Florence Roucher‐Boulez

879 total citations
36 papers, 517 citations indexed

About

Florence Roucher‐Boulez is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Genetics. According to data from OpenAlex, Florence Roucher‐Boulez has authored 36 papers receiving a total of 517 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 17 papers in Endocrinology, Diabetes and Metabolism and 15 papers in Genetics. Recurrent topics in Florence Roucher‐Boulez's work include Sexual Differentiation and Disorders (14 papers), Hormonal Regulation and Hypertension (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Florence Roucher‐Boulez is often cited by papers focused on Sexual Differentiation and Disorders (14 papers), Hormonal Regulation and Hypertension (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Florence Roucher‐Boulez collaborates with scholars based in France, United States and Switzerland. Florence Roucher‐Boulez's co-authors include Yves Morel, Ingrid Plotton, Delphine Mallet, Véronique Tardy, Pierre Val, Anne‐Marie Lefrançois‐Martinez, Antoine Martinez, Isabelle Sahut‐Barnola, Typhanie Dumontet and Nathanaëlle Montanier and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Florence Roucher‐Boulez

34 papers receiving 515 citations

Peers

Countries citing papers authored by Florence Roucher‐Boulez

Since Specialization

Citations

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

Fields of papers citing papers by Florence Roucher‐Boulez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Florence Roucher‐Boulez. 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 Florence Roucher‐Boulez. The network helps show where Florence Roucher‐Boulez may publish in the future.

Co-authorship network of co-authors of Florence Roucher‐Boulez

This figure shows the co-authorship network connecting the top 25 collaborators of Florence Roucher‐Boulez. A scholar is included among the top collaborators of Florence Roucher‐Boulez 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 Florence Roucher‐Boulez. Florence Roucher‐Boulez 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	First intragenic inversion of CYP11B1 gene causing 11β-hydroxylase deficiency: a molecular diagnosis easily overlooked 2025 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), (unknown), Ingrid Plotton, (unknown), (unknown), Florence Roucher‐Boulez	0
2	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
3	Neonatal salt wasting syndrome: Aldosterone synthase deficiency caused by a new splicing variant in CYP11B2 2024 ·Archives de Pédiatrie ·(unknown), (unknown), Pascal Barat, Jérôme Harambat, (unknown), Delphine Mallet, Florence Roucher‐Boulez, Lise Allard	1
4	Testicular impairment in Primary Adrenal Insufficiency caused by Nicotinamide Nucleotide Transhydrogenase (NNT) deficiency - a case report: implication of oxidative stress and importance of fertility preservation 2023 ·Basic and Clinical Andrology ·Lucile Ferreux, (unknown), Emmanuel Dulioust, Xavier Bertagna, Florence Roucher‐Boulez, Mathilde Bourdon, Nicolas Thiounn, Catherine Patrat	2
5	Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation 2022 ·Journal of Clinical Investigation ·Cécily Lucas, Kay‐Sara Sauter, (unknown), Delphine Mallet, (unknown), (unknown), Ingrid Plotton, Yves Morel, Daniel Aeberli, Franca Wagner, Hans Clevers, Amit V. Pandey, Pierre Val, Florence Roucher‐Boulez, Christa E. Flück	8
6	Epileptic encephalopathy as a new feature of the sudden infant death with dysgenesis of the testes syndrome caused by TSPYL1 variants 2022 ·American Journal of Medical Genetics Part A ·(unknown), Delphine Mallet, Florence Roucher‐Boulez, (unknown), Marie Bournez, (unknown), (unknown), Charlotte Pöe, (unknown), Antonio Vitobello, Christophe Philippe, Yannis Duffourd, Christel Thauvin‐Robinet, Laurence Faivre, Sophie Nambot	2
7	Steroid Profiling in the Amniotic Fluid: Reference Range for 12 Steroids and Interest in 21-Hydroxylase Deficiency 2022 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), (unknown), Aurore Bouty, (unknown), Florence Roucher‐Boulez, Delphine Mallet, (unknown), Frédérique Dijoud, Pierre Mouriquand, Pierre‐Yves Mure, Damien Sanlaville, René Écochard, Ingrid Plotton	5
8	Sexually dimorphic activation of innate antitumor immunity prevents adrenocortical carcinoma development 2022 ·Science Advances ·(unknown), (unknown), (unknown), Cécily Lucas, Rachel Guiton, Florence Roucher‐Boulez, (unknown), Christelle Damon‐Soubeyrand, Isabelle Sahut‐Barnola, Jean‐Christophe Pointud, Yoan Renaud, (unknown), Igor Tauveron, Anne‐Marie Lefrançois‐Martinez, Antoine Martinez, Pierre Val	21
9	Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria 2022 ·Frontiers in Endocrinology ·(unknown), Malcolm Donaldson, Ingrid Plotton, (unknown), (unknown), (unknown), Delphine Mallet, (unknown), (unknown), Yves Morel, Florence Roucher‐Boulez	5
10	Hypopituitarism in Patients with Blepharophimosis and <b><i>FOXL2</i></b> Mutations 2020 ·Hormone Research in Paediatrics ·(unknown), Florence Roucher‐Boulez, Alexandru Saveanu, (unknown), Olivier Chabre, Patrizia Amati‐Bonneau, Dominique Bonneau, (unknown), Yves Morel, Carine Villanueva, Thierry Brue, Rachel Reynaud, Marc Nicolino	10
11	Isolated hypoaldosteronism as first sign of X-linked adrenal hypoplasia congenita caused by a novel mutation in NR0B1/DAX-1 gene: a case report 2019 ·BMC Medical Genetics ·Lorenzo Iughetti, Laura Lucaccioni, Patrizia Bruzzi, (unknown), (unknown), Simona Filomena Madeo, Barbara Predieri, Florence Roucher‐Boulez	6
12	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
13	Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene 2018 ·Frontiers in Endocrinology ·(unknown), Delphine Mallet, Alexandre Janin, Rita Menassa, (unknown), Gianni Russo, Anne Lienhardt-Roussie, C Lecointre, Ingrid Plotton, Yves Morel, Florence Roucher‐Boulez	15
14	Adrenocortical development: Lessons from mouse models 2018 ·Annales d Endocrinologie ·Typhanie Dumontet, Isabelle Sahut‐Barnola, Amandine Septier, Nathanaëlle Montanier, Ingrid Plotton, Florence Roucher‐Boulez, Véronique Ducros, Anne‐Marie Lefrançois‐Martinez, (unknown), Mohamad Zubair, Ken-ichirou Morohashi, David T. Breault, Pierre Val, Antoine Martinez	7
15	Statistical method to compare massive parallel sequencing pipelines 2017 ·BMC Bioinformatics ·(unknown), Noémie Leblay, S. Dimassi, Amandine Campan-Fournier, Audrey Labalme, Florence Roucher‐Boulez, Damien Sanlaville, Gaëtan Lesca, Claire Bardel, Pascal Roy	4
16	NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects 2016 ·European Journal of Endocrinology ·Florence Roucher‐Boulez, (unknown), Dinane Samara‐Boustani, (unknown), (unknown), Pierre‐François Souchon, Dominique Simon, Sylvie Nivot, Claudine Heinrichs, (unknown), Xavier Bertagna, L. Groisne, Bruno Leheup, Catherine Naud-Saudreau, G Blondin, (unknown), (unknown), Yves Morel	54
17	Evolution of steroids during pregnancy: Maternal, placental and fetal synthesis 2016 ·Annales d Endocrinologie ·Yves Morel, Florence Roucher‐Boulez, Ingrid Plotton, (unknown), Véronique Tardy, Delphine Mallet	83
18	Successful IVF pregnancy despite inadequate ovarian steroidogenesis due to congenital lipoid adrenal hyperplasia (CLAH): a case report 2016 ·Human Reproduction ·F. Albarel, Jeanne Perrin, (unknown), Florence Roucher‐Boulez, Rachel Reynaud, Thierry Brue, Blandine Courbière	14
19	A splicing mutation in the DMD gene detected by next-generation sequencing and confirmed by mRNA and protein analysis 2015 ·Clinica Chimica Acta ·Florence Roucher‐Boulez, Rita Menassa, Nathalie Streichenberger, Véronique Manel, (unknown), Yves Morel, Laurence Michel‐Calemard	5
20	Macroprolactinaemia: a biological diagnostic strategy from the study of 222 patients 2015 ·European Journal of Endocrinology ·(unknown), C. Harthé, Florence Roucher‐Boulez, Yves Morel, Françoise Borson‐Chazot, Gérald Raverot, Véronique Raverot	7

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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