Unité de psychologie clinique des situations de handicap

Publications

Contributions originales publiées dans des journaux à politique éditoriale

2020

Schneider, M., Myin, E., & Myin-Germeys, I. (in press). Is theory of mind a prerequisite for social interactions? A study in psychotic disorder. Psychological Medicine. IF: 5.641.

Mancini, V., Sandini, C., Padula, M.C., Zöller, D., Schneider, M., Schaer, M., & Eliez, S. (in press). Positive psychotic symptoms are associated with divergent developmental trajectories of hippocampal volume during late adolescence in patients with 22q11DS. Molecular Psychiatry. IF: 11.973.

Armando, M., Ciampoli, M., Padula, M.C., Amminger, P., De Crescenzo, F., Maeder, J., Schneider, M., Schaer, M., Managò, F., Eliez, S., & Papaleo, F. (in press). Favorable effects of omega-3 polyunsaturated fatty acids in attentional control and conversion rate to psychosis in 22q11.2 deletion syndrome. Neuropharmacology. IF: 4.249.

Sandini, C., Chambaz, M., Schneider, M., Armando, M., Zöller, D., Schaer, M., Sandi, C., Van de Ville, D., & Eliez, S. (in press). Pituitary dysmaturation affects psychopathology and neurodevelopment in 22q11.2 deletion syndrome. Psychoneuroendocrinology. IF: 4.013.

Cleynen, I., Engchuan, W., Hestand, M.S., Heung, T., Holleman, A.M., Johnston, H.R., Monfeuga, T., McDonald-McGinn, D.M., Gur, R.E., Morrow, B.E., Swillen, A., Vorstman, J.A.S., Bearden, C.E., Chow, E.W.C., van den Bree, M., Emanuel, B.S., Vermeesch, J.R., Warren, S.T., Owen, M.J., Chopra, P., Cutler, D.J., Duncan, R., Kotlar, A.V., Mulle, J.G., Voss, A.J., Zwick, M.E., Diacou, A., Golden, A., Guo, T., Lin, J.R., Wang, T., Zhang, Z., Zhao, Y., Marshall, C., Merico, D., Jin, A., Lilley, B., Salmons, H.I., Tran, O., Holmans, P., Pardinas, A., Walters, J.T.R., Demaerel, W., Boot, E., Butcher, N.J., Costain, G.A., Lowther, C., Evers, R., van Amelsvoort, T.A.M.J., van Duin, E., Vingerhoets, C., Breckpot, J., Devriendt, K., Vergaelen, E., Vogels, A., Crowley, T.B., McGinn, D.E., Moss, E.M., Sharkus, R.J., Unolt, M., Zackai, E.H., Calkins, M.E., Gallagher, R.S., Gur, R.C., Tang, S.X., Fritsch, R., Ornstein, C., Repetto, G.M., Breetvelt, E., Duijff, S.N., Fiksinski, A., Moss, H., Niarchou, M., Murphy, K.C., Prasad, S.E., Daly, E.M., Gudbrandsen, M., Murphy, C.M., Murphy, D.G., Buzzanca, A., Fabio, F.D., Digilio, M.C., Pontillo, M., Marino, B., Vicari, S., Coleman, K., Cubells, J.F., Ousley, O.Y., Carmel, M., Gothelf, D., Mekori-Domachevsky, E., Michaelovsky, E., Weinberger, R., Weizman, A., Kushan, L., Jalbrzikowski, M., Armando, M., Eliez, S., Sandini, C., Schneider, M., Béna, F.S., Antshel, K.M., Fremont, W., Kates, W.R., Belzeaux, R., Busa, T., Philip, N., Campbell, L.E., McCabe, K.L., Hooper, S.R., Schoch, K., Shashi, V., Simon, T.J., Tassone, F., Arango, C., Fraguas, D., García-Miñaúr, S., Morey-Canyelles, J., Rosell, J., Suñer, D.H., Raventos-Simic, J., International 22q11.2DS Brain and Behavior Consortium, Epstein, M.P., Williams, N.M., & Bassett, A.S. (in press). Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry. IF: 11.973.

Zhao, Y., Diacou, A., Johnston, H.R., Musfee, F.I., McDonald-McGinn, D.M., McGinn, D., Crowley, T.B., Repetto, G.M., Swillen, A., Breckpot, J., Vermeesch, J.R., Kates, W.R., Digilio, M.C., Unolt, M., Marino, B., Pontillo, M., Armando, M., Di Fabio, F., Vicari, S., van den Bree, M., Moss, H., Owen, M.J., Murphy, K.C., Murphy, C.M., Murphy, D., Schoch, K., Shashi, V., Tassone, F., Simon, T.J., Shprintzen, R.J., Campbell, L., Philip, N., Heine-Suñer, D., García-Miñaúr, S., Fernández, L., International 22q11.2 Brain and Behavior Consortium, Bearden, C.E., Vingerhoets, C., van Amelsvoort, T., Eliez, S., Schneider, M., Vorstman, J.A.S., Gothelf, D., Zackai, E., Agopian, A.J., Gur, R.E., Bassett, A.S., Emanuel, B.S., Goldmuntz, E., Mitchell, L.E., Wang, T., & Morrow, B.E. (2020). Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects. American Journal of Human Genetics 106(1), 26-40. IF: 9.924.

Dubourg, L., Maeder, J., Pouillard, V., Eliez, S., & Schneider, M. (2020). Goal-directed behavior in 22q11.2 deletion syndrome: implication for social dysfunctions and the emergence of negative symptoms. Frontiers in Psychiatry 11, 230. IF: 3.36.

Maeder, J., Sandini, C., Zöller, D., Schneider, M., Bostelmann, M., Pouillard, V., Caroni, P., Kliegel, M., & Eliez, S. (2020). Long-term verbal memory deficit and associated hippocampal alterations in 22q11.2 deletion syndrome. Child Neuropsychology 26(3), 289-231. IF: 2.577.

2019

Schneider, M.F, Armando, M.F, Schultze-Lutter, F., Pontillo, M., Vicari, S., Debbané, M., & Eliez, S. (2019). Prevalence, course and psychosis-predictive value of negative symptoms in 22q11.2 deletion syndrome. Schizophrenia Research 206, 286-293. IF: 4.080.
Findicates shared first authorship.

Cantonas, L.M., Tomescu, M.I., Biria, M., Jan, R.K., Schneider, M., Eliez, S., Rihs, T.A., & Michel, C.M. (2019). Abnormal development of early auditory processing in 22q11.2 deletion syndrome. Translational Psychiatry 9(1), 138. IF: 4.691.

Dubourg, L., Vrticka, P., Pouillard, V., Eliez, S., & Schneider, M. (2019). Divergent default mode network connectivity during social perception in 22q11.2 deletion syndrome. Psychiatry Research: Neuroimaging 291, 9-17. IF: 2.270.

Niarchou, M., Chawner, S.J.R.A., Fiksinski, A., Vorstman, J.A.S., Maeder, J., Schneider, M., Eliez, S., Armando, M., Pontillo, M., Vicari, S., McDonald-McGinn, D.M., Emanuel, B.S., Zackai, E.H., Bearden, C.E., Shashi, V., Hooper, S.R., Owen, M.J., Gur, R.E., Wray, N.R., van den Bree, M.B.M., & Thapar, A. for the International 22q11.2 Deletion Syndrome Brain and Behavior Consortium. (2019). Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome. Schizophrenia Research 204, 320-325. IF: 4.080.

Mosheva, M., Pouillard, V., Fishman, Y., Dubourg, L., Sofrin-Frumer, D., Serur, Y., Weizman, A., Eliez, S., Gothelf, D., & Schneider, M. (2019). Education and employment trajectories from childhood to adulthood in individuals with 22q11.2 deletion syndrome. European Child and Adolescent Psychiatry 28(1), 31-42. IF: 3.339.

2018

Zhao, Y., Guo, T., Fiksinski, A., Breetvelt, E., McDonald-McGinn, D.M., Crowley, T.B., Diacou, A., Schneider, M., Eliez, S., Swillen, A., Breckpot, J., Vermeesch, J., Chow, E.W.C., Gothelf, D., Duijff, S., Evers, R., van Amelsvoort, T.A., van den Bree, M., Owen, M., Niarchou, M., Bearden, C.E., Ornstein, C., Pontillo, M., Buzzanca, A., Vicari, S., Armando, M., Murphy, K.C., Murphy, C., Garcia-Minaur, S., Philip, N., Campbell, L., Morey-Cañellas, J., Raventos, J., Rosell, J., Heine-Suner, D., Shprintzen, R.J., Gur, R.E., Zackai, E., Emanuel, B.S., Wang, T., Kates, W.R., Bassett, A.S., Vorstman, J.A.S., & Morrow, B.E. for the International 22q11.2 Brain and Behavior Consortium. (2018). Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American Journal of Medical Genetics Part A 176(10), 2172-2181. IF: 2.264.

Zaharia, A., Schneider, M., Glaser, B., Franchini, M., Menghetti, S., Schaer, M., Debbané, M., & Eliez, S. (2018). Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations. Journal of Neurodevelopmental Disorders 10(1), 26. IF: 3.582.

Sandini, C., Zöller, D., Scariati, E., Padula, M.C., Schneider, M., Schaer, M., Van de Ville, D., & Eliez, S. (2018). Development of structural covariance from childhood to adolescence : a longitudinal study in 22q11.2DS. Frontiers in Neuroscience 12, 327. IF: 4.014.

Sandini, C., Scariati, E., Padula, M.C., Schneider, M., Schaer, M., Van de Ville, D., & Eliet, S. (2018). Cortical dysconnectivity measured by structural covariance is associated with the presence of psychotic symptoms in 22q11.2 deletion syndrome. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging 3(5), 433-442.

Armando, Sandini, Chambaz, M., Schaer, M., Schneider, M.F, & Eliez, S.F (2018). Coping strategies mediate the effect of stressful life events and schizotypal traits and psychotic symptoms in 22q11.2 deletion syndrome. Schizophrenia Bulletin 15(44 suppl_2), S525-S535. IF: 7.575.
F indicates shared last authorship

Glaser, B., Eliez, S., Chomelkery, H., Freitag, C., & Schneider, M. (2018). Online social skills group training for adolescents and young adults with 22q11.2 deletion syndrome (22q11.2DS). Journal of Behavioral and Brain Science 8, 126-145.

Padula, M.C., Schaer, M., Armando, M., Sandini, C., Zöller, D., Scariati, E., Schneider, M., & Eliez, S. (2018). Cortical morphology development in patients with 22q11.2 deletion syndrome at ultra-high risk of psychosis. Psychological Medicine 48(14), 2375-2383. IF: 5.23.

Souchay, C., Dubourg, L., Ballhausen, N., Schneider, M., Cerf, C., Schnitzpahn, K., Faivre, L., Kliegel, M., & Eliez, S. (2018). Time-based prospective memory in children and adolescents with 22q11.2 deletion syndrome. The Clinical Neuropsychologist 32(5), 981-992. IF: 1.564.

Dubourg, L., Vrticka, P., Debbané, M., Chambaz, L., Eliez, S. & Schneider, M. (2018). Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders 10(1), 13. IF: 3.582.

Leendertse, P., Myin-Germeys, I., Lataster, T., Simons, C.J.P., Oorschot, M., Lardinois, M., Schneider, M., van Os, J., Reininghaus, U. For Genetic Risk and Outcome of Psychosis (GROUP) investigators. Psychiatry Research 261, 116-123. IF : 2.528.

Guo, T., Diacou, A., Nomaru, H., McDonald-McGinn, D.M., Hestand, M., Demaerel, W., Zhang, L., Zhao, Y., Ujueta, F., Shan, J., Montagna, C., Zheng, D., Crowley, T.B., Kushan-Wells, L., Bearden, C.E., Kates, W.R., Gothelf, D., Schneider, M., Eliez, S., Breckpot, J., Swillen, A., Vorstman, J., Zackai, E., Benavides Gonzalez, F., Repetto, G.M., Emanuel, B.S., Bassett, A.S., Vermeesch, J.R., Marshall, C.R., Morrow, B.E., International 22q11.2 Brain and Behavior Consortium. (2018). Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2. Human Molecular Genetics 27(7), 1150-1163. IF: 5.340.

Zöller, D., Padula, M.C., Sandini, C., Schneider, M., Scariati, E., Van de Ville, D., Schaer, M., & Eliez, S. (2018). Psychotic symptoms influence the development of anterior cingulate BOLD variability in 22q11.2 deletion syndrome. Schizophrenia Research 193, 319-328. IF: 3.986.

2017

Biria, M., Tomescu, M.I., Custo, A., Cantonas, L.M., Song, K.W., Schneider, M., Murray, M.M., Eliez, S., Michel, C.M., & Rihs, R.A. (2017). Visual processing deficits in 22q11.2 deletion syndrome. Neuroimage: Clinical 17, 976-986. IF: 4.348.

Padula, M.C., Scariati, E., Schaer, M., Sandini, C., Ottet, M.C., Schneider, M., Van de Ville, D., & Eliez, S. (2017). Altered structural network architecture is predictive of the presence of psychotic symptoms in patients with 22q11.2 deletion syndrome. Neuroimage Clinical 16, 142-150. IF: 4.348.

Mihailov, A., Padula, M.C., Scariati, E., Schaer, M., Schneider, M., & Eliez, S. (2017). Morphological brain changes associated with negative symptoms in patients with 22q11.2 deletion syndrome. Schizophrenia Research 188, 52-58. IF: 4.453.

Bassett, A.S., Lowther, C., Merico, D., Costain, G., Chow, E.W.C., van Amelsvoort, T., McDonald-McGinn, D., Gur, R.E., Swillen, A., Van den Bree, M., Murphy, K., Gothelf, D., Bearden, C.E., Eliez, S., Kates, W., Philip, N., Shashi, V., Campbell, L., Vorstman, J., Cubells, J., Repetto, G.M., Simon, T., Boot, E., Heung, T., Evers, R., Vingerhoets, C. van Duin, E., Zackai, E., Vergaelen, E., Devriendt, K., Vermeesch, J.R., Owen, M., Murphy, C., Michaelovsky, E., Kushan, L., Schneider, M., Fremont, W., Busa, T., Hooper, S., McCabe, K., Duijff, S., Isaev, K., Pellecchia, G., Wei, J., Gazzellone, M.J., Scherer, S.W., Emanuel, B.S., Guo, T., Morrow, B.E., Marshall, C.R., & the International 22q11.2DS Brain and Behavior Consortium. (2017). Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome. American Journal of Psychiatry 174(11), 1054-1063. IF: 14.176.

Bostelmann, M., Glaser, B., Zaharia, A., Eliez, S., & Schneider, M. (2017). Does differential visual exploration contribute to visual memory impairments in 22q11.2 microdeletion syndrome? Journal of Intellectual Disability Research 61(12), 1174-1184. IF: 1.99.

Padula, M.C., Schaer, M., Scariati, E., Mutlu, A.K., Zöller, D., Schneider, M., & Eliez, S. (2017). Quantifying indices of short and long-range white matter connectivity at each cortical vertex. Plos One 12(11), e0187493. IF: 3.54.

Guo, T., Repetto, G.Mm, McDonald McGinn, D.M., Chung, J.H., Nomaru, H., Campbell, C.L., Blonska, A., Bassett, A.S., Chow, E.W.C., Mlynarski, E.E., Swillen, A., Vermeesch, J., Devriendt, K., Gothelf, D., Carmel, M., Michaelovsky, E., Schneider, M., Eliez ,S., Antonarakis, S.E., Coleman, K., Tomita-Mitchell, A., Mitchell, M.E., Digilio, M.C., Dallapiccola, B., Marino, B., Philip, N., Busa, T., Kushan-Wells, L., Bearden, C.E., Piotrowicz, M., Hawuła, W., Roberts, A.E., Tassone, F., Simon, T.J., van Duin, E.D.A., van Amelsvoort, T.A., Kates, W.R., Zackai, E., Johnston, H.R., Cutler, D.J., Agopian, A.J., Goldmuntz, E., Mitchell, L.E., Wang, T., Emanuel, B.S., Morrow, B.E. & International 22q11.2 Consortium/Brain and Behavior Consortium (2017). Genome-wide association study to find modifiers for tetralogy of fallot in 22q11.2 deletion syndrome identifies cariants in the GPR98 locus on 5q14.3. Circulation: Cardiovascular Genetics 10(5), e001690. IF: 4.743.

Badoud, D.F, Schneider, M.F, Menghetti, S., Glaser, B., Debbané, M., & Eliez, S. (2017). Understanding others: a pilot investigation of cognitive and affective facets of social cognition in patients with 22q11.2 deletion syndrome (22q11DS). Journal of Neurodevelopmental Disorders 9(1):35. IF : 2.787.
F  indicates shared first authorship

Schneider, M., Reininghaus, U., van Nierop, M., Janssens, M., & Myin-Germeys, I. for GROUP (2017). Does the Social Functioning Scale reflect real-life social functioning? An experience sampling study in patients with a non-affective psychotic disorder and healthy control individuals. Psychological Medicine 47(16), 2777-2786. IF: 5.491.

Weisman, O., Guri, Y., Gur, R.E., McDonal-McGinn, D., Calkins, M., Tang, S., Emanuel, B., Zackai, E.H., Eliez, S., Schneider, M., Schaer, M., Kates, W.R., Antshel, K.M., Fremont, W., Shashi, V., Hooper, S.R., Armando, M., Vicari, S., Pontillo, M., Kushan, L., Jalbrzikowski, M., Bearden, C.E., Cubells, J.F., Ousley, O.Y., Walker, E.F., Simon, T.J., Stoddard, J., Niendam, T., van den Bree, M.B.M., & Gothelf, D., for the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. (2017). Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multi-site Naturalistic Study. Schizophrenia Bulletin 43(5), 1079-1089. IF: 7.757.

Sannino, S., Padula, M.C., Manago, F., Schaer, M., Schneider, M., Armando, M., Scariati, E., Sloan-Bena, F., Mereu, M., Pontillo, M., Vicari, S., Contarini, G., Chiabrera, C., Pagani, M., Gozzi, A., Eliez, S., & Papaleo, F. (2017). Adolescence is the starting point of sex-dichotomous COMT genetic effects. Translational Psychiatry 7(5), e1141. IF 5.538

Armando, M.F, Schneider, M.F#, Pontillo, M., Vicari, S., Debbané, M., Schultze-Lutter, F., & Eliez, S. (2017). No age effect in the prevalence and clinical significance of ultra-high risk symptoms and criteria for psychosis in 22q11.2 deletion syndrome: confirmation of the genetically driven risk for psychosis? PLoS One 12(4), e0174797. IF: 4.411
Findicates shared first authorship

Guipponi, M., Santoni, F., Schneider, M., Gehrig, C., Bustillo, X.B., Kates, W., Morrow, B., Armando, M., Shashi, V., Eliez, S., & Antonarakis, S. (2017). No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients. Translational Psychiatry 7(2), e1039. IF: 5.538.

Padula, M.C., Schaer, M., Scariati, E., Maeder, J., Schneider, M., & Eliez, S. (2017). Multimodal investigation of triple network connectivity in patients with 22q11DS and association with executive functions. Human Brain Mapping 38(4), 2177-2189. IF: 4.962.

Dubourg, L., Schneider, M., Padula, M., Chambaz, L., Schaer, M., & Eliez, S. (2017). Implication of reward alterations in the expression of negative symptoms in 22q11.2 deletion syndrome : a behavioural and DTI study. Psychological Medicine 47(8), 1442-1453. IF: 5.491.

Schneider, M., Van der Linden, M., Menghetti, S., Debbané, M., & Eliez, S. (2017). Negative and paranoid symptoms are associated with negative performance beliefs and social cognition in 22q11.2 deletion syndrome. Early Intervention in Psychiatry 11(2), 156-164. IF : 1.653.

2016

Bostelmann, M., Schneider, M., Padula, M.C., Maeder, J., Schaer, M., Scariati, E., Debbané, M., Glaser, B., Menghetti, S., & Eliez, S. (2016). Visual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks assessing ventral and dorsal visual brain structures? A cross-sectional and longitudinal study. Journal of Neurodevelopmental Disorders 8:41. IF : 2.787.

Franchini, M., Schaer, M., Glaser, B., Kott-Radecka, M., Debbané, M., Schneider, M., Menghetti, S., Sander, D., & Eliez, S. (2016). Visual processing of emotional dynamic faces in 22q11.2 deletion syndrome. Journal of Intellectual and Disability Research 60(4), 308-321. IF : 2.07.

Maeder, J., Schneider, M., Bostelmann, M., Debbané, M., Glaser, B., Menghetti, S., Schaer, M., & Eliez, S. (2016). Developmental trajectories of executive functions in 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders 8:10. IF : 2.787.

Schneider, M.F, Armando, M.F, Pontillo, M., Vicari, S., Debbané , M., Schultze-Lutter, F. & Eliez, S. (2016). Ultra high-risk status and transition to psychosis in 22q11.2 deletion syndrome. World Psychiatry 15(3), 259-265. IF : 20.2015.
Findicates shared first authorship

Scariati, E., Schaer, M., Karahanoglu, I., Schneider, M., Richiardi, J., Debbané, M., Van De Ville, D., & Eliez, S. (2016). Large-scale functional network reorganization in 22q11.2 deletion syndrome revealed by modularity analysis. Cortex 82, 86-99. IF : 4.314.

Schneider, M., Eliez, S., Birr, J., Menghetti, S., Debbané, M., & Van der Linden, M. (2016). Multitasking abilities in adolescents with 22q11.2 deletion syndrome: results from an experimental ecological paradigm. American Journal on Intellectual and Developmental Disabilities 121(2), 151-164. IF : 2.08.

Fonseca-Pedrero, E., Debbané, M., Schneider, M., Badoud, D., & Eliez, S. (2016). Schizotypal traits in adolescents with 22q11.2 deletion syndrome : validity, reliability and risk for psychosis. Psychological Medicine 46(5), 1005-1013. IF : 5.491.

2015

Padula, M.C., Schaer, M., Scariati, E., Schneider, M., Van de Ville, D., Debbané, M., & Eliez, S. (2015). Structural and functional connectivity in the default mode network in 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders 7(1):23. IF : 3.27.

Tomescu, M.I., Rihs, T.A., Roinishvili, M., Karahanoglu, F.I., Schneider, M., Menghetti, S., Van de Ville, D., Brand, A., Chkonia, E., Eliez, S., Herzog, M.H., Michel, C.M., & Cappe, C. (2015). Schizophrenia patients and 22q11.2 deletion syndrome adolescents at risk express the same deviant patterns of resting state EEG microstates : a candidate endophenotype of schizophrenia. Schizophrenia Research : cognition 2(3), 159-165.

Vostman, J.A., Breetvelt, E.J., Duijff, S.N., Eliez, S., Schneider, M., Jalbrzikowski, M., Armando, M., Vicari, S., Shashi, V., Hooper, S.R., Chow, E.W., Fung, W.L., Butcher, N.J., Young, D.A., McDonald-McGinn, D.M., Vogels, A., van Amelsvoort, T., Gothelf, D., Weinberger, R., Weizman, A., Klaassen, P.W., Koops, S., Kates, W.E., Antshel, K.M., Simon, T.J., Ousley, O.Y., Swillen, A., Gur, R.E., Bearden, C.E., Kahn, R.S., & Bassett, A.S. (2015). Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome. JAMA Psychiatry 72(4), 377-385. IF : 13.234.

2014

Tomescu, M.I., Rihs, T.A., Becker, R., Britz, J., Custo, A., Grouiller, F., Schneider, M., Debbané, M., Eliez, S., & Michel, C.M. (2014). Deviant dynamics of EEG resting state pattern in 22q11.2 deletion syndrome adolescents : a vulnerability marker of schizophrenia ? Schizophrenia Research 157(1-3), 175-181. IF : 4.426.

Fountain, D.M., Schaer, M., Mutlu, A.K., Schneider, M., Debbané, M., & Eliez, S. (2014). Congenital heart disease is associated with reduced cortical and hippocampal volume in patients with 22q11.2 deletion syndrome. Cortex 57, 128-142. IF : 5.128.

Scariati, E., Schaer, M., Richiardi, J., Schneider, M., Debbané, M., Van de Ville, D., & Eliez, S. Identifying 22q11.2 deletion syndrome and psychosis using resting-state connectivity patterns. Brain Topography 27(6), 808-821. IF : 3.468.

Schneider, M., Van der Linden, M., Menghetti, S., Glaser, B., Debbané, M., & Eliez, S. (2014). Predominant negative symptoms in 22q11.2 deletion syndrome and their associations with cognitive functioning and functional outcome. Journal of Psychiatric Research 48(1), 86-93. IF : 3.957.

Schneider, M., Schaer, M., Multu, K., Menghetti, S., Glaser, B., Debbané, M., & Eliez, S. (2014). Clinical and cognitive risk factors for psychotic symptoms in 22q11.2 deletion syndrome: a transversal and longitudinal approach. European Journal of Child and Adolescent Psychiatry 23(6), 425-436. IF : 3.336.

2013

Gothelf, D., Schneider, M., Green, T., Debbané, M., Frisch, A., Glaser, B., Zilkha, H., Schaer, M., Weizman, A., & Eliez, S. (2013). Risk Factors and the Evolution of Psychosis in 22q11.2 Deletion Syndrome: A Longitudinal Two-Site Study. Journal of the American Academy of Child and Adolescent Psychiatry 52(11), 1192-1203. IF : 7.260.

Dahoun, T., Eliez, S., Chen, F., Badoud, D., Schneider, M., Laroi, F., & Debbané, M. (2013). Action simulation in hallucination-prone adolescents. Frontiers in Human Neuroscience 7, 1-13. IF : 2.628.

Mutlu, A.K., Schneider, M., Debbané, M., Badoud, D., Eliez, S., & Schaer. M. (2013). Sex differences in thickness and folding developments throughout the cortex. NeuroImage 82, 200-207. IF : 6.132.

Ottet, M.-C., Schaer, M., Cammoun, L., Schneider, M., Debbané, M., Thiran, J.-P., & Eliez, S. (2013). Reduced fronto-temporal and limbic connectivity in the 22q11.2 deletion syndrome: vulnerability markers for developing schizophrenia? PLos One 8(3), eS8429. IF : 3.534.

Delio, M., Guo, T., McDonald-McGinn, D.M., Zackai, E., Herman, S., Kaminetzky, M., Higgins, A.M., Coleman, K., Chow, C., Jarlbrzkowski, M., Bearden, C.E., Bailey, A., Vangkilde, A., Olson, L., Olsen, C., Skovby, F., Werge, T., Templin, L., Busa, T., Philip, N., Swillen, A., Vermeesch, J.R., Devriendt, K., Schneider, M., Dahoun, S., Eliez, S., Schoch, K., Hooper, S.R., Shashi, V., Samanich, J., Marion, R., Boot, E., van Amelsvoort, T., Klaassen, P., Duijff, S.N., Vorstman, J., Yuen, T., Silversides, C., Chow, E., Bassett, A., Frisch, A., Weizman, A., Gothelf, D., Niarchou, M., van den Bree, M., Owen, M.J., Suner, D.H., Andreo, J.R., Armando, M., Vicari, S., Digilio, M.C., Auton, A., Kates, W.R., Wang, T., Shprintzen, R.J., Emanuel, B.S., and Morrow, B.E. in behalf of the International 22q11.2 Consortium. (2013). Enhanced maternal origin of the deletion in Velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome. American Journal of Human Genetics 92(3), 439-447. IF : 10.987.

Rihs, T., Tomescu, M.I., Britz, J., Rochas, V., Custo, A., Schneider, M., Debbané, M., Eliez, S., & Michel, C.M. (2013). Altered auditory processing in frontal and left temporal cortex in 22q11.2 deletion syndrome : a group at high genetic risk for schizophrenia. Psychiatry Research 212(2), 141-149. IF : 2.682.

2012

Debbané, M., Lazouret, M., Lagioia, A., Schneider, M., Van de Ville, D., & Eliez, S. (2012). Resting-state networks in adolescents with 22q11.2 deletion syndrome: associations with prodromal symptoms and executive functions. Schizophrenia Research 139, 33-39. IF : 4.59.

Fabbro, A., Rizzi, E., Schneider, M., Debbané, M., & Eliez, S. (2012). Depression and anxiety disorders in children and adolescents with velo-cardio-facial syndrome (VCFS). European Child and Adolescent Psychiatry 21(7), 379-385. IF : 3.553.

Schneider, M., Debbané, M., Lagioia, A., Salomon, R., D’Argembeau, A., & Eliez, S. (2012). Comparing the neural bases of self-referential processing in typically developing and 22q11.2 adolescents. Developmental Cognitive Neuroscience 2, 277-289. IF : 3.833.

Schneider, M., Van der Linden, M., Glaser, B., Rizzi, E., Dahoun, S.P., Hinard, C., Bartoloni, L., Antonarakis, S.E., Debbané, M., & Eliez S. (2012). Preliminary structure and predictive value of attenuated negative symptoms in 22q11 deletion syndrome. Psychiatry Research 196, 277-284. IF : 2.456.

2011

Lagioia, A., Eliez, S., Schneider, M., Simons, J.S., Van der Linden, M., & Debbané, M. (2011). Neural correlates of reality monitoring during adolescence. NeuroImage 55, 1393-1400. IF : 5.895.

Schaer, M., Glaser, B., Ottet, M.-C., Schneider, M., Bach Cuadra, M., Debbané, M., Thiran, J.-P., & Eliez, S. (2010). Regional cortical volumes and congenital heart disease: a MRI study in 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders 2(4), 224-234. IF : 1.269.

 

Articles de revue publiés dans des journaux à politique éditoriale

Fiskinski, A.M., Schneider, M., Murphy, C.M., Armando, M., Vicari, S., Canyelles, J.M., Gothelf, D., Eliez, S. Breetvelt. E.J., Arango, C., & Vorstman, J.A.S. (2018). Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A 176(10), 2182-2191. IF: 2.264.

Demily, C., Rossi, M., Schneider, M., Edery, P., Leleu, A., d’Amato, T., Franck, N., & Eliez, S. (2015). Perspectives actuelles dans la microdélétion 22q11.2 : prise en charge du phénotype neurocomportemental. L’Encéphale 41(3), 266-273. IF : 0.598.

Schneider, M., Debbané, M., Bassett, A.S., Chow, E.W., Fung, W.L., van den Bree, M., Owen, M., Murphy, K.C., Niarchou, M., Kates, W.R., Antshel, K.M., Fremont, W., McDonald-McGinn, D.M., Gur, R.E., Zackai, E.H., Vorstman, J., Duijff, S.N., Klaassen, P.W., Swillen, A., Gothelf, D., Green, T., Weizman, A., Van Amelsvoort, T., Evers, L., Boot, E., Shashi, V., Hooper, S.R., Bearden, C.E., Jalbrzikowski, M., Armando, M., Vicari, S., Murphy, D.G., Ousley, O., Campbell, L.E., Simon, T.J., & Eliez, S. (2014). Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome : results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. American Journal of Psychiatry 171(6), 627-639. IF : 12.295.

Schneider, M. & Eliez, S. (2010). La microdélétion 22q11.2 [22q11.2 microdeletion]. Archives de Pédiatrie 17, 431-434. IF : 0.305.

Chapitres de livre

Hermans, K., Achterhof, R., Myin-Germeys, I., Kasanova, Z., Kirtley, O., & Schneider, M. (2019). Improving ecological validity in research on social cognition. In E. Lewandowski and A. Moustafa (Eds.), Social cognition and psychosis. Amsterdam: Elsevier.

Debbané, M., Schneider, M., Eliez, S., & Van der Linden, M. (2011). Assessing anomalous perceptions in youths: a preliminary validation study of the Cardiff Anomalous Perception Scale (CAPS). In M. Payne (Ed.), Hallucinations: Types, Stages, and Treatment (pp. 113-130). New York: Nova Publishers.

Thèse de doctorat

Schneider, M. (2014). Une approche plurifactorielle des symptômes négatifs dans la microdélétion 22q11.2. Thèse de doctorat réalisée sous la direction de M. Van der Linden et S. Eliez.