Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Fish, Laurel A."'
Autor:
Bazelmans, Tessel, Arthur, Rowan, Pasco, Greg, Shephard, Elizabeth, Milosavljevic, Bosiljka, Ali, Jannath Begum, Pickles, Andrew, Johnson, Mark H., Jones, Emily J. H., Charman, Tony, Baykoca, Jeni, Blasi, Anna, Bolton, Patrick, Cheung, Celeste, Chiu, Kenny, Dafner, Leila, Davies, Kim, Elsabbagh, Mayada, Fernandes, Janice, Fish, Laurel
Publikováno v:
Autism Research: Official Journal of the International Society for Autism Research; Jul2024, Vol. 17 Issue 7, p1501-1514, 14p
Publikováno v:
In Acta Psychologica April 2017 175:42-49
Autor:
Fish, Laurel A.1 laurel.fish@kcl.ac.uk, Nyström, Pär2, Gliga, Teodora3, Gui, Anna4, Begum Ali, Jannath4, Mason, Luke4, Garg, Shruti5, Green, Jonathan5, Johnson, Mark H.4,6, Charman, Tony7, Harrison, Rebecca4, Meaburn, Emma4, Falck‐Ytter, Terje8,9,10, Jones, Emily J. H.4
Publikováno v:
Journal of Child Psychology. Nov2021, Vol. 62 Issue 11, p1308-1319. 12p. 1 Diagram, 2 Charts, 3 Graphs.
Autor:
Fish, Laurel A.1 (AUTHOR) laurel.fish@kcl.ac.uk, Jones, Emily J. H.2 (AUTHOR)
Publikováno v:
PLoS ONE. 2/5/2021, Vol. 16 Issue 2, p1-29. 29p.
Autor:
Fish, Laurel A., Nystrom, Par, Gliga, Teodora, Gui, Anna, Begum Ali, Jannath, Mason, Luke, Garg, Shruti, Green, Jonathan, Johnson, Mark H., Charman, Tony, Harrison, Rebecca, Meaburn, Emma, Falck-Ytter, Terje, Jones, Emily J. H., BASIS/STAARS team
Although autism spectrum disorder (ASD) is heritable, the mechanisms through which genes contribute to symptom emergence remain unclear. Investigating candidate intermediate phenotypes such as the pupillary light reflex (PLR) prospectively from early
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::189666761fce0a0ce31346c82c7105c5
https://zenodo.org/record/7038965
https://zenodo.org/record/7038965
The pupillary light reflex (PLR) is a low-level automatic behaviour controlled by the autonomic nervous system (ANS)(1). The PLR is characterised by rapid pupil constriction induced by changes to optical luminance(1). An atypical PLR is associated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8d58cd38425965eeea8bc3234fac85e
Autor:
Fish, Laurel A, Nyström, Pär, Gliga, Teodora, Gui, Anna, Begum Ali, Jannath, Mason, Luke, Garg, Shruti, Green, Jonathan, Johnson, Mark H, Charman, Tony, Harrison, Rebecca, Meaburn, Emma, Falck-Ytter, Terje, Jones, Emily JH, BASIS/STAARS* Team
BACKGROUND: Although autism spectrum disorder (ASD) is heritable, the mechanisms through which genes contribute to symptom emergence remain unclear. Investigating candidate intermediate phenotypes such as the pupillary light reflex (PLR) prospectivel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ca473a4a100de20a810f2924b9ff20d
https://www.repository.cam.ac.uk/handle/1810/327737
https://www.repository.cam.ac.uk/handle/1810/327737
Autor:
Fish, Laurel J.1 (AUTHOR) lfish@rule26.com, Halcoussis, Dennis2 (AUTHOR) dhalcoussis@csun.edu, Phillips, G. Michael2,3 (AUTHOR) mphillips@csun.edu
Publikováno v:
Contemporary Economic Policy. Jan2021, Vol. 39 Issue 1, p220-235. 16p.
Publikováno v:
Journal of Economic & Social Measurement. 2019, Vol. 44 Issue 1, p19-24. 6p.
Autor:
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
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-13 (2017)
Molecular Autism
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M 2017, ' Early development of infants with Neurofibromatosis Type 1 : A case series ', Molecular Autism, vol. 8, no. 62 . https://doi.org/10.1186/s13229-017-0178-0
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M H, 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 G, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S M, Baralle, D, Redman, C, Sharif, S, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R & Eden-Basis Team 2017, ' Early development of infants with neurofibromatosis type 1 : a case series ', Molecular Autism, vol. 8, no. 1, 62 . https://doi.org/10.1186/s13229-017-0178-0
Molecular Autism
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M 2017, ' Early development of infants with Neurofibromatosis Type 1 : A case series ', Molecular Autism, vol. 8, no. 62 . https://doi.org/10.1186/s13229-017-0178-0
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M H, 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 G, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S M, Baralle, D, Redman, C, Sharif, S, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R & Eden-Basis Team 2017, ' Early development of infants with neurofibromatosis type 1 : a case series ', Molecular Autism, vol. 8, no. 1, 62 . https://doi.org/10.1186/s13229-017-0178-0
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 study