Florence Roucher‐Boulez

Author

Also Known As

F Roucher, F. ROUCHER, F. Roucher, F. Roucher Boulez, F. Roucher-Boulez, Florence Boulez, Florence Roucher, Florence Roucher Boulez, Florence Roucher-Boulez, Florence Roucher‐Boulez

Publications

899

Citations

H-Index

Concepts

All Affiliations

Université Claude Bernard Lyon 1 Hospices Civils de Lyon Inserm Centre National de la Recherche Scientifique Hôpital Cochin

About

Florence Roucher‐Boulez is an author at Université Claude Bernard Lyon 1 specializing in reproductive biology, morphogenesis, and endocrinology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	1	1	99
2	Public Health	1	1	99
3	Endocrinology	1	1	99
4	Neuroscience	1	1	99
5	Developmental Biology	1	1	99

Florence Roucher‐Boulez

Publications

627

Citations

H-Index

Page 1

	Year	Citations
PKA signaling drives reticularis differentiation and sexually dimorphic adrenal cortex renewal Typhanie Dumontet, Isabelle Sahut‐Barnola, Amandine Septier, JCI Insight GeneticsPka EffectsReproductive BiologyEmbryologyReproductive Endocrinology	2018	99
NNT mutations: a cause of primary adrenal insufficiency, oxidative stress and extra-adrenal defects Florence Roucher‐Boulez, Delphine Mallet-Motak, Dinane Samara‐Boustani, European Journal of Endocrinology	2016	91
New NOBOX Mutations Identified in a Large Cohort of Women With Primary Ovarian Insufficiency Decrease KIT-L Expression Justine Bouilly, Florence Roucher‐Boulez, Anne Gompel, The Journal of Clinical Endocrinology & Metabolism	2014	60
Triple-A syndrome: a wide spectrum of adrenal dysfunction Florence Roucher‐Boulez, Aude Brac de la Perrière, Aude Jacquez, European Journal of Endocrinology	2017	56
Age- and Sex-Specific TSH Upper-Limit Reference Intervals in the General French Population: There Is a Need to Adjust Our Actual Practices Véronique Raverot, Maxime Bonjour, Juliette Abeillon du Payrat, Journal of Clinical Medicine	2020	39
P450 Oxidoreductase Deficiency: Loss of Activity Caused by Protein Instability From a Novel L374H Mutation Shaheena Parween, Florence Roucher‐Boulez, Christa E. Flück, The Journal of Clinical Endocrinology & Metabolism	2016	35
Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria Asmahane Ladjouze, Malcolm Donaldson, Ingrid Plotton, Frontiers in Endocrinology	2022	34
Sexually dimorphic activation of innate antitumor immunity prevents adrenocortical carcinoma development James Wilmouth, Julie Olabe, Diana García-García, Science Advances	2022	33
Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene Claire Goursaud, Delphine Mallet, Alexandre Janin, Frontiers in Endocrinology	2018	29
Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA Sarra Dimassi, Thomas Simonet, Nadia Boutry‐Kryza, Applied & Translational Genomics	2015	27

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