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DNA Resequencing
Known as:
Resequencing
A specific application of gene sequencing that precisely determines the sequence of bases in DNA. Resequencing is used to identify single nucleotide…
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
TREM2 and Alzheimer's disease
E. Niemitz
Nature Genetics
2012
Corpus ID: 6194884
although much effort has been made in sequencing autism exomes, it has been difficult to robustly establish asD (autism spectrum…
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2011
2011
Common genetic variation in the 3′-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well…
Qiaoli Li
,
Guizhong Yang
,
+7 authors
Lei Wang
Human Genetics
2011
Corpus ID: 1944025
Gonadotropin-releasing hormone receptor (GNRHR) is a member of the G protein-coupled Ca(2+)-dependent family of receptors. It…
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2011
2011
The Genomic Architecture of Sporadic Heart Failure
H. Watkins
,
C. Seidman
2011
Corpus ID: 34525126
Common or sporadic systolic heart failure (heart failure) is the clinical syndrome of insufficient forward cardiac output…
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Review
2011
Review
2011
META-ANALYSIS OF A RARE-VARIANT ASSOCIATION TEST.
T. Lumley
,
J. Brody
,
J. Dupuis
,
A. Cupples
2011
Corpus ID: 50361156
Genome-wide assocation studies have often been carried out by meta-analysis rather than by pooling individual-level data. For one…
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2010
2010
Common Susceptibility Variants Examined for Association with Dilated Cardiomyopathy
E. Rampersaud
,
D. Kinnamon
,
K. Hamilton
,
S. Khuri
,
R. Hershberger
,
E. Martin
Annals of Human Genetics
2010
Corpus ID: 13762070
Rare mutations in more than 20 genes have been suggested to cause dilated cardiomyopathy (DCM), but explain only a small…
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2010
2010
Resequencing of pooled DNA for detecting disease associations with rare variants
Tao Wang
,
Chang-Yun Lin
,
T. Rohan
,
Kenny Q. Ye
Genetic Epidemiology
2010
Corpus ID: 22449400
A combination of common and rare variants is thought to contribute to genetic susceptibility to complex diseases. Recently, next…
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2006
2006
Resequencing of the characterised CTGF gene to identify novel or known variants, and analysis of their association with diabetic nephropathy
A. McKnight
,
David A. Savage
,
C. Patterson
,
Hugh R Brady
,
A. P. Maxwell
Journal of Human Genetics
2006
Corpus ID: 7255715
AbstractConnective tissue growth factor (CTGF) has been implicated in the pathogenesis of diabetic nephropathy; however, to date…
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2006
2006
Whole-Genome Analysis of the Methyl tert-Butyl Ether-Degrading Beta-Proteobacterium Methylibium petroleiphilum PM 1 †
K. Hristova
,
Scow
,
+9 authors
P. Chain
2006
Corpus ID: 18425544
Published Ahead of Print 8 December 2006. 2007, 189(5):1931. DOI: 10.1128/JB.01259-06. J. Bacteriol. Richardson and Krassimira R…
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2005
2005
CDX2 polymorphisms, RNA expression, and risk of colorectal cancer.
L. Rozek
,
S. Lipkin
,
+9 authors
S. Gruber
Cancer Research
2005
Corpus ID: 34916693
In adult mammals, CDX2 acts as a transcription factor and is expressed in intestinal epithelial cells. Down-regulation of CDX2 is…
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2000
2000
DETC 2000 / DTM-14547 DO-IT-RIGHT-FIRST-TIME ( DRFT ) APPROACH TO DESIGN STRUCTURE MATRIX ( DSM ) RESTRUCTURING
A. Yassine
,
D. Whitney
,
Jerry Lavine
,
Tony Zambito
2000
Corpus ID: 1153670
* Corresponding author: MIT, CTPID, Rm. E40-252, Cambridge, MA. 02139. Tel. (617)258-7734, Fax (617)253-7140, E-mail: yassine@mit…
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