Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 393 Records) |
| Query Trace: Communication[original query] |
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| A flexible modeling approach for biomarker-based computation of absolute risk of Alzheimer's disease dementia. Alzheimer's & dementia : the journal of the Alzheimer's Association 2022 9 . Hartz Sarah M, Mozersky Jessica, Schindler Suzanne E, Linnenbringer Erin, Wang Junwei, Gordon Brian A, Raji Cyrus A, Moulder Krista L, West Tim, Benzinger Tammie L S, Cruchaga Carlos, Hassenstab Jason J, Bierut Laura J, Xiong Chengjie, Morris John |
| Genetic polymorphisms in COMT and BDNF influence synchronization dynamics of human neuronal oscillations. iScience 2022 Sep 25 (9): 104985. Simola Jaana, Siebenhühner Felix, Myrov Vladislav, Kantojärvi Katri, Paunio Tiina, Palva J Matias, Brattico Elvira, Palva Sa |
| The cross-talk of cancer-associated fibroblasts assist in prognosis and immunotherapy in patients with breast carcinoma. Cancer gene therapy 2022 Aug . Gu Xuyu, Zheng Shiya, Zhang Haifeng, Sun Xiaotong, Zhou Q |
| 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 |
| Two genetic variants in NEXN and ABCC6 genes found in a patient with right coronary artery to right ventricle fistula combined with giant coronary aneurysm and patent ductus arteriosus. Frontiers in cardiovascular medicine 2022 12 9 1048795. Peng Yongxuan, Ye Jiajun, Xu Yuejuan, Huang Jihong, Wu Yurong, Liu Wei, Bai Kai, Chen Sun, Lu Yan |
| Language impairment in the genetic forms of behavioural variant frontotemporal dementia. Journal of neurology 2022 12 . Samra Kiran, MacDougall Amy M, Bouzigues Arabella, Bocchetta Martina, Cash David M, Greaves Caroline V, Convery Rhian S, van Swieten John C, Seelaar Harro, Jiskoot Lize, Moreno Fermin, Sanchez-Valle Raquel, Laforce Robert, Graff Caroline, Masellis Mario, Tartaglia Maria Carmela, Rowe James B, Borroni Barbara, Finger Elizabeth, Synofzik Matthis, Galimberti Daniela, Vandenberghe Rik, de Mendonça Alexandre, Butler Christopher R, Gerhard Alexander, Ducharme Simon, Le Ber Isabelle, Tiraboschi Pietro, Santana Isabel, Pasquier Florence, Levin Johannes, Otto Markus, Sorbi Sandro, Rohrer Jonathan D, Russell Lucy L, |
| The CCN2 Polymorphism rs12526196 Is a Risk Factor for Ascending Thoracic Aortic Aneurysm. International journal of molecular sciences 2022 12 23 (23): . Tejera-Muñoz Antonio, Rodríguez Isabel, Del Río-García Álvaro, Mohamedi Yamina, Martín María, Chiminazzo Valentina, Suárez-Álvarez Beatriz, López-Larrea Carlos, Ruiz-Ortega Marta, Rodrigues-Díez Raúl |
| Physical, language, neurodevelopment and phenotype-genotype correlation of Chinese patients with Mowat-Wilson syndrome. Frontiers in genetics 2022 11 13 1016677. Wu Lihua, Wang Jianhong, Wang Lei, Xu Qi, Zhou Bo, Zhang Zhen, Li Qi, Wang Hui, Han Lu, Jiang Qian, Wang L |
| Relationships of APOE Genotypes With Small RNA and Protein Cargo of Brain Tissue Extracellular Vesicles From Patients With Late-Stage AD. Neurology. Genetics 2022 11 8 (6): e200026. Huang Yiyao, Driedonks Tom A P, Cheng Lesley, Rajapaksha Harinda, Turchinovich Andrey, Routenberg David A, Nagaraj Rajini, Redding-Ochoa Javier, Arab Tanina, Powell Bonita H, Pletnikova Olga, Troncoso Juan C, Zheng Lei, Hill Andrew F, Mahairaki Vasiliki, Witwer Kenneth |
| Saliva DNA: An alternative biospecimen for single nucleotide polymorphism chromosomal microarray analysis in autism. American journal of medical genetics. Part A 2023 9 . Dale Cameron Wright, Maria Lourdes Baluyot, Johanna Carmichael, Artur Darmanian, Ngaire Jose, Con Ngo, Luke St Heaps, Amber Yendle, Katherine Holman, Sylvia Ziso, Feroza Khan, Anne Masi, Natalie Silove, Valsa Eap |
| Cognitive-Behavioral Profile in Pediatric Patients with Syndrome 5p-; Genotype-Phenotype Correlationships. Genes 2023 8 14 (8): . Cristina Bel-Fenellós, Chantal Biencinto-López, Belén Sáenz-Rico, Adolfo Hernández, Ana Karen Sandoval-Talamantes, Jair Tenorio-Castaño, Pablo Lapunzina, Julián Neva |
| SLC22A3 rs2048327 Polymorphism Is Associated with Diabetic Retinopathy in Caucasians with Type 2 Diabetes Mellitus. Biomedicines 2023 8 11 (8): . Emin Grbi?, Mojca Globo?nik Petrovi?, Ines Cilenšek, Danijel Petrov |
| Wildtype peers rescue social play and 50-kHz ultrasonic vocalization deficits in juvenile female Cacna1c heterozygous rats. Frontiers in behavioral neuroscience 2023 8 17 1190272. Rebecca Bogdan, Rukhshona Kayumova, Rainer K W Schwarting, Markus Wöhr, Theresa M Kis |
| Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder. Gene 2023 8 147723. Yulian Fang, Yaqiong Cui, Zhaoqing Yin, Mengzhu Hou, Pan Guo, Hanjie Wang, Nan Liu, Chunquan Cai, Mingbang Wa |
| A pilot study on glutamate receptor and carrier gene variants and risk of childhood autism spectrum. Metabolic brain disease 2023 8 . Jun Liu, Jing Yan, Fei Qu, Weiming Mo, Hong Yu, Pingfang Hu, Zengyu Zha |
| The genetics of autism spectrum disorder in an East African familial cohort. Cell genomics 2023 7 3 (7): 100322. Islam Oguz Tuncay, Darlene DeVries, Ashlesha Gogate, Kiran Kaur, Ashwani Kumar, Chao Xing, Kimberly Goodspeed, Leah Seyoum-Tesfa, Maria H Chahro |
| Genes associated with spontaneous brain activity changes in clinically different patients with major depressive disorder: A transcription-neuroimaging association study. CNS neuroscience & therapeutics 2023 6 . Wenshuang Zhu, Feng Liu, Jilian Fu, Wen Qin, Kaizhong Xue, Jie Tang, Yong Zhang, Chunshui |
| Establishment and validation of a clinical severity scoring system for succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 2023 5 . Itay Tokatly Latzer, Jean-Baptiste Roullet, K Michael Gibson, Phillip L Pea |
| How Subjective and Objective Factors in Research and Practice May Perpetuate Health Disparities amongst Patients with Traumatic Brain Injury. American journal of physical medicine & rehabilitation 2023 5 . Karen T Johnson, HyunBin You, Melissa Kandel, Tolu O Oyesan |
| Polymorphisms in Oxytocin and Vasopressin Receptor Genes as a Factor Shaping the Clinical Picture and the Risk of ASD in Males. Brain sciences 2023 5 13 (4): . Krzysztof M Wilczy?ski, Aleksandra Stasik, Lena Cicho?, Aleksandra Augu?ciak-Duma, Ma?gorzata Janas-Koz |
| Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with corpus callosum agenesis. Ginekologia polska 2023 5 . Zheng Jiao, Tingting Song, Ying Xu, Jia Li, Pengfei Liu, Jiangfang Zhang, Hong Ya |
| Association of GABRG3, GABRB3, HTR2A gene variants with autism spectrum disorder. Gene 2023 4 870 147399. Coskunpinar Ender M, Tur Seymanur, Cevher Binici Nagihan, Yazan Songür Cis |
| Oculocutaneous albinism: the neurological, behavioral, and neuro-ophthalmological perspective. European journal of pediatrics 2023 4 . Galli Jessica, Loi Erika, Dusi Laura, Pasini Nadia, Rossi Andrea, Scaglioni Vera, Mauri Lucia, Fazzi Eli |
| Single-cell analyses and host genetics highlight the role of innate immune cells in COVID-19 severity. Nature genetics 2023 4 . Ryuya Edahiro, Yuya Shirai, Yusuke Takeshima, Shuhei Sakakibara, Yuta Yamaguchi, Teruaki Murakami, Takayoshi Morita, Yasuhiro Kato, Yu-Chen Liu, Daisuke Motooka, Yoko Naito, Ayako Takuwa, Fuminori Sugihara, Kentaro Tanaka, James B Wing, Kyuto Sonehara, Yoshihiko Tomofuji, , Ho Namkoong, Hiromu Tanaka, Ho Lee, Koichi Fukunaga, Haruhiko Hirata, Yoshito Takeda, Daisuke Okuzaki, Atsushi Kumanogoh, Yukinori Oka |
| Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies. Cell genomics 2023 4 3 (4): 100277. Calwing Liao, Mariana Moyses-Oliveira, Celine E F De Esch, Riya Bhavsar, Xander Nuttle, Aiqun Li, Alex Yu, Nicholas D Burt, Serkan Erdin, Jack M Fu, Minghui Wang, Theodore Morley, Lide Han, , Patrick A Dion, Guy A Rouleau, Bin Zhang, Kristen J Brennand, Michael E Talkowski, Douglas M Ruderf |
| Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders. Frontiers in genetics 2023 3 14 955631. Akter Hosneara, Rahman Muhammad Mizanur, Sarker Shaoli, Basiruzzaman Mohammed, Islam Md Mazharul, Rahaman Md Atikur, Rahaman Md Ashiquir, Eshaque Tamannyat Binte, Dity Nushrat Jahan, Sarker Shouvik, Amin Md Robed, Hossain Mohammad Monir, Lopa Maksuda, Jahan Nargis, Hossain Shafaat, Islam Amirul, Mondol Ashaduzzaman, Faruk Md Omar, Saha Narayan, Kundu Gopen Kumar, Kanta Shayla Imam, Kazal Rezaul Karim, Fatema Kanij, Rahman Md Ashrafur, Hasan Maruf, Hossain Mollah Md Abid, Hosen Md Ismail, Karuvantevida Noushad, Begum Ghausia, Zehra Binte, Nassir Nasna, Nabi A H M Nurun, Uddin K M Furkan, Uddin Mohamm |
| Maternal synapsin autoantibodies are associated with neurodevelopmental delay. Frontiers in immunology 2023 2 14 1101087. Bünger Isabel, Makridis Konstantin L, Kreye Jakob, Nikolaus Marc, Sedlin Eva, Ullrich Tim, Hoffmann Christian, Tromm Johannes Vincent, Rasmussen Helle Foverskov, Milovanovic Dragomir, Höltje Markus, Prüss Harald, Kaindl Angela |
| Analysis of neurotransmitters validates the importance of the dopaminergic system in autism spectrum disorder. World journal of pediatrics : WJP 2023 2 . Saha Sharmistha, Chatterjee Mahasweta, Dutta Nilanjana, Sinha Swagata, Mukhopadhyay Kanch |
| Exome-wide analysis identify multiple variations in olfactory receptor genes (OR12D2 and OR5V1) associated with autism spectrum disorder in Saudi females. Frontiers in medicine 2023 2 10 1051039. Almandil Noor B, Alismail Maram Adnan, Alsuwat Hind Saleh, AlSulaiman Abdulla, AbdulAzeez Sayed, Borgio J Franc |
| Severe COVID-19 May Impact Hepatic Fibrosis /Hepatic Stellate Cells Activation as Indicated by a Pathway and Population Genetic Study. Genes 2023 1 14 (1): . Moya Leire, Farashi Samaneh, Suravajhala Prashanth, Janaththani Panchadsaram, Batra Jyots |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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