Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Neoplasms and MAPT[original query] |
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| Pharmacogenetic assessment of toxicity and outcome after platinum plus taxane chemotherapy in ovarian cancer: the Scottish Randomised Trial in Ovarian Cancer. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2007 Oct 25 (29): 4528-35. Marsh Sharon, Paul Jim, King Cristi R, Gifford Gillian, McLeod Howard L, Brown Robe |
| A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2. Neurology 2010 Sep 75 (13): 1189-94. Kay D M, Stevens C F, Hamza T H, Montimurro J S, Zabetian C P, Factor S A, Samii A, Griffith A, Roberts J W, Molho E S, Higgins D S, Gancher S, Moses L, Zareparsi S, Poorkaj P, Bird T, Nutt J, Schellenberg G D, Payami |
| Identification of novel mutations in endometrial cancer patients by whole-exome sequencing. International journal of oncology 2017 Mar . Chang Ya-Sian, Huang Hsien-Da, Yeh Kun-Tu, Chang Jan-Gow |
| CYP3A5 genotype and its impact on vincristine pharmacokinetics and development of neuropathy in Kenyan children with cancer. Pediatric blood & cancer 2018 03 65 (3): . Skiles Jodi L, Chiang ChienWei, Li Claire H, Martin Steve, Smith Ellen L, Olbara Gilbert, Jones David R, Vik Terry A, Mostert Saskia, Abbink Floor, Kaspers Gertjan J, Li Lang, Njuguna Festus, Sajdyk Tammy J, Renbarger Jamie |
Genome-wide association and multi-omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2022 Jun . Chung Jaeyoon, Das Anjali, Sun Xinyu, Sobreira Débora R, Leung Yuk Yee, Igartua Catherine, Mozaffari Sahar, Chou Yi-Fan, Thiagalingam Sam, Mez Jesse, Zhang Xiaoling, Jun Gyungah R, Stein Thor D, Kunkle Brian W, Martin Eden R, Pericak-Vance Margaret A, Mayeux Richard, Haines Jonathan L, Schellenberg Gerard D, Nobrega Marcelo A, Lunetta Kathryn L, Pinto Jayant M, Wang Li-San, Ober Carole, Farrer Lindsay |
| Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. EBioMedicine 2022 10 85 104290. Clark Lorraine N, Gao Yizhe, Wang Gao T, Hernandez Nora, Ashley-Koch Allison, Jankovic Joseph, Ottman Ruth, Leal Suzanne M, Rodriguez Sandra M Barral, Louis Elan |
| A Multigene-Panel Study Identifies Single Nucleotide Polymorphisms Associated with Prostate Cancer Risk. International journal of molecular sciences 2023 4 24 (8): . Maria Antonietta Manca, Fabio Scarpa, Davide Cossu, Elena Rita Simula, Daria Sanna, Stefano Ruberto, Marta Noli, Hajra Ashraf, Tatiana Solinas, Massimo Madonia, Roberto Cusano, Leonardo A Sec |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 18, 2023
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