In situ crosslinking of electrospun gelatin for improved fiber morphology retention and tunable degradation von Kishan, A. P, Nezarati, R. M, Radzicki, C. M, Renfro, A. L, Robinson, J. L, Whitely, M. E, Cosgriff-Hernandez, E. M

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Patterning small-molecule biocapture surfaces: microcontact insertion printing vs. photolithography von Shuster, M. J., Vaish, A., Cao, H. H., Guttentag, A. I., McManigle, J. E., Gibb, A. L., Martinez, M. M., Nezarati, R. M., Hinds, J. M., Liao, W.-S., Weiss, P. S., Andrews, A. M.

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Correction: In situ crosslinking of electrospun gelatin for improved fiber morphology retention and tunable degradation von Kishan, A. P, Nezarati, R. M, Radzicki, C. M, Renfro, A. L, Robinson, J. L, Whitely, M. E, Cosgriff-Hernandez, E. M

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Patterning small-molecule biocapture surfaces: microcontact insertion printing vs. photolithography von Shuster, M J, Vaish, A, Cao, H H, Guttentag, A I, McManigle, J E, Gibb, A L, Martinez-Rivera, M, Martinez, M M, Nezarati, R M, Hinds, J M, Liao, W-S, Weiss, P S, Andrews, A M

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Increased LIS1 expression affects human and mouse brain development von Lu, Xin-Yan, Horner, Michele, Day-Salvatore, Debra-Lynn, Sahoo, Trilochan, Withers, Marjorie A, Cheung, Sau Wai, Gunderson, Kevin L, Hunter, Jill V, Sapir, Tamar, Peiffer, Daniel A, Yanagawa, Yuchio, Reiner, Orly, Shchelochkov, Oleg A, Levy, Talia, Lupski, James R, Nezarati, Marjan M, Martinez, Salvador, Savage, Sarah K, Shinder, Vera, Harris, David J, Ann Shotts, Vern, Bi, Weimin, Amato, Stephen S, Beaudet, Arthur L, Zhang, Feng

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Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy von Assia Batzir, Nurit, Kishor Bhagwat, Pranjali, Larson, Austin, Coban Akdemir, Zeynep, Bagłaj, Maciej, Bofferding, Leon, Bosanko, Katherine B., Bouassida, Skander, Callewaert, Bert, Cannon, Ashley, Enchautegui Colon, Yazmin, Garnica, Adolfo D., Harr, Margaret H., Heck, Sandra, Hurst, Anna C. E., Jhangiani, Shalini N., Isidor, Bertrand, Littlejohn, Rebecca O., Liu, Pengfei, Magoulas, Pilar, Mar Fan, Helen, Marom, Ronit, McLean, Scott, Nezarati, Marjan M., Nugent, Kimberly M., Petersen, Michael B., Rocha, Maria L., Roeder, Elizabeth, Smigiel, Robert, Tully, Ian, Weisfeld‐Adams, James, Wells, Katerina O., Posey, Jennifer E., Lupski, James R., Beaudet, Arthur L., Wangler, Michael F.

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FLNA genomic rearrangements cause periventricular nodular heterotopia von CLAPHAM, K. R, YU, T. W, DU SOUICH, C, VAN KARNEBEEK, C, GUERRINI, R, WALSH, C. A, GANESH, V. S, BARRY, B, CHAN, Y, MEI, D, PARRINI, E, FUNALOT, B, DUPUIS, L, NEZARATI, M. M

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Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants von Girirajan, Santhosh, Rosenfeld, Jill A, Coe, Bradley P, Parikh, Sumit, Friedman, Neil, Goldstein, Amy, Filipink, Robyn A, McConnell, Juliann S, Angle, Brad, Meschino, Wendy S, Nezarati, Marjan M, Asamoah, Alexander, Jackson, Kelly E, Gowans, Gordon C, Martin, Judith A, Carmany, Erin P, Stockton, David W, Schnur, Rhonda E, Penney, Lynette S, Martin, Donna M, Raskin, Salmo, Leppig, Kathleen, Thiese, Heidi, Smith, Rosemarie, Aberg, Erika, Niyazov, Dmitriy M, Escobar, Luis F, El-Khechen, Dima, Johnson, Kisha D, Lebel, Robert R, Siefkas, Kiana, Ball, Susie, Shur, Natasha, McGuire, Marianne, Brasington, Campbell K, Spence, J. Edward, Martin, Laura S, Clericuzio, Carol, Ballif, Blake C, Shaffer, Lisa G, Eichler, Evan E

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Correlation between CAG repeat length and clinical features in Machado-Joseph disease von MACIEL, P, GASPAR, C, NEZARATI, M. M, CORWIN, L. I, LOPES-CENDES, I, ROOKE, K, ROSENBERG, R, MACLEOD, P, FARRER, L. A, SEQUEIROS, J, ROULEAU, G. A, DESTEFANO, A. L, SILVEIRA, I, COUTINHO, P, RADVANY, J, DAWSON, D. M, SUDARSKY, L, GUIMARAES, J, LOUREIRO, J. E. L

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Cenani-Lenz syndrome: report of a new case and review of the literature von Nezarati, Marjan M, McLeod, D Ross

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Increased LIS1 expression affects human and mouse brain development: Making diversity count von WEIMIN BI, SAPIR, Tamar, NEZARATI, Marjan M, SHOTTS, Vern Ann, AMATO, Stephen S, SAVAGE, Sarah K, HARRIS, David J, DAY-SALVATORE, Debra-Lynn, HORNER, Michele, LU, Xin-Yan, SAHOO, Trilochan, YANAGAWA, Yuchio, SHCHELOCHKOV, Oleg A, BEAUDET, Arthur L, SAU WAI CHEUNG, MARTINEZ, Salvador, LUPSKI, James R, REINER, Orly, FENG ZHANG, WITHERS, Marjorie A, HUNTER, Jill V, LEVY, Talia, SHINDER, Vera, PEIFFER, Daniel A, GUNDERSON, Kevin L

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Diagnostic implications of pitfalls in causal variant identification based on 4577 molecularly characterized families von AlAbdi, L, Maddirevula, S, Shamseldin, HE, Khouj, E, Helaby, R, Hamid, H, Almulhim, A, Hashem, MO, Abdulwahab, F, Abouyousef, O, Alqahtani, M, Altuwaijri, N, Jaafar, A, Alshidi, T, Alzahrani, F, Al-Sagheir, AI, Mansour, AM, Alawaji, A, Aldhilan, A, Alhashem, A, Alhemidan, A, Nabil, A, Khan, AO, Aljohar, A, Alsaleem, B, Tabarki, B, Lourenco, CM, Faqeih, E, AlShail, E, Almesaifri, F, Mutairi, FA, Alzaidan, H, Morsy, H, Alshihry, H, Alkuraya, H, Girisha, KM, Al-Fayez, K, Al-Rubeaan, K, kraoua, L, Alnemer, M, Tulbah, M, Zaki, MS, Alfadhel, M, Abouelhoda, M, Nezarati, MM, Al-Qattan, M, Shboul, M, Abanemai, M, Al-Muhaizea, MA, Al-owain, M, Bafaqeeh, MS, Alshammari, M, Abukhalid, M, Alsahan, N, Derar, N, Meriki, N, Bohlega, SA, Tala, SA, Alhassan, S, Wali, S, Mohamed, S, Coskun, S, Saadeh, S, Tkemaladze, T, Kurdi, W, Alhumaidi, ZA, Rahbeeni, Z, Alkuraya, FS

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VACTERL manifestations in two generations of a family von Nezarati, M.M., McLeod, D.R.

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Detecting rearrangements in children using subtelomeric FISH and SKY von Clarkson, Blaise, Pavenski, Katerina, Dupuis, Lucie, Kennedy, Shelley, Meyn, Stephen, Nezarati, Marjan M., Nie, Gloria, Weksberg, Rosanna, Withers, Stephen, Quercia, Nada, Teebi, Ahmad S., Teshima, Ikuko

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De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy von de Lange, IM, Helbig, KL, Weckhuysen, S, Møller, RS, Velinov, M, Dolzhanskaya, N, Marsh, E, Helbig, I, Devinsky, O, Tang, S, Mefford, HC, Myers, CT, van Paesschen, W, Striano, P, van Gassen, K, van Kempen, M, de Kovel, CG, Piard, J, Minassian, BA, Nezarati, MM, Pessoa, A, Jacquette, A, Maher, B, Balestrini, S, Sisodiya, S, Warde, MT, De St Martin, A, Chelly, J, EuroEPINOMICS-RES MAE Working Group, van 't Slot, R, Van Maldergem, L, Brilstra, EH, Koeleman, BP

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