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1q32.2

A chromosome band present on 1q
National Institutes of Health

Related topics

Related topics

5 relations
ChromosomesELF3 wt AlleleMIR29C wt AllelePTPN14 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Developing a Risk-scoring Model for Ankylosing Spondylitis Based on a Combination of HLA-B27, Single-nucleotide Polymorphism, and Copy Number Variant Markers
Objective. To develop a genotype-based ankylosing spondylitis (AS) risk prediction model that is more sensitive and specific than… 
2016
2016
Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex
Van der Woude syndrome (MIM: 119300, VWS) is a dominantly inherited and the most common orofacial clefting syndrome; it accounts… 
Review
2016
Review
2016
Variant Markers NumberCombination of HLA-B 27 , Single-nucleotide Polymorphism , and Copy Developing a Risk-scoring Model for Ankylosing Spondylitis Based on a
Objective. To develop a genotype-based ankylosing spondylitis (AS) risk prediction model that is more sensitive and specific than… 
2016
2016
CD46 Is Amplified in High-Risk Myeloma with Gain of Chromosome 1q and Selectively Targeted By a Novel Anti-CD46 Antibody-Drug Conjugate
Background: Multiple myeloma (MM) is incurable by standard approaches, with relapse and development of treatment resistance… 
2015
2015
Immunogenetic influences on acquisition of HIV-1 infection: Consensus findings from two African cohorts point to an enhancer element in IL19 (1q32.2)
Numerous reports have suggested that immunogenetic factors may influence human immunodeficiency virus (HIV)-1 acquisition, yet… 
2014
2014
Genome‐Wide Copy Number Variation Analysis Identifies Deletion Variants Associated With Ankylosing Spondylitis
To identify ankylosing spondylitis (AS)–associated copy number variations (CNVs) in Korean subjects and their synergistic roles… 
2011
2011
[Chromosomal location of nonsyndromic cleft lip with or without palates for two multiplex families].
OBJECTIVE To find chromosome region closely linked to nonsyndromic cleft lip with or without palates (NSCL±P) by genome-wide scan… 
Review
2010
Review
2010
A heritable cause of cleft lip and palate—Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis
BackgroundOrofacial clefts are common congenital malformations usually characterized by a multifactorial etiology. These… 
2008
2008
Abstract 3139: Identification and Replication of a Genetic Locus for Myocardial Infarction on Chromosome 1q32.2
2007
2007
Genética da periodontite agressiva em brasileiro: resultados preliminares em famílias de ascendência africana
Estudos de genetica de periodontite agressiva em brasileiros ainda sao escassos. Nesse estudo, o padrao de segregacao de… 
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