Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Disease and WWOX[original query] |
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| WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. American journal of human genetics 2008 Aug 83 (2): 180-92. Lee Jenny C, Weissglas-Volkov Daphna, Kyttälä Mira, Dastani Zari, Cantor Rita M, Sobel Eric M, Plaisier Christopher L, Engert James C, van Greevenbroek Marleen M J, Kane John P, Malloy Mary J, Pullinger Clive R, Huertas-Vazquez Adriana, Aguilar-Salinas Carlos A, Tusie-Luna Teresa, de Bruin Tjerk W A, Aouizerat Bradley E, van der Kallen Carla C J, Croce Carlo M, Aqeilan Rami I, Marcil Michel, Viikari Jorma S A, Lehtimäki Terho, Raitakari Olli T, Kuusisto Johanna, Laakso Markku, Taskinen Marja-Riitta, Genest Jacques, Pajukanta Päi |
| Genome-wide association study of gene by smoking interactions in coronary artery calcification. PloS one 2013 8 (10): e74642. Polfus Linda M, Smith Jennifer A, Shimmin Lawrence C, Bielak Lawrence F, Morrison Alanna C, Kardia Sharon L R, Peyser Patricia A, Hixson James |
| Expanding the genetic basis of copy number variation in familial breast cancer. Hereditary cancer in clinical practice 2014 12 (1): 15. Masson Amy L, Talseth-Palmer Bente A, Evans Tiffany-Jane, Grice Desma M, Hannan Garry N, Scott Rodney |
Genome-wide association analysis identifies six new loci associated with forced vital capacity.
Nature genetics 2014 Jul 46 (7): 669-77. Loth Daan W, Artigas María Soler, Gharib Sina A, Wain Louise V, Franceschini Nora, Koch Beate, Pottinger Tess D, Smith Albert Vernon, Duan Qing, Oldmeadow Chris, Lee Mi Kyeong, Strachan David P, James Alan L, Huffman Jennifer E, Vitart Veronique, Ramasamy Adaikalavan, Wareham Nicholas J, Kaprio Jaakko, Wang Xin-Qun, Trochet Holly, Kähönen Mika, Flexeder Claudia, Albrecht Eva, Lopez Lorna M, de Jong Kim, Thyagarajan Bharat, Alves Alexessander Couto, Enroth Stefan, Omenaas Ernst, Joshi Peter K, Fall Tove, Viñuela Ana, Launer Lenore J, Loehr Laura R, Fornage Myriam, Li Guo, Wilk Jemma B, Tang Wenbo, Manichaikul Ani, Lahousse Lies, Harris Tamara B, North Kari E, Rudnicka Alicja R, Hui Jennie, Gu Xiangjun, Lumley Thomas, Wright Alan F, Hastie Nicholas D, Campbell Susan, Kumar Rajesh, Pin Isabelle, Scott Robert A, Pietiläinen Kirsi H, Surakka Ida, Liu Yongmei, Holliday Elizabeth G, Schulz Holger, Heinrich Joachim, Davies Gail, Vonk Judith M, Wojczynski Mary, Pouta Anneli, Johansson Asa, Wild Sarah H, Ingelsson Erik, Rivadeneira Fernando, Völzke Henry, Hysi Pirro G, Eiriksdottir Gudny, Morrison Alanna C, Rotter Jerome I, Gao Wei, Postma Dirkje S, White Wendy B, Rich Stephen S, Hofman Albert, Aspelund Thor, Couper David, Smith Lewis J, Psaty Bruce M, Lohman Kurt, Burchard Esteban G, Uitterlinden André G, Garcia Melissa, Joubert Bonnie R, McArdle Wendy L, Musk A Bill, Hansel Nadia, Heckbert Susan R, Zgaga Lina, van Meurs Joyce B J, Navarro Pau, Rudan Igor, Oh Yeon-Mok, Redline Susan, Jarvis Deborah L, Zhao Jing Hua, Rantanen Taina, O'Connor George T, Ripatti Samuli, Scott Rodney J, Karrasch Stefan, Grallert Harald, Gaddis Nathan C, Starr John M, Wijmenga Cisca, Minster Ryan L, Lederer David J, Pekkanen Juha, Gyllensten Ulf, Campbell Harry, Morris Andrew P, Gläser Sven, Hammond Christopher J, Burkart Kristin M, Beilby John, Kritchevsky Stephen B, Gudnason Vilmundur, Hancock Dana B, Williams O Dale, Polasek Ozren, Zemunik Tatijana, Kolcic Ivana, Petrini Marcy F, Wjst Matthias, Kim Woo Jin, Porteous David J, Scotland Generation, Smith Blair H, Viljanen Anne, Heliövaara Markku, Attia John R, Sayers Ian, Hampel Regina, Gieger Christian, Deary Ian J, Boezen H Marike, Newman Anne, Jarvelin Marjo-Riitta, Wilson James F, Lind Lars, Stricker Bruno H, Teumer Alexander, Spector Timothy D, Melén Erik, Peters Marjolein J, Lange Leslie A, Barr R Graham, Bracke Ken R, Verhamme Fien M, Sung Joohon, Hiemstra Pieter S, Cassano Patricia A, Sood Akshay, Hayward Caroline, Dupuis Josée, Hall Ian P, Brusselle Guy G, Tobin Martin D, London Stephanie |
| Genetic diversity of urinary bladder cancer and the risk of recurrence based on mutation analysis. Neoplasma 2016 63 (6): 952-960. Traczyk-Borszynska M, Borkowska E, Jablonowski Z, Jedrzejczyk A, Pietrusinski M, Kaluzewski B, Sosnowski M, Borowiec |
| Relevance of Sp Binding Site Polymorphism in WWOX for Treatment Outcome in Pancreatic Cancer. Journal of the National Cancer Institute 2016 May 108 (5): . Schirmer Markus A, Lüske Claudia M, Roppel Sebastian, Schaudinn Alexander, Zimmer Christian, Pflüger Ruben, Haubrock Martin, Rapp Jacobe, Güngör Cenap, Bockhorn Maximilian, Hackert Thilo, Hank Thomas, Strobel Oliver, Werner Jens, Izbicki Jakob R, Johnsen Steven A, Gaedcke Jochen, Brockmöller Jürgen, Ghadimi B Micha |
| Functional genetic variant of WW domain-containing oxidoreductase (WWOX) gene is associated with hepatocellular carcinoma risk. PloS one 2017 12 (4): e0176141. Lee Hsiang-Lin, Cheng Hsin-Lin, Liu Yu-Fan, Chou Ming-Chih, Yang Shun-Fa, Chou Ying-E |
| Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Human molecular genetics 2018 2 27 (9): 1664-1674. Teslovich Tanya M, Kim Daniel Seung, Yin Xianyong, Stancáková Alena, Jackson Anne U, Wielscher Matthias, Naj Adam, Perry John R B, Huyghe Jeroen R, Stringham Heather M, Davis James P, Raulerson Chelsea K, Welch Ryan P, Fuchsberger Christian, Locke Adam E, Sim Xueling, Chines Peter S, Narisu Narisu, Kangas Antti J, Soininen Pasi, , Ala-Korpela Mika, Gudnason Vilmundur, Musani Solomon K, Jarvelin Marjo-Riitta, Schellenberg Gerard D, Speliotes Elizabeth K, Kuusisto Johanna, Collins Francis S, Boehnke Michael, Laakso Markku, Mohlke Karen |
| Genomic and Expression Analyses Identify a Disease-Modifying Variant for Fibrostenotic Crohn's Disease. Journal of Crohn's & colitis 2018 Jan . Visschedijk Marijn C, Spekhorst Lieke M, Cheng Shih-Chin, van Loo Ellen S, Jansen B H Dianne, Blokzijl Tjasso, Kil Hyunsuk, de Jong Dirk J, Pierik Marieke, Maljaars Jeroen P W J, van der Woude C Janneke, van Bodegraven Adriaan A, Oldenburg Bas, Löwenberg Mark, Nieuwenhuijs Vincent B, Imhann Floris, van Sommeren Suzanne, Alberts Rudi, Xavier Ramnik J, Dijkstra Gerard, Nico Faber Klaas, Aldaz C Marcelo, Weersma Rinse K, Festen Eleonora A |
| Functional genetic variant of WW domain containing oxidoreductase gene associated with urothelial cell carcinoma clinicopathologic characteristics and long-term survival. Urologic oncology 2019 Aug . Hung Sheng-Chun, Chou Ying-Erh, Li Jian-Ri, Chen Chuan-Shu, Lin Chia-Yen, Chang Li-Wen, Chiu Kun-Yuan, Cheng Chen-Li, Ou Yen-Chuan, Wang Shian-Shiang, Yang Shun- |
| Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates A?, tau, immunity and lipid processing.
Nature genetics 2019 (3): 414-430. Kunkle Brian W, Grenier-Boley Benjamin, Sims Rebecca, Bis Joshua C, Damotte Vincent, Naj Adam C, Boland Anne, Vronskaya Maria, van der Lee Sven J, Amlie-Wolf Alexandre, Bellenguez Céline, Frizatti Aura, Chouraki Vincent, Martin Eden R, Sleegers Kristel, Badarinarayan Nandini, Jakobsdottir Johanna, Hamilton-Nelson Kara L, Moreno-Grau Sonia, Olaso Robert, Raybould Rachel, Chen Yuning, Kuzma Amanda B, Hiltunen Mikko, Morgan Taniesha, Ahmad Shahzad, Vardarajan Badri N, Epelbaum Jacques, Hoffmann Per, Boada Merce, Beecham Gary W, Garnier Jean-Guillaume, Harold Denise, Fitzpatrick Annette L, Valladares Otto, Moutet Marie-Laure, Gerrish Amy, Smith Albert V, Qu Liming, Bacq Delphine, Denning Nicola, Jian Xueqiu, Zhao Yi, Del Zompo Maria, Fox Nick C, Choi Seung-Hoan, Mateo Ignacio, Hughes Joseph T, Adams Hieab H, Malamon John, Sanchez-Garcia Florentino, Patel Yogen, Brody Jennifer A, Dombroski Beth A, Naranjo Maria Candida Deniz, Daniilidou Makrina, Eiriksdottir Gudny, Mukherjee Shubhabrata, Wallon David, Uphill James, Aspelund Thor, Cantwell Laura B, Garzia Fabienne, Galimberti Daniela, Hofer Edith, Butkiewicz Mariusz, Fin Bertrand, Scarpini Elio, Sarnowski Chloe, Bush Will S, Meslage Stéphane, Kornhuber Johannes, White Charles C, Song Yuenjoo, Barber Robert C, Engelborghs Sebastiaan, Sordon Sabrina, Voijnovic Dina, Adams Perrie M, Vandenberghe Rik, Mayhaus Manuel, Cupples L Adrienne, Albert Marilyn S, De Deyn Peter P, Gu Wei, Himali Jayanadra J, Beekly Duane, Squassina Alessio, Hartmann Annette M, Orellana Adelina, Blacker Deborah, Rodriguez-Rodriguez Eloy, Lovestone Simon, Garcia Melissa E, Doody Rachelle S, Munoz-Fernadez Carmen, Sussams Rebecca, Lin Honghuang, Fairchild Thomas J, Benito Yolanda A, Holmes Clive, Karamuji?-?omi? Hata, Frosch Matthew P, Thonberg Hakan, Maier Wolfgang, Roshchupkin Gennady, Ghetti Bernardino, Giedraitis Vilmantas, Kawalia Amit, Li Shuo, Huebinger Ryan M, Kilander Lena, Moebus Susanne, Hernández Isabel, Kamboh M Ilyas, Brundin RoseMarie, Turton James, Yang Qiong, Katz Mindy J, Concari Letizia, Lord Jenny, Beiser Alexa S, Keene C Dirk, Helisalmi Seppo, Kloszewska Iwona, Kukull Walter A, Koivisto Anne Maria, Lynch Aoibhinn, Tarraga Lluís, Larson Eric B, Haapasalo Annakaisa, Lawlor Brian, Mosley Thomas H, Lipton Richard B, Solfrizzi Vincenzo, Gill Michael, Longstreth W T, Montine Thomas J, Frisardi Vincenza, Diez-Fairen Monica, Rivadeneira Fernando, Petersen Ronald C, Deramecourt Vincent, Alvarez Ignacio, Salani Francesca, Ciaramella Antonio, Boerwinkle Eric, Reiman Eric M, Fievet Nathalie, Rotter Jerome I, Reisch Joan S, Hanon Olivier, Cupidi Chiara, Andre Uitterlinden A G, Royall Donald R, Dufouil Carole, Maletta Raffaele Giovanni, de Rojas Itziar, Sano Mary, Brice Alexis, Cecchetti Roberta, George-Hyslop Peter St, Ritchie Karen, Tsolaki Magda, Tsuang Debby W, Dubois Bruno, Craig David, Wu Chuang-Kuo, Soininen Hilkka, Avramidou Despoina, Albin Roger L, Fratiglioni Laura, Germanou Antonia, Apostolova Liana G, Keller Lina, Koutroumani Maria, Arnold Steven E, Panza Francesco, Gkatzima Olymbia, Asthana Sanjay, Hannequin Didier, Whitehead Patrice, Atwood Craig S, Caffarra Paolo, Hampel Harald, Quintela Inés, Carracedo Ángel, Lannfelt Lars, Rubinsztein David C, Barnes Lisa L, Pasquier Florence, Frölich Lutz, Barral Sandra, McGuinness Bernadette, Beach Thomas G, Johnston Janet A, Becker James T, Passmore Peter, Bigio Eileen H, Schott Jonathan M, Bird Thomas D, Warren Jason D, Boeve Bradley F, Lupton Michelle K, Bowen James D, Proitsi Petra, Boxer Adam, Powell John F, Burke James R, Kauwe John S K, Burns Jeffrey M, Mancuso Michelangelo, Buxbaum Joseph D, Bonuccelli Ubaldo, Cairns Nigel J, McQuillin Andrew, Cao Chuanhai, Livingston Gill, Carlson Chris S, Bass Nicholas J, Carlsson Cynthia M, Hardy John, Carney Regina M, Bras Jose, Carrasquillo Minerva M, Guerreiro Rita, Allen Mariet, Chui Helena C, Fisher Elizabeth, Masullo Carlo, Crocco Elizabeth A, DeCarli Charles, Bisceglio Gina, Dick Malcolm, Ma Li, Duara Ranjan, Graff-Radford Neill R, Evans Denis A, Hodges Angela, Faber Kelley M, Scherer Martin, Fallon Kenneth B, Riemenschneider Matthias, Fardo David W, Heun Reinhard, Farlow Martin R, Kölsch Heike, Ferris Steven, Leber Markus, Foroud Tatiana M, Heuser Isabella, Galasko Douglas R, Giegling Ina, Gearing Marla, Hüll Michael, Geschwind Daniel H, Gilbert John R, Morris John, Green Robert C, Mayo Kevin, Growdon John H, Feulner Thomas, Hamilton Ronald L, Harrell Lindy E, Drichel Dmitriy, Honig Lawrence S, Cushion Thomas D, Huentelman Matthew J, Hollingworth Paul, Hulette Christine M, Hyman Bradley T, Marshall Rachel, Jarvik Gail P, Meggy Alun, Abner Erin, Menzies Georgina E, Jin Lee-Way, Leonenko Ganna, Real Luis M, Jun Gyungah R, Baldwin Clinton T, Grozeva Detelina, Karydas Anna, Russo Giancarlo, Kaye Jeffrey A, Kim Ronald, Jessen Frank, Kowall Neil W, Vellas Bruno, Kramer Joel H, Vardy Emma, LaFerla Frank M, Jöckel Karl-Heinz, Lah James J, Dichgans Martin, Leverenz James B, Mann David, Levey Allan I, Pickering-Brown Stuart, Lieberman Andrew P, Klopp Norman, Lunetta Kathryn L, Wichmann H-Erich, Lyketsos Constantine G, Morgan Kevin, Marson Daniel C, Brown Kristelle, Martiniuk Frank, Medway Christopher, Mash Deborah C, Nöthen Markus M, Masliah Eliezer, Hooper Nigel M, McCormick Wayne C, Daniele Antonio, McCurry Susan M, Bayer Anthony, McDavid Andrew N, Gallacher John, McKee Ann C, van den Bussche Hendrik, Mesulam Marsel, Brayne Carol, Miller Bruce L, Riedel-Heller Steffi, Miller Carol A, Miller Joshua W, Al-Chalabi Ammar, Morris John C, Shaw Christopher E, Myers Amanda J, Wiltfang Jens, O'Bryant Sid, Olichney John M, Alvarez Victoria, Parisi Joseph E, Singleton Andrew B, Paulson Henry L, Collinge John, Perry William R, Mead Simon, Peskind Elaine, Cribbs David H, Rossor Martin, Pierce Aimee, Ryan Natalie S, Poon Wayne W, Nacmias Benedetta, Potter Huntington, Sorbi Sandro, Quinn Joseph F, Sacchinelli Eleonora, Raj Ashok, Spalletta Gianfranco, Raskind Murray, Caltagirone Carlo, Bossù Paola, Orfei Maria Donata, Reisberg Barry, Clarke Robert, Reitz Christiane, Smith A David, Ringman John M, Warden Donald, Roberson Erik D, Wilcock Gordon, Rogaeva Ekaterina, Bruni Amalia Cecilia, Rosen Howard J, Gallo Maura, Rosenberg Roger N, Ben-Shlomo Yoav, Sager Mark A, Mecocci Patrizia, Saykin Andrew J, Pastor Pau, Cuccaro Michael L, Vance Jeffery M, Schneider Julie A, Schneider Lori S, Slifer Susan, Seeley William W, Smith Amanda G, Sonnen Joshua A, Spina Salvatore, Stern Robert A, Swerdlow Russell H, Tang Mitchell, Tanzi Rudolph E, Trojanowski John Q, Troncoso Juan C, Van Deerlin Vivianna M, Van Eldik Linda J, Vinters Harry V, Vonsattel Jean Paul, Weintraub Sandra, Welsh-Bohmer Kathleen A, Wilhelmsen Kirk C, Williamson Jennifer, Wingo Thomas S, Woltjer Randall L, Wright Clinton B, Yu Chang-En, Yu Lei, Saba Yasaman, Pilotto Alberto, Bullido Maria J, Peters Oliver, Crane Paul K, Bennett David, Bosco Paola, Coto Eliecer, Boccardi Virginia, De Jager Phil L, Lleo Alberto, Warner Nick, Lopez Oscar L, Ingelsson Martin, Deloukas Panagiotis, Cruchaga Carlos, Graff Caroline, Gwilliam Rhian, Fornage Myriam, Goate Alison M, Sanchez-Juan Pascual, Kehoe Patrick G, Amin Najaf, Ertekin-Taner Nilifur, Berr Claudine, Debette Stéphanie, Love Seth, Launer Lenore J, Younkin Steven G, Dartigues Jean-Francois, Corcoran Chris, Ikram M Arfan, Dickson Dennis W, Nicolas Gael, Campion Dominique, Tschanz JoAnn, Schmidt Helena, Hakonarson Hakon, Clarimon Jordi, Munger Ron, Schmidt Reinhold, Farrer Lindsay A, Van Broeckhoven Christine, C O'Donovan Michael, DeStefano Anita L, Jones Lesley, Haines Jonathan L, Deleuze Jean-Francois, Owen Michael J, Gudnason Vilmundur, Mayeux Richard, Escott-Price Valentina, Psaty Bruce M, Ramirez Alfredo, Wang Li-San, Ruiz Agustin, van Duijn Cornelia M, Holmans Peter A, Seshadri Sudha, Williams Julie, Amouyel Phillippe, Schellenberg Gerard D, Lambert Jean-Charles, Pericak-Vance Margaret A, , , , |
| First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. European journal of human genetics : EJHG 2020 Mar . Hengel Holger, Buchert Rebecca, Sturm Marc, Haack Tobias B, Schelling Yvonne, Mahajnah Muhammad, Sharkia Rajech, Azem Abdussalam, Balousha Ghassan, Ghanem Zaid, Falana Mohammed, Balousha Osama, Ayesh Suhail, Keimer Reinhard, Deigendesch Werner, Zaidan Jimmy, Marzouqa Hiyam, Bauer Peter, Schöls Ludg |
| Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis.
JAMA neurology 2020 10 78 (1): 102-113. Kunkle Brian W, Schmidt Michael, Klein Hans-Ulrich, Naj Adam C, Hamilton-Nelson Kara L, Larson Eric B, Evans Denis A, De Jager Phil L, Crane Paul K, Buxbaum Joe D, Ertekin-Taner Nilufer, Barnes Lisa L, Fallin M Daniele, Manly Jennifer J, Go Rodney C P, Obisesan Thomas O, Kamboh M Ilyas, Bennett David A, Hall Kathleen S, Goate Alison M, Foroud Tatiana M, Martin Eden R, Wang Li-Sao, Byrd Goldie S, Farrer Lindsay A, Haines Jonathan L, Schellenberg Gerard D, Mayeux Richard, Pericak-Vance Margaret A, Reitz Christiane, , Graff-Radford Neill R, Martinez Izri, Ayodele Temitope, Logue Mark W, Cantwell Laura B, Jean-Francois Melissa, Kuzma Amanda B, Adams L D, Vance Jeffery M, Cuccaro Michael L, Chung Jaeyoon, Mez Jesse, Lunetta Kathryn L, Jun Gyungah R, Lopez Oscar L, Hendrie Hugh C, Reiman Eric M, Kowall Neil W, Leverenz James B, Small Scott A, Levey Allan I, Golde Todd E, Saykin Andrew J, Starks Takiyah D, Albert Marilyn S, Hyman Bradley T, Petersen Ronald C, Sano Mary, Wisniewski Thomas, Vassar Robert, Kaye Jeffrey A, Henderson Victor W, DeCarli Charles, LaFerla Frank M, Brewer James B, Miller Bruce L, Swerdlow Russell H, Van Eldik Linda J, Paulson Henry L, Trojanowski John Q, Chui Helena C, Rosenberg Roger N, Craft Suzanne, Grabowski Thomas J, Asthana Sanjay, Morris John C, Strittmatter Stephen M, Kukull Walter |
| Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease.
Nature genetics 2021 5 53 (6): 787-793. Liu Ganqiang, Peng Jiajie, Liao Zhixiang, Locascio Joseph J, Corvol Jean-Christophe, Zhu Frank, Dong Xianjun, Maple-Grødem Jodi, Campbell Meghan C, Elbaz Alexis, Lesage Suzanne, Brice Alexis, Mangone Graziella, Growdon John H, Hung Albert Y, Schwarzschild Michael A, Hayes Michael T, Wills Anne-Marie, Herrington Todd M, Ravina Bernard, Shoulson Ira, Taba Pille, Kõks Sulev, Beach Thomas G, Cormier-Dequaire Florence, Alves Guido, Tysnes Ole-Bjørn, Perlmutter Joel S, Heutink Peter, Amr Sami S, van Hilten Jacobus J, Kasten Meike, Mollenhauer Brit, Trenkwalder Claudia, Klein Christine, Barker Roger A, Williams-Gray Caroline H, Marinus Johan, , Scherzer Clemens |
| Association between WWOX/MAF variants and dementia-related neuropathologic endophenotypes. Neurobiology of aging 2021 Oct . Dugan Adam J, Nelson Peter T, Katsumata Yuriko, Shade Lincoln M P, Teylan Merilee A, Boehme Kevin L, Mukherjee Shubhabrata, Kauwe John S K, Hohman Timothy J, Schneider Julie A, Fardo David W, |
| Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing. Human genomics 2022 09 16 (1): 36. Chen Shasha, Jin Qinchun, Hou Shiqiang, Li Mingfei, Zhang Yuan, Guan Lihua, Pan Wenzhi, Ge Junbo, Zhou Dax |
| Genome-wide linkage search for cancer susceptibility loci in a cohort of non BRCA1/2 families in Sri Lanka. BMC research notes 2022 Jun 15 (1): 190. Wijesiriwardhana Prabhavi, Musolf Anthony M, Bailey-Wilson Joan E, Wetthasinghe T Kalum, Dissanayake Vajira H |
| Mitochondrial 1555 G>A variant as a potential risk factor for childhood glioblastoma. Neuro-oncology advances 0 4 (1): vdac045. Li Shaobo, Gai Xiaowu, Myint Swe Swe, Arroyo Katti, Morimoto Libby, Metayer Catherine, de Smith Adam J, Walsh Kyle M, Wiemels Joseph |
| EHBP1, TUBB, and WWOX SNPs, Gene-Gene and Gene-Environment Interactions on Coronary Artery Disease and Ischemic Stroke. Frontiers in genetics 2022 5 13 843661. Liu Chun-Xiao, Yin Rui-Xing, Cao Xiao-Li, Shi Zong-Hu, Huang Feng, Wei Bi-Liu, Deng Guo-Xiong, Zheng Peng-Fei, Guan Yao-Zo |
| Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia. Journal of lipid research 2022 4 63 (6): 100209. Dong Weilai, Wong Karen H Y, Liu Youbin, Levy-Sakin Michal, Hung Wei-Chien, Li Mo, Li Boyang, Jin Sheng Chih, Choi Jungmin, Lopez-Giraldez Francesc, Vaka Dedeepya, Poon Annie, Chu Catherine, Lao Richard, Balamir Melek, Movsesyan Irina, Malloy Mary J, Zhao Hongyu, Kwok Pui-Yan, Kane John P, Lifton Richard P, Pullinger Clive |
| Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease.
Brain : a journal of neurology 2022 4 . Stevenson-Hoare Joshua, Heslegrave Amanda, Leonenko Ganna, Fathalla Dina, Bellou Eftychia, Luckcuck Lauren, Marshall Rachel, Sims Rebecca, Morgan Bryan Paul, Hardy John, de Strooper Bart, Williams Julie, Zetterberg Henrik, Escott-Price Valenti |
| Whole-Genome Sequencing Among Kazakhstani Children with Early-Onset Epilepsy Revealed New Gene Variants and Phenotypic Variability. Molecular neurobiology 2023 4 . Mirgul Bayanova, Aidos K Bolatov, Assiya Bazenova, Lyazzat Nazarova, Alissa Nauryzbayeva, Naanlep Matthew Tanko, Saule Rakhimova, Nazerke Satvaldina, Diana Samakyzy, Ulan Kozhamkulov, Ulykbek Kairov, Ainur Akilzhanova, Dos Sarbass |
| Multi-step gene set analysis identified HTR3 family genes involving childhood acute lymphoblastic leukemia susceptibility. Archives of toxicology 2024 9 . Xiao Liu, Honghao Guo, Meiyun Kang, Wenfeng Fu, Huiqin Li, Hongsheng Ji, Jiou Zhao, Yongjun Fang, Mulong Du, Yao X |
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