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9p21.2

A chromosome band present on 9p
National Institutes of Health

Papers overview

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2017
2017
Rationale: Despite significant advances in knowledge of the genetic architecture of asthma, specific contributors to the… Expand
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Highly Cited
2014
Highly Cited
2014
Identification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided novel insights into the… Expand
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2014
2014
OBJECTIVE Substantial clinical, pathological, and genetic overlap exists between amyotrophic lateral sclerosis (ALS) and… Expand
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Highly Cited
2013
Highly Cited
2013
Amyotrophic lateral sclerosis (ALS) is the third most common adult-onset neurodegenerative disease. Individuals with ALS rapidly… Expand
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2013
2013
BACKGROUND The presence and severity of coronary artery calcified plaque (CAC) differs markedly between individuals of African… Expand
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2013
2013
PURPOSE We identified single nucleotide polymorphisms associated with change in the AUA Symptom Score after radiotherapy for… Expand
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2013
2013
Amyotrophic lateral sclerosis (ALS) is a severe neurodegenerative disease that causes progressive muscle weakness, eventually… Expand
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2011
2011
We performed a replication study of the 2 genetic variants, rs2814707 on 9p21.2 and rs12608932 on 19p13.3 that are recently… Expand
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Highly Cited
2010
Highly Cited
2010
Summary Background Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of motor neurons that results in… Expand
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Highly Cited
2009
Highly Cited
2009
We conducted a genome-wide association study among 2,323 individuals with sporadic amyotrophic lateral sclerosis (ALS) and 9,013… Expand
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