Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and APH1B[original query] |
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| Male-specific association between a gamma-secretase polymorphism and premature coronary atherosclerosis. PloS one 2008 3 (11): e3662. van Loo Karen M J, Dejaegere Tim, van Zweeden Martine, van Schijndel Jessica E, Wijmenga Cisca, Trip Mieke D, Martens Gerard J |
| Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease. Neurobiology of aging 2011 Mar 32 (3): 556.e13-23. Bekris L M, Galloway N M, Millard S, Lockhart D, Li G, Galasko D R, Farlow M R, Clark C M, Quinn J F, Kaye J A, Schellenberg G D, Leverenz J B, Seubert P, Tsuang D W, Peskind E R, Yu C |
| Cerebrospinal fluid Aß42 levels and APP processing pathway genes in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2015 Jun 30 (7): 936-44. Bekris Lynn M, Tsuang Debby W, Peskind Elaine R, Yu Chang E, Montine Thomas J, Zhang Jing, Zabetian Cyrus P, Leverenz James |
| Full exome sequencing of 11 families with Hidradenitis suppurativa. Journal of the European Academy of Dermatology and Venereology : JEADV 2020 Dec . Theut Riis P, Loft I C, Yazdanyar S, Kjaersgaard Andersen R, Pedersen O B, Ring H C, Huber R, Sultan M, Loesche C, Saunte D M L, Jemec G B |
| The association of clinical phenotypes to known AD/FTD genetic risk loci and their inter-relationship. PloS one 2020 11 15 (11): e0241552. Li Qingqin S, Tian Chao, , Hinds David, Seabrook Guy |
Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer's disease risk genes.
Nature genetics 2021 03 53 (3): 392-402. Schwartzentruber Jeremy, Cooper Sarah, Liu Jimmy Z, Barrio-Hernandez Inigo, Bello Erica, Kumasaka Natsuhiko, Young Adam M H, Franklin Robin J M, Johnson Toby, Estrada Karol, Gaffney Daniel J, Beltrao Pedro, Bassett Andr |
| Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritage. Journal of the European Academy of Dermatology and Venereology : JEADV 2021 Feb . Vural Seçil, Baumgartner Mark, Lichtner Peter, Eckstein Gertrud, Hariry Housien, Chen WenChieh, Ruzicka Thomas, Melnik Bodo, Plewig Gerd, Wagner Matthias, Giehl Kathrin |
| Dysregulated expression levels of APH1B in peripheral blood are associated with brain atrophy and amyloid-? deposition in Alzheimer's disease. Alzheimer's research & therapy 2021 11 13 (1): 183. Park Young Ho, Pyun Jung-Min, Hodges Angela, Jang Jae-Won, Bice Paula J, Kim SangYun, Saykin Andrew J, Nho Kwangsik, |
| The Role of NOTCH Pathway Genes in the Inherited Susceptibility to Aortic Stenosis. Journal of cardiovascular development and disease 2024 7 11 (7): . Olga Irtyuga, Rostislav Skitchenko, Mary Babakekhyan, Dmitrii Usoltsev, Svetlana Tarnovskaya, Anna Malashicheva, Yulya Fomicheva, Oksana Rotar, Olga Moiseeva, Ulyana Shadrina, Mykyta Artomov, Anna Kostareva, Evgeny Shlyakh |
| Hypothesis-based investigation of known AD risk variants reveals the genetic underpinnings of neuropathological lesions observed in Alzheimer's-type dementia. Acta neuropathologica 2024 10 148 (1): 55. Celeste Laureyssen, Fahri Küçükali, Jasper Van Dongen, Klara Gawor, Sandra O Tomé, Alicja Ronisz, Markus Otto, Christine A F von Arnim, Philip Van Damme, Rik Vandenberghe, Dietmar Rudolf Thal, Kristel Sleege |
| Genome-wide association neural networks identify genes linked to family history of Alzheimer's disease. Briefings in bioinformatics 2025 1 26 (1): . Upamanyu Ghose, William Sproviero, Laura Winchester, Najaf Amin, Taiyu Zhu, Danielle Newby, Brittany S Ulm, Angeliki Papathanasiou, Liu Shi, Qiang Liu, Marco Fernandes, Cassandra Adams, Ashwag Albukhari, Majid Almansouri, Hani Choudhry, Cornelia van Duijn, Alejo Nevado-Holga |
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