Genetics of schizophrenia in the South African Xhosa von Gulsuner, S., Stein, D. J., Susser, E. S., Sibeko, G., Pretorius, A., Walsh, T., Majara, L., Mndini, M. M., Mqulwana, S. G., Ntola, O. A., Casadei, S., Ngqengelele, L. L., Korchina, V., van der Merwe, C., Malan, M., Fader, K. M., Feng, M., Willoughby, E., Muzny, D., Baldinger, A., Andrews, H. F., Gur, R. C., Gibbs, R. A., Zingela, Z., Nagdee, M., Ramesar, R. S., King, M. -C., McClellan, J. M.

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Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity von Zhang, Michael Y, Keel, Siobán B, Walsh, Tom, Lee, Ming K, Gulsuner, Suleyman, Watts, Amanda C, Pritchard, Colin C, Salipante, Stephen J, Jeng, Michael R, Hofmann, Inga, Williams, David A, Fleming, Mark D, Abkowitz, Janis L, King, Mary-Claire, Shimamura, Akiko

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Germline mutation rate in African-American women in Arkansas with a personal and/or family history of breast cancer von Zorn, K.K., Simonson, M.E., Compadre, A., Gray, K.E., Runnells, G.A., Harrell, M.I., Gulsuner, S., Radke, M.R., Swisher, E.M.

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Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease von Gulsuner, Hilal Unal, Gulsuner, Suleyman, Mercan, Fatma Nazli, Onat, Onur Emre, Walsh, Tom, Shahin, Hashem, Lee, Ming K., Dogu, Okan, Kansu, Tulay, Topaloglu, Haluk, Elibol, Bulent, Akbostanci, Cenk, King, Mary-Claire, Ozcelik, Tayfun, Tekinay, Ayse B.

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Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group Study von Norquist, Barbara M, Brady, Mark F, Harrell, Maria I, Walsh, Tom, Lee, Ming K, Gulsuner, Suleyman, Bernards, Sarah S, Casadei, Silvia, Burger, Robert A, Tewari, Krishnansu S, Backes, Floor, Mannel, Robert S, Glaser, Gretchen, Bailey, Cheryl, Rubin, Stephen, Soper, John, Lankes, Heather A, Ramirez, Nilsa C, King, Mary Claire, Birrer, Michael J, Swisher, Elizabeth M

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Essential Role of BRCA2 in Ovarian Development and Function von Weinberg-Shukron, Ariella, Rachmiel, Mariana, Renbaum, Paul, Gulsuner, Suleyman, Walsh, Tom, Lobel, Orit, Dreifuss, Amatzia, Ben-Moshe, Avital, Zeligson, Sharon, Segel, Reeval, Shore, Tikva, Kalifa, Rachel, Goldberg, Michal, King, Mary-Claire, Gerlitz, Offer, Levy-Lahad, Ephrat, Zangen, David

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Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy von Zhang, Michael Y, Churpek, Jane E, Keel, Siobán B, Walsh, Tom, Lee, Ming K, Loeb, Keith R, Gulsuner, Suleyman, Pritchard, Colin C, Sanchez-Bonilla, Marilyn, Delrow, Jeffrey J, Basom, Ryan S, Forouhar, Melissa, Gyurkocza, Boglarka, Schwartz, Bradford S, Neistadt, Barbara, Marquez, Rafael, Mariani, Christopher J, Coats, Scott A, Hofmann, Inga, Lindsley, R Coleman, Williams, David A, Abkowitz, Janis L, Horwitz, Marshall S, King, Mary-Claire, Godley, Lucy A, Shimamura, Akiko

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Inherited predisposition to malignant mesothelioma and overall survival following platinum chemotherapy von Hassan, Raffit, Morrow, Betsy, Thomas, Anish, Walsh, Tom, Lee, Ming K., Gulsuner, Suleyman, Gadiraju, Meghana, Panou, Vasiliki, Gao, Shaojian, Mian, Idrees, Khan, Javed, Raffeld, Mark, Patel, Snehal, Xi, Liqiang, Wei, Jun S., Hesdorffer, Mary, Zhang, Jingli, Calzone, Kathleen, Desai, Arpita, Padiernos, Emerson, Alewine, Christine, Schrump, David S., Steinberg, Seth M., Kindler, Hedy L., King, Mary-Claire, Churpek, Jane E.

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Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients von Keel, Siobán B, Scott, Angela, Sanchez-Bonilla, Marilyn, Ho, Phoenix A, Gulsuner, Suleyman, Pritchard, Colin C, Abkowitz, Janis L, King, Mary-Claire, Walsh, Tom, Shimamura, Akiko

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Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants von Johnston, Jennifer J, van der Smagt, Jasper J, Rosenfeld, Jill A, Pagnamenta, Alistair T, Alswaid, Abdulrahman, Baker, Eva H, Blair, Edward, Borck, Guntram, Brinkmann, Julia, Craigen, William, Dung, Vu Chi, Emrick, Lisa, Everman, David B, van Gassen, Koen L, Gulsuner, Suleyman, Harr, Margaret H, Jain, Mahim, Kuechler, Alma, Leppig, Kathleen A, McDonald-McGinn, Donna M, Can, Ngoc Thi Bich, Peleg, Amir, Roeder, Elizabeth R, Rogers, R Curtis, Sagi-Dain, Lena, Sapp, Julie C, Schäffer, Alejandro A, Schanze, Denny, Stewart, Helen, Taylor, Jenny C, Verbeek, Nienke E, Walkiewicz, Magdalena A, Zackai, Elaine H, Zweier, Christiane, Zenker, Martin, Lee, Brendan, Biesecker, Leslie G

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Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failure von Tenenbaum-Rakover, Yardena, Weinberg-Shukron, Ariella, Renbaum, Paul, Lobel, Orit, Eideh, Hasan, Gulsuner, Suleyman, Dahary, Dvir, Abu-Rayyan, Amal, Kanaan, Moien, Levy-Lahad, Ephrat, Bercovich, Dani, Zangen, David

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Reprogramming identifies functionally distinct stages of clonal evolution in myelodysplastic syndromes von Hsu, Jasper, Reilly, Andreea, Hayes, Brian J., Clough, Courtnee A., Konnick, Eric Q., Torok-Storb, Beverly, Gulsuner, Suleyman, Wu, David, Becker, Pamela S., Keel, Siobán B., Abkowitz, Janis L., Doulatov, Sergei

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Reply to Tzoulis et al: Genetic and clinical heterogeneity of essential tremor von Gulsuner, Hilal Unal, Gulsuner, Suleyman, Mercan, Fatma Nazli, Onat, Onur Emre, Walsh, Tom, Shahin, Hashem, Lee, Ming K., Dogu, Okan, Kansu, Tulay, Topaloglu, Haluk, Elibol, Bulent, Akbostanci, Cenk, King, Mary-Claire, Ozcelik, Tayfun, Tekinay, Ayse B.

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Multi-Domain Short Peptide Molecules for in Situ Synthesis and Biofunctionalization of Gold Nanoparticles for Integrin-Targeted Cell Uptake von Unal Gulsuner, Hilal, Ceylan, Hakan, Guler, Mustafa O, Tekinay, Ayse B

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426. Functional Characterization of De Novo Damaging Mutations in Patients With Sporadic Schizophrenia Using CRISPRi in iPSCs von Sunshine, Anna, Gulsuner, Suleyman, Walsh, Tom, King, Mary-Claire, McClellan, Jon

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Genomic analysis of inherited hearing loss in the Palestinian population von Rayyan, Amal Abu, Kamal, Lara, Casadei, Silvia, Brownstein, Zippora, Zahdeh, Fouad, Shahin, Hashem, Canavati, Christina, Dweik, Dima, Jaraysa, Tamara, Rabie, Grace, Carlson, Ryan J., Gulsuner, Suleyman, Lee, Ming K., Avraham, Karen B., Walsh, Tom, King, Mary-Claire, Kanaan, Moien N.

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Bone-Like Mineral Nucleating Peptide Nanofibers Induce Differentiation of Human Mesenchymal Stem Cells into Mature Osteoblasts von Ceylan, Hakan, Kocabey, Samet, Unal Gulsuner, Hilal, Balcik, Ozlem S, Guler, Mustafa O, Tekinay, Ayse B

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Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy, and enteropathy, and implications for clinical management von Baxter, Sarah K., Walsh, Tom, Casadei, Silvia, Eckert, Mary M., Allenspach, Eric J., Hagin, David, Segundo, Gesmar, Lee, Ming K., Gulsuner, Suleyman, Shirts, Brian H., Sullivan, Kathleen E., Keller, Michael D., Torgerson, Troy R., King, Mary-Claire

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439. Functional Characterization of Damaging Mutations in Patients With Sporadic Schizophrenia Using CRISPRi in iPSCS von Sunshine, Anna, Gulsuner, Suleyman, Walsh, Tom, King, Mary-Claire, McClellan, Jon

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Effects of germline and somatic events in candidate BRCA-like genes on breast-tumor signatures von Bodily, Weston R., Shirts, Brian H., Walsh, Tom, Gulsuner, Suleyman, King, Mary-Claire, Parker, Alyssa, Roosan, Moom, Piccolo, Stephen R.

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