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3. CELF Control in the Neuron

Jones, Devin
2022
Theses
NeurosciencesNeurobiologyGeneticsRNA-protein interactionsGene expressionMutagenesisNeurons

16. Genome-wide Burden Of Rare Short Deletions Is Enriched In Major Depressive Disorder In Four Cohorts

Zhang, Xianglong; Abdellaoui, Abdel; Rucker, James; de Jong, Simone; Potash, James B.; Weissman, Myrna M.; Shi, Jianxin; Knowles, James A.; Pato, Carlos; Pato, Michele; Sobell, Janet; Smit, Johannes H.; Hottenga, Jouke-Jan; de Geus, Eco J.C.; Lewis, Cathryn M.; Buttenschøn, Henriette N.; Craddock, Nick; Jones, Ian; Jones, Lisa; McGuffin, Peter; Mors, Ole; Owen, Michael J.; Preisig, Martin; Rietschel, Marcella; Rice, John P.; Rivera, Margarita; Uher, Rudolf; Gejman, Pablo V.; Sanders, Alan R.; Boomsma, Dorret; Penninx, Brenda W.J.H.; Breen, Gerome; Levinson, Douglas F.
2019
Articles
PsychiatryEpidemiologyDepression, MentalGeneticsNeurosciences

18. De novo and inherited private variants in MAP1B in periventricular nodular heterotopia

Heinzen, Erin L.; O’Neill, Adam C.; Zhu, Xiaolin; Allen, Andrew S.; Bahlo, Melanie; Chelly, Jamel; Chen, Ming Hui; Dobyns, William B.; Freytag, Saskia; Guerrini, Renzo; Leventer, Richard J.; Poduri, Annapurna; Robertson, Stephen P.; Walsh, Christopher A.; Zhang, Mengqi; Epilepsy Phenome/Genome Project; Epi4K Consortium
2018
Articles
GeneticsNeurosciencesEpilepsyGenomics

19. Population-specific genetic modification of Huntington's disease in Venezuela

Chao, Michael J.; Kim, Kyung-Hee; Shin, Jun Wan; Lucente, Diane; Wheeler, Vanessa; Li, Hong; Roach, Jared C.; Hood, Leroy; Wexler, Nancy S.; Jardim, Laura B.; Holmans, Peter; Jones, Lesley; Orth, Michael; Kwak, Seung; MacDonald, Marcy; Gusella, James; Lee, Jong Min
2018
Articles
Huntington's diseaseGeneticsTherapeutics--ResearchNeurosciencesNeurogenetics

24. Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias

Gan, Shi-Rui; Wang, Jie; Figueroa, Karla P.; Pulst, Stefan M.; Tomishon, Darya; Lee, Danielle; Perlman, Susan; Wilmot, George; Gomez, Christopher M.; Schmahmann, Jeremy; Paulson, Henry; Shakkottai, Vikram G.; Ying, Sarah H.; Zesiewicz, Theresa; Bushara, Khalaf; Geschwind, Michael; Xia, Guangbin; Subramony, S. H.; Ashizawa, Tetsuo; Kuo, Sheng-Han
2017
Articles
AtaxiaTremorGeneticsNeurosciencesNeurology

44. Genome-Wide Association Analysis Identifies a Mutation in the Thiamine Transporter 2 (SLC19A3) Gene Associated with Alaskan Husky Encephalopathy

Vernau, Karen M.; Runstadler , Jonathan A.; Brown, Emily A.; Cameron, Jessie M.; Huson, Heather J.; Higgins, Robert J.; Ackerley, Cameron; Sturges, Beverly K.; Dickinson, Peter J.; Puschner, Birgit; Giulivi, Cecilia; Shelton, G. Diane; Robinson, Brian H.; DiMauro, Salvatore; Bollen, Andrew W.; Bannasch, Danika L.
2013
Articles
GeneticsPathologyEpidemiologyNeurosciences

50. Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk

Van Broeckhoven, Christine; De Deyn, Peter P.; Sleegers, Kristel; Mattheijssens, Maria; Peeters, Karin; Mayeux, Richard Paul; St. George-Hyslop, Peter; Amouyel, Philippe; Van Dongen, Jasper; Vermeulen, Steven; Pasquier, Florence; Le Bastard, Nathalie; Vandenberghe, Rik; Rogaeva, Ekaterina; Lambert, Jean-Charles; Engelborghs, Sebastiaan; Brouwers, Nathalie; Bettens, Karolien
2012
Articles
Meta-analysisAlzheimer's disease--ResearchNervous system--Degeneration--Genetic aspectsAmino acid sequenceNeurosciencesGeneticsMedical sciences