Literature DB >> 21427756

Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes.

Irene Madrigal1, Mar Xunclà, Maria Isabel Tejada, Francisco Martínez, Isabel Fernández-Carvajal, Luís Alberto Pérez-Jurado, Laia Rodriguez-Revenga, Montserrat Milà.   

Abstract

During the last few years, several studies have reported an excess of intermediate FMR1 alleles in patients with cognitive and/or behavioural phenotypes. Here, we report the frequency of intermediate alleles (IAs) in three pathologies, intellectual disabilities (IDs), attention-deficit/hyperactivity disorder and autism, from different Spanish regions. We found 142 IAs among 9015 patients with ID (1.6%), 4 among the 415 ADHD patients (0.96%) and 4 among the 300 autistic patients (1.3%), similar to the frequency reported in our control population. No evidence was found of an excess of IA at the FRAXA locus in any of the study populations, although geographical variability was detected. Moreover, the analysis of 100 transmissions of IAs showed that 95% of these alleles were stable. Only 3% expanded within the same range and 2% expanded to a full mutation in two generations. No evidence of an association between IAs and behavioural or cognitive phenotypes was found, suggesting that IAs are not clearly implicated in these pathologies.

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Year:  2011        PMID: 21427756      PMCID: PMC3172924          DOI: 10.1038/ejhg.2011.41

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  27 in total

1.  Frequencies of "grey-zone" and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada.

Authors:  P C Patsalis; C Sismani; J A Hettinger; J J Holden; J S Lawson; M Chalifoux; M Wing; M Walker; J Leggo
Journal:  Am J Med Genet       Date:  1999-05-28

2.  Expansion to full mutation of a FMR1 intermediate allele over two generations.

Authors:  Alessandra Terracciano; Maria Grazia Pomponi; Grazia Maria Elisabetta Marino; Pietro Chiurazzi; Maria Michela Rinaldi; Marina Dobosz; Giovanni Neri
Journal:  Eur J Hum Genet       Date:  2004-04       Impact factor: 4.246

3.  Screening for female fragile X premutation and full mutation carriers. A commentary on the work of Wildhagen et Al.

Authors:  M I Tejada; M Duran
Journal:  Community Genet       Date:  1999

4.  FMR1 alleles in Tasmania: a screening study of the special educational needs population.

Authors:  R J Mitchell; J J A Holden; C Zhang; Y Curlis; H R Slater; T Burgess; K C Kirkby; A Carmichael; K D Heading; D Z Loesch
Journal:  Clin Genet       Date:  2005-01       Impact factor: 4.438

5.  Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions.

Authors:  E E Eichler; H A Hammond; J N Macpherson; P A Ward; D L Nelson
Journal:  Hum Mol Genet       Date:  1995-12       Impact factor: 6.150

6.  Length of uninterrupted CGG repeats determines instability in the FMR1 gene.

Authors:  E E Eichler; J J Holden; B W Popovich; A L Reiss; K Snow; S N Thibodeau; C S Richards; P A Ward; D L Nelson
Journal:  Nat Genet       Date:  1994-09       Impact factor: 38.330

7.  Fragile X carrier screening and FMR1 allele distribution in the Japanese population.

Authors:  Susumu Otsuka; Yumiko Sakamoto; Haruhiko Siomi; Mituo Itakura; Kenji Yamamoto; Hideo Matumoto; Tsukasa Sasaki; Nobumasa Kato; Eiji Nanba
Journal:  Brain Dev       Date:  2009-02-10       Impact factor: 1.961

8.  Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms.

Authors:  Danuta Z Loesch; David E Godler; Mahmoud Khaniani; Emma Gould; Freya Gehling; Cheryl Dissanayake; Trent Burgess; Flora Tassone; Richard Huggins; Howard Slater; K H Andy Choo
Journal:  Am J Med Genet A       Date:  2009-10       Impact factor: 2.802

9.  Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

Authors:  Y H Fu; D P Kuhl; A Pizzuti; M Pieretti; J S Sutcliffe; S Richards; A J Verkerk; J J Holden; R G Fenwick; S T Warren
Journal:  Cell       Date:  1991-12-20       Impact factor: 41.582

Review 10.  FMR1 and the fragile X syndrome: human genome epidemiology review.

Authors:  D C Crawford; J M Acuña; S L Sherman
Journal:  Genet Med       Date:  2001 Sep-Oct       Impact factor: 8.822

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  3 in total

1.  Maternal FMR1 alleles expansion in newborns during transmission: a prospective cohort study.

Authors:  Rabia Shahid; Muhammad Yasin; Zia Ur Rehman; Humaira Jadoon; Haleema Tahir; Neelam Meraj; Niamat Khan; Maria Zubair; Irba Zulfiqar; Maha Nowshid; Arfa Azeem; Musarrat Jabeen; Abdul Hameed; Shamim Saleha
Journal:  Pediatr Res       Date:  2022-06-09       Impact factor: 3.756

2.  Clinical Phenotype of Adult Fragile X Gray Zone Allele Carriers: a Case Series.

Authors:  Sarah M Debrey; Maureen A Leehey; Olga Klepitskaya; Christopher M Filley; Raj C Shah; Benzi Kluger; Elizabeth Berry-Kravis; Elaine Spector; Flora Tassone; Deborah A Hall
Journal:  Cerebellum       Date:  2016-10       Impact factor: 3.847

3.  EMQN best practice guidelines for the molecular genetic testing and reporting of fragile X syndrome and other fragile X-associated disorders.

Authors:  Valérie Biancalana; Dieter Glaeser; Shirley McQuaid; Peter Steinbach
Journal:  Eur J Hum Genet       Date:  2014-09-17       Impact factor: 4.246

  3 in total

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