The prevalence of 16p12.1 microdeletion in patients with left-sided cardiac lesions

по D’Alessandro, Lisa C.A., Werner, Petra, Xie, Hongbo M., Hakonarson, Hakon, White, Peter S., Goldmuntz, Elizabeth
Опубликовано в: Congenit Heart Dis (2013)

Clonal Replacement Underlies Spontaneous Remission in Paroxysmal Nocturnal Haemoglobinuria

по Babushok, Daria V., Stanley, Natasha, Xie, Hongbo M., Huang, Hugh, Bagg, Adam, Olson, Timothy S., Bessler, Monica
Опубликовано в: Br J Haematol (2016)

Rare Copy Number Variants in Patients with Congenital Conotruncal Heart Defects

по Xie, Hongbo M., Werner, Petra, Stambolian, Dwight, Bailey-Wilson, Joan E., Hakonarson, Hakon, White, Peter S., Taylor, Deanne M., Goldmuntz, Elizabeth
Опубликовано в: Birth Defects Res (2017)

Efficient digest of high-throughput sequencing data in a reproducible report

по Zhang, Zhe, Leipzig, Jeremy, Sasson, Ariella, Yu, Angela M, Perin, Juan C, Xie, Hongbo M, Sarmady, Mahdi, Warren, Patrick V, White, Peter S
Опубликовано 2013

Disrupted lymphocyte homeostasis in hepatitis‐associated acquired aplastic anemia is associated with short telomeres

по Babushok, Daria V., Grignon, Anne‐Laure, Li, Yimei, Atienza, Jamie, Xie, Hongbo M., Lam, Ho‐Sun, Hartung, Helge, Bessler, Monica, Olson, Timothy S.
Опубликовано в: Am J Hematol (2016)

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

по Rappaport Eric F, Xie Hongbo M, Wenocur Adam, D'arcy Monica, O'Hara Ryan, Murphy Kevin, Perin Juan C, Gai Xiaowu, Shaikh Tamim H, White Peter S
Опубликовано 2010-02-01

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics

по Gai, Xiaowu, Perin, Juan C, Murphy, Kevin, O'Hara, Ryan, D'arcy, Monica, Wenocur, Adam, Xie, Hongbo M, Rappaport, Eric F, Shaikh, Tamim H, White, Peter S
Опубликовано 2010

Menin is necessary for long term maintenance of meningioma-1 driven leukemia

по Libbrecht, Clara, Xie, Hongbo M., Kingsley, Molly C., Haladyna, Jessica N., Riedel, Simone S., Alikarami, Fatemeh, Lenard, Alexandra, McGeehan, Gerard M., Ernst, Patricia, Bernt, Kathrin M.
Опубликовано в: Leukemia (2021)

Copy number variations in individuals with conotruncal heart defects reveal some shared developmental pathways irrespective of 22q11.2 deletion status

по Xie, Hongbo M., Taylor, Deanne M., Zhang, Zhe, McDonald-McGinn, Donna M., Zackai, Elaine H., Stambolian, Dwight, Hakonarson, Hakon, Morrow, Bernice E., Emanuel, Beverly S., Goldmuntz, Elizabeth
Опубликовано в: Birth Defects Res (2019)

Copy Number Variation Is An Important Contributor to the Genetic Causality of Inherited Retinal Degenerations

по Bujakowska, Kinga M., Fernandez-Godino, Rosario, Place, Emily, Cosugar, Mark, Navarro-Gomez, Daniel, White, Joseph, Bedoukian, Emma C., Zhu, Xiaosong, Xie, Hongbo M., Gai, Xiaowu, Leroy, Bart P., Pierce, Eric A.
Опубликовано в: Genet Med (2016)

Specific patterns of H3K79 methylation influence genetic interaction of oncogenes in AML

по Kingsley, Molly C., Xie, Hongbo M., Chen, Bo-Rui, Riedel, Simone S., Pastuer, Taylor, Bollig, Madelyn K., Shank, Tyler, Libbrecht, Clara, Stabler, Sally P., Deshpande, Aniruddha J., Intlekofer, Andrew M., Bernt, Kathrin M.
Опубликовано в: Blood Adv (2020)

Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States

по Oluwafemi, Omobola O., Musfee, Fadi I., Mitchell, Laura E., Goldmuntz, Elizabeth, Xie, Hongbo M., Hakonarson, Hakon, Morrow, Bernice E., Guo, Tingwei, Taylor, Deanne M., McDonald-McGinn, Donna M., Emanuel, Beverly S., Agopian, A. J.
Опубликовано в: Genes (Basel) (2021)

Single Nucleotide Polymorphism Array Analysis of Bone Marrow Failure Patients Reveals Characteristic Patterns of Genetic Changes

по Babushok, Daria V., Xie, Hongbo M., Roth, Jacquelyn J., Perdigones, Nieves, Olson, Timothy S., Cockroft, Joshua D., Gai, Xiaowu, Perin, Juan C., Li, Yimei, Paessler, Michele E., Hakonarson, Hakon, Podsakoff, Gregory M., Mason, Philip J., Biegel, Jaclyn A., Bessler, Monica
Опубликовано 2013

Mitochondrial genome sequence analysis: A custom bioinformatics pipeline substantially improves Affymetrix MitoChip v2.0 call rate and accuracy

по Xie, Hongbo M, Perin, Juan C, Schurr, Theodore G, Dulik, Matthew C, Zhadanov, Sergey I, Baur, Joseph A, King, Michael P, Place, Emily, Clarke, Colleen, Grauer, Michael, Schug, Jonathan, Santani, Avni, Albano, Anthony, Kim, Cecilia, Procaccio, Vincent, Hakonarson, Hakon, Gai, Xiaowu, Falk, Marni J
Опубликовано 2011

Emergence of Clonal Hematopoiesis in the Majority of Patients with Acquired Aplastic Anemia

по Babushok, Daria V., Perdigones, Nieves, Perin, Juan C., Olson, Timothy S., Ye, Wenda, Roth, Jacquelyn J., Lind, Curt, Cattier, Carine, Li, Yimei, Hartung, Helge, Paessler, Michele E., Frank, Dale M., Xie, Hongbo M., Cross, Shanna, Cockroft, Joshua D., Podsakoff, Gregory M., Monos, Dimitrios, Biegel, Jaclyn A., Mason, Philip J., Bessler, Monica
Опубликовано в: Cancer Genet (2015)

Somatic HLA mutations expose the role of class I–mediated autoimmunity in aplastic anemia and its clonal complications

по Babushok, Daria V., Duke, Jamie L., Xie, Hongbo M., Stanley, Natasha, Atienza, Jamie, Perdigones, Nieves, Nicholas, Peter, Ferriola, Deborah, Li, Yimei, Huang, Hugh, Ye, Wenda, Morrissette, Jennifer J. D., Kearns, Jane, Porter, David L., Podsakoff, Gregory M., Eisenlohr, Laurence C., Biegel, Jaclyn A., Chou, Stella T., Monos, Dimitrios S., Bessler, Monica, Olson, Timothy S.
Опубликовано в: Blood Adv (2017)

Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders

по Bannwarth, Sylvie, Procaccio, Vincent, Lebre, Anne Sophie, Jardel, Claude, Chaussenot, Annabelle, Hoarau, Claire, Maoulida, Hassani, Charrier, Nathanaël, Gai, Xiaowu, Xie, Hongbo M, Ferre, Marc, Fragaki, Konstantina, Hardy, Gaëlle, Mousson de Camaret, Bénédicte, Marlin, Sandrine, Dhaenens, Claire Marie, Slama, Abdelhamid, Rocher, Christophe, Paul Bonnefont, Jean, Rötig, Agnès, Aoutil, Nadia, Gilleron, Mylène, Desquiret-Dumas, Valérie, Reynier, Pascal, Ceresuela, Jennifer, Jonard, Laurence, Devos, Aurore, Espil-Taris, Caroline, Martinez, Delphine, Gaignard, Pauline, Le Quan Sang, Kim-Hanh, Amati-Bonneau, Patrizia, Falk, Marni J, Florentz, Catherine, Chabrol, Brigitte, Durand-Zaleski, Isabelle, Paquis-Flucklinger, Véronique
Опубликовано 2013