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3 results on '"Greensmith, Marian"'

1. Atypical Development of Attentional Control Associates with Later Adaptive Functioning, Autism and ADHD Traits

Author

Hendry, Alexandra, Jones, Emily J.H., Bedford, Rachael, Andersson Konke, Linn, Begum Ali, Jannath, Bӧlte, Sven, Brocki, Karin C., Demurie, Ellen, Johnson, Mark, Pijl, Mirjam K.J., Roeyers, Herbert, Charman, Tony, Achermann, Sheila, Agyapong, Mary, Astenvald, Rebecka, Axelson, Lisa, Bazelmans, Tessel, Blommers, Karlijn, Bontinck, Chloè, van den Boomen, Carlijn, Boterberg, Sofie, Braukmann, Ricarda, de Bruijn, Yvette, Bruyneel, Eva, Buitelaar, Jan K., Dafner, Leila, Darki, Fahime, Davies, Kim, Ersoy, Mutluhan, Falck-Ytter, Terje, Fernandes, Janice, Freeman, Zoë, Gliga, Teea, Gredebäck, Gustaf, Greensmith, Marian, Haartsen, Rianne, van Ierland-Veerhoek, Sanne, de Jonge, Maretha V., Kalwarowsky, Sarah, Kemner, Chantal, Kolesnik, Anna, de Korte, Manon, Lundin-Kleberg, Johan, Munsters, Nicolette M., Nyström, Pär, Pasco, Greg, Pirazzoli, Laura, Ristolainen, Johanna, Stadin, Andrietta, Taylor, Chloë, Thorup, Emilia, vaz, Natalie, Vinkenvleugel, Loes, Ward, Emma, Warreyn, Petra, van Wielink, Lilli N., LS FAC Vgl vrouwenst. Taal en Beeld, Engelse taalkunde, Leerstoel Kemner, Afd Psychologische functieleer, Experimental Psychology (onderzoeksprogramma PF), Helmholtz Institute, Afd. OT Individual Development, ICON - Media and Performance Studies, LS FAC Vgl vrouwenst. Taal en Beeld, Engelse taalkunde, Leerstoel Kemner, Afd Psychologische functieleer, Experimental Psychology (onderzoeksprogramma PF), Helmholtz Institute, Afd. OT Individual Development, ICON - Media and Performance Studies, Hendry, Alexandra [0000-0003-1985-2521], and Apollo - University of Cambridge Repository

Subjects
Male, DISORDER, 050103 clinical psychology, Autism, Social Sciences, CHILDREN, psyc, 0302 clinical medicine, Quality of life, QUALITY-OF-LIFE, Developmental and Educational Psychology, Psychology, Attention, Spectrum disorder, DEFICIT/HYPERACTIVITY, FAMILIAL RISK, Early childhood, media_common, 05 social sciences, Atypical development, Adaptation, Physiological, 3. Good health, Phenotype, Child, Preschool, Female, BEHAVIOR, 050104 developmental & child psychology, Clinical psychology, phenotype, media_common.quotation_subject, 03 medical and health sciences, medicine, Humans, ADHD, Attention deficit hyperactivity disorder, 0501 psychology and cognitive sciences, Autistic Disorder, EARLY-CHILDHOOD, SPECTRUM DISORDER, Original Paper, EXECUTIVE FUNCTION, Psykologi, TEMPERAMENT, Attentional control, Infant, medicine.disease, Mental health, HIGH-RISK, Intermediate phenotype, Attention Deficit Disorder with Hyperactivity, Temperament, Intermediate, 030217 neurology & neurosurgery
Abstract

Funder: H2020 European Research Council; doi: http://dx.doi.org/10.13039/100010663, Funder: Research Foundation Flanders, Funder: Universiteit Gent; doi: http://dx.doi.org/10.13039/501100004385, Funder: Marguerite-Marie Delacroix, Funder: Autistica; doi: http://dx.doi.org/10.13039/100011706, Funder: Riksbankens Jubileumsfond; doi: http://dx.doi.org/10.13039/501100004472; Grant(s): NHS14-1802:1, Funder: K.F. Hein Fonds, Funder: Scott Family Junior Research Fellowship, Autism is frequently associated with difficulties with top-down attentional control, which impact on individuals’ mental health and quality of life. The developmental processes involved in these attentional difficulties are not well understood. Using a data-driven approach, 2 samples (N = 294 and 412) of infants at elevated and typical likelihood of autism were grouped according to profiles of parent report of attention at 10, 15 and 25 months. In contrast to the normative profile of increases in attentional control scores between infancy and toddlerhood, a minority (7–9%) showed plateauing attentional control scores between 10 and 25 months. Consistent with pre-registered hypotheses, plateaued growth of attentional control was associated with elevated autism and ADHD traits, and lower adaptive functioning at age 3 years.

Published
2020

2. Early development of infants with neurofibromatosis type 1: a case series

Author

Kolesnik, Anna May, Jones, Emily Jane Harrison, Garg, Shruti, Green, Jonathan, Charman, Tony, Johnson, Mark Henry, Baron-Cohen, Simon, Begum-Ali, Jannath, Bolton, Patrick, Cheung, Celeste, Dafner, Leila, Davies, Kim, Elsabbagh, Mayada, Fernandes, Janice, Fish, Laurel, Gammer, Isobel, Greensmith, Marian, Gliga, Teodora, Kalwarowsky, Sarah, Liew, Michelle, Pasco, Greg, Pickles, Andrew, Ribeiro, Helena, Salomone, Erica, Taylor, Chloe, Tucker, Leslie, Wass, Sam, Burkitt-Wright, Emma, Evans, D. Gareth, Vassallo, Grace, Eelloo, Judith, West, Siobhan, Howard, Elizabeth, Hupton, Eileen, Huson, Sue, Lewis, Lauren, Tricker, Karen, Dobbie, Angus, Drimer, Ruth, Sharif, Saghira Malik, Baralle, Diane, Redman, Carolyn, Sharif, Saba, Symth, Carolyn, Lam, Wayne, Bradbury, Alyson, Harrower, Neil, Quarrell, Oliver, Bethell, Helen, Jones, Rachel, Musson, Susan, Prem, Catherine, Splitt, Miranda, Horridge, Karen, Steiger, Christine, Jim, Carly, Kolesnik, A, Jones, E, Garg, S, Green, J, Charman, T, Johnson, M, Baron-Cohen, S, Begum-Ali, J, Bolton, P, Cheung, C, Dafner, L, Davies, K, Elsabbagh, M, Fernandes, J, Fish, L, Gammer, I, Greensmith, M, Gliga, T, Kalwarowsky, S, Liew, M, Pasco, G, Pickles, A, Ribeiro, H, Salomone, E, Taylor, C, Tucker, L, Wass, S, Burkitt-Wright, E, Evans, D, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S, Baralle, D, Redman, C, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R, Musson, S, Prem, C, Splitt, M, Horridge, K, Steiger, C, Jim, C, Johnson, Mark [0000-0003-4229-2585], and Apollo - University of Cambridge Repository

Subjects
Male, Pediatrics, Autism Spectrum Disorder, Adaptive functioning, Autism, Prospective longitudinal, Developmental cognitive neuroscience, Language Development Disorder, lcsh:RC346-429, psyc, 0302 clinical medicine, Cognition, Development, Infant, NF1, Sensory processing, Social engagement, Translational neurodevelopment, Activities of Daily Living, Communication, Female, Humans, Language Development Disorders, Motor Activity, Neurofibromatosis 1, Prospective Studies, Risk, Temperament, Molecular Biology, Developmental Neuroscience, Developmental Biology, Psychiatry and Mental Health, Prospective cohort study, media_common, 05 social sciences, Neuropsychology, Autism spectrum disorder, Cohort, Psychology, 050104 developmental & child psychology, Human, medicine.medical_specialty, media_common.quotation_subject, behavioral disciplines and activities, 03 medical and health sciences, mental disorders, medicine, 0501 psychology and cognitive sciences, Neurofibromatosis, lcsh:Neurology. Diseases of the nervous system, Research, medicine.disease, Prospective Studie, 030217 neurology & neurosurgery
Abstract

Background Prospective studies of infants at familial risk for autism spectrum disorder (ASD) have yielded insights into the earliest signs of the disorder but represent heterogeneous samples of unclear aetiology. Complementing this approach by studying cohorts of infants with monogenic syndromes associated with high rates of ASD offers the opportunity to elucidate the factors that lead to ASD. Methods We present the first report from a prospective study of ten 10-month-old infants with neurofibromatosis type 1 (NF1), a monogenic disorder with high prevalence of ASD or ASD symptomatology. We compared data from infants with NF1 to a large cohort of infants at familial risk for ASD, separated by outcome at age 3 of ASD (n = 34), atypical development (n = 44), or typical development (n = 89), and low-risk controls (n = 75). Domains assessed at 10 months by parent report and examiner observation include cognitive and adaptive function, sensory processing, social engagement, and temperament. Results Infants with NF1 showed striking impairments in motor functioning relative to low-risk infants; this pattern was seen in infants with later ASD from the familial cohort (HR-ASD). Both infants with NF1 and the HR-ASD group showed communication delays relative to low-risk infants. Conclusions Ten-month-old infants with NF1 show a range of developmental difficulties that were particularly striking in motor and communication domains. As with HR-ASD infants, social skills at this age were not notably impaired. This is some of the first information on early neurodevelopment in NF1. Strong inferences are limited by the sample size, but the findings suggest implications for early comparative developmental science and highlight motor functioning as an important domain to inform the development of relevant animal models. The findings have clinical implications in indicating an important focus for early surveillance and remediation in this early diagnosed genetic disorder. Electronic supplementary material The online version of this article (10.1186/s13229-017-0178-0) contains supplementary material, which is available to authorized users.

Published
2017

3. Early development of infants with neurofibromatosis type 1: A case series

Author

Kolesnik, A, Jones, E, Garg, S, Green, J, Charman, T, Johnson, M, Baron-Cohen, S, Begum-Ali, J, Bolton, P, Cheung, C, Dafner, L, Davies, K, Elsabbagh, M, Fernandes, J, Fish, L, Gammer, I, Greensmith, M, Gliga, T, Kalwarowsky, S, Liew, M, Pasco, G, Pickles, A, Ribeiro, H, Salomone, E, Taylor, C, Tucker, L, Wass, S, Burkitt-Wright, E, Evans, D, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S, Baralle, D, Redman, C, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R, Musson, S, Prem, C, Splitt, M, Horridge, K, Steiger, C, Jim, C, Kolesnik, Anna May, Jones, Emily Jane Harrison, Garg, Shruti, Green, Jonathan, Charman, Tony, Johnson, Mark Henry, Baron-Cohen, Simon, Begum-Ali, Jannath, Bolton, Patrick, Cheung, Celeste, Dafner, Leila, Davies, Kim, Elsabbagh, Mayada, Fernandes, Janice, Fish, Laurel, Gammer, Isobel, Greensmith, Marian, Gliga, Teodora, Kalwarowsky, Sarah, Liew, Michelle, Pasco, Greg, Pickles, Andrew, Ribeiro, Helena, Salomone, Erica, Taylor, Chloe, Tucker, Leslie, Wass, Sam, Burkitt-Wright, Emma, Evans, D. Gareth, Vassallo, Grace, Eelloo, Judith, West, Siobhan, Howard, Elizabeth, Hupton, Eileen, Huson, Sue, Lewis, Lauren, Tricker, Karen, Dobbie, Angus, Drimer, Ruth, Sharif, Saghira Malik, Baralle, Diane, Redman, Carolyn, Sharif, Saba, Symth, Carolyn, Lam, Wayne, Bradbury, Alyson, Harrower, Neil, Quarrell, Oliver, Bethell, Helen, Jones, Rachel, Musson, Susan, Prem, Catherine, Splitt, Miranda, Horridge, Karen, Steiger, Christine, Jim, Carly, Kolesnik, A, Jones, E, Garg, S, Green, J, Charman, T, Johnson, M, Baron-Cohen, S, Begum-Ali, J, Bolton, P, Cheung, C, Dafner, L, Davies, K, Elsabbagh, M, Fernandes, J, Fish, L, Gammer, I, Greensmith, M, Gliga, T, Kalwarowsky, S, Liew, M, Pasco, G, Pickles, A, Ribeiro, H, Salomone, E, Taylor, C, Tucker, L, Wass, S, Burkitt-Wright, E, Evans, D, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S, Baralle, D, Redman, C, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R, Musson, S, Prem, C, Splitt, M, Horridge, K, Steiger, C, Jim, C, Kolesnik, Anna May, Jones, Emily Jane Harrison, Garg, Shruti, Green, Jonathan, Charman, Tony, Johnson, Mark Henry, Baron-Cohen, Simon, Begum-Ali, Jannath, Bolton, Patrick, Cheung, Celeste, Dafner, Leila, Davies, Kim, Elsabbagh, Mayada, Fernandes, Janice, Fish, Laurel, Gammer, Isobel, Greensmith, Marian, Gliga, Teodora, Kalwarowsky, Sarah, Liew, Michelle, Pasco, Greg, Pickles, Andrew, Ribeiro, Helena, Salomone, Erica, Taylor, Chloe, Tucker, Leslie, Wass, Sam, Burkitt-Wright, Emma, Evans, D. Gareth, Vassallo, Grace, Eelloo, Judith, West, Siobhan, Howard, Elizabeth, Hupton, Eileen, Huson, Sue, Lewis, Lauren, Tricker, Karen, Dobbie, Angus, Drimer, Ruth, Sharif, Saghira Malik, Baralle, Diane, Redman, Carolyn, Sharif, Saba, Symth, Carolyn, Lam, Wayne, Bradbury, Alyson, Harrower, Neil, Quarrell, Oliver, Bethell, Helen, Jones, Rachel, Musson, Susan, Prem, Catherine, Splitt, Miranda, Horridge, Karen, Steiger, Christine, and Jim, Carly

Abstract

Background: Prospective studies of infants at familial risk for autism spectrum disorder (ASD) have yielded insights into the earliest signs of the disorder but represent heterogeneous samples of unclear aetiology. Complementing this approach by studying cohorts of infants with monogenic syndromes associated with high rates of ASD offers the opportunity to elucidate the factors that lead to ASD. Methods: We present the first report from a prospective study of ten 10-month-old infants with neurofibromatosis type 1 (NF1), a monogenic disorder with high prevalence of ASD or ASD symptomatology. We compared data from infants with NF1 to a large cohort of infants at familial risk for ASD, separated by outcome at age 3 of ASD (n = 34), atypical development (n = 44), or typical development (n = 89), and low-risk controls (n = 75). Domains assessed at 10 months by parent report and examiner observation include cognitive and adaptive function, sensory processing, social engagement, and temperament. Results: Infants with NF1 showed striking impairments in motor functioning relative to low-risk infants; this pattern was seen in infants with later ASD from the familial cohort (HR-ASD). Both infants with NF1 and the HR-ASD group showed communication delays relative to low-risk infants. Conclusions: Ten-month-old infants with NF1 show a range of developmental difficulties that were particularly striking in motor and communication domains. As with HR-ASD infants, social skills at this age were not notably impaired. This is some of the first information on early neurodevelopment in NF1. Strong inferences are limited by the sample size, but the findings suggest implications for early comparative developmental science and highlight motor functioning as an important domain to inform the development of relevant animal models. The findings have clinical implications in indicating an important focus for early surveillance and remediation in this early diagnosed genetic disorder.

Published
2017

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