Mbarek Hamdi相关文献与解析，生知库 | 链接生命科学的每一步

Impact of Somatic Gene Mutations on Prognosis Prediction in De Novo AML: Unraveling Insights from a Systematic Review and Meta-Analysis

体细胞基因突变对新发急性髓系白血病预后预测的影响：系统评价和荟萃分析揭示的见解

doi:10.3390/cancers17193189

Elfatih, Amal; Ahmed, Nisar; Srour, Luma; Mohammed, Idris; Villiers, William; Al-Barazenji, Tara; Mbarek, Hamdi; El Akiki, Susanna; Jithesh, Puthen Veettil; Muneer, Mohammed; Fareed, Shehab; Mifsud, Borbala

Understanding Heritable Variation Among Hosts in Infectious Diseases Through the Lens of Twin Studies

通过双胞胎研究了解传染病宿主间的遗传变异

期刊:Genes

影响因子:2.8

doi:10.3390/genes16020177

Smatti, Maria K; Yassine, Hadi M; Mbarek, Hamdi; Boomsma, Dorret I

Polygenic scores for dizygotic twinning: insights into the genetic architecture of female fertility

双卵双胞胎的多基因评分：对女性生育力遗传结构的深入了解

期刊:Journal of Assisted Reproduction and Genetics

影响因子:2.7

doi:10.1007/s10815-025-03515-4

Hubers, Nikki; Page, Christian M; Pool, René; Mbarek, Hamdi; Lambalk, Nils; Mijatovic, Velja; Ligthart, Lannie; van Dongen, Jenny; Håberg, Siri; Corfield, Elizabeth C; Beck, Jeffrey J; Ehli, Erik A; Martin, Nicholas G; Willemsen, Gonneke; Harris, Jennifer R; Hottenga, Jouke-Jan; Boomsma, Dorret I

发表日期：2025

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Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks

可能的遗传因素与 GLP1-RA 和减肥手术引起的体重减轻之间的关联：一项纳入 9 个生物样本库中 10960 名个体的多民族研究

期刊:JACC Advances

影响因子:

doi:10.1101/2024.09.11.24313458

German, Jakob; Cordioli, Mattia; Tozzo, Veronica; Urbut, Sarah; Arumäe, Kadri; Smit, Roelof A J; Lee, Jiwoo; Li, Josephine H; Janucik, Adrian; Ding, Yi; Akinkuolie, Akintunde; Heyne, Henrike; Eoli, Andrea; Saad, Chadi; Al-Sarraj, Yasser; Abdel-Latif, Rania; Mohammed, Shaban; Hail, Moza Al; Barry, Alexandra; Wang, Zhe; Cajuso, Tatiana; Corbetta, Andrea; Natarajan, Pradeep; Ripatti, Samuli; Philippakis, Anthony; Szczerbinski, Lukasz; Pasaniuc, Bogdan; Kutalik, Zoltan; Mbarek, Hamdi; Loos, Ruth J F; Vainik, Uku; Ganna, Andrea

发表日期：2025

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Polygenic Scores for Dizygotic Twinning: Insights into the Genetic Architecture of Female Fertility

双卵双胞胎的多基因评分：对女性生育力遗传结构的深入了解

期刊:

影响因子:

doi:10.1101/2024.12.02.24318308

Hubers, Nikki; Page, Christian M; Pool, René; Mbarek, Hamdi; Lambalk, Nils; Mijatovic, Velja; Ligthart, Lannie; van Dongen, Jenny; Corfield, Elizabeth C; Beck, Jeffrey J; Ehli, Erik A; Martin, Nicholas G; Willemsen, Gonneke; Håberg, Siri; Harris, Jennifer R; Hottenga, Jouke-Jan; Boomsma, Dorret I

发表日期：2025

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Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery

可能的遗传因素与GLP-1受体激动剂和减肥手术引起的体重减轻之间的关联

期刊:Nature Medicine

影响因子:

doi:10.1038/s41591-025-03645-3

German, Jakob; Cordioli, Mattia; Tozzo, Veronica; Urbut, Sarah; Arumäe, Kadri; Smit, Roelof A J; Lee, Jiwoo; Li, Josephine H; Janucik, Adrian; Ding, Yi; Akinkuolie, Akintunde; Heyne, Henrike O; Eoli, Andrea; Saad, Chadi; Al-Sarraj, Yasser; Abdel-Latif, Rania; Mohammed, Shaban; Hail, Moza Al; Barry, Alexandra; Wang, Zhe; Cajuso, Tatiana; Corbetta, Andrea; Natarajan, Pradeep; Ripatti, Samuli; Philippakis, Anthony; Szczerbinski, Lukasz; Pasaniuc, Bogdan; Kutalik, Zoltán; Mbarek, Hamdi; Loos, Ruth J F; Vainik, Uku; Ganna, Andrea

Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort

基因组测序在卡塔尔人群中发现了13个新的自闭症谱系障碍候选风险基因

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms252111551

Ben-Mahmoud, Afif; Gupta, Vijay; Abdelaleem, Alice; Thompson, Richard; Aden, Abdi; Mbarek, Hamdi; Saad, Chadi; Tolefat, Mohamed; Alshaban, Fouad; Stanton, Lawrence W; Kim, Hyung-Goo

Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants

对 14392 个全基因组的分析显示，3.5% 的卡塔尔人携带具有医学意义的变异基因。

期刊:European Journal of Human Genetics

影响因子:4.6

doi:10.1038/s41431-024-01656-1

Elfatih, Amal; Saad, Chadi; Mifsud, Borbala; Mbarek, Hamdi

发表日期：2024

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Forging the path to precision medicine in Qatar: a public health perspective on pharmacogenomics initiatives

在卡塔尔开辟精准医疗之路：从公共卫生角度看药物基因组学计划

期刊:Frontiers in Public Health

影响因子:3.4

doi:10.3389/fpubh.2024.1364221

Bastaki, Kholoud; Velayutham, Dinesh; Irfan, Areeba; Adnan, Mohd; Mohammed, Sawsan; Mbarek, Hamdi; Qoronfleh, M Waild; Jithesh, Puthen Veettil

发表日期：2024

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The role of protective genetic variants in modulating epigenetic aging

保护性遗传变异在调节表观遗传衰老中的作用

Impact of Somatic Gene Mutations on Prognosis Prediction in De Novo AML: Unraveling Insights from a Systematic Review and Meta-Analysis

体细胞基因突变对新发急性髓系白血病预后预测的影响：系统评价和荟萃分析揭示的见解

Understanding Heritable Variation Among Hosts in Infectious Diseases Through the Lens of Twin Studies

通过双胞胎研究了解传染病宿主间的遗传变异

Polygenic scores for dizygotic twinning: insights into the genetic architecture of female fertility

双卵双胞胎的多基因评分：对女性生育力遗传结构的深入了解

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks

可能的遗传因素与 GLP1-RA 和减肥手术引起的体重减轻之间的关联：一项纳入 9 个生物样本库中 10960 名个体的多民族研究

Polygenic Scores for Dizygotic Twinning: Insights into the Genetic Architecture of Female Fertility

双卵双胞胎的多基因评分：对女性生育力遗传结构的深入了解

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery

可能的遗传因素与GLP-1受体激动剂和减肥手术引起的体重减轻之间的关联

Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort

基因组测序在卡塔尔人群中发现了13个新的自闭症谱系障碍候选风险基因

Analysis of 14,392 whole genomes reveals 3.5% of Qataris carry medically actionable variants

对 14392 个全基因组的分析显示，3.5% 的卡塔尔人携带具有医学意义的变异基因。

Forging the path to precision medicine in Qatar: a public health perspective on pharmacogenomics initiatives

在卡塔尔开辟精准医疗之路：从公共卫生角度看药物基因组学计划