Caroline Lacoste - Concepedia

Author

Caroline Lacoste

Inserm

Also Known As

C Lacoste, C. Lacoste, C.-R. Lacoste, CAROLINE LACOSTE, Caroline Lacoste, LACOSTE, Caroline, Lacoste, Caroline

Publications

1.8K

Citations

H-Index

Concepts

All Affiliations

Inserm Hôpital de la Timone Assistance Publique – Hôpitaux de Paris Aix-Marseille Université Centre National de la Recherche Scientifique

About

Caroline Lacoste is an author at Inserm specializing in medicine, pathology, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	699
2	Engineering	5	5	267
3	Health Sciences	3	3	87
4	Social Sciences	2	2	117
5	Natural Sciences	1	1	31

Caroline Lacoste

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Phenylphenols, biphenols, bisphenol-A and 4-tert-octylphenol exhibit α and β estrogen activities and antiandrogen activity in reporter cell lines Françoise Paris, Patrick Balaguer, Béatrice Térouanne, Molecular and Cellular Endocrinology β Estrogen ActivitiesBiochemistry4-Tert-octylphenol Exhibit αMedicineHormonal Receptor	2002	199
Point processes for unsupervised line network extraction in remote sensing Caroline Lacoste, Xavier Descombes, Josiane Zerubia IEEE Transactions on Pattern Analysis and Machine Intelligence EngineeringMachine LearningNetwork AnalysisQuality CandyImage Analysis	2005	160
SKIV2L Mutations Cause Syndromic Diarrhea, or Trichohepatoenteric Syndrome Alexandre Fabre, Bernard Charroux, Christine Martinez‐Vinson, The American Journal of Human Genetics Genetic DisorderPathogenesisTrichohepatoenteric SyndromeGastroenterologyPathology	2012	157
A mutation in the Gardos channel is associated with hereditary xerocytosis Raphaël Rapetti‐Mauss, Caroline Lacoste, Véronique Picard, Blood	2015	117
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2 Mathieu Milh, Nadia Boutry‐Kryza, Julie Sutera-Sardo, Orphanet Journal of Rare Diseases	2013	91
A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels Affef Abidi, Jérôme Devaux, Florence Molinari, Neurobiology of Disease Epileptic EncephalopathyChannelopathiesMolecular PhysiologyHyperpolarization (Biology)Neurophysiology	2015	71
Mutations in PHD‐like domain of the <i>ATRX</i> gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome Catherine Badens, Caroline Lacoste, N. Philip, Clinical Genetics	2006	63
Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility Clothilde Estève, Ludmila Francescatto, Perciliz L. Tan, The American Journal of Human Genetics Bone FragilityMendelian DisorderGenetic DisorderGeneticsPathogenesis	2018	63
Epileptic patients with de novo <i><scp>STXBP</scp>1</i> mutations: Key clinical features based on 24 cases Chloé Di Meglio, Gaëtan Lesca, Nathalie Villeneuve, Epilepsia	2015	61
IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients Cyril Mignot, Aoife McMahon, Claire Bar, Genetics in Medicine	2018	57

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