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Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome
In: ISSN: 0002-953X ; EISSN: 1535-7228 ; American Journal of Psychiatry ; https://hal-pasteur.archives-ouvertes.fr/pasteur-03325371 ; American Journal of Psychiatry, American Psychiatric Publishing, 2021, 178 (1), pp.87-98. ⟨10.1176/appi.ajp.2020.19080834⟩ (2021)
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2
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
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3
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
In: Molecular psychiatry, vol 25, iss 10 (2020)
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4
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
In: Molecular psychiatry, vol 25, iss 10 (2020)
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5
Towards controlled terminology for reporting germline cancer susceptibility variants: an ENIGMA report.
Spurdle, Amanda B; Greville-Heygate, Stephanie; Antoniou, Antonis. - : BMJ, 2019. : J Med Genet, 2019
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6
Genetic regulation in pubertal delay.
Howard, SR. - 2019
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7
Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis.
In: Human molecular genetics, vol 27, iss 24 (2018)
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8
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
In: Nature genetics, vol 50, iss 7 (2018)
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9
Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018).
In: Twin research and human genetics : the official journal of the International Society for Twin Studies, vol 21, iss 5 (2018)
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10
Cortical responses before 6 months of life associate with later autism. ...
Lloyd-Fox, Sarah; Blasi, A; Pasco, G. - : Apollo - University of Cambridge Repository, 2018
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11
Cortical responses before 6 months of life associate with later autism.
Lloyd-Fox, Sarah; Blasi, A; Pasco, G. - : Wiley, 2018. : Eur J Neurosci, 2018
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12
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
In: Molecular psychiatry, vol 22, iss 3 (2017)
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13
Language Development and Impairment in Children With Mild to Moderate Sensorineural Hearing Loss. ...
Halliday, Lorna; Tuomainen, Outi; Rosen, Stuart. - : Apollo - University of Cambridge Repository, 2017
Abstract: Purpose: The goal of this study was to examine language development and factors related to language impairments in children with mild to moderate sensorineural hearing loss (MMHL). Method: Ninety children, aged 8-16 years (46 children with MMHL; 44 aged-matched controls), were administered a battery of standardized language assessments, including measures of phonological processing, receptive and expressive vocabulary and grammar, word and nonword reading, and parental report of communication skills. Group differences were examined after controlling for nonverbal ability. Results: Children with MMHL performed as well as controls on receptive vocabulary and word and nonword reading. They also performed within normal limits, albeit significantly worse than controls, on expressive vocabulary, and on receptive and expressive grammar, and worse than both controls and standardized norms on phonological processing and parental report of communication skills. However, there was considerable variation in performance, ...
Keyword: Adolescent; Child; Educational Status; Genetic Predisposition to Disease; Hearing Loss, Sensorineural; Humans; Language Development; Language Development Disorders; Language Tests; Psychometrics; Risk Factors; Surveys and Questionnaires
URL: https://www.repository.cam.ac.uk/handle/1810/310549
https://dx.doi.org/10.17863/cam.57644
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14
Language Development and Impairment in Children With Mild to Moderate Sensorineural Hearing Loss.
Halliday, Lorna; Tuomainen, Outi; Rosen, Stuart. - : American Speech Language Hearing Association, 2017. : J Speech Lang Hear Res, 2017
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15
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.
In: Brain imaging and behavior, vol 10, iss 1 (2016)
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16
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
In: American journal of human genetics, vol 99, iss 3 (2016)
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17
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.
In: Brain imaging and behavior, vol 10, iss 1 (2016)
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18
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations.
In: Hearing research, vol 330, iss Pt B (2015)
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19
Differential susceptibility to effects of maternal sensitivity? A study of candidate plasticity genes.
In: Development and psychopathology, vol 27, iss 3 (2015)
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20
Acculturation, Behavioral Factors, and Family History of Breast Cancer among Mexican and Mexican-American Women.
In: Women's health issues : official publication of the Jacobs Institute of Women's Health, vol 25, iss 5 (2015)
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