HuGE Literature Finder
Records 1-24
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Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.
Journal of endocrinological investigation 2019 Mar . Popovic M, Matana A, Torlak V, Boutin T, Brdar D, Gunjaca I, Kalicanin D, Kolcic I, Boraska Perica V, Punda A, Polašek O, Barbalic M, Hayward C, Zemunik |
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Novel Genetic Variants are Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SCL1A3 and EPHB2.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2016 Aug . Nielson Carrie M, Liu Ching-Ti, Smith Albert V, Ackert-Bicknell Cheryl L, Reppe Sjur, Johanna Jakobsdottir, Wassel Christina, Register Thomas C, Oei Ling, Alonso Lopez Nerea, Oei Edwin H, Parimi Neeta, Samelson Elizabeth J, Nalls Mike A, Zmuda Joseph, Lang Thomas, Bouxsein Mary, Latourelle Jeanne, Claussnitzer Melina, Siggeirsdottir Kristin, Srikanth Priya, Lorentzen Erik, Vandenput Liesbeth, Langefeld Carl, Raffield Laura, Terry Greg, Cox Amanda J, Allison Matthew A, Criqui Michael H, Bowden Don, Ikram M Arfan, Mellström Dan, Karlsson Magnus K, Carr John, Budoff Matthew, Phillips Caroline, Cupples L Adrienne, Chou Wen-Chi, Myers Richard H, Ralston Stuart H, Gautvik Kaare M, Cawthon Peggy M, Cummings Steven, Karasik David, Rivadeneira Fernando, Gudnason Vilmundur, Orwoll Eric S, Harris Tamara B, Ohlsson Claes, Kiel Douglas P, Hsu Yi-Hsia |
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Mutually exclusive ERK Pathway Mutations are present in different stages of multifocal Pulmonary Langerhans Cell Histiocytosis supporting clonal nature of the disease.
Histopathology 2016 Feb . Kamionek Michal, Ahmadi Moghaddam Parnian, Sakhdari Ali, Kovach Alexandra E, Welch Matthew, Meng Xiuling, Dresser Karen, Tomaszewicz Keith, Dresser Karen, Cosar Ediz F, Mark Eugene J, Fraire Armando E, Hutchinson Llo |
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Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas.
Nature genetics 2015 Sep 47 (9): 996-1002. Krauthammer Michael, Kong Yong, Bacchiocchi Antonella, Evans Perry, Pornputtapong Natapol, Wu Cen, McCusker James P, Ma Shuangge, Cheng Elaine, Straub Robert, Serin Merdan, Bosenberg Marcus, Ariyan Stephan, Narayan Deepak, Sznol Mario, Kluger Harriet M, Mane Shrikant, Schlessinger Joseph, Lifton Richard P, Halaban Ru |
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RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counseling.
European journal of human genetics : EJHG 2015 Sep . Widowati Titis, Melhem Shamiram, Patria Suryono Y, de Graaf Bianca M, Sinke Richard J, Viel Martijn, Dijkhuis Jos, Sadewa Ahmad H, Purwohardjono Rochadi, Soenarto Yati, Hofstra Robert Mw, Sribudiani Yun |
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Genetic variation in insulin-induced kinase signaling.
Molecular systems biology 2015 Jul 11 (7): 820. Wang Isabel Xiaorong, Ramrattan Girish, Cheung Vivian |
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MicroRNA-224 is associated with colorectal cancer progression and response to 5-fluorouracil-based chemotherapy by KRAS-dependent and -independent mechanisms.
British journal of cancer 2015 Apr 112 (9): 1480-90. Amankwatia E B, Chakravarty P, Carey F A, Weidlich S, Steele R J C, Munro A J, Wolf C R, Smith |
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[Cytogenetic abnormalities in high-risk multiple myeloma].
Nihon rinsho. Japanese journal of clinical medicine 2015 Jan 73 (1): 28-32. Ishida Tad |
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Mutated ephrin receptor genes in non-small cell lung carcinoma and their occurrence with driver mutations-targeted resequencing study on formalin-fixed, paraffin-embedded tumor material of 81 patients.
Genes, chromosomes & cancer 2013 Dec 52 (12): 1141-9. Mäki-Nevala Satu, Kaur Sarhadi Virinder, Tuononen Katja, Lagström Sonja, Ellonen Pekka, Rönty Mikko, Wirtanen Aino, Knuuttila Aija, Knuutila Saka |
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A9 region in EPHB2 mutation is frequent in tumors with microsatellite instability. Analysis of prognosis.
Anticancer research 2013 Nov 33 (11): 5159-63. Rafael Sara, Vidaurreta Marta, Veganzones Silvia, De La Orden Virgnia, Mediero Beatriz, Gutierrez Maria Luisa, Maestro Maria Lui |
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Genetic variants in the region of the C1q genes are associated with rheumatoid arthritis.
Clinical and experimental immunology 2013 Jul 173 (1): 76-83. Trouw L A, Daha N, Kurreeman F A S, Böhringer S, Goulielmos G N, Westra H J, Zhernakova A, Franke L, Stahl E A, Levarht E W N, Stoeken-Rijsbergen G, Verduijn W, Roos A, Li Y, Houwing-Duistermaat J J, Huizinga T W J, Toes R E |
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SNPs in axon guidance pathway genes and susceptibility for Parkinson's disease in the Korean population.
Journal of human genetics 2011 Feb 56 (2): 125-9. Kim Jong-Min, Park Sue K, Yang Jae Jeong, Shin Eun-Soon, Lee Jee-Young, Yun Ji Young, Kim Ji Seon, Park Sung Sup, Jeon Beom |
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EphB2 SNPs and sporadic prostate cancer risk in African American men.
PloS one 2011 6 (5): e19494. Robbins Christiane M, Hooker Stanley, Kittles Rick A, Carpten John |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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Influence of A9 Region Mutation in EphB2 Gene in the Prognosis of Patients with Colorectal Adenocarcinoma.
Annals of surgical oncology 2010 Dec . Vidaurreta M, Rafael S, Veganzones S, de la Orden V, Fernández C, Gómez-Casaseca R, Cerdán J, Maestro M |
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
PloS one 2010 5 (7): e11493. Jugessur Astanand, Shi Min, Gjessing Håkon Kristian, Lie Rolv Terje, Wilcox Allen James, Weinberg Clarice Ring, Christensen Kaare, Boyles Abee Lowman, Daack-Hirsch Sandra, Nguyen Truc Trung, Christiansen Lene, Lidral Andrew Carl, Murray Jeffrey Cla |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Germline EPHB2 receptor variants in familial colorectal cancer.
PloS one 2008 3 (8): e2885. Zogopoulos George, Jorgensen Claus, Bacani Julinor, Montpetit Alexandre, Lepage Pierre, Ferretti Vincent, Chad Lauren, Selvarajah Subani, Zanke Brent, Hudson Thomas J, Pawson Tony, Gallinger Stev |
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Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease.
PloS one 2008 3 (7): e2707. Li Yonghong, Rowland Charles, Xiromerisiou Georgia, Lagier Robert J, Schrodi Steven J, Dradiotis Efthimios, Ross David, Bui Nam, Catanese Joseph, Aggelakis Konstantinos, Grupe Andrew, Hadjigeorgiou Georgi |
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A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.
Journal of medical genetics 2006 Jun 43 (6): 507-11. Kittles R A, Baffoe-Bonnie A B, Moses T Y, Robbins C M, Ahaghotu C, Huusko P, Pettaway C, Vijayakumar S, Bennett J, Hoke G, Mason T, Weinrich S, Trent J M, Collins F S, Mousses S, Bailey-Wilson J, Furbert-Harris P, Dunston G, Powell I J, Carpten J |
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A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate.
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2006 May 43 (3): 310-6. Watanabe Akira, Akita Sadanori, Tin Nguyen Thi Duc, Natsume Nagato, Nakano Yoko, Niikawa Norio, Uchiyama Takeshi, Yoshiura Koh-ichi |
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EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis.
BMC cancer 2006 6 (): 145. Kokko Antti, Laiho Päivi, Lehtonen Rainer, Korja Sanna, Carvajal-Carmona Luis G, Järvinen Heikki, Mecklin Jukka-Pekka, Eng Charis, Schleutker Johanna, Tomlinson Ian P M, Vahteristo Pia, Aaltonen Lauri |
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The association of clinicopathological features and survival in colorectal cancer patients with kras mutation status.
Journal of cancer research and therapeutics 0 12 (1): 96-102. Akman Tulay, Oztop Ilhan, Baskin Yasemin, Unek Ilkay Tugba, Demir Necla, Ellidokuz Hulya, Yilmaz Ahmet Ug |
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- Page last updated:Feb 20, 2020
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