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15q21
A chromosome band present on 15q
National Institutes of Health
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Related topics
Related topics
7 relations
15q
BCL2L10 wt Allele
Chromosomes
MAPK6 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci
Y. Liu
,
C. Helms
,
+17 authors
A. Bowcock
PLoS Genetics
2008
Corpus ID: 17386118
A genome-wide association study was performed to identify genetic factors involved in susceptibility to psoriasis (PS) and…
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Highly Cited
2004
Highly Cited
2004
Analysis of the human VPS13 gene family.
A. Velayos-Baeza
,
A. Vettori
,
R. Copley
,
C. Dobson-Stone
,
A. Monaco
Genomics
2004
Corpus ID: 2097921
Highly Cited
2004
Highly Cited
2004
Support for EKN1 as the susceptibility locus for dyslexia on 15q21
K. Wigg
,
J. Couto
,
+7 authors
C. Barr
Molecular Psychiatry
2004
Corpus ID: 24772292
Dyslexia has been linked to a number of chromosomal regions including 15q. Recently a gene, EKN1, with unknown function in the…
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Highly Cited
2003
Highly Cited
2003
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain
M. Taipale
,
N. Kaminen
,
+8 authors
J. Kere
Proceedings of the National Academy of Sciences…
2003
Corpus ID: 15766642
Approximately 3–10% of people have specific difficulties in reading, despite adequate intelligence, education, and social…
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Highly Cited
2001
Highly Cited
2001
Rab27a: A key to melanosome transport in human melanocytes.
P. Bahadoran
,
E. Aberdam
,
+7 authors
R. Ballotti
Journal of Cell Biology
2001
Corpus ID: 195690847
Normal pigmentation depends on the uniform distribution of melanin-containing vesicles, the melanosomes, in the epidermis…
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Highly Cited
2000
Highly Cited
2000
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
Gaël Ménasché
,
É. Pastural
,
+8 authors
G. Basile
Nature Genetics
2000
Corpus ID: 7698624
Griscelli syndrome (GS, MIM 214450), a rare, autosomal recessive disorder, results in pigmentary dilution of the skin and the…
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Highly Cited
2000
Highly Cited
2000
Two genes are responsible for Griscelli syndrome at the same 15q21 locus.
É. Pastural
,
F. Ersoy
,
+8 authors
G. de Saint Basile
Genomics
2000
Corpus ID: 27499573
Griscelli syndrome is a rare autosomal recessive disease characterized by pigment dilution, variable cellular immunodeficiency…
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Highly Cited
1997
Highly Cited
1997
Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene
É. Pastural
,
F. Barrat
,
+7 authors
G. Basile
Nature Genetics
1997
Corpus ID: 21815627
Griscelli disease (OMIM 214450) is a rare autosomal recessive disorder characterized by pigmentary dilution, variable cellular…
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Highly Cited
1997
Highly Cited
1997
Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23.
J. Sharp
,
R. Wheeler
,
+5 authors
R. Williams
Human Molecular Genetics
1997
Corpus ID: 24961182
The childhood neuronal ceroid lipofuscinoses (NCLs) are a group of autosomal recessive neurodegenerative disorders characterised…
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Review
1995
Review
1995
Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders.
H. Dietz
,
R. Pyeritz
Human Molecular Genetics
1995
Corpus ID: 19861975
The extracellular microfibril, 10-14 nm in diameter, performs a number of functions, including serving as the scaffolding for…
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