HuGE Literature Finder
Neurological Disorders
Records
1
-
30
| Identification of five genetic variants with differential effects on obesity-related traits based on age. Frontiers in genetics 2022 10 13 970657. Chung Ju Yeon, Jung Hae-Un, Kim Dong Jun, Baek Eun Ju, Kim Han Kyul, Kang Ji-One, Lim Ji Eun, Oh Bermse |
| Genetic analysis of and clinical characteristics associated with ANXA11 variants in a Chinese cohort with amyotrophic lateral sclerosis. Neurobiology of disease 2022 10 175 105907. Jiang Qirui, Lin Junyu, Wei Qianqian, Li Chunyu, Hou Yanbing, Cao Bei, Zhang Lingyu, Ou Ruwei, Liu Kuncheng, Yang Tianmi, Xiao Yi, Shang Huifa |
| Delayed Decline of Cognitive Function by Antihypertensive Agents: A Cohort Study Linked with Genotype Data. The journal of prevention of Alzheimer's disease 2022 10 9 (4): 679-691. Sternberg Z, Podolsky R, Yu J, Tian M, Hojnacki D, Schaller |
| A gene regulatory network approach harmonizes genetic and epigenetic signals and reveals repurposable drug candidates for multiple sclerosis. Human molecular genetics 2022 10 . Manuel Astrid M, Dai Yulin, Jia Peilin, Freeman Leorah A, Zhao Zhongmi |
| Pharmacokinetics, Safety, and Tolerability of Cariprazine in Pediatric Patients with Bipolar I Disorder or Schizophrenia. Journal of child and adolescent psychopharmacology 2022 10 32 (8): 434-443. Riccobene Todd, Riesenberg Robert, Yeung Paul P, Earley Willie R, Hankinson Arlene |
| Genetic Variation in ADAMTS13 is Related to VWF Levels, Atrial Fibrillation and Cerebral Ischemic Events. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2022 28 10760296221141893. Warlo Ellen M K, Bratseth Vibeke, Pettersen Alf-Åge R, Holme Pål Andre, Arnesen Harald, Seljeflot Ingebjørg, Opstad Trine |
| Molecular Evaluation of Ex3 VNTR Polymorphism of the DRD4 Gene in Patients With Autism Spectrum Disorder. Iranian journal of child neurology 2022 16 (4): 23-31. Amiri Shahrokh, Shekari Khaniani Mahmoud, Mohammadi Arman, Asadian Mahan, Mehdizadeh Fanid Leila, Shafiee-Kandjani Ali Re |
| The role of next-generation sequencing in the examination of signaling genes in Brca1/2-negative breast cancer cases. Annals of human genetics 2022 Dec . Cine Naci, Ugurtas Cansu, Gokbayrak Merve, Aydin Duygu, Demir Gulhan, Kuru Seda, Sunnetci-Akkoyunlu Deniz, Eren-Keskin Seda, Simsek Turgay, Cabuk Devrim, Aksu Maksut Gorkem, Canturk Nuh Zafer, Savli Hak |
| Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2022 Dec . Abdulkadir Mohamed, Tischfield Jay A, Heiman Gary A, Hoekstra Pieter J, Dietrich Andr |
| Causal associations of obstructive sleep apnea with cardiovascular disease: A Mendelian randomization study. Sleep 2022 Dec . Li Ye, Miao Yuyang, Zhang Qia |
| Investigation of the Relationship Between MBP Gene Polymorphisms and Delayed Encephalopathy After Acute Carbon Monoxide Poisoning. Neurotoxicology 2022 Dec . Zhang Fan, Zeng Jiao, Zhang Xiaoli, Gu Jiapeng, Han Yongkai, Zhang Ping, Li Wenqiang, Gu Renj |
| Association of IL-8-251T/A (rs4073) gene polymorphism with Systemic lupus erythematosus in a cohort of Egyptian patients. International immunopharmacology 2022 Dec 114 109528. Haroun Riham Abdel-Hamid, Abdel Noor Rasha |
| Impact of ABCC2 1249G>A and -24C>T polymorphisms on lacosamide efficacy and plasma concentrations in Uygur pediatric epilepsy patients in China. Therapeutic drug monitoring 2022 Oct . Zhao Ting, Li Hong-Jian, Feng Jie, Zhang Hui-Lan, Yu Jing, Sun Yan, Yu Lu-H |
| Laboratory and clinical evaluation of a microarray for the detection of ATP7B mutations in Wilson disease in China. Journal of clinical laboratory analysis 2022 Oct e24735. Jia Siyu, Li Xiaojin, Zhang Wei, Zhang Bei, Wu Zhen, Duan Weijia, Ou Xiaojuan, Zhou Donghu, Huang Ji |
| Correlation between ER? gene polymorphism and multiple sclerosis and neuromyelitis optica. Medicine 2022 Oct 101 (41): e31126. Xing Weifang, Hong Mingfan, Wei Zhisheng, Zhang Wenshe |
| Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson's disease. Neural regeneration research 2023 May 18 (5): 1154-1160. Shen Ting, Pu Jia-Li, Jiang Ya-Si, Yue Yu-Mei, He Ting-Ting, Qu Bo-Yi, Zhao Shuai, Yan Ya-Ping, Lai Hsin-Yi, Zhang Bao-Ro |
| A Pilot Study of Associations Between the Occurrence of Palpitations and Cytokine Gene Variations in Women Prior to Breast Cancer Surgery. Biological research for nursing 2022 Oct 10998004221134684. Sheng Ying, Carpenter Janet S, Smith Brenda J, Paul Steven M, Melisko Michelle, Moslehi Javid, Levine Jon D, Conley Yvette P, Kober Kord M, Miaskowski Christi |
| Air pollution exposure during pregnancy and childhood, APOE ?4 status and alzheimer polygenic risk score, and brain structural morphology in preadolescents. Environmental research 2022 Oct 114595. Essers Esmée, Binter Anne-Claire, Neumann Alexander, White Tonya, Alemany Silvia, Guxens Mòni |
| ALDH7A1 rs12514417 polymorphism may increase ischemic stroke risk in alcohol-exposed individuals. Nutrition & metabolism 2022 Oct 19 (1): 70. Lin Chun-Hsiang, Nfor Oswald Ndi, Ho Chien-Chang, Hsu Shu-Yi, Tantoh Disline Manli, Liaw Yi-Chia, Mochly-Rosen Daria, Chen Che-Hong, Liaw Yung- |
| Psychiatric Disorders and Type 2 Diabetes mellitus: A Bidirectional Mendelian Randomization. European journal of clinical investigation 2022 Oct e13893. Tao Haoran, Fan Shujin, Zhu Tianxin, You Lili, Zheng Dinghao, Yan Li, Ren Me |
| Mitochondrial DNA population variation is not associated with Alzheimer's in the Japanese population: A consistent finding across global populations. PloS one 2022 17 (10): e0276169. Wong Johanna, Steyn Jannetta S, Pienaar Ilse S, Elson Joanna |
| Genome-wide analyses identify iScience 2022 Oct 25 (10): 105210. Thériault Sébastien, Imboden Medea, Biggs Mary L, Austin Thomas R, Aeschbacher Stefanie, Schaffner Emmanuel, Brody Jennifer A, Bartz Traci M, Risch Martin, Grossmann Kirsten, Lin Henry J, Soliman Elsayed Z, Post Wendy S, Risch Lorenz, Krieger Jose E, Pereira Alexandre C, Heckbert Susan R, Sotoodehnia Nona, Probst-Hensch Nicole M, Conen Dav |
| Rare variants and HLA haplotypes associated in patients with neuromyelitis optica spectrum disorders. Frontiers in immunology 2022 13 900605. Tabansky Inna, Tanaka Akemi J, Wang Jiayao, Zhang Guanglan, Dujmovic Irena, Mader Simone, Jeganathan Venkatesh, DeAngelis Tracey, Funaro Michael, Harel Asaff, Messina Mark, Shabbir Maya, Nursey Vishaan, DeGouvia William, Laurent Micheline, Blitz Karen, Jindra Peter, Gudesblatt Mark, , King Alejandra, Drulovic Jelena, Yunis Edmond, Brusic Vladimir, Shen Yufeng, Keskin Derin B, Najjar Souhel, Stern Joel N |
| Identification of risk genes for Alzheimer's disease by gene embedding. Cell genomics 2022 Sep 2 (9): . Lagisetty Yashwanth, Bourquard Thomas, Al-Ramahi Ismael, Mangleburg Carl Grant, Mota Samantha, Soleimani Shirin, Shulman Joshua M, Botas Juan, Lee Kwanghyuk, Lichtarge Olivi |
| Disrupted topological organization of resting-state functional brain networks in Parkinson's disease patients with glucocerebrosidase gene mutations. Neuroradiology 2022 Oct . Hou Yanbing, Feng Fei, Zhang Lingyu, Ou Ruwei, Lin Junyu, Gong Qiyong, Shang Huifa |
| Metabolome-wide association study on Proceedings of the National Academy of Sciences of the United States of America 2022 Oct 119 (43): e2206083119. Dehghan Abbas, Pinto Rui Climaco, Karaman Ibrahim, Huang Jian, Durainayagam Brenan R, Ghanbari Mohsen, Nazeer Areesha, Zhong Qi, Liggi Sonia, Whiley Luke, Mustafa Rima, Kivipelto Miia, Solomon Alina, Ngandu Tiia, Kanekiyo Takahisa, Aikawa Tomonori, Radulescu Carola I, Barnes Samuel J, Graça Gonçalo, Chekmeneva Elena, Camuzeaux Stephane, Lewis Matthew R, Kaluarachchi Manuja R, Ikram M Arfan, Holmes Elaine, Tzoulaki Ioanna, Matthews Paul M, Griffin Julian L, Elliott Pa |
| A Mendelian randomization study of genetic predisposition to autoimmune diseases and COVID-19. Scientific reports 2022 Oct 12 (1): 17703. Li Shun, Yuan Shuai, Schooling C M, Larsson Susanna |
| Novel Genome-Wide Interactions Mediated via BOLL and EDNRA Polymorphisms in Intracranial Aneurysm. Journal of Korean Neurosurgical Society 2022 Oct . Hong Eun Pyo, Youn Dong Hyuk, Kim Bong Jun, Lee Jae Jun, Nam Sehyeon, Yoo Hyojong, Kim Heung Cheol, Rhim Jong Kook, Park Jeong Jin, Jeon Jin Pyeo |
| BCOR variants are associated with X-linked recessive partial epilepsy. Epilepsy research 2022 Oct 187 107036. Li Xiang, Bian Wen-Jun, Liu Xiao-Rong, Wang Jie, Luo Sheng, Li Bing-Mei, Yi Yong-Hong, Wu Qian-Yi, Zhai Qiong-Xiang, Gao Liang-Di, Zhang Hai-Feng, He Na, Liao Wei-Ping, |
| Genetic polymorphism in BIN1 rather than APOE is associated with poor recognition memory among men without dementia. Scientific reports 2022 Oct 12 (1): 17802. Mehta Kanika, Mohebbi Mohammadreza, Pasco Julie A, Williams Lana J, Walder Ken, Ng Boon Lung, Gupta Veer Ba |
| The roles of MMP8/MMP10 polymorphisms in ischemic stroke susceptibility. Brain and behavior 2022 Oct e2797. Zhao Yong, Zhang Qi, Zhang Xiaobo, Zhang Yu, Lu Ying, Ma Xiaojuan, Li Weiping, Niu Xiaochen, Zhang Gejuan, Chang Mingze, Shi Wenzhen, Tian |
- Page last reviewed:Feb 1, 2023
- Page last updated:Feb 01, 2023
- Content source: