Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism von Willsey, A. Jeremy, Sanders, Stephan J., Li, Mingfeng, Dong, Shan, Tebbenkamp, Andrew T., Muhle, Rebecca A., Reilly, Steven K., Lin, Leon, Fertuzinhos, Sofia, Miller, Jeremy A., Murtha, Michael T., Bichsel, Candace, Niu, Wei, Cotney, Justin, Ercan-Sencicek, A. Gulhan, Gockley, Jake, Gupta, Abha R., Han, Wenqi, He, Xin, Hoffman, Ellen J., Klei, Lambertus, Lei, Jing, Liu, Wenzhong, Liu, Li, Lu, Cong, Xu, Xuming, Zhu, Ying, Mane, Shrikant M., Lein, Ed S., Wei, Liping, Noonan, James P., Roeder, Kathryn, Devlin, Bernie, Sestan, Nenad, State, Matthew W.

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Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene von Fernandez, Thomas V, Williams, Zsanett P, Kline, Tina, Rajendran, Shreenath, Augustine, Farhan, Wright, Nicole, Sullivan, Catherine A W, Olfson, Emily, Abdallah, Sarah B, Liu, Wenzhong, Hoffman, Ellen J, Gupta, Abha R, Singer, Harvey S

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The role of social entrepreneurial leadership and benchmarking in women empowerment von Dixit, Abha R., Malik, Nishtha, Seth, Manisha, Sethi, Deepa

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Engineering spatial-organized cardiac organoids for developmental toxicity testing von Hoang, Plansky, Kowalczewski, Andrew, Sun, Shiyang, Winston, Tackla S., Archilla, Adriana M., Lemus, Stephanie M., Ercan-Sencicek, A. Gulhan, Gupta, Abha R., Liu, Wenzhong, Kontaridis, Maria I., Amack, Jeffrey D., Ma, Zhen

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Myosteatosis in Cirrhosis: A Review of Diagnosis, Pathophysiological Mechanisms and Potential Interventions von Ebadi, Maryam, Tsien, Cynthia, Bhanji, Rahima A, Dunichand-Hoedl, Abha R, Rider, Elora, Motamedrad, Maryam, Mazurak, Vera C, Baracos, Vickie, Montano-Loza, Aldo J

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism von Sanders, Stephan J., Murtha, Michael T., Gupta, Abha R., Murdoch, John D., Raubeson, Melanie J., Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, DiLullo, Nicholas M., Parikshak, Neelroop N., Stein, Jason L., Walker, Michael F., Ober, Gordon T., Teran, Nicole A., Song, Youeun, El-Fishawy, Paul, Murtha, Ryan C., Choi, Murim, Overton, John D., Bjornson, Robert D., Carriero, Nicholas J., Meyer, Kyle A., Bilguvar, Kaya, Mane, Shrikant M., Šestan, Nenad, Lifton, Richard P., Günel, Murat, Roeder, Kathryn, Geschwind, Daniel H., Devlin, Bernie, State, Matthew W.

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Signaling Pathways and Sex Differential Processes in Autism Spectrum Disorder von Enriquez, Kristen D., Gupta, Abha R., Hoffman, Ellen J.

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Skeletal Muscle Pathological Fat Infiltration (Myosteatosis) Is Associated with Higher Mortality in Patients with Cirrhosis von Ebadi, Maryam, Tsien, Cynthia, Bhanji, Rahima A, Dunichand-Hoedl, Abha R, Rider, Elora, Motamedrad, Maryam, Mazurak, Vera C, Baracos, Vickie, Montano-Loza, Aldo J

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Sex-dependent role for EPHB2 in brain development and autism-associated behavior von Assali, Ahlem, Cho, Jennifer Y, Tsvetkov, Evgeny, Gupta, Abha R, Cowan, Christopher W

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20.2 HUMAN-INDUCED PLURIPOTENT STEM CELL MODELS OF AUTISM-ASSOCIATED MUTATIONS von Gupta, Abha R., MD, PhD

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De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette’s Disorder and Autism von Cappi, Carolina, Oliphant, Melody E., Péter, Zsanett, Zai, Gwyneth, Conceição do Rosário, Maria, Sullivan, Catherine A.W., Gupta, Abha R., Hoffman, Ellen J., Virdee, Manmeet, Olfson, Emily, Abdallah, Sarah B., Willsey, A. Jeremy, Shavitt, Roseli G., Miguel, Euripedes C., Kennedy, James L., Richter, Margaret A., Fernandez, Thomas V.

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Clinical and biological characterization of skeletal muscle tissue biopsies of surgical cancer patients von Anoveros‐Barrera, Ana, Bhullar, Amritpal S., Stretch, Cynthia, Esfandiari, Nina, Dunichand‐Hoedl, Abha R., Martins, Karen J.B., Bigam, David, Khadaroo, Rachel G., McMullen, Todd, Bathe, Oliver F., Damaraju, Sambasivarao, Skipworth, Richard J., Putman, Charles T., Baracos, Vickie E., Mazurak, Vera C.

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Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy von Novarino, Gaia, El-Fishawy, Paul, Kayserili, Hulya, Meguid, Nagwa A., Scott, Eric M., Schroth, Jana, Silhavy, Jennifer L., Kara, Majdi, Khalil, Rehab O., Ben-Omran, Tawfeg, Ercan-Sencicek, A. Gulhan, Hashish, Adel F., Sanders, Stephan J., Gupta, Abha R., Hashem, Hebatalla S., Matern, Dietrich, Gabriel, Stacey, Sweetman, Larry, Rahimi, Yasmeen, Harris, Robert A., State, Matthew W., Gleeson, Joseph G.

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Identification of amygdala-expressed genes associated with autism spectrum disorder von Herrero, Maria Jesus, Velmeshev, Dmitry, Hernandez-Pineda, David, Sethi, Saarthak, Sorrells, Shawn, Banerjee, Payal, Sullivan, Catherine, Gupta, Abha R, Kriegstein, Arnold R, Corbin, Joshua G

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Parenting Stress and its Associated Components Prior to an Autism Spectrum Disorder (ASD) Diagnostic Evaluation von Voliovitch, Yair, Leventhal, John M., Fenick, Ada M., Gupta, Abha R., Feinberg, Emily, Hickey, Emily J., Shabanova, Veronika, Weitzman, Carol

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Increased Expression of Hepatic Stearoyl-CoA Desaturase (SCD)-1 and Depletion of Eicosapentaenoic Acid (EPA) Content following Cytotoxic Cancer Therapy Are Reversed by Dietary Fish... von Monirujjaman, Md, Renani, Leila Baghersad, Isesele, Peter, Dunichand-Hoedl, Abha R, Mazurak, Vera C

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Sarcopenia Severity Based on Computed Tomography Image Analysis in Patients with Cirrhosis von Ebadi, Maryam, Bhanji, Rahima A, Dunichand-Hoedl, Abha R, Mazurak, Vera C, Baracos, Vickie E, Montano-Loza, Aldo J

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Recent Advances in the Genetics of Autism von Gupta, Abha R, State, Matthew W

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Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans von Ercan-Sencicek, A Gulhan, Jambi, Samira, Franjic, Daniel, Nishimura, Sayoko, Li, Mingfeng, El-Fishawy, Paul, Morgan, Thomas M, Sanders, Stephan J, Bilguvar, Kaya, Suri, Mohnish, Johnson, Michele H, Gupta, Abha R, Yuksel, Zafer, Mane, Shrikant, Grigorenko, Elena, Picciotto, Marina, Alberts, Arthur S, Gunel, Murat, Šestan, Nenad, State, Matthew W

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No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contacti... von Murdoch, John D, Gupta, Abha R, Sanders, Stephan J, Walker, Michael F, Keaney, John, Fernandez, Thomas V, Murtha, Michael T, Anyanwu, Samuel, Ober, Gordon T, Raubeson, Melanie J, DiLullo, Nicholas M, Villa, Natalie, Waqar, Zainabdul, Sullivan, Catherine, Gonzalez, Luis, Willsey, A Jeremy, Choe, So-Yeon, Neale, Benjamin M, Daly, Mark J, State, Matthew W

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