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- [1] Identification of novel candidate genes in heterotaxy syndrome patients with congenital heart diseases by whole exome sequencingBIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2020, 1866 (12):Liang, Shuzhang论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Life Sci, Shanghai, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaShi, Xin论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Cardiol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Xinhua Hosp, Sch Med, Dept Pediat Cardiol, Shanghai, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaYu, Chunxiao论文数: 0 引用数: 0 h-index: 0机构: Wuhan Univ, Sch Basic Med Sci, Wuhan, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaShao, Xuelian论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Life Sci, Shanghai, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaZhou, Haitao论文数: 0 引用数: 0 h-index: 0机构: Wuhan Univ, Sch Basic Med Sci, Wuhan, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaLi, Xueyu论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Life Sci, Shanghai, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaChang, Cheng论文数: 0 引用数: 0 h-index: 0机构: Wuhan Univ, Sch Basic Med Sci, Wuhan, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaLai, Kaa Seng论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Life Sci, Shanghai, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaMa, Jinmin论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Sch Life Sci, Shanghai, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R ChinaZhang, Ruilin论文数: 0 引用数: 0 h-index: 0机构: Wuhan Univ, Sch Basic Med Sci, Wuhan, Peoples R China Hubei Prov Key Lab Dev Originated Dis, Wuhan, Peoples R China Fudan Univ, Sch Life Sci, Shanghai, Peoples R China
- [2] Whole Exome Sequencing in Females with Autism Implicates Novel and Candidate GenesINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2015, 16 (01) : 1312 - 1335Butler, Merlin G.论文数: 0 引用数: 0 h-index: 0机构: Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USA Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USARafi, Syed K.论文数: 0 引用数: 0 h-index: 0机构: Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USA Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USAHossain, Waheeda论文数: 0 引用数: 0 h-index: 0机构: Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USA Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USAStephan, Dietrich A.论文数: 0 引用数: 0 h-index: 0机构: Univ Pittsburgh, Dept Human Genet, Pittsburgh, PA 15260 USA Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USAManzardo, Ann M.论文数: 0 引用数: 0 h-index: 0机构: Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USA Univ Kansas, Med Ctr, Dept Psychiat & Behav Sci, Kansas City, KS 66160 USA
- [3] Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisisMOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (05):Salinas-Torres, Victor M.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Univ Hosp Dr Jose Eleuterio Gonzalez, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, MexicoGallardo-Blanco, Hugo L.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Univ Hosp Dr Jose Eleuterio Gonzalez, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, MexicoSalinas-Torres, Rafael A.论文数: 0 引用数: 0 h-index: 0机构: Inst Tecnol Tijuana, Dept Syst & Comp, Tijuana, Mexico Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, MexicoCerda-Flores, Ricardo M.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Nuevo Leon, Sch Nursing, Monterrey, Mexico Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, MexicoLugo-Trampe, Jose J.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Univ Hosp Dr Jose Eleuterio Gonzalez, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, MexicoVillarreal-Martinez, Daniel Z.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Univ Hosp Dr Jose Eleuterio Gonzalez, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, MexicoIbarra-Ramirez, Marisol论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Univ Hosp Dr Jose Eleuterio Gonzalez, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, MexicoMartinez de Villarreal, Laura E.论文数: 0 引用数: 0 h-index: 0机构: Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Univ Hosp Dr Jose Eleuterio Gonzalez, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico Univ Autonoma Nuevo Leon, Sch Med, Dept Genet, Ave Madero & Gonzalitos S-N, Monterrey 64460, Nuevo Leon, Mexico
- [4] WHOLE EXOME SEQUENCING REVEALS NOVEL CANDIDATE GENES IN FAMILIAL MDS/AMLHAEMATOLOGICA, 2016, 101 : 205 - 206论文数: 引用数: h-index:机构:Cardoso, S.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Ctr Genom & Child Hlth, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandTawana, K.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandWang, J.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Barts Canc Inst, Ctr Mol Oncol, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandChelala, C.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Barts Canc Inst, Ctr Mol Oncol, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandPlagnol, V.论文数: 0 引用数: 0 h-index: 0机构: UCL Genet Inst, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandWallis, Y.论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens NHS Fdn Trust, West Midlands Reg Genet Lab, Canc Programme, Birmingham, W Midlands, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandRyan, G.论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens NHS Fdn Trust, West Midlands Reg Genet Lab, Canc Programme, Birmingham, W Midlands, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandEllison, A.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Ctr Genom & Child Hlth, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandAl Seraihi, A.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandWalne, A.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Ctr Genom & Child Hlth, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandTummala, H.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Ctr Genom & Child Hlth, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandFitzgibbon, J.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandDokal, I.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Ctr Genom & Child Hlth, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, EnglandVulliamy, T.论文数: 0 引用数: 0 h-index: 0机构: Queen Mary Univ London, Blizard Inst, Ctr Genom & Child Hlth, London, England Queen Mary Univ London, Barts Canc Inst, Ctr Haematooncol, London, England
- [5] Identification of Novel Candidate Genes for Familial Thyroid Cancer by Whole Exome SequencingINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (09)Tous, Cristina论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain Ctr Biomed Network Res Rare Dis CIBERER, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, SpainMunoz-Redondo, Carmen论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain Ctr Biomed Network Res Rare Dis CIBERER, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, SpainBravo-Gil, Nereida论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain Ctr Biomed Network Res Rare Dis CIBERER, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, SpainGavilan, Angela论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, SpainFernandez, Raquel Maria论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain Ctr Biomed Network Res Rare Dis CIBERER, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, SpainAntinolo, Juan论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, SpainNavarro-Gonzalez, Elena论文数: 0 引用数: 0 h-index: 0机构: Ctr Biomed Network Res Rare Dis CIBERER, Seville 41013, Spain Univ Hosp Virgen Rocio, Dept Endocrinol & Nutr, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, SpainAntinolo, Guillermo论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain Ctr Biomed Network Res Rare Dis CIBERER, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, SpainBorrego, Salud论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain Ctr Biomed Network Res Rare Dis CIBERER, Seville 41013, Spain Univ Seville, Univ Hosp Virgen Rocio, Inst Biomed Seville,CSIC, Dept Maternofetal Med Genet & Reprod, Seville 41013, Spain
- [6] Whole exome sequencing identifies novel candidate genes involved in Asperger syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 368 - 369Poirier, K.论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, France Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, FranceDelobel, B.论文数: 0 引用数: 0 h-index: 0机构: Hop St Vincent de Paul, GH Inst Catholique Lille, Ctr Genet Chromos, Lille, France Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, FranceLenne, B.论文数: 0 引用数: 0 h-index: 0机构: Hop St Vincent de Paul, GH Inst Catholique Lille, Ctr Genet Chromos, Lille, France Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, FranceNectoux, J.论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, France Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, FranceLetourneur, F.论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, France Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, FranceBilluart, P.论文数: 0 引用数: 0 h-index: 0机构: Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, France Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, FranceBienvenu, T.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, Inst Cochin, INSERM, U1016,CNRS,UMR8104, Paris, France Inst Cochin, INSERM, CNRS, U1016,UMR8104, Paris, France
- [7] Exome sequencing of nonsyndromic cleft palate trios reveals interesting candidate genesEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 146 - 146Ishorst, Nina论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, Sch Med, Bonn, Germany Univ Hosp Bonn, Bonn, Germany Univ Bonn, Inst Human Genet, Sch Med, Bonn, GermanyMehrem, Sarah L.论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, Sch Med, Bonn, Germany Univ Hosp Bonn, Bonn, Germany Univ Bonn, Inst Human Genet, Sch Med, Bonn, GermanyDrichel, Dmitriy论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Cologne, Germany Univ Bonn, Inst Human Genet, Sch Med, Bonn, GermanySivalingam, Sugirthan论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Bonn, Bonn, Germany Univ Bonn, Fac Med, Core Unit Bioinformat Anal, Bonn, Germany Univ Bonn, Inst Genom Stat & Bioinformat, Sch Med, Bonn, Germany Univ Hosp Bonn, Inst Med Biometry Informat & Epidemiol, Bonn, Germany Univ Bonn, Inst Human Genet, Sch Med, Bonn, GermanyCarels, Carine论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium Univ Bonn, Inst Human Genet, Sch Med, Bonn, Germanyvan Rooij, Iris论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Dept Hlth Evidence, Med Ctr, Nijmegen, Netherlands Univ Bonn, Inst Human Genet, Sch Med, Bonn, GermanyBuness, Andreas论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Bonn, Bonn, Germany Univ Bonn, Fac Med, Core Unit Bioinformat Anal, Bonn, Germany Univ Bonn, Inst Genom Stat & Bioinformat, Sch Med, Bonn, Germany Univ Hosp Bonn, Inst Med Biometry Informat & Epidemiol, Bonn, Germany Univ Bonn, Inst Human Genet, Sch Med, Bonn, GermanyLudwig, Kerstin论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, Sch Med, Bonn, Germany Univ Hosp Bonn, Bonn, Germany Univ Bonn, Inst Human Genet, Sch Med, Bonn, GermanyMangold, Elisabeth论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Inst Human Genet, Sch Med, Bonn, Germany Univ Hosp Bonn, Bonn, Germany Univ Bonn, Inst Human Genet, Sch Med, Bonn, Germany
- [8] Pathogenic variants identification in primary congenital glaucoma patients using whole exome sequencingScientific Reports, 15 (1)Shahzad Ahmad论文数: 0 引用数: 0 h-index: 0机构: Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical Sciences Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesMuhammad Saleem Gandapur论文数: 0 引用数: 0 h-index: 0机构: Khyber Medical University,Rare Diseases Genetics and Genomics, Centre for Omic Sciences Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesMusharraf Jelani论文数: 0 引用数: 0 h-index: 0机构: Islamia College Peshawar,Department of Physical Chemistry and Technology of Polymers Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesAnees Muhammad论文数: 0 引用数: 0 h-index: 0机构: Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical Sciences Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesIhtisham Ul Haq论文数: 0 引用数: 0 h-index: 0机构: Silesian University of Technology,Joint Doctoral school Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesYousaf Jamal Mahsood论文数: 0 引用数: 0 h-index: 0机构: Silesian University of Technology,Postgraduate Program in Technological Innovation Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesSajjad Ahmad论文数: 0 引用数: 0 h-index: 0机构: Federal University of Minas Gerais,Department of Ophthalmology Khyber Girls Medical Collage Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesWadi B. Alonazi论文数: 0 引用数: 0 h-index: 0机构: Hayatabad Medical Complex,Health Administration Department, College of Business Administration Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesNousheen Bibi论文数: 0 引用数: 0 h-index: 0机构: Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical Sciences Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesMuhammad Tahir Sarwar论文数: 0 引用数: 0 h-index: 0机构: King Saud University,Department of Bioinformatics Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical SciencesTaj Ali Khan论文数: 0 引用数: 0 h-index: 0机构: Shaheed Benazir Bhutto Women University,Institute of Pathology & Diagnostic Medicines Khyber Medical University,Department of Molecular Biology & Genetics, Institute of Basic Medical Sciences
- [9] Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention StudyBIRTH DEFECTS RESEARCH, 2024, 116 (07):Blue, Elizabeth E.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Med, Div Med Genet, Seattle, WA USA Brotman Baty Inst Precis Med, Seattle, WA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAMoore, Kristin J.论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USANorth, Kari E.论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USADesrosiers, Tania A.论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USACarmichael, Suzan L.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Pediat, Stanford, CA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAWhite, Janson J.论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAChong, Jessica X.论文数: 0 引用数: 0 h-index: 0机构: Brotman Baty Inst Precis Med, Seattle, WA USA Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USABamshad, Michael J.论文数: 0 引用数: 0 h-index: 0机构: Brotman Baty Inst Precis Med, Seattle, WA USA Univ Washington, Dept Pediat, Div Med Genet, Seattle, WA USA Seattle Childrens Hosp, Div Genet Med, Seattle, WA USA Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAJenkins, Mary M.论文数: 0 引用数: 0 h-index: 0机构: CDCP, Natl Ctr Birth Defects & Dev Disabil, Atlanta, GA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAAlmli, Lynn M.论文数: 0 引用数: 0 h-index: 0机构: CDCP, Natl Ctr Birth Defects & Dev Disabil, Atlanta, GA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USABrody, Lawrence C.论文数: 0 引用数: 0 h-index: 0机构: Natl Human Genome Res Inst, Div Genom & Soc, NIH, Bethesda, MD USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAFreedman, Sharon F.论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Ophthalmol, Durham, NC USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAReefhuis, Jennita论文数: 0 引用数: 0 h-index: 0机构: CDCP, Natl Ctr Birth Defects & Dev Disabil, Atlanta, GA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USARomitti, Paul A.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Coll Publ Hlth, Dept Epidemiol, Iowa City, IA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAShaw, Gary M.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Sch Med, Dept Pediat, Stanford, CA USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USA论文数: 引用数: h-index:机构:Kay, Denise M.论文数: 0 引用数: 0 h-index: 0机构: New York State Dept Hlth, Wadsworth Ctr, Div Genet, Albany, NY USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USABrowne, Marilyn L.论文数: 0 引用数: 0 h-index: 0机构: New York State Dept Hlth, Birth Defects Registry, Albany, NY USA SUNY Albany, Sch Publ Hlth, Dept Epidemiol & Biostat, Rensselaer, NY USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAFeldkamp, Marcia L.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Sch Med, Dept Pediat, Div Med Genet, Salt Lake City, UT USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAFinnell, Richard H.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Ctr Precis Environm Hlth, Dept Mol & Cellular Biol & Med, Houston, TX USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USANembhard, Wendy N.论文数: 0 引用数: 0 h-index: 0机构: Univ Arkansas Med Sci, Dept Epidemiol, Little Rock, AR USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAPangilinan, Faith论文数: 0 引用数: 0 h-index: 0机构: Natl Human Genome Res Inst, Div Genom & Soc, NIH, Bethesda, MD USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USAOlshan, Andrew F.论文数: 0 引用数: 0 h-index: 0机构: Univ N Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA Univ Washington, Dept Med, Div Med Genet, Seattle, WA USA
- [10] Whole Exome Sequencing Analysis in Early Onset Alzheimer Reveals Novel Candidate GenesANNALS OF NEUROLOGY, 2019, 86 : S101 - S102Fernandez, Victoria论文数: 0 引用数: 0 h-index: 0机构: Washington Univ, Sch Med, St Louis, MO USA Washington Univ, Sch Med, St Louis, MO USA