Ordered-subset analysis of savant skills in autism for 15q11-q13

被引:18
作者
Ma, DQ
Jaworski, J
Menold, MM
Donnelly, S
Abramson, RK
Wright, HH
Delong, GR
Gilbert, JR
Pericak-Vance, MA
Cuccaro, ML
机构
[1] Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Div Pediat Neurol, Durham, NC USA
[3] Univ S Carolina, WS Hall Psychiat Inst, Columbia, SC 29208 USA
关键词
autism; genetics; subsetting; phenotype; linkage;
D O I
10.1002/ajmg.b.30166
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Autism is a complex disorder characterized by genetic and phenotypic heterogeneity. Analysis of phenotypically homogeneous subtypes has been used to both confirm and narrow potential autism linkage regions such as the chromosomal region 15q11-q13. Increased evidence for linkage in this region had been found in a subgroup of 21 autism families (total families = 94) stratified based on a savant skill factor (SSF) from the Autism Diagnostic Interview, Revised (ADI-R). We examined the savant phenotypic finding in our sample of 91 multiplex autism families. Using two-point parametric analysis in stratification with a cutoff point of a savant skill score of 0.16, our families failed to demonstrate linkage to 15q11-q13. In addition, ordered subset analysis (OSA) using SSF as a covariate also failed to show evidence for linkage. Our findings do not support savant skills as an informative phenotypic subset for linkage in our sample. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:38 / 41
页数:4
相关论文
共 50 条
  • [1] Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13
    Nurmi, EL
    Dowd, M
    Tadevosyan-Leyfer, O
    Haines, JL
    Folstein, SE
    Sutcliffe, JS
    JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2003, 42 (07) : 856 - 863
  • [2] Transmission Disequilibrium, Testing of the Chromosome 15q11-q13 Region in Autism
    Kim, Soo-Jeong
    Brune, Camille W.
    Kistner, Emily O.
    Christian, Susan L.
    Courchesne, Eric H.
    Cox, Nancy J.
    Cook, Edwin H.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2008, 147B (07) : 1116 - 1125
  • [3] Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
    Depienne, Christel
    Moreno-De-Luca, Daniel
    Heron, Delphine
    Bouteiller, Delphine
    Gennetier, Aurelie
    Delorme, Richard
    Chaste, Pauline
    Siffroi, Jean-Pierre
    Chantot-Bastaraud, Sandra
    Benyahia, Baya
    Trouillard, Oriane
    Nygren, Gudrun
    Kopp, Svenny
    Johansson, Maria
    Rastam, Maria
    Burglen, Lydie
    Leguern, Eric
    Verloes, Alain
    Leboyer, Marion
    Brice, Alexis
    Gillberg, Christopher
    Betancur, Catalina
    BIOLOGICAL PSYCHIATRY, 2009, 66 (04) : 349 - 359
  • [4] Clinical and Genetic Study of a Family With a Paternally Inherited 15q11-q13 Duplication
    Marini, Carla
    Cecconi, Antonella
    Contini, Elisa
    Pantaleo, Marilena
    Metitieri, Tiziana
    Guarducci, Silvia
    Giglio, Sabrina
    Guerrini, Renzo
    Genuardi, Maurizio
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2013, 161A (06) : 1459 - 1464
  • [5] Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism
    Salmon, B
    Hallmayer, J
    Rogers, T
    Kalaydjieva, L
    Petersen, PB
    Nicholas, P
    Pingree, C
    McMahon, W
    Spiker, D
    Lotspeich, L
    Kraemer, H
    McCague, P
    Dimiceli, S
    Nouri, N
    Pitts, T
    Yang, J
    Hinds, D
    Myers, RM
    Risch, N
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 88 (05): : 551 - 556
  • [6] Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes
    Kalsner, Louisa
    Chamberlain, Stormy J.
    PEDIATRIC CLINICS OF NORTH AMERICA, 2015, 62 (03) : 587 - +
  • [7] Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness
    Ingason, Andres
    Kirov, George
    Giegling, Ina
    Hansen, Thomas
    Isles, Anthony R.
    Jakobsen, Klaus D.
    Kristinsson, Kari T.
    le Roux, Louise
    Gustafsson, Omar
    Craddock, Nick
    Moeller, Hans-Juergen
    McQuillin, Andrew
    Muglia, Pierandrea
    Cichon, Sven
    Rietschel, Marcella
    Ophoff, Roel A.
    Djurovic, Srdjan
    Andreassen, Ole A.
    Pietilaeinen, Olli P. H.
    Peltonen, Leena
    Dempster, Emma
    Collier, David A.
    Clair, David St.
    Rasmussen, Henrik B.
    Glenthoj, Birte Y.
    Kiemeney, Lambertus A.
    Franke, Barbara
    Tosato, Sarah
    Bonetto, Chiara
    Saemundsen, Evald
    Hreidarsson, Stefan J.
    Noethen, Markus M.
    Gurling, Hugh
    O'Donovan, Michael C.
    Owen, Michael J.
    Sigurdsson, Engilbert
    Petursson, Hannes
    Stefansson, Hreinn
    Rujescu, Dan
    Stefansson, Kari
    Werge, Thomas
    AMERICAN JOURNAL OF PSYCHIATRY, 2011, 168 (04) : 408 - 417
  • [8] Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism
    Nurmi, EL
    Amin, T
    Olson, LM
    Jacobs, MM
    McCauley, JL
    Lam, AY
    Organ, EL
    Folstein, SE
    Haines, JL
    Sutcliffe, JS
    MOLECULAR PSYCHIATRY, 2003, 8 (06) : 624 - 634
  • [9] Parent-of-Origin Testing for 15q11-q13 Gains by Quantitative DNA Methylation Analysis
    Askree, S. Hussain
    Dharamrup, Shika
    Hjelm, Lawrence N.
    Coffee, Bradford
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2012, 14 (03) : 192 - 198
  • [10] No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population
    Tochigi, Mamoru
    Kato, Chieko
    Koishi, Shinko
    Kawakubo, Yuki
    Yamamoto, Kenji
    Matsumoto, Hideo
    Hashimoto, Ohiko
    Kim, Soo-Yung
    Watanabe, Keiichiro
    Kano, Yukiko
    Nanba, Eiji
    Kato, Nobumasa
    Sasaki, Tsukasa
    JOURNAL OF HUMAN GENETICS, 2007, 52 (12) : 985 - 989