Articles scientifiques, ouvrages et autres supports
Depuis 2010, les équipes ont publié plus de 400 publications internationales sur l’autisme et les TND, coordonnent d’importants programmes de recherche européens ou nationaux, des essais cliniques ou des études de cohorte et participent à de nombreux autres (~ 100 projets sur les TND soutenus par des agences ou associations nationales ou européennes).
Vous pourrez trouver ci-dessous les références de ces documents classés par années puis par ordre alphabétique du premier auteur:
Baer, S., & de Saint-Martin, A. (2023). [Epilepsy in children and adults. Part 1. Childhood epilepsy]. La Revue Du Praticien, 73(10), 1147‑1153.
Bemmouna, D., Lagzouli, A., & Weiner, L. (2023). The biosocial correlates and predictors of emotion dysregulation in autistic adults compared to borderline personality disorder and nonclinical controls. Molecular Autism, 14, 47. https://doi.org/10.1186/s13229-023-00580-3
Bemmouna, D., & Weiner, L. (2023). Linehan’s biosocial model applied to emotion dysregulation in autism : A narrative review of the literature and an illustrative case conceptualization. Frontiers in Psychiatry, 14, 1238116. https://doi.org/10.3389/fpsyt.2023.1238116
Bertschy, G., Martz, E., Weibel, S., & Weiner, L. (2023). Psychopathological Dissection of Bipolar Disorder and ADHD : Focussing on Racing Thoughts and Verbal Fluency. Neuropsychiatric Disease and Treatment, 19, 1153‑1168. https://doi.org/10.2147/NDT.S401330
Bureau, R., & Clément, C. (2023). “Survival classes for a neurotypical world” : What French autistic adults want and need after receiving an autism diagnosis. Autism, 13623613231183071. https://doi.org/10.1177/13623613231183071
Bureau, R., Riebel, M., Weiner, L., Coutelle, R., Dachez, J., & Clément, C. (2023). French Validation of the Camouflaging Autistic Traits Questionnaire (CAT-Q). Journal of Autism and Developmental Disorders. https://doi.org/10.1007/s10803-023-06048-w
Burger, P., Colin, F., Strehle, A., Mazzucotelli, T., Collot, N., Coutelle, R., Durand, B., Bouman, A., Landau Prat, D., Kleefstra, T., Parrend, P., Piton, A., Koolen, D. A., & Mandel, J.-L. (2023). GenIDA : An international participatory database to gain knowledge on health issues related to genetic forms of neurodevelopmental disorders. Journal of Neural Transmission, 130(3), 459‑471. https://doi.org/10.1007/s00702-022-02569-3
Courraud, J., Engel, C., Quartier, A., Drouot, N., Houessou, U., Plassard, D., Sorlin, A., Brischoux-Boucher, E., Gouy, E., Van Maldergem, L., Rossi, M., Lesca, G., Edery, P., Putoux, A., Bilan, F., Gilbert-Dussardier, B., Atallah, I., Kalscheuer, V. M., Mandel, J.-L., & Piton, A. (2023). Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome. Molecular Psychiatry. https://doi.org/10.1038/s41380-023-02323-5
Coutelle, R., Coulon, N., Schröder, C. M., & Putois, O. (2023). Investigating the borders of autism spectrum disorder : Lessons from the former diagnosis of pervasive developmental disorder not otherwise specified. Frontiers in Psychiatry, 14, 1149580. https://doi.org/10.3389/fpsyt.2023.1149580
Derguy, C., Aubé, B., Rohmer, O., & Loyal, D. (2023). Evaluation of teachers’ knowledge and attitudes regarding the school inclusion of autistic children : Validation of a brief assessment toolkit. British Journal of Educational Psychology, 93(2), 467‑481. https://doi.org/10.1111/bjep.12569
Dubreucq, J., Coutelle, R., Lajnef, M., Godin, O., Amestoy, A., Atzori, P., Baleyte, J.-M., Bonnot, O., Bouvard, M., Coulon, N., Fonseca, D. D., Demily, C., Delorme, R., Fabrowski, M., Givaudan, M., Gollier-Briant, F., Guenolé, F., Humeau, E., Leignier, S., … Speranza, M. (2023). Gender differences in psychosocial function and self-reported health status in late-diagnosed autistic adults : Results from the FACE-ASD national cohort. Psychological Medicine, 53(12), 5674‑5684. https://doi.org/10.1017/S0033291722002902
Durpoix, A., Lachaux, E., Weiner, L., & Weibel, S. (2023). Transdiagnostic skills training group of dialectical behavior therapy : A long-term naturalistic study. Borderline Personality Disorder and Emotion Dysregulation, 10, 37. https://doi.org/10.1186/s40479-023-00243-y
Ellul, P., Maruani, A., Vantalon, V., Humeau, E., Amestoy, A., Anchordoqui, A., Atzori, P., Baleyte, J.-M., Benmansour, S., Bonnot, O., Bouvard, M., Cartigny, A., Coulon, N., Coutelle, R., Da Fonseca, D., Demily, C., Givaudan, M., Gollier-Briant, F., Guénolé, F., … Delorme, R. (2023). Maternal immune activation during pregnancy is associated with more difficulties in socio-adaptive behaviors in autism spectrum disorder. Scientific Reports, 13(1), 17687. https://doi.org/10.1038/s41598-023-45060-z
Granjon, M., Doignon-Camus, N., Popa-Roch, M., & Rohmer, O. (2023). Neural empathic response to disability : An ERP study of prejudice. Biological Psychology, 177, 108507. https://doi.org/10.1016/j.biopsycho.2023.108507
Gustin, M.-P., Putois, B., Guyon, A., Lecendreux, M., Challamel, M.-J., Plancoulaine, S., Bioulac-Rogier, S., Schroder, C., Royant-Parola, S., Huguelet, S., & Franco, P. (2023). French Sleepiness Scale for Adolescents-8 items : A discriminant and diagnostic validation. L’Encéphale, 49(2), 109‑116. https://doi.org/10.1016/j.encep.2022.06.004
Hamaoui, J., Stefaniak, N., & Segond, H. (2023). The influence of vestibular system and fetal presentation on handedness, cognitive and motor development : A comparison between cephalic and breech presentation. Developmental Science, 26(3), e13317. https://doi.org/10.1111/desc.13317
Hinault, T., D’Argembeau, A., Bowler, D. M., La Corte, V., Desaunay, P., Provasi, J., Platel, H., Tran The, J., Charretier, L., Giersch, A., & Droit-Volet, S. (2023). Time processing in neurological and psychiatric conditions. Neuroscience & Biobehavioral Reviews, 154, 105430. https://doi.org/10.1016/j.neubiorev.2023.105430
Husson, T., Lecoquierre, F., Nicolas, G., Richard, A.-C., Afenjar, A., Audebert-Bellanger, S., Badens, C., Bilan, F., Bizaoui, V., Boland, A., Bonnet-Dupeyron, M.-N., Brischoux-Boucher, E., Bonnet, C., Bournez, M., Boute, O., Brunelle, P., Caumes, R., Charles, P., Chassaing, N., … Charbonnier, C. (2023). Episignatures in practice : Independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders. European Journal of Human Genetics: EJHG. https://doi.org/10.1038/s41431-023-01474-x
Kretz, P. F., Wagner, C., Mikhaleva, A., Montillot, C., Hugel, S., Morella, I., Kannan, M., Fischer, M.-C., Milhau, M., Yalcin, I., Brambilla, R., Selloum, M., Herault, Y., Reymond, A., Collins, S. C., & Yalcin, B. (2023). Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein. Genome Biology, 24(1), 261. https://doi.org/10.1186/s13059-023-03092-8
Martin Lorenzo, S., Muniz Moreno, M. D. M., Atas, H., Pellen, M., Nalesso, V., Raffelsberger, W., Prevost, G., Lindner, L., Birling, M.-C., Menoret, S., Tesson, L., Negroni, L., Concordet, J.-P., Anegon, I., & Herault, Y. (2023). Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders. Frontiers in Neuroscience, 17, 1148683. https://doi.org/10.3389/fnins.2023.1148683
Martz, E., Weiner, L., Bonnefond, A., & Weibel, S. (2023). Disentangling racing thoughts from mind wandering in adult attention deficit hyperactivity disorder. Frontiers in Psychology, 14, 1166602. https://doi.org/10.3389/fpsyg.2023.1166602
Martz, E., Weiner, L., & Weibel, S. (2023). Identifying different patterns of emotion dysregulation in adult ADHD. Borderline Personality Disorder and Emotion Dysregulation, 10, 28. https://doi.org/10.1186/s40479-023-00235-y
Mollereau, B., Hayflick, S. J., Escalante, R., Mauthe, M., Papandreou, A., Iuso, A., Celle, M., Aniorte, S., Issa, A. R., Lasserre, J. P., Lesca, G., Thobois, S., Burger, P., & Walter, L. (2023). A burning question from the first international BPAN symposium : Is restoration of autophagy a promising therapeutic strategy for BPAN? Autophagy, 19(12), 3234‑3239. https://doi.org/10.1080/15548627.2023.2247314
Oshodi, Y. O., Schroder, C. M., Rohde, L. A., & Fung, D. (2023). Strategic plan of the international association for child and adolescent psychiatry and allied professions (IACAPAP) for 2023-2026. Child and Adolescent Psychiatry and Mental Health, 17(1), 137. https://doi.org/10.1186/s13034-023-00681-0
Palmer, E. E., Pusch, M., Picollo, A., Forwood, C., Nguyen, M. H., Suckow, V., Gibbons, J., Hoff, A., Sigfrid, L., Megarbane, A., Nizon, M., Cogné, B., Beneteau, C., Alkuraya, F. S., Chedrawi, A., Hashem, M. O., Stamberger, H., Weckhuysen, S., Vanlander, A., … Kalscheuer, V. M. (2023). Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition. Molecular Psychiatry, 28(2), 668‑697. https://doi.org/10.1038/s41380-022-01852-9
Potretzke, S., Zhang, Y., Li, J., Fecteau, K. M., Erikson, D. W., Hibert, M., & Ryabinin, A. E. (2023). Male-selective effects of oxytocin agonism on alcohol intake : Behavioral assessment in socially housed prairie voles and involvement of RAGE. Neuropsychopharmacology, 48(6), 920‑928. https://doi.org/10.1038/s41386-022-01490-3
Riebel, M., Rohmer, O., Charles, E., Lefebvre, F., Weibel, S., & Weiner, L. (2023). Compassion-focused therapy (CFT) for the reduction of the self-stigma of mental disorders : The COMpassion for Psychiatric disorders, Autism and Self-Stigma (COMPASS) study protocol for a randomized controlled study. Trials, 24, 393. https://doi.org/10.1186/s13063-023-07393-y
Rinaldi, B., Bayat, A., Zachariassen, L. G., Sun, J.-H., Ge, Y.-H., Zhao, D., Bonde, K., Madsen, L. H., Awad, I. A. A., Bagiran, D., Sbeih, A., Shah, S. M., El-Sayed, S., Lyngby, S. M., Pedersen, M. G., Stenum-Berg, C., Walker, L. C., Krey, I., Delahaye-Duriez, A., … Kristensen, A. S. (2023). Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes. Brain: A Journal of Neurology, awad403. https://doi.org/10.1093/brain/awad403
Rusu, A., Chevalier, C., de Chaumont, F., Nalesso, V., Brault, V., Hérault, Y., & Ey, E. (2023). Day-to-day spontaneous social behaviours is quantitatively and qualitatively affected in a 16p11.2 deletion mouse model. Frontiers in Behavioral Neuroscience, 17, 1294558. https://doi.org/10.3389/fnbeh.2023.1294558
Shalev, D., Koolen, D. A., de Vries, B. B. A., Blum Meirovitch, S., Mandel, J.-L., Burger, P., Rosenfeld, A., Ben Simon, G. J., & Landau Prat, D. (2023). Ocular manifestations in Koolen–de Vries syndrome : An international study. Canadian Journal of Ophthalmology. https://doi.org/10.1016/j.jcjo.2023.11.021
Stanczak, A., Aelenei, C., Pironom, J., Toczek-Capelle, M.-C., Rohmer, O., & Jury, M. (2023). Can students with special educational needs overcome the “success” expectations? Social Psychology of Education. https://doi.org/10.1007/s11218-023-09806-x
Vazeux, M., Le Nail, P., & Doignon-Camus, N. (2023). Short report on a syllable-based intervention to improve phonemic awareness and reading in children with DLD. Research in Developmental Disabilities, 135, 104455. https://doi.org/10.1016/j.ridd.2023.104455
Walter, A., Martz, E., Weibel, S., & Weiner, L. (2023). Tackling emotional processing in adults with attention deficit hyperactivity disorder and attention deficit hyperactivity disorder + autism spectrum disorder using emotional and action verbal fluency tasks. Frontiers in Psychiatry, 14, 1098210. https://doi.org/10.3389/fpsyt.2023.1098210
Yang, Y., Booker, S. A., Clegg, J. M., Quintana-Urzainqui, I., Sumera, A., Kozic, Z., Dando, O., Martin Lorenzo, S., Herault, Y., Kind, P. C., Price, D. J., & Pratt, T. (2023). Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion. BMC Neuroscience, 24(1), 5. https://doi.org/10.1186/s12868-022-00771-3
Bemmouna, D., Coutelle, R., Weibel, S., & Weiner, L. (2022). Feasibility, Acceptability and Preliminary Efficacy of Dialectical Behavior Therapy for Autistic Adults without Intellectual Disability : A Mixed Methods Study. Journal of Autism and Developmental Disorders, 52(10), 4337‑4354. https://doi.org/10.1007/s10803-021-05317-w
Bemmouna, D., Weibel, S., Kosel, M., Hasler, R., Weiner, L., & Perroud, N. (2022). The utility of the autism-spectrum quotient to screen for autism spectrum disorder in adults with attention deficit/hyperactivity disorder. Psychiatry Research, 312, 114580. https://doi.org/10.1016/j.psychres.2022.114580
Cheviet, A., Bonnefond, A., Bertrand, F., Maumy-Bertrand, M., & Doignon-Camus, N. (2022). How visual attention span and phonological skills contribute to N170 print tuning : An EEG study in French dyslexic students. Brain and Language, 234, 105176. https://doi.org/10.1016/j.bandl.2022.105176
Raïssa-Marie Chevrota et Carmen M Schroder (2022a, mai 2). Décryptages et recommandations sur le sommeil des enfants et des adolescents. EM-Consulte. https://www.em-consulte.com/article/1399186/alertePM
Coursimault, J., Guerrot, A.-M., Morrow, M. M., Schramm, C., Zamora, F. M., Shanmugham, A., Liu, S., Zou, F., Bilan, F., Le Guyader, G., Bruel, A.-L., Denommé-Pichon, A.-S., Faivre, L., Tran Mau-Them, F., Tessarech, M., Colin, E., El Chehadeh, S., Gérard, B., Schaefer, E., … Lecoquierre, F. (2022). MYT1L-associated neurodevelopmental disorder : Description of 40 new cases and literature review of clinical and molecular aspects. Human Genetics, 141(1), 65‑80. https://doi.org/10.1007/s00439-021-02383-z
Coutelle, R., Boedec, M., Vermeulen, K., Kummeling, J., Koolen, D. A., Kleefstra, T., Fournier, C., Colin, F., Strehle, A., Geneviève, D., Burger, P., & Mandel, J.-L. (2022). The impact of lockdown on young people with genetic neurodevelopmental disabilities : A study with the international participatory database GenIDA. BMC Psychiatry, 22, 572. https://doi.org/10.1186/s12888-022-04213-6
Durand, B., Schaefer, E., Burger, P., Baer, S., Schroder, C., Mandel, J.-L., Piton, A., & Coutelle, R. (2022). Neurocognitive and neurobehavioral characterization of two frequent forms of neurodevelopmental disorders : The DYRK1A and the Wiedemann–Steiner syndromes. Clinical Genetics, 102(4), 296‑304. https://doi.org/10.1111/cge.14190
Eguida, M., Schmitt-Valencia, C., Hibert, M., Villa, P., & Rognan, D. (2022). Target-Focused Library Design by Pocket-Applied Computer Vision and Fragment Deep Generative Linking. Journal of Medicinal Chemistry, 65(20), 13771‑13783. https://doi.org/10.1021/acs.jmedchem.2c00931
El Chehadeh, S., Han, K. A., Kim, D., Jang, G., Bakhtiari, S., Lim, D., Kim, H. Y., Kim, J., Kim, H., Wynn, J., Chung, W. K., Vitiello, G., Cutcutache, I., Page, M., Gecz, J., Harper, K., Han, A., Kim, H. M., Wessels, M., … Um, J. W. (2022). SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice. Nature Communications, 13, 4112. https://doi.org/10.1038/s41467-022-31566-z
Gavens, N., Doignon-Camus, N., Chaillou, A.-C., Zeitler, A., & Popa-Roch, M. (2022). Effectiveness of mind mapping for learning in a real educational setting. The Journal of Experimental Education, 90(1), Article 1. https://doi.org/10.1080/00220973.2020.1848765
Graff, I., Juhl, G., & Clément, C. (2022). Fondements et contenus d’un programme de psycho-éducation à destination des parents d’enfants présentant un Trouble Développemental du Langage : « Agir pour communiquer avec mon enfant. Comprendre le trouble développemental du langage ». Revue de psychoéducation, 51(1), Article 1. https://doi.org/10.7202/1088627ar
Hibert, M. (2022). [Oxytocin and its receptor : Molecular and therapeutic approaches]. Biologie Aujourd’hui, 216(3‑4), 125‑130. https://doi.org/10.1051/jbio/2022013
Kayumi, S., Pérez-Jurado, L. A., Palomares, M., Rangu, S., Sheppard, S. E., Chung, W. K., Kruer, M. C., Kharbanda, M., Amor, D. J., McGillivray, G., Cohen, J. S., García-Miñaúr, S., van Eyk, C. L., Harper, K., Jolly, L. A., Webber, D. L., Barnett, C. P., Santos-Simarro, F., Pacio-Míguez, M., … Corbett, M. A. (2022). Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants. Genetics in medicine : official journal of the American College of Medical Genetics, 24(11), 2351‑2366. https://doi.org/10.1016/j.gim.2022.08.006
L Leclair-Visonneau, M-F Vecchierini, C Schröder, C Charley Monaca (2022c, mai 2). French Consensus : How to diagnose restless legs syndrome. EM-Consulte. https://www.em-consulte.com/article/1238279/alertePM
L Leclair-Visonneau, M-F Vecchierini, C Schröder, C Charley Monaca (2022b, mai 2). Erratum to “French Consensus : How to diagnose restless legs syndrome” [Rev. Neurol. 174 (7–8) (2018) 508–14]. EM-Consulte. https://www.em-consulte.com/article/1260989/alertePM
Leitão, E., Schröder, C., Parenti, I., Dalle, C., Rastetter, A., Kühnel, T., Kuechler, A., Kaya, S., Gérard, B., Schaefer, E., Nava, C., Drouot, N., Engel, C., Piard, J., Duban-Bedu, B., Villard, L., Stegmann, A. P. A., Vanhoutte, E. K., Verdonschot, J. A. J., … Depienne, C. (2022). Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X. Nature Communications, 13, 6570. https://doi.org/10.1038/s41467-022-34264-y
N. Limousin, M. Flamand, C. Schröder, d , C. Charley Monaca, ⁎ (2022d, mai 2). French consensus : Treatment of newly diagnosed restless legs syndrome. EM-Consulte. https://www.em-consulte.com/article/1238280/alertePM
Maillard, P.-Y., Baer, S., Schaefer, É., Desnous, B., Villeneuve, N., Lépine, A., Fabre, A., Lacoste, C., El Chehadeh, S., Piton, A., Porter, L. F., Perriard, C., Wardé, M.-T. A., Spitz, M.-A., Laugel, V., Lesca, G., Putoux, A., Ville, D., Mignot, C., … Milh, M. (2022). Molecular and clinical descriptions of patients with GABAA receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2) : A cohort study, review of literature, and genotype-phenotype correlation. Epilepsia, 63(10), 2519‑2533. https://doi.org/10.1111/epi.17336
Martz, E., Weibel, S., & Weiner, L. (2022). An overactive mind : Investigating racing thoughts in ADHD, hypomania and comorbid ADHD and bipolar disorder via verbal fluency tasks. Journal of Affective Disorders, 300, 226‑234. https://doi.org/10.1016/j.jad.2021.12.060
Mary, L., Nourisson, E., Feger, C., Laugel, V., Chaigne, D., Keren, B., Afenjar, A., Billette, T., Trost, D., Cieuta-Walti, C., Gerard, B., Piton, A., & Schaefer, E. (2021). Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy : Broadening the phenotypic spectrum of a potassium channelopathy. American Journal of Medical Genetics. Part A, 185(6), 1803‑1815. https://doi.org/10.1002/ajmg.a.62181
Meziane, H., Birling, M.-C., Wendling, O., Leblanc, S., Dubos, A., Selloum, M., Pavlovic, G., Sorg, T., Kalscheuer, V. M., Billuart, P., Laumonnier, F., Chelly, J., van Bokhoven, H., & Herault, Y. (2022). Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models. Biomedicines, 10(12), 3148. https://doi.org/10.3390/biomedicines10123148
Mucca, M. A., Patat, O., Whalen, S., Arnaud, L., Barcia, G., Buratti, J., Cogné, B., Doummar, D., Karsenty, C., Kenis, S., Leguern, E., Lesca, G., Nava, C., Nizon, M., Piton, A., Valence, S., Villard, L., Weckhuysen, S., Keren, B., & Mignot, C. (2022). Patients with KCNH1-related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome. Journal of Medical Genetics, 59(5), Article 5. https://doi.org/10.1136/jmedgenet-2020-107511
Parenti, I., Leitão, E., Kuechler, A., Villard, L., Goizet, C., Courdier, C., Bayat, A., Rossi, A., Julia, S., Bruel, A.-L., Tran Mau-Them, F., Nambot, S., Lehalle, D., Willems, M., Lespinasse, J., Ghoumid, J., Caumes, R., Smol, T., El Chehadeh, S., … Depienne, C. (2022). The different clinical facets of SYN1-related neurodevelopmental disorders. Frontiers in Cell and Developmental Biology, 10, 1019715. https://doi.org/10.3389/fcell.2022.1019715
Quenneville, A. F., Kalogeropoulou, E., Nicastro, R., Weibel, S., Chanut, F., & Perroud, N. (2022). Anxiety disorders in adult ADHD : A frequent comorbidity and a risk factor for externalizing problems. Psychiatry Research, 310, 114423. https://doi.org/10.1016/j.psychres.2022.114423
Reynaud, E., Pottelette, J., Rabot, J., Rolling, J., Royant-Parola, S., Hartley, S., Coutelle, R., & Schröder, C. M. (2022). Differential effects of COVID-related lockdown on sleep–wake rhythms in adults with autism spectrum disorder compared to the general population. Autism Research, n/a(n/a), Article n/a. https://doi.org/10.1002/aur.2692
Richter, M., Clément, C., & Flavier, E. (2022). Is transition an (adult) problem? – Experiences of autistic students during the transition from primary to secondary school. Journal of Research in Special Educational Needs, 22(4), 368‑379. https://doi.org/10.1111/1471-3802.12574
Riet, F., Mittelhaeuser, C., Lux, A., Bour, R., Selloum, M., Sorg, T., Herault, Y., & Meziane, H. (2022). Behavioral Testing Design for Evaluation of Cognitive Disabilities. Current Protocols, 2(2), e382. https://doi.org/10.1002/cpz1.382
Rohmer, O., Doignon-Camus, N., Audusseau, J., Trautmann, S., Chaillou, A.-C., & Popa-Roch, M. (2022). Removing the academic framing in student evaluations improves achievement in children with dyslexia : The mediating role of self-judgement of competence. Dyslexia, 28(3), 309‑324. https://doi.org/10.1002/dys.1713
Rolling, J., Corduan, G., Roth, M., Schroder, C. M., & Mengin, A. C. (2022). Violent Radicalization and Post-traumatic Dissociation : Clinical Case of a Young Adolescent Girl Radicalized. Frontiers in Psychiatry, 13, 793291. https://doi.org/10.3389/fpsyt.2022.793291
Rolling, J., Rabot, J., & Schroder, C. M. (2022). Melatonin Treatment for Pediatric Patients with Insomnia : Is There a Place for It? Nature and Science of Sleep, 14, 1927‑1944. https://doi.org/10.2147/NSS.S340944
Scala, M., Drouot, N., MacLennan, S. C., Wessels, M. W., Krygier, M., Pavinato, L., Telegrafi, A., de Man, S. A., van Slegtenhorst, M., Iacomino, M., Madia, F., Scudieri, P., Uva, P., Giacomini, T., Nobile, G., Mancardi, M. M., Balagura, G., Galloni, G. B., Verrotti, A., … Piton, A. (2022). De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes. Human Mutation, 43(9), 1299‑1313. https://doi.org/10.1002/humu.24414
Schneider, S., Clément, C., Goltzene, M.-A., Meyer, N., Gras-Vincendon, A., Schröder, C. M., & Coutelle, R. (2022). Determinants of the evolutions of behaviours, school adjustment and quality of life in autistic children in an adapted school setting : An exploratory study with the International Classification of Functioning, disability and health (ICF). BMC Psychiatry, 22, 323. https://doi.org/10.1186/s12888-022-03924-0
Schröder, C. M., Broquère, M. A., Claustrat, B., Delorme, R., Franco, P., Lecendreux, M., & Tordjman, S. (2022). Approches thérapeutiques des troubles du sommeil et des rythmes chez l’enfant avec TSA. L’Encéphale, 48(3), 294‑303. https://doi.org/10.1016/j.encep.2021.08.005
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