Human Genome Epidemiology Literature Finder
|
Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and AKAP9[original query] |
|---|
| Variants in the GH-IGF axis confer susceptibility to lung cancer. Genome research 2006 Jun 16 (6): 693-701. Rudd Matthew F, Webb Emily L, Matakidou Athena, Sellick Gabrielle S, Williams Richard D, Bridle Helen, Eisen Tim, Houlston Richard S, |
| Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
| AKAP9 is a genetic modifier of congenital long-QT syndrome type 1. Circulation. Cardiovascular genetics 2014 Oct 7 (5): 599-606. de Villiers Carin P, van der Merwe Lize, Crotti Lia, Goosen Althea, George Alfred L, Schwartz Peter J, Brink Paul A, Moolman-Smook Johanna C, Corfield Valerie |
| Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans. Alzheimer's & dementia : the journal of the Alzheimer's Association 2014 Nov 10 (6): 609-618.e11. Logue Mark W, Schu Matthew, Vardarajan Badri N, Farrell John, Bennett David A, Buxbaum Joseph D, Byrd Goldie S, Ertekin-Taner Nilufer, Evans Denis, Foroud Tatiana, Goate Alison, Graff-Radford Neill R, Kamboh M Ilyas, Kukull Walter A, Manly Jennifer J, , |
| Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium. Human molecular genetics 2014 Nov 23 (22): 6096-111. Milne Roger L, Burwinkel Barbara, Michailidou Kyriaki, Arias-Perez Jose-Ignacio, Zamora M Pilar, Menéndez-Rodríguez Primitiva, Hardisson David, Mendiola Marta, González-Neira Anna, Pita Guillermo, Alonso M Rosario, Dennis Joe, Wang Qin, Bolla Manjeet K, Swerdlow Anthony, Ashworth Alan, Orr Nick, Schoemaker Minouk, Ko Yon-Dschun, Brauch Hiltrud, Hamann Ute, , Andrulis Irene L, Knight Julia A, Glendon Gord, Tchatchou Sandrine, , , Matsuo Keitaro, Ito Hidemi, Iwata Hiroji, Tajima Kazuo, Li Jingmei, Brand Judith S, Brenner Hermann, Dieffenbach Aida Karina, Arndt Volker, Stegmaier Christa, Lambrechts Diether, Peuteman Gilian, Christiaens Marie-Rose, Smeets Ann, Jakubowska Anna, Lubinski Jan, Jaworska-Bieniek Katarzyna, Durda Katazyna, Hartman Mikael, Hui Miao, Yen Lim Wei, Wan Chan Ching, Marme Federick, Yang Rongxi, Bugert Peter, Lindblom Annika, Margolin Sara, García-Closas Montserrat, Chanock Stephen J, Lissowska Jolanta, Figueroa Jonine D, Bojesen Stig E, Nordestgaard Børge G, Flyger Henrik, Hooning Maartje J, Kriege Mieke, van den Ouweland Ans M W, Koppert Linetta B, Fletcher Olivia, Johnson Nichola, dos-Santos-Silva Isabel, Peto Julian, Zheng Wei, Deming-Halverson Sandra, Shrubsole Martha J, Long Jirong, Chang-Claude Jenny, Rudolph Anja, Seibold Petra, Flesch-Janys Dieter, Winqvist Robert, Pylkäs Katri, Jukkola-Vuorinen Arja, Grip Mervi, Cox Angela, Cross Simon S, Reed Malcolm W R, Schmidt Marjanka K, Broeks Annegien, Cornelissen Sten, Braaf Linde, Kang Daehee, Choi Ji-Yeob, Park Sue K, Noh Dong-Young, Simard Jacques, Dumont Martine, Goldberg Mark S, Labrèche France, Fasching Peter A, Hein Alexander, Ekici Arif B, Beckmann Matthias W, Radice Paolo, Peterlongo Paolo, Azzollini Jacopo, Barile Monica, Sawyer Elinor, Tomlinson Ian, Kerin Michael, Miller Nicola, Hopper John L, Schmidt Daniel F, Makalic Enes, Southey Melissa C, Hwang Teo Soo, Har Yip Cheng, Sivanandan Kavitta, Tay Wan-Ting, Shen Chen-Yang, Hsiung Chia-Ni, Yu Jyh-Cherng, Hou Ming-Feng, Guénel Pascal, Truong Therese, Sanchez Marie, Mulot Claire, Blot William, Cai Qiuyin, Nevanlinna Heli, Muranen Taru A, Aittomäki Kristiina, Blomqvist Carl, Wu Anna H, Tseng Chiu-Chen, Van Den Berg David, Stram Daniel O, Bogdanova Natalia, Dörk Thilo, Muir Kenneth, Lophatananon Artitaya, Stewart-Brown Sarah, Siriwanarangsan Pornthep, Mannermaa Arto, Kataja Vesa, Kosma Veli-Matti, Hartikainen Jaana M, Shu Xiao-Ou, Lu Wei, Gao Yu-Tang, Zhang Ben, Couch Fergus J, Toland Amanda E, , Yannoukakos Drakoulis, Sangrajrang Suleeporn, McKay James, Wang Xianshu, Olson Janet E, Vachon Celine, Purrington Kristen, Severi Gianluca, Baglietto Laura, Haiman Christopher A, Henderson Brian E, Schumacher Fredrick, Le Marchand Loic, Devilee Peter, Tollenaar Robert A E M, Seynaeve Caroline, Czene Kamila, Eriksson Mikael, Humphreys Keith, Darabi Hatef, Ahmed Shahana, Shah Mitul, Pharoah Paul D P, Hall Per, Giles Graham G, Benítez Javier, Dunning Alison M, Chenevix-Trench Georgia, Easton Douglas |
| Alzheimer's disease: rare variants with large effect sizes. Current opinion in genetics & development 2015 Aug 33 49-55. Del-Aguila Jorge L, Koboldt Daniel C, Black Kathleen, Chasse Rachel, Norton Joanne, Wilson Richard K, Cruchaga Carl |
| Cell-free DNA mutations as biomarkers in breast cancer patients receiving tamoxifen. Oncotarget 2016 May . Jansen Maurice Phm, Martens John Wm, Helmijr Jean Ca, Beaufort Corine M, van Marion Ronald, Krol Niels Mg, Monkhorst Kim, Trapman-Jansen Anita Mac, Meijer-van Gelder Marion E, Weerts Marjolein Ja, Ramirez-Ardila Diana E, Dubbink Hendrikus Jan, Foekens John A, Sleijfer Stefan, Berns Els M |
| Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China. Mayo Clinic proceedings 2016 Oct . Zhang Liyong, Tester David J, Lang Di, Chen Yili, Zheng Jinxiang, Gao Rui, Corliss Robert F, Tang Shuangbo, Kyle John W, Liu Chao, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
| Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function. Journal of Alzheimer's disease & Parkinsonism 2017 11 7 (4): . Cukier H N, Kunkle B K, Hamilton K L, Rolati S, Kohli M A, Whitehead P L, Jaworski J, Vance J M, Cuccaro M L, Carney R M, Gilbert J R, Farrer L A, Martin E R, Beecham G W, Haines J L, Pericak-Vance M |
| Targeted Sequencing of Alzheimer Disease Genes in African Americans Implicates Novel Risk Variants. Frontiers in neuroscience 2018 12 592. Logue Mark W, Lancour Daniel, Farrell John, Simkina Irina, Fallin M Daniele, Lunetta Kathryn L, Farrer Lindsay |
| Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease. Annals of clinical and translational neurology 2018 Apr 5 (4): 406-417. Vardarajan Badri N, Barral Sandra, Jaworski James, Beecham Gary W, Blue Elizabeth, Tosto Giuseppe, Reyes-Dumeyer Dolly, Medrano Martin, Lantigua Rafael, Naj Adam, Thornton Timothy, DeStefano Anita, Martin Eden, Wang Li-San, Brown Lisa, Bush William, van Duijn Cornelia, Goate Allison, Farrer Lindsay, Haines Jonathan L, Boerwinkle Eric, Schellenberg Gerard, Wijsman Ellen, Pericak-Vance Margaret A, Mayeux Richard, , Wang Li-S |
| Integrative molecular characterization of Chinese prostate cancer specimens. Asian journal of andrology 2019 May . Lv Shi-Dong, Wang Hong-Yi, Yu Xin-Pei, Zhai Qi-Liang, Wu Yao-Bin, Wei Qiang, Huang Wen-H |
| 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 |
| Host Genetic and Gut Microbial Signatures in Familial Inflammatory Bowel Disease. Clinical and translational gastroenterology 2020 8 11 (7): e00213. Park Yoo Min, Ha Eunji, Gu Ki-Nam, Shin Ga Young, Lee Chang Kyun, Kim Kwangwoo, Kim Hyo Jo |
| Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study. EBioMedicine 2021 Apr 66 103309. Amanat Sana, Gallego-Martinez Alvaro, Sollini Joseph, Perez-Carpena Patricia, Espinosa-Sanchez Juan M, Aran Ismael, Soto-Varela Andres, Batuecas-Caletrio Angel, Canlon Barbara, May Patrick, Cederroth Christopher R, Lopez-Escamez Jose |
| Acquired mutations and transcriptional remodeling in long-term estrogen-deprived locoregional breast cancer recurrences. Breast cancer research : BCR 2021 1 23 (1): 1. Priedigkeit Nolan, Ding Kai, Horne William, Kolls Jay K, Du Tian, Lucas Peter C, Blohmer Jens-Uwe, Denkert Carsten, Machleidt Anna, Ingold-Heppner Barbara, Oesterreich Steffi, Lee Adrian |
| Transcript levels in plasma contribute substantial predictive value as potential Alzheimer's disease biomarkers in African Americans. EBioMedicine 2022 3 78 103929. Reddy Joseph S, Jin Jiangli, Lincoln Sarah J, Ho Charlotte C G, Crook Julia E, Wang Xue, Malphrus Kimberly G, Nguyen Thuy, Tamvaka Nikoleta, Greig-Custo Maria T, Lucas John A, Graff-Radford Neill R, Ertekin-Taner Nilüfer, Carrasquillo Minerva |
| Identification of Survival-Specific Genes in Clear Cell Renal Cell Carcinoma Using a Customized Next-Generation Sequencing Gene Panel. Journal of personalized medicine 2022 Jan 12 (1): . Hwang Jia, Kim Heeeun, Han Jinseon, Lee Jieun, Hong Sunghoo, Kim Saewoong, Yoon Sungjoo Kim, Choi Keonwoo, Yang Jihoon, Park Unsang, Kim Kwangjoong, Yim Kwangil, Kim Yuil, Choi Yeongj |
| Identification of Rare Damaging Missense and Loss of Function Variants in GWAS Loci Using Genome Sequencing Data from Two Cohorts of Familial Late-Onset Alzheimer's Disease. medRxiv : the preprint server for health sciences 2024 1 . Tamil Iniyan Gunasekaran, Dolly Reyes-Dumeyer, Kelley M Faber, Alison Goate, Brad Boeve, Carlos Cruchaga, Margaret Pericak-Vance, Jonathan L Haines, Roger Rosenberg, Debby Tsuang, Diones Rivera Mejia, Martin Medrano, Rafael A Lantigua, Robert A Sweet, David A Bennett, Robert S Wilson, Tatiana Foroud, Badri N Vardarajan, Richard Maye |
- Page last reviewed:Feb 1, 2024
- Content source: