Search - Inria - Institut national de recherche en sciences et technologies du numérique Access content directly

Filter your results

29 Results
authFullName_s : Caroline Lacoste
Image document

Extraction de réseaux linéiques à partir d'images satellitaires et aériennes par processus ponctuels marqués

Caroline Lacoste
Interface homme-machine [cs.HC]. Université Nice Sophia Antipolis, 2004. Français. ⟨NNT : ⟩
Theses tel-00261397v1

Coverage analysis of lists of genes involved in heterogeneous genetic diseases following benchtop exome sequencing using the ion proton

Caroline Lacoste , Jean-Pierre Desvignes , David Salgado , Christophe Pecheux , Laurent Villard et al.
Journal of Genetics, 2016, 95 (1), pp.203-208
Journal articles hal-01469051v1

IPAL Knowledge-based Medical Image Retrieval in ImageCLEFmed 2006

Caroline Lacoste , Jean-Pierre Chevallet , Joo-Hwee Lim , Wei Xiong , Daniel Raccoceanu et al.
Working Notes for the CLEF 2006 Workshop, 20-22 September Medical Image Track, 2006, Alicante, Spain
Conference papers hal-00954109v1
Image document

Incidence of ATRX mutations in myelodysplastic syndromes, the value of microcytosis

Charles Herbaux , Nicolas Duployez , Catherine Badens , Nicolas Poret , Claude Gardin et al.
American Journal of Hematology, 2015, 90 (8), pp.737-738. ⟨10.1002/ajh.24073⟩
Journal articles inserm-02913994v1

Novel partial loss-of-function variants in the tyrosyl-tRNA synthetase 1 (YARS1) gene involved in multisystem disease

Clothilde Estève , Céline Roman , Cécile Deleusse , Melissa Baravalle , Karine Bertaux et al.
European Journal of Medical Genetics, 2021, 64 (10), pp.104294. ⟨10.1016/j.ejmg.2021.104294⟩
Journal articles hal-03623403v1
Image document

A Kv7.2 mutation associated with early onset epileptic encephalopathy with suppression-burst enhances Kv7/M channel activity

Jérôme Devaux , Affef Abidi , Agathe Roubertie , Florence Molinari , Hélène Becq et al.
Epilepsia, 2016, 57 (5), pp.e87 - e93. ⟨10.1111/epi.13366⟩
Journal articles hal-01668018v1

Knowledge-Assisted Medical Image Retrieval

Joo-Hwee Lim , Caroline Lacoste , Jean-Pierre Chevallet , Thi Hoang Diem Le
ICME 2007, International Conference on Multimedia, and Expo, 2007, Beijing, China
Conference papers hal-00953880v1
Image document

Hydrographic Network Extraction from Radar Satellite Images using a Hierarchical Model within a Stochastic Geometry Framework

Caroline Lacoste , Xavier Descombes , Josiane Zerubia , Nicolas Baghdadi
[Research Report] RR-5697, INRIA. 2006, pp.27
Reports inria-00070318v1

Description Osteo-Oto-Hepato-Enteric (O2HE) syndrome, a new recessive autosomal syndrome secondary to loss of function mutations in the UNC45A gene

L. Faivre , Clothilde Esteve , L. Francescatto , P. L. Tan , A. Bourchany et al.
European Journal of Human Genetics, 2019, 27 (1), pp.795-796
Journal articles hal-02461437v1
Image document

The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsies

Lionel Arnaud , Marie-Thérèse Abi Warde , Giulia Barcia , Julitta de Bellescize , Nicolas Chatron et al.
European Journal of Medical Genetics, 2022, 65 (3), pp.104445. ⟨10.1016/j.ejmg.2022.104445⟩
Journal articles hal-03949438v1

A mutation in the Gardos channel is associated with hereditary xerocytosis.

Raphael Rapetti-Mauss , Caroline Lacoste , Veronique Picard , Corinne Guitton , Elise Lombard et al.
Blood, 2015, 126 (11), pp.1273-80
Journal articles hal-01252935v1

Hereditary stomatocytosis: advances in knowledge of forms with dehydrated red blood cells

Catherine Badens , Loïc Garçon , Raphaël Rapetti-Mauss , Caroline Lacoste , Hélène Guizouarn et al.
Hématologie, 2016, 22 (5), pp.319-324. ⟨10.1684/hma.2016.1173⟩
Journal articles hal-01469076v1
Image document

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 , Gisèle Alcaraz , François-Xavier Michon et al.
Neurobiology of Disease, 2015, 80, pp.80 - 92. ⟨10.1016/j.nbd.2015.04.017⟩
Journal articles hal-01664283v1
Image document

Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2.

Mathieu Milh , Nadia Boutry-Kryza , Julie Sutera-Sardo , Cyril Mignot , Stéphane Auvin et al.
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.80. ⟨10.1186/1750-1172-8-80⟩
Journal articles inserm-00829466v1

SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome.

Alexandre Fabre , Bernard Charroux , Christine Martinez-Vinson , Bertrand Roquelaure , Egritas Odul et al.
American Journal of Human Genetics, 2012, 90 (4), pp.689-92. ⟨10.1016/j.ajhg.2012.02.009⟩
Journal articles hal-00843403v1
Image document

Extraction automatique des réseaux linéiques à partir d'images satellitaires et aériennes par processus Markov objet

Caroline Lacoste , Xavier Descombes , Josiane Zerubia , Nicolas Baghdadi
Bulletin - Société Française de Photogrammétrie et de Télédétection, 2003, 170, pp.13-22
Journal articles hal-02924089v1
Image document

A Comparative Study of Point Processes for Line Network Extraction in Remote Sensing

Caroline Lacoste , Xavier Descombes , Josiane Zerubia
RR-4516, INRIA. 2002
Reports inria-00072072v1
Image document

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Cyril Mignot , Aoife Mcmahon , Claire Bar , Philippe Campeau , David Davidson et al.
Genetics in Medicine, 2019, 21 (8), pp.1897-1898. ⟨10.1038/s41436-018⟩
Journal articles hal-01919142v1

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Cyril Mignot , Aoife C. Mcmahon , Claire Bar , Philippe M. Campeau , Claire Davidson et al.
Genetics in Medicine, 2019, 21 (4), pp.837-849. ⟨10.1038/s41436-018-0268-1⟩
Journal articles hal-02478899v1

In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutation

F. Sauvestre , S. Moutton , Catherine Badens , B. Broussin , D. Carles et al.
Neuropathology and Applied Neurobiology, 2017, 43 (7), pp.631-635. ⟨10.1111/nan.12409⟩
Journal articles hal-01741732v1
Image document

A Polyline Process for Unsupervised Line Network Extraction in Remote Sensing

Caroline Lacoste , Xavier Descombes , Josiane Zerubia
[Research Report] RR-5698, INRIA. 2006, pp.26
Reports inria-00070317v1

Clinical study of 19 patients with SCN 8A ‐related epilepsy: Two modes of onset regarding EEG and seizures

Julien Denis , Nathalie Villeneuve , Pierre Cacciagli , Cecile Mignon-Ravix , Caroline Lacoste et al.
Epilepsia, 2019, ⟨10.1111/epi.14727⟩
Journal articles hal-02417625v1
Image document

Molecular and clinical description of patients with GABA A receptor gene variants ( GABRA1 , GABRB2 , GABRB3 , GABRG2 ): a cohort study, review of literature, and genotype‐phenotype correlations

Pierre‐yves Maillard , Sarah Baer , Élise Schaefer , Béatrice Desnous , Nathalie Villeneuve et al.
Epilepsia, In press, 63 (10), pp.2519-2533. ⟨10.1111/epi.17336⟩
Journal articles hal-03700622v1
Image document

Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases

Chloé Di Meglio , Gaetan Lesca , Nathalie Villeneuve , Caroline Lacoste , Affef Abidi et al.
Epilepsia, 2015, 56 (12), pp.1931-1940. ⟨10.1111/epi.13214⟩
Journal articles hal-01664313v1
Image document

Variable Clinical Expression in Patients with Mosaicism for KCNQ2 Mutations

Mathieu Milh , Caroline Lacoste , Pierre Cacciagli , Affef Abidi , Julie Sutera-Sardo et al.
American Journal of Medical Genetics Part A, 2015, 167 (10), pp.2314-2318. ⟨10.1002/ajmg.a.37152⟩
Journal articles istex hal-01664288v1

Medical Image Retrieval based on Knowledge-Assisted Text and Image Indexing

Caroline Lacoste , Joo-Hwee Lim , Jean-Pierre Chevallet , Thi Hoang Diem Le
IEEE Transactions on Circuits and Systems for Video Technology, 2007, 17 (7), pp.889--900
Journal articles hal-00953799v1

Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility

Clothilde Esteve , Ludmila Francescatto , Perciliz Tan , Aurélie Bourchany , Cécile de Leusse et al.
American Journal of Human Genetics, 2018, 102 (3), pp.364 - 374. ⟨10.1016/j.ajhg.2018.01.009⟩
Journal articles hal-01721495v1
Image document

Création de résumés vidéos par une approche statistique

Caroline Lacoste , Ronan Fablet , Patrick Bouthemy , J.F. Yao
RFIA 2002 : 13ème congrès francophone AFRIF-AFIA de reconnaissance des formes et intelligence artificielle, Jan 2002, Angers, France. pp.153 - 162
Conference papers hal-02341682v1

Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome

Caroline Lacoste , B. Leheup , I. Agouti , D. Mowat , F. Giuliano et al.
Clinical Genetics, 2014, 86 (5), pp.502 - 503. ⟨10.1111/cge.12319⟩
Journal articles istex hal-01706687v1