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4q22
A chromosome band present on 4q
National Institutes of Health
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Related topics
Related topics
5 relations
ABCG2 wt Allele
ADH4 wt Allele
ATOH1 wt Allele
Chromosomes
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Analysis of genome‐wide association study‐linked loci in Parkinson's disease of Mainland China
Jun Liu
,
Q. Xiao
,
+8 authors
S. Chen
Movement Disorders
2013
Corpus ID: 41786422
Genome‐wide association studies (GWAS) have identified numerous single‐nucleotide polymorphisms (SNPs) that can modulate the risk…
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Highly Cited
2011
Highly Cited
2011
A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.
J. Nousbeck
,
B. Burger
,
+5 authors
E. Sprecher
American Journal of Human Genetics
2011
Corpus ID: 44296294
Highly Cited
2008
Highly Cited
2008
Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22
K. Pulli
,
K. Karma
,
R. Norio
,
P. Sistonen
,
H. H. Göring
,
I. Järvelä
Journal of Medical Genetics
2008
Corpus ID: 14842214
Background: Music perception and performance are comprehensive human cognitive functions and thus provide an excellent model…
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Highly Cited
2007
Highly Cited
2007
Anaplastic lymphoma kinase-positive diffuse large B-cell lymphoma with a complex karyotype and cryptic 3' ALK gene insertion to chromosome 4 q22-24.
Dariusz Stachurski
,
P. Miron
,
+4 authors
Sa A. Wang
Human Pathology
2007
Corpus ID: 8763176
Highly Cited
2007
Highly Cited
2007
A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for Wolfram syndrome 2.
S. Amr
,
Cindy Heisey
,
+7 authors
R. Shiang
American Journal of Human Genetics
2007
Corpus ID: 35638486
A single missense mutation was identified in a novel, highly conserved zinc-finger gene, ZCD2, in three consanguineous families…
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Highly Cited
2005
Highly Cited
2005
The human HERC family of ubiquitin ligases: novel members, genomic organization, expression profiling, and evolutionary aspects.
Karin Hochrainer
,
H. Mayer
,
U. Baranyi
,
B. Binder
,
J. Lipp
,
Renate Kroismayr
Genomics
2005
Corpus ID: 35460666
Highly Cited
2004
Highly Cited
2004
Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: possible association with an inherited disease and cancer
L. Rozier
,
Eliane El-Achkar
,
F. Apiou
,
M. Debatisse
Oncogene
2004
Corpus ID: 951438
Fragile sites are classified as common or rare depending on their occurrence in the populations. While rare sites are mainly…
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2002
2002
Cloning, expression and characterisation of a human Nudix hydrolase specific for adenosine 5'-diphosphoribose (ADP-ribose).
Shengrong Lin
,
L. Gasmi
,
+10 authors
A. McLennan
Biochimica et Biophysica Acta
2002
Corpus ID: 36213714
Highly Cited
2000
Highly Cited
2000
Genomic organization and chromosome localization of the newly identified human heparanase gene.
Jianghan Dong
,
Angela Kukula
,
M. Toyoshima
,
M. Nakajima
Gene
2000
Corpus ID: 46477629
1996
1996
A gene similar to PKD1 maps to chromosome 4q22: a candidate gene for PKD2.
M. Schneider
,
A. M. Rodriguez
,
+4 authors
S. Weremowicz
Genomics
1996
Corpus ID: 21878512
We report a partial cDNA sequence that encodes a protein, dubbed "polycystwin," with 21% identify and 46% similarity to amino…
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