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- [1] Rare variant discovery in known cancer genes from whole-exome sequencing-of African American hereditary prostate cancer familiesCANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2016, 25 (03)Cropp, Cheryl D.McDonnell, Shannon K.Middha, SumitDeRycke, MelissaKaryadi, Danielle M.Schaid, DanielThibodeau, Stephen N.Isaacs, William B.Ostrander, Elaine A.Stanford, JanetCooney, Kathleen A.Bailey-Wilson, Joan E.Carpten, John D.
- [2] Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytomaNATURE GENETICS, 2011, 43 (07) : 663 - U189Comino-Mendez, InakiGracia-Aznarez, Francisco J.Schiavi, FrancescaLanda, InigoLeandro-Garcia, Luis J.Leton, RocoHonrado, EmilianoRamos-Medina, RocioCaronia, DanielaPita, GuillermoGomez-Grana, Alvarode Cubas, Aguirre A.Inglada-Perez, LuciaMaliszewska, AgnieszkaTaschin, ElisaBobisse, SaraPica, GiuseppeLoli, PaolaHernandez-Lavado, RafaelDiaz, Jose A.Gomez-Morales, MercedesGonzalez-Neira, AnnaRoncador, GiovannaRodriguez-Antona, CristinaBenitez, JavierMannelli, MassimoOpocher, GiuseppeRobledo, MercedesCascon, Alberto
- [3] Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytomaNature Genetics, 2011, 43 : 663 - 667Iñaki Comino-MéndezFrancisco J Gracia-AznárezFrancesca SchiaviIñigo LandaLuis J Leandro-GarcíaRocío LetónEmiliano HonradoRocío Ramos-MedinaDaniela CaroniaGuillermo PitaÁlvaro Gómez-GrañaAguirre A de CubasLucía Inglada-PérezAgnieszka MaliszewskaElisa TaschinSara BobisseGiuseppe PicaPaola LoliRafael Hernández-LavadoJosé A DíazMercedes Gómez-MoralesAnna González-NeiraGiovanna RoncadorCristina Rodríguez-AntonaJavier BenítezMassimo MannelliGiuseppe OpocherMercedes RobledoAlberto Cascón
- [4] Exome Sequencing of African-American Prostate Cancer Reveals Loss-of-Function ERF MutationsCANCER DISCOVERY, 2017, 7 (09) : 973 - 983Huang, Franklin W.Mosquera, Juan MiguelGarofalo, AndreaOh, CoyinBaco, MariaAmin-Mansour, AliRabasha, BokangBahl, SamiraMullane, Stephanie A.Robinson, Brian D.Aldubayan, SaudKhani, FrancescaKarir, BeerinderKim, EejungChimene-Weiss, JeremyHofree, MatanRomanel, AlessandroOsborne, Joseph R.Kim, Jong WookAzabdaftari, GissouWoloszynska-Read, AnnaSfanos, KarenDe Marzo, Angelo M.Demichelis, FrancescaGabriel, StaceyVan Allen, Eliezer M.Mesirov, JillTamayo, PabloRubin, Mark A.Powell, Isaac J.Garraway, Levi A.
- [5] Analysis of Whole Exome Sequencing Data of Hereditary Lung Cancer Families Identifies Germline Copy Number Variations (Cnvs) in Multiple GenesGENETIC EPIDEMIOLOGY, 2019, 43 (07) : 896 - 896Mandal, DiptasriTran, Dinh-VanTermine, KirstenMusolf, Anthony M.de Andrade, MarizaSchwartz, Ann G.Pinney, Susan M.Amos, Christopher I.Govindan, RamaswamyBailey-Wilson, Joan E.
- [6] Whole-Exome Sequencing of Germline Variants in Non-BRCA Families with Hereditary Breast CancerBIOMEDICINES, 2022, 10 (05)Liu, YaxuanHelgadottir, Hafdis T.Kharaziha, PedramChoi, JungminLopez-Giraldez, FrancescMane, Shrikant M.Hoiom, VeronicaJuhlin, Carl ChristoferLarsson, CatharinaBajalica-Lagercrantz, Svetlana
- [7] Identification of Novel Mutations by Exome Sequencing in African American Colorectal Cancer PatientsCANCER, 2015, 121 (01) : 34 - 42Ashktorab, HassanDaremipouran, MohammadDevaney, JoeVarma, SudhirRahi, HamedLee, EdwardShokrani, BabakSchwartz, RussellNickerson, Michael L.Brim, Hassan
- [8] Exome sequencing identifies novel and known mutations in families with intellectual disabilityBMC Medical Genomics, 14Memoona RasheedValeed KhanRicardo HarripaulMaimoona SiddiquiMadiha Amin MalikZahid UllahMuhammad ZahidJohn B. VincentMuhammad Ansar
- [9] Exome sequencing identifies novel and known mutations in families with intellectual disabilityBMC MEDICAL GENOMICS, 2021, 14 (01)Rasheed, MemoonaKhan, ValeedHarripaul, RicardoSiddiqui, MaimoonaMalik, Madiha AminUllah, ZahidZahid, MuhammadVincent, John B.Ansar, Muhammad
- [10] Breast cancer predisposing germline mutations identified by exome sequencingANNALS OF ONCOLOGY, 2017, 28Kuligina, E. S.Sokolenko, A. P.Bizin, I. V.Anisimova, M. O.Romanko, A. A.Imyanitov, E.