Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 35 Records) |
Query Trace: MACROD2[original query] |
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A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
Gut 2012 Aug . Julià A, Domènech E, Ricart E, Tortosa R, García-Sánchez V, Pérez Gisbert J, Nos Mateu P, Gutiérrez A, Gomollón F, Mendoza JL, Garcia-Planella E, Barreiro-de Acosta M, Muñoz F, Vera M, Saro C, Esteve M, Andreu M, Alonso A, López-Lasanta M, Codó L, Gelpí JL, García-Montero AC, Bertanpetit J, Absher D, Panés J, Marsal S |
The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families. Psychiatric genetics 2012 Aug 22 (4): 177-81. Prandini Paola, Pasquali Alessandra, Malerba Giovanni, Marostica Andrea, Zusi Chiara, Xumerle Luciano, Muglia Pierandrea, Da Ros Lucio, Ratti Emiliangelo, Trabetti Elisabetta, Pignatti Pier Franco, |
Copy number variation in subjects with major depressive disorder who attempted suicide. PloS one 2012 7 (9): 9. Perlis RH, Ruderfer D, Hamilton SP, Ernst C |
Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.
Proceedings of the National Academy of Sciences of the United States of America 2013 Mar 110 (12): 4768-73. Jahanshad Neda, Rajagopalan Priya, Hua Xue, Hibar Derrek P, Nir Talia M, Toga Arthur W, Jack Clifford R, Saykin Andrew J, Green Robert C, Weiner Michael W, Medland Sarah E, Montgomery Grant W, Hansell Narelle K, McMahon Katie L, de Zubicaray Greig I, Martin Nicholas G, Wright Margaret J, Thompson Paul M, |
A genome-wide survey of transgenerational genetic effects in autism. PloS one 2013 8 (10): e76978. Tsang Kathryn M, Croen Lisa A, Torres Anthony R, Kharrazi Martin, Delorenze Gerald N, Windham Gayle C, Yoshida Cathleen K, Zerbo Ousseny, Weiss Lauren |
MACROD2 gene associated with autistic-like traits in a general population sample. Psychiatric genetics 2014 Dec 24 (6): 241-8. Jones Rachel M, Cadby Gemma, Blangero John, Abraham Lawrence J, Whitehouse Andrew J O, Moses Eric |
High Prevalence and Clinical Relevance of Genes Affected by Chromosomal Breaks in Colorectal Cancer. PloS one 2015 10 (9): e0138141. van den Broek Evert, Dijkstra Maurits J J, Krijgsman Oscar, Sie Daoud, Haan Josien C, Traets Joleen J H, van de Wiel Mark A, Nagtegaal Iris D, Punt Cornelis J A, Carvalho Beatriz, Ylstra Bauke, Abeln Sanne, Meijer Gerrit A, Fijneman Remond J |
A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. BMC genomics 2015 16 381. Wang Yi-Ting, Sung Pei-Yuan, Lin Peng-Lin, Yu Ya-Wen, Chung Ren-H |
Lack of replication of previous autism spectrum disorder GWAS hits in European populations. Autism research : official journal of the International Society for Autism Research 2016 Jul . Torrico Bàrbara, Chiocchetti Andreas G, Bacchelli Elena, Trabetti Elisabetta, Hervás Amaia, Franke Barbara, Buitelaar Jan K, Rommelse Nanda, Yousaf Afsheen, Duketis Eftichia, Freitag Christine M, Caballero-Andaluz Rafaela, Martinez-Mir Amalia, Scholl Francisco G, Ribasés Marta, , Battaglia Agatino, Malerba Giovanni, Delorme Richard, Benabou Marion, Maestrini Elena, Bourgeron Thomas, Cormand Bru, Toma Claud |
Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy.
Investigative ophthalmology & visual science 2016 Jun 57 (7): 3129-37. Khong Jwu Jin, Burdon Kathryn P, Lu Yi, Leonardos Lefta, Laurie Kate J, Walsh John P, Gajdatsy Adam D, Ebeling Peter R, McNab Alan A, Hardy Thomas G, Stawell Richard J, Davis Garry J, Selva Dinesh, Tsirbas Angelo, Montgomery Grant W, Macgregor Stuart, Craig Jamie |
Antiphospholipid antibodies in a large population-based cohort: genome-wide associations and effects on monocyte gene expression.
Thrombosis and haemostasis 2016 Apr 116 (1): . Müller-Calleja Nadine, Rossmann Heidi, Müller Christian, Wild Philipp, Blankenberg Stefan, Pfeiffer Norbert, Binder Harald, Beutel Manfred E, Manukyan Davit, Zeller Tanja, Lackner Karl |
Genetic analysis of advanced glycation end products in the DHS MIND study.
Gene 2016 Feb . Adams Jeremy N, Raffield Laura M, Martelle Susan E, Freedman Barry I, Langefeld Carl D, Carr J Jeffrey, Cox Amanda J, Bowden Donald |
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Molecular autism 2017 8 21. Authors are not available |
Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density.
Bone 2018 May 110 378-385. Pei Yu-Fang, Hu Wen-Zhu, Yan Min-Wei, Li Chang-Wei, Liu Lu, Yang Xiao-Lin, Hai Rong, Wang Xiu-Yan, Shen Hui, Tian Qing, Deng Hong-Wen, Zhang L |
High Genetic Risk Scores of ASIC2, MACROD2, CHRM3, and C2orf83 Genetic Variants Associated with Polycystic Ovary Syndrome Impair Insulin Sensitivity and Interact with Energy Intake in Korean Women.
Gynecologic and obstetric investigation 2019 84 (3): 225-236. Kim Sung-Hoon, Liu Meiling, Jin Hyun Seok, Park Sunm |
Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2019 Oct 49 (10): 1342-1351. Sugier Pierre-Emmanuel, Sarnowski Chloé, Granell Raquel, Laprise Catherine, Ege Markus J, Margaritte-Jeannin Patricia, Dizier Marie-Hélène, Minelli Cosetta, Moffatt Miriam F, Lathrop Mark, Cookson William O C M, Henderson A John, von Mutius Erika, Kogevinas Manolis, Demenais Florence, Bouzigon Emmanuel |
Replication of previous GWAS hits suggests the association between rs4307059 near MSNP1AS and autism in a Chinese Han population. Progress in neuro-psychopharmacology & biological psychiatry 2019 1 92 194-198. Wang Ziqi, Zhang Jishui, Lu Tianlan, Zhang Tian, Jia Meixiang, Ruan Yanyan, Zhang Dai, Li Jun, Wang Lifa |
An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray. Scientific reports 2020 Feb 10 (1): 3198. Bacchelli Elena, Cameli Cinzia, Viggiano Marta, Igliozzi Roberta, Mancini Alice, Tancredi Raffaella, Battaglia Agatino, Maestrini Ele |
Congenital heart disease risk loci identified by genome-wide association study in European patients.
The Journal of clinical investigation 2020 Nov . Lahm Harald, Jia Meiwen, Dreßen Martina, Wirth Felix, Puluca Nazan, Gilsbach Ralf, Keavney Bernard D, Cleuziou Julie, Beck Nicole, Bondareva Olga, Dzilic Elda, Burri Melchior, König Karl C, Ziegelmüller Johannes A, Abou-Ajram Claudia, Neb Irina, Zhang Zhong, Doppler Stefanie A, Mastantuono Elisa, Lichtner Peter, Eckstein Gertrud, Hörer Jürgen, Ewert Peter, Priest James R, Hein Lutz, Lange Rüdiger, Meitinger Thomas, Cordell Heather J, Müller-Myhsok Bertram, Krane Mark |
Human papilloma virus (HPV) integration signature in Cervical Cancer: identification of MACROD2 gene as HPV hot spot integration site. British journal of cancer 2020 11 124 (4): 777-785. Kamal Maud, Lameiras Sonia, Deloger Marc, Morel Adeline, Vacher Sophie, Lecerf Charlotte, Dupain Célia, Jeannot Emmanuelle, Girard Elodie, Baulande Sylvain, Dubot Coraline, Kenter Gemma, Jordanova Ekaterina S, Berns Els M J J, Bataillon Guillaume, Popovic Marina, Rouzier Roman, Cacheux Wulfran, Le Tourneau Christophe, Nicolas Alain, Servant Nicolas, Scholl Suzy M, Bièche Ivan, |
Copy Number Variation Pattern for Discriminating MACROD2 States of Colorectal Cancer Subtypes. Frontiers in bioengineering and biotechnology 2020 1 7 407. Zhang ShiQi, Pan XiaoYong, Zeng Tao, Guo Wei, Gan Zijun, Zhang Yu-Hang, Chen Lei, Zhang YunHua, Huang Tao, Cai Yu-Do |
Sex-specific genetic factors affect the risk of early-onset periodontitis in Europeans.
Journal of clinical periodontology 2021 Aug . Freitag-Wolf Sandra, Munz Matthias, Junge Olaf, Graetz Christian, Jockel-Schneider Yvonne, Staufenbiel Ingmar, Bruckmann Corinna, Lieb Wolfgang, Franke Andre, Loos Bruno G, Jepsen Søren, Dommisch Henrik, Schaefer Arne |
Association of MACROD2 gene variants with obesity and physical activity in a Korean population. Molecular genetics & genomic medicine 2021 2 9 (4): e1635. Kim Hye-Rim, Jin Hyun-Seok, Eom Yong-B |
The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients. Clinical neurology and neurosurgery 2021 Jan 202 106487. Albuz Burcu, Ozdemir Ozturk, Silan Fat |
Unraveling the genomic basis of congenital heart disease. The Journal of clinical investigation 2021 Jan 131 (2): . Darbar Dawo |
Association of the MACROD2 rs6110695 A>G polymorphism with an increasing WBC count in a Korean population. Immunity, inflammation and disease 2022 Jul 10 (7): e669. Yang Jihye, Han Youngmin, Lee Jong Ho, Yoo Hye J |
Genom-wide analysis identifies single nucleotide polymorphism variations and altered pathways associated with poor semen quality in breeding bulls. Reproduction in domestic animals = Zuchthygiene 2022 Jun . Ebenezer Samuel King John Peter, Kumaresan Arumugam, Talluri Thirumala Rao, Sinha Manish Kumar, Raval Kathan, Nag Pradeep, Karuthadurai Thirumalaisamy, Aranganathan Veerama |
Contribution of copy number variations to the risk of severe eating disorders. Psychiatry and clinical neurosciences 2022 May . Kushima Itaru, Imaeda Miho, Tanaka Satoshi, Kato Hidekazu, Oya-Ito Tomoko, Nakatochi Masahiro, Aleksic Branko, Ozaki Nor |
Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota. The pharmacogenomics journal 2022 Jan . Lopes Guilherme S, Lopes Jaime L, Bielinski Suzette J, Armasu Sebastian M, Zhu Ye, Cavanaugh Dana C, Moyer Ann M, Jacobson Debra J, Wang Liwei, Jiang Ruoxiang, St Sauver Jennifer L, Larson Nicholas |
Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk. International journal of molecular sciences 2023 4 24 (8): . Andrea Gelemanovi?, Tatjana ?atipovi? Ardali?, Ajka Pribisali?, Caroline Hayward, Ivana Kol?i?, Ozren Polaš |
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- Page last updated:Mar 25, 2024
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