copy number variation

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1
profile of the spleen transcriptome in beef steers with variation in gain and feed intake
;Amanda K Lindholm-Perry;Rebecca J Kern;Brittney N Keel;Warren M Snelling;Larry A Kuehn;Harvey C Fre...
2016 chemical record (new york, ny) DOI: 10.3389/fgene.2016.0... 223 views
2
web-based database and viewer of east asian copy number variations
;Ji-Hong Kim;Hae-Jin Hu;Yeun-Jun Chung
2012 Journal of environmental management DOI: 10.5808/GI.2012.10.1... 170 views
3
adding complexity to complexity: gene family evolution in polyploids
;Barbara K. Mable;Anne K. Brysting;Marte H. Jørgensen;Anna K. Z. Carbonell;Anna K. Z. Carbonell;Chri...
2018 eating behaviors DOI: 10.3389/fevo.2018.00... 174 views
4
genetics of psoriasis and psoriatic arthritis
;Chandran Vinod
2010 heterocycles 151 views
5
mirna-mediated risk for schizophrenia in 22q11.2 deletion syndrome
;Linda M Brzustowicz;Linda M Brzustowicz;Anne S Bassett;Anne S Bassett;Anne S Bassett
2012 chemical record (new york, ny) DOI: 10.3389/fgene.2012.0... 189 views
6
copy number variation in hereditary non-polyposis colorectal cancer
;Garry N. Hannan;Konsta Duesing;Desma M. Grice;Amy L. Masson;Bente A. Talseth-Palmer;Tiffany-Jane Ev...
2013 thermal science and engineering progress DOI: 10.3390/genes4040536 154 views
7
etumortype, an algorithm of discriminating cancer types for circulating tumor cells or cell-free dnas in blood
;Jinfeng Zou;Edwin Wang
2017 journal of ethics DOI: 10.1016/j.gpb.2017.0... 201 views
8
Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations.
Simba, Hannah;Kuivaniemi, Helena;Lutje, Vittoria;Tromp, Gerard;Sewram, Vikash;
2019 Frontiers in genetics DOI: 10.3389/fgene.2019.0... 208 views
9
Genome-wide copy number variation study in anorectal malformations.
Wong, Emily H M;Cui, Long;Ng, Chun-Laam;Tang, Clara S M;Liu, Xue-Lai;So, Man-Ting;Yip, Benjamin Hon-...
2013 Human molecular genetics DOI: 10.1093/hmg/dds451 170 views
10
ClickGene: an open cloud-based platform for big pan-cancer data genome-wide association study, visualization and exploration.
Bi, Jia-Hao;Tong, Yi-Fan;Qiu, Zhe-Wei;Yang, Xing-Feng;Minna, John;Gazdar, Adi F;Song, Kai;
2019 biodata mining DOI: 10.1186/s13040-019-0... 246 views
11
Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder
Tammimies, K.
2019 Scientific reports DOI: 10.1038/s41598-019-4... 195 views
12
"Doubled-haploid" allohexaploid Brassica lines lose fertility and viability and accumulate genetic variation due to genomic instability.
Mwathi, Margaret W;Schiessl, Sarah V;Batley, Jacqueline;Mason, Annaliese S;
2019 chromosoma DOI: 10.1007/s00412-019-0... 271 views
13
Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting
Zhang, Xiaoqing;Wang, Bo;Zhang, Lichen;You, Guoling;Palais, Robert A.;Zhou, Luming;Fu, Qihua;
2018 BMC genomics 333 views
14
The Genetics of Non-Syndromic Primary Ovarian Insufficiency: A Systematic Review.
Venturella, Roberta;De Vivo, Valentino;Carlea, Annunziata;D'Alessandro, Pietro;Saccone, Gabriele;Ard...
2019 international journal of fertility & sterility DOI: 10.22074/ijfs.2019.5... 210 views
15
Uniparental isodisomy caused autosomal recessive diseases: NGS-based analysis allows the concurrent detection of homogenous variants and copy-neutral loss of heterozygosity.
Xiao, Bing;Wang, Lili;Liu, Huili;Fan, Yanjie;Xu, Yan;Sun, Yu;Qiu, Wenjuan;
2019 molecular genetics & genomic medicine DOI: 10.1002/mgg3.945 195 views
16
Syndromic Oral Clefts: Challenges of Genetic Assessment in Brazil and Suggestions to Improve Health Policies.
Gil-da-Silva-Lopes, Vera Lúcia;Fontes, Marshall Italo Barros;Dos Santos, Ana Paula;Appenzeller, Simo...
2019 public health genomics DOI: 10.1159/000501973 305 views
17
Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary system.
Hu, Ting;Zhang, Zhu;Wang, Jiamin;Li, Qinqin;Zhu, Hongmei;Lai, Yi;Wang, He;Liu, Shanling;
2019 prenatal diagnosis DOI: 10.1002/pd.5550 331 views
18
An Evolutionary Perspective on the Impact of Genomic Copy Number Variation on Human Health.
Saitou, Marie;Gokcumen, Omer;
2019 Journal of molecular evolution DOI: 10.1007/s00239-019-0... 220 views
19
Copy Number Variations in the Survival Motor Neuron Genes: Implications for Spinal Muscular Atrophy and Other Neurodegenerative Diseases
Butchbach, Matthew E R;Butchbach, Matthew E R;Butchbach, Matthew E R;Butchbach, Matthew E R;
2016 Frontiers in molecular biosciences 293 views
20
Horizontal and vertical integrative analysis methods for mental disorders omics data.
Wang, Shuaichao;Shi, Xingjie;Wu, Mengyun;Ma, Shuangge;
2019 Scientific reports DOI: 10.1038/s41598-019-4... 279 views

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chromosoma
ISSN: 1432-0886 219 views

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beef cattle spleen feed intake database genome browsergenetics polyploidy gene family evolution balancing selectionevolutionecology environment gene human leucocyte antigendermatology schizophrenia genetic mirna Cancer DNA repair diagnostic testing cancerbiology (general)