A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV data

por Nishiyama, Takeshi, Takahashi, Kunihiko, Tango, Toshiro, Pinto, Dalila, Scherer, Stephen W, Takami, Satoshi, Kishino, Hirohisa
Publicado 2011

Parallel changes in serum proteins and diffusion tensor imaging in methamphetamine-associated psychosis

por Breen, Michael S., Uhlmann, Anne, Ozcan, Sureyya, Chan, Man, Pinto, Dalila, Bahn, Sabine, Stein, Dan J.
Publicado 2017

Candidate genes and biological processes in de novo CNVs from autistic individuals

por Noh, Hyun J, Marshall, Christian R, Pinto, Dalila, Scherer, Stephen W, Ponting, Chris P, Webber, Caleb
Publicado 2010

Characterization of Large Copy Number Variation in Mexican Type 2 Diabetes subjects

por de Jesús Ascencio-Montiel, Iván, Pinto, Dalila, Parra, Esteban J., Valladares-Salgado, Adán, Cruz, Miguel, Scherer, Stephen W.
Publicado 2017

A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3

por Pagnamenta, Alistair T., Holt, Richard, Yusuf, Mohammed, Pinto, Dalila, Wing, Kirsty, Betancur, Catalina, Scherer, Stephen W., Volpi, Emanuela V., Monaco, Anthony P.
Publicado 2011

A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder

por Bacchelli, Elena, Ceroni, Fabiola, Pinto, Dalila, Lomartire, Silvia, Giannandrea, Maila, D'Adamo, Patrizia, Bonora, Elena, Parchi, Piero, Tancredi, Raffaella, Battaglia, Agatino, Maestrini, Elena
Publicado 2014

Genome-Wide Survey of Large Rare Copy Number Variants in Alzheimer’s Disease Among Caribbean Hispanics

por Ghani, Mahdi, Pinto, Dalila, Lee, Joseph H., Grinberg, Yakov, Sato, Christine, Moreno, Danielle, Scherer, Stephen W., Mayeux, Richard, St. George-Hyslop, Peter, Rogaeva, Ekaterina
Publicado 2012

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

por Vieland, Veronica J., Hallmayer, Joachim, Huang, Yungui, Pagnamenta, Alistair T., Pinto, Dalila, Khan, Hameed, Monaco, Anthony P., Paterson, Andrew D., Scherer, Stephen W., Sutcliffe, James S., Szatmari, Peter
Publicado 2011

mTADA is a framework for identifying risk genes from de novo mutations in multiple traits

por Nguyen, Tan-Hoang, Dobbyn, Amanda, Brown, Ruth C., Riley, Brien P., Buxbaum, Joseph D., Pinto, Dalila, Purcell, Shaun M., Sullivan, Patrick F., He, Xin, Stahl, Eli A.
Publicado 2020

Network Topologies and Convergent Aetiologies Arising from Deletions and Duplications Observed in Individuals with Autism

por Noh, Hyun Ji, Ponting, Chris P., Boulding, Hannah C., Meader, Stephen, Betancur, Catalina, Buxbaum, Joseph D., Pinto, Dalila, Marshall, Christian R., Lionel, Anath C., Scherer, Stephen W., Webber, Caleb
Publicado 2013

Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms

por Monsuur, Alienke J., de Bakker, Paul I. W., Zhernakova, Alexandra, Pinto, Dalila, Verduijn, Willem, Romanos, Jihane, Auricchio, Renata, Lopez, Ana, van Heel, David A., Crusius, J. Bart A, Wijmenga, Cisca
Publicado 2008

Correction: Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms

por Monsuur, Alienke J., de Bakker, Paul I. W., Zhernakova, Alexandra, Pinto, Dalila, Verduijn, Willem, Romanos, Jihane, Auricchio, Renata, Lopez, Ana, van Heel, David A., Crusius, J. Bart A, Wijmenga, Cisca
Publicado 2009

Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis

por Holmes, Greg, Gonzalez-Reiche, Ana S., Lu, Na, Zhou, Xianxiao, Rivera, Joshua, Kriti, Divya, Sebra, Robert, Williams, Anthony A., Donovan, Michael J., Potter, S. Steven, Pinto, Dalila, Zhang, Bin, van Bakel, Harm, Jabs, Ethylin Wang
Publicado 2020

Identifying Signatures of Natural Selection in Tibetan and Andean Populations Using Dense Genome Scan Data

por Bigham, Abigail, Bauchet, Marc, Pinto, Dalila, Mao, Xianyun, Akey, Joshua M., Mei, Rui, Scherer, Stephen W., Julian, Colleen G., Wilson, Megan J., López Herráez, David, Brutsaert, Tom, Parra, Esteban J., Moore, Lorna G., Shriver, Mark D.
Publicado 2010

Towards a comprehensive structural variation map of an individual human genome

por Pang, Andy W, MacDonald, Jeffrey R, Pinto, Dalila, Wei, John, Rafiq, Muhammad A, Conrad, Donald F, Park, Hansoo, Hurles, Matthew E, Lee, Charles, Venter, J Craig, Kirkness, Ewen F, Levy, Samuel, Feuk, Lars, Scherer, Stephen W
Publicado 2010

High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy

por Pai, Balagopal, Tome-Garcia, Jessica, Cheng, Wan Sze, Nudelman, German, Beaumont, Kristin G., Ghatan, Saadi, Panov, Fedor, Caballero, Elodia, Sarpong, Kwadwo, Marcuse, Lara, Yoo, Jiyeoun, Jiang, Yan, Schaefer, Anne, Akbarian, Schahram, Sebra, Robert, Pinto, Dalila, Zaslavsky, Elena, Tsankova, Nadejda M.
Publicado 2022

Correction: High-resolution transcriptomics informs glial pathology in human temporal lobe epilepsy

por Pai, Balagopal, Tome‑Garcia, Jessica, Cheng, Wan Sze, Nudelman, German, Beaumont, Kristin G., Ghatan, Saadi, Panov, Fedor, Caballero, Elodia, Sarpong, Kwadwo, Marcuse, Lara, Yoo, Jiyeoun, Jiang, Yan, Schaefer, Anne, Akbarian, Schahram, Sebra, Robert, Pinto, Dalila, Zaslavsky, Elena, Tsankova, Nadejda M.
Publicado 2022

Evaluating performance and applications of sample-wise cell deconvolution methods on human brain transcriptomic data

por Dai, Rujia, Chu, Tianyao, Zhang, Ming, Wang, Xuan, Jourdon, Alexandre, Wu, Feinan, Mariani, Jessica, Vaccarino, Flora M., Lee, Donghoon, Fullard, John F., Hoffman, Gabriel E., Roussos, Panos, Wang, Yue, Wang, Xusheng, Pinto, Dalila, Wang, Sidney H., Zhang, Chunling, Chen, Chao, Liu, Chunyu
Publicado 2023

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

por Pagnamenta, Alistair T, Khan, Hameed, Walker, Susan, Gerrelli, Dianne, Wing, Kirsty, Bonaglia, Maria Clara, Giorda, Roberto, Berney, Tom, Mani, Elisa, Molteni, Massimo, Pinto, Dalila, Le Couteur, Ann, Hallmayer, Joachim, Sutcliffe, James S, Szatmari, Peter, Paterson, Andrew D, Scherer, Stephen W, Vieland, Veronica J, Monaco, Anthony P
Publicado 2010

The impact of common variants on gene expression in the human brain: from RNA to protein to schizophrenia risk

por Liang, Qiuman, Jiang, Yi, Shieh, Annie W., Zhou, Dan, Chen, Rui, Wang, Feiran, Xu, Meng, Niu, Mingming, Wang, Xusheng, Pinto, Dalila, Wang, Yue, Cheng, Lijun, Vadukapuram, Ramu, Zhang, Chunling, Grennan, Kay, Giase, Gina, White, Kevin P, Peng, Junmin, Li, Bingshan, Liu, Chunyu, Chen, Chao, Wang, Sidney H.
Publicado 2023