S E Folstein
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Explore the profile of S E Folstein including associated specialties, affiliations and a list of published articles.
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86
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27650
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Recent Articles
1.
Skaar D, Shao Y, Haines J, Stenger J, Jaworski J, Martin E, et al.
Mol Psychiatry
. 2004 Nov;
10(6):563-71.
PMID: 15558079
Several genome-wide screens have indicated the presence of an autism susceptibility locus within the distal long arm of chromosome 7 (7q). Mapping at 7q22 within this region is the candidate...
2.
McCauley J, Olson L, Dowd M, Amin T, Steele A, Blakely R, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2004 Apr;
127B(1):104-12.
PMID: 15108191
Autism is a complex genetic neurodevelopmental disorder in which affected individuals display deficits in language, social relationships, and patterns of compulsive and stereotyped behaviors and rigidity. Linkage analysis in our...
3.
Wassink T, Piven J, Vieland V, Pietila J, Goedken R, Folstein S, et al.
Mol Psychiatry
. 2004 Apr;
9(10):968-72.
PMID: 15098001
Impaired reciprocal social interaction is one of the core features of autism. While its determinants are complex, one biomolecular pathway that clearly influences social behavior is the arginine-vasopressin (AVP) system....
4.
Nurmi E, Amin T, Olson L, Jacobs M, McCauley J, Lam A, et al.
Mol Psychiatry
. 2003 Jul;
8(6):624-34, 570.
PMID: 12851639
Autism [MIM 209850] is a neurodevelopmental disorder exhibiting a complex genetic etiology with clinical and locus heterogeneity. Chromosome 15q11-q13 has been proposed to harbor a gene for autism susceptibility based...
5.
McInnis M, Lan T, Willour V, McMahon F, Simpson S, Addington A, et al.
Mol Psychiatry
. 2003 Mar;
8(3):288-98.
PMID: 12660801
The purpose of this study was to assess 65 pedigrees ascertained through a Bipolar I (BPI) proband for evidence of linkage, using nonparametric methods in a genome-wide scan and for...
6.
Hutcheson H, Bradford Y, Folstein S, Gardiner M, Santangelo S, Sutcliffe J, et al.
Am J Med Genet B Neuropsychiatr Genet
. 2003 Jan;
117B(1):90-6.
PMID: 12555242
Previous genetic and cytogenetic studies provide evidence that points to one or more autism susceptibility genes residing on chromosome 7q (AUTS1, 115-149 cM on the Marshfield map). However, further localization...
7.
Folstein S, Rosen-Sheidley B
Nat Rev Genet
. 2001 Dec;
2(12):943-55.
PMID: 11733747
Since autism was first recognized as a disorder in 1943, speculation about its aetiology has ranged from biological to psychological and back again. After twin studies during the 1970s and...
8.
Nurmi E, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner M, et al.
Genomics
. 2001 Sep;
77(1-2):105-13.
PMID: 11543639
Autistic disorder is a neurodevelopmental disorder with a complex genetic etiology. Observations of maternal duplications affecting chromosome 15q11-q13 in patients with autism and evidence for linkage and linkage disequilibrium to...
9.
Wassink T, Piven J, Vieland V, Huang J, Swiderski R, Pietila J, et al.
Am J Med Genet
. 2001 Jul;
105(5):406-13.
PMID: 11449391
We examined WNT2 as a candidate disease gene for autism for the following reasons. First, the WNT family of genes influences the development of numerous organs and systems, including the...
10.
Folstein S, Mankoski R
Am J Hum Genet
. 2000 Jul;
67(2):278-81.
PMID: 10889044
No abstract available.