir, Ian T. Rose, (unknown), Marcus Quinkler, Gerard S. Conway, Lidia Castro-Feijóo, David Araújo‐Vilar, Manuel Pombo, Fernando Domı́nguez, Emma L. Williams, Trevor Cole, Jeremy Kirk, (unknown), Gill Rumsby, Wiebke Arlt, Nils Krone	72
15	Hypochondroplasia and acanthosis nigricans: a new syndrome due to the p.Lys650Thr mutation in the fibroblast growth factor receptor 3 gene? 2008 ·European Journal of Endocrinology ·Lidia Castro-Feijóo, Lourdes Loidi, Anxo Vidal, Silvia Parajes, E. Rosón, Ana Belén Cid Álvarez, (unknown), Jesús Barreiro, (unknown), Fernando Domı́nguez, Manuel Pombo	23
16	High Frequency of Copy Number Variations and Sequence Variants at CYP21A2 Locus: Implication for the Genetic Diagnosis of 21-Hydroxylase Deficiency 2008 ·PLoS ONE ·Silvia Parajes, Celsa Quinteiro, Fernando Domı́nguez, Lourdes Loidi	62
17	Functional characterization of threeCYP21A2sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co-expression system 2008 ·Human Mutation ·(unknown), Lourdes Loidi, Vivek Dhir, Silvia Parajes, Celsa Quinteiro, Fernando Domı́nguez, Joachim Grötzinger, Wolfgang G. Sippell, Felix G. Riepe, Wiebke Arlt, Nils Krone	15
18	A Simple and Robust Quantitative PCR Assay to Determine CYP21A2 Gene Dose in the Diagnosis of 21-Hydroxylase Deficiency 2007 ·Clinical Chemistry ·Silvia Parajes, (unknown), Fernando Domı́nguez, Lourdes Loidi	26
19	High variability in CYP21A2 mutated alleles in Spanish 21‐hydroxylase deficiency patients, six novel mutations and a founder effect 2006 ·Clinical Endocrinology ·Lourdes Loidi, Celsa Quinteiro, Silvia Parajes, Jesús Barreiro, (unknown), José Manuel Cabezas-Agrícola, Aurelio M. Sueiro, David Araújo‐Vilar, (unknown), Javier Costas, Manuel Pombo, Fernando Domı́nguez	45
20	A comparative study of the utility of two superdisintegrants in microcrystalline cellulose pellets prepared by extrusion–spheronization 2005 ·European Journal of Pharmaceutics and Biopharmaceutics ·C. Souto, (unknown), Silvia Parajes, Ramón Martı́nez-Pacheco	44

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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