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Genomics into Healthcare: the 5th Pan Arab Human Genetics Conference and 2013 Golden Helix Symposium.基因组学融入医疗保健：第五届泛阿拉伯人类遗传学会议暨2013年金色螺旋研讨会
Hum Mutat. 2014 May;35(5):637-40. doi: 10.1002/humu.22530. Epub 2014 Mar 31.
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Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference.多因素疾病的遗传学：第六届泛阿拉伯人类遗传学会议论文集
J Transl Med. 2016 Apr 20;14:96. doi: 10.1186/s12967-016-0854-4.
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Genetic Analysis in Translational Medicine: The 2010 GOLDEN HELIX Symposium.转化医学中的遗传分析：2010 年 GOLDEN HELIX 研讨会。
Hum Mutat. 2011 Jun;32(6):698-703. doi: 10.1002/humu.21473. Epub 2011 Mar 24.
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Building Skills and Resources for Genomics, Epigenetics, and Bioinformatics Research for Africa: Report of the Joint 11th Conference of the African Society of Human Genetics and 12th H3Africa Consortium, 2018.为非洲的基因组学、表观遗传学和生物信息学研究构建技能和资源：非洲人类遗传学学会第 11 次会议和 H3Africa 联盟第 12 次会议联合报告，2018 年。
Am J Trop Med Hyg. 2020 Jun;102(6):1417-1424. doi: 10.4269/ajtmh.19-0837.
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Consanguineous marriages in the United Arab Emirates.阿拉伯联合酋长国的近亲婚姻。
J Biosoc Sci. 1997 Oct;29(4):491-7. doi: 10.1017/s0021932097004914.
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CTGA: the database for genetic disorders in Arab populations.CTGA：阿拉伯人群遗传疾病数据库。
Nucleic Acids Res. 2006 Jan 1;34(Database issue):D602-6. doi: 10.1093/nar/gkj015.
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Global Oncology Medical Diplomacy Working Group Inaugural Meeting: Defining Worldwide Barriers to Germline Genomics in Cancer Prevention and Management.全球肿瘤医学外交工作组首次会议：确定癌症预防和管理中胚系基因组学的全球障碍。
Ann Glob Health. 2023 Feb 21;89(1):16. doi: 10.5334/aogh.3967. eCollection 2023.
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Clinical applications of next-generation sequencing: the 2013 human genome variation society scientific meeting.下一代测序技术的临床应用：2013 年人类基因组变异学会科学会议。
Hum Mutat. 2013 Nov;34(11):1583-7. doi: 10.1002/humu.22400. Epub 2013 Sep 4.
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A 1000 Arab genome project to study the Emirati population.一项旨在研究阿联酋人口的 1000 个阿拉伯人基因组计划。
J Hum Genet. 2018 Apr;63(4):533-536. doi: 10.1038/s10038-017-0402-y. Epub 2018 Feb 6.
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Mitochondrial DNA control region variation in Dubai, United Arab Emirates.阿拉伯联合酋长国迪拜的线粒体DNA控制区变异
Forensic Sci Int Genet. 2008 Jan;2(1):e9-10. doi: 10.1016/j.fsigen.2007.08.005. Epub 2007 Sep 24.
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The genetic landscape of inherited retinal dystrophies in Arabs.阿拉伯人群遗传性视网膜营养不良的遗传图谱。
BMC Med Genomics. 2023 May 1;16(1):89. doi: 10.1186/s12920-023-01518-7.
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The genetics of rod-cone dystrophy in Arab countries: a systematic review.阿拉伯国家的 rods-cone dystrophy 遗传学：系统评价。
Eur J Hum Genet. 2021 Jun;29(6):897-910. doi: 10.1038/s41431-020-00754-0. Epub 2020 Nov 13.
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Genomic Medicine Without Borders: Which Strategies Should Developing Countries Employ to Invest in Precision Medicine? A New "Fast-Second Winner" Strategy.无国界基因组医学：发展中国家应采用哪些策略投资精准医学？一种新的“快速第二赢家”策略。
OMICS. 2017 Nov;21(11):647-657. doi: 10.1089/omi.2017.0141.
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Success stories in genomic medicine from resource-limited countries.资源有限国家基因组医学的成功案例。
Hum Genomics. 2015 Jun 18;9(1):11. doi: 10.1186/s40246-015-0033-3.
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Individualized medicine enabled by genomics in Saudi Arabia.沙特阿拉伯基因组学助力的个性化医疗。
BMC Med Genomics. 2015;8 Suppl 1(Suppl 1):S3. doi: 10.1186/1755-8794-8-S1-S3. Epub 2015 Jan 15.
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Prevalence and correlation of human papilloma virus and its types with prognostic markers in patients with invasive ductal carcinoma of the breast in kuwait.科威特乳腺浸润性导管癌患者中人乳头瘤病毒及其类型与预后标志物的患病率及相关性
Sultan Qaboos Univ Med J. 2013 Nov;13(4):527-33. doi: 10.12816/0003311. Epub 2013 Nov 8.
2
Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies.全球临床相关基因组变异等位基因频率 FINDbase 数据库的发展。
Nucleic Acids Res. 2014 Jan;42(Database issue):D1020-6. doi: 10.1093/nar/gkt1125. Epub 2013 Nov 14.
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Breast cancer in Arab populations: molecular characteristics and disease management implications.阿拉伯人群中的乳腺癌：分子特征及对疾病管理的影响。
Lancet Oncol. 2013 Sep;14(10):e417-24. doi: 10.1016/S1470-2045(13)70165-7.
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The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.摩洛哥遗传疾病数据库 (MGDD)：一个与遗传疾病和疾病易感性相关的 DNA 变异数据库。
Eur J Hum Genet. 2014 Mar;22(3):322-6. doi: 10.1038/ejhg.2013.151. Epub 2013 Jul 17.
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CYP3A4*22: promising newly identified CYP3A4 variant allele for personalizing pharmacotherapy.CYP3A4*22：有潜力的新鉴定 CYP3A4 变异等位基因用于药物治疗个体化。
Pharmacogenomics. 2013 Jan;14(1):47-62. doi: 10.2217/pgs.12.187.
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Public Health Genomics and personalized healthcare: a pipeline from cell to society.公共卫生基因组学与个性化医疗：从细胞到社会的流程
Drug Metabol Drug Interact. 2012;27(3):121-3. doi: 10.1515/dmdi-2012-0028.
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A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataract.PRG4基因的一种新型突变是先天性屈曲挛缩-关节病-髋内翻-心包炎综合征的潜在病因，其表型可能扩展至包括先天性白内障。
Birth Defects Res A Clin Mol Teratol. 2012 Jul;94(7):553-6. doi: 10.1002/bdra.23031. Epub 2012 Jun 8.
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Pharmacogenomics and public health: implementing 'populationalized' medicine.药物基因组学与公共卫生：实施“群体化”医学。
Pharmacogenomics. 2012 May;13(7):803-13. doi: 10.2217/pgs.12.52.
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A personal view on systems medicine and the emergence of proactive P4 medicine: predictive, preventive, personalized and participatory.个人视角下的系统医学与主动的 P4 医学的出现：预测性、预防性、个性化和参与性。
N Biotechnol. 2012 Sep 15;29(6):613-24. doi: 10.1016/j.nbt.2012.03.004. Epub 2012 Mar 18.
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Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays.基于自组装 DNA 纳米阵列的无链碱基读取进行人类基因组测序。
Science. 2010 Jan 1;327(5961):78-81. doi: 10.1126/science.1181498. Epub 2009 Nov 5.
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