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Simple Search
Hits 1 – 16 of 16
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
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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4
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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5
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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6
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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7
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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8
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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9
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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10
Cerebral asymmetry and language development: cause, correlate, or consequence?
Bishop, DV
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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11
New insight on the Xq28 association with systemic sclerosis.
Carmona, FD
;
Cénit, MC
;
Diaz-Gallo, LM
...
In: Ann Rheum Dis , 72 (12) 2032 - 2038. (2013) (2013)
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12
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci
J. Martin
;
S. Assassi
;
L. Diaz-Gallo
. - : Oxford University Press, 2013
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13
Individual common variants exert weak effects on the risk for autism spectrum disorders.
Anney, Richard
;
Klei, Lambertus
;
Pinto, Dalila
...
In: Human molecular genetics, vol 21, iss 21 (2012)
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14
Individual common variants exert weak effects on the risk for autism spectrum disorderspi.
Anney, R
;
Klei, L
;
Pinto, D
...
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 ; ORA review team (2012)
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15
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
Gorlova, Olga
;
Martin, Jose-Ezequiel
;
Rueda, Blanca
...
In: PLoS genetics, vol 7, iss 7 (2011)
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16
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
Newbury, DF
;
Paracchini, S
;
Scerri, TS
...
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 (2011)
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