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15q14
A chromosome band present on 15q
National Institutes of Health
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10 relations
15q
C15orf55 wt Allele
CASC5 wt Allele
Chromosomes
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Usefulness of Nuclear Protein in Testis (NUT) Immunohistochemistry in the Cytodiagnosis of NUT Midline Carcinoma: A Brief Case Report
H. Park
,
Y. Bae
,
+4 authors
S. Hong
The Korean Journal of Pathology
2014
Corpus ID: 6832595
Nuclear protein in testis (NUT) midline carcinomas are uncommon, recently described, fatal neoplasm that are characterized by…
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2013
2013
Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort
Claire L. Simpson
,
R. Wojciechowski
,
S. Yee
,
Poorva Soni
,
J. Bailey-Wilson
,
D. Stambolian
Molecular Vision
2013
Corpus ID: 22320913
Purpose Refractive error is a complex trait with multiple genetic and environmental risk factors, and is the most common cause of…
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2006
2006
Characterization of allelic variants at chromosome 15q14 in schizophrenia
R. Freedman
,
S. Leonard
,
M. Waldo
,
J. Gault
,
A. Olincy
,
L. Adler
Genes, Brain and Behavior
2006
Corpus ID: 8120906
Evidence of genetic linkage for schizophrenia at chromosome 15q14 has been reported in nine independent studies, but the…
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2006
2006
P50 sensory gating deficit in children with centrotemporal spikes and sharp waves in the EEG
B. Fiedler
,
O. Debus
,
B. Neubauer
,
M. Kienle
,
G. Kurlemann
Neuroscience Letters
2006
Corpus ID: 30166731
Highly Cited
2002
Highly Cited
2002
The effects of nicotine on specific eye tracking measures in schizophrenia
J. Sherr
,
C. Myers
,
M. Avila
,
Amie Elliott
,
T. Blaxton
,
G. Thaker
Biological Psychiatry
2002
Corpus ID: 22944498
2002
2002
Identification and mutational analysis of candidate genes for juvenile myoclonic epilepsy on 6p11–p12: LRRC1, GCLC, KIAA0057 and CLIC5
Toshimitsu Suzuki
,
R. Morita
,
+14 authors
K. Yamakawa
Epilepsy Research
2002
Corpus ID: 9340681
2002
2002
Mutational analysis of the connexin 36 gene (CX36) and exclusion of the coding sequence as a candidate region for catatonic schizophrenia in a large pedigree
Jobst Meyer
,
Marion Mai
,
G. Ortega
,
R. Mössner
,
K. Lesch
Schizophrenia Research
2002
Corpus ID: 12288868
Highly Cited
2001
Highly Cited
2001
Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium
G. Turecki
,
P. Grof
,
+13 authors
M. Alda
Molecular Psychiatry
2001
Corpus ID: 23903314
Genetic mapping studies in bipolar disorder (BD) have been hampered by the unclear boundaries of the phenotypic spectrum, and…
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2001
2001
Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy
O. Steinlein
,
B. Neubauer
,
T. Sander
,
Luyan Song
,
J. Stoodt
,
D. Mount
Epilepsy Research
2001
Corpus ID: 24004785
2000
2000
Unbalanced translocation t(15;22) in "severe" Prader-Willi syndrome.
A. Smith
,
A. Jauch
,
L. St. Heaps
,
L. Robson
,
B. Kearney
Annales de Genetique
2000
Corpus ID: 44286195
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