Molly C. Losh, Ph.D. - Publications

Communication Sciences and Disorders Northwestern University, Evanston, IL 
autism, language, social cognition

33 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Hall DA, Robertson E, Shelton AL, Losh MC, Mila M, Moreno EG, Gomez-Anson B, Martínez-Cerdeño V, Grigsby J, Lozano R, Hagerman R, Maria LS, Berry-Kravis E, O'Keefe JA. Update on the Clinical, Radiographic, and Neurobehavioral Manifestations in FXTAS and FMR1 Premutation Carriers. Cerebellum (London, England). PMID 27287737 DOI: 10.1007/S12311-016-0799-4  1
2015 Smith MJ, Fleming MF, Wright MA, Losh M, Humm LB, Olsen D, Bell MD. Brief Report: Vocational Outcomes for Young Adults with Autism Spectrum Disorders at Six Months After Virtual Reality Job Interview Training. Journal of Autism and Developmental Disorders. PMID 25986176 DOI: 10.1007/S10803-015-2470-1  1
2015 Klusek J, Roberts JE, Losh M. Cardiac autonomic regulation in autism and Fragile X syndrome: a review. Psychological Bulletin. 141: 141-75. PMID 25420222 DOI: 10.1037/A0038237  1
2014 Hogan-Brown AL, Hoedemaker RS, Gordon PC, Losh M. Eye-voice span during rapid automatized naming: evidence of reduced automaticity in individuals with autism spectrum disorder and their siblings. Journal of Neurodevelopmental Disorders. 6: 33. PMID 25177372 DOI: 10.1186/1866-1955-6-33  1
2014 Wheeler AC, Bailey DB, Berry-Kravis E, Greenberg J, Losh M, Mailick M, Milà M, Olichney JM, Rodriguez-Revenga L, Sherman S, Smith L, Summers S, Yang JC, Hagerman R. Associated features in females with an FMR1 premutation. Journal of Neurodevelopmental Disorders. 6: 30. PMID 25097672 DOI: 10.1186/1866-1955-6-30  1
2014 Losh M, Gordon PC. Quantifying narrative ability in autism spectrum disorder: a computational linguistic analysis of narrative coherence. Journal of Autism and Developmental Disorders. 44: 3016-25. PMID 24915929 DOI: 10.1007/S10803-014-2158-Y  1
2014 Klusek J, Martin GE, Losh M. A comparison of pragmatic language in boys with autism and fragile X syndrome. Journal of Speech, Language, and Hearing Research : Jslhr. 57: 1692-707. PMID 24686468 DOI: 10.1044/2014_Jslhr-L-13-0064  1
2014 Klusek J, Martin GE, Losh M. Consistency between research and clinical diagnoses of autism among boys and girls with fragile X syndrome. Journal of Intellectual Disability Research : Jidr. 58: 940-52. PMID 24528851 DOI: 10.1111/Jir.12121  1
2014 Klusek J, Losh M, Martin GE. Sex differences and within-family associations in the broad autism phenotype. Autism : the International Journal of Research and Practice. 18: 106-16. PMID 23188882 DOI: 10.1177/1362361312464529  1
2013 Klusek J, Martin GE, Losh M. Physiological arousal in autism and fragile X syndrome: group comparisons and links with pragmatic language. American Journal On Intellectual and Developmental Disabilities. 118: 475-95. PMID 24432860 DOI: 10.1352/1944.7558-118.6.475  1
2013 Martin GE, Losh M, Estigarribia B, Sideris J, Roberts J. Longitudinal profiles of expressive vocabulary, syntax and pragmatic language in boys with fragile X syndrome or Down syndrome. International Journal of Language & Communication Disorders / Royal College of Speech & Language Therapists. 48: 432-43. PMID 23889838 DOI: 10.1111/1460-6984.12019  1
2013 Hogan-Brown AL, Losh M, Martin GE, Mueffelmann DJ. An investigation of narrative ability in boys with autism and fragile X syndrome. American Journal On Intellectual and Developmental Disabilities. 118: 77-94. PMID 23464607 DOI: 10.1352/1944-7558-118.2.77  1
2013 Zucker N, Moskovich A, Bulik CM, Merwin R, Gaddis K, Losh M, Piven J, Wagner HR, LaBar KS. Perception of affect in biological motion cues in anorexia nervosa. The International Journal of Eating Disorders. 46: 12-22. PMID 23109257 DOI: 10.1002/Eat.22062  1
2012 Losh M, Martin GE, Klusek J, Hogan-Brown AL, Sideris J. Social communication and theory of mind in boys with autism and fragile x syndrome. Frontiers in Psychology. 3: 266. PMID 22934085 DOI: 10.3389/Fpsyg.2012.00266  1
2012 Losh M, Klusek J, Martin GE, Sideris J, Parlier M, Piven J. Defining genetically meaningful language and personality traits in relatives of individuals with fragile X syndrome and relatives of individuals with autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 660-8. PMID 22693142 DOI: 10.1002/Ajmg.B.32070  1
2010 Losh M, Esserman D, Piven J. Rapid automatized naming as an index of genetic liability to autism. Journal of Neurodevelopmental Disorders. 2: 109-16. PMID 20721307 DOI: 10.1007/S11689-010-9045-4  1
2010 Couture SM, Penn DL, Losh M, Adolphs R, Hurley R, Piven J. Comparison of social cognitive functioning in schizophrenia and high functioning autism: more convergence than divergence. Psychological Medicine. 40: 569-79. PMID 19671209 DOI: 10.1017/S003329170999078X  1
2009 Losh M, Adolphs R, Poe MD, Couture S, Penn D, Baranek GT, Piven J. Neuropsychological profile of autism and the broad autism phenotype. Archives of General Psychiatry. 66: 518-26. PMID 19414711 DOI: 10.1001/Archgenpsychiatry.2009.34  1
2008 Losh M, Sullivan PF, Trembath D, Piven J. Current developments in the genetics of autism: from phenome to genome. Journal of Neuropathology and Experimental Neurology. 67: 829-37. PMID 18716561 DOI: 10.1097/Nen.0B013E318184482D  1
2008 Konneker T, Barnes T, Furberg H, Losh M, Bulik CM, Sullivan PF. A searchable database of genetic evidence for psychiatric disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 671-5. PMID 18548508 DOI: 10.1002/Ajmg.B.30802  1
2008 Losh M, Childress D, Lam K, Piven J. Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 424-33. PMID 17948871 DOI: 10.1002/Ajmg.B.30612  1
2008 Zucker NL, Losh M. Repetitive behaviours in anorexia nervosa, autism, and obsessive-compulsive personality disorder Psychiatry. 7: 183-187. DOI: 10.1016/J.Mppsy.2008.02.012  1
2008 Piven J, Hurley R, Losh M, Parlier M, Steven Reznick J. Response to: Genichi Sugihara, Kenji J. Tsuchiya, Nori Takei, letter to the editor: Broad autism phenotype from schizophrenia-spectrum disorders Journal of Autism and Developmental Disorders. 38: 2000-2001. DOI: 10.1007/S10803-008-0595-1  1
2007 Zucker NL, Losh M, Bulik CM, LaBar KS, Piven J, Pelphrey KA. Anorexia nervosa and autism spectrum disorders: guided investigation of social cognitive endophenotypes. Psychological Bulletin. 133: 976-1006. PMID 17967091 DOI: 10.1037/0033-2909.133.6.976  1
2007 Losh M, Piven J. Social-cognition and the broad autism phenotype: identifying genetically meaningful phenotypes. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 48: 105-12. PMID 17244276 DOI: 10.1111/J.1469-7610.2006.01594.X  1
2007 Hurley RS, Losh M, Parlier M, Reznick JS, Piven J. The broad autism phenotype questionnaire. Journal of Autism and Developmental Disorders. 37: 1679-90. PMID 17146701 DOI: 10.1007/S10803-006-0299-3  1
2007 Wassink TH, Losh M, Piven J, Sheffield VC, Ashley E, Westin ER, Patil SR. Systematic screening for subtelomeric anomalies in a clinical sample of autism. Journal of Autism and Developmental Disorders. 37: 703-8. PMID 17004120 DOI: 10.1007/S10803-006-0196-9  1
2006 Losh M, Capps L. Understanding of emotional experience in autism: insights from the personal accounts of high-functioning children with autism. Developmental Psychology. 42: 809-18. PMID 16953688 DOI: 10.1037/0012-1649.42.5.809  1
2005 Wassink TH, Losh M, Frantz RS, Vieland VJ, Goedken R, Piven J, Sheffield VC. A case of autism and uniparental disomy of chromosome 1. Human Genetics. 117: 200-6. PMID 15887000 DOI: 10.1007/S00439-005-1257-4  1
2004 Reilly J, Losh M, Bellugi U, Wulfeck B. "Frog, where are you?" Narratives in children with specific language impairment, early focal brain injury, and Williams syndrome. Brain and Language. 88: 229-47. PMID 14965544 DOI: 10.1016/S0093-934X(03)00101-9  1
2003 Losh M, Capps L. Narrative ability in high-functioning children with autism or Asperger's syndrome. Journal of Autism and Developmental Disorders. 33: 239-51. PMID 12908827 DOI: 10.1023/A:1024446215446  1
2000 Capps L, Losh M, Thurber C. "The frog ate the bug and made his mouth sad": narrative competence in children with autism. Journal of Abnormal Child Psychology. 28: 193-204. PMID 10834770 DOI: 10.1023/A:1005126915631  1
2000 Losh M, Bellugi U, Reilly J, Anderson D. Narrative as a social engagement tool: the excessive use of evaluation in narratives from children with williams syndrome Narrative Inquiry. 10: 265-290. DOI: 10.1075/Ni.10.2.01Los  1
Show low-probability matches.