Marcin Imielinski

发表

Abstract A22: Identifying somatic mutation hotspots across protein family alignments.

Marcin Imielinski, Charles Du, Matthew Meyerson, 2013 .

Corrigendum: Signatures of mutational processes in human cancer

Roland Eils, Natalie Jäger, Adam P. Butler, 2013, Nature.

The evolutionary history of 2,658 cancers

Benjamin J. Raphael, Salem Malikic, Martin Peifer, 2017, Nature.

SvABA: genome-wide detection of structural variants and indels by local assembly

Joachim Weischenfeldt, Gad Getz, Rameen Beroukhim, 2018, Genome research.

Strong synaptic transmission impact by copy number variations in schizophrenia

Raquel E. Gur, Mark Weiser, Muredach P. Reilly, 2010, Proceedings of the National Academy of Sciences.

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Robert T. Schultz, Margaret A. Pericak-Vance, Takeshi Sakurai, 2009, Nature.

SvABA: Genome-wide detection of structural variants and indels by local assembly

Peter J. Campbell, Joachim Weischenfeldt, Rameen Beroukhim, 2017 .

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

Tariq Ahmad, Katherine I. Morley, Vibeke Andersen, 2011, Nature Genetics.

Deep epistasis in human metabolism.

Calin Belta, Marcin Imielinski, C. Belta, 2010, Chaos.

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects.

Constantin Polychronakos, David C Wilson, Joseph T. Glessner, 2010, Human molecular genetics.

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

John A. Sweeney, Geraldine Dawson, Daniel H. Geschwind, 2009, PLoS genetics.

Systematic analysis of conservation relations in Escherichia coli genome-scale metabolic network reveals novel growth media.

Calin Belta, Harvey Rubin, Marcin Imielinski, 2006, Biophysical journal.

Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas

Chandra Sekhar Pedamallu, Carrie Cibulskis, Angela N. Brooks, 2016, Nature Genetics.

Insertions and Deletions Target Lineage-Defining Genes in Human Cancers

Marcin Imielinski, Matthew Meyerson, M. Meyerson, 2017, Cell.

Identification of focally amplified lineage-specific super-enhancers in human epithelial cancers

Marcin Imielinski, Matthew Meyerson, Andrew D Cherniack, 2015, Nature Genetics.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Susanne Walitza, Aribert Rothenberger, Takeshi Sakurai, 2011, Nature Genetics.

Inferring structural variant cancer cell fraction

Roland Eils, Yuan Ji, Jan Schröder, 2020, Nature Communications.

Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing

Ken Chen, Mark Gerstein, Satoru Miyano, 2018, Nature Genetics.

Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions

Nicholas P. Tatonetti, Iman Hajirasouliha, Christopher E. Mason, 2020, bioRxiv.

Patterns of structural variation in human cancer

Jan O. Korbel, Peter J. Campbell, Joachim Weischenfeldt, 2017, bioRxiv.

A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci

Constantin Polychronakos, Struan F. A. Grant, Joseph T. Glessner, 2011, PLoS genetics.

Abstract 3000: Pervasive intra-tumour heterogeneity and subclonal selection across cancer types

Yuan Ji, Ville Mustonen, Salem Malikic, 2018, Molecular and Cellular Biology / Genetics.

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

Xiaowu Gai, Laura K Conlin, Livija Medne, 2009, Genome research.

A Pan-Cancer Analysis of Transcriptome Changes Associated with Somatic Mutations in U2AF1 Reveals Commonly Altered Splicing Events

Chandra Sekhar Pedamallu, Angela N. Brooks, Gad Getz, 2014, PloS one.

Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions

Jean Thierry-Mieg, Iman Hajirasouliha, Christopher E. Mason, 2020, bioRxiv.

Association Analysis of the FTO Gene with Obesity in Children of Caucasian and African Ancestry Reveals a Common Tagging SNP

Struan F. A. Grant, Joseph T. Glessner, Hakon Hakonarson, 2008, PloS one.

Variants of DENND1B associated with asthma in children.

Ingo Ruczinski, James Flory, Terri H Beaty, 2010, The New England journal of medicine.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Robert T. Schultz, Takeshi Sakurai, Joseph Piven, 2009, Nature.

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

Struan F. A. Grant, Joseph T. Glessner, Hakon Hakonarson, 2010, PloS one.

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

Joseph T. Glessner, Hakon Hakonarson, Ryan M. Smith, 2008, Nature Genetics.

Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2

Wendy Winckler, Gad Getz, Steven A Carr, 2012, Proceedings of the National Academy of Sciences.

Common variants at five new loci associated with early-onset inflammatory bowel disease

Johan Van Limbergen, David C Wilson, David C. Wilson, 2009, Nature Genetics.

Portraits of genetic intra-tumour heterogeneity and subclonal selection across cancer types

Yuan Ji, Ville Mustonen, Paul T. Spellman, 2018, bioRxiv.