Patricia Bretones

542 total citations
14 papers, 301 citations indexed

About

Patricia Bretones is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Endocrine and Autonomic Systems. According to data from OpenAlex, Patricia Bretones has authored 14 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Endocrinology, Diabetes and Metabolism and 4 papers in Endocrine and Autonomic Systems. Recurrent topics in Patricia Bretones's work include Thyroid Disorders and Treatments (5 papers), Sexual Differentiation and Disorders (4 papers) and Neuroscience of respiration and sleep (4 papers). Patricia Bretones is often cited by papers focused on Thyroid Disorders and Treatments (5 papers), Sexual Differentiation and Disorders (4 papers) and Neuroscience of respiration and sleep (4 papers). Patricia Bretones collaborates with scholars based in France and Switzerland. Patricia Bretones's co-authors include M David, Yves Morel, Delphine Mallet, Frédérique Dijoud, Laurence Michel‐Calemard, Véronique Raverot, Karim Chikh, Nicolás de Roux, Delphine Zénaty and Cécile Lambe and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Human Reproduction and Molecular and Cellular Endocrinology.

In The Last Decade

Patricia Bretones

13 papers receiving 294 citations

Peers

Countries citing papers authored by Patricia Bretones

Since Specialization

Citations

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

Fields of papers citing papers by Patricia Bretones

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patricia Bretones

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Urinary gonadotropin assay on 24-h collections as a tool to detect early central puberty onset in girls: determination of predictive thresholds 2024 ·Human Reproduction ·(unknown), (unknown), Véronique Raverot, Patricia Bretones, René Écochard, (unknown), Marc Nicolino, (unknown), Florence Roucher‐Boulez, Carine Villanueva, (unknown), Ingrid Plotton	0
2	Case Report: Longitudinal follow-up and testicular sperm extraction in a patient with a pathogenic NR5A1 (SF-1) frameshift variant: p.(Phe70Serfs5) 2023 ·Frontiers in Endocrinology* ·(unknown), Delphine Mallet, (unknown), Claire-Lise Gay, Elsa Labrune, Patricia Bretones, Sandrine Giscard d’Estaing, B. Cuzin, Frédérique Dijoud, Florence Roucher‐Boulez, Ingrid Plotton	5
3	IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency 2022 ·European Journal of Endocrinology ·(unknown), Rachel Reynaud, (unknown), (unknown), Patricia Bretones, (unknown), Thomas Édouard, Gérald Raverot, Anne Barlier, Thierry Brue, Frédéric Castinetti, Alexandru Saveanu	2
4	Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France 2022 ·Archives de Pédiatrie ·(unknown), (unknown), Patricia Bretones, (unknown), (unknown), Rachel Reynaud, C. Thomas Somma, Pascal Barat, (unknown), Natacha Bouhours‐Nouet, (unknown), Michel Polak, Juliane Léger, David Cheillan, R. Coutant	4
5	Congenital Hypothyroidism due to a Low Level of Maternal Thyrotropin Receptor-Blocking Antibodies 2020 ·European Thyroid Journal ·(unknown), Patricia Bretones, J. Abeillon, (unknown), (unknown), Karim Chikh, Véronique Raverot	10
6	Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder 2019 ·Frontiers in Endocrinology ·Florence Roucher‐Boulez, Delphine Mallet, Nicolas Chatron, Frédérique Dijoud, Daniela Gorduza, Patricia Bretones, Yves Morel	16
7	Growth curves for congenital adrenal hyperplasia from a national retrospective cohort 2016 ·Journal of Pediatric Endocrinology and Metabolism ·Patricia Bretones, Benjamin Riche, (unknown), M David, Pascal Roy, Véronique Tardy, Behrouz Kassaï, Ségolène Gaillard, Delphine Bernoux, Yves Morel, Pierre Chatelain, Marc Nicolino, Catherine Cornu, (unknown)	15
8	Predictive value of maternal second-generation thyroid-binding inhibitory immunoglobulin assay for neonatal autoimmune hyperthyroidism 2014 ·European Journal of Endocrinology ·(unknown), Karim Chikh, Nadine Bossard, Patricia Bretones, P. Gaucherand, Olivier Claris, Anne Charrié, Véronique Raverot, Jacques Orgiazzi, Françoise Borson‐Chazot, Claire Bournaud	71
9	Late prenatal dexamethasone and phenotype variations in 46,XX CAH: Concerns about current protocols and benefits for surgical procedures 2014 ·Journal of Pediatric Urology ·Daniela Gorduza, (unknown), (unknown), Claire-Lise Gay, Pierre Chatelain, M David, Patricia Bretones, Anne Lienhardt-Roussie, Aude Brac de la Perrière, Yves Morel, Pierre Mouriquand	12
10	Hémorragie surrénalienne révélée par un ictère néonatal : à propos d’un cas 2012 ·Archives de Pédiatrie ·(unknown), Stéphane Haÿs, (unknown), Patricia Bretones, M. Bensaïd, Iolanda Jordán, (unknown), (unknown), (unknown)	2
11	Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1) 2006 ·Molecular and Cellular Endocrinology ·Delphine Zénaty, Patricia Bretones, Cécile Lambe, (unknown), M David, Juliane Léger, Nicolás de Roux	47
12	Gonadal Dysgenesis Without Adrenal Insufficiency in a 46, XY Patient Heterozygous for the Nonsense C16X Mutation: A Case of SF1 Haploinsufficiency 2004 ·The Journal of Clinical Endocrinology & Metabolism ·Delphine Mallet, Patricia Bretones, Laurence Michel‐Calemard, Frédérique Dijoud, M David, Yves Morel	83
13	Question 4 Quelles stratégies diagnostiques et thérapeutiques des troubles du métabolisme glucidique au cours de la mucoviscidose? Stratégies diagnostiques et thérapeutiques des troubles du métabolisme glucidique au cours de la mucoviscidose 2003 ·Archives de Pédiatrie ·Patricia Bretones	2
14	A Familial Case of Congenital Hypothyroidism Caused by a Homozygous Mutation of the Thyrotropin Receptor Gene 2001 ·Thyroid ·Patricia Bretones, L Duprez, Jasmine Parma, Muriel D. David, Gilbert Vassart, Patrice Rodien	32

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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