Human Genome Epidemiology Literature Finder
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Developmental language disorder - a comprehensive study of more than 46,000 individuals.
Psychiatry research 2023 3 323 115171. Nudel Ron, Christensen Rikke Vang, Kalnak Nelli, Schwinn Michael, Banasik Karina, Dinh Khoa Manh, , Erikstrup Christian, Pedersen Ole Birger, Burgdorf Kristoffer Sølvsten, Ullum Henrik, Ostrowski Sisse Rye, Hansen Thomas Folkmann, Werge Thom |
Association of the dihydrolipoamide dehydrogenase gene with Alzheimer's disease in an Ashkenazi Jewish population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 Nov 131B (1): 60-6. Brown Abraham M, Gordon Derek, Lee Hsinhwa, Caudy Michael, Hardy John, Haroutunian Vahram, Blass John |
Somatic mutations of amino acid metabolism-related genes in gastric and colorectal cancers and their regional heterogeneity--a short report. Cellular oncology (Dordrecht) 2014 Dec 37 (6): 455-61. Oh Hye Rim, An Chang Hyeok, Yoo Nam Jin, Lee Sug Hyu |
Wingless-type MMTV integration site family member 2 (WNT2) gene is associated with resistance to MAP in faecal culture and antibody response in Holstein cattle. Animal genetics 2015 Apr 46 (2): 122-32. Pauciullo A, Küpper J, Brandt H, Donat K, Iannuzzi L, Erhardt |
Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.
Pediatrics 2016 Apr 137 (4): . Kornilov Sergey A, Rakhlin Natalia, Koposov Roman, Lee Maria, Yrigollen Carolyn, Caglayan Ahmet Okay, Magnuson James S, Mane Shrikant, Chang Joseph T, Grigorenko Elena |
Genetic association of the glycine cleavage system genes and myelomeningocele. Birth defects research. Part A, Clinical and molecular teratology 2016 Sep . Shah Rita H, Northrup Hope, Hixson James E, Morrison Alanna C, Au Kit Si |
Somatic Ephrin Receptor Mutations Are Associated with Metastasis in Primary Colorectal Cancer. Cancer research 2017 04 77 (7): 1730-1740. Mathot Lucy, Kundu Snehangshu, Ljungström Viktor, Svedlund Jessica, Moens Lotte, Adlerteg Tom, Falk-Sörqvist Elin, Rendo Verónica, Bellomo Claudia, Mayrhofer Markus, Cortina Carme, Sundström Magnus, Micke Patrick, Botling Johan, Isaksson Anders, Moustakas Aristidis, Batlle Eduard, Birgisson Helgi, Glimelius Bengt, Nilsson Mats, Sjöblom Tobi |
Clinical characteristics and mutation analysis of five Chinese patients with maple syrup urine disease. Metabolic brain disease 2018 1 33 (3): 741-751. Li Xiaomei, Yang Yali, Gao Qing, Gao Min, Lv Yvqiang, Dong Rui, Liu Yi, Zhang Kaihui, Gai Zhongt |
Cohesion of Cortical Language Networks During Word Processing Is Predicted by a Common Polymorphism in the SETBP1 Gene. New directions for child and adolescent development 2020 4 2020 (169): 131-155. Rakhlin Natalia, Landi Nicole, Lee Maria, Magnuson James S, Naumova Oxana Yu, Ovchinnikova Irina V, Grigorenko Elena |
Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity. Orphanet journal of rare diseases 2020 11 15 (1): 309. Margutti Ana Vitoria Barban, Silva Wilson Araújo, Garcia Daniel Fantozzi, de Molfetta Greice Andreotti, Marques Adriana Aparecida, Amorim Tatiana, Prazeres Vânia Mesquita Gadelha, Boy da Silva Raquel Tavares, Miura Irene Kazue, Seda Neto João, Santos Emerson de Santana, Santos Mara Lúcia Schmitz Ferreira, Lourenço Charles Marques, Tonon Tássia, Sperb-Ludwig Fernanda, de Souza Carolina Fischinger Moura, Schwartz Ida Vanessa Döederlein, Camelo José Sim |
Genetic variants in Hippo signalling pathway-related genes affect the risk of colorectal cancer. Archives of toxicology 2020 10 95 (1): 271-281. Shen Hengyang, Meng Yixuan, Hu Tao, Li Shuwei, Du Mulong, Xin Junyi, Gu Dongying, Wang Meilin, Fu Z |
Pyruvate dehydrogenase complex deficiency: updating the clinical, metabolic and mutational landscapes in a cohort of Portuguese patients. Orphanet journal of rare diseases 2020 10 15 (1): 298. Pavlu-Pereira Hana, Silva Maria João, Florindo Cristina, Sequeira Sílvia, Ferreira Ana Cristina, Duarte Sofia, Rodrigues Ana Luísa, Janeiro Patrícia, Oliveira Anabela, Gomes Daniel, Bandeira Anabela, Martins Esmeralda, Gomes Roseli, Soares Sérgia, Tavares de Almeida Isabel, Vicente João B, Rivera Isab |
The neural basis of nonword repetition in children with developmental speech or language disorder: An fMRI study. Neuropsychologia 2020 1 138 107312. Pigdon Lauren, Willmott Catherine, Reilly Sheena, Conti-Ramsden Gina, Liegeois Frederique, Connelly Alan, Morgan Angela |
Genetic analysis by targeted next-generation sequencing and novel variation identification of maple syrup urine disease in Chinese Han population. Scientific reports 2021 9 11 (1): 18939. Fang Xiaohua, Zhu Xiaofan, Feng Yin, Bai Ying, Zhao Xuechao, Liu Ning, Kong Xiangdo |
Study of Acute Liver Failure in Children Using Next Generation Sequencing Technology. The Journal of pediatrics 2021 5 236 124-130. Hegarty Robert, Gibson Philippa, Sambrotta Melissa, Strautnieks Sandra, Foskett Pierre, Ellard Sian, Baptista Julia, Lillis Suzanne, Bansal Sanjay, Vara Roshni, Dhawan Anil, Grammatikopoulos Tassos, Thompson Richard |
Identification of polymorphisms in the MSTN and ADRB3 genes associated with growth and ultrasound carcass traits in Kajli sheep. Animal biotechnology 2021 11 1-16. Ali Asad, Javed Khalid, Zahoor Imran, Anjum Khalid Mahmood, Sharif Num |
Reevaluation of Serum Arylesterase Activity in Neurodevelopmental Disorders. Antioxidants (Basel, Switzerland) 2021 1 10 (2): . Piras Ignazio Stefano, Gabriele Stefano, Altieri Laura, Lombardi Federica, Sacco Roberto, Lintas Carla, Manzi Barbara, Curatolo Paolo, Nobile Maria, Rigoletto Catia, Molteni Massimo, Persico Antonio |
A novel cuproptosis-related gene signature of prognosis and immune microenvironment in head and neck squamous cell carcinoma cancer. Journal of cancer research and clinical oncology 2022 11 149 (1): 203-218. Jiang Xu, Ke Jing, Jia Lifeng, An Xiang, Ma Haiyu, Li Zhongwan, Yuan W |
Cuproptosis Combined with lncRNAs Predicts the Prognosis and Immune Microenvironment of Breast Cancer. Computational and mathematical methods in medicine 2022 10 2022 5422698. Zhang Liangping, Zhang Yujun, Bao Jianhang, Gao Wenshuo, Wang Dong, Pan H |
The signature of cuproptosis-related immune genes predicts the tumor microenvironment and prognosis of prostate adenocarcinoma. Frontiers in immunology 2023 8 14 1181370. Kai Yao, Rumeng Zhang, Liang Li, Mingdong Liu, Shiyao Feng, Haixin Yan, Zhihui Zhang, Dongdong X |
Genetic variations in the retrograde endocannabinoid signaling pathway in Chinese patients with major depressive disorder. Frontiers in neurology 2023 5 14 1153509. Huifang Xu, Tongtong Li, Qiyong Gong, Haizhen Xu, Yongbo Hu, Wenqi Lü, Xin Yang, Jin Li, Wenming Xu, Weihong Kua |
The influence of insulin-related genetic variants on fetal growth, fetal blood flow, and placental weight in a prospective pregnancy cohort. Scientific reports 2023 11 13 (1): 19638. Pauline K Reim, Line Engelbrechtsen, Dorte Gybel-Brask, Theresia M Schnurr, Louise Kelstrup, Estrid V Høgdall, Torben Hans |
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder. Human genetics 2024 2 . Ashraf Yahia, Danyang Li, Sanna Lejerkrans, Shyam Rajagopalan, Nelli Kalnak, Kristiina Tammimi |
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- Page last updated:Apr 22, 2024
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