M. Ronemus

发表

Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses

Michael Wigler, Ivan Iossifov, Michael Ronemus, 2011, Neuron.

De Novo Gene Disruptions in Children on the Autistic Spectrum

Kenny Q. Ye, M. Schatz, J. Troge, 2012, Neuron.

The role of de novo mutations in the genetics of autism spectrum disorders

Michael Wigler, Ivan Iossifov, Michael Ronemus, 2014, Nature Reviews Genetics.

Reducing INDEL calling errors in whole genome and exome sequencing data

M. Schatz, I. Iossifov, G. Lyon, 2014, Genome Medicine.

Demethylation-Induced Developmental Pleiotropy in Arabidopsis

S. Dellaporta, Jychian Chen, M. Ronemus, 1996, Science.

Indel variant analysis of short-read sequencing data with Scalpel

Ewa A. Bergmann, M. Schatz, Yoon-ha Lee, 2015, Nature Protocols.

Removing System Noise from Comparative Genomic Hybridization Data by Self-Self Analysis

Kenny Q. Ye, B. Lakshmi, B. Yamrom, 2011, 1105.0900.

Reducing INDEL errors in whole-genome and exome sequencing

M. Schatz, I. Iossifov, G. Lyon, 2014 .

Breaking point

M. Ronemus, 2000, Nature Medicine.

SMASH, a fragmentation and sequencing method for genomic copy number analysis

J. Kendall, M. Wigler, Beicong Ma, 2016, Genome research.

Reducing system noise in copy number data using principal components of self-self hybridizations

Kenny Q. Ye, B. Lakshmi, B. Yamrom, 2011, Proceedings of the National Academy of Sciences.

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

Boris Yamrom, Kenny Q. Ye, Andreas Buja, 2011, Neuron.

Rare de novo germline copy-number variation in testicular cancer.

B. Yamrom, J. Kendall, A. Leotta, 2012, American journal of human genetics.

Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data

Yufeng Shen, Boris Yamrom, Jeremy Leipzig, 2014, Circulation research.

The contribution of de novo coding mutations to autism spectrum disorder

Boris Yamrom, Kenny Q. Ye, Michael C. Schatz, 2014, Nature.

MicroRNA-Targeted and Small Interfering RNA–Mediated mRNA Degradation Is Regulated by Argonaute, Dicer, and RNA-Dependent RNA Polymerase in Arabidopsis[W][OA]

R. Martienssen, M. Vaughn, M. Ronemus, 2006, The Plant Cell Online.

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease

B. Yamrom, J. Kendall, A. Leotta, 2013, Human Genetics.

RareDeNovoandTransmittedCopy-NumberVariation in Autistic Spectrum Disorders

A. Buja, B. Yamrom, J. Kendall, 2011 .

Rates of contributory de novo mutation in high and low-risk autism families

A. Buja, B. Yamrom, Seungtai Yoon, 2021, Communications biology.

Low load for disruptive mutations in autism genes and their biased transmission

Kenny Q. Ye, B. Yamrom, Yoon-ha Lee, 2015, Proceedings of the National Academy of Sciences.

GENOMIC ANALYSIS OF CANCER AND HUMAN GENETIC DISORDERS

J. Troge, B. Yamrom, A. Krasnitz, 2013 .

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

Stephan J Sanders, M. Daly, W. Chung, 2015, Science.

Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies.

V. Jobanputra, K. Wrzeszczynski, A. Abhyankar, 2020, Journal of Molecular Diagnostics.

Transposons, tandem repeats, and the silencing of imprinted genes.

R. Martienssen, B. May, Z. Lippman, 2004, Cold Spring Harbor symposia on quantitative biology.

RNA interference: Methylation mystery

R. Martienssen, M. Ronemus, 2005, Nature.

Reducing INDEL errors in whole-genome and exome sequencing

M. Schatz, I. Iossifov, G. Narzisi, 2014 .

Partial bisulfite conversion for unique template sequencing

Talitha L Forcier, M. Wigler, D. Levy, 2017, Nucleic acids research.

Sharing parental genomes by siblings concordant or discordant for autism

Kenny Q. Ye, A. Buja, B. Yamrom, 2023, Cell genomics.

De novo mutations in Congenital Heart Disease with Neurodevelopmental and Other Birth Defects

Stephan J Sanders, M. Daly, W. Chung, 2016 .