Annals of human genetics

Keyphrases

Publications

2024

Madoussou Toure, Ghita Amalou, Imane Ait Raise, N'kan Max Ange Mobio, Abderrahim Malki, Abdelhamid Barakat
First report of an Ivorian family with nonsyndromic hearing loss caused by GJB2 compound heterozygous variants. Annals of human genetics (2024)
Jing Peng, Lianghua Li, Huai Ning, Xiaocheng Li
Association between cholelithiasis, cholecystectomy, and risk of breast and gynecological cancers: Evidence from meta-analysis and Mendelian randomization study. Annals of human genetics (2024)
Saeed Ghadimi Haddadan, Esmaeil Babaei, Mehrdad Setareh
Population-genetic and comparative interpopulation studies of the 15 autosomal STR markers in the population living in the Northwest of Iran. Annals of human genetics (2024)
Chuan Fu Yap, Andrew P Morris
Methods for multiancestry genome-wide association study meta-analysis. Annals of human genetics (2024)
Xi Wang, Qiong Lan, Yifeng Lin, Xi Yuan, Shuyan Mei, Fanzhang Lei, Bonan Dong, Ming Zhao, Meiming Cai, Chunmei Shen, Bo-Feng Zhu
Investigating the effectiveness of forensic genetics and population genetic diversity using a multi-InDel system in Chinese Hezhou and Southern Shaanxi Han populations. Annals of human genetics (2024)
Caroline Hey Bækgaard, Emilie Boye Lester, Steffen Møller-Larsen, Mathilde Faurholdt Lauridsen, Martin Jakob Larsen
NanoImprint: A DNA methylation tool for clinical interpretation and diagnosis of common imprinting disorders using nanopore long-read sequencing. Annals of human genetics (2024)
Muhammad Osama Siddiqui, Rabeet Tariq, Raman Kumar, Saira Mansoor
Need of the hour? Genetic and genomic testing referrals from primary healthcare centers with inclusion of precision medicine in Pakistan. Annals of human genetics (2024)
Maria Kiladi
A historical perspective on Lionel Penrose: Scientist, geneticist and dedicated opponent of eugenics. Annals of human genetics (2024)
Rahma Said, Javier Hernández-Losa, Rosa Somoza Lopez de Haro, Teresa Moline, Skander Zouari, Ahlem Blel, Soumaya Rammeh, Amine Derouiche, Slah Ouerhani
Epithelial-mesenchymal transition dysregulation in prostate cancer: Insights from molecular unraveling and epidemiological analyses in Tunisia, North Africa. Annals of human genetics (2024)
Yuan Dang, Jingyun Huang, Chen Lin, Shaohua Xu
Investigation of the association between the Toll-like receptor 1 rs4833095 variation and gastric adenocarcinoma recurrence. Annals of human genetics (2024)
Irene Paradisi, Sergio Arias, Vassiliki Ikonomu
Spinocerebellar ataxia type 10 and Huntington disease-like 2 in Venezuela: Further evidence of two different ancestral founder effects. Annals of human genetics (2024)
Binbin Lin, Li Pan, Huijing He, Yaoda Hu, Ji Tu, Ling Zhang, Ze Cui, Xiaolan Ren, Xianghua Wang, Jing Nai, Guangliang Shan
Heritability and genetic correlations of obesity indices and cardiometabolic traits in the Northern Chinese families. Annals of human genetics (2024)
Alper Türkel, Ilknur Deliktaş Onur, Hicran Anik, Irem Öner, Haktan Bağiş Erdem, Taha Bahsi, Özge Özalp, Berna Öksüzoğlu, Öztürk Ateş, Cengiz Karaçin
Effects of BRCA variation on prognosis in patients with nonmetastatic breast cancer. Annals of human genetics (2024)
João Paulo Limongi França Guilherme, Edilamar Menezes Oliveira
Increased prevalence of the null allele of the p.Arg577Ter variant in the ACTN3 gene in Brazilian long-distance athletes: A retrospective study. Annals of human genetics (2024)
Céleste E Cohen, Dallas M Swallow, Catherine Walker
The molecular basis of lactase persistence: Linking genetics and epigenetics. Annals of human genetics (2024)
Gerald Mboowa, Ivan Sserwadda, Stephen Kanyerezi, Stephen Tukwasibwe, Benson Kidenya
The dawn of a cure for sickle cell disease through CRISPR-based treatment: A critical test of equity in public health genomics. Annals of human genetics (2024)
Mendi J Muthinja, Carlos Othon Guelngar, Maouly Fall, Fatumah Jama, Huda Aldeen Shuja, Jamila Nambafu, Daniel Gams Massi, Oluwadamilola O Ojo, Njideka U Okubadejo, Funmilola Tolulope Taiwo, Alassane Mamadou Diop, Coudjou J D G de Chacus, Fodé Abass Cissé, Amara Cissé, Juzar Hooker, Dilraj Sokhi, Henry Houlden, Mie Rizig
An exploration of the genetics of the mutant Huntingtin (mHtt) gene in a cohort of patients with chorea from different ethnic groups in sub-Saharan Africa. Annals of human genetics (2024)
Barbara I Peña-Espinoza, Emmanuel Torre-Horta, María G Ortiz-López, Marta Menjivar
ABCA1 variant rs9282541 is associated with metabolic syndrome in Maya children. Annals of human genetics (2024)
Mariam Traore, Harouna Sangare, Oudou Diabate, Abdoulaye Diawara, Cheickna Cissé, Oyekanmi Nashiru, Jian Li, Jeffrey Shaffer, Mamadou Wélé, Seydou Doumbia, Tinashe Chikowore, Opeyemi Soremekun, Segun Fatumo
Causal effect of severe and non-severe malaria on dyslipidemia in African Ancestry individuals: A Mendelian randomization study. Annals of human genetics (2024)
Imane El Alami, Wafa Khaali, Majida Jalbout, Amina Gihbid, Wided Ben Ayoub, Abdellatif Benider, Selma Mohamed Brahim, Mokhtar Hamdi Cherif, Nadia Benchakroun, Mohammed El Mzibri, El Khalil Ben Driss, Khalid Belghmi, Marilys Corbex, Meriem Khyatti
Genetic variations in CYP2A6, CYP2E1, GSTM1, GSTT1 genes and the risk of Nasopharyngeal carcinoma in North African population. Annals of human genetics (2024)
Elli Tsintzas, Teresa Niccoli
Using Drosophila amyloid toxicity models to study Alzheimer's disease. Annals of human genetics (2024)
Jun Zhang, Yiji Pan, Hongxia Yang, Shuqiong Hu, Sheng Zheng, Tao He
Genetically predicted retinal vascular occlusion in relation to cardiovascular diseases: A bidirectional two-sample Mendelian randomization analysis. Annals of human genetics (2024)
Imane El Alami, Wafa Khaali, Majida Jalbout, Amina Gihbid, Wided Ben Ayoub, Abdellatif Benider, Selma Mohamed Brahim, Mokhtar Hamdi Cherif, Nadia Benchakroun, Mohammed El Mzibri, El Khalil Ben Driss, Khalid Belghmi, Marilys Corbex, Meriem Khyatti
Genetic variations in CYP2A6, CYP2E1, GSTM1, GSTT1 genes and the risk of Nasopharyngeal carcinoma in North African population. Annals of human genetics (2024)
Larry Baum, Chi Chiu Lee, Rui Ye, Yuanxin Zhong, Se Fong Hung, Chun Pan Tang, Ting Pong Ho, James M Swanson, Robert K Moyzis, Pak-Chung Sham, Patrick Wing-Leung Leung
Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele. Annals of human genetics (2024)
Yi-Shian Liu, Yu-Chun Lin, Meng-Chih Lin, Chao-Chien Wu, Tsu-Nai Wang
Association of blood lipid profiles and asthma: A bidirectional two-sample Mendelian randomization study. Annals of human genetics (2024)
Faisal Almalki
Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia. Annals of human genetics (2024)
Tao Peng, Zhe Liu, Yu Zhang, Xudong Liu, Lijun Zhao, Ying Ma, Jinke Fan, Xinqiang Song, Lei Wang
The systematic identification of survival-related alternative splicing events and splicing factors in glioblastoma. Annals of human genetics (2024)
Zhaokun Wang, Jiaying Shi, Dachang Tao, Shengyu Xie, Yuan Yang, Yunqiang Liu
Nonsense suppression induces read-through of a novel BMPR1A variant in a Chinese family with hereditary colorectal cancer. Annals of human genetics (2024)

volume 88, number 4, 2024

Jun Zhang, Yiji Pan, Hongxia Yang, Shuqiong Hu, Sheng Zheng, Tao He
Genetically predicted retinal vascular occlusion in relation to cardiovascular diseases: A bidirectional two-sample Mendelian randomization analysis. Annals of human genetics 88 (4) (2024)
Barbara I Peña-Espinoza, Emmanuel Torre-Horta, María G Ortiz-López, Marta Menjivar
ABCA1 variant rs9282541 is associated with metabolic syndrome in Maya children. Annals of human genetics 88 (4) (2024)
Zhaokun Wang, Jiaying Shi, Dachang Tao, Shengyu Xie, Yuan Yang, Yunqiang Liu
Nonsense suppression induces read-through of a novel BMPR1A variant in a Chinese family with hereditary colorectal cancer. Annals of human genetics 88 (4) (2024)
Tao Peng, Zhe Liu, Yu Zhang, Xudong Liu, Lijun Zhao, Ying Ma, Jinke Fan, Xinqiang Song, Lei Wang
The systematic identification of survival-related alternative splicing events and splicing factors in glioblastoma. Annals of human genetics 88 (4) (2024)
Yuan Dang, Jingyun Huang, Chen Lin, Shaohua Xu
Investigation of the association between the Toll-like receptor 1 rs4833095 variation and gastric adenocarcinoma recurrence. Annals of human genetics 88 (4) (2024)
Yi-Shian Liu, Yu-Chun Lin, Meng-Chih Lin, Chao-Chien Wu, Tsu-Nai Wang
Association of blood lipid profiles and asthma: A bidirectional two-sample Mendelian randomization study. Annals of human genetics 88 (4) (2024)
Zhaokun Wang, Jiaying Shi, Dachang Tao, Shengyu Xie, Yuan Yang, Yunqiang Liu
Nonsense suppression induces read-through of a novel BMPR1A variant in a Chinese family with hereditary colorectal cancer. Annals of human genetics 88 (4) (2024)

volume 88, number 5, 2024

Elli Tsintzas, Teresa Niccoli
Using Drosophila amyloid toxicity models to study Alzheimer's disease. Annals of human genetics 88 (5) (2024)
Caroline Hey Bækgaard, Emilie Boye Lester, Steffen Møller-Larsen, Mathilde Faurholdt Lauridsen, Martin Jakob Larsen
NanoImprint: A DNA methylation tool for clinical interpretation and diagnosis of common imprinting disorders using nanopore long-read sequencing. Annals of human genetics 88 (5) (2024)
Caroline Hey Bækgaard, Emilie Boye Lester, Steffen Møller-Larsen, Mathilde Faurholdt Lauridsen, Martin Jakob Larsen
NanoImprint: A DNA methylation tool for clinical interpretation and diagnosis of common imprinting disorders using nanopore long-read sequencing. Annals of human genetics 88 (5) (2024)
Faisal Almalki
Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia. Annals of human genetics 88 (5) (2024)
Faisal Almalki
Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia. Annals of human genetics 88 (5) (2024)
Caroline Hey Bækgaard, Emilie Boye Lester, Steffen Møller-Larsen, Mathilde Faurholdt Lauridsen, Martin Jakob Larsen
NanoImprint: A DNA methylation tool for clinical interpretation and diagnosis of common imprinting disorders using nanopore long-read sequencing. Annals of human genetics 88 (5) (2024)
Larry Baum, Chi Chiu Lee, Rui Ye, Yuanxin Zhong, Se Fong Hung, Chun Pan Tang, Ting Pong Ho, James M Swanson, Robert K Moyzis, Pak-Chung Sham, Patrick Wing-Leung Leung
Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele. Annals of human genetics 88 (5) (2024)
Elli Tsintzas, Teresa Niccoli
Using Drosophila amyloid toxicity models to study Alzheimer's disease. Annals of human genetics 88 (5) (2024)
Larry Baum, Chi Chiu Lee, Rui Ye, Yuanxin Zhong, Se Fong Hung, Chun Pan Tang, Ting Pong Ho, James M Swanson, Robert K Moyzis, Pak-Chung Sham, Patrick Wing-Leung Leung
Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat allele. Annals of human genetics 88 (5) (2024)
Faisal Almalki
Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia. Annals of human genetics 88 (5) (2024)

volume 88, number 3, 2023

Maryam Kazemi Naeini, Mahdi Akbarzadeh, Iraj Kazemi, Doug Speed, Sayed Mohsen Hosseini
Using the Bayesian variational spike and slab model in a genome-wide association study for finding associated loci with bipolar disorder. Annals of human genetics 88 (3) (2023)
Maryam Kazemi Naeini, Mahdi Akbarzadeh, Iraj Kazemi, Doug Speed, Sayed Mohsen Hosseini
Using the Bayesian variational spike and slab model in a genome-wide association study for finding associated loci with bipolar disorder. Annals of human genetics 88 (3) (2023)
Motahareh Amjadi, Zahra Hayatmehr, Balázs Egyed, Mahmood Tavallaei, Anna Szécsényi-Nagy
A comprehensive review of HVS-I mitochondrial DNA variation of 19 Iranian populations. Annals of human genetics 88 (3) (2023)
Qun Ji, Fengxia Du, Yangyaxin Yu, Ying Li
Exploring the clinical significance of miR-148 expression variations in distinct subtypes of irritable bowel syndrome. Annals of human genetics 88 (3) (2023)
Motahareh Amjadi, Zahra Hayatmehr, Balázs Egyed, Mahmood Tavallaei, Anna Szécsényi-Nagy
A comprehensive review of HVS-I mitochondrial DNA variation of 19 Iranian populations. Annals of human genetics 88 (3) (2023)