Kevin C. H. Ha

发表

RNAcompete-S: Combined RNA sequence/structure preferences for RNA binding proteins derived from a single-step in vitro selection.

Kaitlin U Laverty, Kate B. Cook, T. Hughes, 2017, Methods.

Shifts in Ribosome Engagement Impact Key Gene Sets in Neurodevelopment and Ubiquitination in Rett Syndrome.

Robert J. Weatheritt, Q. Morris, B. Blencowe, 2020, Cell reports.

An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms

B. Blencowe, Xinchen Wang, Kevin C. H. Ha, 2017, Genome Research.

Identification of gene fusion transcripts by transcriptome sequencing in BRCA1-mutated breast cancers and cell lines

A. Ashworth, W. Foulkes, J. Reis-Filho, 2011, BMC Medical Genomics.

Whippet: an efficient method for the detection and quantification of alternative splicing reveals extensive transcriptomic complexity

Robert J. Weatheritt, B. Blencowe, Kevin C. H. Ha, 2017, bioRxiv.

Comparison of Affymetrix Gene Array with the Exon Array shows potential application for detection of transcript isoform variation

J. Coulombe-Huntington, Kevin C. H. Ha, J. Majewski, 2009, BMC Genomics.

MECP2 Is Post-transcriptionally Regulated during Human Neurodevelopment by Combinatorial Action of RNA-Binding Proteins and miRNAs.

Q. Morris, B. Blencowe, Kevin C. H. Ha, 2016, Cell reports.

Germ-line DNA copy number variation frequencies in a large North American population

Gary D. Bader, Steven Gallinger, Gary D Bader, 2007, Human Genetics.

RNAcompete methodology and application to determine sequence preferences of unconventional RNA-binding proteins.

Timothy R. Hughes, Quaid D. Morris, T. Hughes, 2017, Methods.

QAPA: a new method for the systematic analysis of alternative polyadenylation from RNA-seq data

Quaid Morris, Benjamin J. Blencowe, Q. Morris, 2018, Genome Biology.

Genetic interaction mapping and exon-resolution functional genomics with a hybrid Cas9–Cas12a platform

Henry N. Ward, B. Blencowe, C. Myers, 2020, Nature Biotechnology.

Multilayered Control of Alternative Splicing Regulatory Networks by Transcription Factors.

Robert J. Weatheritt, T. Hughes, B. Blencowe, 2017, Molecular cell.

Regulation of alternative polyadenylation by the C2H2-zinc-finger protein Sp1.

B. Blencowe, D. Ray, Xinghua Guo, 2022, Molecular cell.

The RNA-binding protein SERBP1 functions as a novel oncogenic factor in glioblastoma by bridging cancer metabolism and epigenetic regulation

Gabriela D. A. Guardia, Yi-ming Li, T. Hughes, 2020, Genome Biology.

QAPA: a new method for the systematic analysis of alternative polyadenylation from RNA-seq data

Q. Morris, B. Blencowe, Kevin C. H. Ha, 2018, Genome Biology.

An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms

B. Blencowe, Xinchen Wang, Kevin C. H. Ha, 2017, Genome research.

Comparative genomics of elastin: Sequence analysis of a highly repetitive protein.

John Parkinson, Ming Miao, Trevis M. Alleyne, 2007, Matrix biology : journal of the International Society for Matrix Biology.

Differential contribution of transcriptomic regulatory layers in the definition of neuronal identity

Robert J. Weatheritt, Q. Morris, B. Blencowe, 2021, Nature communications.

RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression.

Emilie Lalonde, Jacek Majewski, Tomi Pastinen, 2011, Genome research.

Oncogenic Activation of the RNA Binding Protein NELFE and MYC Signaling in Hepatocellular Carcinoma.

T. Hughes, Q. Morris, D. Ray, 2017, Cancer cell.

Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next‐generation exome sequencing

Nada Jabado, Constantin Polychronakos, Emilie Lalonde, 2010, Human mutation.

Novel Mutations in SCO1 as a Cause of Fatal Infantile Encephalopathy and Lactic Acidosis

E. Shoubridge, H. Antonicka, Kevin C. H. Ha, 2013, Human mutation.

Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype

Kevin C. H. Ha, J. Majewski, K. Al-Thihli, 2011, Journal of Medical Genetics.

Mutations in SCARF2 are responsible for Van Den Ende-Gupta syndrome.

Kevin C. H. Ha, J. Majewski, L. Jerome-Majewska, 2010, American journal of human genetics.

Efficient and Accurate Quantitative Profiling of Alternative Splicing Patterns of Any Complexity on a Laptop.

Robert J. Weatheritt, Robert J Weatheritt, B. Blencowe, 2018, Molecular cell.

Shifts in Ribosome Engagement Impact Key Gene Sets in Neurodevelopment and Ubiquitination in Rett Syndrome

Robert J. Weatheritt, Q. Morris, B. Blencowe, 2019, SSRN Electronic Journal.

Genetic interaction mapping and exon-resolution functional genomics with a hybrid Cas9–Cas12a platform

B. Blencowe, C. Myers, J. Moffat, 2020, Nature Biotechnology.

ARHGDIA: a novel gene implicated in nephrotic syndrome

Kevin C. H. Ha, S. Narod, J. Majewski, 2013, Journal of Medical Genetics.

Comparison of Affymetrix Gene Array with the Exon Array shows potential application for detection of transcript isoform variation

J. Coulombe-Huntington, Kevin C. H. Ha, J. Majewski, 2009, BMC Genomics.

Multilayered Control of Alternative Splicing Regulatory Networks by Transcription Factors.

Robert J. Weatheritt, Frederick S. Vizeacoumar, T. Hughes, 2017, Molecular cell.

Efficient and Accurate Quantitative Profiling of Alternative Splicing Patterns of Any Complexity on a Laptop.

Robert J. Weatheritt, B. Blencowe, Kevin C. H. Ha, 2018, Molecular cell.