Impact of TP53 mutation variant allele frequency on phenotype and outcomes in myelodysplastic syndromes von Sallman, D A, Komrokji, R, Vaupel, C, Cluzeau, T, Geyer, S M, McGraw, K L, Al Ali, N H, Lancet, J, McGinniss, M J, Nahas, S, Smith, A E, Kulasekararaj, A, Mufti, G, List, A, Hall, J, Padron, E

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MDS-associated somatic mutations and clonal hematopoiesis are common in idiopathic cytopenias of undetermined significance von Kwok, Brian, Hall, Jeff M., Witte, John S., Xu, Yin, Reddy, Prashanti, Lin, Keming, Flamholz, Rachel, Dabbas, Bashar, Yung, Aine, Al-Hafidh, Jenan, Balmert, Emily, Vaupel, Christine, El Hader, Carlos, McGinniss, Matthew J., Nahas, Shareef A., Kines, Julie, Bejar, Rafael

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Multiple imputation in three or more stages von McGinniss, J., Harel, O.

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Stratifying Risk for Celiac Disease in a Large At-Risk United States Population by Using HLA Alleles von Pietzak, Michelle M, Schofield, Timothy C, McGinniss, Matthew J, Nakamura, Robert M

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Identification of meaningful cognitive endpoints in studies of pharmacological treatments for cognitive impairment in schizophrenia: an adaptive two-stage methodology von Brown, D, Wang, L, McGinniss, J, Sand, M, Pollentier, S

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Technical Standards and Guidelines for Fragile X: The First of a Series of Disease-Specific Supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the Am... von Maddalena, Anne, Richards, Carolyn Sue, McGinniss, Matthew J, Brothman, Arthur, Desnick, Robert J, Grier, Robert E, Hirsch, Betsy, Jacky, Peter, McDowell, Geraldine A, Popovich, Bradley, Watson, Michael, Wolff, Daynna J

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William J. Byron, S.J.: A Biographical Essay, written by Patrick Samway, S.J von McGinniss, Michael J

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Identification of HRAS mutations and absence of GNAQ or GNA11 mutations in deep penetrating nevi von Bender, Ryan P, McGinniss, Matthew J, Esmay, Paula, Velazquez, Elsa F, Reimann, Julie DR

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Evinacumab reduces remnant cholesterol in patients with hypercholesterolemia or hypertriglyceridemia von Rosenson, R.S., Rader, D., Ali, S., Banerjee, P., Mcginniss, J., Pordy, R.

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Evinacumab reduces EU apheresis eligibility in patients with homozygous familial hypercholesterolemia von Raal, F., Rosenson, R., Moriarty, P., Ali, S., Banerjee, P., Zhao, J., George, R.T., Mcginniss, J., Pordy, R.

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Novel and recurrent rearrangements in the CFTR gene : clinical and laboratory implications for cystic fibrosis screening von HANTASH, Feras M, REDMAN, Joy B, STARN, Kelsey, ANDERSON, Ben, BULLER, Arlene, MCGINNISS, Matthew J, QUAN, Franklin, MEI PENG, WEIMIN SUN, STROM, Charles M

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D108 DIAGNOSIS AND MANAGEMENT OF NONTUBERCULOUS MYCOBACTERIA INFECTIONS: Halting A Rapid Grower: Inhaled Amikacin Mitigates M. Fortuitum Pulmonary Infection In An Hiv/aids Patient von McGinniss, J E, Villanueva, M, Malinis, M

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Prolonged Fungal Colonization is Associated with Increased Risk of Chronic Lung Allograft Dysfunction von Le Mahajan, A., Brown, M., Hsu, J., Oyster, M., Kalman, L., McGinniss, J., Collman, R., Anderson, M., Clausen, E., Jones, T., Diamond, J., Feng, R., Christie, J.

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Extensive sequencing of the CFTR gene : lessons learned from the first 157 patient samples von MCGINNISS, Matthew J, CHEN, Christina, STROM, Charles M, REDMAN, Joy B, BULLER, Arlene, QUAN, Franklin, MEI PENG, GIUSTI, Robert, HANTASH, Feras M, DONGHUI HUANG, WEIMIN SUN

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1094P Demographics, prior therapies and reasons for cemiplimab treatment: Prospective cemiplimAb-rwlc survivorship and epidemiology (C.A.S.E.) study in patients with advanced cutan... von Rabinowits, G., Homsi, J., Nikanjam, M., Gentry, R., Strasswimmer, J., Venna, S., Migden, M.R., Chandra, S., Ruiz, E., Zhang, H.R., McGinniss, J., Seluzhytsky, A., Desai, J.

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CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotype von Sun, Weimin, Anderson, Ben, Redman, Joy, Milunsky, Aubrey, Buller, Arlene, McGinniss, Matthew J, Quan, Franklin, Anguiano, Arturo, Huang, Stephen, Hantash, Feras, Strom, Charles

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P.3.d.053 - Identification of meaningful cognitive endpoints in studies of pharmacological treatments for cognitive impairment in schizophrenia: an adaptive two-stage methodology von Brown, D., Wang, L., McGinniss, J., Sand, M., Pollentier, S.

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FP04.03 Clinical Benefit of First-Line Cemiplimab in Patients with Locally Advanced NSCLC: Subgroup Analysis from EMPOWER-Lung 1 von Bondarenko, I., Sezer, A., Kilickap, S., Gümüş, M., Özgüroğlu, M., Gogishvili, M., Turk, H.M., Cicin, I., Bentsion, D., Gladkov, O., Clingan, P., Sriuranpong, V., Rizvi, N., Mcginniss, J., Pouliot, J., Lee, S., Seebach, F., Lowy, I., Gullo, G., Rietschel, P.

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Molecular screening for diseases frequent in Ashkenazi Jews: Lessons learned from more than 100,000 tests performed in a commercial laboratory von Strom, Charles M., Crossley, Beryl, Redman, Joy B., Quan, Franklin, Buller, Arlene, McGinniss, Matthew J., Sun, Weimin

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Development of a Web-Based Query Tool for Quality Assurance of Clinical Molecular Genetic Test Results von McGinniss, Matthew J, Chen, Rebecca, Pratt, Victoria M, Buller, Arlene, Quan, Franklin, Strom, Charles M, Sun, Weimin, Crossley, Beryl

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