1 |
EIN CLOZE TEST ZUR SPRACHSTANDSERHEBUNG PORTUGIESISCHER L2 LERNER DES DEUTSCHEN ...
|
|
|
|
BASE
|
|
Show details
|
|
2 |
Ein Cloze Test zur Sprachstandserhebung portugiesischer L2 Lerner des Deutschen
|
|
|
|
BASE
|
|
Show details
|
|
3 |
The innovative moments coding system and the assimilation of problematic experiences scale: a case study comparing two methods to track change in psychotherapy
|
|
|
|
BASE
|
|
Show details
|
|
4 |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
|
Anney, Richard; Klei, Lambertus; Pinto, Dalila; Almeida, Joana; Bacchelli, Elena; Baird, Gillian; Bolshakova, Nadia; Bölte, Sven; Bolton, Patrick F; Bourgeron, Thomas; Brennan, Sean; Brian, Jessica; Casey, Jillian; Conroy, Judith; Correia, Catarina; Corsello, Christina; Crawford, Emily L; de Jonge, Maretha; Delorme, Richard; Duketis, Eftichia; Duque, Frederico; Estes, Annette; Farrar, Penny; Fernandez, Bridget A; Folstein, Susan E; Fombonne, Eric; Gilbert, John; Gillberg, Christopher; Glessner, Joseph T; Green, Andrew; Green, Jonathan; Guter, Stephen J; Heron, Elizabeth A; Holt, Richard; Howe, Jennifer L; Hughes, Gillian; Hus, Vanessa; Igliozzi, Roberta; Jacob, Suma; Kenny, Graham P; Kim, Cecilia; Kolevzon, Alexander; Kustanovich, Vlad; Lajonchere, Clara M; Lamb, Janine A; Law-Smith, Miriam; Leboyer, Marion; Le Couteur, Ann; Leventhal, Bennett L; Liu, Xiao-Qing; Lombard, Frances; Lord, Catherine; Lotspeich, Linda; Lund, Sabata C; Magalhaes, Tiago R; Mantoulan, Carine; McDougle, Christopher J; Melhem, Nadine M; Merikangas, Alison; Minshew, Nancy J; Mirza, Ghazala K; Munson, Jeff; Noakes, Carolyn; Nygren, Gudrun; Papanikolaou, Katerina; Pagnamenta, Alistair T; Parrini, Barbara; Paton, Tara; Pickles, Andrew; Posey, David J; Poustka, Fritz; Ragoussis, Jiannis; Regan, Regina; Roberts, Wendy; Roeder, Kathryn; Roge, Bernadette; Rutter, Michael L; Schlitt, Sabine; Shah, Naisha; Sheffield, Val C; Soorya, Latha; Sousa, Inês; Stoppioni, Vera; Sykes, Nuala; Tancredi, Raffaella; Thompson, Ann P; Thomson, Susanne; Tryfon, Ana; Tsiantis, John; Van Engeland, Herman; Vincent, John B; Volkmar, Fred; Vorstman, JAS; Wallace, Simon; Wing, Kirsty; Wittemeyer, Kerstin; Wood, Shawn; Zurawiecki, Danielle; Zwaigenbaum, Lonnie; Bailey, Anthony J
|
|
In: Human molecular genetics, vol 21, iss 21 (2012)
|
|
Abstract:
While it is apparent that rare variation can play an important role in the genetic architecture of autism spectrum disorders (ASDs), the contribution of common variation to the risk of developing ASD is less clear. To produce a more comprehensive picture, we report Stage 2 of the Autism Genome Project genome-wide association study, adding 1301 ASD families and bringing the total to 2705 families analysed (Stages 1 and 2). In addition to evaluating the association of individual single nucleotide polymorphisms (SNPs), we also sought evidence that common variants, en masse, might affect the risk. Despite genotyping over a million SNPs covering the genome, no single SNP shows significant association with ASD or selected phenotypes at a genome-wide level. The SNP that achieves the smallest P-value from secondary analyses is rs1718101. It falls in CNTNAP2, a gene previously implicated in susceptibility for ASD. This SNP also shows modest association with age of word/phrase acquisition in ASD subjects, of interest because features of language development are also associated with other variation in CNTNAP2. In contrast, allele scores derived from the transmission of common alleles to Stage 1 cases significantly predict case status in the independent Stage 2 sample. Despite being significant, the variance explained by these allele scores was small (Vm< 1%). Based on results from individual SNPs and their en masse effect on risk, as inferred from the allele score results, it is reasonable to conclude that common variants affect the risk for ASD but their individual effects are modest.
|
|
Keyword:
Alleles; Biological Sciences; Child; Child Development Disorders; Female; Gene Frequency; Genetic Predisposition to Disease; Genetics & Heredity; Genome-Wide Association Study; Genotype; Humans; Language Development; Male; Medical and Health Sciences; Membrane Proteins; Nerve Tissue Proteins; Pervasive; Polymorphism; Risk Factors; Single Nucleotide
|
|
URL: https://escholarship.org/uc/item/7452m9z1
|
|
BASE
|
|
Hide details
|
|
5 |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
|
|
|
In: ISSN: 0964-6906 ; EISSN: 1460-2083 ; Human Molecular Genetics ; https://www.hal.inserm.fr/inserm-00723650 ; Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (21), pp.4781-92. ⟨10.1093/hmg/dds301⟩ (2012)
|
|
BASE
|
|
Show details
|
|
6 |
Individual common variants exert weak effects on the risk for autism spectrum disorders
|
|
|
|
BASE
|
|
Show details
|
|
7 |
Individual common variants exert weak effects on risk for Autism Spectrum Disorders
|
|
|
|
BASE
|
|
Show details
|
|
8 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
|
|
|
|
BASE
|
|
Show details
|
|
9 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
|
|
|
|
BASE
|
|
Show details
|
|
10 |
Individual common variants exert weak effects on the risk for autism spectrum disorderspi
|
|
|
|
BASE
|
|
Show details
|
|
11 |
Narrative change in emotion-focused therapy: how is change constructed through the lens of the innovative moments coding system?
|
|
|
|
In: Psychotherapy research : journal of the Society for Psychotherapy Research 20 (2010) 6, 692-701
|
|
IDS Bibliografie zur Gesprächsforschung
|
|
Show details
|
|
|
|