Genome-wide detection of tandem DNA repeats that are expanded in autism von 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.

Volltext

Support to caregivers who have received genetic information about neurodevelopmental and psychiatric vulnerability in their young children: A narrative review von Perlman, Polina, Vorstman, Jacob, Hoang, Ny, Summers, Jane, Baribeau, Danielle, Cunningham, Jessie, Mulsant, Benoit H.

Volltext

A framework for an evidence-based gene list relevant to autism spectrum disorder von Schaaf, Christian P., Betancur, Catalina, Yuen, Ryan K. C., Parr, Jeremy R., Skuse, David H., Gallagher, Louise, Bernier, Raphael A., Buchanan, Janet A., Buxbaum, Joseph D., Chen, Chun-An, Dies, Kira A., Elsabbagh, Mayada, Firth, Helen V., Frazier, Thomas, Hoang, Ny, Howe, Jennifer, Marshall, Christian R., Michaud, Jacques L., Rennie, Olivia, Szatmari, Peter, Chung, Wendy K., Bolton, Patrick F., Cook, Edwin H., Scherer, Stephen W., Vorstman, Jacob A. S.

Volltext

31.1 When and How to Incorporate Genetic Testing into Child and Adolescent Psychiatry von Hoang, Ny

Volltext

Autistic traits in youth with familial adenomatous polyposis: A Dutch–Canadian case–control study von Danieli, Polina Perlman, Hoang, Ny, Selvanayagam, Thanuja, Yang, Alvin, Breetvelt, Elemi, Tabbers, Merit, Cohen, Christine, Aelvoet, Arthur S., Trost, Brett, Ward, Thomas, Semotiuk, Kara, Durno, Carol, Aronson, Melyssa, Cohen, Zane, Dekker, Evelien, Vorstman, Jacob

Volltext

Sleep phenotype of individuals with autism spectrum disorder bearing mutations in the PER2 circadian rhythm gene von Hoang, Ny, Yuen, Ryan K.C., Howe, Jennifer, Drmic, Irene, Ambrozewicz, Patricia, Russell, Carolyn, Vorstman, Jacob, Weiss, Shelly K., Anagnostou, Evdokia, Malow, Beth A., Scherer, Stephen W.

Volltext

Heterogeneity in clinical sequencing tests marketed for autism spectrum disorders von Hoang, Ny, Buchanan, Janet A., Scherer, Stephen W.

Volltext

Neurodevelopmental functioning in probands and non‐proband carriers of 22q11.2 microduplication von Drmic, Irene E., MacKinnon Modi, Bonnie, McConnell, Beth, Jilderda, Sanne, Hoang, Ny, Noor, Abdul, Bassett, Anne S., Speevak, Marsha, Stavropoulos, Dimitri J., Carter, Melissa T.

Volltext

An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure von Summers, Jane, Baribeau, Danielle, Perlman, Polina, Hoang, Ny, Cui, Sunny, Krakowski, Aneta, Ambrozewicz, Patricia, Ho, Ariel, Selvanayagam, Thanuja, Sándor-Bajusz, Kinga A, Palad, Katrina, Patel, Nishi, McGaughey, Sarah, Gallagher, Louise, Scherer, Stephen W, Szatmari, Peter, Vorstman, Jacob

Volltext

Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders von Srivastava, Siddharth, Love-Nichols, Jamie A., Dies, Kira A., Ledbetter, David H., Martin, Christa L., Chung, Wendy K., Firth, Helen V., Frazier, Thomas, Hansen, Robin L., Prock, Lisa, Brunner, Han, Hoang, Ny, Scherer, Stephen W., Sahin, Mustafa, Miller, David T.

Volltext

Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly von Woodbury-Smith, Marc, Deneault, Eric, Yuen, Ryan K C, Walker, Susan, Zarrei, Mehdi, Pellecchia, Giovanna, Howe, Jennifer L, Hoang, Ny, Uddin, Mohammed, Marshall, Christian R, Chrysler, Christina, Thompson, Ann, Szatmari, Peter, Scherer, Stephen W

Volltext

Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants von Chan, Ada J. S., Cytrynbaum, Cheryl, Hoang, Ny, Ambrozewicz, Patricia M., Weksberg, Rosanna, Drmic, Irene, Ritzema, Anne, Schachar, Russell, Walker, Susan, Uddin, Mohammed, Zarrei, Mehdi, Yuen, Ryan K. C., Scherer, Stephen W.

Volltext

Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes von Woodbury-Smith, Marc, Nicolson, Rob, Zarrei, Mehdi, Yuen, Ryan K. C., Walker, Susan, Howe, Jennifer, Uddin, Mohammed, Hoang, Ny, Buchanan, Janet A., Chrysler, Christina, Thompson, Ann, Szatmari, Peter, Scherer, Stephen W.

Volltext

Does personal genome testing drive service utilization in an adult preventive medicine clinic? von Hoang, Ny, Hayeems, Robin, Davies, Jill, Pu, Shuye, Wasim, Syed, Velsher, Lea, Aw, James, Chénier, Sébastien, Stavropoulos, Dimitri J, Babul-Hirji, Riyana, Weksberg, Rosanna, Shuman, Cheryl

Volltext

Communicating complex genomic information: A counselling approach derived from research experience with Autism Spectrum Disorder von Hoang, Ny, Cytrynbaum, Cheryl, Scherer, Stephen W.

Volltext

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders von Srivastava, Siddharth, Love-Nichols, Jamie A., Dies, Kira A., Ledbetter, David H., Martin, Christa L., Chung, Wendy K., Firth, Helen V., Frazier, Thomas, Hansen, Robin L., Prock, Lisa, Brunner, Han, Hoang, Ny, Scherer, Stephen W., Sahin, Mustafa, Miller, David T.

Volltext

Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosage von Dale, Breanne, Modi, Bonnie MacKinnon, Jilderda, Sanne, McConnell, Beth, Hoang, Ny, Swaroop, Pooja, Falcon, Jhoan, Thiruvahindrapuram, Bhooma, Walker, Susan, Scherer, Stephen W., Stavropoulos, D. James, Drmic, Irene E., Carter, Melissa T.

Volltext

Whole-genome sequencing of quartet families with autism spectrum disorder von Yuen, Ryan K C, Thiruvahindrapuram, Bhooma, Merico, Daniele, Walker, Susan, Tammimies, Kristiina, Hoang, Ny, Chrysler, Christina, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Liu, Yi, Gazzellone, Matthew J, D'Abate, Lia, Deneault, Eric, Howe, Jennifer L, Liu, Richard S C, Thompson, Ann, Zarrei, Mehdi, Uddin, Mohammed, Marshall, Christian R, Ring, Robert H, Zwaigenbaum, Lonnie, Ray, Peter N, Weksberg, Rosanna, Carter, Melissa T, Fernandez, Bridget A, Roberts, Wendy, Szatmari, Peter, Scherer, Stephen W

Volltext

Developmental implications of genetic testing for physical indications von Baribeau, Danielle A, Hoang, Ny, Selvanayagam, Thanuja, Stavropoulos, D James, Costain, Gregory, Scherer, Stephen W, Vorstman, Jacob

Volltext

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders (vol 21, 2019,... von Srivastava, Siddharth, Love-Nichols, Jamie A., Dies, Kira A., Ledbetter, David H., Martin, Christa L., Chung, Wendy K., Firth, Helen V., Frazier, Thomas, Hansen, Robin L., Prock, Lisa, Brunner, Han, Hoang, Ny, Scherer, Stephen W., Sahin, Mustafa, Miller, David T.

Volltext