Lista de obras - Hongbo M. Xie - Dominio Público Uruguay

Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.

artículo científico publicado en 2014

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

artículo científico publicado en 2010

Clonal Replacement Underlies Spontaneous Remission in Paroxysmal Nocturnal Haemoglobinuria

artículo científico publicado en 2016

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

scientific article published on 20 June 2019

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

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

artículo científico publicado en 2015

High mobility group protein B1 is an activator of apoptotic response to antimetabolite drugs.

artículo científico publicado en 2007

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

artículo científico publicado en 2009

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

artículo científico publicado en 2011

Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders

artículo científico publicado en 2013

Rare copy number variants in patients with congenital conotruncal heart defects.

artículo científico publicado en 2017

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

artículo científico publicado en 2010

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

artículo científico publicado en 2010

Rare structural variation of synapse and neurotransmission genes in autism ⬇️

artículo científico publicado el 1 de marzo de 2011

Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes

scientific article published on 14 October 2013

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

artículo científico publicado en 2013

Lista de obras de Hongbo M. Xie

Analysis of chromosomal structural variation in patients with congenital left-sided cardiac lesions.

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

Clonal Replacement Underlies Spontaneous Remission in Paroxysmal Nocturnal Haemoglobinuria

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

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

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

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

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

High mobility group protein B1 is an activator of apoptotic response to antimetabolite drugs.

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

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

Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders

Rare copy number variants in patients with congenital conotruncal heart defects.

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

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

Rare structural variation of synapse and neurotransmission genes in autism ⬇️

Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes

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