Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and KIN[original query] |
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| Predictive genetic test decisions for Huntington's disease: context, appraisal and new moral imperatives. Social science & medicine (1982) 2004 Jan 58 (1): 137-49. Taylor Sandra |
| The HER2 I655V polymorphism and breast cancer risk in Ashkenazim. Epidemiology (Cambridge, Mass.) 2003 Nov 14 (6): 694-700. Rutter Joni L, Chatterjee Nilanjan, Wacholder Sholom, Struewing Jeffr |
| Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method. Archives of neurology 2008 Apr 65 (4): 467-74. Wang Yuanjia, Clark Lorraine N, Louis Elan D, Mejia-Santana Helen, Harris Juliette, Cote Lucien J, Waters Cheryl, Andrews Howard, Ford Blair, Frucht Steven, Fahn Stanley, Ottman Ruth, Rabinowitz Daniel, Marder Kar |
| Cerebrospinal fluid tau levels are a marker for molecular subtype in sporadic Creutzfeldt-Jakob disease. Neurobiology of aging 2015 Feb . Karch André, Hermann Peter, Ponto Claudia, Schmitz Matthias, Arora Amandeep, Zafar Saima, Llorens Franc, Müller-Heine Annika, Zerr In |
| Impairment of memory generalization in preclinical autosomal dominant Alzheimer's disease mutation carriers. Neurobiology of aging 2018 3 65 149-157. Petok Jessica R, Myers Catherine E, Pa Judy, Hobel Zachary, Wharton David M, Medina Luis D, Casado Maria, Coppola Giovanni, Gluck Mark A, Ringman John |
| Modern view on epidermal dysplasia carcinogenesis. Experimental oncology 2019 Sep 41 (3): 216-223. Oshyvalova O, Rossokha |
| Penetrance of Glucocerebrosidase (GBA) Mutations in Parkinson's Disease: A Kin Cohort Study. Movement disorders : official journal of the Movement Disorder Society 2020 8 35 (11): 2111-2114. Balestrino Roberta, Tunesi Sara, Tesei Silvana, Lopiano Leonardo, Zecchinelli Anna L, Goldwurm Stefa |
| Karyomegalic interstitial nephritis with a novel FAN1 gene mutation and concurrent ALECT2 amyloidosis. BMC nephrology 2020 3 21 (1): 74. Law Steven, Gillmore Julian, Gilbertson Janet A, Bass Paul, Salama Alan |
| Limited Effect of Y Chromosome Variation on Coronary Artery Disease and Mortality in UK Biobank-Brief Report. Arteriosclerosis, thrombosis, and vascular biology 2022 7 42 (9): 1198-1206. Timmers Paul R H J, Wilson James |
| The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young. medRxiv : the preprint server for health sciences 2023 4 . Puckelwartz Megan J, Pesce Lorenzo L, Hernandez Edgar J, Webster Gregory, Dellefave-Castillo Lisa M, Russell Mark W, Geisler Sarah S, Kearns Samuel D, Etheridge Felix K, Etheridge Susan P, Monroe Tanner O, Pottinger Tess D, Kannankeril Prince J, Shoemaker M Benjamin, Fountain Darlene, Roden Dan M, MacLeod Heather, Burns Kristin M, Yandell Mark, Tristani-Firouzi Martin, George Alfred L, McNally Elizabeth |
| The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young. Genome medicine 2024 1 16 (1): 13. Megan J Puckelwartz, Lorenzo L Pesce, Edgar J Hernandez, Gregory Webster, Lisa M Dellefave-Castillo, Mark W Russell, Sarah S Geisler, Samuel D Kearns, Felix Karthik, Susan P Etheridge, Tanner O Monroe, Tess D Pottinger, Prince J Kannankeril, M Benjamin Shoemaker, Darlene Fountain, Dan M Roden, Meghan Faulkner, Heather M MacLeod, Kristin M Burns, Mark Yandell, Martin Tristani-Firouzi, Alfred L George, Elizabeth M McNal |
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