Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 36 Records) |
| Query Trace: ADAM10[original query] |
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| Association of ADAM10 and CAMK2A polymorphisms with conduct disorder: evidence from family-based studies. Journal of abnormal child psychology 2011 Aug 39 (6): 773-82. Jian Xue-Qiu, Wang Ke-Sheng, Wu Tie-Jian, Hillhouse Joel J, Mullersman Jerald |
| Genetic association between ADAM10 gene polymorphism and Alzheimer's disease in a Northern Han Chinese population. Brain research 2011 Nov 1421 78-81. Song Jing-Hui, Yu Jin-Tai, Liu Min, Yan Chuan-Zhu, Tan L |
| Contribution of putative genetic factors and candidate gene variants to inter-individual variation of circulating fractalkine (CX3CL1) levels in a large UK twins' sample. Human immunology 2012 Dec . Franco L, Williams FM, Trofimov S, Surdulescu G, Spector T, Livshits G |
| An association study on ADAM10 promoter polymorphisms and atherosclerotic cerebral infarction in a Chinese population. CNS neuroscience & therapeutics 2013 Oct 19 (10): 785-94. Li You, Liao Feng, Yin Xiao-Jian, Cui Li-Li, Ma Guo-Da, Nong Xiao-Xian, Zhou Hai-Hong, Chen Yan-Fang, Zhao Bin, Li Ke-Sh |
| An ADAM10 promoter polymorphism is a functional variant in severe sepsis patients and confers susceptibility to the development of sepsis. Critical care (London, England) 2015 19 73. Cui Lili, Gao Yan, Xie Yuliu, Wang Yan, Cai Yujie, Shao Xin, Ma Xiaotang, Li You, Ma Guoda, Liu Gen, Cheng Wanwen, Liu Yu, Liu Tingting, Pan Qunwen, Tao Hua, Liu Zhou, Zhao Bin, Shao Yiming, Li Kesh |
| Cerebrospinal fluid Aß42 levels and APP processing pathway genes in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2015 Jun 30 (7): 936-44. Bekris Lynn M, Tsuang Debby W, Peskind Elaine R, Yu Chang E, Montine Thomas J, Zhang Jing, Zabetian Cyrus P, Leverenz James |
| Genetic association between APP, ADAM10 gene polymorphism, and sporadic Alzheimer's disease in the Chinese population. Neurotoxicity research 2015 Apr 27 (3): 284-91. Zeng Fan, Shen Cheng, Liu Yu-Hui, Li Jing, Zhu Jie, Wang Ye-Ran, Yan Jia-Chuan, Gao Chang-Yue, Zhou Hua-Dong, Deng Juan, Wang Yan-Jia |
| Promoter Variants of the ADAM10 Gene and Their Roles in Temporal Lobe Epilepsy. Frontiers in neurology 2016 7 108. Tao Hua, Zhao Jianghao, Zhou Xu, Ma Zhonghua, Chen Ying, Sun Fuhai, Cui Lili, Zhou Haihong, Cai Yujie, Chen Yanyan, Zhao Shu, Yao Lifen, Zhao Bin, Li Kesh |
| Association of a BACE1 Gene Polymorphism with Parkinson's Disease in a Norwegian Population. Parkinson's disease 2015 2015 973298. Lange Johannes, Lunde Kristin Aaser, Sletten Camilla, Møller Simon Geir, Tysnes Ole-Bjørn, Alves Guido, Larsen Jan Petter, Maple-Grødem Jo |
| Pharmacogenomics study on cadherin 2 network with regard to HIV infection and methadone treatment outcome. PloS one 2017 12 (3): e0174647. Kuo Hsiang-Wei, Shih Chia-Lung, Tsung Jieh-Hen, Liu Sheng-Wen, Chu Shih-Kai, Yang Hsin-Chou, Tsou Hsiao-Hui, Wang Zih-Hsiang, Chen Andrew C H, Liu Yu- |
| A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains. Journal of Alzheimer's disease : JAD 2017 Jan . Haddick Patrick C G, Larson Jessica L, Rathore Nisha, Bhangale Tushar R, Phung Qui T, Srinivasan Karpagam, Hansen David V, Lill Jennie R, , Pericak-Vance Margaret A, Haines Jonathan, Farrer Lindsay A, Kauwe John S, Schellenberg Gerard D, Cruchaga Carlos, Goate Alison M, Behrens Timothy W, Watts Ryan J, Graham Robert R, Kaminker Joshua S, van der Brug Marc |
| A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease. Molecular psychiatry 2018 Jul . Hartl Daniela, May Patrick, Gu Wei, Mayhaus Manuel, Pichler Sabrina, Spaniol Christian, Glaab Enrico, Bobbili Dheeraj Reddy, Antony Paul, Koegelsberger Sandra, Kurz Alexander, Grimmer Timo, Morgan Kevin, Vardarajan Badri N, Reitz Christiane, Hardy John, Bras Jose, Guerreiro Rita, Balling Rudi, Schneider Jochen G, Riemenschneider Matthias, |
GWAS on family history of Alzheimer's disease.
Translational psychiatry 2018 May 8 (1): 99. Marioni Riccardo E, Harris Sarah E, Zhang Qian, McRae Allan F, Hagenaars Saskia P, Hill W David, Davies Gail, Ritchie Craig W, Gale Catharine R, Starr John M, Goate Alison M, Porteous David J, Yang Jian, Evans Kathryn L, Deary Ian J, Wray Naomi R, Visscher Peter |
| Influence of ADAM10 Polymorphisms on Plasma Level of Soluble Receptor for Advanced Glycation End Products and The Association With Alzheimer's Disease Risk. Frontiers in genetics 2018 9 540. Huang Wen-Hui, Chen Wei, Jiang Lian-Ying, Yang Yi-Xia, Yao Li-Fen, Li Ke-Sh |
| Impact of ADAM10 gene polymorphisms on hepatocellular carcinoma development and clinical characteristics. International journal of medical sciences 2018 15 (12): 1334-1340. Shiu Jr-Shiang, Hsieh Ming-Ju, Chiou Hui-Ling, Wang Hsiang-Ling, Yeh Chao-Bin, Yang Shun-Fa, Chou Ying-E |
| Profiles of ?-Amyloid Peptides and Key Secretases in Brain Autopsy Samples Differ with Sex and APOE ?4 Status: Impact for Risk and Progression of Alzheimer Disease. Neuroscience 2018 1 373 20-36. Nyarko Jennifer N K, Quartey Maa O, Pennington Paul R, Heistad Ryan M, Dea Doris, Poirier Judes, Baker Glen B, Mousseau Darrell |
| A Functional Polymorphism-Mediated Disruption of EGR1/ADAM10 Pathway Confers the Risk of Sepsis Progression. mBio 2019 Aug 10 (4): . Chen Feng, Wang Yan, Zhang Wenying, Cai Yujie, Zhao Tian, Mai Hui, Tao Shoubao, Wei Wenyan, Li Jia, Chen Xiongjin, Li Xiaohui, Tang Pei, Fan Weihao, Yang Jingqi, Ou Mingqian, Lu Furong, Lai Zhipeng, Chen Huiyi, Zou Ting, Sun Furong, Shao Yiming, Cui Li |
| 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, , , , |
| Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Cold Spring Harbor molecular case studies 2019 12 5 (6): . Cochran J Nicholas, McKinley Emily C, Cochran Meagan, Amaral Michelle D, Moyers Bryan A, Lasseigne Brittany N, Gray David E, Lawlor James M J, Prokop Jeremy W, Geier Ethan G, Holt James M, Thompson Michelle L, Newberry J Scott, Yokoyama Jennifer S, Worthey Elizabeth A, Geldmacher David S, Love Marissa Natelson, Cooper Gregory M, Myers Richard M, Roberson Erik |
| Rare mutations of ADAM17 from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling. Clinical science (London, England : 1979) 2019 1 133 (2): 225-238. Xie Yifang, Ma Anyun, Wang Boshi, Peng Rui, Jing Yingchun, Wang Deqian, Finnell Richard H, Qiao Bin, Wang Yongming, Wang Hongyan, Zheng Yufa |
| The association of clinical phenotypes to known AD/FTD genetic risk loci and their inter-relationship. PloS one 2020 11 15 (11): e0241552. Li Qingqin S, Tian Chao, , Hinds David, Seabrook Guy |
| Soluble Receptor for Advanced Glycation End-products (sRAGE) and Colorectal Cancer Risk: A Case-Control Study Nested within a European Prospective Cohort. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2020 Oct . Aglago Elom K, Rinaldi Sabina, Freisling Heinz, Jiao Li, Hughes David J, Fedirko Veronika, Schalkwijk Casper G, Weiderpass Elisabete, Dahm Christina C, Overvad Kim, Eriksen Anne Kirstine, Kyrø Cecilie, Boutron-Ruault Marie-Christine, Rothwell Joseph A, Severi Gianluca, Katzke Verena, Kühn Tilman, Schulze Matthias B, Aleksandrova Krasimira, Masala Giovanna, Krogh Vittorio, Panico Salvatore, Tumino Rosario, Naccarati Alessio, Bueno-de-Mesquita Bas, van Gils Carla H, Sandanger Torkjel M, Gram Inger T, Skeie Guri, Quirós J Ramón, Jakszyn Paula, Sánchez Maria-Jose, Amiano Pilar, Huerta José María, Ardanaz Eva, Johansson Ingegerd, Harlid Sophia, Perez-Cornago Aurora, Mayén Ana-Lucia, Cordova Reynalda, Gunter Marc J, Vineis Paolo, Cross Amanda J, Riboli Elio, Jenab Maz |
| Association of ADAM10 gene variants with sporadic Parkinson's disease in Chinese Han population. The journal of gene medicine 2021 Feb e3319. Zhou Miaomiao, Lin Yuwan, Lu Lin, Zhang Zhiling, Guo Wenyuan, Peng Guoyou, Zhang Wenlong, Zhu Ziting, Wu Zhuohua, Mo Mingshu, Yang Xinling, Zhu Xiaoqin, Chen Chaojun, Chen Xiang, Xu Ping |
| 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 |
| ADAM10 Gene Variants in AD Patients and Their Relationship to CSF Protein Levels. International journal of molecular sciences 2023 4 24 (7): . Agüero-Rabes Pablo, Pérez-Pérez Julián, Cremades-Jimeno Lucía, García-Ayllón María-Salud, Gea-González Adriana, Sainz María José, Mahillo-Fernández Ignacio, Téllez Raquel, Cárdaba Blanca, Sáez-Valero Javier, Gómez-Tortosa Estrel |
| Computational analysis and molecular dynamics simulation of high-risk single nucleotide polymorphisms of the ADAM10 gene. Journal of biomolecular structure & dynamics 2023 3 1-13. Namme Jannatun Nayem, Reza Hasan Mahmud, Bepari Asim Kum |
| ADAM10 Gene Polymorphism and Its Relationship to Hepatocellular Carcinoma in Egyptian HCV Patients Receiving Direct-Acting Antiviral Therapies (DAAs). Asian Pacific journal of cancer prevention : APJCP 2023 1 24 (1): 149-155. Ghanem Samar, El Gedawy Gamalat, Yehia Sania, Bedair Hanan, Awad Samah, Abdel-Razek Wael, Elhelbawy Mostafa, El-Sabaawy Dalia, Elfert Ashraf Yous |
| Cell type-specific histone acetylation profiling of Alzheimer's disease subjects and integration with genetics. Frontiers in molecular neuroscience 2023 1 15 948456. Ramamurthy Easwaran, Welch Gwyneth, Cheng Jemmie, Yuan Yixin, Gunsalus Laura, Bennett David A, Tsai Li-Huei, Pfenning Andreas |
| Whole exome sequencing analyses identified novel genes for Alzheimer's disease and related dementia. Alzheimer's & dementia : the journal of the Alzheimer's Association 2024 8 . Ya-Ru Zhang, Bang-Sheng Wu, Shi-Dong Chen, Liu Yang, Yue-Ting Deng, Yu Guo, Xin-Rui Wu, Wei-Shi Liu, Ju-Jiao Kang, Jian-Feng Feng, Wei Cheng, Jin-Tai |
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