Expanding the phenotype of feingold syndrome-2 by Grote, Lauren E., Repnikova, Elena A., Amudhavalli, Shivarajan M.

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Spectrum of KV2.1 Dysfunction in KCNB1‐Associated Neurodevelopmental Disorders by Kang, Seok Kyu, Vanoye, Carlos G., Misra, Sunita N., Echevarria, Dennis M., Calhoun, Jeffrey D., O'Connor, John B., Fabre, Katarina L., McKnight, Dianalee, Demmer, Laurie, Goldenberg, Paula, Grote, Lauren E., Thiffault, Isabelle, Saunders, Carol, Strauss, Kevin A., Torkamani, Ali, der Smagt, Jasper, Gassen, Koen, Carson, Robert P., Diaz, Jullianne, Leon, Eyby, Jacher, Joseph E., Hannibal, Mark C., Litwin, Jessica, Friedman, Neil R., Schreiber, Allison, Lynch, Bryan, Poduri, Annapurna, Marsh, Eric D., Goldberg, Ethan M., Millichap, John J., George, Alfred L., Kearney, Jennifer A.

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Spectrum of K V 2.1 Dysfunction in KCNB1-Associated Neurodevelopmental Disorders by Kang, Seok Kyu, Vanoye, Carlos G, Misra, Sunita N, Echevarria, Dennis M, Calhoun, Jeffrey D, O'Connor, John B, Fabre, Katarina L, McKnight, Dianalee, Demmer, Laurie, Goldenberg, Paula, Grote, Lauren E, Thiffault, Isabelle, Saunders, Carol, Strauss, Kevin A, Torkamani, Ali, van der Smagt, Jasper, van Gassen, Koen, Carson, Robert P, Diaz, Jullianne, Leon, Eyby, Jacher, Joseph E, Hannibal, Mark C, Litwin, Jessica, Friedman, Neil R, Schreiber, Allison, Lynch, Bryan, Poduri, Annapurna, Marsh, Eric D, Goldberg, Ethan M, Millichap, John J, George, Jr, Alfred L, Kearney, Jennifer A

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Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia by Guissart, Claire, Latypova, Xenia, Rollier, Paul, Khan, Tahir N., Stamberger, Hannah, McWalter, Kirsty, Cho, Megan T., Kjaergaard, Susanne, Weckhuysen, Sarah, Lesca, Gaetan, Besnard, Thomas, Õunap, Katrin, Schema, Lynn, Chiocchetti, Andreas G., McDonald, Marie, de Bellescize, Julitta, Vincent, Marie, Van Esch, Hilde, Sattler, Shannon, Forghani, Irman, Thiffault, Isabelle, Freitag, Christine M., Barbouth, Deborah Sara, Cadieux-Dion, Maxime, Willaert, Rebecca, Guillen Sacoto, Maria J., Safina, Nicole P., Dubourg, Christèle, Grote, Lauren, Carré, Wilfrid, Saunders, Carol, Pajusalu, Sander, Farrow, Emily, Boland, Anne, Karlowicz, Danielle Hays, Deleuze, Jean-François, Wojcik, Monica H., Pressman, Rena, Isidor, Bertrand, Vogels, Annick, Van Paesschen, Wim, Al-Gazali, Lihadh, Al Shamsi, Aisha Mohamed, Claustres, Mireille, Pujol, Aurora, Sanders, Stephan J., Rivier, François, Leboucq, Nicolas, Cogné, Benjamin, Sasorith, Souphatta, Sanlaville, Damien, Retterer, Kyle, Odent, Sylvie, Katsanis, Nicholas, Bézieau, Stéphane, Koenig, Michel, Davis, Erica E., Pasquier, Laurent, Küry, Sébastien

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Occurrence and characterization of medulloblastoma in a patient with Curry‐Jones syndrome by Porath, Binu, Farooki, Sana, Gener, Melissa, Amudhavalli, Shivarajan Manickavasagam, Grote, Lauren, Cooley, Linda D., Ginn, Kevin, Farooqi, Midhat S.

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Variable approaches to genetic counseling for microarray regions of homozygosity associated with parental relatedness by Grote, Lauren, Myers, Melanie, Lovell, Anne, Saal, Howard, Sund, Kristen Lipscomb

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A patient with polymerase E1 deficiency (POLE1): clinical features and overlap with DNA breakage/instability syndromes by Thiffault, Isabelle, Saunders, Carol, Jenkins, Janda, Raje, Nikita, Canty, Kristi, Sharma, Mukta, Grote, Lauren, Welsh, Holly I, Farrow, Emily, Twist, Greyson, Miller, Neil, Zwick, David, Zellmer, Lee, Kingsmore, Stephen F, Safina, Nicole P

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Spectrum of KV 2.1 Dysfunction in KCNB1-Associated Neurodevelopmental Disorders by Kang, Seok Kyu, Vanoye, Carlos G, Misra, Sunita N, Echevarria, Dennis M, Calhoun, Jeffrey D, O'Connor, John B, Fabre, Katarina L, McKnight, Dianalee, Demmer, Laurie, Goldenberg, Paula, Grote, Lauren E, Thiffault, Isabelle, Saunders, Carol, Strauss, Kevin A, Torkamani, Ali, van der Smagt, Jasper, van Gassen, Koen, Carson, Robert P, Diaz, Jullianne, Leon, Eyby, Jacher, Joseph E, Hannibal, Mark C, Litwin, Jessica, Friedman, Neil R, Schreiber, Allison, Lynch, Bryan, Poduri, Annapurna, Marsh, Eric D, Goldberg, Ethan M, Millichap, John J, George, Alfred L, Kearney, Jennifer A

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Occurrence and characterization of medulloblastoma in a patient with Curry-Jones syndrome by Porath, Binu, Farooki, Sana, Gener, Melissa, Amudhavalli, Shivarajan Manickavasagam, Grote, Lauren, Cooley, Linda D, Ginn, Kevin, Farooqi, Midhat S

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Tumor-targeted CD28 bispecific antibodies enhance the antitumor efficacy of PD-1 immunotherapy by Waite, Janelle C, Wang, Bei, Haber, Lauric, Hermann, Aynur, Ullman, Erica, Ye, Xuan, Dudgeon, Drew, Slim, Rabih, Ajithdoss, Dharani K, Godin, Stephen J, Ramos, Ilyssa, Wu, Qi, Oswald, Erin, Poon, Patrick, Golubov, Jacquelynn, Grote, Devon, Stella, Jennifer, Pawashe, Arpita, Finney, Jennifer, Herlihy, Evan, Ahmed, Hassan, Kamat, Vishal, Dorvilliers, Amanda, Navarro, Elizabeth, Xiao, Jenny, Kim, Julie, Yang, Shao Ning, Warsaw, Jacqueline, Lett, Clarissa, Canova, Lauren, Schulenburg, Teresa, Foster, Randi, Krueger, Pamela, Garnova, Elena, Rafique, Ashique, Babb, Robert, Chen, Gang, Stokes Oristian, Nicole, Siao, Chia-Jen, Daly, Christopher, Gurer, Cagan, Martin, Joel, Macdonald, Lynn, MacDonald, Douglas, Poueymirou, William, Smith, Eric, Lowy, Israel, Thurston, Gavin, Olson, William, Lin, John C, Sleeman, Matthew A, Yancopoulos, George D, Murphy, Andrew J, Skokos, Dimitris

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Implementation of perinatal collaborative care: a health services approach to perinatal depression care by Miller, Emily S., Jensen, Rebekah, Hoffman, M. Camille, Osborne, Lauren M., McEvoy, Katherine, Grote, Nancy, Moses-Kolko, Eydie L.

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Feedback from readers by Goodsmith, Lauren, Grote, Dan

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