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15q11-q13
A chromosome band present on 15q.
National Institutes of Health
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Related topics
Related topics
3 relations
15q
Chromosomes
UBE3A wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Transmission disequilibrium testing of the chromosome 15q11‐q13 region in autism
Soo-Jeong Kim
,
Camille W. Brune
,
+4 authors
E. Cook
American Journal of Medical Genetics Part B…
2008
Corpus ID: 13945623
Evidence implicates the serotonin transporter gene (SLC6A4) and the 15q11‐q13 genes as candidates for autism as well as…
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Highly Cited
2007
Highly Cited
2007
Quantification of the methylation status of the PWS/AS imprinted region: comparison of two approaches based on bisulfite sequencing and methylation-sensitive MLPA.
N. Dikow
,
A. Nygren
,
+4 authors
J. Zschocke
Molecular and Cellular Probes
2007
Corpus ID: 8439619
2005
2005
Relationship between severity of epilepsy and developmental outcome in Angelman syndrome
Y. Ohtsuka
,
Katsuhiro Kobayashi
,
+4 authors
E. Oka
Brain & development (Tokyo. )
2005
Corpus ID: 36270329
2005
2005
Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD.
D. Bittel
,
N. Kibiryeva
,
Z. Talebizadeh
,
D. J. Driscoll
,
M. Butler
Genomics
2005
Corpus ID: 37456779
2005
2005
A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
Mihaela Ștefan
,
T. Portis
,
R. Longnecker
,
R. Nicholls
Genomics
2005
Corpus ID: 23855797
2003
2003
Reserpine responsive myoclonus and hyperpyrexia in a patient with Angelman syndrome
M. Stecker
,
S. Myers
Clinical neurology and neurosurgery (Dutch…
2003
Corpus ID: 21305340
1999
1999
Imprinted methylation and its effect on expression of the mouse Zfp127 gene.
A. Hershko
,
A. Razin
,
R. Shemer
Gene
1999
Corpus ID: 35822383
Highly Cited
1999
Highly Cited
1999
In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit.
Johannes Schweizer
,
Debra Zynger
,
Uta Francke
Human Molecular Genetics
1999
Corpus ID: 31997839
Human chromosome region 15q11-q13 contains a cluster of oppositely imprinted genes. Loss of the paternal or the maternal alleles…
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1996
1996
Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.
L. White
,
Peter K. Rogan
,
R. D. Nicholls
,
Bai-lin Wu
,
Bruce R. Korf
,
J. H. Knoll
American Journal of Human Genetics
1996
Corpus ID: 37568298
Allele-specific replication differences have been observed in imprinted chromosomal regions. We have exploited this…
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1995
1995
Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
N. Spinner
,
E. Zackai
,
Sou-De Cheng
,
J. H. Knoll
American journal of medical genetics
1995
Corpus ID: 2769060
We have studied a patient with Angelman syndrome (AS) and a 47,XY,+inv dup(15) (pter-->q11::q11-->pter) karyotype. Molecular…
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