Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement von Guerreiro, Rita João, Lohmann, Ebba, Brás, José Miguel, Gibbs, Jesse Raphael, Rohrer, Jonathan D, Gurunlian, Nicole, Dursun, Burcu, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, Singleton, Andrew, Hardy, John

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The Parkinson's Disease DNA Variant Browser von Kim, Jonggeol J., Makarious, Mary B., Bandres‐Ciga, Sara, Gibbs, Jesse Raphael, Ding, Jinhui, Hernandez, Dena G., Brooks, Janet, Grenn, Francis P., Iwaki, Hirotaka, Singleton, Andrew B., Nalls, Mike A., Blauwendraat, Cornelis

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A simple and efficient algorithm for genome-wide homozygosity analysis in disease von Liu, Wei, Ding, Jinhui, Gibbs, Jesse Raphael, Wang, Sue Jane, Hardy, John, Singleton, Andrew

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Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease von Guerreiro, Rita João, Lohmann, Ebba, Kinsella, Emma, Brás, José Miguel, Luu, Nga, Gurunlian, Nicole, Dursun, Burcu, Bilgic, Basar, Santana, Isabel, Hanagasi, Hasmet, Gurvit, Hakan, Gibbs, Jesse Raphael, Oliveira, Catarina, Emre, Murat, Singleton, Andrew

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Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement von Guerreiro, Rita João, Lohmann, Ebba, Brás, José Miguel, Gibbs, Jesse Raphael, Rohrer, Jonathan D., Gurunlian, Nicole, Dursun, Burcu, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, Singleton, Andrew, Hardy, John

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Age-modulated association between prefrontal NAA and the BDNF gene von Salehi, Basira, Preuss, Nora, van der Veen, Jan Willem, Shen, Jun, Neumeister, Alexander, Drevets, Wayne C., Hodgkinson, Colin, Goldman, David, Wendland, Jens R., Singleton, Andrew, Gibbs, Jesse R., Cookson, Mark R., Hasler, Gregor

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