Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: DLG2[original query] |
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Evaluation of DLG2 as a positional candidate for disposition index in African-Americans from the IRAS Family Study. Diabetes research and clinical practice 2010 Jan 87 (1): 69-76. Palmer Nicholette D, Mychaleckyj Josyf C, Langefeld Carl D, Ziegler Julie T, Williams Adrienne H, Bryer-Ash Michael, Bowden Donald |
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
PLoS genetics 2012 8 (2): e1002490. Demirkan Ay?e, van Duijn Cornelia M, Ugocsai Peter, Isaacs Aaron, Pramstaller Peter P, Liebisch Gerhard, Wilson James F, Johansson Åsa, Rudan Igor, Aulchenko Yurii S, Kirichenko Anatoly V, Janssens A Cecile J W, Jansen Ritsert C, Gnewuch Carsten, Domingues Francisco S, Pattaro Cristian, Wild Sarah H, Jonasson Inger, Polasek Ozren, Zorkoltseva Irina V, Hofman Albert, Karssen Lennart C, Struchalin Maksim, Floyd James, Igl Wilmar, Biloglav Zrinka, Broer Linda, Pfeufer Arne, Pichler Irene, Campbell Susan, Zaboli Ghazal, Kolcic Ivana, Rivadeneira Fernando, Huffman Jennifer, Hastie Nicholas D, Uitterlinden Andre, Franke Lude, Franklin Christopher S, Vitart Veronique, , Nelson Christopher P, Preuss Michael, , Bis Joshua C, O'Donnell Christopher J, Franceschini Nora, , Witteman Jacqueline C M, Axenovich Tatiana, Oostra Ben A, Meitinger Thomas, Hicks Andrew A, Hayward Caroline, Wright Alan F, Gyllensten Ulf, Campbell Harry, Schmitz Gerd, |
Clinical significance of de novo and inherited copy-number variation. Human mutation 2013 Dec 34 (12): 1679-87. Vulto-van Silfhout Anneke T, Hehir-Kwa Jayne Y, van Bon Bregje W M, Schuurs-Hoeijmakers Janneke H M, Meader Stephen, Hellebrekers Claudia J M, Thoonen Ilse J M, de Brouwer Arjan P M, Brunner Han G, Webber Caleb, Pfundt Rolph, de Leeuw Nicole, de Vries Bert B |
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Jun 165B (4): 303-13. Noor Abdul, Lionel Anath C, Cohen-Woods Sarah, Moghimi Narges, Rucker James, Fennell Alanna, Thiruvahindrapuram Bhooma, Kaufman Liana, Degagne Bryan, Wei John, Parikh Sagar V, Muglia Pierandrea, Forte Julia, Scherer Stephen W, Kennedy James L, Xu Wei, McGuffin Peter, Farmer Anne, Strauss John, Vincent John |
Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families. Neurogenetics 2014 May 15 (2): 117-27. Egger Gerald, Roetzer Katharina M, Noor Abdul, Lionel Anath C, Mahmood Huda, Schwarzbraun Thomas, Boright Oliver, Mikhailov Anna, Marshall Christian R, Windpassinger Christian, Petek Erwin, Scherer Stephen W, Kaschnitz Wolfgang, Vincent John |
New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Sep 168 (6): 459-470. Alemany Silvia, Ribasés Marta, Vilor-Tejedor Natàlia, Bustamante Mariona, Sánchez-Mora Cristina, Bosch Rosa, Richarte Vanesa, Cormand Bru, Casas Miguel, Ramos-Quiroga Josep A, Sunyer Jor |
A genome-wide association study of chronic obstructive pulmonary disease in Hispanics.
Annals of the American Thoracic Society 2015 Mar 12 (3): 340-8. Chen Wei, Brehm John M, Manichaikul Ani, Cho Michael H, Boutaoui Nadia, Yan Qi, Burkart Kristin M, Enright Paul L, Rotter Jerome I, Petersen Hans, Leng Shuguang, Obeidat Ma'en, Bossé Yohan, Brandsma Corry-Anke, Hao Ke, Rich Stephen S, Powell Rhea, Avila Lydiana, Soto-Quiros Manuel, Silverman Edwin K, Tesfaigzi Yohannes, Barr R Graham, Celedón Juan |
A Population-Based Study of Four Genes Associated with Heroin Addiction in Han Chinese. PloS one 0 11 (9): e0163668. Li Yunxiao, Qiao Xiaomeng, Yin Fangyuan, Guo Hao, Huang Xin, Lai Jianghua, Wei Shugua |
Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders. Scientific reports 2016 Jun 6 27491. Xing Jingrui, Kimura Hiroki, Wang Chenyao, Ishizuka Kanako, Kushima Itaru, Arioka Yuko, Yoshimi Akira, Nakamura Yukako, Shiino Tomoko, Oya-Ito Tomoko, Takasaki Yuto, Uno Yota, Okada Takashi, Iidaka Tetsuya, Aleksic Branko, Mori Daisuke, Ozaki Nor |
An Association Study Between Genetic Polymorphisms in Functional Regions of Five Genes and the Risk of Schizophrenia. Journal of molecular neuroscience : MN 2016 Apr . Yan Peng, Qiao Xiaomeng, Wu Hua, Yin Fangyuan, Zhang Jing, Ji Yuanyuan, Wei Shuguang, Lai Jiangh |
Genome-Wide Interaction Analysis of Air Pollution Exposure and Childhood Asthma with Functional Follow-up. American journal of respiratory and critical care medicine 2016 Nov . Gref Anna, Kebede Merid Simon, Gruzieva Olena, Ballereau Stéphane, Becker Allan, Bellander Tom, Bergström Anna, Bossé Yohan, Bottai Matteo, Chan-Yeung Moira, Fuertes Elaine, Ierodiakonou Despo, Jiang Ruiwei, Joly Stéphane, Jones Meaghan, Kobor Michael S, Korek Michal, Kozyrskyj Anita L, Kumar Ashish, Lemonnier Nathanaël, MacIntyre Elaina, Ménard Camille, Nickle David, Obeidat Ma'en, Pellet Johann, Standl Marie, Sääf Annika, Söderhäll Cilla, Tiesler Carla Mt, van den Berge Maarten, Vonk Judith M, Vora Hita, Xu Cheng-Jian, Antó Josep M, Auffray Charles, Brauer Michael, Bousquet Jean, Brunekreef Bert, Gauderman W James, Heinrich Joachim, Kere Juha, Koppelman Gerard H, Postma Dirkje, Carlsten Christopher, Pershagen Göran, Melén Er |
Genome-wide association study of Parkinson's disease in East Asians.
Human molecular genetics 2016 Dec . Foo Jia Nee, Tan Louis C, Irwan Ishak D, Au Wing-Lok, Low Hui Qi, Prakash Kumar-M, Ahmad-Annuar Azlina, Bei Jinxin, Chan Anne Yy, Chen Chiung Mei, Chen Yi-Chun, Chung Sun Ju, Deng Hao, Lim Shen-Yang, Mok Vincent, Pang Hao, Pei Zhong, Peng Rong, Shang Hui-Fang, Song Kyuyoung, Tan Ai Huey, Wu Yih-Ru, Aung Tin, Cheng Ching-Yu, Chew Fook Tim, Chew Soo-Hong, Chong Siow-Ann, Ebstein Richard P, Lee Jimmy, Saw Seang-Mei, Seow Adeline, Subramaniam Mythily, Tai E-Shyong, Vithana Eranga N, Wong Tien-Yin, Heng Khai Koon, Meah Wee-Yang, Khor Chiea Chuen, Liu Hong, Zhang Furen, Liu Jianjun, Tan Eng-Ki |
Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan.
Cephalalgia : an international journal of headache 2017 Jan 333102417695105. Chen Shih-Pin, Fuh Jong-Ling, Chung Ming-Yi, Lin Ying-Chao, Liao Yi-Chu, Wang Yen-Feng, Hsu Chia-Lin, Yang Ueng-Cheng, Lin Ming-Wei, Chiou Jen-Jie, Wang Po-Jen, Chen Ping-Kun, Fan Pi-Chuan, Wu Jer-Yuan, Chen Yuan-Tsong, Kao Lung-Sen, Shen-Jang Fann Cathy, Wang Shuu-Ji |
Whole exome sequencing identified genetic variations in Chinese hemangioblastoma patients. American journal of medical genetics. Part A 2017 7 173 (10): 2605-2613. Ma Dexuan, Yang Jingyun, Wang Ying, Huang Xiang, Du Guhong, Zhou Liang |
Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate. Molecular vision 2017 10 23 660-665. Matovinovic Elizabeth, Kho Pik Fang, Lea Rodney A, Benton Miles C, Eccles David A, Haupt Larisa M, Hewitt Alex W, Sherwin Justin C, Mackey David A, Griffiths Lyn |
A Longitudinal Imaging Genetics Study of Neuroanatomical Asymmetry in Alzheimer's Disease. Biological psychiatry 2018 6 84 (7): 522-530. Wachinger Christian, Nho Kwangsik, Saykin Andrew J, Reuter Martin, Rieckmann Anna, |
Genome-wide linkage analysis in Spanish melanoma-prone families identifies a new familial melanoma susceptibility locus at 11q. European journal of human genetics : EJHG 2018 Apr . Potrony Miriam, Puig-Butille Joan Anton, Farnham James M, Giménez-Xavier Pol, Badenas Celia, Tell-Martí Gemma, Aguilera Paula, Carrera Cristina, Malvehy Josep, Teerlink Craig C, Puig Susa |
DLG2, but not TMEM229B, GPNMB, and ITGA8 polymorphism, is associated with Parkinson's disease in a Taiwanese population. Neurobiology of aging 2017 Dec . Wu Hsiu-Chuan, Chen Chiung-Mei, Chen Yi-Chun, Fung Hon-Chung, Chang Kuo-Hsuan, Wu Yih- |
Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes.
Journal of medical genetics 2019 Feb . Freidin Maxim, Kraatari Minna, Skarp Sini, Määttä Juhani, Kettunen Johannes, Niinimäki Jaakko, Karppinen Jaro, Williams Frances, Männikkö Min |
TRPM8 genetic variant is associated with chronic migraine and allodynia. The journal of headache and pain 2019 Dec 20 (1): 115. Ling Yu-Hsiang, Chen Shih-Pin, Fann Cathy Shen-Jang, Wang Shuu-Jiun, Wang Yen-Fe |
SNPs in SNCA, MCCC1, DLG2, GBF1 and MBNL2 are associated with Parkinson's disease in southern Chinese population. Journal of cellular and molecular medicine 2020 Jul . Zhao Aonan, Li Yuanyuan, Niu Mengyue, Li Guanglu, Luo Ningdi, Zhou Liche, Kang Wenyan, Liu J |
Genetic variants in glutamate-, A?-, and tau-related pathways determine polygenic risk for Alzheimer's disease. Neurobiology of aging 2020 Nov . Lawingco Ted, Chaudhury Sultan, Brookes Keeley J, Guetta-Baranes Tamar, Guerreiro Rita, Bras Jose, Hardy John, Francis Paul, Thomas Alan, Belbin Olivia, Morgan Kev |
Gut microbiota is associated with bone mineral density : an observational and genome-wide environmental interaction analysis in the UK Biobank cohort.
Bone & joint research 2021 Nov 10 (11): 734-741. Cheng Bolun, Wen Yan, Yang Xuena, Cheng Shiqiang, Liu Li, Chu Xiaomeng, Ye Jing, Liang Chujun, Yao Yao, Jia Yumeng, Zhang Fe |
DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism. Hormone research in paediatrics 2021 Oct . Turan Ihsan, Demir Korcan, Mengen Eda, Kotan Leman Damla, Gürbüz Fatih, Yüksel Bilgin, Topaloglu Ali Kem |
Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer's disease-associated genes: DTNB and DLG2. Molecular psychiatry 2022 3 27 (4): 1963-1969. Prokopenko Dmitry, Lee Sanghun, Hecker Julian, Mullin Kristina, Morgan Sarah, Katsumata Yuriko, , Weiner Michael W, Fardo David W, Laird Nan, Bertram Lars, Hide Winston, Lange Christoph, Tanzi Rudolph |
Behavioural and molecular characterisation of the Dlg2 haploinsufficiency rat model of genetic risk for psychiatric disorder. Genes, brain, and behavior 2022 Jan e12797. Waldron Sophie, Pass Rachel, Griesius Simonas, Mellor Jack R, Robinson Emma S J, Thomas Kerrie L, Wilkinson Lawrence S, Humby Trevor, Hall Jeremy, Dwyer Dominic |
A Genome-Wide Interaction Study of Erythrocyte ?3 Polyunsaturated Fatty Acid Species and Memory in The Framingham Heart Study Offspring Cohort. The Journal of nutrition 2023 12 . Carmen E Annevelink, Jason Westra, Aleix Sala-Vila, William S Harris, Nathan L Tintle, Gregory C Shear |
DLG2 intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism. Genetics in medicine : official journal of the American College of Medical Genetics 2023 10 101010. Yunjia Chen, Ender Karaca, Nathaniel H Robin, Dana Goodloe, Ali Al-Beshri, S Joy Dean, Anna C E Hurst, Andrew J Carroll, Fady M Mikha |
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