Genomic architecture of autism from comprehensive whole-genome sequence annotation

Autor: Trost, Brett, Thiruvahindrapuram, Bhooma, Chan, Ada J.S., Engchuan, Worrawat, Higginbotham, Edward J., Howe, Jennifer L., Loureiro, Livia O., Reuter, Miriam S., Roshandel, Delnaz, Whitney, Joe, Zarrei, Mehdi, Bookman, Matthew, Somerville, Cherith, Shaath, Rulan, Abdi, Mona, Aliyev, Elbay, Patel, Rohan V., Nalpathamkalam, Thomas, Pellecchia, Giovanna, Hamdan, Omar, Kaur, Gaganjot, Wang, Zhuozhi, MacDonald, Jeffrey R., Wei, John, Sung, Wilson W.L., Lamoureux, Sylvia, Hoang, Ny, Selvanayagam, Thanuja, Deflaux, Nicole, Geng, Melissa, Ghaffari, Siavash, Bates, John, Young, Edwin J., Ding, Qiliang, Shum, Carole, D'Abate, Lia, Bradley, Clarrisa A., Rutherford, Annabel, Aguda, Vernie, Apresto, Beverly, Chen, Nan, Desai, Sachin, Du, Xiaoyan, Fong, Matthew L.Y., Pullenayegum, Sanjeev, Samler, Kozue, Wang, Ting, Ho, Karen, Paton, Tara, Pereira, Sergio L., Herbrick, Jo-Anne, Wintle, Richard F., Fuerth, Jonathan, Noppornpitak, Juti, Ward, Heather, Magee, Patrick, Al Baz, Ayman, Kajendirarajah, Usanthan, Kapadia, Sharvari, Vlasblom, Jim, Valluri, Monica, Green, Joseph, Seifer, Vicki, Quirbach, Morgan, Rennie, Olivia, Kelley, Elizabeth, Masjedi, Nina, Lord, Catherine, Szego, Michael J., Zawati, Ma'n H., Lang, Michael, Strug, Lisa J., Marshall, Christian R., Costain, Gregory, Calli, Kristina, Iaboni, Alana, Yusuf, Afiqah, Ambrozewicz, Patricia, Gallagher, Louise, Amaral, David G., Brian, Jessica, Elsabbagh, Mayada, Georgiades, Stelios, Messinger, Daniel S., Ozonoff, Sally, Sebat, Jonathan, Sjaarda, Calvin, Smith, Isabel M., Szatmari, Peter, Zwaigenbaum, Lonnie, Kushki, Azadeh, Frazier, Thomas W., Vorstman, Jacob A.S., Fakhro, Khalid A., Fernandez, Bridget A., Lewis, M.E. Suzanne, Weksberg, Rosanna, Fiume, Marc, Yuen, Ryan K.C., Anagnostou, Evdokia, Sondheimer, Neal, Glazer, David, Hartley, Dean M., Scherer, Stephen W.

Publikováno v: In Cell 10 November 2022 185(23):4409-4427

Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant.

Autor: Yip, Silas, Calli, Kristina, Qiao, Ying, Trost, Brett, Scherer, Stephen W., Lewis, M. E. Suzanne

Publikováno v: Genes; Dec2023, Vol. 14 Issue 12, p2122, 11p

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Blood Mitochondrial DNA Content in HIV-Exposed Uninfected Children with Autism Spectrum Disorder.

Autor: Budd, Matthew A.^1,2 m.budd@alumni.ubc.ca, Calli, Kristina³ kcalli@mail.ubc.ca, Samson, Lindy^4,5 Samson@cheo.on.ca, Bowes, Jennifer⁵, Hsieh, Anthony Y. Y.^1,2, Forbes, John C.⁶ jcforbes@shaw.ca, Bitnun, Ari⁷ ari.bitnun@sickkids.ca, Singer, Joel^8,9 jsinger@hivnet.ubc.ca, Kakkar, Fatima¹⁰ fatima.kakkar@umontreal.ca, Alimenti, Ariane^6,11 emaan@cw.bc.ca, Maan, Evelyn J.^11,12, Lewis, M. E. Suzanne³, Gentile, Carole¹³ cgentile@cheo.on.ca, Côté, Hélène C.F.^1,2,12 helene.cote@ubc.ca, Brophy, Jason C.^4,5

Publikováno v: Viruses (1999-4915). Feb2018, Vol. 10 Issue 2, p77. 16p.

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