Cryptic chromosome abnormalities in a patient with mixed phenotype acute leukemia

Por Ning, Yi, Slovak, Marilyn L., Schultz, Roger A., Gojo, Ivana, Baer, Maria R.
Publicado no Leuk Lymphoma (2013)

Human and mouse homologs of Escherichia coli DinB (DNA polymerase IV), members of the UmuC/DinB superfamily

Por Gerlach, Valerie L., Aravind, L., Gotway, Garrett, Schultz, Roger A., Koonin, Eugene V., Friedberg, Errol C.
Publicado em 1999

MODY-like diabetes associated with an apparently balanced translocation: possible involvement of MPP7 gene and cell polarity in the pathogenesis of diabetes

Por Bhoj, Elizabeth J, Romeo, Stefano, Baroni, Marco G, Bartov, Guy, Schultz, Roger A, Zinn, Andrew R
Publicado em 2009

Structure of the Highly Conserved HERC2 Gene and of Multiple Partially Duplicated Paralogs in Human

Por Ji, Yonggang, Rebert, Nancy A., Joslin, John M., Higgins, Michael J., Schultz, Roger A., Nicholls, Robert D.
Publicado em 2000

The Gene Mutated in Variant Late-Infantile Neuronal Ceroid Lipofuscinosis (CLN6) and in nclf Mutant Mice Encodes a Novel Predicted Transmembrane Protein

Por Wheeler, Ruth B., Sharp, Julie D., Schultz, Roger A., Joslin, John M., Williams, Ruth E., Mole, Sara E.
Publicado em 2002

Value of Oligonucleotide-Based Array Comparative Genomic Hybridization for Diagnosis of Acute Promyelocytic Leukemia in a Patient Negative for t(15;17)(q24.1;q21.2)/Promyelocytic L...

Por Alayed, Khaled, Medeiros, L. Jeffrey, Schultz, Roger A., Cortes, Jorge, Lu, Gary, Bueso-Ramos, Carlos E., Konoplev, Sergej
Publicado no Clin Lymphoma Myeloma Leuk (2013)

Cloning the human and mouse MMS19 genes and functional complementation of a yeast mms19 deletion mutant

Por Queimado, Lurdes, Rao, Malini, Schultz, Roger A., Koonin, Eugene V., Aravind, L., Nardo, Tiziana, Stefanini, Miria, Friedberg, Errol C.
Publicado em 2001

Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells

Por McDaniel, Lisa D. , Tomkins, Darrell J. , Stanbridge, Eric J. , Somerville, Martin J. , Friedberg, Errol C. , Schultz, Roger A. 
Publicado em 2005

Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH

Por Neill, Nicholas J., Ballif, Blake C., Lamb, Allen N., Parikh, Sumit, Ravnan, J. Britt, Schultz, Roger A., Torchia, Beth S., Rosenfeld, Jill A., Shaffer, Lisa G.
Publicado em 2011

DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13

Por Garcia, Nilda M., Allgood, Jocelyn, Santos, Lane J., Lonergan, D., Batanian, J.R., Henkemeyer, Mark, Bartsch, Oliver, Schultz, Roger A., Zinn, Andrew R., Baker, Linda A.
Publicado em 2006

Loss of Blm enhances basal cell carcinoma and rhabdomyosarcoma tumorigenesis in Ptch1(+/−) mice

Por Davari, Parastoo, Hebert, Jennifer L., Albertson, Donna G., Huey, Bing, Roy, Ritu, Mancianti, Maria L., Horvai, Andrew E., McDaniel, Lisa D., Schultz, Roger A., Epstein, Ervin H.
Publicado em 2010

Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis

Por Schultz, Roger A, Delioukina, Maria, Gaal, Karl, Bedell, Victoria, Smith, David D, Forman, Stephen J, McDaniel, Lisa D, Ballif, Blake C, Shaffer, Lisa G, Slovak, Marilyn L
Publicado em 2011

A Tlr7 translocation accelerates systemic autoimmunity in murine lupus

Por Subramanian, Srividya, Tus, Katalin, Li, Quan-Zhen, Wang, Andrew, Tian, Xiang-Hong, Zhou, Jinchun, Liang, Chaoying, Bartov, Guy, McDaniel, Lisa D., Zhou, Xin J., Schultz, Roger A., Wakeland, Edward K.
Publicado em 2006

Upregulation of TRAG3 gene in urothelial carcinoma of the bladder

Por Karam, Jose A., Huang, Sandra, Fan, Jinhai, Stanfield, Jennifer, Schultz, Roger A., Pong, Rey-Chen, Sun, Xiankai, Mason, Ralph P., Xie, Xian-Jin, Niu, Gang, Chen, Xiaoyuan, Frenkel, Eugene P., Sagalowsky, Arthur I., Hsieh, Jer-Tsong
Publicado em 2010

Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis

Por Kolquist, Kathryn A, Schultz, Roger A, Slovak, Marilyn L, McDaniel, Lisa D, Brown, Theresa C, Tubbs, Raymond R, Cook, James R, Theil, Karl S, Cawich, Victoria, Valentin, Caitlin, Minier, Sara, Neill, Nicholas J, Byerly, Steve, Morton, S Annie, Sahoo, Trilochan, Ballif, Blake C, Shaffer, Lisa G
Publicado em 2011

MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways

Por Paciorkowski, Alex R., Traylor, Ryan N., Rosenfeld, Jill A., Hoover, Jacqueline M., Harris, Catharine J., Winter, Susan, Lacassie, Yves, Bialer, Martin, Lamb, Allen N., Schultz, Roger A., Berry-Kravis, Elizabeth, Porter, Brenda E., Falk, Marni, Venkat, Anu, Vanzo, Rena J., Cohen, Julie S., Fatemi, Ali, Dobyns, William B., Shaffer, Lisa G., Ballif, Blake C., Marsh, Eric D.
Publicado em 2013

Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features

Por Lamb, Allen N., Rosenfeld, Jill A., Neill, Nicholas J., Talkowski, Michael E., Blumenthal, Ian, Girirajan, Santhosh, Keelean-Fuller, Debra, Fan, Zheng, Pouncey, Jill, Stevens, Cathy, Mackay-Loder, Loren, Terespolsky, Deborah, Bader, Patricia, Rosenbaum, Kenneth, Vallee, Stephanie, Moeschler, John B., Ladda, Roger, Sell, Susan, Martin, Judith, Ryan, Shawnia, Jones, Marilyn C., Moran, Rocio, Shealy, Amy, Madan-Khetarpal, Suneeta, McConnell, Juliann, Surti, Urvashi, Delahaye, Andrée, Heron-Longe, Bénédicte, Pipiras, Eva, Benzacken, Brigitte, Passemard, Sandrine, Verloes, Alain, Isidor, Bertrand, Le Caignec, Cedric, Glew, Gwen M., Opheim, Kent E., Eichler, Evan E., Morton, Cynthia C., Gusella, James F., Schultz, Roger A., Ballif, Blake C., Shaffer, Lisa G.
Publicado em 2012