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- [1] Identification of Novel TTN Mutations in Three Chinese Familial Dilated Cardiomyopathy Pedigrees by Whole Exome SequencingCARDIOVASCULAR INNOVATIONS AND APPLICATIONS, 2020, 4 (04) : 229 - 237Peng, YingMiao, JinxinZhai, YafeiFang, GuangmingWang, ChuchuWang, YaoheZhao, XiaoyanDong, Jianzeng
- [2] Novel Mutations Identified by Whole Exome Sequencing in Acral MelanomaJOURNAL OF INVESTIGATIVE DERMATOLOGY, 2019, 139 (09) : S301 - S301Lim, Y.Yoon, D.Lee, D.
- [3] Whole-Exome Sequencing Identifies Two Novel TTN Mutations in Chinese Families with Dilated CardiomyopathyCARDIOLOGY, 2017, 136 (01) : 10 - 14Liu, Ji-ShiFan, Liang-LiangZhang, HaoLiu, XiaoxianHuang, HaoLi-JianTaoXia, KunXiang, Rong
- [4] Novel mutations identified by whole-exome sequencing in acral melanomaJOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2020, 83 (06) : 1792 - 1794Lim, YoungkyoungYoon, DokyoungLee, Dong-Youn
- [5] Potential digenic inheritance of familial hypertrophic cardiomyopathy identified by whole-exome sequencingMOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (03):Ren, Ming-BaoChai, Xiao-RuiLi, LinWang, XinYin, Chenghong
- [6] Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathySCIENTIFIC REPORTS, 2017, 7Truszkowska, Grazyna T.Bilinska, Zofia T.Muchowicz, AngelikaPollak, AgnieszkaBiernacka, AnnaKozar-Kaminska, KatarzynaStawinski, PiotrGasperowicz, PiotrKosinska, JoannaZielinski, TomaszPloski, Rafal
- [7] Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathyScientific Reports, 7Grażyna T. TruszkowskaZofia T. BilińskaAngelika MuchowiczAgnieszka PollakAnna BiernackaKatarzyna Kozar-KamińskaPiotr StawińskiPiotr GasperowiczJoanna KosińskaTomasz ZielińskiRafał Płoski
- [8] Whole Exome Sequencing Identifies a Troponin T Mutation Hot Spot in Familial Dilated CardiomyopathyPLOS ONE, 2013, 8 (10): : e78104Campbell, NzaliSinagra, GianfrancoJones, Kenneth L.Slavov, DobromirGowan, KatherineMerlo, MarcoCarniel, ElisaFain, Pamela R.Aragona, PierluigiDi Lenarda, AndreaMestroni, LuisaTaylor, Matthew R. G.
- [9] WHOLE EXOME SEQUENCING IDENTIFIES A TROPONIN T MUTATION HOT SPOT IN FAMILIAL DILATED CARDIOMYOPATHYJOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2013, 61 (10) : E594 - E594Mestroni, LuisaCampbell, NzaliSinagra, GianfrancoJones, KennethSlavov, DobromirGowan, KatherineMerlo, MarcoCarniel, ElisaFain, PamAragona, PierluigiDi Lenarda, AndreaTaylor, Matthew R. G.
- [10] WHOLE EXOME SEQUENCING IDENTIFIED CANDIDATE GENE MUTATIONS IN A PEDIGREE OF FAMILIAL MYELOPROLIFERATIVE NEOPLASMEXPERIMENTAL HEMATOLOGY, 2017, 53 : S116 - S116Cher, Chae YinLam, Nelson KaLam, Stephen Sze YuenHe, Bai-LiangYing, DinggeChung, Brian Hon-YinAu, Chun HungChan, Tsun LeungMa, Edmond Shiu KwanLiang, Raymond Hin SuenKwong, Yok LamLeung, Anskar Yu Hung