Author details

Full Name

Charles Gawad

Affiliation

Stanford University

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34807338	Bringing precision oncology to cellular resolution with single-cell genomics.	Clin Exp Metastasis	2022
36163278	Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.	Nat Genet	2022
35442732	Simultaneous monitoring of disease and microbe dynamics through plasma DNA sequencing in pediatric patients with acute lymphoblastic leukemia.	Sci Adv	2022
36204688	Duplex Sequencing Uncovers Recurrent Low-frequency Cancer-associated Mutations in Infant and Childhood <i>KMT2A</i>-rearranged Acute Leukemia.	Hemasphere	2022
34807338	Bringing precision oncology to cellular resolution with single-cell genomics.	Clin Exp Metastasis	2022
35442732	Simultaneous monitoring of disease and microbe dynamics through plasma DNA sequencing in pediatric patients with acute lymphoblastic leukemia.	Sci Adv	2022
36204688	Duplex Sequencing Uncovers Recurrent Low-frequency Cancer-associated Mutations in Infant and Childhood <i>KMT2A</i>-rearranged Acute Leukemia.	Hemasphere	2022
36163278	Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.	Nat Genet	2022
34099548	Accurate genomic variant detection in single cells with primary template-directed amplification.	Proc Natl Acad Sci U S A	2021
34099548	Accurate genomic variant detection in single cells with primary template-directed amplification.	Proc Natl Acad Sci U S A	2021
31855231	Evaluation of Plasma Microbial Cell-Free DNA Sequencing to Predict Bloodstream Infection in Pediatric Patients With Relapsed or Refractory Cancer.	JAMA Oncol	2020
31855231	Evaluation of Plasma Microbial Cell-Free DNA Sequencing to Predict Bloodstream Infection in Pediatric Patients With Relapsed or Refractory Cancer.	JAMA Oncol	2020
31028641	Sequencing the Genomes of Single Cells.	Methods Mol Biol	2019
31028641	Sequencing the Genomes of Single Cells.	Methods Mol Biol	2019
31151460	Single-cell RNA sequencing reveals the impact of chromosomal instability on glioblastoma cancer stem cells.	BMC Med Genomics	2019
31341285	Resolving medulloblastoma cellular architecture by single-cell genomics.	Nature	2019
31341285	Resolving medulloblastoma cellular architecture by single-cell genomics.	Nature	2019
31151460	Single-cell RNA sequencing reveals the impact of chromosomal instability on glioblastoma cancer stem cells.	BMC Med Genomics	2019
29284596	Measurable residual disease detection by high-throughput sequencing improves risk stratification for pediatric B-ALL.	Blood	2018
30220501	A Single-Cell Transcriptional Atlas of the Developing Murine Cerebellum.	Curr Biol	2018
30063705	High-resolution transcriptional dissection of in vivo Atoh1-mediated hair cell conversion in mature cochleae identifies Isl1 as a co-reprogramming factor.	PLoS Genet	2018
30245008	LC3-Associated Phagocytosis in Myeloid Cells Promotes Tumor Immune Tolerance.	Cell	2018
30573729	Murine hematopoietic stem cell activity is derived from pre-circulation embryos but not yolk sacs.	Nat Commun	2018
29489755	Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.	Nature	2018
29284596	Measurable residual disease detection by high-throughput sequencing improves risk stratification for pediatric B-ALL.	Blood	2018
30063705	High-resolution transcriptional dissection of in vivo Atoh1-mediated hair cell conversion in mature cochleae identifies Isl1 as a co-reprogramming factor.	PLoS Genet	2018
30220501	A Single-Cell Transcriptional Atlas of the Developing Murine Cerebellum.	Curr Biol	2018
30245008	LC3-Associated Phagocytosis in Myeloid Cells Promotes Tumor Immune Tolerance.	Cell	2018
30573729	Murine hematopoietic stem cell activity is derived from pre-circulation embryos but not yolk sacs.	Nat Commun	2018
29489755	Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.	Nature	2018
29178827	Genome-wide segregation of single nucleotide and structural variants into single cancer cells.	BMC Genomics	2017
29178827	Genome-wide segregation of single nucleotide and structural variants into single cancer cells.	BMC Genomics	2017
26806412	Single-cell genome sequencing: current state of the science.	Nat Rev Genet	2016
26806412	Single-cell genome sequencing: current state of the science.	Nat Rev Genet	2016
27736885	Dynamic ASXL1 Exon Skipping and Alternative Circular Splicing in Single Human Cells.	PLoS One	2016
27681629	Early somatic mosaicism is a rare cause of long-QT syndrome.	Proc Natl Acad Sci U S A	2016
27736885	Dynamic ASXL1 Exon Skipping and Alternative Circular Splicing in Single Human Cells.	PLoS One	2016
27681629	Early somatic mosaicism is a rare cause of long-QT syndrome.	Proc Natl Acad Sci U S A	2016
24799715	Noninvasive in vivo monitoring of tissue-specific global gene expression in humans.	Proc Natl Acad Sci U S A	2014
25425670	Dissecting the clonal origins of childhood acute lymphoblastic leukemia by single-cell genomics.	Proc Natl Acad Sci U S A	2014
24799715	Noninvasive in vivo monitoring of tissue-specific global gene expression in humans.	Proc Natl Acad Sci U S A	2014
25136831	A quantitative comparison of single-cell whole genome amplification methods.	PLoS One	2014
25425670	Dissecting the clonal origins of childhood acute lymphoblastic leukemia by single-cell genomics.	Proc Natl Acad Sci U S A	2014
25136831	A quantitative comparison of single-cell whole genome amplification methods.	PLoS One	2014
22319583	Circular RNAs are the predominant transcript isoform from hundreds of human genes in diverse cell types.	PLoS One	2012
22932801	Massive evolution of the immunoglobulin heavy chain locus in children with B precursor acute lymphoblastic leukemia.	Blood	2012
22319583	Circular RNAs are the predominant transcript isoform from hundreds of human genes in diverse cell types.	PLoS One	2012
22932801	Massive evolution of the immunoglobulin heavy chain locus in children with B precursor acute lymphoblastic leukemia.	Blood	2012
16078857	Towards molecular medicine: a case for a biological periodic table.	Am J Pharmacogenomics	2005
16078857	Towards molecular medicine: a case for a biological periodic table.	Am J Pharmacogenomics	2005

1 - 50 of 50

Kimaada Allette

Icahn School of Medicine at Mount Sinai

Career Start Year 2016

Number of shared co-authors 0

Richard de Borja

The Hospital for Sick Children

Career Start Year 2012

Number of shared co-authors 2

Marta Gut

Universitat de Barcelona (UB)

Career Start Year 2010

Number of shared co-authors 9

Maxime Caron

Centre Hospitalier Universitaire Sainte-Justine

Career Start Year 2010

Number of shared co-authors 0

Andrew McPherson

Memorial Sloan Kettering Cancer Center

Career Start Year 2010

Number of shared co-authors 0

Christopher A Miller

Washington University School of Medicine

Career Start Year 2009

Number of shared co-authors 0

Vyacheslav Amstislavskiy

Max-Planck-Institute for Molecular Genetics

Career Start Year 2009

Number of shared co-authors 9

Ignaty Leshchiner

Broad Institute of Massachusetts Institute of Technology and Harvard

Career Start Year 2008

Number of shared co-authors 1

Ken Chen

University of Texas MD Anderson Cancer Center

Career Start Year 2007

Number of shared co-authors 5

Ayshwarya Subramanian

Broad Institute of MIT and Harvard

Career Start Year 2006

Number of shared co-authors 1

Kun Zhang

China Pharmaceutical University

Career Start Year 2005

Number of shared co-authors 3

Yongjun Zhao

Canada British Columbia Cancer Research Centre, University of British Columbia

Career Start Year 2005

Number of shared co-authors 21

James Hicks

Michelson Center for Convergent Bioscience, University of Southern California

Career Start Year 2004

Number of shared co-authors 0

Robert Sebra

Icahn School of Medicine at Mount Sinai

Career Start Year 2004

Number of shared co-authors 0

Jason Walker

McDonnell Genome Institute, Washington University School of Medicine

Career Start Year 2004

Number of shared co-authors 3

Catrina Fronick

McDonnell Genome Institute, Washington University in St. Louis School of Medicine

Career Start Year 2004

Number of shared co-authors 0

Chip Stewart

Broad Institute of MIT and Harvard

Career Start Year 2004

Number of shared co-authors 8

Trevor J Pugh

Princess Margaret Cancer Centre, University Health Network

Career Start Year 2003

Number of shared co-authors 13

Peter J Campbell

Wellcome Sanger Institute

Career Start Year 2003

Number of shared co-authors 3

Peter Van Loo

The Francis Crick Institute

Career Start Year 2003

Number of shared co-authors 2

Jacqueline E Payton

Washington University School of Medicine.

Career Start Year 2001

Number of shared co-authors 1

Gad Getz

Broad Institute of the Massachusetts Institute of Technology and Harvard

Career Start Year 2000

Number of shared co-authors 16

David H Spencer

Washington University School of Medicine.

Career Start Year 2000

Number of shared co-authors 1

Thierry Voet

KU Leuven Institute for Single Cell Omics (LISCO)

Career Start Year 1999

Number of shared co-authors 1

Martin Hirst

University of British Columbia

Career Start Year 1998

Number of shared co-authors 18

Jay Shendure

University of Washington

Career Start Year 1996

Number of shared co-authors 5

Aaron M Newman

Stanford University

Career Start Year 1994

Number of shared co-authors 2

Robert S Fulton

McDonnell Genome Institute, Washington University School of Medicine

Career Start Year 1994

Number of shared co-authors 28

Marco A Marra

University of British Columbia

Career Start Year 1993

Number of shared co-authors 36

Elaine R Mardis

The Ohio State University

Career Start Year 1988

Number of shared co-authors 33

row(s) 1 - 30 of 30

John Easton

St Jude Children's Research Hospital

Co-authored papers 6

Veronica Gonzalez-Pena

Stanford University School of Medicine

Co-authored papers 6

Stephen R Quake

Stanford University

Co-authored papers 5

Jinghui Zhang

Changhai Hospital, Second Military Medical University

Co-authored papers 2

Laure Bihannic

St. Jude Children's Research Hospital

Co-authored papers 2

Xiang Chen

St. Jude Children's Research Hospital

Co-authored papers 2

Norman J Lacayo

Co-authored papers 2

Xiaotu Ma

St. Jude Children's Research Hospital

Co-authored papers 2

Timothy N Phoenix

Co-authored papers 2

Paul A Northcott

St Jude Children's Research Hospital

Co-authored papers 2

Stephen P Hunger

Children's Hospital of Philadelphia

Co-authored papers 2

Jennifer Hadley

St. Jude Children's Research Hospital

Co-authored papers 2

Euan A Ashley

Stanford University

Co-authored papers 1

Leandro C Hermida

University of Pittsburgh

Co-authored papers 1

Lisa Mayr

Co-authored papers 1

David Wu

University of Washington

Co-authored papers 1

Christopher A Walsh

Broad Institute of MIT and Harvard

Co-authored papers 1

Yunfeng Dai

Colleges of Medicine, University of Florida

Co-authored papers 1

Xiao-Nan Li

Northwestern University

Co-authored papers 1

Jaime M Guidry Auvil

National Cancer Institute

Co-authored papers 1

Marco V Perez

Co-authored papers 1

Ching C Lau

Baylor College of Medicine

Co-authored papers 1

Robert J Wechsler-Reya

Sanford Burnham Prebys Medical Discovery Institute

Co-authored papers 1

Sharon J Diskin

Children's Hospital of Philadelphia

Co-authored papers 1

Megan E Grove

Stanford Medicine Clinical Genomics Program

Co-authored papers 1

Xueyuan Cao

University of Chinese Academy of Sciences

Co-authored papers 1

Soheil Meshinchi

Fred Hutchinson Cancer Research Centre

Co-authored papers 1

Stanley Pounds

St. Jude Children's Research Hospital.

Co-authored papers 1

Stefan M Pfister

Hopp Children's Cancer Center Heidelberg (KiTZ)

Co-authored papers 1

1 - 30

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