| Year |
Citation |
Score |
| 2023 |
Martin GE, Lee M, Bicknell K, Goodkind A, Maltman N, Losh M. A longitudinal investigation of pragmatic language across contexts in autism and related neurodevelopmental conditions. Frontiers in Neurology. 14: 1155691. PMID 37545730 DOI: 10.3389/fneur.2023.1155691 |
0.375 |
|
| 2023 |
Lau JCY, Losh M, Speights M. Differences in speech articulatory timing and associations with pragmatic language ability in autism. Research in Autism Spectrum Disorders. 102. PMID 37484484 DOI: 10.1016/j.rasd.2023.102118 |
0.345 |
|
| 2023 |
Patel SP, Landau E, Martin GE, Rayburn C, Elahi S, Fragnito G, Losh M. A profile of prosodic speech differences in individuals with autism spectrum disorder and first-degree relatives. Journal of Communication Disorders. 102: 106313. PMID 36804204 DOI: 10.1016/j.jcomdis.2023.106313 |
0.38 |
|
| 2022 |
Hogan AL, Winston M, Barstein J, Losh M. Slower Peak Pupillary Response to Emotional Faces in Parents of Autistic Individuals. Frontiers in Psychology. 13: 836719. PMID 36304881 DOI: 10.3389/fpsyg.2022.836719 |
0.387 |
|
| 2022 |
Patel SP, Cole J, Lau JCY, Fragnito G, Losh M. Verbal entrainment in autism spectrum disorder and first-degree relatives. Scientific Reports. 12: 11496. PMID 35798758 DOI: 10.1038/s41598-022-12945-4 |
0.413 |
|
| 2022 |
Guilfoyle J, Winston M, Sideris J, Martin GE, Nayar K, Bush L, Wassink T, Losh M. Childhood Academic Performance: A Potential Marker of Genetic Liability to Autism. Journal of Autism and Developmental Disorders. PMID 35194728 DOI: 10.1007/s10803-022-05459-5 |
0.408 |
|
| 2021 |
Bush L, Martin GE, Landau E, Losh M. A Longitudinal Study of Parent-Child Interactions and Language Outcomes in Fragile X Syndrome and Other Neurodevelopmental Disorders. Frontiers in Psychiatry. 12: 718572. PMID 34819882 DOI: 10.3389/fpsyt.2021.718572 |
0.363 |
|
| 2021 |
Maltman N, Guilfoyle J, Nayar K, Martin GE, Winston M, Lau JCY, Bush L, Patel S, Lee M, Sideris J, Hall DA, Zhou L, Sharp K, Berry-Kravis E, Losh M. The Phenotypic Profile Associated With the Premutation in Women: An Investigation of Clinical-Behavioral, Social-Cognitive, and Executive Abilities. Frontiers in Psychiatry. 12: 718485. PMID 34421690 DOI: 10.3389/fpsyt.2021.718485 |
0.324 |
|
| 2021 |
Nayar K, Kang X, Xing J, Gordon PC, Wong PCM, Losh M. A cross-cultural study showing deficits in gaze-language coordination during rapid automatized naming among individuals with ASD. Scientific Reports. 11: 13401. PMID 34183686 DOI: 10.1038/s41598-021-91911-y |
0.348 |
|
| 2020 |
Nayar K, Sealock JM, Maltman N, Bush L, Cook EH, Davis LK, Losh M. Elevated Polygenic Burden for Autism Spectrum Disorder Is Associated With the Broad Autism Phenotype in Mothers of Individuals With Autism Spectrum Disorder. Biological Psychiatry. PMID 33229037 DOI: 10.1016/J.Biopsych.2020.08.029 |
0.473 |
|
| 2020 |
Lau JCY, To CKS, Kwan JSK, Kang X, Losh M, Wong PCM. Lifelong Tone Language Experience does not Eliminate Deficits in Neural Encoding of Pitch in Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 33216279 DOI: 10.1007/s10803-020-04796-7 |
0.381 |
|
| 2020 |
Patel SP, Nayar K, Martin GE, Franich K, Crawford S, Diehl JJ, Losh M. An Acoustic Characterization of Prosodic Differences in Autism Spectrum Disorder and First-Degree Relatives. Journal of Autism and Developmental Disorders. PMID 32056118 DOI: 10.1007/S10803-020-04392-9 |
0.437 |
|
| 2019 |
Winston M, Nayar K, Hogan AL, Barstein J, La Valle C, Sharp K, Berry-Kravis E, Losh M. Physiological regulation and social-emotional processing in female carriers of the FMR1 premutation. Physiology & Behavior. 112746. PMID 31765665 DOI: 10.1016/J.Physbeh.2019.112746 |
0.431 |
|
| 2019 |
Crowley JJ, Szatkiewicz J, Kähler AK, Giusti-Rodriguez P, Ancalade N, Booker JK, Carr JL, Giamberardino SN, Crawford GE, Losh M, Stockmeier CA, Taylor AK, Piven J, Sullivan PF. Correction: Common-variant associations with fragile X syndrome. Molecular Psychiatry. PMID 31548576 DOI: 10.1038/S41380-019-0526-X |
0.306 |
|
| 2019 |
Martin GE, Barstein J, Patel S, Lee M, Henry L, Losh M. Longitudinal analysis of communication repair skills across three neurodevelopmental disabilities. International Journal of Language & Communication Disorders. PMID 31538707 DOI: 10.1111/1460-6984.12500 |
0.46 |
|
| 2019 |
Nayar K, McKinney W, Hogan AL, Martin GE, La Valle C, Sharp K, Berry-Kravis E, Norton ES, Gordon PC, Losh M. Language processing skills linked to FMR1 variation: A study of gaze-language coordination during rapid automatized naming among women with the FMR1 premutation. Plos One. 14: e0219924. PMID 31348790 DOI: 10.1371/Journal.Pone.0219924 |
0.39 |
|
| 2019 |
Patel SP, Kim JH, Larson CR, Losh M. Mechanisms of voice control related to prosody in autism spectrum disorder and first-degree relatives. Autism Research : Official Journal of the International Society For Autism Research. PMID 31187944 DOI: 10.1002/Aur.2156 |
0.479 |
|
| 2019 |
Lee M, Nayar K, Maltman N, Hamburger D, Martin GE, Gordon PC, Losh M. Understanding Social Communication Differences in Autism Spectrum Disorder and First-Degree Relatives: A Study of Looking and Speaking. Journal of Autism and Developmental Disorders. PMID 30864059 DOI: 10.1007/S10803-019-03969-3 |
0.481 |
|
| 2018 |
Crowley JJ, Szatkiewicz J, Kähler AK, Giusti-Rodriguez P, Ancalade N, Booker JK, Carr JL, Crawford GE, Losh M, Stockmeier CA, Taylor AK, Piven J, Sullivan PF. Common-variant associations with fragile X syndrome. Molecular Psychiatry. PMID 30531935 DOI: 10.1038/S41380-018-0290-3 |
0.328 |
|
| 2018 |
Martin GE, Bush L, Klusek J, Patel S, Losh M. A Multimethod Analysis of Pragmatic Skills in Children and Adolescents With Fragile X Syndrome, Autism Spectrum Disorder, and Down Syndrome. Journal of Speech, Language, and Hearing Research : Jslhr. 1-15. PMID 30418476 DOI: 10.1044/2018_Jslhr-L-18-0008 |
0.506 |
|
| 2018 |
Nayar K, Gordon PC, Martin GE, Hogan AL, La Valle C, McKinney W, Lee M, Norton ES, Losh M. Links between looking and speaking in autism and first-degree relatives: insights into the expression of genetic liability to autism. Molecular Autism. 9: 51. PMID 30338047 DOI: 10.1186/S13229-018-0233-5 |
0.489 |
|
| 2018 |
Barstein J, Martin GE, Lee M, Losh M. A Duck Wearing Boots?! Pragmatic Language Strategies for Repairing Communication Breakdowns Across Genetically Based Neurodevelopmental Disabilities. Journal of Speech, Language, and Hearing Research : Jslhr. 1-15. PMID 29800075 DOI: 10.1044/2018_Jslhr-L-17-0064 |
0.383 |
|
| 2017 |
Lee M, Bush L, Martin GE, Barstein J, Maltman N, Klusek J, Losh M. A Multi-Method Investigation of Pragmatic Development in Individuals With Down Syndrome. American Journal On Intellectual and Developmental Disabilities. 122: 289-309. PMID 28654411 DOI: 10.1352/1944-7558-122.4.289 |
0.466 |
|
| 2017 |
Lee M, Martin GE, Berry-Kravis E, Losh M. Erratum to: A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome. Journal of Neurodevelopmental Disorders. 9: 10. PMID 28286580 DOI: 10.1186/S11689-017-9192-Y |
0.386 |
|
| 2017 |
Martin GE, Barstein J, Hornickel J, Matherly S, Durante G, Losh M. Signaling of noncomprehension in communication breakdowns in fragile X syndrome, Down syndrome, and autism spectrum disorder. Journal of Communication Disorders. 65: 22-34. PMID 28161297 DOI: 10.1016/J.Jcomdis.2017.01.003 |
0.52 |
|
| 2017 |
Lee M, Martin GE, Hogan A, Hano D, Gordon PC, Losh M. What's the story? A computational analysis of narrative competence in autism. Autism : the International Journal of Research and Practice. 1362361316677957. PMID 28095705 DOI: 10.1177/1362361316677957 |
0.468 |
|
| 2017 |
Losh M, Martin GE, Lee M, Klusek J, Sideris J, Barron S, Wassink T. Developmental Markers of Genetic Liability to Autism in Parents: A Longitudinal, Multigenerational Study. Journal of Autism and Developmental Disorders. PMID 28070788 DOI: 10.1007/S10803-016-2996-X |
0.476 |
|
| 2016 |
Lee M, Martin GE, Berry-Kravis E, Losh M. A developmental, longitudinal investigation of autism phenotypic profiles in fragile X syndrome. Journal of Neurodevelopmental Disorders. 8: 47. PMID 28050218 DOI: 10.1186/S11689-016-9179-0 |
0.489 |
|
| 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 |
0.384 |
|
| 2015 |
Hall D, Todorova-Koteva K, Pandya S, Bernard B, Ouyang B, Walsh M, Pounardjian T, Deburghraeve C, Zhou L, Losh M, Leehey M, Berry-Kravis E. Neurological and endocrine phenotypes of fragile X carrier women. Clinical Genetics. PMID 26212380 DOI: 10.1111/Cge.12646 |
0.302 |
|
| 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 |
0.349 |
|
| 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 |
0.46 |
|
| 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 |
0.454 |
|
| 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 |
0.335 |
|
| 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 |
0.493 |
|
| 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 |
0.492 |
|
| 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 |
0.386 |
|
| 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 |
0.513 |
|
| 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 |
0.536 |
|
| 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 |
0.455 |
|
| 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 |
0.476 |
|
| 2012 |
Losh M, Martin GE, Klusek J, Hogan-Brown AL. Pragmatic Language in autism and fragile X syndrome: Genetic and clinical applications. Perspectives On Language Learning and Education. 19: 48-55. PMID 24660047 DOI: 10.1044/Lle19.2.48 |
0.452 |
|
| 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 |
0.539 |
|
| 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 |
0.513 |
|
| 2012 |
Losh M, Esserman D, Anckarsäter H, Sullivan PF, Lichtenstein P. Lower birth weight indicates higher risk of autistic traits in discordant twin pairs. Psychological Medicine. 42: 1091-102. PMID 22132806 DOI: 10.1017/S0033291711002339 |
0.366 |
|
| 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 |
0.476 |
|
| 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 |
0.325 |
|
| 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 |
0.461 |
|
| 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 |
0.356 |
|
| 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 |
0.322 |
|
| 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 |
0.394 |
|
| 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 |
0.391 |
|
| 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 |
0.342 |
|
| 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 |
0.395 |
|
| 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 |
0.431 |
|
| 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 |
0.484 |
|
| 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 |
0.661 |
|
| 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 |
0.387 |
|
| 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 |
0.465 |
|
| 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 |
0.7 |
|
| 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 |
0.679 |
|
| 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 |
0.511 |
|
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