OpenURL Connection Search

Select item for more details and to access through your institution.

Big Data Analytics for Genomic Medicine.
Published in:
International Journal of Molecular Sciences, 2017, v. 18, n. 2, p. 412, doi. 10.3390/ijms18020412
By:
- He, Karen Y.;
- Dongliang Ge;
- He, Max M.
Publication type:
Article
Detecting fitness epistasis in recently admixed populations with genome-wide data.
Published in:
BMC Genomics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12864-020-06874-7
By:
- Ni, Xumin;
- Zhou, Mengshi;
- Wang, Heming;
- He, Karen Y.;
- Broeckel, Uli;
- Hanis, Craig;
- Kardia, Sharon;
- Redline, Susan;
- Cooper, Richard S.;
- Tang, Hua;
- Zhu, Xiaofeng
Publication type:
Article
Rare coding variants in RCN3 are associated with blood pressure.
Published in:
BMC Genomics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12864-022-08356-4
By:
- He, Karen Y.;
- Kelly, Tanika N.;
- Wang, Heming;
- Liang, Jingjing;
- Zhu, Luke;
- Cade, Brian E.;
- Assimes, Themistocles L.;
- Becker, Lewis C.;
- Beitelshees, Amber L.;
- Bielak, Lawrence F.;
- Bress, Adam P.;
- Brody, Jennifer A.;
- Chang, Yen-Pei Christy;
- Chang, Yi-Cheng;
- de Vries, Paul S.;
- Duggirala, Ravindranath;
- Fox, Ervin R.;
- Franceschini, Nora;
- Furniss, Anna L.;
- Gao, Yan
Publication type:
Article
Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea.
Published in:
2022
By:
- Jingjing Liang;
- Heming Wang;
- Cade, Brian E.;
- Kurniansyah, Nuzulul;
- He, Karen Y.;
- Jiwon Lee;
- Sands, Scott A.;
- Brody, Jennifer A.;
- Han Chen;
- Gottlieb, Daniel J.;
- Evans, Daniel S.;
- Xiuqing Guo;
- Gharib, Sina A.;
- Hale, Lauren;
- Hillman, David R.;
- Lutsey, Pamela L.;
- Mukherjee, Sutapa;
- Ochs-Balcom, Heather M.;
- Palmer, Lyle J.;
- Purcell, Shaun
Publication type:
journal article
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
Published in:
Human Genetics, 2019, v. 138, n. 2, p. 199, doi. 10.1007/s00439-019-01975-0
By:
- He, Karen Y.;
- Li, Xiaoyin;
- Kelly, Tanika N.;
- Liang, Jingjing;
- Cade, Brian E.;
- Assimes, Themistocles L.;
- Becker, Lewis C.;
- Beitelshees, Amber L.;
- Bress, Adam P.;
- Chang, Yen-Pei Christy;
- Chen, Yii-Der Ida;
- de Vries, Paul S.;
- Fox, Ervin R.;
- Franceschini, Nora;
- Furniss, Anna;
- Gao, Yan;
- Guo, Xiuqing;
- Haessler, Jeffrey;
- Hwang, Shih-Jen;
- Irvin, Marguerite Ryan
Publication type:
Article
Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records.
Published in:
PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167847
By:
- He, Karen Y.;
- Zhao, Yiqing;
- McPherson, Elizabeth W.;
- Li, Quan;
- Xia, Fan;
- Weng, Chunhua;
- Wang, Kai;
- He, Max M.
Publication type:
Article
Multivariate Analysis of Anthropometric Traits Using Summary Statistics of Genome-Wide Association Studies from GIANT Consortium.
Published in:
PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0163912
By:
- Park, Haeil;
- Li, Xiaoyin;
- Song, Yeunjoo E.;
- He, Karen Y.;
- Zhu, Xiaofeng
Publication type:
Article
SparkText: Biomedical Text Mining on Big Data Framework.
Published in:
PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0162721
By:
- Ye, Zhan;
- Tafti, Ahmad P.;
- He, Karen Y.;
- Wang, Kai;
- He, Max M.
Publication type:
Article
Characterization of APOE Christchurch carriers in 455,306 UK Biobank participants.
Published in:
Molecular Neurodegeneration, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13024-023-00684-7
By:
- He, Karen Y.;
- Khramtsova, Ekaterina A.;
- Cabrera-Socorro, Alfredo;
- Zhang, Yanfei;
- Li, Shuwei;
- Sarver, Brice A. J.;
- Smets, Bart;
- Li, Qingqin S.;
- De Muynck, Louis;
- Parrado, Antonio R.;
- Lovestone, Simon;
- Black, Mary Helen
Publication type:
Article
Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants.
Published in:
Genome Medicine, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13073-019-0664-4
By:
- He, Max M.;
- Li, Quan;
- Yan, Muqing;
- Cao, Hui;
- Hu, Yue;
- He, Karen Y.;
- Cao, Kajia;
- Li, Marilyn M.;
- Wang, Kai
Publication type:
Article
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.
Published in:
PLoS Genetics, 2017, v. 13, n. 3, p. 1, doi. 10.1371/journal.pgen.1006678
By:
- He, Karen Y.;
- Wang, Heming;
- Cade, Brian E.;
- Nandakumar, Priyanka;
- Giri, Ayush;
- Ware, Erin B.;
- Haessler, Jeffrey;
- Liang, Jingjing;
- Smith, Jennifer A.;
- Franceschini, Nora;
- Le, Thu H.;
- Kooperberg, Charles;
- Edwards, Todd L.;
- Kardia, Sharon L. R.;
- Lin, Xihong;
- Chakravarti, Aravinda;
- Redline, Susan;
- Zhu, Xiaofeng
Publication type:
Article

Found: 11