Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular Malaysia

scientific article (publication date: 2014)

Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular Malaysia is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2014PLoSO...9j0371M
P356DOI10.1371/JOURNAL.PONE.0100371
P932PMC publication ID4067311
P698PubMed publication ID24956385
P5875ResearchGate publication ID263396669

P50authorStephen W. SchererQ7610775
Hoh Boon PengQ59694169
Christian MarshallQ89518827
Anath C. LionelQ114341260
Maude E PhippsQ30504080
Bhooma ThiruvahindrapuramQ48237178
P2093author name stringSiti Shuhada Mokhtar
P2860cites workNutritional status of women and children in Malaysian rural populationsQ95508091
A preliminary study of copy number variation in TibetansQ21134117
Isolated populations and complex disease gene identificationQ21183904
Genetic and fossil evidence for the origin of modern humansQ22065529
Single, Rapid Coastal Settlement of Asia Revealed by Analysis of Complete Mitochondrial GenomesQ22065802
Functional impact of global rare copy number variation in autism spectrum disordersQ24596191
Global variation in copy number in the human genomeQ24658083
A haplotype map of the human genomeQ24679827
Bias of selection on human copy-number variantsQ25257186
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The 'human revolution' in lowland tropical Southeast Asia: the antiquity and behavior of anatomically modern humans at Niah Cave (Sarawak, Borneo)Q28278394
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibilityQ28301418
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variantsQ28732264
Worldwide human relationships inferred from genome-wide patterns of variationQ29547228
Relative impact of nucleotide and copy number variation on gene expression phenotypesQ29614883
Multiple dispersals and modern human originsQ30048798
Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studiesQ33303453
Copy number variation in African AmericansQ33421551
Copy number variations in East-Asian population and their evolutionary and functional implicationsQ33697675
Copy number variation across European populationsQ33988707
A map of copy number variations in Chinese populationsQ34075621
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The current excitement about copy-number variation: how it relates to gene duplications and protein familiesQ34782604
Genomic drift and copy number variation of sensory receptor genes in humansQ36299992
Mutational and selective effects on copy-number variants in the human genomeQ36863503
Genomics for the worldQ37003231
Association of the 5'-upstream regulatory region of the alpha7 nicotinic acetylcholine receptor subunit gene (CHRNA7) with schizophreniaQ37356715
Copy number variants, diseases and gene expressionQ37417891
Psoriasis is associated with increased beta-defensin genomic copy numberQ39789019
Genomic copy number variations in three Southeast Asian populationsQ43053229
Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14.Q44017821
Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversityQ46110821
An update of the general health status in the indigenous populations of MalaysiaQ46527877
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.Q48954065
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P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectMalaysiaQ833
P304page(s)e100371
P577publication date2014-01-01
P1433published inPLOS OneQ564954
P1476titleNovel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular Malaysia
P478volume9

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cites work (P2860)
Q36066625A 3.4-kb Copy-Number Deletion near EPAS1 Is Significantly Enriched in High-Altitude Tibetans but Absent from the Denisovan Sequence
Q52687665A genome-wide characterization of copy number variations in native populations of Peninsular Malaysia.
Q39185001Differential positive selection of malaria resistance genes in three indigenous populations of Peninsular Malaysia.
Q28603500Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy

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