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Associations of <i>NINJ2</i> Sequence Variants with Incident Ischemic Stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) Consortium.
Published in:
PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099798
By:
- Bis, Joshua C.;
- DeStefano, Anita;
- Liu, Xiaoming;
- Brody, Jennifer A.;
- Choi, Seung Hoan;
- Verhaaren, Benjamin F. J.;
- Debette, Stéphanie;
- Ikram, M. Arfan;
- Shahar, Eyal;
- Butler Jr, Kenneth R.;
- Gottesman, Rebecca F.;
- Muzny, Donna;
- Kovar, Christie L.;
- Psaty, Bruce M.;
- Hofman, Albert;
- Lumley, Thomas;
- Gupta, Mayetri;
- Wolf, Philip A.;
- van Duijn, Cornelia;
- Gibbs, Richard A.
Publication type:
Article
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Published in:
Human Molecular Genetics, 2022, v. 31, n. 18, p. 3120, doi. 10.1093/hmg/ddac100
By:
- Pankratz, Nathan;
- Wei, Peng;
- Brody, Jennifer A;
- Chen, Ming-Huei;
- Vries, Paul S de;
- Huffman, Jennifer E;
- Stimson, Mary Rachel;
- Auer, Paul L;
- Boerwinkle, Eric;
- Cushman, Mary;
- Maat, Moniek P M de;
- Folsom, Aaron R;
- Franco, Oscar H;
- Gibbs, Richard A;
- Haagenson, Kelly K;
- Hofman, Albert;
- Johnsen, Jill M;
- Kovar, Christie L;
- Kraaij, Robert;
- McKnight, Barbara
Publication type:
Article
Comprehensive molecular characterization of human colon and rectal cancer.
Published in:
Nature, 2012, v. 487, n. 7407, p. 330, doi. 10.1038/nature11252
By:
- Muzny, Donna M.;
- Bainbridge, Matthew N.;
- Chang, Kyle;
- Dinh, Huyen H.;
- Drummond, Jennifer A.;
- Fowler, Gerald;
- Kovar, Christie L.;
- Lewis, Lora R.;
- Morgan, Margaret B.;
- Newsham, Irene F.;
- Reid, Jeffrey G.;
- Santibanez, Jireh;
- Shinbrot, Eve;
- Trevino, Lisa R.;
- Wu, Yuan-Qing;
- Wang, Min;
- Gunaratne, Preethi;
- Donehower, Lawrence A.;
- Creighton, Chad J.;
- Wheeler, David A.
Publication type:
Article
Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy.
Published in:
Genome Medicine, 2013, v. 5, n. 6, p. 1, doi. 10.1186/gm461
By:
- Lupski, James R.;
- Gonzaga-Jauregui, Claudia;
- Yaping Yang;
- Bainbridge, Matthew N.;
- Jhangiani, Shalini;
- Buhay, Christian J.;
- Kovar, Christie L.;
- Min Wang;
- Hawes, Alicia C.;
- Reid, Jeffrey G.;
- Eng, Christine;
- Muzny, Donna M.;
- Gibbs, Richard A.
Publication type:
Article

Found: 4

Associations of <i>NINJ2</i> Sequence Variants with Incident Ischemic Stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) Consortium.

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.

Comprehensive molecular characterization of human colon and rectal cancer.

Exome sequencing resolves apparent incidental findings and reveals further complexity of SH3TC2 variant alleles causing Charcot-Marie-Tooth neuropathy.