Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: RIN3[original query] |
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Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
Nature genetics 2011 Jul 43 (7): 685-9. Albagha Omar M E, Wani Sachin E, Visconti Micaela R, Alonso Nerea, Goodman Kirsteen, Brandi Maria Luisa, Cundy Tim, Chung Pui Yan Jenny, Dargie Rosemary, Devogelaer Jean-Pierre, Falchetti Alberto, Fraser William D, Gennari Luigi, Gianfrancesco Fernando, Hooper Michael J, Van Hul Wim, Isaia Gianluca, Nicholson Geoff C, Nuti Ranuccio, Papapoulos Socrates, Montes Javier del Pino, Ratajczak Thomas, Rea Sarah L, Rendina Domenico, Gonzalez-Sarmiento Rogelio, Di Stefano Marco, Ward Lynley C, Walsh John P, Ralston Stuart H, |
Beyond GWAS in COPD: probing the landscape between gene-set associations, genome-wide associations and protein-protein interaction networks. Human heredity 2014 78 (3-4): 131-9. McDonald Merry-Lynn Noelle, Mattheisen Manuel, Cho Michael H, Liu Yang-Yu, Harshfield Benjamin, Hersh Craig P, Bakke Per, Gulsvik Amund, Lange Christoph, Beaty Terri H, Silverman Edwin K, |
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
PLoS genetics 2014 Jun 10 (6): e1004423. Kemp John P, Medina-Gomez Carolina, Estrada Karol, St Pourcain Beate, Heppe Denise H M, Warrington Nicole M, Oei Ling, Ring Susan M, Kruithof Claudia J, Timpson Nicholas J, Wolber Lisa E, Reppe Sjur, Gautvik Kaare, Grundberg Elin, Ge Bing, van der Eerden Bram, van de Peppel Jeroen, Hibbs Matthew A, Ackert-Bicknell Cheryl L, Choi Kwangbom, Koller Daniel L, Econs Michael J, Williams Frances M K, Foroud Tatiana, Zillikens M Carola, Ohlsson Claes, Hofman Albert, Uitterlinden André G, Davey Smith George, Jaddoe Vincent W V, Tobias Jonathan H, Rivadeneira Fernando, Evans David |
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
The Lancet. Respiratory medicine 2014 Mar 2 (3): 214-25. Cho Michael H, McDonald Merry-Lynn N, Zhou Xiaobo, Mattheisen Manuel, Castaldi Peter J, Hersh Craig P, Demeo Dawn L, Sylvia Jody S, Ziniti John, Laird Nan M, Lange Christoph, Litonjua Augusto A, Sparrow David, Casaburi Richard, Barr R Graham, Regan Elizabeth A, Make Barry J, Hokanson John E, Lutz Sharon, Dudenkov Tanda Murray, Farzadegan Homayoon, Hetmanski Jacqueline B, Tal-Singer Ruth, Lomas David A, Bakke Per, Gulsvik Amund, Crapo James D, Silverman Edwin K, Beaty Terri H, |
Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone. Human molecular genetics 2015 Jun 24 (11): 3286-95. Vallet Mahéva, Soares Dinesh C, Wani Sachin, Sophocleous Antonia, Warner Jon, Salter Donald M, Ralston Stuart H, Albagha Omar M |
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
BMC genetics 2015 Dec 16 138. Lutz Sharon M, Cho Michael H, Young Kendra, Hersh Craig P, Castaldi Peter J, McDonald Merry-Lynn, Regan Elizabeth, Mattheisen Manuel, DeMeo Dawn L, Parker Margaret, Foreman Marilyn, Make Barry J, Jensen Robert L, Casaburi Richard, Lomas David A, Bhatt Surya P, Bakke Per, Gulsvik Amund, Crapo James D, Beaty Terri H, Laird Nan M, Lange Christoph, Hokanson John E, Silverman Edwin K, , |
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Nature communications 2015 6 8658. Artigas María Soler, Wain Louise V, Miller Suzanne, Kheirallah Abdul Kader, Huffman Jennifer E, Ntalla Ioanna, Shrine Nick, Obeidat Ma'en, Trochet Holly, McArdle Wendy L, Alves Alexessander Couto, Hui Jennie, Zhao Jing Hua, Joshi Peter K, Teumer Alexander, Albrecht Eva, Imboden Medea, Rawal Rajesh, Lopez Lorna M, Marten Jonathan, Enroth Stefan, Surakka Ida, Polasek Ozren, Lyytikäinen Leo-Pekka, Granell Raquel, Hysi Pirro G, Flexeder Claudia, Mahajan Anubha, Beilby John, Bossé Yohan, Brandsma Corry-Anke, Campbell Harry, Gieger Christian, Gläser Sven, González Juan R, Grallert Harald, Hammond Chris J, Harris Sarah E, Hartikainen Anna-Liisa, Heliövaara Markku, Henderson John, Hocking Lynne, Horikoshi Momoko, Hutri-Kähönen Nina, Ingelsson Erik, Johansson Åsa, Kemp John P, Kolcic Ivana, Kumar Ashish, Lind Lars, Melén Erik, Musk Arthur W, Navarro Pau, Nickle David C, Padmanabhan Sandosh, Raitakari Olli T, Ried Janina S, Ripatti Samuli, Schulz Holger, Scott Robert A, Sin Don D, Starr John M, , Viñuela Ana, Völzke Henry, Wild Sarah H, Wright Alan F, Zemunik Tatijana, Jarvis Deborah L, Spector Tim D, Evans David M, Lehtimäki Terho, Vitart Veronique, Kähönen Mika, Gyllensten Ulf, Rudan Igor, Deary Ian J, Karrasch Stefan, Probst-Hensch Nicole M, Heinrich Joachim, Stubbe Beate, Wilson James F, Wareham Nicholas J, James Alan L, Morris Andrew P, Jarvelin Marjo-Riitta, Hayward Caroline, Sayers Ian, Strachan David P, Hall Ian P, Tobin Martin |
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.
Nature communications 2017 Jul 8 (1): 121. Medina-Gomez Carolina, Kemp John P, Dimou Niki L, Kreiner Eskil, Chesi Alessandra, Zemel Babette S, Bønnelykke Klaus, Boer Cindy G, Ahluwalia Tarunveer S, Bisgaard Hans, Evangelou Evangelos, Heppe Denise H M, Bonewald Lynda F, Gorski Jeffrey P, Ghanbari Mohsen, Demissie Serkalem, Duque Gustavo, Maurano Matthew T, Kiel Douglas P, Hsu Yi-Hsiang, C J van der Eerden Bram, Ackert-Bicknell Cheryl, Reppe Sjur, Gautvik Kaare M, Raastad Truls, Karasik David, van de Peppel Jeroen, Jaddoe Vincent W V, Uitterlinden André G, Tobias Jonathan H, Grant Struan F A, Bagos Pantelis G, Evans David M, Rivadeneira Fernan |
Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport. JAMA neurology 2017 Jul . Kunkle Brian W, Vardarajan Badri N, Naj Adam C, Whitehead Patrice L, Rolati Sophie, Slifer Susan, Carney Regina M, Cuccaro Michael L, Vance Jeffery M, Gilbert John R, Wang Li-San, Farrer Lindsay A, Reitz Christiane, Haines Jonathan L, Beecham Gary W, Martin Eden R, Schellenberg Gerard D, Mayeux Richard P, Pericak-Vance Margaret |
Identification of rs7350481 at chromosome 11q23.3 as a novel susceptibility locus for metabolic syndrome in Japanese individuals by an exome-wide association study. Oncotarget 2017 Apr . Yamada Yoshiji, Sakuma Jun, Takeuchi Ichiro, Yasukochi Yoshiki, Kato Kimihiko, Oguri Mitsutoshi, Fujimaki Tetsuo, Horibe Hideki, Muramatsu Masaaki, Sawabe Motoji, Fujiwara Yoshinori, Taniguchi Yu, Obuchi Shuichi, Kawai Hisashi, Shinkai Shoji, Mori Seijiro, Arai Tomio, Tanaka Masas |
Association and interaction effects of Alzheimer's disease-associated genes and lifestyle on cognitive aging in older adults in a Taiwanese population. Oncotarget 2017 Feb . Lin Eugene, Tsai Shih-Jen, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Kao Chung-Fe |
The effect of the top 20 Alzheimer disease risk genes on gray-matter density and FDG PET brain metabolism. Alzheimer's & dementia (Amsterdam, Netherlands) 2016 5 53-66. Stage Eddie, Duran Tugce, Risacher Shannon L, Goukasian Naira, Do Triet M, West John D, Wilhalme Holly, Nho Kwangsik, Phillips Meredith, Elashoff David, Saykin Andrew J, Apostolova Liana |
Centenarian controls increase variant effect sizes by an average twofold in an extreme case-extreme control analysis of Alzheimer's disease. European journal of human genetics : EJHG 2018 9 27 (2): 244-253. Tesi Niccolò, van der Lee Sven J, Hulsman Marc, Jansen Iris E, Stringa Najada, van Schoor Natasja, Meijers-Heijboer Hanne, Huisman Martijn, Scheltens Philip, Reinders Marcel J T, van der Flier Wiesje M, Holstege Hen |
Blood-brain barrier transcytosis genes, risk of dementia and stroke: a prospective cohort study of 74,754 individuals. European journal of epidemiology 2019 Mar . Juul Rasmussen Ida, Tybjærg-Hansen Anne, Rasmussen Katrine Laura, Nordestgaard Børge G, Frikke-Schmidt Ru |
Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget's Disease of Bone and Modifies the Age of Onset. Calcified tissue international 2019 Feb . De Ridder Raphaël, Boudin Eveline, Vandeweyer Geert, Devogelaer Jean-Pierre, Fransen Erik, Mortier Geert, Van Hul W |
Protective Variants in Alzheimer's Disease. Current genetic medicine reports 2020 10 7 (1): 1-12. Andrews Shea J, Fulton-Howard Brian, Goate Alis |
A novel age-informed approach for genetic association analysis in Alzheimer's disease. Alzheimer's research & therapy 2021 Apr 13 (1): 72. Le Guen Yann, Belloy Michael E, Napolioni Valerio, Eger Sarah J, Kennedy Gabriel, Tao Ran, He Zihuai, Greicius Michael D, |
Associations of Alzheimer's disease risk variants with gene expression, amyloidosis, tauopathy, and neurodegeneration. Alzheimer's research & therapy 2021 Jan 13 (1): 15. Tan Meng-Shan, Yang Yu-Xiang, Xu Wei, Wang Hui-Fu, Tan Lin, Zuo Chuan-Tao, Dong Qiang, Tan Lan, Suckling John, Yu Jin-Tai, |
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature genetics 2022 11 54 (12): 1786-1794. Holstege Henne, Hulsman Marc, Charbonnier Camille, Grenier-Boley Benjamin, Quenez Olivier, Grozeva Detelina, van Rooij Jeroen G J, Sims Rebecca, Ahmad Shahzad, Amin Najaf, Norsworthy Penny J, Dols-Icardo Oriol, Hummerich Holger, Kawalia Amit, Amouyel Philippe, Beecham Gary W, Berr Claudine, Bis Joshua C, Boland Anne, Bossù Paola, Bouwman Femke, Bras Jose, Campion Dominique, Cochran J Nicholas, Daniele Antonio, Dartigues Jean-François, Debette Stéphanie, Deleuze Jean-François, Denning Nicola, DeStefano Anita L, Farrer Lindsay A, Fernández Maria Victoria, Fox Nick C, Galimberti Daniela, Genin Emmanuelle, Gille Johan J P, Le Guen Yann, Guerreiro Rita, Haines Jonathan L, Holmes Clive, Ikram M Arfan, Ikram M Kamran, Jansen Iris E, Kraaij Robert, Lathrop Marc, Lemstra Afina W, Lleó Alberto, Luckcuck Lauren, Mannens Marcel M A M, Marshall Rachel, Martin Eden R, Masullo Carlo, Mayeux Richard, Mecocci Patrizia, Meggy Alun, Mol Merel O, Morgan Kevin, Myers Richard M, Nacmias Benedetta, Naj Adam C, Napolioni Valerio, Pasquier Florence, Pastor Pau, Pericak-Vance Margaret A, Raybould Rachel, Redon Richard, Reinders Marcel J T, Richard Anne-Claire, Riedel-Heller Steffi G, Rivadeneira Fernando, Rousseau Stéphane, Ryan Natalie S, Saad Salha, Sanchez-Juan Pascual, Schellenberg Gerard D, Scheltens Philip, Schott Jonathan M, Seripa Davide, Seshadri Sudha, Sie Daoud, Sistermans Erik A, Sorbi Sandro, van Spaendonk Resie, Spalletta Gianfranco, Tesi Niccolo', Tijms Betty, Uitterlinden André G, van der Lee Sven J, Visser Pieter Jelle, Wagner Michael, Wallon David, Wang Li-San, Zarea Aline, Clarimon Jordi, van Swieten John C, Greicius Michael D, Yokoyama Jennifer S, Cruchaga Carlos, Hardy John, Ramirez Alfredo, Mead Simon, van der Flier Wiesje M, van Duijn Cornelia M, Williams Julie, Nicolas Gaël, Bellenguez Céline, Lambert Jean-Charl |
LLM-PBC: Logic Learning Machine-Based Explainable Rules Accurately Stratify the Genetic Risk of Primary Biliary Cholangitis. Journal of personalized medicine 2022 10 12 (10): . Gerussi Alessio, Verda Damiano, Cappadona Claudio, Cristoferi Laura, Bernasconi Davide Paolo, Bottaro Sandro, Carbone Marco, Muselli Marco, Invernizzi Pietro, Asselta Rosanna, On Behalf Of The Italian Pbc Genetics Study Grou |
Cognitively healthy centenarians are genetically protected against Alzheimer's disease. Alzheimer's & dementia : the journal of the Alzheimer's Association 2024 4 . Niccolo' Tesi, Sven van der Lee, Marc Hulsman, Natasja M van Schoor, Martijn Huisman, Yolande Pijnenburg, Wiesje M van der Flier, Marcel Reinders, Henne Holste |
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