Biblio

Zhang M, Abbas-Turki A, Lombard A, Koukam A, Jo K-H.  2020.  Autonomous vehicle with communicative driving for pedestrian crossing: Trajectory optimization. 2020 IEEE 23RD INTERNATIONAL CONFERENCE ON INTELLIGENT TRANSPORTATION SYSTEMS (ITSC).

Auzoult L.  2015.  Autonomy and Resistance to Authority. SWISS JOURNAL OF PSYCHOLOGY. 74:49-53.

Guarisco M, Gao F, Paire D.  2017.  Autonomy and User Experience Enhancement Control of an Electrically Assisted Bicycle With Dual-Wheel Drive. IEEE TRANSACTIONS ON INDUSTRY APPLICATIONS. 53:1476-1484.

Chrenko D, Ravey A, Roche R, Bouquain D.  2014.  Autonomy Estimation for EV based on Road Planning Software. 2014 IEEE TRANSPORTATION ELECTRIFICATION CONFERENCE AND EXPO (ITEC).

Chrenko D, Ravey A, Roche R, Bouquain D.  2014.  Autonomy Estimation for EV based on Road Planning Software. 2014 IEEE TRANSPORTATION ELECTRIFICATION CONFERENCE AND EXPO (ITEC).

Chrenko D, Ravey A, Roche R, Bouquain D.  2014.  Autonomy Estimation for EV based on Road Planning Software. 2014 IEEE TRANSPORTATION ELECTRIFICATION CONFERENCE AND EXPO (ITEC).

Chrenko D, Ravey A, Roche R, Bouquain D.  2014.  Autonomy Estimation for EV based on Road Planning Software. 2014 IEEE TRANSPORTATION ELECTRIFICATION CONFERENCE AND EXPO (ITEC).

Coste B.  2014.  Autonomy in the Dock: Oscar Wilde's First Trial. CAHIERS VICTORIENS & EDOUARDIENS.

Amoura C, Berjot S, Gillet N, Caruana S, Cohen J, Finez L.  2015.  Autonomy-Supportive and Controlling Styles of Teaching Opposite or Distinct Teaching Styles? SWISS JOURNAL OF PSYCHOLOGY. 74:141-158.

Mottet N, Cabrol C, Metz J-P, Toubin C, Arbez-Gindre F, Valduga M, McElreavey K, Riethmuller D, Van Maldergem L, Piard J.  2019.  Autopsy findings of ectodermal dysplasia and sex development disorder in a fetus with 19q12q13 microdeletion. EUROPEAN JOURNAL OF MEDICAL GENETICS. 62:103539.

S. Penda VBitseki, Olivier A.  2017.  Autoregressive functions estimation in nonlinear bifurcating autoregressive models. STATISTICAL INFERENCE FOR STOCHASTIC PROCESSES. 20:179-210.

Smadja DM, Chocron R, Rossi E, Poitier B, Pya Y, Bekbossynova M, Peronino C, Rancic J, Roussel JChristian, Kindo M et al..  2020.  Autoregulation of Pulsatile Bioprosthetic Total Artificial Heart is Involved in Endothelial Homeostasis Preservation. THROMBOSIS AND HAEMOSTASIS. 120:1313-1322.

Girardot J, Billard F, Coillet A, Hertz E, Grelu P.  2020.  Autosetting Mode-Locked Laser Using an Evolutionary Algorithm and Time-Stretch Spectral Characterization. IEEE JOURNAL OF SELECTED TOPICS IN QUANTUM ELECTRONICS. 26:1100108.

Girardot J., Billard F., Coillet A., Nafa M., Hertz E., Grelu P.  2021.  Autosetting Mode-locked Laser with Genetic Algorithm Optimization and Advanced Intracavity Controls. 2021 CONFERENCE ON LASERS AND ELECTRO-OPTICS EUROPE & EUROPEAN QUANTUM ELECTRONICS CONFERENCE (CLEO/EUROPE-EQEC).

Serey-Gaut M.G, Cabrol C., Vallat J., Tatu L., Loeys B., Van Maldergem L..  2019.  Autosomal dominant recurrent parotitis: an under-reported entity. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:374.

Serey-Gaut M.G, Cabrol C., Vallat J., Tatu L., Loeys B., Van Maldergem L..  2019.  Autosomal dominant recurrent parotitis: an under-reported entity. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:374.

Serey-Gaut M.G, Cabrol C., Vallat J., Tatu L., Loeys B., Van Maldergem L..  2019.  Autosomal dominant recurrent parotitis: an under-reported entity. EUROPEAN JOURNAL OF HUMAN GENETICS. 27:374.

Greally MT, Kalis NN, Agab W, Ardati K, Giurgea S, Kornak U, Van Maldergem L.  2014.  Autosomal Recessive Cutis Laxa Type 2A ( ARCL2A) Mimicking Ehlers- Danlos Syndrome by Its Dermatological Manifestations: Report of Three Affected Patients. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 164:1245-1253.

Thevenon J., Duplomb L., Phadke S., Eguether T., Saunier A., Avila M., Carmignac V., Bruel A-L, St-Onge J., Duffourd Y. et al..  2016.  Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral-facial-digital syndrome with short stature and brachymesophalangia. CLINICAL GENETICS. 90:509-517.

Amos J.S, Huang L., Thevenon J., Kariminedjad A., Beaulieu C.L, Masurel-Paulet A., Najmabadi H., Fattahi Z., Beheshtian M., Tonekaboni S.H et al..  2017.  Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping. CLINICAL GENETICS. 91:92-99.

Schaefer E, Collet C, Genevieve D, Vincent M, Lohmann DR, Sanchez E, Bolender C, Eliot M-M, Nuernberg G, Passos-Bueno M-R et al..  2014.  Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome. GENETICS IN MEDICINE. 16:720-724.

Letard P, Drunat S, Vial Y, Duerinckx S, Ernault A, Amram D, Arpin S, Bertoli M, Busa T, Ceulemans B et al..  2018.  Autosomal recessive primary microcephaly due to ASPM mutations: An update. HUMAN MUTATION. 39:319-332.

Bruel A.-L, Masurel-Paulet A., Riviere J.-B, Duffourd Y., Lehalle D., Bensignor C., Huet F., Borgnon J., Roucher F., Kuentz P. et al..  2017.  Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis. CLINICAL GENETICS. 91:333-338.

Lefebvre M., Duffourd Y., Jouan T., Poe C., Jean-Marcais N., Verloes A., St-Onge J., Riviere J.-B, Petit F., Pierquin G. et al..  2017.  Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis. CLINICAL GENETICS. 91:908-912.

Ruaud L, Rice GI, Cabrol C, Piard J, Rodero M, van Eyk L, Boucher-Brischoux E, de Noordhout AMaertens, Mare R, Scalais E et al..  2018.  Autosomal-dominant early-onset spastic paraparesis with brain calcification due to IFIH1 gain-of-function. HUMAN MUTATION. 39:1076-1080.