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16q22.1
A chromosome band present on 16q
National Institutes of Health
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19 relations
16q
ACD wt Allele
CDH1 wt Allele
CDH3 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Two dominantly inherited ataxias linked to chromosome 16q22.1: SCA4 and SCA31 are not allelic
Ulf Edener
,
V. Bernard
,
Y. Hellenbroich
,
G. Gillessen‐Kaesbach
,
C. Zühlke
Journal of Neurology
2011
Corpus ID: 22644988
Autosomal dominant spinocerebellar ataxias (SCAs) are heterogeneous neurological disorders characterised by cerebellar…
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Highly Cited
2010
Highly Cited
2010
Association studies on 11 published colorectal cancer risk loci
S. Holst
,
S. Picelli
,
+24 authors
A. Lindblom
British Journal of Cancer
2010
Corpus ID: 12716909
Background:Recently, several genome-wide association studies (GWAS) have independently found numerous loci at which common single…
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2007
2007
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia
T. Amino
,
K. Ishikawa
,
+8 authors
H. Mizusawa
Journal of Human Genetics
2007
Corpus ID: 8106737
AbstractThe 16q22.1-linked autosomal dominant cerebellar ataxia (16q-ADCA; Online Mendelian Inheritance in Man [OMIN] #117210) is…
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2006
2006
16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study
Ouyang Yi
,
K. Sakoe
,
+12 authors
Y. Takiyama
Journal of Neurological Sciences
2006
Corpus ID: 35623283
2006
2006
Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese
Y. Onodera
,
Masashi Aoki
,
Hideki Mizuno
,
H. Warita
,
Y. Shiga
,
Y. Itoyama
Neurology
2006
Corpus ID: 28025112
Chromosome 16q22.1-linked autosomal dominant cerebellar ataxia (16q-ADCA) is strongly associated with a substitution in the…
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Review
2005
Review
2005
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1→qter) and partial monosomy 20q (20q13.3→qter)
Chih-ping Chen
,
Shuan-Pei Lin
,
+6 authors
Wayseen Wang
Prenatal Diagnosis
2005
Corpus ID: 41848343
To present the perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q and partial monosomy 20q and…
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Highly Cited
2003
Highly Cited
2003
Frequent E-cadherin Gene Inactivation by Loss of Heterozygosity in Pleomorphic Lobular Carcinoma of the Breast
J. Palacios
,
D. Sarrió
,
M. García-Macías
,
B. Bryant
,
M. Sobel
,
M. Merino
Modern Pathology
2003
Corpus ID: 24428642
Pleomorphic lobular carcinoma of the breast is a variant of infiltrating lobular carcinoma that has poor prognosis. The…
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2001
2001
Mapping the chromosome 16 cadherin gene cluster to a minimal deleted region in ductal breast cancer.
I. Chalmers
,
M. Aubele
,
+4 authors
M. Atkinson
Cancer Genetics and Cytogenetics
2001
Corpus ID: 36001999
2000
2000
High-resolution integrated map encompassing the breast cancer loss of heterozygosity region on human chromosome 16q22.1.
E. Frengen
,
P. Rocca-Serra
,
+11 authors
F. Dorion‐Bonnet
Genomics
2000
Corpus ID: 45324941
Loss of heterozygosity (LOH) on the long arm of human chromosome 16 is a common genetic alteration observed in both invasive…
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Highly Cited
1993
Highly Cited
1993
A tight cluster of five unrelated human genes on chromosome 16q22.1.
Frank Larsen
,
J. Solheim
,
Tom Kristensen
,
A. Kolstø
,
H. Prydz
Human Molecular Genetics
1993
Corpus ID: 23094779
A locus on human chromosome 16q22.1 contains at least five tightly clustered genes which are unrelated by sequence homology and…
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