Antisense-mediated Exon Skipping Decreases Tau Protein Expression: A Potential Therapy For Tauopathies

por Sud, Reeteka, Geller, Evan T, Schellenberg, Gerard D
Publicado 2014

Genome-wide association reveals genetic effects on human Aβ(42 )and τ protein levels in cerebrospinal fluids: a case control study

por Han, Mi-Ryung, Schellenberg, Gerard D, Wang, Li-San
Publicado 2010

Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk

por Carayol, Jerome, Schellenberg, Gerard D, Tores, Frederic, Hager, Jörg, Ziegler, Andreas, Dawson, Geraldine
Publicado 2010

Autism risk assessment in siblings of affected children using sex-specific genetic scores

por Carayol, Jerome, Schellenberg, Gerard D, Dombroski, Beth, Genin, Emmanuelle, Rousseau, Francis, Dawson, Geraldine
Publicado 2011

parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism

por Poorkaj, Parvoneh, Moses, Lina, Montimurro, Jennifer S, Nutt, John G, Schellenberg, Gerard D, Payami, Haydeh
Publicado 2005

Measuring informed consent capacity in an Alzheimer's disease clinical trial

por Guarino, Peter D., Vertrees, Julia E., Asthana, Sanjay, Sano, Mary, Llorente, Maria D., Pallaki, Muralidhar, Love, Susan, Schellenberg, Gerard D., Dysken, Maurice W.
Publicado 2016

One for all and all for One: Improving replication of genetic studies through network diffusion

por Lancour, Daniel, Naj, Adam, Mayeux, Richard, Haines, Jonathan L., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Crovella, Mark, Farrer, Lindsay A., Kasif, Simon
Publicado 2018

DRAW+SneakPeek: Analysis workflow and quality metric management for DNA-seq experiments

por Lin, Chiao-Feng, Valladares, Otto, Childress, D. Micah, Klevak, Egor, Geller, Evan T., Hwang, Yih-Chii, Tsai, Ellen A., Schellenberg, Gerard D., Wang, Li-San
Publicado 2013

The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer’s disease

por Stutzbach, Lauren D, Xie, Sharon X, Naj, Adam C, Albin, Roger, Gilman, Sid, Lee, Virginia M Y, Trojanowski, John Q, Devlin, Bernie, Schellenberg, Gerard D
Publicado 2013

INFERNO: inferring the molecular mechanisms of noncoding genetic variants

por Amlie-Wolf, Alexandre, Tang, Mitchell, Mlynarski, Elisabeth E, Kuksa, Pavel P, Valladares, Otto, Katanic, Zivadin, Tsuang, Debby, Brown, Christopher D, Schellenberg, Gerard D, Wang, Li-San
Publicado 2018

VCPA: genomic variant calling pipeline and data management tool for Alzheimer’s Disease Sequencing Project

por Leung, Yuk Yee, Valladares, Otto, Chou, Yi-Fan, Lin, Han-Jen, Kuzma, Amanda B, Cantwell, Laura, Qu, Liming, Gangadharan, Prabhakaran, Salerno, William J, Schellenberg, Gerard D, Wang, Li-San
Publicado 2019

VCPA: genomic variant calling pipeline and data management tool for Alzheimer’s Disease Sequencing Project

por Leung, Yuk Yee, Valladares, Otto, Chou, Yi-Fan, Lin, Han-Jen, Kuzma, Amanda B, Cantwell, Laura, Qu, Liming, Gangadharan, Prabhakaran, Salerno, William J, Schellenberg, Gerard D, Wang, Li-San
Publicado 2019

A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism

por Carayol, Jérôme, Schellenberg, Gerard D., Dombroski, Beth, Amiet, Claire, Génin, Bérengère, Fontaine, Karine, Rousseau, Francis, Vazart, Céline, Cohen, David, Frazier, Thomas W., Hardan, Antonio Y., Dawson, Geraldine, Rio Frio, Thomas
Publicado 2014

Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project

por Lee, Wan-Ping, Tucci, Albert A., Conery, Mitchell, Leung, Yuk Yee, Kuzma, Amanda B., Valladares, Otto, Chou, Yi-Fan, Lu, Wenbin, Wang, Li-San, Schellenberg, Gerard D., Tzeng, Jung-Ying
Publicado 2021

Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease

por Zhang, Xiaoling, Farrell, John J., Tong, Tong, Hu, Junming, Zhu, Congcong, Wang, Li‐San, Mayeux, Richard, Haines, Jonathan L., Pericak‐Vance, Margaret A., Schellenberg, Gerard D., Lunetta, Kathryn L., Farrer, Lindsay A.
Publicado 2021

Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

por He, Xin, Sanders, Stephan J., Liu, Li, De Rubeis, Silvia, Lim, Elaine T., Sutcliffe, James S., Schellenberg, Gerard D., Gibbs, Richard A., Daly, Mark J., Buxbaum, Joseph D., State, Matthew W., Devlin, Bernie, Roeder, Kathryn
Publicado 2013

Transmission of tauopathy strains is independent of their isoform composition

por He, Zhuohao, McBride, Jennifer D., Xu, Hong, Changolkar, Lakshmi, Kim, Soo-jung, Zhang, Bin, Narasimhan, Sneha, Gibbons, Garrett S., Guo, Jing L., Kozak, Michael, Schellenberg, Gerard D., Trojanowski, John Q., Lee, Virginia M. -Y.
Publicado 2020

Gene-Environment Interactions in Progressive Supranuclear Palsy

por Litvan, Irene, Proudfoot, James A., Martin, Eden R., Standaert, David, Riley, David, Hall, Deborah, Marras, Connie, Bayram, Ece, Dubinsky, Richard M., Bordelon, Yvette, Reich, Stephen, Shprecher, David, Kluger, Benzi, Cunningham, Christopher, Schellenberg, Gerard D., Jankovic, Joseph
Publicado 2021

Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer’s Diseases Sequencing Project Subjects

por Wang, Hui, Dombroski, Beth A, Cheng, Po-Liang, Tucci, Albert, Si, Ya-Qin, Farrell, John J, Tzeng, Jung-Ying, Leung, Yuk Yee, Malamon, John S, Wang, Li-San, Vardarajan, Badri N, Farrer, Lindsay A, Schellenberg, Gerard D, Lee, Wan-Ping
Publicado 2023

The Arctic AβPP mutation leads to Alzheimer’s disease pathology with highly variable topographic deposition of differentially truncated Aβ

por Kalimo, Hannu, Lalowski, Maciej, Bogdanovic, Nenad, Philipson, Ola, Bird, Thomas D, Nochlin, David, Schellenberg, Gerard D, Brundin, RoseMarie, Olofsson, Tommie, Soliymani, Rabah, Baumann, Marc, Wirths, Oliver, Bayer, Thomas A, Nilsson, Lars NG, Basun, Hans, Lannfelt, Lars, Ingelsson, Martin
Publicado 2013