共 50 条
- [31] Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young PersonsScientific Reports, 7James E. HixsonGoo JunLawrence C. ShimminYizhi WangGuoqiang YuChunhong MaoAndrew S. WarrenTimothy D. HowardRichard S. Vander HeideJennifer Van EykYue WangDavid M. Herrington
- [32] Exome sequencing can reliably identify mtDNA variants increasing the diagnostic yield in a diagnostic contextEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 187 - 187Wagner, M.Alhaddad, B.Berutti, R.Prokisch, H.Strom, T.Wortmann, S. B.
- [33] Application of Whole Exome Sequencing and Functional Annotations to Identify Genetic Variants Associated with Marfan SyndromeJOURNAL OF PERSONALIZED MEDICINE, 2022, 12 (02):Lin, Min-RouChang, Che-MaiTing, JafitChang, Jan-GowthChou, Wan-HsuanHuang, Kuei-JungCheng, GloriaChang, Hsiao-HuangChang, Wei-Chiao
- [34] A whole exome sequencing study to identify rare variants in multiplex families with alcohol use disorderFRONTIERS IN PSYCHIATRY, 2023, 14Hill, Shirley Y.Hostyk, Joseph
- [35] Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variantsScientific Reports, 6Tea KaartokallioJingwen WangSeppo HeinonenEero KajantieKatja KivinenAnneli PoutaPaul GerdhemHong JiaoJuha KereHannele Laivuori
- [36] Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young PersonsSCIENTIFIC REPORTS, 2017, 7Hixson, James E.Jun, GooShimmin, Lawrence C.Wang, YizhiYu, GuoqiangMao, ChunhongWarren, Andrew S.Howard, Timothy D.Vander Heide, Richard S.Van Eyk, JenniferWang, YueHerrington, David M.
- [38] Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variantsSCIENTIFIC REPORTS, 2016, 6Kaartokallio, TeaWang, JingwenHeinonen, SeppoKajantie, EeroKivinen, KatjaPouta, AnneliGerdhem, PaulJiao, HongKere, JuhaLaivuori, Hannele
- [39] Exome Sequencing Identifies Genetic Variants Associated with Extreme Manifestations of the Cardiovascular Phenotype in Marfan SyndromeGENES, 2022, 13 (06)Jimenez, YanirethPaulsen, CesarTurner, EduardoIturra, SebastianCuevas, OscarLay-son, GuillermoRepetto, Gabriela M.Rojas, MarceloCalderon, Juan F.
- [40] Exome sequencing reveals frequent deleterious germline variants in cancer susceptibility genes in women with invasive breast cancer undergoing neoadjuvant chemotherapyBREAST CANCER RESEARCH AND TREATMENT, 2015, 153 (02) : 435 - 443Ellingson, Marissa S.Hart, Steven N.Kalari, Krishna R.Suman, VeraSchahl, Kimberly A.Dockter, Travis J.Felten, Sara J.Sinnwell, Jason P.Thompson, Kevin J.Tang, XiaojiaVedell, Peter T.Barman, PoulamiSicotte, HuguesEckel-Passow, Jeanette E.Northfelt, Donald W.Gray, Richard J.McLaughlin, Sarah A.Moreno-Aspitia, AlvaroIngle, James N.Moyer, Ann M.Visscher, Daniel W.Jones, KatieConners, AmyMcDonough, MichelleWieben, Eric D.Wang, LieweiWeinshilboum, RichardBoughey, Judy C.Goetz, Matthew P.