Grants per year
Personal profile
Education/Academic qualification
Developmental Psychology, PhD, University of California, Berkeley
… → 2004
Psychology, BA, San Diego State University
Fingerprint Dive into the research topics where Molly C Losh is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 2 Similar Profiles
Autistic Disorder
Medicine & Life Sciences
Fragile X Syndrome
Medicine & Life Sciences
Language
Medicine & Life Sciences
Aptitude
Medicine & Life Sciences
Phenotype
Medicine & Life Sciences
Down Syndrome
Medicine & Life Sciences
pragmatics
Social Sciences
autism
Social Sciences
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Grants 2010 2024
A Family-Genetic Study of Autism and Fragile X Syndrome
Cole, J. S., Kraus, N. & Losh, M. C.
National Institute of Mental Health
9/23/19 → 7/31/24
Project: Research project
Fragile X Syndrome
Autistic Disorder
Endophenotypes
Phenotype
Molecular Biology
Parent-toddler EEG neural synchrony as a window into social communication deficits in autism
Losh, M. C., Norton, E. S. & Roberts, M. Y.
National Institute on Deafness and Other Communication Disorders
7/20/18 → 6/30/20
Project: Research project
Autistic Disorder
Electroencephalography
Communication
Brain
Language Development
Northwestern University Interdepartmental Neuroscience Postbaccalaureate Research Education Program
Acosta, A., Allada, R., Apkarian, A., Awatramani, R., Beeman, M., Bevan, M. D., Bozza, T. C., Cang, J., Chetkovich, D. M., Cobia, D. J., Contractor, A., Corcos, D. M., DeVries, S. H., Dewald, J. P. A., Dhar, S., Disterhoft, J. F., Dombeck, D. A., Elliott, J. M., Feng, Y., Ferreira, A. B., Gallio, M., Garcia-Anoveros, J., George Jr, A. L., Geula, C., Gordon, K. E., Gottfried, J. A., Grafman, J. H., Hartmann, M. J. Z., Heckman, C., Hespos, S. J., Jayaraman, A., Kahnt, T., Kearney, J. A., Kessler, J., Kiskinis, E., Kohtz, J., Kording, K. P., Kozorovitskiy, Y., Krainc, D., Larson, C., Lee, S. S. M., Li, L., Losh, M. C., Maccaferri, G., MacIver, M. A., Martina, M., Mazzulli, J., McLean, D., Mesulam, M., Miller, L. E., Miller, R. J., Mussa-Ivaldi, F., Nusslock, R., Opal, P., Ozdinler, P. H., Paller, K., Parrish, T. B., Prakriya, M., Radulovic, J., Raman, I. M., Reber, P. J., Redei, E., Rogalski, E., Sanchez, J. T., Sanz-Clemente, A., Savas, J. N., Schmidt, T. M., Schwartz, G. W., Segraves, M., Shepherd, G. M. G., Siddique, T., Solla, S. A., Surmeier Jr, D. J., Swanson, G. T., Topczewski, J., Tresch, M. C., Tysseling, V. M., Vassar, R. J., Voss, J. L., Wainwright, D. A., Wang, L., Weintraub, S., Woolley, C. S. & Wright, B. A.
National Institute of General Medical Sciences
5/1/17 → 4/30/22
Project: Research project
neurosciences
graduate
university
education
A Family-Genetic Study of Language in Autism
Ferrie, J. P., Kraus, N. & Losh, M. C.
National Institute of Mental Health
9/20/16 → 8/31/21
Project: Research project
Autistic Disorder
Language
Endophenotypes
Parents
Autism Spectrum Disorder
The role of parent phenotype in parent-mediated language interventions for autism
Kim, K. A., Losh, M. C. & Roberts, M. Y.
National Institute on Deafness and Other Communication Disorders
8/1/15 → 7/31/20
Project: Research project
autism
parents
intervention strategy
language
dyad
Research Output 1999 2020
Longitudinal analysis of communication repair skills across three neurodevelopmental disabilities
Martin, G. E., Barstein, J., Patel, S., Lee, M., Henry, L. & Losh, M., Jan 1 2020, In : International Journal of Language and Communication Disorders. 55, 1, p. 26-42 17 p.Research output: Contribution to journal › Article
communication skills
Down Syndrome
Aptitude
disability
Communication
Common-variant associations with fragile X syndrome
Crowley, J. J., Szatkiewicz, J., Kähler, A. K., Giusti-Rodriguez, P., Ancalade, N. E., Booker, J. K., Carr, J. L., Crawford, G. E., Losh, M. C., Stockmeier, C. A., Taylor, A. K., Piven, J. & Sullivan, P. F., Mar 1 2019, In : Molecular Psychiatry. 24, 3, p. 338-344 7 p.Research output: Contribution to journal › Article
Fragile X Syndrome
Haplotypes
Genome
Intellectual Disability
Odds Ratio
Correction: Common-variant associations with fragile X syndrome (Molecular Psychiatry, (2019), 24, 3, (338-344), 10.1038/s41380-018-0290-3)
Crowley, J. J., Szatkiewicz, J., Kähler, A. K., Giusti-Rodriguez, P., Ancalade, N. E., Booker, J. K., Carr, J. L., Giamberardino, S. N., Crawford, G. E., Losh, M., Stockmeier, C. A., Taylor, A. K., Piven, J. & Sullivan, P. F., Jan 1 2019, (Accepted/In press) In : Molecular Psychiatry.Research output: Contribution to journal › Comment/debate
Fragile X Syndrome
Psychiatry
1
Citation
(Scopus)
Language processing skills linked to FMR1 variation: A study of gaze-language coordination during rapid automatized naming among women with the FMR1 premutation
Nayar, K., McKinney, W., Hogan, A. L., Martin, G. E., Valle, C. L., Sharp, K., Berry-Kravis, E., Norton, E. S., Gordon, P. C. & Losh, M. C., Jan 1 2019, In : PloS one. 14, 7, e0219924.Research output: Contribution to journal › Article
Open Access
Language
Processing
eyes
Fragile X Mental Retardation Protein
Genes
1
Citation
(Scopus)
Mechanisms of voice control related to prosody in autism spectrum disorder and first-degree relatives
Patel, S. P., Kim, J. H., Larson, C. R. & Losh, M., Jan 1 2019, In : Autism Research. 12, 8, p. 1192-1210 19 p.Research output: Contribution to journal › Article
Open Access
Autism Spectrum Disorder
Autistic Disorder
Evoked Potentials
Reaction Time
Language