Mónica Fernández‐Cancio

Author

Centre for Biomedical Network Research on Rare Diseases ORCID

Also Known As

Antonio Moreno-Galdó, Fernández-Cancio M, Fernández-Cancio, M., Fernández-Cancio, Mónica, M. Fernandez-Cancio, M. Fernandez‐Cancio, M. Fernández-Cancio, M. Fernández Cancio, M. Fernández-Cancio, M. Fernández‐Cancio

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Centre for Biomedical Network Research on Rare Diseases Instituto de Salud Carlos III Vall d'Hebron Institut de Recerca Universitat Autònoma de Barcelona Vall d'Hebron Hospital Universitari

About

Mónica Fernández‐Cancio is an author at Centre for Biomedical Network Research on Rare Diseases specializing in medicine, developmental biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	220
2	Biochemistry	2	2	40
3	Engineering	1	1	30
4	Public Health	1	1	29
5	Social Sciences	1	1	10

Mónica Fernández‐Cancio

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Novel (60%) and Recurrent (40%) Androgen Receptor Gene Mutations in a Series of 59 Patients with a 46,XY Disorder of Sex Development Laura Audí, Mónica Fernández‐Cancio, Antonio Carrascosa, The Journal of Clinical Endocrinology & Metabolism	2010	145
Ten Novel Mutations in the NR5A1 Gene Cause Disordered Sex Development in 46,XY and Ovarian Insufficiency in 46,XX Individuals Núria Camats, Amit V. Pandey, Mónica Fernández‐Cancio, The Journal of Clinical Endocrinology & Metabolism	2012	132
Rickets in the Middle East: Role of Environment and Genetic Predisposition Giampiero I. Baroncelli, Abdullah Bereket, Mohamed El Kholy, The Journal of Clinical Endocrinology & Metabolism	2008	130
Characterization of Novel StAR (Steroidogenic Acute Regulatory Protein) Mutations Causing Non-Classic Lipoid Adrenal Hyperplasia Christa E. Flück, Amit V. Pandey, Bernhard Dick, PLoS ONE	2011	90
The d3/fl-Growth Hormone (GH) Receptor Polymorphism Does Not Influence the Effect of GH Treatment (66 μg/kg per Day) or the Spontaneous Growth in Short Non-GH-Deficient Small-for-Gestational-Age Children: Results from a Two-Year Controlled Prospective Study in 170 Spanish Patients Antonio Carrascosa, Cristina Estéban, R. Espadero, The Journal of Clinical Endocrinology & Metabolism	2006	81
Expanding the Clinical and Genetic Spectra of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected and Unexpected Findings Francesc Rudilla, Clara Franco‐Jarava, Mónica Martínez‐Gallo, Frontiers in Immunology	2019	71
Broad phenotypes in heterozygous NR5A1 46,XY patients with a disorder of sex development: an oligogenic origin? Núria Camats, Mónica Fernández‐Cancio, Laura Audí, European Journal of Human Genetics Broad PhenotypesInfertilityXy PatientsDevelopmental BiologyMendelian Disorder	2018	64
<i><scp>AR</scp></i> and <i><scp>SRD</scp>5A2</i> gene mutations in a series of 51 Turkish 46,<scp>XY DSD</scp> children with a clinical diagnosis of androgen insensitivity Teoman Akçay, Mónica Fernández‐Cancio, Serap Turan, Andrology	2014	56
Human NR5A1/SF-1 Mutations Show Decreased Activity on BDNF (Brain-Derived Neurotrophic Factor), an Important Regulator of Energy Balance: Testing Impact of Novel SF-1 Mutations Beyond Steroidogenesis Jana Malíková, Núria Camats, Mónica Fernández‐Cancio, PLoS ONE	2014	44
Mechanism of the Dual Activities of Human CYP17A1 and Binding to Anti-Prostate Cancer Drug Abiraterone Revealed by a Novel V366M Mutation Causing 17,20 Lyase Deficiency Mónica Fernández‐Cancio, Núria Camats, Christa E. Flück, Pharmaceuticals	2018	44

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