C. Shaw

Anna Gambin, Chad A Shaw, Tomasz Gambin, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Common variants in the human platelet PAR4 thrombin receptor alter platelet function and differ by race.

C. Shaw, L. Simon, S. Coughlin, 2014, Blood.

Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression.

Yan Huang, Thomas Lücke, Joanna Lubieniecka, 2012, Human molecular genetics.

Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease

C. Shaw, J. Lupski, J. Jankovic, 2020, Neurology: Genetics.

Integrated Sequencing & Array Comparative Genomic Hybridization in Familial Parkinson’s Disease

C. Shaw, J. Lupski, J. Jankovic, 2019 .

Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

P. Stankiewicz, A. Breman, Ankita Patel, 2019, Genome Medicine.

Predicting human genes susceptible to genomic instability associated with Alu/Alu-mediated rearrangements

P. Stankiewicz, A. Breman, C. Shaw, 2018, Genome research.

Mus81 and converging forks limit the mutagenicity of replication fork breakage

C. Shaw, J. Lupski, I. Campbell, 2015, Science.

Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.

P. Stankiewicz, Ankita Patel, C. Shaw, 2015, Human molecular genetics.

Absence of heterozygosity due to template switching during replicative rearrangements.

M. Hurles, R. Pfundt, P. Stankiewicz, 2015, American journal of human genetics.

Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination

J. Rosenfeld, P. Stankiewicz, Ankita Patel, 2014, BMC Biology.

NAHR-mediated copy-number variants in a clinical population: Mechanistic insights into both genomic disorders and Mendelizing traits

J. Rosenfeld, P. Stankiewicz, A. Breman, 2013, Genome research.

Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching.

P. Stankiewicz, Ankita Patel, C. Shaw, 2009, Human molecular genetics.

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype.

Lorraine Potocki, Pawel Stankiewicz, Weimin Bi, 2007, American journal of human genetics.

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

Chad A Shaw, Ankita Patel, Z. Ou, 2005, Genetics in Medicine.

Identification of novel candidate disease genes from de novo exonic copy number variants

J. Rosenfeld, P. Stankiewicz, A. Breman, 2017, Genome Medicine.

Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability

P. Stankiewicz, C. Shaw, E. Obersztyn, 2013, Journal of Applied Genetics.

Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today’s genomic array era?

P. Stankiewicz, Ankita Patel, C. Shaw, 2012, Genetics in Medicine.

Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

P. Stankiewicz, Ankita Patel, C. Shaw, 2007, American journal of medical genetics. Part A.

Centers for Mendelian Genomics: A decade of facilitating gene discovery

Jeffrey M. Weiss, Ryan L. Collins, Jack M. Fu, 2021, medRxiv.

Sequencing individual genomes with recurrent deletions reveals allelic architecture and disease loci for autosomal recessive traits

Nurit Assia Batzir, C. Shaw, J. Lupski, 2021, medRxiv.

Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies

J. Rosenfeld, A. Breman, C. Shaw, 2018, Genetics in Medicine.

Disruption of the circadian clock within the cardiomyocyte influences myocardial contractile function, metabolism, and gene expression.

C. Shaw, P. Hardin, M. Chandler, 2008, American journal of physiology. Heart and circulatory physiology.

The oncogenic STP axis promotes triple-negative breast cancer via degradation of the REST tumor suppressor.

C. Shaw, D. Edwards, S. Hilsenbeck, 2014, Cell reports.

Genome-wide analyses of LINE–LINE-mediated nonallelic homologous recombination

Anna Gambin, Tomasz Gambin, Chad A. Shaw, 2015, Nucleic acids research.

Activin signaling: effects on body composition and mitochondrial energy metabolism.

C. Shaw, B. Graham, Joseph J Shen, 2009, Endocrinology.

Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation

Z. Ou, M. L. Cooper, E. Roeder, 2007, American journal of medical genetics. Part A.

Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome

Rodney C. Samaco, C. Shaw, H. Zoghbi, 2011, Nature Genetics.

Neuroendocrine phenotypes in a boy with 5q14 deletion syndrome implicate the regulatory roles of myocyte-specific enhancer factor 2C in the postnatal hypothalamus.

C. Shaw, Janghoo Lim, Min-Seon Kim, 2013, European journal of medical genetics.

Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome

P. Stankiewicz, C. Shaw, J. Lupski, 2019, Genome Medicine.

Low‐level mosaicism of trisomy 14: Phenotypic and molecular characterization

L. Shao, Ankita Patel, C. Shaw, 2008, American journal of medical genetics. Part A.

Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders

Anna Gambin, Chad A Shaw, Tomasz Gambin, 2012, European Journal of Human Genetics.

Corrigendum: Mutations in the transcriptional repressor REST predispose to Wilms tumor

C. Shaw, S. Seal, N. Rahman, 2016, Nature Genetics.

Mutations in the transcriptional repressor REST predispose to Wilms tumor

C. Shaw, S. Seal, N. Rahman, 2015, Nature Genetics.

EMT cells increase breast cancer metastasis via paracrine GLI activation in neighbouring tumour cells

L. D. White, C. Shaw, H. Ford, 2017, Nature Communications.

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

L. D. White, Ankita Patel, C. Shaw, 2009, Prenatal diagnosis.

Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

L. D. White, Z. Ou, A. C. Chinault, 2008, Genetics in Medicine.

Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNA.

Z. Ou, A. C. Chinault, Ankita Patel, 2009, The Journal of molecular diagnostics : JMD.

Genome‐wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women

Ripudaman Singh, Niels Uldbjerg, Rui Chen, 2016, Prenatal diagnosis.

Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10 362 consecutive cases

P. Stankiewicz, Ankita Patel, C. Shaw, 2014, European Journal of Human Genetics.

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature

A. Breman, Ankita Patel, C. Shaw, 2012, Prenatal diagnosis.

Exercise and Genetic Rescue of SCA1 via the Transcriptional Repressor Capicua

C. Shaw, H. Zoghbi, H. Orr, 2011, Science.

Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis

A. Breman, C. Shaw, D. Edwards, 2019, American journal of human genetics.

Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results

Z. Ou, P. Stankiewicz, M. L. Cooper, 2010, American journal of medical genetics. Part A.

Transcriptional Profiling of Mammary Gland Side Population Cells

C. Shaw, S. Hilsenbeck, J. Rosen, 2006, Stem cells.

Partial Loss of Ataxin-1 Function Contributes to Transcriptional Dysregulation in Spinocerebellar Ataxia Type 1 Pathogenesis

C. Shaw, H. Zoghbi, H. Orr, 2010, PLoS genetics.

Evidence for Diversity in Transcriptional Profiles of Single Hematopoietic Stem Cells

C. Shaw, Nathan C Boles, C. Ramos, 2006, PLoS genetics.

De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.

Stephan J Sanders, R. Redon, J. Rosenfeld, 2017, American journal of human genetics.

De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.

Stephan J Sanders, R. Redon, J. Rosenfeld, 2017, American journal of human genetics.

Circadian rhythms in myocardial metabolism and contractile function: influence of workload and oleate.

C. Shaw, M. Chandler, J. Dyck, 2007, American journal of physiology. Heart and circulatory physiology.

NetComm: a network analysis tool based on communicability

Edward S. Chen, Ian M. Campbell, Regis A. James, 2014, Bioinform..

Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndrome

C. Shaw, T. Hara, Y. Oda, 2014, BMC Medical Genomics.

Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders

L. D. White, P. Stankiewicz, C. Shaw, 2004, Journal of Medical Genetics.

Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management

Fan Xia, Pengfei Liu, Xiaoyan Ge, 2017, JAMA pediatrics.

Transcriptional Transitions during Dictyostelium Spore Germination

C. Shaw, G. Shaulsky, A. Kuspa, 2004, Eukaryotic Cell.

An orderly retreat: Dedifferentiation is a regulated process.

C. Shaw, G. Shaulsky, M. Katoh, 2004, Proceedings of the National Academy of Sciences of the United States of America.

A cell-adhesion pathway regulates intercellular communication during Dictyostelium development.

C. Shaw, G. Shaulsky, Jessica Svetz, 2003, Developmental biology.

TagA, a putative serine protease/ABC transporter of Dictyostelium that is required for cell fate determination at the onset of development

C. Shaw, G. Shaulsky, A. Kuspa, 2003, Development.

Detection of ≥1 Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays

P. Stankiewicz, A. Breman, C. Shaw, 2012, Prenatal diagnosis.

Fusion of Large-Scale Genomic Knowledge and Frequency Data Computationally Prioritizes Variants in Epilepsy

Ankita Patel, Chad A. Shaw, Carlos A. Bacino, 2013, PLoS genetics.

The protease‐activated receptor 4 Ala120Thr variant alters platelet responsiveness to low‐dose thrombin and protease‐activated receptor 4 desensitization, and is blocked by non‐competitive P2Y12 inhibition

C. Shaw, E. Chen, L. Edelstein, 2018, Journal of thrombosis and haemostasis : JTH.

Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses

C. Shaw, J. Lupski, R. Gibbs, 2016, Human mutation.

Integrative genomic analysis of the human immune response to influenza vaccination

Molly S Bray, Chad A Shaw, Luis M Franco, 2013, eLife.

Reanalysis of Clinical Exome Sequencing Data.

J. Rosenfeld, E. Zackai, C. Shaw, 2019, The New England journal of medicine.

Incidental copy-number variants identified by routine genome testing in a clinical population

P. Stankiewicz, Ankita Patel, C. Shaw, 2012, Genetics in Medicine.

De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations

C. Shaw, S. Cheung, T. Bohan, 2015, Orphanet Journal of Rare Diseases.

RAS–MAPK–MSK1 pathway modulates ataxin 1 protein levels and toxicity in SCA1

Hyojin Kang, Ismael Al-Ramahi, Juan Botas, 2013, Nature.

Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems.

P. Stankiewicz, Z. Xia, P. Szafranski, 2010, American journal of human genetics.

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA

Yanming Feng, Fan Xia, Shashikant Kulkarni, 2019, Nature Medicine.

Screening and familial characterization of copy‐number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure

P. Stankiewicz, C. Shaw, A. Zinn, 2013, American journal of medical genetics. Part A.

Confounding by Repetitive Elements and CpG Islands Does Not Explain the Association between Hypomethylation and Genomic Instability

L. D. White, A. C. Chinault, Ankita Patel, 2013, PLoS genetics.

Design tools for MPRA experiments

Edward S. Chen, Chad A. Shaw, Andrew R. Ghazi, 2018, Bioinform..

The Circadian Clock within the Cardiomyocyte Is Essential for Responsiveness of the Heart to Fatty Acids*

Molly S Bray, Chad A Shaw, C. Shaw, 2006, Journal of Biological Chemistry.

Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects

C. Shaw, J. Belmont, S. Lalani, 2016, Philosophical Transactions of the Royal Society B: Biological Sciences.

TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.

Gao T. Wang, Mahshid S. Azamian, M. Hurles, 2013, American journal of human genetics.

Yasunari Sakai Autism Disorders Protein Interactome Reveals Converging Molecular Pathways Among

Diana V. Dugas, B. Dawson, C. Shaw, 2011 .

Integrative genomic analysis of the human immune response to influenza vaccination

C. Shaw, J. Belmont, R. Couch, 2013, eLife.

Abstract 3091: A sumoylation-dependent transcriptional subprogram is required for Myc-driven tumorigenesis

M. Rao, C. Shaw, S. Elledge, 2012 .

A joint modeling approach for longitudinal microbiome data improves ability to detect microbiome associations with disease

Pamela N Luna, Jonathan M Mansbach, Chad A Shaw, 2020, PLoS Comput. Biol..

CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome.

C. Shaw, P. Jin, D. Nelson, 2014, Human molecular genetics.

De Novo Truncating Mutation of TRIM8 Causes Early‐Onset Epileptic Encephalopathy

C. Shaw, T. Hara, N. Matsumoto, 2016, Annals of human genetics.

A paradox of transcriptional and functional innate interferon responses of human intestinal enteroids to enteric virus infection

Chad A Shaw, Kapil Saxena, Lukas M Simon, 2017, Proceedings of the National Academy of Sciences.

Circulating and disseminated tumor cells from breast cancer patient-derived xenograft-bearing mice as a novel model to study metastasis

C. Shaw, S. Hilsenbeck, R. Schiff, 2015, Breast Cancer Research.

Gene Sequence Variability of the Three Surface Proteins of Human Respiratory Syncytial Virus (HRSV) in Texas

B. Dawson, C. Shaw, P. Piedra, 2014, PloS one.

Theoretical Consideration of Amplification Strategies

Chad A. Shaw, C. Shaw, 2002, Neurochemical Research.

Ataxin1L Is a Regulator of HSC Function Highlighting the Utility of Cross-Tissue Comparisons for Gene Discovery

C. Shaw, H. Zoghbi, Juliette J. Kahle, 2013, PLoS genetics.

Host Transcriptional Response to Influenza and Other Acute Respiratory Viral Infections – A Prospective Cohort Study

C. Shaw, J. Belmont, R. Couch, 2015, PLoS pathogens.

MicroRNA Expression Differences in Human Hematopoietic Cell Lineages Enable Regulated Transgene Expression

C. Shaw, L. Edelstein, P. Bray, 2014, PloS one.

Activation of Multiple Proto-oncogenic Tyrosine Kinases in Breast Cancer via Loss of the PTPN12 Phosphatase

M. Rao, C. Shaw, R. Gibbs, 2011, Cell.

OntologyTraverser: an R package for GO analysis

Andrew Young, J. Cho, Chad A. Shaw, 2005, Bioinform..

The insulin-like growth factor pathway is altered in spinocerebellar ataxia type 1 and type 7

C. Shaw, C. Thaller, H. Zoghbi, 2008, Proceedings of the National Academy of Sciences.

Anti-miR-148a regulates platelet FcγRIIA signaling and decreases thrombosis in vivo in mice.

C. Shaw, L. Edelstein, P. Bray, 2015, Blood.

Identifying diagnostically‐relevant resting state brain functional connectivity in the ventral posterior complex via genetic data mining in autism spectrum disorder

Philip R Baldwin, C. Shaw, P. Baldwin, 2016, Autism research : official journal of the International Society for Autism Research.

Respiratory syncytial virus and rhinovirus severe bronchiolitis are associated with distinct nasopharyngeal microbiota.

C. Shaw, N. Ajami, J. Petrosino, 2016, The Journal of allergy and clinical immunology.

Increased Moraxella and Streptococcus species abundance after severe bronchiolitis is associated with recurrent wheezing

C. Shaw, J. Petrosino, C. Camargo, 2019, Journal of Allergy and Clinical Immunology.

Targeting the Mevalonate Pathway to Overcome Acquired Anti-HER2 Treatment Resistance in Breast Cancer

Laura M. Heiser, Nicholas J. Wang, C. Shaw, 2019, Molecular Cancer Research.

An efficient algorithm for accurate computation of the Dirichlet-multinomial log-likelihood function

Peng Yu, Chad A. Shaw, C. Shaw, 2014, Bioinform..

Application of dual-genome oligonucleotidearray-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes

A. C. Chinault, C. Shaw, L. Wong, 2009, Genetics in Medicine.

RISK ASSESSMENT OF T1 TRANSITIONAL CELL CARCINOMA OF THE BLADDER USING P53 IMMUNOHISTOCHEMISTRY AND PATHOLOGIC SUBSTAGING

C. Shaw, T. Wheeler, A. Weizer, 1999 .

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

P. Stankiewicz, C. Shaw, Yaping Yang, 2019, Genome Medicine.

FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia

C. Shaw, P. Donahoe, I. Campbell, 2021, Journal of Pediatric Genetics.

The intrinsic circadian clock within the cardiomyocyte.

C. Shaw, P. Hardin, E. Abel, 2005, American journal of physiology. Heart and circulatory physiology.

The human platelet: strong transcriptome correlations among individuals associate weakly with the platelet proteome

C. Shaw, I. Rigoutsos, P. Fortina, 2014, Biology Direct.

Short running title: Platelet microRNA in platelet reactivity

C. Shaw, S. Leal, G. McKnight, 2011 .

Reliable detection of subchromosomal deletions and duplications using cell‐based noninvasive prenatal testing

A. Breman, C. Shaw, A. Beaudet, 2018, Prenatal diagnosis.

Erratum: De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder (American Journal of Human Genetics (2017) 100(2) (352–363) (S0002929717300034) (10.1016/j.ajhg.2017.01.003))

Stephan J Sanders, R. Redon, J. Rosenfeld, 2017 .

Genome-wide association study of platelet aggregation in African Americans

C. Shaw, S. Leal, L. Becker, 2015, BMC Genetics.

CELF1 is a central node in post-transcriptional regulatory programmes underlying EMT

C. Shaw, S. Hilsenbeck, J. Neilson, 2016, Nature Communications.

Identification of novel candidate disease genes from de novo exonic copy number variants

J. Rosenfeld, P. Stankiewicz, A. Breman, 2017, Genome Medicine.

Rapid attenuation of circadian clock gene oscillations in the rat heart following ischemia-reperfusion.

C. Shaw, P. Hardin, M. Bray, 2007, Journal of molecular and cellular cardiology.

Circadian Clock Gene Expression in the Ovary: Effects of Luteinizing Hormone

C. Shaw, E. Abel, M. Bray, 2007 .

Selection for or against Escape from Nonsense Mediated Decay is a Novel Signature for the Detection of Cancer Genes

C. Shaw, Runjun D. Kumar, Briana A. Burns, 2021, bioRxiv.

Correction: Evidence for Diversity in Transcriptional Profiles of Single Hematopoietic Stem Cells

C. Shaw, C. Ramos, M. Goodell, 2006, PLoS Genetics.

An essential role for Gαi2 in Smoothened-stimulated epithelial cell proliferation in the mammary gland

C. Shaw, S. Hilsenbeck, L. Birnbaumer, 2015, Science Signaling.

A novel developmental mechanism in Dictyostelium revealed in a screen for communication mutants.

C. Shaw, G. Shaulsky, N. Van Driessche, 2003, Developmental biology.

Evidence for Feasibility of Fetal Trophoblastic Cell-Based Noninvasive Prenatal Testing

Jeffrey L. Werbin, A. Breman, C. Shaw, 2017 .

The association between anterior nares and nasopharyngeal microbiota in infants hospitalized for bronchiolitis

C. Shaw, N. Ajami, J. Petrosino, 2018, Microbiome.

Novel MicroRNA Candidates and miRNA-mRNA Pairs in Embryonic Stem (ES) Cells

David L. Steffen, Richard A. Gibbs, Xiaolian Gao, 2008, PloS one.

Global Gene Expression Profiling in Infants With Acute Respiratory Syncytial Virus Broncholitis Demonstrates Systemic Activation of Interferon Signaling Networks

C. Shaw, J. Belmont, R. Couch, 2013, The Pediatric infectious disease journal.

"interactive" version of data associated with the eLife paper "Integrative genomic analysis of the human immune response to influenza vaccination"

C. Shaw, J. Belmont, R. Couch, 2013 .

Clinical genome sequencing: three years experience at a tertiary childrens hospital

C. Shaw, Runjun D. Kumar, J. Scull, 2023, medRxiv.

The impact of the Turkish (TK) population variome on the genomic architecture of rare disease traits

C. Shaw, J. Lupski, R. Gibbs, 2023, bioRxiv.

Sox7‐positive endothelial progenitors establish coronary arteries and govern ventricular compaction

C. Shaw, K. Red-Horse, P. Young, 2023, EMBO reports.

A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

Yanming Feng, Fan Xia, Tomasz Gambin, 2019, Genome Medicine.

Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

P. Stankiewicz, Ankita Patel, C. Shaw, 2019, Genome Medicine.

Retroviral vector insertion sites associated with dominant hematopoietic clones mark “stemness” pathways

C. Shaw, F. Staal, M. Goodell, 2007 .

Retroviral vector insertion sites associated with dominant hematopoietic clones mark “stemness” pathways

C. Shaw, F. Staal, M. Goodell, 2007 .

Exact sampling formulas for multi-type Galton-Watson processes

Peter Olofsson, Chad A. Shaw, C. Shaw, 2002 .

Exact sampling formulas for multi-type Galton-Watson processes

C. Shaw, P. Olofsson, 2002, Journal of mathematical biology.

OntologyTraverser: an R package for GO analysis

C. Shaw, J. Cho, N. Whitehouse, 2005, Bioinform..

Retroviral vector insertion sites associated with dominant hematopoietic clones mark “stemness” pathways

C. Shaw, F. Staal, M. Goodell, 2007 .

Gene expression in Barrett's esophagus: Laser capture versus whole tissue

Toni-Ann Mistretta, Milton J. Finegold, Hashem B. El-Serag, 2009, Scandinavian journal of gastroenterology.

Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses

C. Shaw, J. Lupski, R. Gibbs, 2016, Human mutation.

Hematopoietic stem and progenitor cells confer cross-protective trained immunity in mouse models

C. Shaw, R. Jaksik, A. Catic, 2023, iScience.

Detection of clinically relevant exonic copy‐number changes by array CGH

P. Stankiewicz, Z. Xia, Ankita Patel, 2010, Human mutation.

Genomic hypomethylation in the human germline associates with structural mutability in the human genome

L. D. White, A. C. Chinault, Ankita Patel, 2012 .

Platelet microRNA-mRNA coexpression profiles correlate with platelet reactivity.

C. Shaw, S. Leal, G. McKnight, 2010, Blood.

HER2 Reactivation through Acquisition of the HER2 L755S Mutation as a Mechanism of Acquired Resistance to HER2-targeted Therapy in HER2+ Breast Cancer

Laura M. Heiser, Nicholas J. Wang, C. Shaw, 2017, Clinical Cancer Research.

Human Genome-Wide Association and Mouse Knockout Approaches Identify Platelet Supervillin as an Inhibitor of Thrombus Formation Under Shear Stress

C. Shaw, S. Leal, L. Edelstein, 2012, Circulation.

The association between anterior nares and nasopharyngeal microbiota in infants hospitalized for bronchiolitis

C. Shaw, N. Ajami, J. Petrosino, 2018, Microbiome.

Common variants in the human platelet PAR4 thrombin receptor alter platelet function and differ by race.

C. Shaw, L. Simon, S. Coughlin, 2014, Blood.