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Annals of Human Genetics

IF1.2
论文数16
被引数1443
期刊论文 16
发表时间
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Genetic Insights Into Hypertension and Breast Cancer Risk in African Women: A Mendelian Randomization and Colocalization Analyses非洲女性高血压和乳腺癌风险的遗传学见解：一项孟德尔随机化和共定位分析
deleteAnnals of Human Genetics
IF1.2
delete2026-07-01
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PREAI
deleteAnsah, Emmanuel Owusu; Agyenim, Emmanuel Boateng; Danquah, Andrews; Addo, Stephen Kumi; Agyirifo, Daniel Sakyi; Fosu, Kwadwo; Kyei, Foster
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Identification of PSMA4 as a Therapeutic Target for Atherosclerosis: A Comprehensive Multiomics Mendelian Randomization AnalysisPSMA4作为动脉粥样硬化治疗靶点的鉴定：一项综合的多组学孟德尔随机化分析
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IF1.2
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PREAI
deleteYu, Yongchao; Zhu, Yuan; Tian, Qian; Shao, Lijuan; Zeng, Jiao; Xu, Dandan; Mo, Xiangang
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A Novel Biallelic REL Frameshift Variant p.(Tyr9Ilefs*2) Causing Immunodeficiency-92 With Profound c-Rel Deficiency一种新型双等位基因REL移码变异p.(Tyr9Ilefs*2)导致免疫缺陷-92并伴有严重的c-Rel缺乏
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IF1.2
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deleteEl-Hamri, Mohsine-Ali; Sabky, Zineb; Benyahya, Nada; Abboussi, Oualid; Lyahyai, Jaber; Seffiani, Abdelaziz
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Hip Bone Marrow Adiposity as a Risk Factor for Alzheimer's Disease: Insights From Mendelian Randomization Analysis髋骨骨髓脂肪含量作为阿尔茨海默病风险因素的探讨：基于孟德尔随机化分析
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IF1.2
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PREAI
deleteShi, Wei; Zhu, Zhenhua; Wu, Minghui; Cheng, Wenjun; Xu, Haijun
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Genetic Diversity and Historical Divergence of Malays and Indigenous Populations in Peninsular Malaysia and Northern Borneo马来西亚半岛和婆罗洲北部马来人与土著人群的遗传多样性与历史分化
deleteAnnals of Human Genetics
IF1.2
delete2026-03-01
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PREAI
deleteSaw, Woei-Yuh; Yew, Chee Wei; Rahman, Thuhairah Abdul; Hoque, Mohammad Zahirul; Xu, Shuhua; Khor, Chiea-Chuen; Subbiah, Vijay Kumar; Teo, Yik-Ying; Hoh, Boon-Peng
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Mitonuclear Discordance and Gout, Type 2 Diabetes and Chronic Kidney Disease in Aotearoa New Zealand Indigenous Māori and Pacific People线粒核不协调与痛风、2型糖尿病和慢性肾病在新西兰原住民毛利人和太平洋岛民中的关系
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delete2026-02-01
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deleteDickerson, Rachel R.; Takei, Riku; Cadzow, Murray; Schurr, Theodore G.; Wilcox, Phillip L.; Dalbeth, Nicola; Stamp, Lisa K.; Murphy, Rinki; De Zoysa, Janak R.; Castel, Stephane E.; Emde, Anne-katrin; Wasik, Kaja A.; Merriman, Tony R.; Gosling, Anna L.
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Downregulation of EPAS1 and EGLN1 mRNA Expression Associated With High-Altitude Adaptive Genetic Variants in Sherpa HighlandersSherpa高原人群高海拔适应性遗传变异与EPAS1和EGLN1 mRNA表达下调的关联
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deleteDroma, Yunden; Yue, Fengming; Ota, Masao; Kobayashi, Nobumitsu; Kitaguchi, Yoshiaki; Hanaoka, Masayuki
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Construction of a Prognostic and Diagnostic Gene Signature Based on the Characteristics of Cancer Stem-Like Cells for the Treatment Guidance of Hepatocellular Carcinoma基于癌干细胞样细胞特征构建肝细胞癌治疗指导的预后和诊断基因签名
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deleteLi, Xiawei; Wang, Min; Zhang, Xiang; Bilige; Du, Zhiye; Yang, Yongqi; Zhang, Baotong
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The Genetic Basis of Neurological Disorders: Missense and Nonsense Variants in Three Pakistani Families With Syndromic Intellectual Disability神经性疾病的遗传基础：来自三个巴基斯坦家庭的综合征性智力障碍中的错义和终止密码子变异
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delete2025-12-01
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deleteJaved, Kenza; Muhammad, Nazif; Hussain, Syeda Iqra; Fozia, Fozia; Ullah, Muhammad Irfan; Qiaz, Shah; Jan, Samin; Din, Salah Ud; Reman, Adil U.; Khan, Muhammad Daud; Saleha, Shamim; Muhammad, Noor; Wasif, Naveed; Khan, Saadullah
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Recent Statistical Innovations in Human Genetics (vol89 , pg241-254 , 2025)
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deleteBalding, D. J.; Speed, D.
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Genetic Landscape of Pediatric Dyslipidemia in a Turkish Cohort: Insights From a Single-Center Experience土耳其队列中儿童血脂异常的遗传景观：单中心经验的见解
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deleteErdogan, Kadri Murat; Akcan, Mehmet Berkay; Yazici, Havva; Ozyilmaz, Berk; Ozdemir, Taha Resid; Kaya, Ozge Ozer; Kirbiyik, Ozgur; Er, Esra; Kutbay, Yasar Bekir; Guvenc, Merve Saka; Turk, Tuba Sozen; Kesan, Selcan; Esenkaya, Fethiye; Koc, Altug
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CFAP74 Variants Could Cause Male Infertility With the Asthenoteratozoospermia Phenotype
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deleteChen, Guoyong; Wang, Yulin; Kang, Jingyi; Mei, Xiaoyan; Zhang, Zhedan; Zhang, Yan; Lu, Jun; Liu, Yun; Lan, Fenghua; Huang, Wujian; Zhang, Duo
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Association Between Different Types of Lipids and Alzheimer's Disease, Parkinson's Disease, and Epilepsy: A Mendelian Randomization and Bioinformatics Analysis不同类型脂质与阿尔茨海默病、帕金森病和癫痫的关联：一项孟德尔随机化和生物信息学分析
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deleteZhang, Jiayu; Song, Anqi; Xiang, Yi; Liu, Jiaqi; Li, Baixiang; Li, Xueting
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A Novel Variant of STAG1 Gene and Literature ReviewSTAG1基因的一种新型变异及文献综述
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deleteXie, Meihua; Xie, Liyun; Zhuang, Jianlong; Li, Hening; Zhou, Hongxia; Yue, Xiaojuan
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Identification and Functional Verification of Variants Associated With Clubfoot and Arthrogrypotic Hand Deformation in a Multigeneration Polish Family鉴定与多代波兰家庭中先天性马蹄内翻足和关节挛缩手畸形相关变异的功能验证
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deleteHordyjewska-Kowalczyk, Ewa; Ramanujam, Akshaya; Odrzywolski, Adrian; Verkerk, Annemieke; van Meurs, Joyce; Kandzierski, Grzegorz; Tylzanowski, Przemko
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Multipoint linkage disequilibrium mapping using multilocus allele frequency data
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IF1.2
delete2005-03-29
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deleteJohnson, T
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