A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface by Gupta, Gagan D., Coyaud, Étienne, Gonçalves, João, Mojarad, Bahareh A., Liu, Yi, Wu, Qianzhu, Gheiratmand, Ladan, Comartin, David, Tkach, Johnny M., Cheung, Sally W.T., Bashkurov, Mikhail, Hasegan, Monica, Knight, James D., Lin, Zhen-Yuan, Schueler, Markus, Hildebrandt, Friedhelm, Moffat, Jason, Gingras, Anne-Claude, Raught, Brian, Pelletier, Laurence

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Genome-wide tandem repeat expansions contribute to schizophrenia risk by Mojarad, Bahareh A, Engchuan, Worrawat, Trost, Brett, Backstrom, Ian, Yin, Yue, Thiruvahindrapuram, Bhooma, Pallotto, Linda, Mitina, Aleksandra, Khan, Mahreen, Pellecchia, Giovanna, Haque, Bushra, Guo, Keyi, Heung, Tracy, Costain, Gregory, Scherer, Stephen W, Marshall, Christian R, Pearson, Christopher E, Bassett, Anne S, Yuen, Ryan K C

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Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia by Mojarad, Bahareh A, Yin, Yue, Manshaei, Roozbeh, Backstrom, Ian, Costain, Gregory, Heung, Tracy, Merico, Daniele, Marshall, Christian R, Bassett, Anne S, Yuen, Ryan K C

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Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences by Manshaei, Roozbeh, Merico, Daniele, Reuter, Miriam S., Engchuan, Worrawat, Mojarad, Bahareh A., Chaturvedi, Rajiv, Heung, Tracy, Pellecchia, Giovanna, Zarrei, Mehdi, Nalpathamkalam, Thomas, Khan, Reem, Okello, John B. A., Liston, Eriskay, Curtis, Meredith, Yuen, Ryan K. C., Marshall, Christian R., Jobling, Rebekah K., Oechslin, Erwin, Wald, Rachel M., Silversides, Candice K., Scherer, Stephen W., Kim, Raymond H., Bassett, Anne S.

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CEP19 cooperates with FOP and CEP350 to drive early steps in the ciliogenesis programme by Mojarad, Bahareh A., Gupta, Gagan D., Hasegan, Monica, Goudiam, Oumou, Basto, Renata, Gingras, Anne-Claude, Pelletier, Laurence

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Genome-wide detection of tandem DNA repeats that are expanded in autism by Trost, Brett, Engchuan, Worrawat, Nguyen, Charlotte M, Thiruvahindrapuram, Bhooma, Dolzhenko, Egor, Backstrom, Ian, Mirceta, Mila, Mojarad, Bahareh A, Yin, Yue, Dov, Alona, Chandrakumar, Induja, Prasolava, Tanya, Shum, Natalie, Hamdan, Omar, Pellecchia, Giovanna, Howe, Jennifer L, Whitney, Joseph, Klee, Eric W, Baheti, Saurabh, Amaral, David G, Anagnostou, Evdokia, Elsabbagh, Mayada, Fernandez, Bridget A, Hoang, Ny, Lewis, M E Suzanne, Liu, Xudong, Sjaarda, Calvin, Smith, Isabel M, Szatmari, Peter, Zwaigenbaum, Lonnie, Glazer, David, Hartley, Dean, Stewart, A Keith, Eberle, Michael A, Sato, Nozomu, Pearson, Christopher E, Scherer, Stephen W, Yuen, Ryan K C

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Clinical whole-genome sequencing and FISH identify two different fusion partners for NUP98 in a patient with acute myeloid leukemia: A case report by Mojarad, Bahareh A, Crees, Zachary D, Schroeder, Molly C, Xiang, Zhifu, Vader, Justin, Sina, Jason, Jacoby, Meagan, Frater, John L, Duncavage, Eric J, Spencer, David H, Lavine, Kory, Neidich, Julie A, Amarillo, Ina

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Genome-wide detection of tandem DNA repeats expanded in autism by Trost, Brett, Engchuan, Worrawat, Nguyen, Charlotte M., Thiruvahindrapuram, Bhooma, Dolzhenko, Egor, Backstrom, Ian, Mirceta, Mila, Mojarad, Bahareh A., Yin, Yue, Dov, Alona, Chandrakumar, Induja, Prasolava, Tanya, Shum, Natalie, Hamdan, Omar, Pellecchia, Giovanna, Howe, Jennifer L., Whitney, Joseph, Klee, Eric W., Baheti, Saurabh, Amaral, David G., Anagnostou, Evdokia, Elsabbagh, Mayada, Fernandez, Bridget A., Hoang, Ny, Suzanne Lewis, M. E., Liu, Xudong, Sjaarda, Calvin, Smith, Isabel M., Szatmari, Peter, Zwaigenbaum, Lonnie, Glazer, David, Hartley, Dean, Stewart, A. Keith, Eberle, Michael A., Sato, Nozomu, Pearson, Christopher E., Scherer, Stephen W., Yuen, Ryan K. C.

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Profiling PIK3CA variants in disorders of somatic mosaicism by Mojarad, Bahareh A., Hernandez, Patricia V., Evenson, Michael J., Corliss, Meagan M., Stein, Sarah L., Theos, Amy, Coughlin, Carrie C., Sisk, Bryan, Menezes, Maithilee, Schroeder, Molly C., Heusel, Jonathan W., Neidich, Julie A., Cao, Yang

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Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data by Hartley, Taila, Soubry, Élisabeth, Acker, Meryl, Osmond, Matthew, Couse, Madeline, Gillespie, Meredith K., Ito, Yoko, Marshall, Aren E., Lemire, Gabrielle, Huang, Lijia, Chisholm, Caitlin, Eaton, Alison J., Price, E. Magda, Dowling, James J., Ramani, Arun K., Mendoza‐Londono, Roberto, Costain, Gregory, Axford, Michelle M., Szuto, Anna, McNiven, Vanda, Damseh, Nadirah, Jobling, Rebekah, Kock, Leanne, Mojarad, Bahareh A., Young, Ted, Shao, Zhuo, Hayeems, Robin Z., Graham, Ian D., Tarnopolsky, Mark, Brady, Lauren, Armour, Christine M., Geraghty, Michael, Richer, Julie, Sawyer, Sarah, Lines, Matthew, Mercimek‐Andrews, Saadet, Carter, Melissa T., Graham, Gail, Kannu, Peter, Lazier, Joanna, Li, Chumei, Aul, Ritu B., Balci, Tugce B., Dlamini, Nomazulu, Badalato, Lauren, Guerin, Andrea, Walia, Jagdeep, Chitayat, David, Cohn, Ronald, Faghfoury, Hanna, Forster‐Gibson, Cynthia, Gonorazky, Hernan, Grunebaum, Eyal, Inbar‐Feigenberg, Michal, Karp, Natalya, Morel, Chantal, Rusnak, Alison, Sondheimer, Neal, Warman‐Chardon, Jodi, Bhola, Priya T., Bourque, Danielle K., Chacon, Inara J., Chad, Lauren, Chakraborty, Pranesh, Chong, Karen, Doja, Asif, Goh, Elaine Suk‐Ying, Saleh, Maha, Potter, Beth K., Marshall, Christian R., Dyment, David A., Kernohan, Kristin, Boycott, Kym M.

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Clinical whole-genome sequencing and FISH identify two different fusion partners for NUP98 in a patient with acute myeloid leukemia: A case report by Mojarad, Bahareh A, Crees, Zachary D, Schroeder, Molly C, Xiang, Zhifu, Vader, Justin, Sina, Jason, Jacoby, Meagan, Frater, John L, Duncavage, Eric J, Spencer, David H, Lavine, Kory, Neidich, Julie A, Amarillo, Ina

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