Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 43 Records) |
Query Trace: ROBO1[original query] |
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African ancestry GWAS of dementia in a large military cohort identifies significant risk loci.
Molecular psychiatry 2022 12 28 (3): 1293-1302. Sherva Richard, Zhang Rui, Sahelijo Nathan, Jun Gyungah, Anglin Tori, Chanfreau Catherine, Cho Kelly, Fonda Jennifer R, Gaziano J Michael, Harrington Kelly M, Ho Yuk-Lam, Kremen William S, Litkowski Elizabeth, Lynch Julie, Neale Zoe, Roussos Panos, Marra David, Mez Jesse, Miller Mark W, Salat David H, Tsuang Debby, Wolf Erika, Zeng Qing, Panizzon Matthew S, Merritt Victoria C, Farrer Lindsay A, Hauger Richard L, Logue Mark |
Lack of association between genetic polymorphisms in ROBO1, MRPL19/C2ORF3 and THEM2 with developmental dyslexia. Gene 2013 Oct 529 (2): 215-9. Venkatesh Shyamala K, Siddaiah Anand, Padakannaya Prakash, Ramachandra Nallur |
Study of candidate genes for dyslexia in Brazilian individuals. Genetics and molecular research : GMR 2013 12 (4): 5356-64. Svidnicki M C C M, Salgado C A, Lima R F, Ciasca S M, Secolin R, Pomilio M C A, Junqueira P A, Pinto M S, Pereira M M, Sartorato E |
Frameshift mutations of axon guidance genes ROBO1 and ROBO2 in gastric and colorectal cancers with microsatellite instability. Pathology 2013 Dec 45 (7): 645-50. Je Eun Mi, Gwak Min, Oh Hyerim, Choi Mi Ryoung, Choi Youn Jin, Lee Sug Hyung, Yoo Nam J |
Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Dec 165B (8): 627-34. Sun Yimin, Gao Yong, Zhou Yuxi, Chen Huan, Wang Guoqing, Xu Junquan, Xia Jiguang, Huen Michael S Y, Siok Wai Ting, Jiang Yuyang, Tan Li H |
Association of the ROBO1 gene with reading disabilities in a family-based analysis. Genes, brain, and behavior 2014 Apr 13 (4): 430-8. Tran C, Wigg K G, Zhang K, Cate-Carter T D, Kerr E, Field L L, Kaplan B J, Lovett M W, Barr C |
A common polymorphism in pre-miR-146a underlies Hirschsprung disease risk in Han Chinese. Experimental and molecular pathology 2014 Dec 97 (3): 511-4. Zhu Hairong, Cai Peng, Zhu Dongmei, Xu Chao, Li Hongxing, Tang Junwei, Xie Hua, Qin Yufeng, Sharan Ankur, Tang Weibing, Xia Yank |
KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia. Journal of human genetics 2014 Apr 59 (4): 189-97. Mascheretti Sara, Riva Valentina, Giorda Roberto, Beri Silvana, Lanzoni Lara Francesca Emilia, Cellino Maria Rosaria, Marino Cecil |
An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia. Human genetics 2015 Jul 134 (7): 749-60. Mascheretti S, Bureau A, Trezzi V, Giorda R, Marino |
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. Journal of human genetics 2015 Jul 60 (7): 399-401. Matsson Hans, Huss Mikael, Persson Helena, Einarsdottir Elisabet, Tiraboschi Ettore, Nopola-Hemmi Jaana, Schumacher Johannes, Neuhoff Nina, Warnke Andreas, Lyytinen Heikki, Schulte-Körne Gert, Nöthen Markus M, Leppänen Paavo Ht, Peyrard-Janvid Myriam, Kere Ju |
Whole-exome and targeted sequencing identify ROBO1 and ROBO2 mutations as progression-related drivers in myelodysplastic syndromes. Nature communications 2015 6 8806. Xu Feng, Wu Ling-Yun, Chang Chun-Kang, He Qi, Zhang Zheng, Liu Li, Shi Wen-Hui, Guo Juan, Zhu Yang, Zhao You-Shan, Gu Shu-Cheng, Fei Cheng-Ming, Wu Dong, Zhou Li-Yu, Su Ji-Ying, Song Lu-Xi, Xiao Chao, Li Xi |
Genetic variant in DIP2A gene is associated with developmental dyslexia in Chinese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Oct . Kong Rui, Shao Shanshan, Wang Jia, Zhang Xiaohui, Guo Shengnan, Zou Li, Zhong Rong, Lou Jiao, Zhou Jie, Zhang Jiajia, Song Ranr |
Human ROBO1 regulates white matter structure in corpus callosum. Brain structure & function 2016 May . Darki Fahimeh, Massinen Satu, Salmela Elina, Matsson Hans, Peyrard-Janvid Myriam, Klingberg Torkel, Kere Ju |
Two classes of intrahepatic cholangiocarcinoma defined by relative abundance of mutations and copy number alterations. Oncotarget 2016 Mar . Kim Young-Ho, Hong Eun-Kyung, Kong Sun-Young, Han Sung-Sik, Kim Seoung-Hoon, Rhee Je-Keun, Hwang Soo-Kyung, Park Sang-Jae, Kim Tae-M |
Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
Nature communications 2016 7 10605. Zhang Yong-Biao, Hu Jintian, Zhang Jiao, Zhou Xu, Li Xin, Gu Chaohao, Liu Tun, Xie Yangchun, Liu Jiqiang, Gu Mingliang, Wang Panpan, Wu Tingting, Qian Jin, Wang Yue, Dong Xiaoqun, Yu Jun, Zhang Qingg |
Coexpression and expression quantitative trait loci analyses of the angiogenesis gene-gene interaction network in prostate cancer. Translational cancer research 2016 Oct 5 (Suppl 5): S951-S963. Lin Hui-Yi, Cheng Chia-Ho, Chen Dung-Tsa, Chen Y Ann, Park Jong |
A mutational comparison of adult and adolescent and young adult (AYA) colon cancer. Cancer 2017 Nov . Tricoli James V, Boardman Lisa A, Patidar Rajesh, Sindiri Sivasish, Jang Jin S, Walsh William D, McGregor Paul M, Camalier Corinne E, Mehaffey Michele G, Furman Wayne L, Bahrami Armita, Williams P Mickey, Lih Chih-Jian, Conley Barbara A, Khan Jav |
Association analysis of dyslexia candidate genes in a Dutch longitudinal sample. European journal of human genetics : EJHG 2017 1 25 (4): 452-460. Carrion-Castillo Amaia, Maassen Ben, Franke Barbara, Heister Angelien, Naber Marlies, van der Leij Aryan, Francks Clyde, Fisher Simon |
A pilot Indian family-based association study between dyslexia and Reelin pathway genes, DCDC2 and ROBO1, identifies modest association with a triallelic unit TAT in the gene RELN. Asian journal of psychiatry 2018 Aug 37 121-129. Devasenapathy Subhashree, Midha Rashi, Naskar Teesta, Mehta Anuradha, Prajapati Bharat, Ummekulsum Mariam, Sagar Rajesh, Singh Nandini C, Sinha Subra |
Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies.
PloS one 2018 13 (4): e0196245. Pande Mala, Joon Aron, Brewster Abenaa M, Chen Wei V, Hopper John L, Eng Cathy, Shete Sanjay, Casey Graham, Schumacher Fredrick, Lin Yi, Harrison Tabitha A, White Emily, Ahsan Habibul, Andrulis Irene L, Whittemore Alice S, John Esther M, Ko Win Aung, Makalic Enes, Schmidt Daniel F, Kapuscinski Miroslaw K, Ochs-Balcom Heather M, Gallinger Steven, Jenkins Mark A, Newcomb Polly A, Lindor Noralane M, Peters Ulrike, Amos Christopher I, Lynch Patrick |
Pharmacogenetics of response to neoadjuvant paclitaxel treatment for locally advanced breast cancer. Oncotarget 2018 1 8 (63): 106454-106467. Perez-Ortiz Andric C, Ramírez Israel, Cruz-López Juan C, Villarreal-Garza Cynthia, Luna-Angulo Alexandra, Lira-Romero Esmeralda, Jiménez-Chaidez Salvador, Díaz-Chávez José, Matus-Santos Juan A, Sánchez-Chapul Laura, Mendoza-Lorenzo Patricia, Estrada-Mena Francisco |
Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2.
PLoS genetics 2019 Jun 15 (6): e1008107. Tiensuu Heli, Haapalainen Antti M, Karjalainen Minna K, Pasanen Anu, Huusko Johanna M, Marttila Riitta, Ojaniemi Marja, Muglia Louis J, Hallman Mikko, Rämet Mi |
Both rare and common genetic variants contribute to autism in the Faroe Islands.
NPJ genomic medicine 2019 4 1. Leblond Claire S, Cliquet Freddy, Carton Coralie, Huguet Guillaume, Mathieu Alexandre, Kergrohen Thomas, Buratti Julien, Lemière Nathalie, Cuisset Laurence, Bienvenu Thierry, Boland Anne, Deleuze Jean-François, Stora Tormodur, Biskupstoe Rannva, Halling Jónrit, Andorsdóttir Guðrið, Billstedt Eva, Gillberg Christopher, Bourgeron Thom |
Alcohol Intake and Alcohol-SNP Interactions Associated with Prostate Cancer Aggressiveness. Journal of clinical medicine 2021 Feb 10 (3): . Lin Hui-Yi, Wang Xinnan, Tseng Tung-Sung, Kao Yu-Hsiang, Fang Zhide, Molina Patricia E, Cheng Chia-Ho, Berglund Anders E, Eeles Rosalind A, Muir Kenneth R, Pashayan Nora, Haiman Christopher A, Brenner Hermann, Consortium The Practical, Park Jong |
Genome-wide interaction study with major depression identifies novel variants associated with cognitive function.
Molecular psychiatry 2021 Nov . Thalamuthu Anbupalam, Mills Natalie T, Berger Klaus, Minnerup Heike, Grotegerd Dominik, Dannlowski Udo, Meinert Susanne, Opel Nils, Repple Jonathan, Gruber Marius, Nenadi? Igor, Stein Frederike, Brosch Katharina, Meller Tina, Pfarr Julia-Katharina, Forstner Andreas J, Hoffmann Per, Nöthen Markus M, Witt Stephanie, Rietschel Marcella, Kircher Tilo, Adams Mark, McIntosh Andrew M, Porteous David J, Deary Ian J, Hayward Caroline, Campbell Archie, Grabe Hans Jörgen, Teumer Alexander, Homuth Georg, van der Auwera-Palitschka Sandra, Oliver Schubert K, Baune Bernhard |
Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort.
Frontiers in dental medicine 2021 1 2 . Alotaibi Rasha N, Howe Brian J, Moreno Uribe Lina M, Ramirez Consuelo Valencia, Restrepo Claudia, Deleyiannis Frederic W B, Padilla Carmencita, Orioli Ieda M, Buxó Carmen J, Hecht Jacqueline T, Wehby George L, Neiswanger Katherine, Murray Jeffery C, Shaffer John R, Weinberg Seth M, Marazita Mary |
Whole Exome Sequencing in Patients With Ectopic Posterior Pituitary. Journal of the Endocrine Society 2022 8 6 (10): bvac116. Silva Tatiane S, Faucz Fabio R, Hernández-Ramírez Laura C, Pankratz Nathan, Lane John, Kay Denise M, Lyra Arthur, Kochi Cristiane, Stratakis Constantine A, Longui Carlos A, Mills James |
An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations. Proceedings of the National Academy of Sciences of the United States of America 2022 5 119 (21): e2203928119. Quiat Daniel, Kim Seong Won, Zhang Qi, Morton Sarah U, Pereira Alexandre C, DePalma Steven R, Willcox Jon A L, McDonough Barbara, DeLaughter Daniel M, Gorham Joshua M, Curran Justin J, Tumblin Melissa, Nicolau Yamileth, Artunduaga Maria A, Quintanilla-Dieck Lourdes, Osorno Gabriel, Serrano Luis, Hamdan Usama, Eavey Roland D, Seidman Christine E, Seidman J |
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program.
Communications biology 2022 7 5 (1): 756. DiCorpo Daniel, Gaynor Sheila M, Russell Emily M, Westerman Kenneth E, Raffield Laura M, Majarian Timothy D, Wu Peitao, Sarnowski Chloé, Highland Heather M, Jackson Anne, Hasbani Natalie R, de Vries Paul S, Brody Jennifer A, Hidalgo Bertha, Guo Xiuqing, Perry James A, O'Connell Jeffrey R, Lent Samantha, Montasser May E, Cade Brian E, Jain Deepti, Wang Heming, D'Oliveira Albanus Ricardo, Varshney Arushi, Yanek Lisa R, Lange Leslie, Palmer Nicholette D, Almeida Marcio, Peralta Juan M, Aslibekyan Stella, Baldridge Abigail S, Bertoni Alain G, Bielak Lawrence F, Chen Chung-Shiuan, Chen Yii-Der Ida, Choi Won Jung, Goodarzi Mark O, Floyd James S, Irvin Marguerite R, Kalyani Rita R, Kelly Tanika N, Lee Seonwook, Liu Ching-Ti, Loesch Douglas, Manson JoAnn E, Minster Ryan L, Naseri Take, Pankow James S, Rasmussen-Torvik Laura J, Reiner Alexander P, Reupena Muagututi'a Sefuiva, Selvin Elizabeth, Smith Jennifer A, Weeks Daniel E, Xu Huichun, Yao Jie, Zhao Wei, Parker Stephen, Alonso Alvaro, Arnett Donna K, Blangero John, Boerwinkle Eric, Correa Adolfo, Cupples L Adrienne, Curran Joanne E, Duggirala Ravindranath, He Jiang, Heckbert Susan R, Kardia Sharon L R, Kim Ryan W, Kooperberg Charles, Liu Simin, Mathias Rasika A, McGarvey Stephen T, Mitchell Braxton D, Morrison Alanna C, Peyser Patricia A, Psaty Bruce M, Redline Susan, Shuldiner Alan R, Taylor Kent D, Vasan Ramachandran S, Viaud-Martinez Karine A, Florez Jose C, Wilson James G, Sladek Robert, Rich Stephen S, Rotter Jerome I, Lin Xihong, Dupuis Josée, Meigs James B, Wessel Jennifer, Manning Alisa |
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families. Medicina (Kaunas, Lithuania) 2023 8 59 (8): . Francesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, Mirella Vinci, Antonino Musumeci, Angelo Gloria, Donatella Greco, Daniela Rita Raciti, Alessandro Zagami, Biagio Rizzo, Santina Città, Concetta Federico, Luigi Vetri, Salvatore Saccone, Serafino Buo |
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- Page last updated:Apr 16, 2024
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