165 related articles for article (PubMed ID: 27423854)
1. Testing neutrality at copy-number-variable loci under the finite-allele and finite-site models.
Hu XS; Hu Y; Chen X
Theor Popul Biol; 2016 Dec; 112():1-13. PubMed ID: 27423854
[TBL] [Abstract][Full Text] [Related]
2. Identification of copy number variation hotspots in human populations.
Fu W; Zhang F; Wang Y; Gu X; Jin L
Am J Hum Genet; 2010 Oct; 87(4):494-504. PubMed ID: 20920665
[TBL] [Abstract][Full Text] [Related]
3. The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
Liu J; Zhou Y; Liu S; Song X; Yang XZ; Fan Y; Chen W; Akdemir ZC; Yan Z; Zuo Y; Du R; Liu Z; Yuan B; Zhao S; Liu G; Chen Y; Zhao Y; Lin M; Zhu Q; Niu Y; Liu P; Ikegawa S; Song YQ; Posey JE; Qiu G; ; Zhang F; Wu Z; Lupski JR; Wu N
Hum Genet; 2018 Jul; 137(6-7):553-567. PubMed ID: 30019117
[TBL] [Abstract][Full Text] [Related]
4. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
Sokolowski M; Wasserman J; Wasserman D
PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
[TBL] [Abstract][Full Text] [Related]
5. Haplotype phasing and inheritance of copy number variants in nuclear families.
Palta P; Kaplinski L; Nagirnaja L; Veidenberg A; Möls M; Nelis M; Esko T; Metspalu A; Laan M; Remm M
PLoS One; 2015; 10(4):e0122713. PubMed ID: 25853576
[TBL] [Abstract][Full Text] [Related]
6. Origins and functional impact of copy number variation in the human genome.
Conrad DF; Pinto D; Redon R; Feuk L; Gokcumen O; Zhang Y; Aerts J; Andrews TD; Barnes C; Campbell P; Fitzgerald T; Hu M; Ihm CH; Kristiansson K; Macarthur DG; Macdonald JR; Onyiah I; Pang AW; Robson S; Stirrups K; Valsesia A; Walter K; Wei J; ; Tyler-Smith C; Carter NP; Lee C; Scherer SW; Hurles ME
Nature; 2010 Apr; 464(7289):704-12. PubMed ID: 19812545
[TBL] [Abstract][Full Text] [Related]
7. Detection of copy number variation using SNP genotyping.
Cooper GM; Mefford HC
Methods Mol Biol; 2011; 767():243-52. PubMed ID: 21822880
[TBL] [Abstract][Full Text] [Related]
8. [DNA polymorphisms].
Suehiro Y; Furuya T; Sasaki K; Hinota Y
Rinsho Byori; 2013 Nov; 61(11):1001-7. PubMed ID: 24450105
[TBL] [Abstract][Full Text] [Related]
9. Population-genetic nature of copy number variations in the human genome.
Kato M; Kawaguchi T; Ishikawa S; Umeda T; Nakamichi R; Shapero MH; Jones KW; Nakamura Y; Aburatani H; Tsunoda T
Hum Mol Genet; 2010 Mar; 19(5):761-73. PubMed ID: 19966329
[TBL] [Abstract][Full Text] [Related]
10. A practical case-control association test for detecting a susceptibility allele at a copy number variation locus.
Ohashi J
J Hum Genet; 2009 Mar; 54(3):169-73. PubMed ID: 19197338
[TBL] [Abstract][Full Text] [Related]
11. An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational history.
Gaunt TR; Rodriguez S; Guthrie PA; Day IN
Hum Mutat; 2010 Apr; 31(4):414-20. PubMed ID: 20077501
[TBL] [Abstract][Full Text] [Related]
12. Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome.
Peng Z; Zhou W; Fu W; Du R; Jin L; Zhang F
Hum Mol Genet; 2015 Mar; 24(5):1225-33. PubMed ID: 25324539
[TBL] [Abstract][Full Text] [Related]
13. Acetylcholine-metabolizing butyrylcholinesterase (BCHE) copy number and single nucleotide polymorphisms and their role in attention-deficit/hyperactivity syndrome.
Jacob CP; Weber H; Retz W; Kittel-Schneider S; Heupel J; Renner T; Lesch KP; Reif A
J Psychiatr Res; 2013 Dec; 47(12):1902-8. PubMed ID: 24041656
[TBL] [Abstract][Full Text] [Related]
14. The clinical context of copy number variation in the human genome.
Lee C; Scherer SW
Expert Rev Mol Med; 2010 Mar; 12():e8. PubMed ID: 20211047
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
Komura D; Shen F; Ishikawa S; Fitch KR; Chen W; Zhang J; Liu G; Ihara S; Nakamura H; Hurles ME; Lee C; Scherer SW; Jones KW; Shapero MH; Huang J; Aburatani H
Genome Res; 2006 Dec; 16(12):1575-84. PubMed ID: 17122084
[TBL] [Abstract][Full Text] [Related]
16. CNVs are associated with genomic architecture in a songbird.
da Silva VH; Laine VN; Bosse M; Oers KV; Dibbits B; Visser ME; M A Crooijmans RP; Groenen MAM
BMC Genomics; 2018 Mar; 19(1):195. PubMed ID: 29703149
[TBL] [Abstract][Full Text] [Related]
17. Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.
Žilina O; Koltšina M; Raid R; Kurg A; Tõnisson N; Salumets A
BMC Genomics; 2015 Sep; 16(1):703. PubMed ID: 26376747
[TBL] [Abstract][Full Text] [Related]
18. Simultaneous detection of single nucleotide polymorphisms and copy number variations in the CYP2D6 gene by multiplex polymerase chain reaction combined with capillary electrophoresis.
Liao HW; Tsai IL; Chen GY; Kuo CT; Wei MF; Hwang TJ; Chen WJ; Shen LJ; Kuo CH
Anal Chim Acta; 2013 Feb; 763():67-75. PubMed ID: 23340288
[TBL] [Abstract][Full Text] [Related]
19. CNVmap: A Method and Software To Detect and Map Copy Number Variants from Segregation Data.
Falque M; Jebreen K; Paux E; Knaak C; Mezmouk S; Martin OC
Genetics; 2020 Mar; 214(3):561-576. PubMed ID: 31882400
[TBL] [Abstract][Full Text] [Related]
20. Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach.
Kalari KR; Hebbring SJ; Chai HS; Li L; Kocher JP; Wang L; Weinshilboum RM
BMC Genomics; 2010 Jun; 11():357. PubMed ID: 20525348
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
