Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and MACROD2[original query] |
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Two-marker association tests yield new disease associations for coronary artery disease and hypertension.
Human genetics 2011 Dec 130 (6): 725-33. Slavin Thomas P, Feng Tao, Schnell Audrey, Zhu Xiaofeng, Elston Robert |
| A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample. PloS one 2011 6 (5): e19382. Obeidat Ma'en, Wain Louise V, Shrine Nick, Kalsheker Noor, Soler Artigas Maria, Repapi Emmanouela, Burton Paul R, Johnson Toby, Ramasamy Adaikalavan, Zhao Jing Hua, Zhai Guangju, Huffman Jennifer E, Vitart Veronique, Albrecht Eva, Igl Wilmar, Hartikainen Anna-Liisa, Pouta Anneli, Cadby Gemma, Hui Jennie, Palmer Lyle J, Hadley David, McArdle Wendy L, Rudnicka Alicja R, Barroso Inês, Loos Ruth J F, Wareham Nicholas J, Mangino Massimo, Soranzo Nicole, Spector Tim D, Gläser Sven, Homuth Georg, Völzke Henry, Deloukas Panos, Granell Raquel, Henderson John, Grkovic Ivica, Jankovic Stipan, Zgaga Lina, Polašek Ozren, Rudan Igor, Wright Alan F, Campbell Harry, Wild Sarah H, Wilson James F, Heinrich Joachim, Imboden Medea, Probst-Hensch Nicole M, Gyllensten Ulf, Johansson Åsa, Zaboli Ghazal, Mustelin Linda, Rantanen Taina, Surakka Ida, Kaprio Jaakko, Jarvelin Marjo-Riitta, Hayward Caroline, Evans David M, Koch Beate, Musk Arthur William, Elliott Paul, Strachan David P, Tobin Martin D, Sayers Ian, Hall Ian P, |
| 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 |
| 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, |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 30, 2023
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