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摩洛哥的遗传学与基因组医学：当下的希望能让未来充满光明。

Genetics and genomic medicine in Morocco: the present hope can make the future bright.

作者信息

Belhassan Khadija, Ouldim Karim, Sefiani Abdel Aziz

机构信息

Medical Genetics and Onco-Genetics Department Hassan II University Medical Center Fez Morocco.

Medical Genetics Department National Institute of Hygiene Rabat Morocco.

出版信息

Mol Genet Genomic Med. 2016 Nov 10;4(6):588-598. doi: 10.1002/mgg3.255. eCollection 2016 Nov.

DOI:10.1002/mgg3.255
PMID:27896281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5118203/
Abstract

Genetics and genomic medicine in Morocco: the present hope can make the future bright.

摘要

摩洛哥的遗传学与基因组医学

当下的希望能让未来充满光明。

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NAT2 Genotypes in Moroccan Patients with Hepatotoxicity Due to Antituberculosis Drugs.摩洛哥抗结核药物所致肝毒性患者的NAT2基因分型
Genet Test Mol Biomarkers. 2016 Nov;20(11):680-684. doi: 10.1089/gtmb.2016.0060. Epub 2016 Aug 19.
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First application of next-generation sequencing in Moroccan breast/ovarian cancer families and report of a novel frameshift mutation of the gene.下一代测序技术在摩洛哥乳腺癌/卵巢癌家族中的首次应用及该基因一个新的移码突变报告。
Oncol Lett. 2016 Aug;12(2):1192-1196. doi: 10.3892/ol.2016.4739. Epub 2016 Jun 16.
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Further evidence of POP1 mutations as the cause of anauxetic dysplasia.
Aging (Albany NY). 2022 Mar 28;14(6):2524-2536. doi: 10.18632/aging.203984.
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Tracing ovarian cancer research in Morocco: A bibliometric analysis.摩洛哥卵巢癌研究追踪：文献计量分析
Gynecol Oncol Rep. 2021 May 7;37:100777. doi: 10.1016/j.gore.2021.100777. eCollection 2021 Aug.
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How to design a national genomic project-a systematic review of active projects.如何设计国家基因组项目——对正在进行的项目的系统评价。
Hum Genomics. 2021 Mar 24;15(1):20. doi: 10.1186/s40246-021-00315-6.
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Morocco's First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges.摩洛哥首家生物银行：建立、伦理问题、生物医学研究机会和挑战。
Biomed Res Int. 2020 Dec 8;2020:8812609. doi: 10.1155/2020/8812609. eCollection 2020.
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Empowering newborn screening programs in African countries through establishment of an international collaborative effort.通过建立国际合作努力来加强非洲国家的新生儿筛查项目。
J Community Genet. 2020 Jul;11(3):253-268. doi: 10.1007/s12687-020-00463-7. Epub 2020 May 15.
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An International Summit in Human Genetics and Genomics: Empowering clinical practice and research in developing countries.一场人类遗传学与基因组学国际峰会：助力发展中国家的临床实践与研究
Mol Genet Genomic Med. 2019 Jan;7(1):e00599. doi: 10.1002/mgg3.599.
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Looking back and looking forward.回首往昔，展望未来。
Mol Genet Genomic Med. 2018 Jan;6(1):3-8. doi: 10.1002/mgg3.374.
POP1突变作为生长迟缓性发育异常病因的进一步证据。
Am J Med Genet A. 2016 Sep;170(9):2462-5. doi: 10.1002/ajmg.a.37839. Epub 2016 Jul 6.
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Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism.肢端肥大性额鼻发育不全与ZSWIM6突变：表型谱与镶嵌现象
Clin Genet. 2016 Sep;90(3):270-5. doi: 10.1111/cge.12721. Epub 2016 Feb 3.
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Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6.海姆勒综合征由过氧化物酶体生物发生基因PEX1和PEX6的亚效突变引起。
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Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.地中海奠基者突变数据库（MFMD）：利用奠基者突变进行地中海人群的遗传学诊断、遗传多样性及迁徙历史研究
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TPMT alleles in the Moroccans.
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A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to pain.一名患有先天性无痛觉的摩洛哥儿童中SCN9A基因出现一种新的无义突变。
Pediatr Neurol. 2014 Nov;51(5):741-4. doi: 10.1016/j.pediatrneurol.2014.06.009. Epub 2014 Jul 12.
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The CYP7A1 gene rs3808607 variant is associated with susceptibility of tuberculosis in Moroccan population.CYP7A1基因rs3808607变异与摩洛哥人群的结核病易感性相关。
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