Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: ROBO2[original query] |
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Genetic analyses of roundabout (ROBO) axon guidance receptors in autism. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Oct 147B (7): 1019-27. Anitha A, Nakamura Kazuhiko, Yamada Kazuo, Suda Shiro, Thanseem Ismail, Tsujii Masatsugu, Iwayama Yoshimi, Hattori Eiji, Toyota Tomoko, Miyachi Taishi, Iwata Yasuhide, Suzuki Katsuaki, Matsuzaki Hideo, Kawai Masayoshi, Sekine Yoshimoto, Tsuchiya Kenji, Sugihara Gen-Ichi, Ouchi Yasuomi, Sugiyama Toshiro, Koizumi Keita, Higashida Haruhiro, Takei Nori, Yoshikawa Takeo, Mori Nor |
ROBO2 gene variants are associated with familial vesicoureteral reflux. Journal of the American Society of Nephrology : JASN 2008 Apr 19 (4): 825-31. Bertoli-Avella Aida M, Conte Maria Luisa, Punzo Francesca, de Graaf Bianca M, Lama Giuliana, La Manna Angela, Polito Cesare, Grassia Carolina, Nobili Bruno, Rambaldi Pier Francesco, Oostra Ben A, Perrotta Silver |
A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.
Schizophrenia bulletin 2009 Jan 35 (1): 96-108. Potkin Steven G, Turner Jessica A, Guffanti Guia, Lakatos Anita, Fallon James H, Nguyen Dana D, Mathalon Daniel, Ford Judith, Lauriello John, Macciardi Fabio, |
Mutations in the ROBO2 and SLIT2 genes are rare causes of familial vesico-ureteral reflux. Pediatric nephrology (Berlin, Germany) 2009 Aug 24 (8): 1501-8. Zu Shulu, Bartik Zsuzsa, Zhao Shengtian, Sillen Ulla, Nordenskjöld Agne |
Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux. Journal of the American Society of Nephrology : JASN 2010 Jan 21 (1): 113-23. Cordell Heather J, Darlay Rebecca, Charoen Pimphen, Stewart Aisling, Gullett Ambrose M, Lambert Heather J, Malcolm Sue, Feather Sally A, Goodship Timothy H J, Woolf Adrian S, Kenda Rajko B, Goodship Judith A, |
In search of genes associated with risk for psychopathic tendencies in children: a two-stage genome-wide association study of pooled DNA. Journal of child psychology and psychiatry, and allied disciplines 2010 Jul 51 (7): 780-8. Viding Essi, Hanscombe Ken B, Curtis Charles J C, Davis Oliver S P, Meaburn Emma L, Plomin Robe |
Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. PloS one 2012 7 (4): e31327. van Eerde Albertien M, Duran Karen, van Riel Els, de Kovel Carolien G F, Koeleman Bobby P C, Knoers Nine V A M, Renkema Kirsten Y, van der Horst Henricus J R, Bökenkamp Arend, van Hagen Johanna M, van den Berg Leonard H, Wolffenbuttel Katja P, van den Hoek Joop, Feitz Wouter F, de Jong Tom P V M, Giltay Jacques C, Wijmenga Cis |
Common variants in Mendelian kidney disease genes and their association with renal function. Journal of the American Society of Nephrology : JASN 2013 Dec 24 (12): 2105-17. Parsa Afshin, Fuchsberger Christian, Köttgen Anna, O'Seaghdha Conall M, Pattaro Cristian, de Andrade Mariza, Chasman Daniel I, Teumer Alexander, Endlich Karlhans, Olden Matthias, Chen Ming-Huei, Tin Adrienne, Kim Young J, Taliun Daniel, Li Man, Feitosa Mary, Gorski Mathias, Yang Qiong, Hundertmark Claudia, Foster Meredith C, Glazer Nicole, Isaacs Aaron, Rao Madhumathi, Smith Albert V, O'Connell Jeffrey R, Struchalin Maksim, Tanaka Toshiko, Li Guo, Hwang Shih-Jen, Atkinson Elizabeth J, Lohman Kurt, Cornelis Marilyn C, Johansson Asa, Tönjes Anke, Dehghan Abbas, Couraki Vincent, Holliday Elizabeth G, Sorice Rossella, Kutalik Zoltan, Lehtimäki Terho, Esko Tõnu, Deshmukh Harshal, Ulivi Sheila, Chu Audrey Y, Murgia Federico, Trompet Stella, Imboden Medea, Kollerits Barbara, Pistis Giorgio, Harris Tamara B, Launer Lenore J, Aspelund Thor, Eiriksdottir Gudny, Mitchell Braxton D, Boerwinkle Eric, Schmidt Helena, Hofer Edith, Hu Frank, Demirkan Ayse, Oostra Ben A, Turner Stephen T, Ding Jingzhong, Andrews Jeanette S, Freedman Barry I, Giulianini Franco, Koenig Wolfgang, Illig Thomas, Döring Angela, Wichmann H-Erich, Zgaga Lina, Zemunik Tatijana, Boban Mladen, Minelli Cosetta, Wheeler Heather E, Igl Wilmar, Zaboli Ghazal, Wild Sarah H, Wright Alan F, Campbell Harry, Ellinghaus David, Nöthlings Ute, Jacobs Gunnar, Biffar Reiner, Ernst Florian, Homuth Georg, Kroemer Heyo K, Nauck Matthias, Stracke Sylvia, Völker Uwe, Völzke Henry, Kovacs Peter, Stumvoll Michael, Mägi Reedik, Hofman Albert, Uitterlinden Andre G, Rivadeneira Fernando, Aulchenko Yurii S, Polasek Ozren, Hastie Nick, Vitart Veronique, Helmer Catherine, Wang Jie Jin, Stengel Bénédicte, Ruggiero Daniela, Bergmann Sven, Kähönen Mika, Viikari Jorma, Nikopensius Tiit, Province Michael, Colhoun Helen, Doney Alex, Robino Antonietta, Krämer Bernhard K, Portas Laura, Ford Ian, Buckley Brendan M, Adam Martin, Thun Gian-Andri, Paulweber Bernhard, Haun Margot, Sala Cinzia, Mitchell Paul, Ciullo Marina, Vollenweider Peter, Raitakari Olli, Metspalu Andres, Palmer Colin, Gasparini Paolo, Pirastu Mario, Jukema J Wouter, Probst-Hensch Nicole M, Kronenberg Florian, Toniolo Daniela, Gudnason Vilmundur, Shuldiner Alan R, Coresh Josef, Schmidt Reinhold, Ferrucci Luigi, van Duijn Cornelia M, Borecki Ingrid, Kardia Sharon L R, Liu Yongmei, Curhan Gary C, Rudan Igor, Gyllensten Ulf, Wilson James F, Franke Andre, Pramstaller Peter P, Rettig Rainer, Prokopenko Inga, Witteman Jacqueline, Hayward Caroline, Ridker Paul M, Bochud Murielle, Heid Iris M, Siscovick David S, Fox Caroline S, Kao W Linda, Böger Carsten |
Replication of a ROBO2 polymorphism associated with conduct problems but not psychopathic tendencies in children. Psychiatric genetics 2013 Dec 23 (6): 251-4. Dadds Mark R, Moul Caroline, Cauchi Avril, Hawes David J, Brennan Jo |
Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.
Human genomics 2013 7 16. Ding Lili, Abebe Tilahun, Beyene Joseph, Wilke Russell A, Goldberg Arnon, Woo Jessica G, Martin Lisa J, Rothenberg Marc E, Rao Marepalli, Hershey Gurjit K Khurana, Chakraborty Ranajit, Mersha Tesfaye |
Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux. Kidney international 2013 Aug 84 (2): 327-37. Dobson Mark G, Darlow John M, Hunziker Manuela, Green Andrew J, Barton David E, Puri Pr |
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 |
Common variation near ROBO2 is associated with expressive vocabulary in infancy.
Nature communications 2014 5 4831. St Pourcain Beate, Cents Rolieke A M, Whitehouse Andrew J O, Haworth Claire M A, Davis Oliver S P, O'Reilly Paul F, Roulstone Susan, Wren Yvonne, Ang Qi W, Velders Fleur P, Evans David M, Kemp John P, Warrington Nicole M, Miller Laura, Timpson Nicholas J, Ring Susan M, Verhulst Frank C, Hofman Albert, Rivadeneira Fernando, Meaburn Emma L, Price Thomas S, Dale Philip S, Pillas Demetris, Yliherva Anneli, Rodriguez Alina, Golding Jean, Jaddoe Vincent W V, Jarvelin Marjo-Riitta, Plomin Robert, Pennell Craig E, Tiemeier Henning, Davey Smith Geor |
Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux. Pediatric nephrology (Berlin, Germany) 2015 Sep . Elahi Shan, Homstad Alison, Vaidya Himani, Stout Jennifer, Hall Gentzon, Wu Guanghong, Conlon Peter, Routh Jonathan C, Wiener John S, Ross Sherry S, Nagaraj Shashi, Wigfall Delbert, Foreman John, Adeyemo Adebowale, Gupta Indra R, Brophy Patrick D, Rabinovich C Egla, Gbadegesin Rasheed |
Whole genomes redefine the mutational landscape of pancreatic cancer. Nature 2015 Feb 518 (7540): 495-501. Waddell Nicola, Pajic Marina, Patch Ann-Marie, Chang David K, Kassahn Karin S, Bailey Peter, Johns Amber L, Miller David, Nones Katia, Quek Kelly, Quinn Michael C J, Robertson Alan J, Fadlullah Muhammad Z H, Bruxner Tim J C, Christ Angelika N, Harliwong Ivon, Idrisoglu Senel, Manning Suzanne, Nourse Craig, Nourbakhsh Ehsan, Wani Shivangi, Wilson Peter J, Markham Emma, Cloonan Nicole, Anderson Matthew J, Fink J Lynn, Holmes Oliver, Kazakoff Stephen H, Leonard Conrad, Newell Felicity, Poudel Barsha, Song Sarah, Taylor Darrin, Waddell Nick, Wood Scott, Xu Qinying, Wu Jianmin, Pinese Mark, Cowley Mark J, Lee Hong C, Jones Marc D, Nagrial Adnan M, Humphris Jeremy, Chantrill Lorraine A, Chin Venessa, Steinmann Angela M, Mawson Amanda, Humphrey Emily S, Colvin Emily K, Chou Angela, Scarlett Christopher J, Pinho Andreia V, Giry-Laterriere Marc, Rooman Ilse, Samra Jaswinder S, Kench James G, Pettitt Jessica A, Merrett Neil D, Toon Christopher, Epari Krishna, Nguyen Nam Q, Barbour Andrew, Zeps Nikolajs, Jamieson Nigel B, Graham Janet S, Niclou Simone P, Bjerkvig Rolf, Grützmann Robert, Aust Daniela, Hruban Ralph H, Maitra Anirban, Iacobuzio-Donahue Christine A, Wolfgang Christopher L, Morgan Richard A, Lawlor Rita T, Corbo Vincenzo, Bassi Claudio, Falconi Massimo, Zamboni Giuseppe, Tortora Giampaolo, Tempero Margaret A, , Gill Anthony J, Eshleman James R, Pilarsky Christian, Scarpa Aldo, Musgrove Elizabeth A, Pearson John V, Biankin Andrew V, Grimmond Sean |
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 |
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 |
ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia. Pediatric research 2016 Mar . Mitsioni Artemis G, Siomou Ekaterini, Bouba Ioanna, Petridi Stavroula, Siamopoulou Antigoni, Georgiou Ioann |
A novel relationship for schizophrenia, bipolar and major depressive disorder Part 3: Evidence from chromosome 3 high density association screen. The Journal of comparative neurology 2017 Aug . Chen Xing, Long Feng, Cai Bin, Chen Xiaohong, Chen Ga |
Clues for Polygenic Inheritance of Pituitary Stalk Interruption Syndrome From Exome Sequencing in 20 Patients. The Journal of clinical endocrinology and metabolism 2017 Nov . Zwaveling-Soonawala Nitash, Alders Marielle, Jongejan Aldo, Kovacic Lidija, Duijkers Floor A, Maas Saskia M, Fliers Eric, van Trotsenburg A S Paul, Hennekam Raoul |
Convergence of evidence from a methylome-wide CpG-SNP association study and GWAS of major depressive disorder. Translational psychiatry 2018 8 8 (1): 162. Aberg Karolina A, Shabalin Andrey A, Chan Robin F, Zhao Min, Kumar Gaurav, van Grootheest Gerard, Clark Shaunna L, Xie Lin Y, Milaneschi Yuri, Penninx Brenda W J H, van den Oord Edwin J C |
Identification of ROBO2 as a Potential Locus Associated with Inhaled Corticosteroid Response in Childhood Asthma. Journal of personalized medicine 2021 8 11 (8): . Hernandez-Pacheco Natalia, Gorenjak Mario, Li Jiang, Repnik Katja, Vijverberg Susanne J, Berce Vojko, Jorgensen Andrea, Karimi Leila, Schieck Maximilian, Samedy-Bates Lesly-Anne, Tavendale Roger, Villar Jesús, Mukhopadhyay Somnath, Pirmohamed Munir, Verhamme Katia M C, Kabesch Michael, Hawcutt Daniel B, Turner Steve, Palmer Colin N, Tantisira Kelan G, Burchard Esteban G, Maitland-van der Zee Anke H, Flores Carlos, Poto?nik Uroš, Pino-Yanes Mar |
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 |
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 |
Genome-Wide Association Study Identifies ROBO2 as a Novel Susceptibility Gene for Anthracycline-Related Cardiomyopathy in Childhood Cancer Survivors.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2022 12 JCO2201527. Wang Xuexia, Singh Purnima, Zhou Liting, Sharafeldin Noha, Landier Wendy, Hageman Lindsey, Burridge Paul, Yasui Yutaka, Sapkota Yadav, Blanco Javier G, Oeffinger Kevin C, Hudson Melissa M, Chow Eric J, Armenian Saro H, Neglia Joseph P, Ritchey A Kim, Hawkins Douglas S, Ginsberg Jill P, Robison Leslie L, Armstrong Gregory T, Bhatia Smi |
Genome-wide association study meta-analysis of suicide death and suicidal behavior.
Molecular psychiatry 2022 Oct . Li Qingqin S, Shabalin Andrey A, DiBlasi Emily, Gopal Srihari, Canuso Carla M, , Palotie Aarno, Drevets Wayne C, Docherty Anna R, Coon Hila |
Genome-Wide Association Study and Identification of Candidate Genes for Intramuscular Fat Fatty Acid Composition in Ningxiang Pigs. Animals : an open access journal from MDPI 2023 10 13 (20): . Qinghua Zeng, Hu Gao, Shishu Yin, Yinglin Peng, Fang Yang, Yawei Fu, Xiaoxiao Deng, Yue Chen, Xiaohong Hou, Qian Wang, Zhao Jin, Gang Song, Jun He, Yulong Yin, Kang |
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