HuGE Literature Finder
Records 1-20
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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 |
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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 |
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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 |
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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 |
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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 |
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Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
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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 |
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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, , |
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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 |
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Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.
Journal of the American College of Cardiology 2014 Apr 63 (14): 1430-7. Weeke Peter, Mosley Jonathan D, Hanna David, Delaney Jessica T, Shaffer Christian, Wells Quinn S, Van Driest Sara, Karnes Jason H, Ingram Christie, Guo Yan, Shyr Yu, Norris Kris, Kannankeril Prince J, Ramirez Andrea H, Smith Joshua D, Mardis Elaine R, Nickerson Deborah, George Alfred L, Roden Dan |
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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 |
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Role of DISC1 Interacting Proteins in Schizophrenia Risk from Genome-Wide Analysis of Missense SNPs.
Annals of human genetics 2013 Jul . Costas J, Suárez-Rama JJ, Carrera N, Paz E, Páramo M, Agra S, Brenlla J, Ramos-Ríos R, Arrojo M |
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7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium.
Journal of medical genetics 2011 Oct 48 (10): 698-702. Milne Roger L, Lorenzo-Bermejo Justo, Burwinkel Barbara, Malats Núria, Arias Jose Ignacio, Zamora M Pilar, Benítez Javier, Humphreys Manjeet K, García-Closas Montserrat, Chanock Stephen J, Lissowska Jolanta, Sherman Mark E, Mannermaa Arto, Kataja Vesa, Kosma Veli-Matti, Nevanlinna Heli, Heikkinen Tuomas, Aittomäki Kristiina, Blomqvist Carl, Anton-Culver Hoda, Ziogas Argyrios, Devilee Peter, van Asperen Christie J, Tollenaar Rob A E M, Seynaeve Caroline, Hall Per, Czene Kamila, Liu Jianjun, Irwanto Astrid K, Kang Daehee, Yoo Keun-Young, Noh Dong-Young, Couch Fergus J, Olson Janet E, Wang Xianshu, Fredericksen Zachary, Nordestgaard Børge G, Bojesen Stig E, Flyger Henrik, Margolin Sara, Lindblom Annika, Fasching Peter A, Schulz-Wendtland Ruediger, Ekici Arif B, Beckmann Matthias W, Wang-Gohrke Shan, Shen Chen-Yang, Yu Jyh-Cherng, Hsu Huan-Ming, Wu Pei-Ei, Giles Graham G, Severi Gianluca, Baglietto Laura, English Dallas R, Cox Angela, Brock Ian, Elliott Graeme, Reed Malcolm W R, Beesley Jonathan, Chen Xiaoqing, Investigators Kconfab, , Fletcher Olivia, Gibson Lorna, dos Santos Silva Isabel, Peto Julian, Frank Bernd, Heil Joerg, Meindl Alfons, Chang-Claude Jenny, Hein Rebecca, Vrieling Alina, Flesch-Janys Dieter, Southey Melissa C, Smith Letitia, Apicella Carmel, Hopper John L, Dunning Alison M, Pooley Karen A, Pharoah Paul D P, Hamann Ute, Pesch Beate, Ko Yon-Dschun, , Easton Douglas F, Chenevix-Trench Georg |
Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.
Alcoholism, clinical and experimental research 2011 May 35 (5): 963-75. Kendler Kenneth S, Kalsi Gursharan, Holmans Peter A, Sanders Alan R, Aggen Steven H, Dick Danielle M, Aliev Fazil, Shi Jianxin, Levinson Douglas F, Gejman Pablo |
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International Lung Cancer Consortium: coordinated association study of 10 potential lung cancer susceptibility variants.
Carcinogenesis 2010 Apr 31 (4): 625-33. Truong Therese, Sauter Wiebke, McKay James D, Hosgood H Dean, Gallagher Carla, Amos Christopher I, Spitz Margaret, Muscat Joshua, Lazarus Philip, Illig Thomas, Wichmann H Erich, Bickeböller Heike, Risch Angela, Dienemann Hendrik, Zhang Zuo-Feng, Naeim Behnaz Pezeshki, Yang Ping, Zienolddiny Shanbeh, Haugen Aage, Le Marchand Loïc, Hong Yun-Chul, Kim Jin Hee, Duell Eric J, Andrew Angeline S, Kiyohara Chikako, Shen Hongbing, Matsuo Keitaro, Suzuki Takeshi, Seow Adeline, Ng Daniel P K, Lan Qing, Zaridze David, Szeszenia-Dabrowska Neonilia, Lissowska Jolanta, Rudnai Peter, Fabianova Eleonora, Constantinescu Vali, Bencko Vladimir, Foretova Lenka, Janout Vladimir, Caporaso Neil E, Albanes Demetrius, Thun Michael, Landi Maria Teresa, Trubicka Joanna, Lener Marcin, Lubinski Jan, , Wang Ying, Chabrier Amélie, Boffetta Paolo, Brennan Paul, Hung Rayjean |
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Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families.
Cancer letters 2008 Nov 271 (1): 153-7. Frank Bernd, Burwinkel Barbara, Bermejo Justo Lorenzo, Försti Asta, Hemminki Kari, Houlston Richard, Mangold Elisabeth, Rahner Nils, Friedl Waltraut, Friedrichs Nicolaus, Buettner Reinhard, Engel Christoph, Loeffler Markus, Holinski-Feder Elke, Morak Monika, Keller Gisela, Schackert Hans K, Krüger Stefan, Goecke Timm, Moeslein Gabriela, Kloor Matthias, Gebert Johannes, Kunstmann Erdmute, Schulmann Karsten, Rüschoff Josef, Propping Peter, |
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Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis.
Journal of the National Cancer Institute 2008 Mar 100 (6): 437-42. Frank Bernd, Wiestler Miriam, Kropp Silke, Hemminki Kari, Spurdle Amanda B, Sutter Christian, Wappenschmidt Barbara, Chen Xiaoqing, Beesley Jonathan, Hopper John L, , Meindl Alfons, Kiechle Marion, Slanger Tracy, Bugert Peter, Schmutzler Rita K, Bartram Claus R, Flesch-Janys Dieter, Mutschelknauss Elke, Ashton Katie, Salazar Ramona, Webb Emily, Hamann Ute, Brauch Hiltrud, Justenhoven Christina, Ko Yon-Dschun, Brüning Thomas, Silva Isabel dos Santos, Johnson Nichola, Pharoah Paul P D, Dunning Alison M, Pooley Karen A, Chang-Claude Jenny, Easton Douglas F, Peto Julian, Houlston Richard, , Chenevix-Trench Georgia, Fletcher Olivia, Burwinkel Barba |
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Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.
Human molecular genetics 2006 Nov 15 (21): 3263-71. Webb Emily L, Rudd Matthew F, Sellick Gabrielle S, El Galta Rachid, Bethke Lara, Wood Wendy, Fletcher Olivia, Penegar Steven, Withey Laura, Qureshi Mobshra, Johnson Nichola, Tomlinson Ian, Gray Richard, Peto Julian, Houlston Richard |
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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, |
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Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility.
Journal of psychiatric research 0 66-67 38-44. Suárez-Rama José Javier, Arrojo Manuel, Sobrino Beatriz, Amigo Jorge, Brenlla Julio, Agra Santiago, Paz Eduardo, Brión María, Carracedo Ángel, Páramo Mario, Costas Javi |
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- Page last updated:Jan 19, 2021
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