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All papers authored by Hongbo M. Xie

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2019 Alexandra Lenard, Hongbo Michael Xie

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, Taylor Pastuer, Tyler Shank, Clara Libbrecht, Simone S. Riedel

ORCID

, Molly Kingsley

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, Zuo-Fei Yuan, Nan Zhu, Tobias Neff, Kathrin M. Bernt

ORCID

Epigenetic regulation of protein translation in KMT2A-rearranged AML

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Hongbo M. Xie

ORCID

, Deanne M. Taylor, Zhe Zhang, Donna M. McDonald‐McGinn, Elaine H. Zackai, Dwight Stambolian, Hakon Hakonarson, Bernice E. Morrow, Beverly S. Emanuel, Elizabeth Goldmuntz

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

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2016 Kinga M. Bujakowska, Rosario Fernandez-Godino, Emily Place

ORCID

, Mark Consugar, Daniel Navarro-Gomez, Joseph White

ORCID

, Emma C. Bedoukian

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, Xiaosong Zhu, Hongbo M. Xie

ORCID

, Xiaowu Gai, Bart P. Leroy, Eric A. Pierce

Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations

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Daria V. Babushok, Natasha Stanley, Hongbo M. Xie

ORCID

, Hugh Huang, Adam Bagg, Timothy S. Olson, Monica Bessler

Clonal Replacement Underlies Spontaneous Remission in Paroxysmal Nocturnal Haemoglobinuria

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Daria V. Babushok, Anne-Laure Grignon, Yimei Li, Jamie Atienza, Hongbo M. Xie

ORCID

, Ho-Sun Lam, Helge Hartung, Monica Bessler, Timothy S. Olson

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

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2015 Daria V. Babushok, Nieves Perdigones, Juan C. Perin, Timothy S. Olson, Wenda Ye, Jacquelyn J. Roth, Curt Lind, Carine Cattier, Yimei Li, Helge Hartung, Michele E. Paessler, Dale M. Frank, Hongbo M. Xie

ORCID

, Shanna Cross, Joshua D. Cockroft and 5 other authors

Emergence of clonal hematopoiesis in the majority of patients with acquired aplastic anemia

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2014 Peter S. White, Hongbo M. Xie

ORCID

, Petra Werner, Joseph Glessner, Brande Latney, Hakon Hakonarson, Elizabeth Goldmuntz

Analysis of Chromosomal Structural Variation in Patients with Congenital Left-Sided Cardiac Lesions

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2013 Marie T. Lott

ORCID

, Jeremy N. Leipzig, Olga Derbeneva, H. Michael Xie

ORCID

, H. Michael Xie, Dimitra Chalkia, Mahdi Sarmady, Vincent Procaccio

ORCID

, Douglas C. Wallace

mtDNA Variation and Analysis Using MITOMAP and MITOMASTER

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Daria V. Babushok, Hongbo M. Xie

ORCID

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

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

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Zhe Zhang, Jeremy Leipzig, Ariella Sasson, Angela M. Yu, Juan C. Perin, Hongbo M. Xie

ORCID

, Mahdi Sarmady, Patrick V. Warren, Peter S. White

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

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Sylvie Bannwarth, Bénédicte Mousson de Camaret, Vincent Procaccio

ORCID

, Anne Sophie Lebre, Claude Jardel, Annabelle Chaussenot, Claire Hoarau, Hassani Maoulida, Nathanaël Charrier, Xiaowu Gai, Hongbo M. Xie

ORCID

ORCID

, Konstantina Fragaki, Gaëlle Hardy, Bénédicte Mousson de Camaret and 25 other authors

Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders

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Lisa C. A. D'Alessandro, Petra Werner, Hongbo M. Xie

ORCID

, Hakon Hakonarson, Peter S. White, Elizabeth Goldmuntz

The Prevalence of 16p12.1 Microdeletion in Patients with Left-sided Cardiac Lesions

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2011 X. Gai, H. M. Xie

ORCID

, J. C. Perin, N. Takahashi, K. Murphy, A. S. Wenocur, M. D'arcy, R. J. O'Hara, E. Goldmuntz, D. E. Grice, T. H. Shaikh, H. Hakonarson, J. D. Buxbaum, J. Elia, P. S. White

Rare structural variation of synapse and neurotransmission genes in autism

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Hongbo M. Xie

ORCID

, Juan C. Perin, Theodore G. Schurr, Matthew C. Dulik, Sergey I. Zhadanov, Joseph A. Baur, Michael P. King, Emily Place, Colleen Clarke, Michael Grauer, Jonathan Schug, Avni Santani, Anthony Albano, Cecilia Kim, Vincent Procaccio

ORCID

and 3 other authors

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

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2010 Li An, Desmond J. Smith, Hongbo Xie

ORCID

, Vasileios Megalooikonomou, Zoran Obradovic

Identifying Gene Functions using Functional Expression Profiles obtained by Voxelation

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J. Elia, X. Gai, H. M. Xie

ORCID

, J. C. Perin, E. Geiger, J. T. Glessner, M. D'Arcy, R. Deberardinis, E. Frackelton, C. Kim, F. Lantieri, B. M. Muganga, L. Wang, T. Takeda, E. F. Rappaport and 6 other authors

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes (Molecular Psychiatry (2010) 15 (637-646) DOI: 10.1038/mp.2009.57)

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Xiaowu Gai, Juan C. Perin, Kevin Murphy, Ryan O'Hara, Monica D'arcy, Adam Wenocur, Hongbo M. Xie

ORCID

, Eric F. Rappaport, Tamim H. Shaikh, Peter S. White

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

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2009 Judit Garriga, Hongbo Xie

ORCID

, Zoran Obradovic, Xavier Graña

Selective control of gene expression by CDK9 in human cells

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Tamim H. Shaikh, Xiaowu Gai, Juan C. Perin, Joseph T. Glessner, Hongbo Xie

ORCID

, Kevin Murphy, Ryan O'Hara, Tracy Casalunovo, Laura K. Conlin, Monica D'Arcy, Edward C. Frackelton, Elizabeth A. Geiger, Chad Haldeman-Englert, Marcin Imielinski, Cecilia E. Kim and 23 other authors

High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications

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J. Elia, X. Gai, H. M. Xie

ORCID

, J. C. Perin, E. Geiger, J. T. Glessner, M. D'arcy, R. deBerardinis, E. Frackelton, C. Kim, F. Lantieri, B. M. Muganga, L. Wang, T. Takeda, E. F. Rappaport and 6 other authors

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

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