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Hits 1 – 20 of 30
1
Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation.
Klusek, Jessica
;
Fairchild, Amanda
;
Moser, Carly
...
In: Journal of neurodevelopmental disorders, vol 14, iss 1 (2022)
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2
The trans-ancestral genomic architecture of glycemic traits.
Chen, J.
;
Spracklen, C.N.
;
Marenne, G.
...
In: Nature genetics, vol. 53, no. 6, pp. 840-860 (2021)
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3
Developmental regulation of canonical and small ORF translation from mRNAs
Patraquim, Pedro
;
Mumtaz, Muhammad Ali Shahzad
;
Pueyo, Jose Ignacio
. - : BMC, 2020
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4
Bi-allelic Variants in IQSEC1 Cause Intellectual Disability, Developmental Delay, and Short Stature.
Ansar, M.
;
Chung, H.L.
;
Al-Otaibi, A.
...
In: American journal of human genetics, vol. 105, no. 5, pp. 907-920 (2019)
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5
Global genetic differentiation of complex traits shaped by natural selection in humans.
Guo, J.
;
Wu, Y.
;
Zhu, Z.
...
In: Nature communications, vol. 9, no. 1, pp. 1865 (2018)
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6
Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay.
Ansar, M.
;
Riazuddin, S.
;
Sarwar, M.T.
...
In: Genetics in medicine, vol. 20, no. 7, pp. 778-784 (2018)
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7
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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8
High-throughput assessment of small open reading frame translation in Drosophila melanogaster
Mumtaz, Muhammad Ali Shahzad
. - 2016
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9
A novel multi-alignment pipeline for high-throughput sequencing data.
Huang, Shunping
;
Holt, James
;
Kao, Chia-Yu
...
In: Database : the journal of biological databases and curation, vol 2014, iss 0 (2014)
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10
Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adults
Alfred, T
;
Ben-Shlomo, Y
;
Cooper, R
...
In: The Journal of Nutrition , 143 (5) 606 -612. (2013) (2013)
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11
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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12
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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13
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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14
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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15
Population-level neutral model already explains linguistic patterns.
Bentley, RA
;
Ormerod, P
;
Shennan, S
In: Proc Biol Sci , 278 (1713) pp. 1770-1772. (2011) (2011)
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16
Hemiplasy: a new term in the lexicon of phylogenetics.
Avise, John C
;
Robinson, Terence J
In: Systematic biology, vol 57, iss 3 (2008)
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17
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
Groszer, M
;
Keays, DA
;
Deacon, RM
...
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 (2008)
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18
The co-evolution of culturally inherited altruistic helping and cultural transmission under random group formation.
Lehmann, L.
;
Feldman, M.W.
In: Theoretical Population Biology, vol. 73, no. 4, pp. 506-516 (2008)
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19
The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence
Mekel-Bobrov, Nitzan
;
Posthuma, Danielle
;
Gilbert, Sandra L.
. - : Oxford University Press, 2007
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20
APOE ε2-ε4 genotype is a possible risk factor for primary progressive aphasia [6]
Acciarri, A.
;
Masullo, C.
(orcid:0000-0001-7798-3410);
Bizzarro, A.
. - : WILEY-LISS, 2006
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