Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and PCM1[original query] |
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| PCM1 and schizophrenia: a replication study in the Northern Swedish population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Sep 153B (6): 1240-3. Moens Lotte N, Ceulemans Shana, Alaerts Maaike, Van Den Bossche Maarten J A, Lenaerts An-Sofie, De Zutter Sonia, Norrback Karl-Fredrik, Adolfsson Rolf, Del-Favero Jurg |
| RACK1 is a candidate gene associated with the prognosis of patients with early stage non-small cell lung cancer. Oncotarget 2015 Feb 6 (6): 4451-66. Choi Yi-Young, Lee Shin Yup, Lee Won Kee, Jeon Hyo-Sung, Lee Eung Bae, Lee Hyun Cheol, Choi Jin Eun, Kang Hyo-Gyoung, Lee Eun Jin, Bae Eun Young, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Kim In-San, Lee Myung Hoon, Kim Young Tae, Jheon Sanghoon, Park Jae Yo |
| Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency. BioMed research international 2016 3 2015 862039. Sandgren Johanna, Holm Stefan, Marino Ana Maria, Asmundsson Jurate, Grillner Pernilla, Nistér Monica, Díaz de Ståhl Teresi |
| Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot. Circulation research 2019 Feb 124 (4): 553-563. Page Donna J, Miossec Matthieu J, Williams Simon G, Monaghan Richard M, Fotiou Elisavet, Cordell Heather J, Sutcliffe Louise, Topf Ana, Bourgey Mathieu, Bourque Guillaume, Eveleigh Robert, Dunwoodie Sally L, Winlaw David S, Bhattacharya Shoumo, Breckpot Jeroen, Devriendt Koenraad, Gewillig Marc, Brook J David, Setchfield Kerry J, Bu'Lock Frances A, O'Sullivan John, Stuart Graham, Bezzina Connie R, Mulder Barbara J M, Postma Alex V, Bentham James R, Baron Martin, Bhaskar Sanjeev S, Black Graeme C, Newman William G, Hentges Kathryn E, Lathrop G Mark, Santibanez-Koref Mauro, Keavney Bernard |
| Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
| Chemotherapy-free treatment targeting fusions and driver mutations in KRAS wild-type pancreatic ductal adenocarcinoma, a case series. Therapeutic advances in medical oncology 2024 5 16 17588359241253113. Maahum Mehdi, Aniko Szabo, Aditya Shreenivas, James P Thomas, Susan Tsai, Kathleen K Christians, Douglas B Evans, Callisia N Clarke, William A Hall, Beth Erickson, Gulrayz Ahmed, Bicky Thapa, Thomas McFall, Ben George, Razelle Kurzrock, Mandana Kamg |
- Page last reviewed:Feb 1, 2024
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