Literature DB >> 7961335

Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder.

P Baker1, J Piven, S Schwartz, S Patil.   

Abstract

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Year:  1994        PMID： 7961335     DOI： 10.1007/BF02172133

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN： 0162-3257


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  10 in total

1.  Autism associated with marker chromosome.

Authors:  C Gillberg; S Steffenburg; J Wahlström; I C Gillberg; A Sjöstedt; T Martinsson; S Liedgren; O Eeg-Olofsson
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1991-05       Impact factor: 8.829

2.  Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

Authors:  D H Ledbetter; V M Riccardi; S D Airhart; R J Strobel; B S Keenan; J D Crawford
Journal:  N Engl J Med       Date:  1981-02-05       Impact factor: 91.245

3.  Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15.

Authors:  J Wagstaff; J H Knoll; J Fleming; E F Kirkness; A Martin-Gallardo; F Greenberg; J M Graham; J Menninger; D Ward; J C Venter
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

Review 4.  Etiology of autism: genetic influences.

Authors:  S E Folstein; J Piven
Journal:  Pediatrics       Date:  1991-05       Impact factor: 7.124

5.  Cytogenetic and clinical studies in five cases of inv dup(15).

Authors:  L Wisniewski; T Hassold; J Heffelfinger; J V Higgins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

6.  The prevalence of fragile X in a sample of autistic individuals diagnosed using a standardized interview.

Authors:  J Piven; J Gayle; R Landa; M Wzorek; S Folstein
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  1991-09       Impact factor: 8.829

7.  Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A.

Authors:  J R Lupski; C A Wise; A Kuwano; L Pentao; J T Parke; D G Glaze; D H Ledbetter; F Greenberg; P I Patel
Journal:  Nat Genet       Date:  1992-04       Impact factor: 38.330

8.  Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.

Authors:  D H Ledbetter; J T Mascarello; V M Riccardi; V D Harper; S D Airhart; R J Strobel
Journal:  Am J Hum Genet       Date:  1982-03       Impact factor: 11.025

9.  Clinical and molecular analysis of five inv dup(15) patients.

Authors:  W P Robinson; F Binkert; R Giné; C Vazquez; W Müller; W Rosenkranz; A Schinzel
Journal:  Eur J Hum Genet       Date:  1993       Impact factor: 4.246

10.  Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues.

Authors:  I L Cohen; V Sudhalter; A Pfadt; E C Jenkins; W T Brown; P M Vietze
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025
  10 in total
  30 in total

Review 1.  The pathophysiology and treatment of autism.

Authors:  D J Posey; C J McDougle
Journal:  Curr Psychiatry Rep       Date:  2001-04       Impact factor: 5.285

Review 2.  Genomic copy number variation in disorders of cognitive development.

Authors:  Eric M Morrow
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2010-11       Impact factor: 8.829

3.  A 15q13.3 microdeletion segregating with autism.

Authors:  Alistair T Pagnamenta; Kirsty Wing; Elham Sadighi Akha; Samantha J L Knight; Sven Bölte; Gabriele Schmötzer; Eftichia Duketis; Fritz Poustka; Sabine M Klauck; Annemarie Poustka; Jiannis Ragoussis; Anthony J Bailey; Anthony P Monaco
Journal:  Eur J Hum Genet       Date:  2008-12-03       Impact factor: 4.246

Review 4.  Molecular genetic investigations of autism.

Authors:  E Maestrini; A J Marlow; D E Weeks; A P Monaco
Journal:  J Autism Dev Disord       Date:  1998-10

Review 5.  Chromosomal disorders and autism.

Authors:  C Gillberg
Journal:  J Autism Dev Disord       Date:  1998-10

6.  Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR.

Authors:  A Oguro-Ando; C Rosensweig; E Herman; Y Nishimura; D Werling; B R Bill; J M Berg; F Gao; G Coppola; B S Abrahams; D H Geschwind
Journal:  Mol Psychiatry       Date:  2014-10-14       Impact factor: 15.992

7.  Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.

Authors:  E H Cook; V Lindgren; B L Leventhal; R Courchesne; A Lincoln; C Shulman; C Lord; E Courchesne
Journal:  Am J Hum Genet       Date:  1997-04       Impact factor: 11.025

8.  The Genetic Control of Stoichiometry Underlying Autism.

Authors:  Robert B Darnell
Journal:  Annu Rev Neurosci       Date:  2020-07-08       Impact factor: 12.449

9.  Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

Authors:  Karen N Leung; Roxanne O Vallero; Amanda J DuBose; James L Resnick; Janine M LaSalle
Journal:  Hum Mol Genet       Date:  2009-08-05       Impact factor: 6.150

10.  Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.

Authors:  Simon G Gregory; Jessica J Connelly; Aaron J Towers; Jessica Johnson; Dhani Biscocho; Christina A Markunas; Carla Lintas; Ruth K Abramson; Harry H Wright; Peter Ellis; Cordelia F Langford; Gordon Worley; G Robert Delong; Susan K Murphy; Michael L Cuccaro; Antonello Persico; Margaret A Pericak-Vance
Journal:  BMC Med       Date:  2009-10-22       Impact factor: 8.775
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