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- [1] A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencingGENOME MEDICINE, 2019, 11 (1)Cao, Ye论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Chinese Univ Hong Kong, Dept Obstet & Gynecol, Hong Kong, Peoples R China Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USATokita, Mari J.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAChen, Edward S.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAGhosh, Rajarshi论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAChen, Tiansheng论文数: 0 引用数: 0 h-index: 0机构: Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAFeng, Yanming论文数: 0 引用数: 0 h-index: 0机构: Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAGorman, Elizabeth论文数: 0 引用数: 0 h-index: 0机构: Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAGibellini, Federica论文数: 0 引用数: 0 h-index: 0机构: Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAWard, Patricia A.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USABraxton, Alicia论文数: 0 引用数: 0 h-index: 0机构: Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAWang, Xia论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAMeng, Linyan论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAXiao, Rui论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USABi, Weimin论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAXia, Fan论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAEng, Christine M.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAYang, Yaping论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA论文数: 引用数: h-index:机构:Shaw, Chad论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Rice Univ, Dept Stat, Houston, TX 77251 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USALiu, Pengfei论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USAStankiewicz, Pawel论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA Baylor Genet, Houston, TX 77021 USA Baylor Coll Med, Dept Mol & Human Genet, One Baylor Plaza, Houston, TX 77030 USA
- [2] Global inference of disease-causing single nucleotide variants from exome sequencing dataBMC BIOINFORMATICS, 2016, 17Wu, Mengmeng论文数: 0 引用数: 0 h-index: 0机构: MOE Key Lab Bioinformat, Beijing, Peoples R China Tsinghua Natl Lab Informat Sci & Technol, Bioinformat Div, Beijing, Peoples R China Tsinghua Natl Lab Informat Sci & Technol, Ctr Synthet & Syst Biol, Beijing, Peoples R China Tsinghua Univ, Dept Comp Sci, Beijing, Peoples R China MOE Key Lab Bioinformat, Beijing, Peoples R ChinaChen, Ting论文数: 0 引用数: 0 h-index: 0机构: MOE Key Lab Bioinformat, Beijing, Peoples R China Tsinghua Natl Lab Informat Sci & Technol, Bioinformat Div, Beijing, Peoples R China Tsinghua Natl Lab Informat Sci & Technol, Ctr Synthet & Syst Biol, Beijing, Peoples R China Tsinghua Univ, Dept Comp Sci, Beijing, Peoples R China MOE Key Lab Bioinformat, Beijing, Peoples R ChinaJiang, Rui论文数: 0 引用数: 0 h-index: 0机构: MOE Key Lab Bioinformat, Beijing, Peoples R China Tsinghua Natl Lab Informat Sci & Technol, Bioinformat Div, Beijing, Peoples R China Tsinghua Natl Lab Informat Sci & Technol, Ctr Synthet & Syst Biol, Beijing, Peoples R China Tsinghua Univ, Dept Comp Sci, Beijing, Peoples R China Tsinghua Univ, Dept Automat, Beijing, Peoples R China MOE Key Lab Bioinformat, Beijing, Peoples R China
- [3] Global inference of disease-causing single nucleotide variants from exome sequencing dataBMC Bioinformatics, 17Mengmeng Wu论文数: 0 引用数: 0 h-index: 0机构: Tsinghua National Laboratory for Information Science and Technology,MOE Key Laboratory of Bioinformatics; Bioinformatics Division and Center for Synthetic & Systems BiologyTing Chen论文数: 0 引用数: 0 h-index: 0机构: Tsinghua National Laboratory for Information Science and Technology,MOE Key Laboratory of Bioinformatics; Bioinformatics Division and Center for Synthetic & Systems BiologyRui Jiang论文数: 0 引用数: 0 h-index: 0机构: Tsinghua National Laboratory for Information Science and Technology,MOE Key Laboratory of Bioinformatics; Bioinformatics Division and Center for Synthetic & Systems Biology
- [4] Predicting Mendelian Disease-Causing Non-Synonymous Single Nucleotide Variants in Exome Sequencing StudiesPLOS GENETICS, 2013, 9 (01):Li, Miao-Xin论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Ctr Reprod Dev & Growth, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Ctr Genom Sci, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R ChinaKwan, Johnny S. H.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Dept Med, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R ChinaBao, Su-Ying论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Dept Biochem, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R ChinaYang, Wanling论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Dept Paediat & Adolescent Med, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R ChinaHo, Shu-Leong论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Dept Med, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R ChinaSong, Yong-Qiang论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Dept Biochem, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R ChinaSham, Pak C.论文数: 0 引用数: 0 h-index: 0机构: Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Ctr Reprod Dev & Growth, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Ctr Genom Sci, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, State Key Lab Cognit & Brain Sci, Pokfulam, Hong Kong, Peoples R China Univ Hong Kong, Dept Psychiat, Pokfulam, Hong Kong, Peoples R China
- [5] Integrating Multiple Genomic Data to Predict Disease-Causing Nonsynonymous Single Nucleotide Variants in Exome Sequencing StudiesPLOS GENETICS, 2014, 10 (03):Wu, Jiaxin论文数: 0 引用数: 0 h-index: 0机构: Tsinghua Univ, MOE Key Lab Bioinformat, Bioinformat Div, Beijing 100084, Peoples R China Tsinghua Univ, MOE Key Lab Bioinformat, Bioinformat Div, Beijing 100084, Peoples R ChinaLi, Yanda论文数: 0 引用数: 0 h-index: 0机构: Tsinghua Univ, MOE Key Lab Bioinformat, Bioinformat Div, Beijing 100084, Peoples R ChinaJiang, Rui论文数: 0 引用数: 0 h-index: 0机构: Tsinghua Univ, MOE Key Lab Bioinformat, Bioinformat Div, Beijing 100084, Peoples R China
- [6] Whole exome sequencing unravels disease-causing genes in consanguineous families in QatarCLINICAL GENETICS, 2014, 86 (02) : 134 - 141Fahiminiya, S.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, Canada Genome Quebec Innovat Ctr, Montreal, PQ, Canada McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaAlmuriekhi, M.论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Sect Clin & Metab Genet, Dept Pediat, Doha, Qatar McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaNawaz, Z.论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Cytogenet & Mol Cytogenet Lab, Dept Lab Med & Pathol, Doha, Qatar McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaStaffa, A.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, Canada Genome Quebec Innovat Ctr, Montreal, PQ, Canada McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaLepage, P.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, Canada Genome Quebec Innovat Ctr, Montreal, PQ, Canada McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaAli, R.论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Sect Clin & Metab Genet, Dept Pediat, Doha, Qatar McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaHashim, L.论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Sect Clin & Metab Genet, Dept Pediat, Doha, Qatar McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaSchwartzentruber, J.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, Canada Genome Quebec Innovat Ctr, Montreal, PQ, Canada McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaAbu Khadija, K.论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Cytogenet & Mol Cytogenet Lab, Dept Lab Med & Pathol, Doha, Qatar McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaZaineddin, S.论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Cytogenet & Mol Cytogenet Lab, Dept Lab Med & Pathol, Doha, Qatar McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaGamal, H.论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Sect Clin & Metab Genet, Dept Pediat, Doha, Qatar McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaMajewski, J.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, Canada Genome Quebec Innovat Ctr, Montreal, PQ, Canada McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, CanadaBen-Omran, T.论文数: 0 引用数: 0 h-index: 0机构: Hamad Med Corp, Sect Clin & Metab Genet, Dept Pediat, Doha, Qatar McGill Univ, Fac Med, Dept Human Genet, Montreal, PQ, Canada
- [7] Clinical relevance of somatic mosaic variants detected from exome sequencing dataCLINICAL IMMUNOLOGY, 2023, 250Ghosh, Rajarshi论文数: 0 引用数: 0 h-index: 0机构: NIAID, NIH, Rockville, MD USA NIAID, NIH, Rockville, MD USAOler, Andrew论文数: 0 引用数: 0 h-index: 0机构: NIAID, NIH, Bioinformat & Computat Biosci Branch, Rockville, MD USA NIAID, NIH, Rockville, MD USARustad, Mark论文数: 0 引用数: 0 h-index: 0机构: NIAID, NIH, Off Data Sci & Emerging Technol, Rockville, MD USA NIAID, NIH, Rockville, MD USALi, Samuel论文数: 0 引用数: 0 h-index: 0机构: NIAID, Bioinformat & Computat Biosci Branch, Rockville, MD USA NIAID, NIH, Rockville, MD USAYan, Jia论文数: 0 引用数: 0 h-index: 0机构: NIAID, Rockville, MD USA NIAID, NIH, Rockville, MD USASimiluk, Morgan论文数: 0 引用数: 0 h-index: 0机构: NIAID, Rockville, MD USA NIAID, NIH, Rockville, MD USASeifert, Bryce论文数: 0 引用数: 0 h-index: 0机构: NIAID, Rockville, MD USA NIAID, NIH, Rockville, MD USACalvo, Katherine论文数: 0 引用数: 0 h-index: 0机构: NIAID, Automated Hematol & Morphol, NIH Clin Ctr, Dept Lab Med, Rockville, MD USA NIAID, NIH, Rockville, MD USAHolland, Steven论文数: 0 引用数: 0 h-index: 0机构: NIAID, Div Intramural Res, NIH, Rockville, MD USA NIAID, Immunopathogenesis Sect, NIH, Rockville, MD USA NIAID, NIH, Rockville, MD USAWalkiewicz, Magdalena论文数: 0 引用数: 0 h-index: 0机构: NIAID, NIH, Rockville, MD USA NIAID, NIH, Rockville, MD USA
- [8] Case report: Exome sequencing revealed disease-causing variants in a patient with spondylospinal thoracic dysostosisFRONTIERS IN PEDIATRICS, 2023, 11Bouchoucha, Sami论文数: 0 引用数: 0 h-index: 0机构: Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, Tunisia Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, TunisiaChikhaoui, Asma论文数: 0 引用数: 0 h-index: 0机构: Univ Tunis El Manar, Inst Pasteur Tunis, Lab Genom Biomed & Oncogenet, LR16IPT05, Tunis, Tunisia Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, TunisiaNajjar, Dorra论文数: 0 引用数: 0 h-index: 0机构: Univ Tunis El Manar, Inst Pasteur Tunis, Lab Genom Biomed & Oncogenet, LR16IPT05, Tunis, Tunisia Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, TunisiaZayoud, Khouloud论文数: 0 引用数: 0 h-index: 0机构: Univ Tunis El Manar, Inst Pasteur Tunis, Lab Genom Biomed & Oncogenet, LR16IPT05, Tunis, Tunisia Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, TunisiaZouari, Mohamed论文数: 0 引用数: 0 h-index: 0机构: Univ Tunis El Manar, Inst Pasteur Tunis, Genom Platform, Tunis, Tunisia Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, TunisiaNessib, Mohamed Nabil论文数: 0 引用数: 0 h-index: 0机构: Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, Tunisia Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, Tunisia论文数: 引用数: h-index:机构:Yacoub-Youssef, Houda论文数: 0 引用数: 0 h-index: 0机构: Univ Tunis El Manar, Inst Pasteur Tunis, Lab Genom Biomed & Oncogenet, LR16IPT05, Tunis, Tunisia Hop Enfant Bechir Hamza, Serv Orthopedie, Tunis, Tunisia
- [9] Exome sequencing in a large cohort of individuals with VATER/VACTERL association for identification of disease-causing variants in disease-associated genes and prioritization of candidate genesPEDIATRIC NEPHROLOGY, 2023, 38 (07) : 2287 - 2288Comic, Jasmina论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Dept Nephrol, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanyRiedhammer, Korbinian M.论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Dept Nephrol, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanyVill, Katharina论文数: 0 引用数: 0 h-index: 0机构: Ludwig Maximilians Univ Munchen, LMU Hosp, Dr Hauner Childrens Hosp, Dept Pediat Neurol & Dev Med, Munich, Germany LMU, Ctr Children Med Complexity, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanyAbazi-Emini, Nora论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp, Med Fac Skopje, Dept Pediat Nephrol, Skopje, North Macedonia Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanySeitz, Barbara论文数: 0 引用数: 0 h-index: 0机构: KfH Kuratorium Dialyse & Nierentransplantat EV, KfH Board Trustees Dialysis & Kidney Transplantat, Neu Isenburg, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanyBraunisch, Matthias C.论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Dept Nephrol, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanyBrugger, Mela-Nie论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanyTasic, Velibor论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp, Med Fac Skopje, Dept Pediat Nephrol, Skopje, North Macedonia Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanyReutter, Heiko论文数: 0 引用数: 0 h-index: 0机构: Univ Erlangen Nurnberg, Dept Neonatol & Pedi atric Intens Care, Erlangen, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, GermanyHoefele, Julia论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, Germany Tech Univ Munich, Klinikum Rechts Isar, Sch Med, Inst Human Genet, Munich, Germany
- [10] Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital CataractGENES, 2020, 11 (05)Berry, Vanita论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, England Moorfields Eye Hosp NHS Fdn Trust, London EC1V 2PD, England UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, EnglandIonides, Alex论文数: 0 引用数: 0 h-index: 0机构: Moorfields Eye Hosp NHS Fdn Trust, London EC1V 2PD, England UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, EnglandPontikos, Nikolas论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, England Moorfields Eye Hosp NHS Fdn Trust, London EC1V 2PD, England UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, EnglandMoghul, Ismail论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Canc Inst, London WC1E 6BT, England UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, EnglandMoore, Anthony T.论文数: 0 引用数: 0 h-index: 0机构: Moorfields Eye Hosp NHS Fdn Trust, London EC1V 2PD, England Univ Calif San Francisco, Ophthalmol Dept, Sch Med, San Francisco, CA 94158 USA UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, EnglandQuinlan, Roy A.论文数: 0 引用数: 0 h-index: 0机构: Univ Durham, Dept Biosci, Upper Mountjoy Sci Site, Durham DH1 3LE, England UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, EnglandMichaelides, Michel论文数: 0 引用数: 0 h-index: 0机构: UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, England Moorfields Eye Hosp NHS Fdn Trust, London EC1V 2PD, England UCL, UCL Inst Ophthalmol, 11-43 Bath St, London EC1V 9EL, England