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Genetic Predisposition to Disease (51)
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Hits 1 – 20 of 51
1
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
Bigdeli, Tim B
;
Genovese, Giulio
;
Georgakopoulos, Penelope
...
In: Molecular psychiatry, vol 25, iss 10 (2020)
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2
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry.
Bigdeli, Tim B
;
Genovese, Giulio
;
Georgakopoulos, Penelope
...
In: Molecular psychiatry, vol 25, iss 10 (2020)
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3
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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4
Genetic regulation in pubertal delay.
Howard, SR
. - 2019
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5
Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis.
Kuiper, Jonas JW
;
Setten, Jessica van
;
Devall, Matthew
...
In: Human molecular genetics, vol 27, iss 24 (2018)
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6
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
Savage, Jeanne E
;
Jansen, Philip R
;
Stringer, Sven
...
In: Nature genetics, vol 50, iss 7 (2018)
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7
Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018).
Lam, Max
;
Trampush, Joey W
;
Yu, Jin
...
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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8
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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9
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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10
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
Trampush, JW
;
Yang, MLZ
;
Yu, J
...
In: Molecular psychiatry, vol 22, iss 3 (2017)
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11
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
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12
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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13
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.
Eicher, John D
;
Montgomery, Angela M
;
Akshoomoff, Natacha
...
In: Brain imaging and behavior, vol 10, iss 1 (2016)
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14
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
Leppa, Virpi M
;
Kravitz, Stephanie N
;
Martin, Christa Lese
...
In: American journal of human genetics, vol 99, iss 3 (2016)
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15
Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.
Eicher, John D
;
Montgomery, Angela M
;
Akshoomoff, Natacha
...
In: Brain imaging and behavior, vol 10, iss 1 (2016)
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16
Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations.
Santarelli, Rosamaria
;
del Castillo, Ignacio
;
Cama, Elona
...
In: Hearing research, vol 330, iss Pt B (2015)
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17
Differential susceptibility to effects of maternal sensitivity? A study of candidate plasticity genes.
Belsky, Jay
;
Newman, Daniel A
;
Widaman, Keith F
...
In: Development and psychopathology, vol 27, iss 3 (2015)
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18
Acculturation, Behavioral Factors, and Family History of Breast Cancer among Mexican and Mexican-American Women.
Nodora, Jesse N
;
Cooper, Renee
;
Talavera, Gregory A
...
In: Women's health issues : official publication of the Jacobs Institute of Women's Health, vol 25, iss 5 (2015)
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19
Comorbidities in preschool children at family risk of dyslexia.
Gooch, D
;
Hulme, C
;
Nash, HM
...
In: J Child Psychol Psychiatry , 55 (3) 237 - 246. (2014) (2014)
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20
The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies.
Steinberg, J
;
Webber, C
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2013)
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